A liposome is an artificially-prepared vesicle composed of a lipid bilayer. The liposome can be used as a vehicle for administration of nutrients and pharmaceutical drugs. Liposomes can be prepared by disrupting biological membranes (such as by sonication).
Liposomes are often composed of phosphatidylcholine-enriched phospholipids and may also contain mixed lipid chains with surfactant properties such as egg phosphatidylethanolamine. A liposome design may employ surface ligands for attaching to unhealthy tissue.
The major types of liposomes are the multilamellar vesicle (MLV), the small unilamellar vesicle (SUV), the large unilamellar vesicle (LUV), and the cochleate vesicle.
Liposomes were first described by British haematologist Alec D Bangham in 1961 (published 1964), at the Babraham Institute, in Cambridge. They were discovered when Bangham and R. W. Horne were testing the institute's new electron microscope by adding negative stain to dry phospholipids. The resemblance to the plasmalemma was obvious, and the microscope pictures served as the first real evidence for the cell membrane being a bilayer lipid structure.
The word liposome derives from two Greek words: lipo ("fat") and soma ("body"); it is so named because its composition is primarily of phospholipid.
A liposome encapsulates a region of aqueous solution inside a hydrophobic membrane; dissolved hydrophilic solutes cannot readily pass through the lipids. Hydrophobic chemicals can be dissolved into the membrane, and in this way liposome can carry both hydrophobic molecules and hydrophilic molecules. To deliver the molecules to sites of action, the lipid bilayer can fuse with other bilayers such as the cell membrane, thus delivering the liposome contents. By making liposomes in a solution of DNA or drugs (which would normally be unable to diffuse through the membrane) they can be (indiscriminately) delivered past the lipid bilayer. A liposome does not necessarily have lipophobic contents, such as water, although it usually does.
Liposomes are used as models for artificial cells. Liposomes can also be designed to deliver drugs in other ways. Liposomes that contain low (or high) pH can be constructed such that dissolved aqueous drugs will be charged in solution (i.e., the pH is outside the drug's pI range). As the pH naturally neutralizes within the liposome (protons can pass through some membranes), the drug will also be neutralized, allowing it to freely pass through a membrane. These liposomes work to deliver drug by diffusion rather than by direct cell fusion.
A similar approach can be exploited in the biodetoxification of drugs by injecting empty liposomes with a transmembrane pH gradient. In this case the vesicles act as sinks to scavenge the drug in the blood circulation and prevent its toxic effect. Another strategy for liposome drug delivery is to target endocytosis events. Liposomes can be made in a particular size range that makes them viable targets for natural macrophage phagocytosis. These liposomes may be digested while in the macrophage's phagosome, thus releasing its drug. Liposomes can also be decorated with opsonins and ligands to activate endocytosis in other cell types.
In addition to gene and drug delivery applications, liposomes can be used as carriers for the delivery of dyes to textiles, pesticides to plants, enzymes and nutritional supplements to foods, and cosmetics to the skin.
Liposomes are also used as outer shells of some microbubble contrast agents used in contrast-enhanced ultrasound.
List of drugs
||The examples and perspective in this section may not represent a worldwide view of the subject. (January 2012)|
As of 2012, 12 drugs with liposomal delivery systems have been approved and five additional liposomal drugs were in clinical trials.
List of clinically approved liposomal drugs
|Name||Trade name||Company||Indication||Liposomal Excipients|
|Liposomal amphotericin B||Abelcet||Enzon||Fungal infections||DMPC and DMPG|
|Liposomal amphotericin B||Ambisome||Gilead Sciences||Fungal and protozoal infections||HSPC, Cholesterol, DSPG|
|Liposomal cytarabine||Depocyt||Pacira (formerly SkyePharma)||Malignant lymphomatous meningitis||DOPC, Cholesterol, DPPG|
|Liposomal daunorubicin||DaunoXome||Gilead Sciences||HIV-related Kaposi’s sarcoma||DSPC, Cholesterol|
|Liposomal doxorubicin||Myocet||Zeneus||Combination therapy with cyclophosphamide in metastatic breast cancer||LIPOVA-E120, Cholesterol|
|Liposomal IRIV vaccine||Epaxal||Crucell||Hepatitis A||LECIVA-S70|
|Liposomal IRIV vaccine||Inflexal V||Berna Biotech||Influenza||LECIVA-S90|
|Liposomal morphine||DepoDur||SkyePharma, Endo||Postsurgical analgesia||DOPC, Cholesterol, DPPG|
|Liposomal verteporfin||Visudyne||QLT, Novartis||Age-related macular degeneration, pathologic myopia, ocular histoplasmosis||Egg PG, DMPC|
|Liposome-proteins SP-B and SP-C||Curosurf||Chiesi Farmaceutici, S.p.A.||pulmonary surfactant for Respiratory Distress Syndrome (RDS)||Leciva-S90|
|Liposome-PEG doxorubicin||Doxil/Caelyx||Ortho Biotech, Schering-Plough||HIV-related Kaposi’s sarcoma, metastatic breast cancer, metastatic ovarian cancer||MPEG-DSPE, HSPC, Cholesterol|
|Micellular estradiol||Estrasorb||Novavax||Menopausal therapy||Soybean oil, Polysorbate80|
|Liposomal vincristine||Marqibo||Spectrum Pharmaceuticals||Acute Lymphoblastic Leukemia (ALL) and Melanoma||Cholesterol and egg sphingomyelin|
Dietary and nutritional supplements
Regarding the use of liposomes as a carrier of dietary and nutritional supplements; until very recently the use of liposomes were primarily directed at targeted drug delivery. However, the versatile abilities of liposomes are now being discovered in other settings. Liposomes are presently being cleverly implemented for the specific oral delivery of certain dietary and nutritional supplements.
A very small number of dietary and nutritional supplement companies are currently pioneering the benefits of this unique science towards this new application. This new direction and employment of liposome science is in part due to the low absorption and bioavailability rates of traditional oral dietary and nutritional tablets and capsules. The low oral bioavailability and absorption of many nutrients is clinically well documented. Therefore the natural encapsulation of lypophilic and hydrophilic nutrients within liposomes has made for a very effective method of bypassing the destructive elements of the gastric system and aiding the encapsulated nutrient to be delivered to the cells and tissues.
It is important to note that certain influential factors have far reaching effects on the percentage of liposome that are yielded in manufacturing. These influences also have an effect on the actual amount of realized liposome entrapment and the actual quality of the liposomes themselves. These are very crucial elements which lead to the long term stability of the liposomes. These complex yet significant factors are the following: (1) The actual manufacturing method and preparation of the liposomes themselves; (2) The constitution, quality, and type of raw phospholipid used in the formulation and manufacturing of the liposomes; (3) The ability to create homogeneous liposome particle sizes that are stable and hold their encapsulated payload. These primary and key elements comprise the foundation of an effective liposome carrier for use in increasing the bioavailability of oral dosages of dietary and nutritional supplements.
- the physicochemical characteristics of the material to be entrapped and those of the liposomal ingredients;
- the nature of the medium in which the lipid vesicles are dispersed
- the effective concentration of the entrapped substance and its potential toxicity;
- additional processes involved during application/delivery of the vesicles;
- optimum size, polydispersity and shelf-life of the vesicles for the intended application; and,
- batch-to-batch reproducibility and possibility of large-scale production of safe and efficient liposomal products
Formation of liposomes and nanoliposomes is not a spontaneous process. Lipid vesicles are formed when phospholipids such as lecithin are placed in water and consequently form one bilayer or a series of bilayers, each separated by water molecules, once enough energy is supplied.
Liposomes can be created by sonicating phosphatidylcholine rich phospholipids in water. Low shear rates create multilamellar liposomes, which have many layers like an onion. Continued high-shear sonication tends to form smaller unilamellar liposomes. In this technique, the liposome contents are the same as the contents of the aqueous phase. Sonication is generally considered a "gross" method of preparation as it can damage the structure of the drug to be encapsulated. Newer methods such as extrusion and Mozafari method  are employed to produce materials for human use.
Further advances in liposome research have been able to allow liposomes to avoid detection by the body's immune system, specifically, the cells of reticuloendothelial system (RES). These liposomes are known as "stealth liposomes", and are constructed with PEG (Polyethylene Glycol) studding the outside of the membrane. The PEG coating, which is inert in the body, allows for longer circulatory life for the drug delivery mechanism. However, research currently seeks to investigate at what amount of PEG coating the PEG actually hinders binding of the liposome to the delivery site. In addition to a PEG coating, most stealth liposomes also have some sort of biological species attached as a ligand to the liposome in order to enable binding via a specific expression on the targeted drug delivery site. These targeting ligands could be monoclonal antibodies (making an immunoliposome), vitamins, or specific antigens. Targeted liposomes can target nearly any cell type in the body and deliver drugs that would naturally be systemically delivered. Naturally toxic drugs can be much less toxic if delivered only to diseased tissues. Polymersomes, morphologically related to liposomes, can also be used this way.
In case of tumor development, certain anticancer drugs such as doxorubicin (Doxil) and daunorubicin are provided through liposomes. Liposomal cisplatin has received orphan drug designation for pancreatic cancer from EMEA.
- Torchilin, V (2006). "Multifunctional nanocarriers". Advanced Drug Delivery Reviews 58 (14): 1532–55. doi:10.1016/j.addr.2006.09.009. PMID 17092599.
- Kimball's Biology Pages, "Cell Membranes."
- Explanation on twst.com commercial page, cf. also Int.Patent PCT/US2008/074543 on p.4, section 0014
- Stryer S. (1981) Biochemistry, 213
- Bangham, A. D.; Horne, R. W. (1964). "Negative Staining of Phospholipids and Their Structural Modification by Surface-Active Agents As Observed in the Electron Microscope". Journal of Molecular Biology 8: 660–668. doi:10.1016/S0022-2836(64)80115-7. PMID 14187392.
- Horne, R. W.; Bangham, A. D.; Whittaker, V. P. (1963). "Negatively Stained Lipoprotein Membranes". Nature 200: 1340. doi:10.1038/2001340a0. PMID 14098499.
- Bangham, A. D.; Horne, R. W.; Glauert, A. M.; Dingle, J. T.; Lucy, J. A. (1962). "Action of saponin on biological cell membranes". Nature 196: 952–955. doi:10.1038/196952a0. PMID 13966357.
- Bertrand, Nicolas; Bouvet, CéLine; Moreau, Pierre; Leroux, Jean-Christophe (2010). "Transmembrane pH-Gradient Liposomes to Treat Cardiovascular Drug Intoxication". ACS Nano 4 (12): 7552–8. doi:10.1021/nn101924a. PMID 21067150.
- Barani, H; Montazer, M (2008). "A review on applications of liposomes in textile processing". Journal of liposome research 18 (3): 249–62. doi:10.1080/08982100802354665. PMID 18770074.
- Meure, LA; Knott, R; Foster, NR; Dehghani, F (2009). "The depressurization of an expanded solution into aqueous media for the bulk production of liposomes". Langmuir : the ACS journal of surfaces and colloids 25 (1): 326–37. doi:10.1021/la802511a. PMID 19072018.
- Yoko Shojia, Hideki Nakashima (2004). "Nutraceutics and Delivery Systems". Journal of Vitamin Delivery Targeting.
- Williamson, G; Manach, C (2005). "Bioavailability and bioefficacy of polyphenols in humans. II. Review of 93 intervention studies". The American journal of clinical nutrition 81 (1 Suppl): 243S–255S. PMID 15640487.
- Bender, David A. (2003). Nutritional Biochemistry of Vitamins. Cambridge, U.K.
- Szoka Jr, F; Papahadjopoulos, D (1980). "Comparative properties and methods of preparation of lipid vesicles (liposomes)". Annual review of biophysics and bioengineering 9: 467–508. doi:10.1146/annurev.bb.09.060180.002343. PMID 6994593.
- Chaize, B; Colletier, JP; Winterhalter, M; Fournier, D (2004). "Encapsulation of enzymes in liposomes: High encapsulation efficiency and control of substrate permeability". Artificial cells, blood substitutes, and immobilization biotechnology 32 (1): 67–75. doi:10.1081/BIO-120028669. PMID 15027802.
- Gomezhens, A; Fernandezromero, J (2006). "Analytical methods for the control of liposomal delivery systems". TrAC Trends in Analytical Chemistry 25 (2): 167. doi:10.1016/j.trac.2005.07.006.
- Mozafari, MR; Johnson, C; Hatziantoniou, S; Demetzos, C (2008). "Nanoliposomes and their applications in food nanotechnology". Journal of liposome research 18 (4): 309–27. doi:10.1080/08982100802465941. PMID 18951288.
- Mozafari, M.R. and Mortazavi, S.M. (2005). Nanoliposomes: From Fundamentals to Recent Developments. Oxford, UK: Trafford Publishing Ltd.
- Colas, JC; Shi, W; Rao, VS; Omri, A; Mozafari, MR; Singh, H (2007). "Microscopical investigations of nisin-loaded nanoliposomes prepared by Mozafari method and their bacterial targeting". Micron (Oxford, England : 1993) 38 (8): 841–7. doi:10.1016/j.micron.2007.06.013. PMID 17689087.
|Wikimedia Commons has media related to Liposomes.|