Droplet-based microfluidics

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Droplet-based microfluidics manipulate discrete volumes of fluids in immiscible phases with low Reynolds number and laminar flow regimes.[1][2] Interest in droplet-based microfluidics systems has been growing substantially in past decades.[3][4] Microdroplets offer the feasibility of handling miniature volumes (μl to fl) of fluids conveniently, provide better mixing, encapsulation, sorting, sensing and are suitable for high throughput experiments.[5][1] Two immiscible phases used for the droplet based systems are referred to as the continuous phase (medium in which droplets flow) and dispersed phase (the droplet phase).[6]

Droplet formation methods[edit]

In order for droplet formation to occur, two immiscible phases, referred to as the continuous phase (medium in which droplets are generated) and dispersed phase (the droplet phase), must be used.[6] The size of the generated droplets is mainly controlled by the flow rate ratio of the continuous phase and dispersed phase, interfacial tension between two phases, and the geometry of the channels used for droplet generation.[7] Droplets can be formed both passively and actively.[8] Active droplet formation (electric, magnetic, centrifugal) often uses similar devices to passive formation but requires an external energy input for droplet manipulation.[8] Passive droplet formation tends to be more common than active as it produces similar results with simpler device designs. Generally, three types of microfluidic geometries are utilized for passive droplet generation: (i) Cross-Flowing, (ii) Flow Focusing, and (iii) Co-Flowing.[8] Droplet based microfluidics often operate under low Reynold’s numbers to ensure laminar flow within the system.[2] Droplet size is often quantified with coefficient of variation (CV) as a description of the standard deviation from the mean droplet size. Each of the listed methods provide a way to generate microfluidic droplets in a controllable and tunable manner with proper variable manipulation.

Cross-flowing droplet formation[edit]

Cross-flowing is a passive formation method that involves the continuous and aqueous phases running at an angle to each other.[9] Most commonly, the channels are perpendicular in a T-shaped junction with the dispersed phase intersecting the continuous phase; other configurations such as a Y-junction are also possible.[8][10][11] The dispersed phase extends into the continuous and is stretched until shear forces break off a droplet.[12][13] In a T-junction, droplet size and formation rate are determined by the flow rate ratio and capillary number.[14] The capillary number relates the viscosity of the continuous phase, the superficial velocity of the continuous phase, and the interfacial tension.[7] Typically, the dispersed phase flow rate is slower than the continuous flow rate. T-junction formation can be further applied by adding additional channels, creating two T-junctions at one location. By adding channels, different dispersed phases can be added at the same point to create alternating droplets of different compositions.[15] Droplet size, usually above 10 μm, is limited by the channel dimensions and often produces droplets with a CV of less than 2% with a rate of up to 7 kHz[4].

Flow focusing droplet formation[edit]

Flow focusing is a usually passive formation method that involves the dispersed phase flowing to meet the continuous phase typically at an angle (nonparallel streams) then undergoing a constraint that creates a droplet.[16] This constraint is generally a narrowing in the channel to create the droplet though symmetric shearing, followed by a channel of equal or greater width.[17] As with cross-flowing, the continuous phase flow rate is typically higher than the dispersed phase flow rate. Decreasing the flow of the continuous phase can increase the size of the droplets.[5] Flow focusing can also be an active method with the constraint point being adjustable using pneumatic side chambers controlled by compressed air.[18] The movable chambers act to pinch the flow, deforming the stream and creating a droplet with a changeable driving frequency. Droplet size is usually around several hundred nanometers with a CV of less than 3% and a rate of up to several hundred Hz to tens of kHz.[8]

Co-flowing droplet formation[edit]

Co-flowing is a passive droplet formation method where the dispersed phase channel is enclosed inside a continuous phase channel.[19] At the end of the dispersed phase channel, the fluid is stretched until it breaks from shear forces and forms droplets either by dripping or jetting.[20] Dripping occurs when capillary forces dominate the system and droplets are created at the channel endpoint.[20] Jetting occurs, by widening or stretching, when the continuous phase is moving slower, creating a stream from the dispersed phase channel opening. Under the widening regime, the dispersed phase is moving faster than the continuous phase causing a deceleration of the dispersed phase, widening the droplet and increasing the diameter.[21] Under the stretching regime, viscous drag dominates causing the stream to narrow creating a smaller droplet.[21] The effect of the continuous phase flow rate on the droplet size depends on whether the system is in a stretching or widening regime thus different equations must be used to predict droplet size.[20] Droplet size is usually around several hundred nanometers with a CV of less than 5% and a rate of up to tens of kHz.[8]

Droplet manipulation[edit]

The benefits of microfluidics can be scaled up to higher throughput using larger channels to allow more droplets to pass or by increasing droplet size.[22] Droplet size can be tuned by adjusting the rate of flow of the continuous and disperse phases, but droplet size is limited by the need to maintain the concentration, inter-analyte distances, and stability of microdroplets.[23] Thus, increased channel size becomes attractive due to the ability to create and transport a large number of droplets,[22] though dispersion[24] and stability of droplets[25] become a concern. Finally, thorough mixing of droplets to expose the greatest possible number of reagents is necessary to ensure the maximum amount of starting materials react.[22] This can be accomplished by using a windy channel to facilitate unsteady laminar flow within the droplets.[1]

Reagent addition[edit]

Microscale reactions performed in droplet-based applications conserve reagents and reduce reaction time all at kilohertz rates.[5][26] Reagent addition to droplet microreactors has been a focus of research due to the difficulty of achieving reproducible additions at kilohertz rates without droplet-to-droplet contamination.[27]

Reagent coflow prior to droplet formation[edit]

Reagents can be added at the time of droplet formation through a “co-flow” geometry.[1] Reagent streams are pumped in separate channels and join at the interface with a channel containing the continuous phase, which shears and creates droplets containing both reagents. By changing the flow rates in reagent channels, reagent ratios within a droplet can be controlled.[28][29]

Droplet fusion[edit]

The fusion of droplets with different contents can also be exploited for reagent addition. Electro-coalescence merges pairs of droplets by applying an electric field to temporarily destabilize the droplet-droplet interface to achieve reproducible droplet fusion in surfactant-stabilized emulsions.[30][31] Electro-coalescence requires droplets (which are normally separated by the continuous phase) to come into contact. By manipulating droplet size in separate streams, differential flow of droplet sizes can bring droplets into contact before merging.[32]

Another method for facilitating droplet fusion is acoustic tweezing.[33] While droplets are flowing in microfluidic channels, they can be immobilised using an acoustic tweezer based on surface acoustic waves.[33] Once a droplet is held with the acoustic tweezer, consecutive droplets collide into it and fusion takes place.

Injection of reagents into existing droplets[edit]

Reagent co-flow and droplet fusion methods are tied to droplet formation events which lack downstream flexibility. To decouple reagent addition from droplet creation, a setup where reagent stream flows through a channel perpendicular to the droplet stream is utilized.[34][35] An injection droplet is then merged with the plug as it passes the channel. Reagent volume is controlled by the flow rate of the perpendicular reagent channel.

An early challenge for such systems is that reagent droplet merging was not reproducible for stable emulsions.[36] By adapting the use of an actuated electric field into this geometry, Abate et al. achieved sub-picoliter control of reagent injection.[36] This approach, termed picoinjection, controls injection volume through reagent stream pressure and droplet velocity. Further work on this method has aimed to reduce pressure fluctuations that impede reproducible injections.[37]

Droplet-to-droplet contamination is a challenge of many injection methods.[38] To combat this, Doonan et al. developed a multifunctional K-channel, which flows reagent streams opposite the path of the droplet stream.[39] Utilizing an interface between the two channels, injection is achieved similarly to picoinjection, but any bilateral contamination washed away through continuous reagent flow. Contamination is avoided at the expense of potentially wasting precious reagent.

Droplet incubation[edit]

In order to make droplet-based microfluidics a viable technique for carrying out chemical reactions or working with living cells on the microscale, it is necessary to implement methods allowing for droplet incubation.[40] Chemical reactions often need time to occur, and living cells similarly require time to grow, multiply, and carry out metabolic processes. Droplet incubation can be accomplished either within the device itself (on-chip) or externally (off-chip), depending on the parameters of the system.[26] Off-chip incubation is useful for incubation times of a day or more or for incubation of millions of droplets at a time.[26] On-chip incubation allows for integration of droplet manipulation and detection steps in a single device.[26]

Off-chip incubation[edit]

Droplets containing cells can be stored off-chip in PTFE tubing for up to several days while maintaining cell viability and allowing for reinjection onto another device for analysis.[41] Evaporation of aqueous and oil-based fluids has been reported with droplet storage in PTFE tubing, so for storage longer than several days, glass capillaries are also used.[42] Finally, following formation in a microfluidic device, droplets may also be guided through a system of capillaries and tubing leading to a syringe. Droplets can be incubated in the syringe and then directly injected onto another chip for further manipulation or detection and analysis.[43]

On-chip incubation[edit]

Delay lines are used to incubate droplets on-chip. After formation, droplets can be introduced into a serpentine channel with length of up to a meter or more.[44][24] Increasing the depth and width of the delay line channel (as compared to channels used to form and transport droplets) enables longer incubation times while minimizing channel back pressure.[24] Because of the larger channel size, droplets fill up the delay line channel[45] and incubate in the time it takes the droplets to traverse this channel.

Delay lines were originally designed for incubating droplets containing chemical reaction mixtures and were capable of achieving delay times of up to one hour.[24][46][47] These devices make use of delay line channels tens of centimeters in length. Increasing the total length of the delay line channels to one or more meters made incubation times of 12 or more hours possible.[44][48] Delay lines have been shown to maintain droplet stability for up to 3 days,[48] and cell viability has been demonstrated using on-chip delay lines for up to 12 hours.[44] Prior to the development of delay lines, on-chip incubation was performed by directing droplets into large reservoirs (several millimeters in both length and width), which offers high storage capacity and lower complexity of device construction and operation if precise time control of droplets is not required.[49]

If it is important to have a uniform distribution of incubation times for the droplets, the delay line channel may contain regularly-spaced constrictions.[24] Droplets flowing through a channel of uniform diameter travel at different speeds based on their radial position; droplets closer to the center of the channel move faster than those near the edges.[24] By narrowing the channel width to a fraction of its original size, droplets with higher velocities are forced to equilibrate with slower-moving droplets because the constriction allows fewer droplets to pass through at a time.[24] Another manipulation to the geometry of the delay line channel involves introducing turns to the droplets' trajectory. This increases the extent to which any reagents contained within the droplets are mixed via chaotic advection.[1] For systems requiring the incubation of 100 to 1000 droplets, traps can be fabricated in the delay line channel that store droplets separately from one another.[50][51] This provides for finer control and monitoring of individual droplets.

Magnetic droplets[edit]

The micro-magnetofluidic method is the control of magnetic fluids by an applied magnetic field on a microfluidic platform,[52] offering wireless and programmable control of the magnetic droplets.[53] Hence, the magnetic force can also be used to perform various logical operations, in addition to the hydrodynamic force and the surface tension force. The magnetic field strength, type of the magnetic field (gradient, uniform or rotating), magnetic susceptibility, interfacial tension, flow rates, and flow rate ratios determine the control of the droplets on a micro-magnetofluidic platform.[54]

Droplet sorting[edit]

Droplet sorting in microfluidics is an important technique, allowing for discrimination based on factors ranging from droplet size to chemicals labeled with fluorescent tags within the droplet, stemming off of the work done to sort cells in Flow Cytometry.[55][56][57] Within the realm of droplet sorting there are two main types, bulk sorting, which uses either active or passive methods, and precise sorting, which relies mainly on active methods. Bulk sorting is applied to samples with a large number of droplets (> 2000 s−1) that can be sorted based off intrinsic properties of the droplets (such as viscosity, density, etc.) without checking each droplet.[58] Precise sorting, on the other hand, aims to separate droplets that meet certain criteria that is checked on each droplet.[58]

Passive sorting is done through control of the microfluidic channel design, allowing for discrimination based on droplet size. Size sorting relies on the bifurcating junctions in the channel to divert the flow, which causes droplets to sort based on how they interact with the cross section of that flow, the shear rate, which relates directly to their size.[56][59][60] Other passive methods include inertia and microfiltration, each having to do with the physical properties, such as inertia, and density, of the droplet.[58][61] Active sorting uses additional devices attached to the microfluidic device to alter the path of a droplet during flow by controlling some aspect, including thermal, magnetic, pneumatic, acoustic, hydrodynamic and electric control.[62][63][64][65] These controls are utilized to sort the droplets in response to some signal detection from the droplets such as fluorescence intensity.

Precise sorting methods utilize these active sorting methods by first making a decision (e.g., fluorescence signal) about the droplets then altering their flow with one of the aforementioned methods. A technique called Fluorescent Activated Droplet Sorting (FADS) has been developed which utilizes electric field-induced active sorting with fluorescent detection to sort up to 2000 droplets per second.[55] The method relies on, but is not limited to, enzymatic activity of compartmentalized target cells to activate a fluorogenic substrate within the droplet. When a fluorescing droplet is detected, two electrodes are switched on applying a field to the droplet, which shifts its course into the selection channel, while non-fluorescing droplets flow through the main channel to waste.[55][66] Other methods utilize different selection criteria, such as absorbance of droplet, number of encapsulated particles, or image recognition of cell shapes.[57][67][68] Sorting can be done to improve encapsulation purity, an important factor for collecting sample for further experiments.[66]

Key applications[edit]

Cell culture[edit]

One of the key advantages of droplet-based microfluidics is the ability to use droplets as incubators for single cells.[41][69]

Devices capable of generating thousands of droplets per second opens new ways characterize cell population, not only based on a specific marker measured at a specific time point but also based on cells' kinetic behavior such as protein secretion, enzyme activity or proliferation. Recently, a method was found to generate a stationary array of microscopic droplets for single-cell incubation that does not require the use of a surfactant.[citation needed]

Biological macromolecule characterization[edit]

Protein crystallization[edit]

Droplet-based devices have also been used to investigate the conditions necessary for protein crystallization.[70][71]

Droplet-based PCR[edit]

Polymerase chain reaction (PCR) has been a vital tool in genomics and biological endeavors since its inception as it has greatly sped up production and analysis of DNA samples for a wide range of applications.[72] The technological advancement of microdroplet scale PCR has enabled the construction of single-molecule PCR-on-a-chip device.[73] Early single molecule DNA replication, including what occurs in microdroplet or emulsion PCR, was more difficult than larger scale PCR so much higher concentrations of components were usually used.[74] However, fully optimized conditions have minimized this overload by insuring single molecules have an appropriate concentration of replication components distributed throughout the reaction cell.[74] Non-droplet based microfluidic PCR also faces challenges with reagent absorption into the device channels, but droplet-based systems lessen this problem with decreased channel contact.[75]

Using water-in-oil systems, droplet PCR operates by assembling ingredients, forming droplets, combining droplets, thermocycling, and then processing results much like normal PCR. This technique is capable of running in excess of 2 million PCR reactions in addition to a 100,000-fold increase in the detection of wild-type alleles over mutant alleles.[76] Droplet-based PCR greatly increases the multiplexing capabilities of normal PCR – allowing for fast production of mutation libraries. Without proofreading, DNA replication is inherently somewhat error-prone, but by introducing error-prone polymerases, droplet-based PCR utilizes higher than normal mutation output to build a mutation library more quickly and efficiently than normal.[77] This makes droplet-based PCR more attractive than slower, traditional PCR.[78] In a similar application, highly multiplexed, microdroplet PCR has been developed that allows for the screening of large numbers of target sequences enabling applications such as bacterial identification.[79] On-chip PCR allows for an excess of 15 x 15 multiplexing, which means that multiple target DNA sequences could be run on the same device at the same time.[80] This multiplexing was made possible with immobilized DNA primer fragments placed in the base of the individual wells of the chips.[81]

Combining droplet-based PCR with polydimethylsiloxane (PDMS) devices has allowed for novel enhancements of droplet PCR as well as remedying some preexisting problems with droplet PCR including high liquid loss due to evaporation.[82] Droplet-based PCR is highly sensitive to air bubbles as they create temperature differentials hindering DNA replication while also dislodging reagents from the replication chamber.[75] Now, droplet-based PCR has been carried out in PDMS devices to transfer reagents into droplets through a PDMS layer in a more controlled manner that better maintains replication progress and stability than traditional valves.[83] A recent droplet-PCR PDMS device allowed for higher accuracy and amplification of small copy numbers in comparison to traditional quantitative PCR experiments.[84] This higher accuracy was due to surfactant-doped PDMS as well as a sandwiched glass-PDMS-glass device design. These device properties have allowed for more streamlined priming of DNA and less water evaporation during PCR cycling.[84]

DNA sequencing[edit]

Multiple microfluidic systems, including droplet-based systems, have been used for DNA sequencing.

Chemical synthesis[edit]

Droplet-based microfluidics has become an important tool in chemical synthesis due to several attractive features. Microscale reactions allow for cost reduction through the usage of small reagent volumes, rapid reactions in the order of milliseconds, and efficient heat transfer that leads to environmental benefits when the amount of energy consumed per unit temperature rise can be extremely small.[85] The degree of control over local conditions within the devices often makes it possible to select one product over another with high precision.[85][86] With high product selectivity and small sizes of reagents and reaction environments come less stringent reaction clean-up and smaller footprint.[85] Microdispersed droplets created by droplet-based chemistry are capable of acting as environments in which chemical reactions occur, as reagent carriers in the process of generating complex nanostructures.[87] Droplets are also capable of being transformed into cell-like structures which can be used to mimic humans' biological components and processes.[87][86]

As a method of chemical synthesis, Droplets in microfluidics devices act as individual reaction chambers protected from contamination through device fouling by the continuous phase. Benefits of synthesis using this regime (compared to batch processes) include high throughput, continuous experiments, low waste, portability, and a high degree of synthetic control.[87] Some examples of possible syntheses are the creation of semiconductor microspheres[88] and nanoparticles.[89] Chemical detection is integrated into the device to ensure careful monitoring of reactions, NMR spectroscopy, microscopy, electrochemical detection, and chemiluminescent detection are used. Often, measurements are taken at different points along the microfluidic device to monitor the progress of the reaction.[87]

Increased rate of reactions using microdroplets is seen in the aldol reaction of silyl enol ethers and aldehydes. Using a droplet-based microfluidic device, reaction times were shortened to twenty minutes versus the twenty-four hours required for a batch process.[23] Other experimenters were able to show a high selectivity of cis-stilbene to the thermodynamically favored trans-stilbene compared to the batch reaction, showing the high degree of control afforded by microreactor droplets. This stereocontrol is beneficial to the pharmaceutical industry.[90] For instance, L-Methotrexate, a drug used in chemotherapy, is more readily absorbed than the D isomer.

Microparticle and Nanoparticle synthesis[edit]

Advanced particles and particle-based materials, such as polymer particles, microcapsules, nanocrystals, and photonic crystal clusters or beads can be synthesized with the assistance of droplet-based microfluidics.[91] Nanoparticles, such as colloidal CdS and CdS/CdSe core-shell nanoparticles, can also be synthesized through multiple steps on a millisecond time scale in a microfluidic droplet-based system.[92]

Nanoparticles, microparticles and colloidal clusters in microfluidic devices are useful for functions such as drug delivery.[93] The first particles incorporated in droplet-based systems were silica gels in the micrometer size range in order to test their applications in the manufacturing of displays and optical coatings.[94] Mixing solid particles with aqueous microdroplets requires changes to microfluidic channels such as additional reagent mixes and choice of specific materials such as silica or polymers that do not interfere with the channels and any bioactive substances the droplets contain.[95]

The synthesis of copolymers requires milling macroscopic molecules to microparticles with porous, irregular surfaces using organic solvents and emulsification techniques. These droplets preloaded with microparticles can also be quickly processed using UV irradiation.[96] Characterization of these microparticles and nanoparticles involves microimaging for analyzing the structure and the identification of the macroscopic material being milled. Techniques such as the controlled encapsulation of individual gas bubbles to create hollow nanoparticles for synthesizing microbubbles with specific contents are vital for drug delivery systems. Both silica and titanium based microparticles are used as durable shells after using gas to increase the flow velocity of the aqueous phase. A higher flow velocity allows greater control over the thickness of the aqueous shells.[95] The emerging versatility of nanoparticles can be seen in the delivery of particle-loaded microdroplets being utilized in depot injections for drug delivery rather than the typical approach of injecting drugs intravenously. This is possible due to the low thickness of the shells which typically are in the range of 1 to 50 µm.[95]

More recent advancements in microfluidic particles allowed the synthesis of nanometer sized particles from biologically derived polymers. Using specific flow-focusing multiphase designs that control flow rate and temperature, the size of nanoparticle formation can be controlled along with the concentration and configuration of the droplets.[96][97] Another technique for creating particle-loaded microdroplets is the use of lipid-hydrogel nanoparticles that can be manipulated into more narrowly-shaped droplets, which is useful when soft or brittle materials must be used.[98] These soft materials are especially important in the production of powders. Recent advancements on the nanoscale such as devices that fabricate both spherical and non-spherical droplets that are ultrafast and homogeneous mixed are being produced for large scale production of powdered particles in industrial applications.[99]

Gel Particle Synthesis[edit]

The synthesis of gel particles also known as hydrogels, microgels, and nanogels, has been an area of interest for researchers and industries alike for the last several decades.[100] A microfluidic based approach to synthesizing these hydrogel particles is a useful tool, due to high throughput, mono-dispersity of particles, and cost reduction through the use of small reagent volumes. One of the key challenges early on in the field of gels was forming monodisperse particles. Initially polymerization-based techniques were used to form bulk microparticles that were polydisperse in size.[101][102][103][104] These techniques generally were centered around using an aqueous solution that was mixed vigorously to create emulsions. Eventually a technique was developed to create monodisperse biodegradable microgels by making O/W emulsions in an in-line droplet generating channel geometry.[105] This junction geometry accompanied with a surfactant laden continuous phase was responsible for creating microgels made from poly-dex-HEMA. Other device geometries including T-junction style formation are also viable and have been used to make silica-based gels.[106]

Once these methods were established, efforts focused on applying functionality to these particles. Examples include bacteria encapsulated particles, drug or protein encapsulated particles, and magnetic gel particles.[107] To insert these functional components into the gel structure, can be as simple as integrating the component into the dispersed phase. In some cases, certain device geometries are preferred, for example a flow focusing junction was used to encapsulate bacteria in agarose microparticles.[108] Multiple emulsions are of interest for pharmaceutical and cosmetic applications[109] and are formed using two consecutive flow focusing junctions.[110] More complicated particles can also be synthesized such as Janus particles, which have surfaces with two or more distinct physical properties.[111]

Some examples of the increasing application of gel particles include drug delivery, biomedical applications, and tissue engineering, and many of these applications require monodisperse particles where a microfluidics-based approach is preferred.[112][113] Bulk emulsification methods are still relevant, though, since not all applications require uniform microparticles. The future of microfluidic synthesis of gels may lie in developing techniques to create bulk amounts of these uniform particles in order to make them more commercially/industrially available.[114]

Extraction and phase transfer using droplet microfluidics[edit]

Liquid-liquid extraction is a method used to separate an analyte from a complex mixture; with this method compounds separate based on their relative solubility in different immiscible liquid phases.[115][116] To overcome some of the disadvantages associated with common bench top methods such as the shake-flask method,[117] Microfluidic liquid-liquid extraction methods have been employed. Microfluidic droplet-based systems have demonstrated the capability to manipulate discrete volumes of fluids in immiscible phases with low Reynolds numbers.[118] and laminar flow regimes.[5] Microscale methods reduce time required, reduce sample and reagent volume, and allow for automation and integration.[119][120] In some studies, the performance of droplet-based microfluidic extraction compares closely with the shake-flask method.[121] A study which compared the shake-flask and microfluidic liquid-Liquid extrication methods for 26 compounds and found a close correlation between the values obtained (R2= 0.994).[122]

It has also been demonstrated that microfluidic liquid-liquid extraction devices can be integrated with other instruments for detection of the extracted analytes.[123][26] For example, microfluidic extraction could be used to extract an analyte initially in an aqueous phase such as cocaine in saliva then interfaced with on-chip IR spectroscopy for detection.[124] Microfluidic liquid-liquid extraction has shown to be advantageous in numerous applications such as pharmacokinetic drug studies where only small cell numbers are needed,[125][26] and in additional studies where smaller reagent volumes are required.[5]

Droplet detection[edit]

Separation methods[edit]

Droplet-based microfluidic systems can be coupled to separation methods for specific tasks. Common separation techniques coupled to droplet-based microfluidic systems include High Performance Liquid Chromatography (HPLC) and electrophoresis.

High performance liquid chromatography[edit]

Chemical separation on the microscale can be used in both biological and chemical analysis.[126][127][128] As an analytical tool, a chemical separation technique, like HPLC, can be coupled to a microfluidic device. Droplet-based microfluidic devices coupled to HPLC have high detection sensitivity, use low volumes of reagents, have short analysis times, and minimal cross-contamination of analytes, which make them efficient in many aspects.[129] One basic use of HPLC in droplet-based microfluidics is chemical separation by HPLC, which is then connected to a device that creates microliter sized droplets of each eluted compound. With this system, it is possible to create large droplet libraries of different compounds in a centralized location.[126] However, there are problems associated with microscale chromatography, like HPLC. These problems include dispersion of separated bands, diffusion, and “dead volume” in channels after separation.[127] One way to bypass these issues is the use of droplets to compartmentalize separation bands, which combats diffusion and the loss of separated analytes.[128] An advantage to using HPLC coupled to a microfluidic device is that more than one separation can be coupled. For example, 2D separation (two-dimensional chromatography) is possible with these devices (i.e. HPLC x LC, LC x LC, and HPLC x HPLC).[130]

Electrophoresis[edit]

Capillary electrophoresis (CE) and microcapillary gel electrophoresis (μCGE) are well-recognized microchip electrophoresis (MCE) methods that can provide numerous analytical advantages including high resolution, high sensitivity, and effective coupling to mass spectrometry (MS).[131][132][133] Microchip electrophoresis can be applied generally as a method for high-throughput screening processes that help discover and evaluate drugs.[132] Using MCE, specifically CE, microcapillary gel electrophoresis (μCGE) devices are created to perform high-number DNA sample processing, which makes it a good candidate for DNA analysis.[133][134] μCGE devices are also practical for separation purposes because they use online separation, characterization, encapsulation, and selection of differing analytes originating from a composite sample.[133] All of these advantages of MCE methods translate to microfluidic devices. The reason MCE methods are coupled to droplet-based microfluidic devices is because of the ability to analyze samples on the nanoliter scale.[135] Using MCE methods on a small scale reduces cost and reagent use.[133] Similarly to HPLC, fluorescence based detection techniques are used for capillary electrophoresis, which make these methods practical and can be applied to fields such as biotechnology, analytical chemistry, and drug development.[136] These MCE and other electrophoresis based methods began to develop once capillary electrophoresis gained popularity in the 1980s and gained even more attention in the early 1990s, as it was reviewed nearly 80 times by the year 1992.[137]

Mass spectrometry (MS) is a near universal detection technique that is recognized throughout the world as the gold standard for identification of manycompounds. MS is an analytical technique in which chemical species are ionized and sorted before detection, and the resulting mass spectrum is used to identify the ions' parent molecules. This makes MS, unlike other detection techniques (such as fluorescence), label-free; i.e. there is no need to bind additional ligands or groups to the molecule of interest in order to receive a signal and identify the compound.

There are many cases in which other spectroscopic methods, such as nuclear magnetic resonance (NMR), fluorescence, infrared, or Raman, are not viable as standalone methods due to the particular chemical composition of the droplets. Often, these droplets are sensitive to fluorescent labels,[55] or contain species that are otherwise indeterminately similar, where MS may be employed along with other methods to characterize a specific analyte of interest.[56] [57]However, MS has only recently (in the past decade) gained popularity as a detection method for droplet-based microfluidics (and microfluidics as a whole) due to challenges associated with coupling mass spectrometers with these miniaturized devices.[138][139][140] Difficulty of separation/purification make entirely microfluidic scale systems coupled to mass spectrometry ideal in the fields of proteomics,[141][55] [58] [59] enzyme kinetics,[60] drug discovery,[37] and newborn disease screening.[61] The two primary methods of ionization for mass analysis used in droplet-based microfluidics today are matrix-assisted laser desorption/ionization (MALDI)[62] [63] and electrospray ionization (ESI).[55] Additional methods for coupling, such as (but not limited to) surface acoustic wave nebulization (SAWN),[142] and paper-spray ionization onto miniaturized MS,[143] are being developed as well.[138][64]

Mass spectrometry[edit]

Mass spectrometry (MS) is a near universal detection technique that is recognized throughout the world as the gold standard for identification of manycompounds. MS is an analytical technique in which chemical species are ionized and sorted before detection, and the resulting mass spectrum is used to identify the ions' parent molecules. This makes MS, unlike other detection techniques (such as fluorescence), label-free; i.e. there is no need to bind additional ligands or groups to the molecule of interest in order to receive a signal and identify the compound.

There are many cases in which other spectroscopic methods, such as nuclear magnetic resonance (NMR), fluorescence, infrared, or Raman, are not viable as standalone methods due to the particular chemical composition of the droplets. Often, these droplets are sensitive to fluorescent labels,[55] or contain species that are otherwise indeterminately similar, where MS may be employed along with other methods to characterize a specific analyte of interest.[56] [57]However, MS has only recently (in the past decade) gained popularity as a detection method for droplet-based microfluidics (and microfluidics as a whole) due to challenges associated with coupling mass spectrometers with these miniaturized devices.[138][139][140] Difficulty of separation/purification make entirely microfluidic scale systems coupled to mass spectrometry ideal in the fields of proteomics,[141][55] [58] [59] enzyme kinetics,[60] drug discovery,[37] and newborn disease screening.[61] The two primary methods of ionization for mass analysis used in droplet-based microfluidics today are matrix-assisted laser desorption/ionization (MALDI)[62] [63] and electrospray ionization (ESI).[55] Additional methods for coupling, such as (but not limited to) surface acoustic wave nebulization (SAWN),[142] and paper-spray ionization onto miniaturized MS,[143] are being developed as well.[138][64]

Electrospray ionization[edit]

One complication offered by the coupling of MS to droplet-based microfluidics is that the dispersed samples are produced at comparatively low flow rates compared to traditional MS-injection techniques. ESI is able to easily accept these low flow rates and is now commonly exploited for on-line microfluidic analysis.[138][131][144][145] ESI and MALDI offer a high throughput answer to the problem of label-free droplet detection, but ESI requires less intensive sample preparation and fabrication elements that are scalable to microfluidic device scale.[141][145][144][68] ESI involves the application of a high voltage to a carrier stream of analyte-containing droplets, which aerosolizes the stream, followed by detection at a potential-differentiated analyser region. The carrier fluid within a droplet-based microfluidic device, typically an oil, is often an obstacle within ESI. The oil, when part of the flow of droplets going into an ESI-MS instrument, can cause a constant background voltage interfering with the detection of sample droplets.[131] This background interference can be rectified by changing the oil used as a carrier fluid and by adjusting the voltage used for the electrospray.[131][141]

Droplet size, Taylor cone shape, and flow rate can be controlled by varying the potential differential and the temperature of a drying (to evaporate analyte-surrounding solvent) stream of gas (usually nitrogen).[69] Because ESI allows for online droplet detection, other problems posed by segmented or off-chip detection based systems can be solved, such as the minimizing of sample (droplet) dilution, which is especially critical to microfluidic droplet detection where analyte samples are already diluted to the lowest experimentally relevant concentration.[70]

Matrix-assisted laser desorption/ionization[edit]

MALDI is typified by the use of an ultraviolet (UV) laser to trigger ablation of analyte species that are mixed with a matrix of crystallized molecules with high optical absorption.[140] The ions within the resulting ablated gasses are then protonated or deprotonated before acceleration into a mass spectrometer. The primary advantages of MALDI detection over ESI in microfluidic devices are that MALDI allows for much easier multiplexing,[65][146] which even further increases the device's overall throughput,[63] as well as less reliance on moving parts, and the absence of Taylor cone stability problems posed by microfluidic-scale flow rates.[147][66] The speed of MALDI detection, along with the scale of microfluidic droplets, allows for improvements upon macro-scale techniques in both throughput and time-of-flight (TOF) resolution.[60] [63] Where typical MS detection setups often utilize separation techniques such as chromatography, MALDI setups require a sufficiently purified sample to be mixed with pre-determined organic matrices, suited for the specific sample, prior to detection.[58] MALDI matrix composition must be tuned to produce appropriate fragmentation and ablation of analytes.

One method to obtain a purified sample from droplet-based microfluidics is to end the microfluidic channel onto a MALDI plate, with aqueous droplets forming on hydrophilic regions on the plate.[140][146][147][148] Solvent and carrier fluid are then allowed to evaporate, leaving behind only the dried droplets of the sample of interest, after which the MALDI matrix is applied to the dried droplets. This sample preparation has notable limitations and complications, which are not currently overcome for all types of samples. Additionally, MALDI matrices are preferentially in much higher concentrations than the analyte sample, which allows for microfluidic droplet transportation to be incorporated into online MALDI matrix production. Due to the low number of known matrices and trial and error nature of finding appropriate new matrix compositions,[67] this can be the determining factor in the use of other forms of spectroscopy over MALDI.[140][138][149]

Raman spectroscopy[edit]

Raman spectroscopy is an optical technique that provides non-destructive analysis with chemical specificity without complex sample preparation, and is capable of detecting components within mixtures. Raman signal corresponds to vibrational excitation of specific molecules within the system based on the scattered visible light emitted from a molecule with a lower energy than the excitation light source. Raman spectroscopy, when coupled with microfluidic devices, can monitor fluid mixing and trapping[150] of liquids and can also detect solid and gas phases[151] within microfluidic platforms. Raman signal can be detected with integrated fiberoptics[152] within the microfluidic chip or by placing the device on Raman microscope.[153]

Raman signal is inherently weak; therefore for short detection times at small sample volumes in microfluidic devices, signal amplification is utilized. Some microfluidic systems utilize metallic colloids[154] or nanoparticles[155] within solution to capitalize on Surface-enhanced Raman spectroscopy (SERS) as a detection technique.[156] Typical confocal Raman microscopy allows for spectroscopic information from small focal volumes less 1 micron cubed, and thus smaller than the microfluidic channel dimensions.[153] Multi-photon Raman spectroscopy, such as stimulated Raman scattering (SRS) or coherent anti-Stokes Raman scattering (CARS) also enhance signal from substances in microfluidic devices.[157]

For droplet-based microfluidics, Raman detection provides online analysis of multiple analytes within droplets or continuous phase. Raman signal is sensitive to concentration changes, therefore solubility and mixing kinetics of a droplet-based microfluidic system can be detected using Raman.[151][153] Considerations include the refractive index difference at the interface of the droplet and continuous phase, as well as between fluid and channel connections.[153][150][158]

Fluorescent Detection[edit]

Fluorescence spectroscopy is one of the most common droplet detection techniques.[159] It provides a rapid response, and, for applicable analytes, it has a strong signal.[160] The use of fluorescence spectroscopy in microfluidics follows a similar format to most other fluorescent analytical techniques. A light source is used to excite analyte molecules in the sample, after which the analyte fluoresces, and the fluorescence response is the measured output. Cameras can be used to capture the fluorescence signal of the droplets,[161] and filters are often used to filter out scattered excitation light. In microfluidic droplet detection, the experimental setup of a fluorescence instrument can vary greatly. A common setup in fluorescent droplet detection is with the use of an epifluorescence microscope.[159] This sometimes utilizes a confocal geometry, which can vary depending on experimental needs. For example, Jeffries et al. reported success with exploring an orthogonal confocal geometry, as opposed to a standard epi geometry.[159] However, other setups for fluorescence detection have been explored, as epifluorescence microscopes can be expensive and difficult to upkeep.[160] Cole et al. have proposed and tested an experimental setup with fiber optics to conduct fluorescence analysis of microfluidic droplets.  

Fluorescence detection of droplets has a number of advantages. First, it can accommodate a large and fast throughput.[159] Analysis of thousands of samples can be conducted in a short period of time, which is advantageous for the analysis of a large number of samples.[158] Another advantage is the accuracy of the method. In an analysis performed by Li et al., it was found that use of fluorescence detection techniques yielded 100% detection accuracy in 13 of 15 collected images. The remaining two had relative errors around 6%.[161] Another advantage of fluorescence detection is that it allows for quantitative analysis of droplet spacing in a sample.[162] This is done by use of temporal measurements and the flow velocity of the analyte.[163] The time spacing between signals allows for calculation of droplet spacing. Further fluorescence analysis of microfluidic droplet samples can be used to measure the fluorescent lifetime of samples, providing additional information that is not obtainable for fluorescence intensity measurements alone.[164]

The applications of fluorescence detection are varied, with many of its uses centered in biological applications. Frenz et al. utilized fluorescence detection of droplets to examine enzyme kinetics. For this experiment, b-lactamase interacted with fluorocillin, a fluorogenic substrate. Fluorescence of the droplets were measured at multiple time intervals to examine the change with time.[24] This detection method goes beyond biological applications, though, and allows for the physical study of droplet formation and evolution. For example, Sakai et al. used fluorescence detection to monitor droplet size.[165]  This was done by collecting fluorescence data to calculate the concentration of a fluorescent dye within a single droplet, thus allowing size growth to be monitored. The use of fluorescence detection techniques can be expanded into applications beyond data collection; a widely used method of cell and droplet sorting in microfluidics is fluorescence activated sorting, where droplets are sorted into different channels or collection outlets based on their fluorescence intensity.[55]

Electrochemical Detection[edit]

Electrochemical detection serves as an inexpensive alternative to not only measure chemical composition in certain cases, but also droplet length, frequency, conductivity, and velocity at high speeds and usually with very little space compensation on the chip.[40][158] The method was first discussed in Luo et al. wherein the team was able to successfully measure the size and ion concentration in pico-liter droplets containing dissolved NaCl ions.[166] It is usually performed with a set or series of microelectrodes which measure the perturbations of current, smaller drops giving smaller perturbations while larger drops giving longer curves. The number of perturbations in the current can also indicate the frequency of the droplets passing the electrode as a way to determine the rate of droplets as well.[167] Several different compounds have been suggested for use within the electrodes, as accurate, precise, and significant readings can be difficult within the microscale. These compounds range from carbon paste electrodes that are applied directly to the chip, to platinum black electrodeposited on platinum wire in tandem with a silver chloride on silver microelectrode to increase activity and surface area.[168]

As for chemical composition, readings are achieved through chronoamperometric analysis of electro-active compounds within the droplets as stated above. The potential varies dependent on the electrically viable ions, dissolved sodium and chlorine ions in this experiment, and their concentrations within each droplet.[158][167] Another group displayed, with a series of controls, that mixed droplet composition involving potassium iodide was detected accurately on the time scale of seconds with optimal voltage, velocity, and pH ranges.[169] In addition to this, a more unique approach is developing within chronoamperometric readings, where magneto-fluidic systems have been created and the potential readings are measured in otherwise electro-inactive fluids by the dissolution of magnetic microparticles into the reagent.[170] This method is enhanced into a digital microfluidic (DMF) setting, where gold and sliver electrodes in junction with dissolved magnetic microparticles in the fluids replaced the typical fluorescence-based detection of droplets in the immunoassay of biomarker analytes.[171]

The above experiment by Shamsi et al, alludes to the main use for electrochemical detection in microfluidics; biosensing for various measurements such as enzyme kinetics and biological assays of many other types of cells.[172][173] Increased control on the system is needed for these processes as with increasing flow rate, enzyme detection decreases. Though as an enzymatic reaction progresses, the amperometric reading will evolve as well, allowing for rapid monitoring of the kinetics.[174] Also, specific surfactants can lack biocompatibility with the system, affecting the enzyme and skewing detection.[175] The reaches of this application have even had effects in aquaculture and economics, as electrochemical sensing has been used to test the freshness of fish rapidly.[174] Use of this detection method is primarily found in the electrowetting of dielectric DMFs, where the sensing electrode apparatus can be reconfigurable and has a longer lifetime while still producing accurate results.[176]

References[edit]

  1. ^ a b c d e Song H, Tice JD, Ismagilov RF (February 2003). "A microfluidic system for controlling reaction networks in time". Angewandte Chemie. 42 (7): 768–72. doi:10.1002/anie.200390203. PMID 12596195.
  2. ^ a b Garstecki P, Fuerstman MJ, Stone HA, Whitesides GM (March 2006). "Formation of droplets and bubbles in a microfluidic T-junction-scaling and mechanism of break-up". Lab on a Chip. 6 (3): 437–46. CiteSeerX 10.1.1.644.3101. doi:10.1039/b510841a. PMID 16511628.
  3. ^ Seemann R, Brinkmann M, Pfohl T, Herminghaus S (January 2012). "Droplet based microfluidics". Reports on Progress in Physics. Physical Society. 75 (1): 016601. Bibcode:2012RPPh...75a6601S. doi:10.1088/0034-4885/75/1/016601. PMID 22790308.
  4. ^ Sesen M, Alan T, Neild A (July 2017). "Droplet control technologies for microfluidic high throughput screening (μHTS)". Lab on a Chip. 17 (14): 2372–2394. doi:10.1039/C7LC00005G. PMID 28631799.
  5. ^ a b c d e Teh SY, Lin R, Hung LH, Lee AP (February 2008). "Droplet microfluidics". Lab on a Chip. 8 (2): 198–220. doi:10.1039/b715524g. PMID 18231657.
  6. ^ a b van Dijke KC, Veldhuis G, Schroën K, Boom RM (2010-03-01). "Simultaneous formation of many droplets in a single microfluidic droplet formation unit". AIChE Journal. 56 (3): 833–836. doi:10.1002/aic.11990. ISSN 1547-5905.
  7. ^ a b Dendukuri D, Tsoi K, Hatton TA, Doyle PS (March 2005). "Controlled synthesis of nonspherical microparticles using microfluidics". Langmuir. 21 (6): 2113–6. doi:10.1021/la047368k. PMID 15751995.
  8. ^ a b c d e f Zhu P, Wang L (December 2016). "Passive and active droplet generation with microfluidics: a review". Lab on a Chip. 17 (1): 34–75. doi:10.1039/c6lc01018k. PMID 27841886.
  9. ^ Thorsen T, Roberts RW, Arnold FH, Quake SR (April 2001). "Dynamic pattern formation in a vesicle-generating microfluidic device" (PDF). Physical Review Letters. 86 (18): 4163–6. Bibcode:2001PhRvL..86.4163T. doi:10.1103/physrevlett.86.4163. PMID 11328121.
  10. ^ Gu H, Duits MH, Mugele F (2011-04-15). "Droplets formation and merging in two-phase flow microfluidics". International Journal of Molecular Sciences. 12 (4): 2572–97. doi:10.3390/ijms12042572. PMC 3127135. PMID 21731459.
  11. ^ Tenje M, Fornell A, Ohlin M, Nilsson J (February 2018). "Particle Manipulation Methods in Droplet Microfluidics". Analytical Chemistry. 90 (3): 1434–1443. doi:10.1021/acs.analchem.7b01333. PMID 29188994.
  12. ^ Christopher GF, Anna SL (2007). "Microfluidic methods for generating continuous droplet streams". Journal of Physics D: Applied Physics. 40 (19): R319–R336. doi:10.1088/0022-3727/40/19/r01.
  13. ^ Abate AR, Weitz DA (May 2011). "Air-bubble-triggered drop formation in microfluidics". Lab on a Chip. 11 (10): 1713–6. doi:10.1039/c1lc20108e. PMID 21448493.
  14. ^ Liu H, Zhang Y (2009). "Droplet formation in a T-shaped microfluidic junction". Journal of Applied Physics. 106 (34906): 034906–034906–8. Bibcode:2009JAP...106c4906L. doi:10.1063/1.3187831.
  15. ^ Zheng B, Tice JD, Ismagilov RF (September 2004). "Formation of droplets of alternating composition in microfluidic channels and applications to indexing of concentrations in droplet-based assays". Analytical Chemistry. 76 (17): 4977–82. doi:10.1021/ac0495743. PMC 1766978. PMID 15373431.
  16. ^ Anna S, Bontoux N, Stone H (2003). "Formation of dispersions using "flow focusing" in microchannels". Applied Physics Letters. 82 (3): 364–366. Bibcode:2003ApPhL..82..364A. doi:10.1063/1.1537519.
  17. ^ Tan Y, Cristini V, Lee AP (2006). "Monodispersed microfluidic droplet generation by shear focusing microfluidic device". Sensors and Actuators B: Chemical. 114 (1): 350–356. doi:10.1016/j.snb.2005.06.008.
  18. ^ Hsiung S, Chen C, Lee G (2006). "Micro-droplet formation utilizing microfluidic flow focusing and controllable moving-wall chopping techniques". Journal of Micromechanics and Microengineering. 16 (11): 2403–2410. Bibcode:2006JMiMi..16.2403H. doi:10.1088/0960-1317/16/11/022.
  19. ^ Anna S (2016). "Droplets and Bubbles in Microfluidic Devices". Annual Review of Fluid Mechanics. 48: 285–309. Bibcode:2016AnRFM..48..285A. doi:10.1146/annurev-fluid-122414-034425.
  20. ^ a b c Castro-Hernandez E, Gundabala V, Fernández-Nieves A, Gordillo JM (2009). "Scaling the drop size in coflow experiments". New Journal of Physics. 11 (7): 075021. Bibcode:2009NJPh...11g5021C. doi:10.1088/1367-2630/11/7/075021.
  21. ^ a b Utada AS, Fernandez-Nieves A, Stone HA, Weitz DA (August 2007). "Dripping to jetting transitions in coflowing liquid streams". Physical Review Letters. 99 (9): 094502. Bibcode:2007PhRvL..99i4502U. doi:10.1103/physrevlett.99.094502. PMID 17931011.
  22. ^ a b c Korczyk PM, Dolega ME, Jakiela S, Jankowski P, Makulska S, Garstecki P (2015). "Scaling up the Throughput of Synthesis and Extraction in Droplet Microfluidic Reactors". Journal of Flow Chemistry. 5 (2): 110–118. doi:10.1556/jfc-d-14-00038.
  23. ^ a b Wiles C, Watts P, Haswell SJ, Pombo-Villar E (December 2001). "The aldol reaction of silyl enol ethers within a micro reactor". Lab on a Chip. 1 (2): 100–1. doi:10.1039/B107861E. PMID 15100867.
  24. ^ a b c d e f g h Frenz L, Blank K, Brouzes E, Griffiths AD (May 2009). "Reliable microfluidic on-chip incubation of droplets in delay-lines". Lab on a Chip. 9 (10): 1344–8. doi:10.1039/b816049j. PMC 5317046. PMID 19417899.
  25. ^ Li M, Jiang W, Chen Z, Suryaprakash S, Lv S, Tang Z, et al. (February 2017). "A versatile platform for surface modification of microfluidic droplets". Lab on a Chip. 17 (4): 635–639. doi:10.1039/c7lc00079k. PMC 5328679. PMID 28154857.
  26. ^ a b c d e f Shembekar N, Chaipan C, Utharala R, Merten CA (April 2016). "Droplet-based microfluidics in drug discovery, transcriptomics and high-throughput molecular genetics". Lab on a Chip. 16 (8): 1314–31. doi:10.1039/c6lc00249h. PMID 27025767.
  27. ^ Mashaghi S, Abbaspourrad A, Weitz DA, van Oijen AM (September 2016). "Droplet microfluidics: A tool for biology, chemistry and nanotechnology". TrAC Trends in Analytical Chemistry. 82: 118–25. doi:10.1016/j.trac.2016.05.019.
  28. ^ Huebner A, Srisa-Art M, Holt D, Abell C, Hollfelder F, deMello AJ, Edel JB (March 2007). "Quantitative detection of protein expression in single cells using droplet microfluidics". Chemical Communications (12): 1218–20. doi:10.1039/b618570c. PMID 17356761.
  29. ^ Agresti JJ, Antipov E, Abate AR, Ahn K, Rowat AC, Baret JC, et al. (March 2010). "Ultrahigh-throughput screening in drop-based microfluidics for directed evolution". Proceedings of the National Academy of Sciences of the United States of America. 107 (9): 4004–9. Bibcode:2010PNAS..107.4004A. doi:10.1073/pnas.0910781107. PMC 2840095. PMID 20142500.
  30. ^ Ahn K, Kerbage C, Hunt TP, Westervelt RM, Link DR, Weitz DA (January 2006). "Dielectrophoretic manipulation of drops for high-speed microfluidic sorting devices". Applied Physics Letters. 88 (2): 024104. Bibcode:2006ApPhL..88b4104A. doi:10.1063/1.2164911.
  31. ^ Gerdts CJ, Tereshko V, Yadav MK, Dementieva I, Collart F, Joachimiak A, et al. (December 2006). "Time-controlled microfluidic seeding in nL-volume droplets to separate nucleation and growth stages of protein crystallization". Angewandte Chemie. 45 (48): 8156–60. doi:10.1002/anie.200602946. PMC 1766323. PMID 17099920.
  32. ^ Gu H, Duits MH, Mugele F (2011). "Droplets formation and merging in two-phase flow microfluidics". International Journal of Molecular Sciences. 12 (4): 2572–97. doi:10.3390/ijms12042572. PMC 3127135. PMID 21731459.
  33. ^ a b Sesen M, Alan T, Neild A (September 2014). "Microfluidic on-demand droplet merging using surface acoustic waves". Lab on a Chip. 14 (17): 3325–33. doi:10.1039/C4LC00456F. PMID 24972001.
  34. ^ Song H, Li HW, Munson MS, Van Ha TG, Ismagilov RF (July 2006). "On-chip titration of an anticoagulant argatroban and determination of the clotting time within whole blood or plasma using a plug-based microfluidic system". Analytical Chemistry. 78 (14): 4839–49. doi:10.1021/ac0601718. PMC 1851927. PMID 16841902.
  35. ^ Sivasamy J, Chim YC, Wong TN, Nguyen NT, Yobas L (March 2010). "Reliable addition of reagents into microfluidic droplets". Microfluidics and Nanofluidics. 8 (3): 409–16. doi:10.1007/s10404-009-0531-5.
  36. ^ a b Abate AR, Hung T, Mary P, Agresti JJ, Weitz DA (November 2010). "High-throughput injection with microfluidics using picoinjectors". Proceedings of the National Academy of Sciences of the United States of America. 107 (45): 19163–6. Bibcode:2010PNAS..10719163A. doi:10.1073/pnas.1006888107. PMC 2984161. PMID 20962271.
  37. ^ Rhee M, Light YK, Yilmaz S, Adams PD, Saxena D, Meagher RJ, Singh AK (December 2014). "Pressure stabilizer for reproducible picoinjection in droplet microfluidic systems". Lab on a Chip. 14 (23): 4533–9. doi:10.1039/c4lc00823e. PMC 4213212. PMID 25270338.
  38. ^ Hayes CJ, Dalton TM (June 2015). "Microfluidic droplet-based PCR instrumentation for high-throughput gene expression profiling and biomarker discovery". Biomolecular Detection and Quantification. 4: 22–32. doi:10.1016/j.bdq.2015.04.003. PMC 4822205. PMID 27077035.
  39. ^ Doonan SR, Bailey RC (April 2017). "K-Channel: A Multifunctional Architecture for Dynamically Reconfigurable Sample Processing in Droplet Microfluidics". Analytical Chemistry. 89 (7): 4091–4099. doi:10.1021/acs.analchem.6b05041. PMC 5812353. PMID 28222260.
  40. ^ a b Theberge AB, Courtois F, Schaerli Y, Fischlechner M, Abell C, Hollfelder F, Huck WT (August 2010). "Microdroplets in microfluidics: an evolving platform for discoveries in chemistry and biology". Angewandte Chemie (International Ed. In English). 49 (34): 5846–68. doi:10.1002/anie.200906653. PMID 20572214.
  41. ^ a b Clausell-Tormos J, Lieber D, Baret JC, El-Harrak A, Miller OJ, Frenz L, et al. (May 2008). "Droplet-based microfluidic platforms for the encapsulation and screening of Mammalian cells and multicellular organisms". Chemistry & Biology. 15 (5): 427–37. doi:10.1016/j.chembiol.2008.04.004. PMID 18482695.
  42. ^ Li L, Mustafi D, Fu Q, Tereshko V, Chen DL, Tice JD, Ismagilov RF (December 2006). "Nanoliter microfluidic hybrid method for simultaneous screening and optimization validated with crystallization of membrane proteins". Proceedings of the National Academy of Sciences of the United States of America. 103 (51): 19243–8. Bibcode:2006PNAS..10319243L. doi:10.1073/pnas.0607502103. PMC 1748211. PMID 17159147.
  43. ^ Mazutis L, Araghi AF, Miller OJ, Baret JC, Frenz L, Janoshazi A, et al. (June 2009). "Droplet-based microfluidic systems for high-throughput single DNA molecule isothermal amplification and analysis". Analytical Chemistry. 81 (12): 4813–21. doi:10.1021/ac900403z. PMID 19518143.
  44. ^ a b c Köster S, Angilè FE, Duan H, Agresti JJ, Wintner A, Schmitz C, et al. (July 2008). "Drop-based microfluidic devices for encapsulation of single cells". Lab on a Chip. 8 (7): 1110–5. doi:10.1039/b802941e. PMID 18584086.
  45. ^ Shim JU, Cristobal G, Link DR, Thorsen T, Jia Y, Piattelli K, Fraden S (July 2007). "Control and measurement of the phase behavior of aqueous solutions using microfluidics". Journal of the American Chemical Society. 129 (28): 8825–35. doi:10.1021/ja071820f. PMC 2531156. PMID 17580868.
  46. ^ Brouzes E, Medkova M, Savenelli N, Marran D, Twardowski M, Hutchison JB, et al. (August 2009). "Droplet microfluidic technology for single-cell high-throughput screening". Proceedings of the National Academy of Sciences of the United States of America. 106 (34): 14195–200. Bibcode:2009PNAS..10614195B. doi:10.1073/pnas.0903542106. PMC 2732882. PMID 19617544.
  47. ^ El Debs B, Utharala R, Balyasnikova IV, Griffiths AD, Merten CA (July 2012). "Functional single-cell hybridoma screening using droplet-based microfluidics". Proceedings of the National Academy of Sciences of the United States of America. 109 (29): 11570–5. Bibcode:2012PNAS..10911570D. doi:10.1073/pnas.1204514109. PMC 3406880. PMID 22753519.
  48. ^ a b Holtze C, Rowat AC, Agresti JJ, Hutchison JB, Angilè FE, Schmitz CH, et al. (October 2008). "Biocompatible surfactants for water-in-fluorocarbon emulsions". Lab on a Chip. 8 (10): 1632–9. doi:10.1039/b806706f. PMID 18813384.
  49. ^ Courtois F, Olguin LF, Whyte G, Bratton D, Huck WT, Abell C, Hollfelder F (February 2008). "An integrated device for monitoring time-dependent in vitro expression from single genes in picolitre droplets". ChemBioChem. 9 (3): 439–46. doi:10.1002/cbic.200700536. PMID 18232037.
  50. ^ Hu H, Eustace D, Merten CA (October 2015). "Efficient cell pairing in droplets using dual-color sorting". Lab on a Chip. 15 (20): 3989–93. doi:10.1039/c5lc00686d. PMID 26313441.
  51. ^ Huebner A, Bratton D, Whyte G, Yang M, Demello AJ, Abell C, Hollfelder F (March 2009). "Static microdroplet arrays: a microfluidic device for droplet trapping, incubation and release for enzymatic and cell-based assays". Lab on a Chip. 9 (5): 692–8. doi:10.1039/b813709a. PMID 19224019.
  52. ^ Varma VB, Ray A, Wang ZM, Wang ZP, Ramanujan RV (November 2016). "Droplet Merging on a Lab-on-a-Chip Platform by Uniform Magnetic Fields". Scientific Reports. 6: 37671. Bibcode:2016NatSR...637671V. doi:10.1038/srep37671. PMC 5124862. PMID 27892475.
  53. ^ Pamme N (January 2006). "Magnetism and microfluidics". Lab on a Chip. 6 (1): 24–38. CiteSeerX 10.1.1.458.4857. doi:10.1039/b513005k. PMID 16372066.
  54. ^ Ray A, Varma VB, Wang Z, Wang Z, Jayaneel PJ, Sudharsan NM, Ramanujan RV (2016-01-01). "Magnetic Droplet Merging by Hybrid Magnetic Fields". IEEE Magnetics Letters. 7: 1–5. doi:10.1109/LMAG.2016.2613065. ISSN 1949-307X.
  55. ^ a b c d Baret JC, Miller OJ, Taly V, Ryckelynck M, El-Harrak A, Frenz L, et al. (July 2009). "Fluorescence-activated droplet sorting (FADS): efficient microfluidic cell sorting based on enzymatic activity". Lab on a Chip. 9 (13): 1850–8. doi:10.1039/B902504A. PMID 19532959.
  56. ^ a b Tan Y, Ho YL, Lee AP (2007-06-29). "Microfluidic sorting of droplets by size". Microfluidics and Nanofluidics. 4 (4): 343. doi:10.1007/s10404-007-0184-1. ISSN 1613-4990.
  57. ^ a b Gielen F, Hours R, Emond S, Fischlechner M, Schell U, Hollfelder F (November 2016). "Ultrahigh-throughput-directed enzyme evolution by absorbance-activated droplet sorting (AADS)". Proceedings of the National Academy of Sciences of the United States of America. 113 (47): E7383–E7389. Bibcode:2016PNAS..113E7383G. doi:10.1073/pnas.1606927113. PMC 5127370. PMID 27821774.
  58. ^ a b c Shen Y, Yalikun Y, Tanaka Y (2019-03-01). "Recent advances in microfluidic cell sorting systems". Sensors and Actuators B: Chemical. 282: 268–281. doi:10.1016/j.snb.2018.11.025. ISSN 0925-4005.
  59. ^ Tan YC, Fisher JS, Lee AI, Cristini V, Lee AP (August 2004). "Design of microfluidic channel geometries for the control of droplet volume, chemical concentration, and sorting". Lab on a Chip. 4 (4): 292–8. doi:10.1039/B403280M. PMID 15269794.
  60. ^ Jeong H, Lee B, Jin SH, Lee C (2019-03-15). "Hydrodynamic control of droplet breakup, immobilization, and coalescence for a multiplex microfluidic static droplet array". Chemical Engineering Journal. 360: 562–568. doi:10.1016/j.cej.2018.11.182. ISSN 1385-8947.
  61. ^ Hatch AC, Patel A, Beer NR, Lee AP (April 2013). "Passive droplet sorting using viscoelastic flow focusing". Lab on a Chip. 13 (7): 1308–15. doi:10.1039/C2LC41160A. PMID 23380996.
  62. ^ Xi HD, Zheng H, Guo W, Gañán-Calvo AM, Ai Y, Tsao CW, et al. (February 2017). "Active droplet sorting in microfluidics: a review". Lab on a Chip. 17 (5): 751–771. doi:10.1039/C6LC01435F. PMID 28197601.
  63. ^ Wu L, Chen P, Dong Y, Feng X, Liu BF (June 2013). "Encapsulation of single cells on a microfluidic device integrating droplet generation with fluorescence-activated droplet sorting". Biomedical Microdevices. 15 (3): 553–60. doi:10.1007/s10544-013-9754-z. PMID 23404263.
  64. ^ Link DR, Grasland-Mongrain E, Duri A, Sarrazin F, Cheng Z, Cristobal G, et al. (April 2006). "Electric control of droplets in microfluidic devices". Angewandte Chemie. 45 (16): 2556–60. doi:10.1002/anie.200503540. PMID 16544359.
  65. ^ Lee C, Lee J, Kim HH, Teh SY, Lee A, Chung IY, et al. (August 2012). "Microfluidic droplet sorting with a high frequency ultrasound beam". Lab on a Chip. 12 (15): 2736–42. doi:10.1039/C2LC21123H. PMC 3400154. PMID 22643737.
  66. ^ a b Mazutis L, Gilbert J, Ung WL, Weitz DA, Griffiths AD, Heyman JA (May 2013). "Single-cell analysis and sorting using droplet-based microfluidics". Nature Protocols. 8 (5): 870–91. doi:10.1038/nprot.2013.046. PMC 4128248. PMID 23558786.
  67. ^ Cao Z, Chen F, Bao N, He H, Xu P, Jana S, et al. (January 2013). "Droplet sorting based on the number of encapsulated particles using a solenoid valve". Lab on a Chip. 13 (1): 171–8. doi:10.1039/C2LC40950J. PMID 23160342.
  68. ^ Girault M, Kim H, Arakawa H, Matsuura K, Odaka M, Hattori A, et al. (January 2017). "An on-chip imaging droplet-sorting system: a real-time shape recognition method to screen target cells in droplets with single cell resolution". Scientific Reports. 7: 40072. Bibcode:2017NatSR...740072G. doi:10.1038/srep40072. PMC 5216404. PMID 28059147.
  69. ^ Joensson HN, Andersson Svahn H (December 2012). "Droplet microfluidics--a tool for single-cell analysis". Angewandte Chemie. 51 (49): 12176–92. doi:10.1002/anie.201200460. PMID 23180509.
  70. ^ Zheng B, Tice JD, Roach LS, Ismagilov RF (May 2004). "A droplet-based, composite PDMS/glass capillary microfluidic system for evaluating protein crystallization conditions by microbatch and vapor-diffusion methods with on-chip X-ray diffraction". Angewandte Chemie. 43 (19): 2508–11. doi:10.1002/anie.200453974. PMC 1766324. PMID 15127437.
  71. ^ Zheng B, Roach LS, Ismagilov RF (September 2003). "Screening of protein crystallization conditions on a microfluidic chip using nanoliter-size droplets". Journal of the American Chemical Society. 125 (37): 11170–1. CiteSeerX 10.1.1.652.8596. doi:10.1021/ja037166v. PMID 16220918.
  72. ^ Clark DP (2013). Molecular biology. Pazdernik, Nanette Jean. (2nd ed.). Waltham, MA: Academic Press. ISBN 9780123785947. OCLC 777375628.
  73. ^ Huebner A, Sharma S, Srisa-Art M, Hollfelder F, Edel JB, Demello AJ (August 2008). "Microdroplets: a sea of applications?". Lab on a Chip. 8 (8): 1244–54. doi:10.1039/b806405a. PMID 18651063.
  74. ^ a b Nakano M, Komatsu J, Matsuura S, Takashima K, Katsura S, Mizuno A (April 2003). "Single-molecule PCR using water-in-oil emulsion". Journal of Biotechnology. 102 (2): 117–24. doi:10.1016/S0168-1656(03)00023-3. PMID 12697388.
  75. ^ a b Zhang C, Xing D (2007-07-01). "Miniaturized PCR chips for nucleic acid amplification and analysis: latest advances and future trends". Nucleic Acids Research. 35 (13): 4223–37. doi:10.1093/nar/gkm389. PMC 1934988. PMID 17576684.
  76. ^ Hindson BJ, Ness KD, Masquelier DA, Belgrader P, Heredia NJ, Makarewicz AJ, et al. (November 2011). "High-throughput droplet digital PCR system for absolute quantitation of DNA copy number". Analytical Chemistry. 83 (22): 8604–10. doi:10.1021/ac202028g. PMC 3216358. PMID 22035192.
  77. ^ Watson, James D. (2014). Molecular biology of the gene. Watson, James D., 1928- (Seventh ed.). Boston. ISBN 9780321762436. OCLC 824087979.
  78. ^ Fallah-Araghi A, Baret JC, Ryckelynck M, Griffiths AD (March 2012). "A completely in vitro ultrahigh-throughput droplet-based microfluidic screening system for protein engineering and directed evolution". Lab on a Chip. 12 (5): 882–91. doi:10.1039/c2lc21035e. PMID 22277990.
  79. ^ Xu Y, Yan H, Zhang Y, Jiang K, Lu Y, Ren Y, et al. (July 2015). "A fully sealed plastic chip for multiplex PCR and its application in bacteria identification". Lab on a Chip. 15 (13): 2826–34. doi:10.1039/c5lc00244c. PMID 26016439.
  80. ^ Kim J, Jeong D, Kim Y, Kwon Y, Rhee G, Zhang D, Kim H (2013). "Development of a multiplex PCR method for testing six GM soybean events". Food Control. 31 (2): 366–371. doi:10.1016/j.foodcont.2012.10.015.
  81. ^ Jung S, Kim BK, Lee S, Yoon S, Im H, Kim SK (2018). "Multiplexed on-chip real-time PCR using hydrogel spot array for microRNA profiling of minimal tissue samples". Sensors and Actuators B: Chemical. 262: 118–124. doi:10.1016/j.snb.2018.01.228.
  82. ^ Prakash AR, Adamia S, Sieben V, Pilarski P, Pilarski LM, Backhouse CJ (2006). "Small volume PCR in PDMS biochips with integrated fluid control and vapour barrier". Sensors and Actuators B: Chemical. 113 (1): 398–409. doi:10.1016/j.snb.2005.03.049.
  83. ^ Trung NB, Saito M, Takabayashi H, Viet PH, Tamiya E, Takamura Y (2010). "Multi-chamber PCR chip with simple liquid introduction utilizing the gas permeability of polydimethylsiloxane". Sensors and Actuators B: Chemical. 149 (1): 284–290. doi:10.1016/j.snb.2010.06.013.
  84. ^ a b Fu Y, Zhou H, Jia C, Jing F, Jin Q, Zhao J, Li G (2017). "A microfluidic chip based on surfactant-doped polydimethylsiloxane (PDMS) in a sandwich configuration for low-cost and robust digital PCR". Sensors and Actuators B: Chemical. 245: 414–422. doi:10.1016/j.snb.2017.01.161.
  85. ^ a b c Elvira KS, Casadevall i Solvas X, Wootton RC, deMello AJ (November 2013). "The past, present and potential for microfluidic reactor technology in chemical synthesis". Nature Chemistry. 5 (11): 905–15. Bibcode:2013NatCh...5..905E. doi:10.1038/nchem.1753. PMID 24153367.
  86. ^ a b Dittrich PS, Manz A (March 2006). "Lab-on-a-chip: microfluidics in drug discovery". Nature Reviews. Drug Discovery. 5 (3): 210–8. doi:10.1038/nrd1985. PMID 16518374.
  87. ^ a b c d Mashaghi S, Abbaspourrad A, Weitz DA, van Oijen AM (2016-09-01). "Droplet microfluidics: A tool for biology, chemistry and nanotechnology". TrAC Trends in Analytical Chemistry. 82: 118–125. doi:10.1016/j.trac.2016.05.019.
  88. ^ Beesabathuni SN, Stockham JG, Kim JH, Lee HB, Chung JH, Shen AQ (2013-11-04). "Fabrication of conducting polyaniline microspheres using droplet microfluidics". RSC Advances. 3 (46): 24423. doi:10.1039/C3RA44808H. ISSN 2046-2069.
  89. ^ Dai J, Yang X, Hamon M, Kong L (2015-11-15). "Particle size controlled synthesis of CdS nanoparticles on a microfluidic chip". Chemical Engineering Journal. 280: 385–390. doi:10.1016/j.cej.2015.06.005.
  90. ^ Skelton V, Greenway GM, Haswell SJ, Styring P, Morgan DO, Warrington BH, Wong SY (2001-01-01). "The generation of concentration gradients usingelectroosmotic flow in micro reactors allowing stereoselective chemicalsynthesis". Analyst. 126 (1): 11–13. Bibcode:2001Ana...126...11S. doi:10.1039/B006727J. ISSN 1364-5528.
  91. ^ Wang JT, Wang J, Han JJ (July 2011). "Fabrication of advanced particles and particle-based materials assisted by droplet-based microfluidics". Small. 7 (13): 1728–54. doi:10.1002/smll.201001913. PMID 21618428.
  92. ^ Shestopalov I, Tice JD, Ismagilov RF (August 2004). "Multi-step synthesis of nanoparticles performed on millisecond time scale in a microfluidic droplet-based system" (PDF). Lab on a Chip. 4 (4): 316–21. doi:10.1039/b403378g. PMID 15269797.
  93. ^ Wan J, Shi L, Benson B, Bruzek MJ, Anthony JE, Sinko PJ, et al. (September 2012). "Microfluidic generation of droplets with a high loading of nanoparticles". Langmuir. 28 (37): 13143–8. doi:10.1021/la3025952. PMC 3856230. PMID 22934976.
  94. ^ Khan SA, Günther A, Schmidt MA, Jensen KF (September 2004). "Microfluidic synthesis of colloidal silica". Langmuir. 20 (20): 8604–11. doi:10.1021/la0499012. PMID 15379481.
  95. ^ a b c Wiesmann UN, DiDonato S, Herschkowitz NN (October 1975). "Effect of chloroquine on cultured fibroblasts: release of lysosomal hydrolases and inhibition of their uptake". Biochemical and Biophysical Research Communications. 66 (4): 1338–43. doi:10.1016/0006-291X(75)90506-9. PMID 4.
  96. ^ a b Dubinsky S, Zhang H, Nie Z, Gourevich I, Voicu D, Deetz M, Kumacheva E (May 2008). "Microfluidic Synthesis of Macroporous Copolymer Particles". Macromolecules. 41 (10): 3555–3561. Bibcode:2008MaMol..41.3555D. doi:10.1021/ma800300d. ISSN 0024-9297.
  97. ^ Rondeau E, Cooper-White JJ (June 2008). "Biopolymer microparticle and nanoparticle formation within a microfluidic device". Langmuir. 24 (13): 6937–45. doi:10.1021/la703339u. PMID 18510374.
  98. ^ Hong JS, Stavis SM, DePaoli Lacerda SH, Locascio LE, Raghavan SR, Gaitan M (July 2010). "Microfluidic directed self-assembly of liposome-hydrogel hybrid nanoparticles". Langmuir. 26 (13): 11581–8. doi:10.1021/la100879p. PMID 20429539.
  99. ^ Xu JH, Li SW, Tan J, Wang YJ, Luo GS (September 2006). "Controllable preparation of monodisperse O/W and W/O emulsions in the same microfluidic device". Langmuir. 22 (19): 7943–6. doi:10.1021/la0605743. PMID 16952223.
  100. ^ Plamper FA, Richtering W (February 2017). "Functional Microgels and Microgel Systems". Accounts of Chemical Research. 50 (2): 131–140. doi:10.1021/acs.accounts.6b00544. PMID 28186408.
  101. ^ Franssen O, Hennink WE (June 1998). "A novel preparation method for polymeric microparticles without the use of organic solvents". International Journal of Pharmaceutics. 168 (1): 1–7. doi:10.1016/S0378-5173(98)00071-4.
  102. ^ Stenekes RJ, Franssen O, van Bommel EM, Crommelin DJ, Hennink WE (April 1998). "The preparation of dextran microspheres in an all-aqueous system: effect of the formulation parameters on particle characteristics". Pharmaceutical Research. 15 (4): 557–61. doi:10.1023/A:1011925709873. PMID 9587951.
  103. ^ Vladisavljević GT, Williams RA (March 2005). "Recent developments in manufacturing emulsions and particulate products using membranes". Advances in Colloid and Interface Science. 113 (1): 1–20. doi:10.1016/j.cis.2004.10.002. PMID 15763236.
  104. ^ Charcosset C, Fessi H (2011). "Membrane emulsification and microchannel emulsification processes". Reviews in Chemical Engineering. 21 (1): 1–32. doi:10.1515/REVCE.2005.21.1.1.
  105. ^ De Geest BG, Urbanski JP, Thorsen T, Demeester J, De Smedt SC (November 2005). "Synthesis of monodisperse biodegradable microgels in microfluidic devices". Langmuir. 21 (23): 10275–9. doi:10.1021/la051527y. PMID 16262275.
  106. ^ Nisisako T, Torii T, Higuchi T (2004-08-01). "Novel microreactors for functional polymer beads". Chemical Engineering Journal. 7th International Conference on Microreaction Technology. 101 (1): 23–29. doi:10.1016/j.cej.2003.11.019.
  107. ^ Wan, Jiandi (June 2012). "Microfluidic-Based Synthesis of Hydrogel Particles for Cell Microencapsulation and Cell-Based Drug Delivery". Polymers. 4 (2): 1084–1108. doi:10.3390/polym4021084.
  108. ^ Eun YJ, Utada AS, Copeland MF, Takeuchi S, Weibel DB (March 2011). "Encapsulating bacteria in agarose microparticles using microfluidics for high-throughput cell analysis and isolation". ACS Chemical Biology. 6 (3): 260–6. doi:10.1021/cb100336p. PMC 3060957. PMID 21142208.
  109. ^ Lee TY, Choi TM, Shim TS, Frijns RA, Kim SH (September 2016). "Microfluidic production of multiple emulsions and functional microcapsules". Lab on a Chip. 16 (18): 3415–40. doi:10.1039/C6LC00809G. PMID 27470590.
  110. ^ Chen CH, Abate AR, Lee D, Terentjev EM, Weitz DA (2009). "Microfluidic Assembly of Magnetic Hydrogel Particles with Uniformly Anisotropic Structure". Advanced Materials. 21 (31): 3201–3204. doi:10.1002/adma.200900499.
  111. ^ Marquis M, Renard D, Cathala B (April 2012). "Microfluidic generation and selective degradation of biopolymer-based Janus microbeads". Biomacromolecules. 13 (4): 1197–203. doi:10.1021/bm300159u. PMID 22401572.
  112. ^ Rashid M, Kaur V, Hallan SS, Sharma S, Mishra N (July 2016). "Microparticles as controlled drug delivery carrier for the treatment of ulcerative colitis: A brief review". Saudi Pharmaceutical Journal. 24 (4): 458–72. doi:10.1016/j.jsps.2014.10.001. PMC 4908146. PMID 27330377.
  113. ^ Oliveira MB, Mano JF (July 2011). "Polymer-based microparticles in tissue engineering and regenerative medicine". Biotechnology Progress. 27 (4): 897–912. doi:10.1002/btpr.618. hdl:1822/12916. PMID 21584949.
  114. ^ Nisisako T, Torii T (February 2008). "Microfluidic large-scale integration on a chip for mass production of monodisperse droplets and particles". Lab on a Chip. 8 (2): 287–93. doi:10.1039/B713141K. PMID 18231668.
  115. ^ Furniss BS, Hannaford AJ, Smith PW, tatchell AR (1989). Vogel's Textbook of Practical Analytical Chemistry (PDF) (5th ed.). UK: Longman. pp. 156–164. ISBN 978-0-582-46236-6.
  116. ^ Ballinger JT, Shugar GJ (1990). Chemical Technicians' Ready Reference Handbook (3rd ed.). New York: McGraw-Hill. pp. 457–462. ISBN 978-0-07-174592-5.
  117. ^ Morikawa G, Suzuka C, Shoji A, Shibusawa Y, Yanagida A (January 2016). "High-throughput determination of octanol/water partition coefficients using a shake-flask method and novel two-phase solvent system". Journal of Pharmaceutical and Biomedical Analysis. 117: 338–44. doi:10.1016/j.jpba.2015.09.019. PMID 26422471.
  118. ^ Purcell EM (January 1977). "Life at low Reynolds number". American Journal of Physics. 45 (1): 3–11. Bibcode:1977AmJPh..45....3P. doi:10.1119/1.10903. hdl:2433/226838.
  119. ^ Casadevall i Solvas X, deMello A (February 2011). "Droplet microfluidics: recent developments and future applications". Chemical Communications. 47 (7): 1936–42. doi:10.1039/c0cc02474k. PMID 20967373.
  120. ^ Mary P, Studer V, Tabeling P (April 2008). "Microfluidic droplet-based liquid-liquid extraction". Analytical Chemistry. 80 (8): 2680–7. doi:10.1021/ac800088s. PMID 18351786.
  121. ^ Poulsen CE, Wootton RC, Wolff A, deMello AJ, Elvira KS (June 2015). "A Microfluidic Platform for the Rapid Determination of Distribution Coefficients by Gravity-Assisted Droplet-Based Liquid-Liquid Extraction". Analytical Chemistry. 87 (12): 6265–70. doi:10.1021/acs.analchem.5b01061. PMID 25984969.
  122. ^ Alimuddin M, Grant D, Bulloch D, Lee N, Peacock M, Dahl R (August 2008). "Determination of log D via automated microfluidic liquid-liquid extraction". Journal of Medicinal Chemistry. 51 (16): 5140–2. doi:10.1021/jm8005228. PMID 18666772.
  123. ^ Lubej M, Novak U, Liu M, Martelanc M, Franko M, Plazl I (May 2015). "Microfluidic droplet-based liquid-liquid extraction: online model validation". Lab on a Chip. 15 (10): 2233–9. doi:10.1039/c4lc01460j. PMID 25850663.
  124. ^ Wägli P, Chang YC, Hans K, Homsy A, Hvozdara L, Herzig HP, et al. (August 2013). "Microfluidic droplet-based liquid-liquid extraction and on-chip IR spectroscopy detection of cocaine in human saliva". Analytical Chemistry. 85 (15): 7558–65. doi:10.1021/ac401606p. PMID 23815182.
  125. ^ Kang L, Chung BG, Langer R, Khademhosseini A (January 2008). "Microfluidics for drug discovery and development: from target selection to product lifecycle management". Drug Discovery Today. 13 (1–2): 1–13. doi:10.1016/j.drudis.2007.10.003. PMC 2700821. PMID 18190858.
  126. ^ a b Ochoa A, Álvarez-Bohórquez E, Castillero E, Olguin LF (May 2017). "Detection of Enzyme Inhibitors in Crude Natural Extracts Using Droplet-Based Microfluidics Coupled to HPLC". Analytical Chemistry. 89 (9): 4889–4896. doi:10.1021/acs.analchem.6b04988. PMID 28374582.
  127. ^ a b Kim JY, Cho SW, Kang DK, Edel JB, Chang SI, deMello AJ, O'Hare D (September 2012). "Lab-chip HPLC with integrated droplet-based microfluidics for separation and high frequency compartmentalisation". Chemical Communications. 48 (73): 9144–6. doi:10.1039/C2CC33774F. PMID 22871959.
  128. ^ a b Ji J, Nie L, Li Y, Yang P, Liu B (October 2013). "Simultaneous online enrichment and identification of trace species based on microfluidic droplets". Analytical Chemistry. 85 (20): 9617–22. doi:10.1021/ac4018082. PMID 24032421.
  129. ^ Edgar JS, Milne G, Zhao Y, Pabbati CP, Lim DS, Chiu DT (30 March 2009). "Compartmentalization of chemically separated components into droplets". Angewandte Chemie. 48 (15): 2719–22. doi:10.1002/anie.200805396. PMC 2865894. PMID 19142923.
  130. ^ Niu XZ, Zhang B, Marszalek RT, Ces O, Edel JB, Klug DR, deMello AJ (November 2009). "Droplet-based compartmentalization of chemically separated components in two-dimensional separations". Chemical Communications (41): 6159–61. doi:10.1039/b918100h. PMID 19826654.
  131. ^ a b c d Li Q, Pei J, Song P, Kennedy RT (June 2010). "Fraction collection from capillary liquid chromatography and off-line electrospray ionization mass spectrometry using oil segmented flow". Analytical Chemistry. 82 (12): 5260–7. doi:10.1021/ac100669z. PMC 2894538. PMID 20491430.
  132. ^ a b Guetschow ED, Steyer DJ, Kennedy RT (October 2014). "Subsecond electrophoretic separations from droplet samples for screening of enzyme modulators". Analytical Chemistry. 86 (20): 10373–9. doi:10.1021/ac502758h. PMC 4204908. PMID 25233947.
  133. ^ a b c d Draper MC, Niu X, Cho S, James DI, Edel JB (July 2012). "Compartmentalization of electrophoretically separated analytes in a multiphase microfluidic platform". Analytical Chemistry. 84 (13): 5801–8. doi:10.1021/ac301141x. PMID 22656086.
  134. ^ Dishinger JF, Kennedy RT (August 2008). "Multiplexed detection and applications for separations on parallel microchips". Electrophoresis. 29 (16): 3296–305. doi:10.1002/elps.200800067. PMC 2597776. PMID 18702055.
  135. ^ Hassan SU, Morgan H, Zhang X, Niu X (April 2015). "Droplet interfaced parallel and quantitative microfluidic-based separations" (PDF). Analytical Chemistry. 87 (7): 3895–901. doi:10.1021/ac504695w. PMID 25775116.
  136. ^ Jacobson SC, Koutny LB, Hergenroeder R, Moore AW, Ramsey JM (October 1994). "Microchip Capillary Electrophoresis with an Integrated Postcolumn Reactor". Analytical Chemistry. 66 (20): 3472–3476. doi:10.1021/ac00092a027.
  137. ^ Kuhr WG, Monnig CA (June 1992). "Capillary electrophoresis". Analytical Chemistry. 64 (12): 389–407. doi:10.1021/ac00036a021.
  138. ^ a b c d e f Wang X, Yi L, Mukhitov N, Schrell AM, Dhumpa R, Roper MG (February 2015). "Microfluidics-to-mass spectrometry: a review of coupling methods and applications". Journal of Chromatography. A. 1382: 98–116. doi:10.1016/j.chroma.2014.10.039. PMC 4318794. PMID 25458901.
  139. ^ a b McCarley RL, Vaidya B, Wei S, Smith AF, Patel AB, Feng J, et al. (January 2005). "Resist-free patterning of surface architectures in polymer-based microanalytical devices". Journal of the American Chemical Society. 127 (3): 842–3. doi:10.1021/ja0454135. PMID 15656615.
  140. ^ a b c d e Küster SK, Fagerer SR, Verboket PE, Eyer K, Jefimovs K, Zenobi R, Dittrich PS (February 2013). "Interfacing droplet microfluidics with matrix-assisted laser desorption/ionization mass spectrometry: label-free content analysis of single droplets". Analytical Chemistry. 85 (3): 1285–9. doi:10.1021/ac3033189. PMID 23289755.
  141. ^ a b c d Ji J, Nie L, Qiao L, Li Y, Guo L, Liu B, et al. (August 2012). "Proteolysis in microfluidic droplets: an approach to interface protein separation and peptide mass spectrometry". Lab on a Chip. 12 (15): 2625–9. doi:10.1039/c2lc40206h. PMID 22695710.
  142. ^ a b Ho J, Tan MK, Go DB, Yeo LY, Friend JR, Chang HC (May 2011). "Paper-based microfluidic surface acoustic wave sample delivery and ionization source for rapid and sensitive ambient mass spectrometry". Analytical Chemistry. 83 (9): 3260–6. doi:10.1021/ac200380q. PMID 21456580.
  143. ^ a b Liu J, Wang H, Manicke NE, Lin JM, Cooks RG, Ouyang Z (March 2010). "Development, characterization, and application of paper spray ionization". Analytical Chemistry. 82 (6): 2463–71. doi:10.1021/ac902854g. PMID 20158226.
  144. ^ a b Zhu Y, Fang Q (October 2010). "Integrated droplet analysis system with electrospray ionization-mass spectrometry using a hydrophilic tongue-based droplet extraction interface". Analytical Chemistry. 82 (19): 8361–6. doi:10.1021/ac101902c. PMID 20806885.
  145. ^ a b Pei J, Li Q, Lee MS, Valaskovic GA, Kennedy RT (August 2009). "Analysis of samples stored as individual plugs in a capillary by electrospray ionization mass spectrometry". Analytical Chemistry. 81 (15): 6558–61. doi:10.1021/ac901172a. PMC 2846185. PMID 19555052.
  146. ^ a b Lazar IM, Kabulski JL (June 2013). "Microfluidic LC device with orthogonal sample extraction for on-chip MALDI-MS detection". Lab on a Chip. 13 (11): 2055–65. doi:10.1039/c3lc50190f. PMC 4123744. PMID 23592150.
  147. ^ a b Zhong M, Lee CY, Croushore CA, Sweedler JV (May 2012). "Label-free quantitation of peptide release from neurons in a microfluidic device with mass spectrometry imaging". Lab on a Chip. 12 (11): 2037–45. doi:10.1039/c2lc21085a. PMC 3558029. PMID 22508372.
  148. ^ Wang S, Chen S, Wang J, Xu P, Luo Y, Nie Z, Du W (September 2014). "Interface solution isoelectric focusing with in situ MALDI-TOF mass spectrometry". Electrophoresis. 35 (17): 2528–33. doi:10.1002/elps.201400083. PMID 24789497.
  149. ^ Lomasney AR, Yi L, Roper MG (August 2013). "Simultaneous monitoring of insulin and islet amyloid polypeptide secretion from islets of Langerhans on a microfluidic device". Analytical Chemistry. 85 (16): 7919–25. doi:10.1021/ac401625g. PMC 3770151. PMID 23848226.
  150. ^ a b Cristobal G, Arbouet L, Sarrazin F, Talaga D, Bruneel JL, Joanicot M, Servant L (September 2006). "On-line laser Raman spectroscopic probing of droplets engineered in microfluidic devices". Lab on a Chip. 6 (9): 1140–6. doi:10.1039/b602702d. PMID 16929392.
  151. ^ a b Liu N, Aymonier C, Lecoutre C, Garrabos Y, Marre S (2012-11-01). "Microfluidic approach for studying CO2 solubility in water and brine using confocal Raman spectroscopy". Chemical Physics Letters. 551: 139–143. doi:10.1016/j.cplett.2012.09.007.
  152. ^ Ashok PC, Singh GP, Rendall HA, Krauss TF, Dholakia K (April 2011). "Waveguide confined Raman spectroscopy for microfluidic interrogation". Lab on a Chip. 11 (7): 1262–70. doi:10.1039/c0lc00462f. PMID 21225053.
  153. ^ a b c d Chrimes AF, Khoshmanesh K, Stoddart PR, Mitchell A, Kalantar-Zadeh K (July 2013). "Microfluidics and Raman microscopy: current applications and future challenges". Chemical Society Reviews. 42 (13): 5880–906. doi:10.1039/c3cs35515b. hdl:1959.3/316024. PMID 23624774.
  154. ^ Park T, Lee S, Seong GH, Choo J, Lee EK, Kim YS, et al. (April 2005). "Highly sensitive signal detection of duplex dye-labelled DNA oligonucleotides in a PDMS microfluidic chip: confocal surface-enhanced Raman spectroscopic study". Lab on a Chip. 5 (4): 437–42. doi:10.1039/b414457k. PMID 15791342.
  155. ^ Cecchini MP, Hong J, Lim C, Choo J, Albrecht T, Demello AJ, Edel JB (April 2011). "Ultrafast surface enhanced resonance Raman scattering detection in droplet-based microfluidic systems". Analytical Chemistry. 83 (8): 3076–81. doi:10.1021/ac103329b. PMID 21413700.
  156. ^ Kim D, Campos AR, Datt A, Gao Z, Rycenga M, Burrows ND, et al. (July 2014). "Microfluidic-SERS devices for one shot limit-of-detection". The Analyst. 139 (13): 3227–3234. Bibcode:2014Ana...139.3227K. doi:10.1039/c4an00357h. PMC 4067008. PMID 24756225.
  157. ^ Cao C, Zhou D, Chen T, Streets AM, Huang Y (May 2016). "Label-Free Digital Quantification of Lipid Droplets in Single Cells by Stimulated Raman Microscopy on a Microfluidic Platform". Analytical Chemistry. 88 (9): 4931–9. doi:10.1021/acs.analchem.6b00862. PMID 27041129.
  158. ^ a b c d Zhu Y, Fang Q (July 2013). "Analytical detection techniques for droplet microfluidics--a review". Analytica Chimica Acta. 787: 24–35. doi:10.1016/j.aca.2013.04.064. PMID 23830418.
  159. ^ a b c d Jeffries GD, Lorenz RM, Chiu DT (December 2010). "Ultrasensitive and high-throughput fluorescence analysis of droplet contents with orthogonal line confocal excitation". Analytical Chemistry. 82 (23): 9948–54. doi:10.1021/ac102173m. PMC 2995829. PMID 21062029.
  160. ^ a b Cole RH, Gartner ZJ, Abate AR (May 2016). "Multicolor Fluorescence Detection for Droplet Microfluidics Using Optical Fibers". Journal of Visualized Experiments (111): e54010. doi:10.3791/54010. PMC 4942052. PMID 27214249.
  161. ^ a b Li R, Wang Y, Xu H, Fei B, Qin B (November 2017). "Micro-Droplet Detection Method for Measuring the Concentration of Alkaline Phosphatase-Labeled Nanoparticles in Fluorescence Microscopy". Sensors. 17 (11): 2685. doi:10.3390/s17112685. PMC 5712791. PMID 29160812.
  162. ^ Basova EY, Foret F (January 2015). "Droplet microfluidics in (bio)chemical analysis". The Analyst. 140 (1): 22–38. Bibcode:2015Ana...140...22B. doi:10.1039/C4AN01209G. PMID 25295973.
  163. ^ Schmitz CH, Rowat AC, Köster S, Weitz DA (January 2009). "Dropspots: a picoliter array in a microfluidic device". Lab on a Chip. 9 (1): 44–9. doi:10.1039/B809670H. PMID 19209334.
  164. ^ Casadevall i Solvas X, Niu X, Leeper K, Cho S, Chang SI, Edel JB, deMello AJ (December 2011). "Fluorescence detection methods for microfluidic droplet platforms". Journal of Visualized Experiments (58): e3437. doi:10.3791/3437. PMC 3346046. PMID 22215381.
  165. ^ Sakai T, Takeda Y, Mafuné F, Abe M, Kondow T (2003). "Monitoring Growth of Surfactant-Free Nanodroplets Dispersed in Water by Single-Droplet Detection". The Journal of Physical Chemistry B. 107 (13): 2921–2926. doi:10.1021/jp021887j. ISSN 1520-6106.
  166. ^ Luo C, Yang X, Fu Q, Sun M, Ouyang Q, Chen Y, Ji H (May 2006). "Picoliter-volume aqueous droplets in oil: electrochemical detection and yeast cell electroporation". Electrophoresis. 27 (10): 1977–83. doi:10.1002/elps.200500665. PMID 16596709.
  167. ^ a b Liu S, Gu Y, Le Roux RB, Matthews SM, Bratton D, Yunus K, Fisher AC, Huck WT (November 2008). "The electrochemical detection of droplets in microfluidic devices". Lab on a Chip. 8 (11): 1937–42. doi:10.1039/b809744e. PMID 18941696.
  168. ^ Suea-Ngam A, Rattanarat P, Chailapakul O, Srisa-Art M (July 2015). "Electrochemical droplet-based microfluidics using chip-based carbon paste electrodes for high-throughput analysis in pharmaceutical applications". Analytica Chimica Acta. 883: 45–54. doi:10.1016/j.aca.2015.03.008. PMID 26088775.
  169. ^ Karuwan C, Sukthang K, Wisitsoraat A, Phokharatkul D, Patthanasettakul V, Wechsatol W, Tuantranont A (June 2011). "Electrochemical detection on electrowetting-on-dielectric digital microfluidic chip". Talanta. 84 (5): 1384–9. doi:10.1016/j.talanta.2011.03.073. PMID 21641456.
  170. ^ Lindsay S, Vázquez T, Egatz-Gómez A, Loyprasert S, Garcia AA, Wang J (May 2007). "Discrete microfluidics with electrochemical detection". The Analyst. 132 (5): 412–6. Bibcode:2007Ana...132..412L. doi:10.1039/b617631c. PMID 17471386.
  171. ^ Shamsi MH, Choi K, Ng AH, Wheeler AR (February 2014). "A digital microfluidic electrochemical immunoassay". Lab on a Chip. 14 (3): 547–54. doi:10.1039/c3lc51063h. PMID 24292705.
  172. ^ Han Z, Li W, Huang Y, Zheng B (July 2009). "Measuring rapid enzymatic kinetics by electrochemical method in droplet-based microfluidic devices with pneumatic valves". Analytical Chemistry. 81 (14): 5840–5. doi:10.1021/ac900811y. PMID 19518139.
  173. ^ Rackus DG, Shamsi MH, Wheeler AR (August 2015). "Electrochemistry, biosensors and microfluidics: a convergence of fields". Chemical Society Reviews. 44 (15): 5320–40. doi:10.1039/c4cs00369a. PMID 25962356.
  174. ^ a b Itoh D, Sassa F, Nishi T, Kani Y, Murata M, Suzuki H (August 2012). "Droplet-based microfluidic sensing system for rapid fish freshness determination". Sensors and Actuators B: Chemical. 171: 619–26.
  175. ^ Gu S, Lu Y, Ding Y, Li L, Zhang F, Wu Q (September 2013). "Droplet-based microfluidics for dose-response assay of enzyme inhibitors by electrochemical method". Analytica Chimica Acta. 796: 68–74. doi:10.1016/j.aca.2013.08.016. PMID 24016585.
  176. ^ Farzbod A, Moon H (May 2018). "Integration of reconfigurable potentiometric electrochemical sensors into a digital microfluidic platform". Biosensors & Bioelectronics. 106: 37–42. doi:10.1016/j.bios.2018.01.048. PMID 29414086.