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m-Cresol - ipcs inchem

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OECD SIDS<br />

m- / p-CRESOL<br />

m/p-<strong>Cresol</strong><br />

An Ames test was performed without S9-mix and with S9-mix from rat and hamster livers. The<br />

studies gave no indication of gene mutations (NTP 1991).<br />

Conclusion:<br />

In vitro, m-,and p- cresol did not induce gene mutations in bacterial and mammalian cell systems<br />

and m/p-<strong>Cresol</strong> mixture did not induce gene mutations in bacteria, both in the presence or absence<br />

of metabolic activation.<br />

(B) Cytogenicity<br />

m-<strong>Cresol</strong>:<br />

There is a study on cytogenicity (Chromosome aberration) using Chinese Hamster Ovary (CHO)<br />

cells in vitro which corresponds to the current OECD guideline 473 (Hazleton Lab. Am. 1988b).<br />

The study gave no indication of any clastogenic activity of the substance.<br />

In addition, there is a mouse lymphoma assay (Hazleton Lab. Am. 1988a) with a negative result. In<br />

a Sister Chromatid Exchange (SCE) test on human fibroblasts without metabolic activation no<br />

increases in exchange rates were seen (Cheng and Kligerman 1984).<br />

p-<strong>Cresol</strong><br />

There is a study on cytogenicity (Chromosome aberration) using Chinese Hamster Ovary (CHO)<br />

cells in vitro which corresponds to the current OECD guideline 473 Incubated without metabolic<br />

activation the assay was positive in all doses. The metabolic activated cultures which were<br />

incubated for 10 hours yielded negative results and those which were incubated for 20 hours yielded<br />

positive results (Hazleton Lab. Inc. 1988f). In addition, there is a mouse lymphoma assay with a<br />

negative result both in the presence or absence of metabolic activation (Hazleton Lab. Inc. 1988e).<br />

In a Sister Chromatid Exchange (SCE) tests with human lymphocytes using a treatment time of up<br />

to 90 hours (Jansson et al. 1986) and with human fibroblasts incubated with p-cresol for two hours<br />

(Cheng and Kligerman 1984), no increases in exchange rates were seen.<br />

m/p-<strong>Cresol</strong><br />

There are no cytogenetic assays in vitro with a m/p cresol mixture.<br />

Conclusion:<br />

m-<strong>Cresol</strong> did not induce chromosomal aberrations in vitro, whereas p-cresol had clastogenic<br />

activity in CHO cells in both the presence or absence of S-9 mix. It is therefore possible that m/pcresol<br />

mixture has the potential to induce chromosomal aberrations in vitro. Neither m- nor p-cresol<br />

did increase SCE in vitro.<br />

(C) Indicator test<br />

m-<strong>Cresol</strong><br />

No induction of Unscheduled DNA Synthesis (UDS) was found in rat primary hepatocytes m<br />

(Hazleton Lab. Am. Inc. 1988c). In contrast, UDS was induced in SHE cells, but only in the<br />

presence of a metabolic activation system (Hamaguchi and Tsutsui 2000).<br />

26<br />

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