A response to “A quantitative assessment of the carcinogenicity of hexavalent chromium by the oral route and its relevance to human exposure”-Reference-Cited by-同舟云学术

A response to “A quantitative assessment of the carcinogenicity of hexavalent chromium by the oral route and its relevance to human exposure”

Published:2011-04 Issue:3 Volume:111 Page:468-470
ISSN:0013-9351
Container-title:Environmental Research
language:en
Short-container-title:Environmental Research

Author:

Proctor Deborah M.,Thompson Chad M.,Suh Mina,Harris Mark A.

Publisher

Elsevier BV

Subject

General Environmental Science,Biochemistry

Reference12 articles.

1. Exposure to hexavalent chromium resulted in significantly higher tissue chromium burden compared to trivalent chromium following similar oral doses to male F344/N and female B6C3F1 mice;Collins;Toxicol. Sci.,2010

2. Estimates of the chromium(VI) reducing capacity in human body compartments as a mechanism for attenuating its potential toxicity and carcinogenicity;De Flora;Carcinogenesis,1997

3. Human ingestion of chromium (VI) in drinking water: pharmacokinetics following repeated exposure;Finley;Toxicol. Appl. Pharmacol.,1997

4. National Toxicology Program (NTP), 2007. NTP technical report on the toxicity studies of sodium dichromate dihydrate administered in drinking water to male and female F344/N rats and B6C3F1 mice and male BALB/c and am3-C57BL/6 mice. January 2007 National Institutes of Health Public Health Service U.S. Department of Health and Human Services. Accessed at: 〈http://ntp.niehs.nih.gov/ntp/htdocs/ST_rpts/TOX72.pdfbm94934〉.

5. NTP, 2008. Final technical report on the toxicology and carcinogenesis studies of sodium dichromate dihydrate in F344/N rats and B6C3F1 mice. Accessed at: 〈http://ntp.niehs.nih.gov/files/546_web_FINAL.pdfS〉.

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