Literature DB >> 29408293

Potential impurities in drug substances: Compound-specific toxicology limits for 20 synthetic reagents and by-products, and a class-specific toxicology limit for alkyl bromides.

J P Bercu1, S M Galloway2, P Parris3, A Teasdale4, M Masuda-Herrera5, K Dobo6, P Heard6, M Kenyon6, J Nicolette7, E Vock8, W Ku9, J Harvey10, A White10, S Glowienke11, E A Martin3, L Custer12, R A Jolly13, V Thybaud14.   

Abstract

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.
Copyright © 2018. Published by Elsevier Inc.

Entities:  

Keywords:  Acceptable intake (AI); Class-specific limit; Compound-specific limit; Drug substance; Impurities; Monofunctional alkyl bromides; Permissible daily exposure (PDE); Threshold of toxicological concern (TTC)

Mesh:

Substances:

Year:  2018        PMID: 29408293     DOI: 10.1016/j.yrtph.2018.02.001

Source DB:  PubMed          Journal:  Regul Toxicol Pharmacol        ISSN: 0273-2300            Impact factor:   3.271


  7 in total

1.  Generation of TD50 values for carcinogenicity study data.

Authors:  Andrew Thresher; John Paul Gosling; Richard Williams
Journal:  Toxicol Res (Camb)       Date:  2019-07-25       Impact factor: 3.524

Review 2.  Utility of a next-generation framework for assessment of genomic damage: A case study using the pharmaceutical drug candidate etoposide.

Authors:  John Nicolette; Mirjam Luijten; Jennifer C Sasaki; Laura Custer; Michelle Embry; Roland Froetschl; George Johnson; Gladys Ouedraogo; Raja Settivari; Veronique Thybaud; Kerry L Dearfield
Journal:  Environ Mol Mutagen       Date:  2021-11-22       Impact factor: 3.579

3.  Presence of Acetamide in Milk and Beef from Cattle Consuming AFEX-Treated Crop Residues.

Authors:  Bryan Bals; Farzaneh Teymouri; Diane Haddad; W Allen Julian; Ramin Vismeh; A Daniel Jones; Preeti Mor; Brandon Van Soest; Amrish Tyagi; Michael VandeHaar; Venkataraman Bringi
Journal:  J Agric Food Chem       Date:  2019-09-11       Impact factor: 5.279

4.  Salmonella typhimurium TA100 and TA1535 and E. coli WP2 uvrA are highly sensitive to detect the mutagenicity of short Alkyl-N-Nitrosamines in the Bacterial Reverse Mutation Test.

Authors:  Frank Bringezu; Stephanie Simon
Journal:  Toxicol Rep       Date:  2022-02-08

5.  Analytical Method Development for 19 Alkyl Halides as Potential Genotoxic Impurities by Analytical Quality by Design.

Authors:  Kyoungmin Lee; Wokchul Yoo; Jin Hyun Jeong
Journal:  Molecules       Date:  2022-07-11       Impact factor: 4.927

6.  Improvement of quantitative structure-activity relationship (QSAR) tools for predicting Ames mutagenicity: outcomes of the Ames/QSAR International Challenge Project.

Authors:  Masamitsu Honma; Airi Kitazawa; Alex Cayley; Richard V Williams; Chris Barber; Thierry Hanser; Roustem Saiakhov; Suman Chakravarti; Glenn J Myatt; Kevin P Cross; Emilio Benfenati; Giuseppa Raitano; Ovanes Mekenyan; Petko Petkov; Cecilia Bossa; Romualdo Benigni; Chiara Laura Battistelli; Alessandro Giuliani; Olga Tcheremenskaia; Christine DeMeo; Ulf Norinder; Hiromi Koga; Ciloy Jose; Nina Jeliazkova; Nikolay Kochev; Vesselina Paskaleva; Chihae Yang; Pankaj R Daga; Robert D Clark; James Rathman
Journal:  Mutagenesis       Date:  2019-03-06       Impact factor: 3.000

7.  A toxicogenomic approach for the risk assessment of the food contaminant acetamide.

Authors:  Rance Nault; Bryan Bals; Farzaneh Teymouri; Michael B Black; Melvin E Andersen; Patrick D McMullen; Seetha Krishnan; Nagesh Kuravadi; Neetha Paul; Santhosh Kumar; Kamala Kannan; K C Jayachandra; Lakshmanan Alagappan; Bhavesh Dhirajlal Patel; Kenneth T Bogen; Bhaskar B Gollapudi; James E Klaunig; Tim R Zacharewski; Venkataraman Bringi
Journal:  Toxicol Appl Pharmacol       Date:  2019-12-24       Impact factor: 4.219

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.