Eosin is the name of several fluorescent acidic compounds which bind to and form salts with basic, or eosinophilic, compounds like proteins containing amino acid residues such as arginine and lysine, and stains them dark red or pink as a result of the actions of bromine on eosin. In addition to staining proteins in the cytoplasm, it can be used to stain collagen and muscle fibers for examination under the microscope. Structures that stain readily with eosin are termed eosinophilic. In the field of histology, Eosin Y is the form of eosin used most often as a histologic stain.[1][2]
History and etymology
editEosin was named by its inventor Heinrich Caro after the nickname (Eos) of a childhood friend, Anna Peters.[3] It was commercialized (mainly for the textile industry) in 1874, in the same year when it was invented.[4]
Variants
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There are actually two very closely related compounds commonly referred to as eosin. Most often used is in histology is Eosin Y[1][2] (also known as eosin Y ws, eosin yellowish, Acid Red 87, C.I. 45380, bromoeosine, bromofluoresceic acid, D&C Red No. 22); it has a very slightly yellowish cast. The other eosin compound is Eosin B (eosin bluish, Acid Red 91, C.I. 45400, Saffrosine, Eosin Scarlet, or imperial red); it has a very faint bluish cast. The two dyes are interchangeable, and the use of one or the other is a matter of preference and tradition.
Eosin Y is a tetrabromo derivative of fluorescein.[5] Eosin B is a dibromo dinitro derivative of fluorescein.[6]
Food dye tetraiodofluorescein was historically known as Bluish Eosine,[7] Eosin J[8] or iodo-eosine[9] but is now called erythrosine or Red 3.
Uses
editUse in histology
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Eosin is most often used as a counterstain to hematoxylin in H&E (haematoxylin and eosin) staining. H&E staining is one of the most commonly used techniques in histology. Tissue stained with haematoxylin and eosin shows cytoplasm stained pink-orange and nuclei stained darkly, either blue or purple. Eosin also stains red blood cells intensely red.
For staining, eosin Y is typically used in concentrations of 1 to 5 percent weight by volume, dissolved in water or ethanol.[10] For prevention of mold growth in aqueous solutions, thymol is sometimes added.[11] A small concentration (0.5 percent) of acetic acid usually gives a deeper red stain to the tissue.
It is listed as an IARC class 3 carcinogen.
Other uses
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Eosin is also used as a red dye in inks; however, the molecule, especially that of eosin Y, tends to degrade over time, leaving behind its bromine atoms, hence causing paint incorporating such a dye to obtain a darker brown tinge over time.[12] A notable user of eosin dye was the Post-Impressionist painter Van Gogh.
See also
editReferences
edit- ^ a b Lillie, Ralph Dougall (1977). H. J. Conn's Biological stains (9th ed.). Baltimore: Williams & Wilkins. pp. 692p.
- ^ a b Bancroft, John; Stevens, Alan, eds. (1982). The Theory and Practice of Histological Techniques (2nd ed.). Longman Group Limited.
- ^ Travis, Anthony S (1998). ""Ambitious and Glory Hunting . . . Impractical and Fantastic": Heinrich Caro at BASF". Technology and Culture. 39 (1): 105–115. doi:10.2307/3107005. JSTOR 3107005.
- ^ Journal of the Society of Chemical Industry. Society of Chemical Industry. 1885.
- ^ Its CAS number is and its SMILES structure is O=C5C(Br)=C2O C1=C(Br)C([O-]) =C(Br)C=C1C(C4=C (C([O-])=O)C=C C=C4)=C2C=C3Br.
- ^ Its CAS number is and its SMILES structure is O=C5C(Br)=C2O C1=C(Br)C([O-]) =C([N+]([O-])=O) C=C1C(C4=C(C([O-]) =O)C=CC=C4)=C2 C=C3[N+]([O-])=O.
- ^ Watts, Henry (1881). A Dictionary of Chemistry and the Allied Branches of Other Sciences. Longmans, Green, and Company.
- ^ Hesse, Bernhard Conrad (1912). Coal-tar Colors Used in Food Products. U.S. Government Printing Office.
- ^ Southworth, J.; Bentley, Thomas Leslie James (1927). Photographic Chemicals and Chemistry. Sir I. Pittman.
- ^ "Haematoxylin Eosin (H&E) staining". protocolsonline.com. 11 April 2010. Retrieved 22 April 2018.
- ^ Hitokoto H, Morozumi S, Wauke T, Sakai S, Kurata H (1980). "Inhibitory effects of spices on growth and toxin production of toxigenic fungi". Appl. Environ. Microbiol. 39 (4): 818–22. doi:10.1128/AEM.39.4.818-822.1980. PMC 291425. PMID 6769391.
- ^ a b "Van Gogh's Fading Colors Inspire Scientific Inquiry".