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Trypan blue is an azo dye that is used as a dye-stuff. It is a direct dye for cotton textiles.[3] In biosciences, it is used as vital stain to selectively colour dead tissues or cells blue.

Trypan blue
TrypanBlueSalt.png
Names
IUPAC name
(3Z,3'Z)-3,3'-[(3,3'-dimethylbiphenyl-4,4'-diyl)di(1Z)hydrazin-2-yl-1-ylidene]bis(5-amino-4-oxo-3,4-dihydronaphthalene-2,7-disulfonic acid)
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.000.715
KEGG
UNII
Properties
C34H24N6Na4O14S4
Molar mass 872.88
Appearance deep blue in aqueous solution[1]
Melting point > 300 °C (572 °F; 573 K)
<0.1 mg/mL in water [2]
Solubility 20 mg/mL in methyl Cellosolve, and 0.6 mg/mL in ethanol
Hazards
Lethal dose or concentration (LD, LC):
6200 mg/kg (oral, rat)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Live cells or tissues with intact cell membranes are not coloured. Since cells are very selective in the compounds that pass through the membrane, in a viable cell trypan blue is not absorbed; however, it traverses the membrane in a dead cell. Hence, dead cells appear as a distinctive blue colour under a microscope. Since live cells are excluded from staining, this staining method is also described as a dye exclusion method. This dye may be a cause of certain birth defects, such as encephalocele.[citation needed]

Contents

Background and chemistryEdit

Trypan blue is derived from toluidine, that is, any of several isomeric bases, C14H16N2, derived from toluene. Trypan blue is so-called because it can kill trypanosomes, the parasites that cause sleeping sickness. An analog of trypan blue, suramin, is used pharmacologically against trypanosomiasis. Trypan blue is also known as diamine blue and Niagara blue.

The extinction coefficient for trypan blue is 6⋅104 M−1 cm−1 at 607 nm in methanol.[4]

Trypan red and trypan blue were first synthesized by the German scientist Paul Ehrlich in 1904.

Uses of trypan blueEdit

 
Observation with an optical microscope of Hyaloperonospora parasitica within a leaf of Arabidopsis thaliana by using the trypan blue staining.

Trypan blue is commonly used in microscopy (for cell counting) and in laboratory mice for assessment of tissue viability.[5] The method cannot distinguish between necrotic and apoptotic cells.

It may be used to observe fungal hyphae[6] and stramenopiles.

Trypan blue is also used in ophthalmic cataract surgery to stain the anterior capsule in the presence of a mature cataract, to aid in visualization, before creating the continuous curvilinear capsulorhexis.

In early 20th century, the existence of a barrier protective toward the brain (blood brain barrier) was inferred, based on the observation that injection of trypan blue in animals led to whole‐body staining except for the brain and spinal cord.

SynonymsEdit

  • Azidine blue 3B
  • Benzamine blue 3B
  • Benzo Blue bB
  • Chlorazol blue 3B
  • Diamine blue 3B
  • Dianil blue H3G
  • Direct blue 14
  • Niagara blue 3B

Further readingEdit

  • Chapter "Detection of Caspase Activation Combined with Other Probes of Apoptosis", Eurekah Bioscience Collection, NCBI bookshelf
  • Protocol for use of the dye (PDF) from Northwestern University
  • Wainwright, M. (December 2010). "Dyes, trypanosomiasis and DNA: a historical and critical review". Biotechnic & Histochemistry. 85 (6): 341–54. doi:10.3109/10520290903297528. PMID 21080764.

ReferencesEdit

  1. ^ https://pubchem.ncbi.nlm.nih.gov/compound/9562061#section=Color
  2. ^ https://pubchem.ncbi.nlm.nih.gov/compound/9562061#section=Solubility
  3. ^ Klaus Hunger; Peter Mischke; Wolfgang Rieper; Roderich Raue; Klaus Kunde; Aloys Engel (2005). "Azo Dyes". Ullmann's Encyclopedia of Industrial Chemistry. Ullmann’s Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_245. ISBN 978-3527306732..
  4. ^ "Sigma-Aldrich, 60% Trypan Blue, Product page". Retrieved 2015-07-15.
  5. ^ Strober, W (May 2001). Trypan blue exclusion test of cell viability. Current Protocols in Immunology. Appendix 3. pp. Appendix 3B. doi:10.1002/0471142735.ima03bs21. ISBN 978-0471142737. PMID 18432654.
  6. ^ Nowicki, Marcin; et al. (15 May 2013), "A simple dual stain for detailed investigations of plant-fungal pathogen interactions", Vegetable Crops Research Bulletin, 77, doi:10.2478/v10032-012-0016-z, retrieved 2013-05-24