毒理
致癌物
药品
化学
职业接触限值
人口
试剂
药理学
有机化学
生物
医学
职业暴露
环境卫生
医疗急救
作者
Joel P. Bercu,Sheila M. Galloway,Patricia Parris,Andrew Teasdale,Melisa Masuda-Herrera,Krista L. Dobo,Pamela L. Heard,Michelle Kenyon,John Nicolette,E. Vock,Warren W. Ku,James Harvey,Angela White,Susanne Glowienke,Elizabeth A. Martin,Laura Custer,Robert A. Jolly,V. Thybaud
标识
DOI:10.1016/j.yrtph.2018.02.001
摘要
This paper provides compound-specific toxicology limits for 20 widely used synthetic reagents and common by-products that are potential impurities in drug substances. In addition, a 15 μg/day class-specific limit was developed for monofunctional alkyl bromides, aligning this with the class-specific limit previously defined for monofunctional alkyl chlorides. Both the compound- and class-specific toxicology limits assume a lifetime chronic exposure for the general population (including sensitive subpopulations) by all routes of exposure for pharmaceuticals. Inhalation-specific toxicology limits were also derived for acrolein, formaldehyde, and methyl bromide because of their localized toxicity via that route. Mode of action was an important consideration for a compound-specific toxicology limit. Acceptable intake (AI) calculations for certain mutagenic carcinogens assumed a linear dose-response for tumor induction, and permissible daily exposure (PDE) determination assumed a non-linear dose-response. Several compounds evaluated have been previously incorrectly assumed to be mutagenic, or to be mutagenic carcinogens, but the evidence reported here for such compounds indicates a lack of mutagenicity, and a non-mutagenic mode of action for tumor induction. For non-mutagens with insufficient data to develop a toxicology limit, the ICH Q3A qualification thresholds are recommended. The compound- and class-specific toxicology limits described here may be adjusted for an individual drug substance based on treatment duration, dosing schedule, severity of the disease and therapeutic indication.
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