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Fluorescein

From Wikipedia, the free encyclopedia
(Redirected from Uranin)
Fluorescein
Skeletal formula
Ball-and-stick model
Sample of dark red powder
Names
Pronunciation /flʊəˈrɛsi.ɪn, flʊəˈrɛsiːn/
IUPAC name
3′,6′-Dihydroxy-3H-spiro[2-benzofuran-1,9′-xanthen]-3-one
Other names
Resorcinolphthalein, C.I. 45350, solvent yellow 94, D&C yellow no. 7, angiofluor, Japan yellow 201, soap yellow
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.017.302 Edit this at Wikidata
EC Number
  • 219-031-8
KEGG
MeSH Fluorescein
UNII
  • InChI=1S/C20H12O5/c21-11-5-7-15-17(9-11)24-18-10-12(22)6-8-16(18)20(15)14-4-2-1-3-13(14)19(23)25-20/h1-10,21-22H checkY
    Key: GNBHRKFJIUUOQI-UHFFFAOYSA-N checkY
  • InChI=1/C20H12O5/c21-11-5-7-15-17(9-11)24-18-10-12(22)6-8-16(18)20(15)14-4-2-1-3-13(14)19(23)25-20/h1-10,21-22H
    Key: GNBHRKFJIUUOQI-UHFFFAOYAZ
  • C12C=CC([O-])=CC=1OC3=CC(=O)C=CC3=C2c4ccccc4C(O)=O
Properties
C20H12O5
Molar mass 332.311 g·mol−1
Melting point 314 to 316 °C (597 to 601 °F; 587 to 589 K)
Slightly
Pharmacology
S01JA01 (WHO)
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
H319
P305, P338, P351
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X markN verify (what is checkYX markN ?)

Fluorescein is an organic compound and dye based on the xanthene tricyclic structural motif, formally belonging to triarylmethane dyes family. It is available as a dark orange/red powder, slightly soluble in water and alcohol. It is used as a fluorescent tracer in many applications.[1]

The color of its aqueous solutions is green by reflection and orange by transmission, and its spectral properties are dependent on pH of the solution.[2][3] This can be noticed in bubble levels, for example, in which fluorescein is added as a colorant to the alcohol filling the tube, in order to increase the visibility of the air bubble contained within. More concentrated solutions of fluorescein can even appear red because, under these conditions, nearly all incident emission is re-absorbed by the solution.[3]

It is on the World Health Organization's List of Essential Medicines.[4]

Uses

[edit]

Fluorescein sodium, the sodium salt of fluorescein, is used extensively as a diagnostic tool in the field of ophthalmology and optometry, where topical fluorescein is used in the diagnosis of globe rupture,[5] corneal abrasions, corneal ulcers and herpetic corneal infections.[6] It is also used in rigid gas permeable contact lens fitting to evaluate the tear layer under the lens.[7] It is available as sterile single-use sachets containing lint-free paper applicators soaked in fluorescein sodium solution or as sterile single-use eye drops.[8]

The thyroxine ester of fluorescein is used to quantify the thyroxine concentration in blood.[1]

Fluorescein is also known as a color additive (D&C Yellow no. 7). The disodium salt form of fluorescein is known as uranine or D&C Yellow no. 8.[9] Fluorescein is a precursor to the red dye eosin Y by bromination.[1]

Safety

[edit]

Oral and intravenous use of fluorescein can cause adverse reactions, including nausea, vomiting, hives, acute hypotension, anaphylaxis and related anaphylactoid reaction,[10][11] causing cardiac arrest[12] and sudden death due to anaphylactic shock.[13][14]

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,[15][16] including one case of anaphylaxis with cardiac arrest (resuscitated) following topical use in an eye drop.[12] Reported rates of adverse reactions vary from 1% to 6%.[17][18][19][20] 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.[19] The risk can be reduced with prophylactic use of antihistamines and prompt emergency management of any ensuing anaphylaxis.[21][22] A simple prick test may help to identify persons at greatest risk of adverse reaction.[20]

Chemistry

[edit]
Fluorescein under UV illumination
Fluorescence excitation and emission spectra of fluorescein

The fluorescence of this molecule is very intense; for the deprotonated form in basic solution, peak excitation occurs at 495 nm and peak emission at 520 nm.[citation needed][23]

Fluorescein has a pKa of 6.4,[2] and its ionization equilibrium leads to pH-dependent absorption and emission over the range of 5 to 9. 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.[24] The lifetimes can be recovered using time-correlated single photon counting or phase-modulation fluorimetry.[25] Upon exhaustive irradiation with visible light, fluorescein decomposes to release phthalic and formic acids and carbon monoxide, effectively acting as a photoCORM. The remaining resorcinol rings react with singlet oxygen formed in situ to give oxidized, ring-opened products.[26]

Fluorescein has an isosbestic point (equal absorption for all pH values) at 460 nm.[27]

Derivatives

[edit]
Fluorescein isothiocyanate and 6-FAM phosphoramidite

Many derivatives of fluorescein are known. These include fluorescein isothiocyanate 1 and succinimidyl ester modified fluorescein. Fluorescein isothiocyanate, often abbreviated as FITC, features an isothiocyanate group (−N=C=S) substituent. FITC reacts with the amine groups of many biologically relevant compounds, including intracellular proteins, to form a thiourea linkage.[28] Succinimidyl ester modified fluorescein, also known as NHS-fluorescein, is a common amine-reactive derivative which yields amide adducts that are more stable than the aforementioned thioureas. Other useful reagents include carboxyfluorescein, carboxyfluorescein succinimidyl ester, pentafluorophenyl esters (PFP) and tetrafluorophenyl esters (TFP).

In oligonucleotide synthesis, several phosphoramidite reagents containing protected fluorescein, e.g. 6-FAM phosphoramidite 2, are used for the preparation of fluorescein-labeled oligonucleotides.[29]

The extent to which fluorescein dilaurate is broken down to yield lauric acid can be detected as a measure of pancreatic esterase activity.[30]

Synthesis

[edit]

Approximately 250 tons were produced in the year 2000. The method involves the fusion of phthalic anhydride and resorcinol,[1] similar to the route described by Adolf von Baeyer in 1871.[31] In some cases, acids such as zinc chloride and methanesulfonic acid are employed to accelerate the Friedel-Crafts reaction.[32][33]

The mechanism of the reaction when undertaken with a strong acid such as sulfuric acid is proposed to begin with attack of protonated phthalic anhydride on the resorcinol.

Research

[edit]

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.[23] In water, fluorescein has an absorption maximum at 494 nm and emission maximum of 512 nm. Amongst its major uses in the sciences, it is used as a methylated spirit dye in Australia and New Zealand.[34]

Biosciences

[edit]

In cellular biology, the isothiocyanate derivative of fluorescein is often used to label and track cells in fluorescence microscopy applications, such as flow cytometry.[35] 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.[35] This application is common in yeast display.[36]

Fluorescein can also be conjugated to nucleoside triphosphates and incorporated into a probe enzymatically for in situ hybridisation.[37] The use of fluorescein amidite, shown below right, allows one to synthesize labeled oligonucleotides for the same purpose.[38] Another technique, termed molecular beacons, makes use of synthetic fluorescein-labeled oligonucleotides.[39] 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.[40]

Fluorescein drops being instilled for an eye examination

Intravenous or oral fluorescein is used in fluorescein angiography in research and to diagnose and categorize vascular disorders including retinal disease, macular degeneration, diabetic retinopathy, inflammatory intraocular conditions, and intraocular tumors.[23] It is also being used increasingly during surgery for brain and spine tumors.[41]

Diluted fluorescein dye has been used to localise multiple muscular ventricular septal defects during open heart surgery and confirm the presence of any residual defects.[42]

The Gemini 4 spacecraft releases dye into the water, to aid location after splashdown, June 1965.

Earth sciences

[edit]

Fluorescein is used as a conservative flow tracer in hydrological tracer tests, to help in understanding of water flow of both surface waters and groundwater and observe areas of contamination or obstruction in these systems.[43] The dye can also be added to rainwater in environmental testing simulations to aid in locating and analyzing any water leaks.[44] As fluorescein solution changes its color depending on concentration, it has been used as a tracer in evaporation experiments.[45]

Fluorescein dye solutions, typically 15% active, are commonly used as an aid in leak detection during hydrostatic testing of subsea oil and gas pipelines and other subsea infrastructures. Leaks can be detected by divers or ROVs carrying an ultraviolet light.[46]

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 local wildlife.[47]

Plant science

[edit]

In plant science, fluorescein and other fluorescent dyes have been used to monitor and study plant vasculature, particularly the xylem, which is the main water transportation pathway in plants. This is because fluorescein is xylem-mobile and unable to cross plasma membranes, making it particularly useful in tracking water movement through the xylem.[48] Fluorescein can be introduced to a plant's veins through the roots or a cut stem. The dye is able to be taken up into the plant the same way as water and moves from the roots to the top of the plant due to a transpirational pull.[49] The fluorescein that has been taken up into the plant can be visualized under a fluorescent microscope.

See also

[edit]

References

[edit]
  1. 1 2 3 4 Gessner, Thomas; Mayer, Udo (2000). "Triarylmethane and Diarylmethane Dyes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a27_179. ISBN 978-3-527-30673-2.
  2. 1 2 Sjöback, Robert; Nygren, Jan; Kubista, Mikael (1995-06-01). "Absorption and fluorescence properties of fluorescein". Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 51 (6): L7–L21. Bibcode:1995AcSpA..51L...7S. doi:10.1016/0584-8539(95)01421-P. ISSN 1386-1425.
  3. 1 2 Le Guern, Florent; Mussard, Vanessa; Gaucher, Anne; Rottman, Martin; Prim, Damien (2020-12-03). "Fluorescein Derivatives as Fluorescent Probes for pH Monitoring along Recent Biological Applications". International Journal of Molecular Sciences. 21 (23) 9217. doi:10.3390/ijms21239217. ISSN 1422-0067. PMC 7729466. PMID 33287208.
  4. ↑ World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
  5. ↑ Zhou, Yujia; DiSclafani, Mark; Jeang, Lauren; Shah, Ankit A (2022-08-10). "Open Globe Injuries: Review of Evaluation, Management, and Surgical Pearls". Clinical Ophthalmology. 16: 2545–2559. doi:10.2147/OPTH.S372011. ISSN 1177-5467. PMC 9379121. PMID 35983163.
  6. ↑ OD, By Bisant A. Labib. "Reach for the Dye". www.reviewofoptometry.com. Retrieved 2026-06-28.
  7. ↑ Ulrich, Bret; Haderlie, Scott; Paxman, Paul; Anderson, Brian (1991-05-01). "The use of fluorescein patterns as a guide in fitting rigid gas permeable contact lenses". Repository. Retrieved 2026-06-28.
  8. ↑ "New Drugs". Can Med Assoc J. 80 (12): 997–998. 1959. PMC 1831125. PMID 20325960.
  9. ↑ "Fluorescein". www.acs.org. 2013. Retrieved 2026-06-28.
  10. ↑ "The diagnosis and management of anaphylaxis. Joint Task Force on Practice Parameters, American Academy of Allergy, Asthma and Immunology, American College of Allergy, Asthma and Immunology, and the Joint Council of Allergy, Asthma and Immunology" (PDF). The Journal of Allergy and Clinical Immunology. 101 (6 Pt 2): S465–528. 1998. doi:10.1016/S0091-6749(18)30566-9. PMID 9673591. Archived (PDF) from the original on 2015-07-24.
  11. ↑ "The diagnosis and management of anaphylaxis: an updated practice parameter". www.guideline.gov. Archived from the original on 2007-08-05. Retrieved 2026-06-28.
  12. 1 2 El Harrar, N; Idali, B; Moutaouakkil, S; El Belhadji, M; Zaghloul, K; Amraoui, A; Benaguida, M (1996). "Anaphylactic shock caused by application of fluorescein on the ocular conjunctiva". Presse Médicale. 25 (32): 1546–7. PMID 8952662.
  13. ↑ Fineschi V, Monasterolo G, Rosi R, Turillazzi E (1999). "Fatal anaphylactic shock during a fluorescein angiography". Forensic Sci. Int. 100 (1–2): 137–42. doi:10.1016/S0379-0738(98)00205-9. PMID 10356782.
  14. ↑ Hitosugi M, Omura K, Yokoyama T, Kawato H, Motozawa Y, Nagai T, Tokudome S (2004). "An autopsy case of fatal anaphylactic shock following fluorescein angiography: a case report". Med Sci Law. 44 (3): 264–5. doi:10.1258/rsmmsl.44.3.264. PMID 15296251. S2CID 71681503.
  15. ↑ Kinsella FP, Mooney DJ (1988). "Anaphylaxis following oral fluorescein angiography". Am. J. Ophthalmol. 106 (6): 745–6. doi:10.1016/0002-9394(88)90716-7. PMID 3195657.
  16. ↑ Gómez-Ulla F, Gutiérrez C, Seoane I (1991). "Severe anaphylactic reaction to orally administered fluorescein". Am. J. Ophthalmol. 112 (1): 94. doi:10.1016/s0002-9394(14)76222-1. PMID 1882930.
  17. ↑ Kwan AS, Barry C, McAllister IL, Constable I (2006). "Fluorescein angiography and adverse drug reactions revisited: the Lions Eye experience". Clin. Experiment. Ophthalmol. 34 (1): 33–8. doi:10.1111/j.1442-9071.2006.01136.x. PMID 16451256. S2CID 32809716.
  18. ↑ Jennings BJ, Mathews DE (1994). "Adverse reactions during retinal fluorescein angiography". J Am Optom Assoc. 65 (7): 465–71. PMID 7930354.
  19. 1 2 Kwiterovich KA, Maguire MG, Murphy RP, Schachat AP, Bressler NM, Bressler SB, Fine SL (1991). "Frequency of adverse systemic reactions after fluorescein angiography. Results of a prospective study". Ophthalmology. 98 (7): 1139–42. doi:10.1016/s0161-6420(91)32165-1. PMID 1891225.
  20. 1 2 Matsuura M, Ando F, Fukumoto K, Kyogane I, Torii Y, Matsuura M (1996). "[Usefulness of the prick test for anaphylactoid reaction in intravenous fluorescein administration]". Nippon Ganka Gakkai Zasshi (in Japanese). 100 (4): 313–7. PMID 8644545.
  21. ↑ Ellis PP, Schoenberger M, Rendi MA (1980). "Antihistamines as prophylaxis against side reactions to intravenous fluorescein". Trans Am Ophthalmol Soc. 78: 190–205. PMC 1312139. PMID 7257056.
  22. ↑ Yang CS, Sung CS, Lee FL, Hsu WM (2007). "Management of anaphylactic shock during intravenous fluorescein angiography at an outpatient clinic". J Chin Med Assoc. 70 (8): 348–9. doi:10.1016/S1726-4901(08)70017-0. PMID 17698436.
  23. 1 2 3 PubChem. "Fluorescein". pubchem.ncbi.nlm.nih.gov. Retrieved 2026-06-28.
  24. ↑ "pH dependence of the fluorescence lifetime of enhanced yellow fluorescent protein in solution and cells". Journal of Photochemistry and Photobiology A: Chemistry. 235: 65–71. 2012-05-01. doi:10.1016/j.jphotochem.2012.02.016. ISSN 1010-6030.
  25. ↑ Datta, Rupsa; Heaster, Tiffany M.; Sharick, Joe T.; Gillette, Amani A.; Skala, Melissa C. (2020). "Fluorescence lifetime imaging microscopy: fundamentals and advances in instrumentation, analysis, and applications". Journal of Biomedical Optics. 25 (7): 1–43. doi:10.1117/1.JBO.25.7.071203. ISSN 1560-2281. PMC 7219965. PMID 32406215.
  26. ↑ Martínek, Marek; Ludvíková, Lucie; Šranková, Mária; Navrátil, Rafael; Muchová, Lucie; Huzlík, Jiří; Vítek, Libor; Klán, Petr; Šebej, Peter (2022-11-03). "Common xanthene fluorescent dyes are visible-light activatable CO-releasing molecules". Organic & Biomolecular Chemistry. 21 (1): 93–97. doi:10.1039/D2OB01823C. ISSN 1477-0539. PMID 36326159. S2CID 253266074.
  27. ↑ "Fluorescein *CAS 2321-07-5* | AAT Bioquest". www.aatbio.com. Retrieved 2026-06-28.
  28. ↑ "Fluorescent Probes". www.sciencedirect.com. doi:10.1016/B978-0-12-382239-0.00010-8. Retrieved 2026-06-28.
  29. ↑ Brush, C. K. "Fluorescein Labelled Phosphoramidites". U.S. patent 5,583,236. Priority date July 19, 1991.
  30. ↑ Kay, G.; Hine, P.; Braganza, J. (1982). "The pancreolauryl test. A method of assessing the combined functional efficacy of pancreatic esterase and bile salts in vivo?". Digestion. 24 (4): 241–245. doi:10.1159/000198803. ISSN 0012-2823. PMID 7152148.
  31. ↑ Berichte der Deutschen Chemischen Gesellschaft (in German). Verlag Chemie. 1871.
  32. ↑ Sun, W. C.; Gee, K. R.; Klaubert, D. H.; Haugland, R. P. (1997). "Synthesis of Fluorinated Fluoresceins". The Journal of Organic Chemistry. 62 (19): 6469–6475. doi:10.1021/jo9706178.
  33. ↑ Burgess, Kevin; Ueno, Yuichiro; Jiao, Guan-Sheng (2004). "Preparation of 5- and 6-Carboxyfluorescein". Synthesis. 2004 (15): 2591–2593. doi:10.1055/s-2004-829194.
  34. ↑ "Ethanol: Human health tier II assessment" (PDF). 2014-02-07.
  35. 1 2 Eggleton, Paul; Nissim, Ahuva; Ryan, Brent J.; Whiteman, Matthew; Winyard, Paul G. (2013-04-01). "Detection and isolation of human serum autoantibodies that recognize oxidatively modified autoantigens". Free Radical Biology and Medicine. 57: 79–91. doi:10.1016/j.freeradbiomed.2012.11.006. ISSN 0891-5849.
  36. ↑ Chao, Ginger; Lau, Wai L.; Hackel, Benjamin J.; Sazinsky, Stephen L.; Lippow, Shaun M.; Wittrup, K. Dane (2006). "Isolating and engineering human antibodies using yeast surface display". Nature Protocols. 1 (2): 755–768. doi:10.1038/nprot.2006.94. ISSN 1750-2799. PMID 17406305.
  37. ↑ Wiegant, Joop; Ried, Thomas; Nederlof, Petra M.; Ploeg, Mels Van der; Tanke, Hans J.; Raap, Anton K. (1991). "In situ hybridisation with fluoresceinated DNA". Nucleic Acids Research. 19 (12): 3237–3241. doi:10.1093/nar/19.12.3237. ISSN 0305-1048. PMC 328316. PMID 2062640.
  38. ↑ "FAM Phosphoramidite: A Key Reagent for Fluorescently Labeled Oligonucleotide Synthesis". FAM Phosphoramidite: A Key Reagent for Fluorescently Labeled Oligonucleotide Synthesis. Retrieved 2026-06-28.
  39. ↑ Monroy-Contreras, Ricardo; Vaca, Luis (2011). "Molecular beacons: powerful tools for imaging RNA in living cells". Journal of Nucleic Acids. 2011 741723. doi:10.4061/2011/741723. ISSN 2090-021X. PMC 3163130. PMID 21876785.
  40. ↑ Noga E. J.; Udomkusonsri P. (2002). "Fluorescein: A Rapid, Sensitive, Nonlethal Method for Detecting Skin Ulceration in Fish" (PDF). Vet Pathol. 39 (6): 726–731(6). doi:10.1354/vp.39-6-726. PMID 12450204. S2CID 46010136. Archived from the original (PDF) on 2007-09-28. Retrieved 2007-07-16.
  41. ↑ Cardali, Salvatore Massimiliano; Ricciardo, Giuseppe; Garufi, Giada; Raffa, Giovanni; Messineo, Francesco; Scalia, Gianluca; Conti, Alfredo; Germanò, Antonino (2022). "Fluorescein-guided surgery for intradural spinal tumors: A single-center experience". Brain and Spine. 2 100908. doi:10.1016/j.bas.2022.100908. PMC 9560644. PMID 36248155.
  42. ↑ Mathew, Thomas (2014). "Use of Fluorescein Dye to Identify Residual Defects". Ann Thorac Surg. 97 (1): e27-8. doi:10.1016/j.athoracsur.2013.10.059. ISSN 0003-4975. PMID 24384220.
  43. ↑ Campos, Carlos J. A.; Tremblay, Louis A.; Champeau, Olivier; Goblick, Gregory (2026-03-03). "Fluorescent Dyes in Hydrological Tracing: Application Methods, Ecotoxicological Effects, and Safe Application Levels". Journal of Xenobiotics. 16 (2): 45. doi:10.3390/jox16020045. ISSN 2039-4713. PMC 13010594. PMID 41874116.
  44. ↑ "Products/Fluorescein - Alfa Chemistry". www.alfa-chemistry.com. Retrieved 2026-06-28.
  45. ↑ Käss, W. Tracing Technique in Geohydrology. Rotterdam: Balkema.
  46. ↑ McStay, D; Kerlin, J; Acheson, R (2007-07-01). "An optical sensor for the detection of leaks from subsea pipelines and risers". Journal of Physics: Conference Series. 76 012009. doi:10.1088/1742-6596/76/1/012009. ISSN 1742-6588.
  47. ↑ The Story Behind Dyeing the River Green. Greenchicagoriver.com. Retrieved on 2014-08-28.
  48. ↑ Salih, Anya; Tjoelker, Mark G.; Renard, Justine; Pfautsch, Sebastian (2015-03-01). "Phloem as Capacitor: Radial Transfer of Water into Xylem of Tree Stems Occurs via Symplastic Transport in Ray Parenchyma". Plant Physiology. 167 (3): 963–971. doi:10.1104/pp.114.254581. ISSN 0032-0889. PMC 4348778. PMID 25588734.
  49. ↑ Duran-Nebreda S, Bassel G (July 2017). "Fluorescein Transport Assay to Assess Bulk Flow of Molecules Through the Hypocotyl in Arabidopsis thaliana". Bio-Protocol. 8 (7) e2791. doi:10.21769/bioprotoc.2791. PMC 8275252. PMID 34286014.
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