Fluorescein

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Fluorescein
Other names	Fluorescein, resorcinolphthalein, C.I. 45350, solvent yellow 94, D & C yellow no. 7, angiofluor, Japan yellow 201, soap yellow, Pyoverdin
Identifiers
CAS number	[2321-07-5]
PubChem	16850
EC number	219-031-8
MeSH	Fluorescein
SMILES	OC(C1=C(C(C(C=CC(O)=C3) =C3O2)=C4C2=CC(C=C4)=O)C=CC=C1)=O
Properties
Molecular formula	C20H12O5
Molar mass	332.306 g/mol
Melting point	314 - 316 °C
Solubility in water	Slightly
Hazards
S-phrases	S26 S36
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox references

Fluorescein is a fluorophore commonly used in microscopy, in a type of dye laser as the gain medium, in forensics and serology to detect latent blood stains, and in dye tracing. Fluorescein has an absorption maximum at 494 nm and emission maximum of 521 nm (in water). Also, fluorescein has an isosbestic point (equal absorption for all pH values) at 460 nm. Fluorescein is also known as a color additive (D&C Yellow no. 7). The disodium salt form of fluorescein is known as D&C Yellow no. 8.

Contents 1 Chemical and physical properties 2 Derivatives 3 Synthesis 4 Applications 4.1 Uses in river systems 4.2 Biochemical research 4.3 Health care applications 5 Safety 6 See also 7 References 8 External links

[edit] Chemical and physical properties

The fluorescence of this molecule is very high, and excitation occurs at 494 nm and emission at 521.

Fluorescein has a pK_a of 6.4 and its ionization equilibrium leads to pH-dependent absorption and emission over the range of 5 to 9. Also, the fluorescence lifetimes of the protonated and deprotonated forms of fluorescein are approximately 3 and 4 ns, which allows for pH determination from non-intensity based measurements. The lifetimes can be recovered using time-correlated single photon counting or phase-modulation fluorimetry.

[edit] Derivatives

There are many fluorescein derivatives, for example fluorescein isothiocyanate, often abbreviated as FITC. FITC is the original fluorescein molecule functionalized with an isothiocyanate group (-N=C=S), replacing a hydrogen atom on the bottom ring of the structure. This derivative is reactive towards amine groups on proteins inside cells. A succinimidyl-ester functional group attached to the fluorescein core, creating NHS-fluorescein, forms another common amine reactive derivative.

Other green dyes include Oregon Green, Tokyo Green, SNAFL, and carboxynaphthofluorescein. These dyes, along with newer fluors such as Alexa 488 and DyLight 488, have been tailored for various chemical and biological applications where higher photostability, different spectral characteristics, or different attachment groups are needed.

[edit] Synthesis

Fluorescein was first synthesized by Adolf von Baeyer in 1871. It can be prepared from phthalic anhydride and resorcinol in the presence of zinc chloride via the Friedel-Crafts reaction.

A second method to prepare fluorescein uses methanesulfonic acid as a Brønsted acid catalyst. This route has a high yield under milder conditions. ^{[1] [2]}

[edit] Applications

[edit] Uses in river systems

One of its more recognizable uses was in the Chicago River, where fluorescein was the first substance used to dye the river green on St. Patrick's Day in 1962. In 1966 environmentalists forced a change to a vegetable based dye to protect the thousands of goldfish that populate the river.^{[citation needed]}

Other uses of fluorescein include using it as a water-soluble dye added to rainwater in environmental testing simulations to aid in locating and analyzing any water leaks, and in Australia and New Zealand as a methylated spirit dye.

[edit] Biochemical research

In cellular biology, the isothiocyanate derivative of fluorescein is often used to label and track cells in fluorescence microscopy applications (for example, flow cytometry). Additional biologically active molecules (such as antibodies) may also be attached to fluorescein, allowing biologists to target the fluorophore to specific proteins or structures within cells. This application is common in yeast display.

Fluorescein can also be conjugated to nucleoside triphosphates and incorporated into a probe for in situ hybridisation. Fluorescein-labelled probes can be imaged using FISH, or targeted by antibodies using immunohistochemistry. The latter is a common alternative to digoxigenin, and the two are used together for labelling two genes in one sample ^[3].

[edit] Health care applications

Fluorescein sodium is used extensively as a diagnostic tool in the field of ophthalmology and optometry, where topical fluorescein is used in the diagnosis of corneal abrasions, corneal ulcers and herpetic corneal infections. It is also used in rigid gas permeable contact lens fitting to evaluate the tear layer under the lens.

Intravenous or oral fluorescein is used in fluorescein angiography in research and to diagnose and categorize vascular disorders in e.g. legs, including retinal disease macular degeneration, diabetic retinopathy, inflammatory intraocular conditions, and intraocular tumors , and increasingly during surgery for brain tumors.

[edit] Safety

Topical, oral, and intravenous use of fluorescein can cause adverse reactions including nausea, vomiting, hives, acute hypotension, anaphylaxis and related anaphylactoid reaction,^[4] cardiac arrest,^[5] and sudden death.^[6][7]

The most common adverse reaction is nausea, due to a difference in the pH from the body and the pH of the sodium fluorescein dye.^{[citation needed]} The nausea usually is transient and subsides quickly. Hives can range from a minor annoyance to severe, and a single dose of antihistamine may give complete relief. Anaphylactic shock and subsequent cardiac arrest and sudden death are very rare but because they occur within minutes, a health care provider who uses fluorescein should be prepared to perform emergency resuscitation.

Intravenous use has the most reported adverse reactions, including sudden death, but this may reflect greater use rather than greater risk. Both oral and topical uses have been reported to cause anaphylaxis,^[8][9] including one case of anaphylaxis with cardiac arrest (resuscitated) following topical use in an eye drop.^[5] Reported rates of adverse reactions vary from 1% to 6%^{[10][11][12][13]} The higher rates may reflect study populations that include a higher percentage of persons with prior adverse reactions. The risk of an adverse reaction is 25 times higher if the person has had a prior adverse reaction.^[12] The risk can be reduced with prior (prophylactic) use of antihistamines^[14] and prompt emergency management of any ensuing anaphylaxis.^[15] A simple prick test may help to identify persons at greatest risk of adverse reaction.^[13]

[edit] See also

• Chemical derivatives of fluorescein:
  • Eosin
  • Carboxyfluorescein
  • Fluorescein isothiocyanate
  • Erythrosine
  • DyLight Fluor, a product line of fluorescent dyes
• Pseudomonas aeruginosa, a bacterium that secretes fluorescein
• Fluorescein diacetate hydrolysis, a biochemistry laboratory test
• Other dyes:
  • Methylene blue

[edit] References

[edit] External links

• Absorption and Emission Spectra of Fluorescein in Ethanol and Basic Ethanol at OGI School of Science and Engineering
• Fluorescein Ionization Equilibria at Invitrogen
• MSDS at Oxford University
• Absorption spectra and fluorescence emission spectra