Genetic toxicology studies with glutaraldehyde

✍ Scribed by Jane S. Vergnes; Bryan Ballantyne

• Publisher: John Wiley and Sons
• Year: 2002
• Tongue: English
• Weight: 167 KB
• Volume: 22
• Category: Article
• ISSN: 0260-437X
• DOI: 10.1002/jat.825

✦ Synopsis

Abstract

Glutaraldehyde (GA; CAS no. 111‐30‐8) has a wide spectrum of industrial, scientific and biomedical applications, with a potential for human exposure particularly in its biocidal applications. The likelihood for genotoxic effects was investigated in vitro and in vivo. A Salmonella typhimurium reverse mutation assay showed no evidence for mutagenic activity with strains TA98, TA1535, TA1537 and TA1538, with or without metabolic activation. However, there was a weak mutagenic response (1.9–2.3‐fold at the highest non‐toxic concentration) with TA100 in the presence of metabolic activation. In a Chinese hamster ovary (CHO) forward gene mutation assay (HGPRT locus) there were no consistent, statistically significant, reproducible or dosage‐related increases in the frequency of 6‐thioguanine resistant cells. There were no reproducible or dosage‐related increases in sister chromatid exchanges in an in vitro test in CHO cells. An in vitro cytogenetics study in CHO cells showed no evidence for an increase in chromosomal aberrations on treatment with GA, either in the presence or absence of metabolic activation. In vivo, a mouse peripheral blood micronucleus test showed no increase in micronucleated polychromatophils at sampling times of 30, 48 and 72 h after acute gavage dosing with GA at 40, 80 and 125 mg kg^−1^ (corresponding to 25, 50 and 85% of the LD~50~). The absence of an in vivo clastogenic potential was confirmed by no increase in chromosomal aberrations in a rat bone marrow cytogenetics study with sampling at 12, 24 and 48 h after acute gavage dosing with GA (12.5, 30 or 60 mg kg^−1^ with males, and 7.5, 20 or 40 mg kg^−1^ with females). Thus, in this series of tests, GA produced genotoxic effects in vitro only in a bacterial reverse mutation assay with no evidence for in vivo genotoxicity. Copyright © 2002 John Wiley & Sons, Ltd.