The acute intravenous toxicity of biological stains, dyes, and other fluorescent substances

https://doi.org/10.1016/0041-008X(78)90185-0Get rights and content

Abstract

Sodium fluorescein and indocyanine green are currently used as indicators for angiography of the retinal and choroidal vasculatures. This study was conducted to suggest additional indicator substances for this technique. Fifty-three dyes and biological stains were evaluated by the following criteria: intravenous LD50, histopathological damage from intravenous administration, binding properties in blood, in vivo metabolism of the substances, fluorescent and absorption spectra, and impurities detected with thin-layer chromatography. Male Swiss-Webster mice were used for the intravenous toxicity studies and for the metabolism and LD50 determinations. Several cyanines were modified by recrystallization with sodium iodide and an oxazine was sulfonated to improve their solubility and biocompatibility. Both techniques were successful in improving the intravenous toxicity and the solubility of the dyes in water. Iodination was not successful on the merocyanines. Patent blue VF and 8-hydroxy-1,3,6-pyrene trisulfonic acid trisodium salt were promising since both had impurities yet their LD50s exceeded 1000 mg/kg. Fluorones with two salt sites (NaO and COONa) were soluble at 10% or more in water. Nonhalogenated fluorones were excreted totally in the urine, while those with eight halogen atoms were removed via the biliary system. Those fluorones with six or less halogen atoms were excreted by both systems. Twenty-three of the fifty-three dyes were tolerated well enough for use in angiography of the ocular fundus. The majority of the substances had at least one impurity. In general, the cationic dyes were poorly tolerated; only 2 of the 23 acceptable substances were cationic. Those dyes that were anionic or dipolar were the best tolerated, with the dipolar molecules being cleared, at least partially, by the liver.

References (19)

  • P. Jablonski et al.

    The clinical chemistry of bromosulfophthalein and other cholephilic dyes

    Advan. Clin. Chem.

    (1969)
  • H.A. Kues

    Thin layer chromatography of some cyanine dyes

    J. Chromatogr.

    (1977)
  • E. Cotchin et al.
  • G.A. Emerson et al.

    Toxicity of certain proposed antileprosy dyes: fluorescein, eosin, erythrosin and others

    Int. J. Leprosy

    (1934)
  • R.W. Flower et al.

    A clinical technique for simultaneous angiography of separate retinal and choridal circulations

    Invest. Ophthalmol.

    (1973)
  • E. Gurr
  • E.C. Hagan
  • B. Highman et al.

    Effect of DMSO, exercise, and training on rat serum enzymes and tissues

    Amer. J. Physiol.

    (1967)
  • R. Höber

    Studies concerning the nature of the secretory activity of the isolated-perfused frog liver

    J. Gen. Physiol.

    (1939)
There are more references available in the full text version of this article.

Cited by (75)

  • Reversible and irreversible fluorescence activity of the Enhanced Green Fluorescent Protein in pH: Insights for the development of pH-biosensors

    2020, International Journal of Biological Macromolecules
    Citation Excerpt :

    Although inorganic fluorophores are easier to work with than fluorescent proteins, their toxicity is a barrier for medical use. The toxicity of fluorescence dyes have been reported decades ago [29], and more recently, cytotoxicity at low concentrations was also reported on novel fluorophores like quantum dots [30,31]. Fluorescent proteins have been extensively applied for biological studies, including in vivo assays, being biocompatible with cells and animals, and presenting very low toxicities [11,32,33], making them well suited for use in pharmaceutical formulations.

  • Fluorescence in neurosurgery: Its diagnostic and therapeutic use. Review of the literature

    2015, Journal of Photochemistry and Photobiology B: Biology
    Citation Excerpt :

    In the 1960s renal blood flow was determined by ICG and diagnosis of subretinal processes was done by ICG. As a tricarbocyanine ICG has a molecular weight of 774.96 Da – the structural formula is 2,2′-indo-6,7,6′,7′-dibenzocarbocyanine sodium salt [69,82]. Maximum near-infrared light absorption is at 790 nm with a maximum emission at 835 nm [14].

View all citing articles on Scopus

This work was supported by The National Institutes of Health under Contract No. NO 1-EY-3-2139.

View full text