DNA Damage and Micronucleus Induction by Small-Molecule Nitrosamine Drug Impurities and Nitrosamine Drug Substance-Related Impurities in HepaRG Cells

IF 2.7 4区 医学 Q3 ENVIRONMENTAL SCIENCES
Hannah S. Xu, Ji-Eun Seo, Xilin Li, Nan Mei, Aisar H. Atrakchi, Karen L. Davis Bruno, Sruthi T. King, Robert T. Dorsam, Naomi L. Kruhlak, Kelly Brant, Robert H. Heflich, Xiaoqing Guo
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引用次数: 0

Abstract

Nitrosamine drug impurities, including both small-molecule nitrosamines and nitrosamine drug substance-related impurities (NDSRIs), are members of a cohort of concern for pharmaceutical safety assessment. As the toxicity of most nitrosamine impurities requires metabolic activation by cytochrome P450 enzymes, this study used human HepaRG cells, which have metabolic activity similar to that of human hepatic cells, to evaluate methods for nitrosamine safety assessment. The genotoxicity of four small-molecule nitrosamines, N-bis(2,2-diethoxyethyl) nitrous amide (BDEA), N-nitrosodiphenylamine, N,N-nitroso-N-ethylaniline (NEPA), and 1-methyl-4-nitrosopiperazine (MNP), and five NDSRIs, N-nitroso-bumetanide, N-nitroso-ciprofloxacin, N-nitroso-dabigatran etexilate, N-nitroso-desmethyl-diphenhydramine, and N-nitroso-sertraline, was evaluated in two-dimensional (2D)/attached and three-dimensional (3D)/spheroid HepaRG cell cultures using two high-throughput genetic toxicity assays, the CometChip DNA damage assay and the flow-cytometric micronucleus (MN) assay. These test substances exhibited a range of responses in other genotoxicity assays, including strong positive, negative, and inconclusive results. Following a 24-h treatment, two NDSRIs, N-nitroso-desmethyl-diphenhydramine and N-nitroso-sertraline, and two small-molecule nitrosamines, BDEA and MNP, induced DNA damage, with the small-molecule nitrosamines positive only in 3D HepaRG spheroids. MN formation was detected only in spheroids exposed to N-nitroso-desmethyl-diphenhydramine. Benchmark concentration (BMC) values derived from the DNA damage data were lower for the genotoxic NDSRIs compared to the genotoxic small-molecule nitrosamines, which correlated with higher cytotoxicity for the NDSRIs. These results show that, while HepaRG spheroids were a more sensitive model for the hazard identification of small-molecule nitrosamines, the responses produced by NDSRIs were more complex, with NDSRIs tested producing similar levels of DNA damage in 2D and 3D cultures and inducing MN formation only in 3D spheroids.

小分子亚硝胺类药物杂质和亚硝胺类药物相关杂质在HepaRG细胞中的DNA损伤和微核诱导。
亚硝胺类药物杂质,包括小分子亚硝胺类和亚硝胺类原料药相关杂质(NDSRIs),是药品安全性评价关注的队列之一。由于大多数亚硝胺杂质的毒性需要细胞色素P450酶的代谢激活,因此本研究使用具有与人肝细胞相似代谢活性的人HepaRG细胞来评价亚硝胺安全性评价方法。4种小分子亚硝胺,N-双(2,2-二氧乙基)亚氮酰胺(BDEA)、N-亚硝基二苯胺、N,N-亚硝基-N-乙基苯胺(NEPA)和1-甲基-4-亚硝基哌嗪(MNP),以及5种NDSRIs, N-亚硝基-布美坦、N-亚硝基-环丙沙星、N-亚硝基-达比加群酯、N-亚硝基-去甲基-苯海拉明和N-亚硝基-舍曲林的遗传毒性。在二维(2D)/附着和三维(3D)/球形HepaRG细胞培养中使用两种高通量遗传毒性试验,CometChip DNA损伤试验和流式细胞微核(MN)试验进行评估。这些试验物质在其他遗传毒性试验中表现出一系列反应,包括强烈的阳性、阴性和不确定的结果。治疗24小时后,两种NDSRIs (n -亚硝基去甲基苯海拉明和n -亚硝基舍曲林)和两种小分子亚硝胺(BDEA和MNP)诱导DNA损伤,小分子亚硝胺仅在3D HepaRG球体中呈阳性。仅在暴露于n -亚硝基去甲基苯海拉明的球体中检测到MN的形成。与遗传毒性小分子亚硝胺相比,遗传毒性NDSRIs的DNA损伤基准浓度(BMC)值较低,这与NDSRIs较高的细胞毒性相关。这些结果表明,虽然HepaRG球体是一个更敏感的小分子亚硝胺危害识别模型,但NDSRIs产生的反应更为复杂,NDSRIs在2D和3D培养中产生相似水平的DNA损伤,并且仅在3D球体中诱导MN形成。
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来源期刊
CiteScore
5.40
自引率
10.70%
发文量
52
审稿时长
12-24 weeks
期刊介绍: Environmental and Molecular Mutagenesis publishes original research manuscripts, reviews and commentaries on topics related to six general areas, with an emphasis on subject matter most suited for the readership of EMM as outlined below. The journal is intended for investigators in fields such as molecular biology, biochemistry, microbiology, genetics and epigenetics, genomics and epigenomics, cancer research, neurobiology, heritable mutation, radiation biology, toxicology, and molecular & environmental epidemiology.
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