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动物源性生物材料中残留戊二醛的遗传毒性评价及代谢研究

genotoxicity evaluation and metabolic study of residual glutaraldehyde in animal-derived biomaterials.

作者信息

Shi Jianfeng, Lian Huan, Huang Yuanli, Zhao Danmei, Wang Han, Wang Chunren, Li Jingli, Ke Linnan

机构信息

Institute for Medical Devices Control, National Institutes for Food and Drug Control, No. 31 Huatuo Road, Beijing 102629, China.

出版信息

Regen Biomater. 2020 Oct 24;7(6):619-625. doi: 10.1093/rb/rbaa041. eCollection 2020 Dec.

Abstract

Glutaraldehyde (GA) is an important additive that is mainly used in animal-derived biomaterials to improve their mechanical and antimicrobial capacities. However, GA chemical toxicity and the metabolic mechanism remain relatively unknown. Therefore, residual GA has always been a major health risk consideration for animal-derived medical devices. In this study, extracts of three bio-patches were tested via the GA determination test and mouse lymphoma assay (MLA). The results showed that dissolved GA was a potential mutagen, which could induce significant cytotoxic and mutagenic effects in mouse lymphoma cells. These toxic reactions were relieved by the S9 metabolic activation (MA) system. Furthermore, we confirmed that GA concentration decreased and glutaric acid was generated during the catalytic process. We revealed GA could be oxidized via cytochrome P450 which was the main metabolic factor of S9. We found that even though GA was possibly responsible for positive reactions of animal-derived biomaterials' biocompatibility evaluation, it may not represent the real situation occurring in human bodies, owing to the presence of various detoxification mechanisms including the S9 system. Overall, in order to achieve a general balance between risk management and practical application, rational decisions based on comprehensive analyses must be considered.

摘要

戊二醛(GA)是一种重要的添加剂,主要用于动物源生物材料,以提高其机械性能和抗菌能力。然而,GA的化学毒性和代谢机制仍相对未知。因此,残留的GA一直是动物源医疗器械主要的健康风险考量因素。在本研究中,通过GA测定试验和小鼠淋巴瘤试验(MLA)对三种生物贴片的提取物进行了测试。结果表明,溶解的GA是一种潜在的诱变剂,可在小鼠淋巴瘤细胞中诱导显著的细胞毒性和诱变作用。这些毒性反应通过S9代谢活化(MA)系统得到缓解。此外,我们证实了在催化过程中GA浓度降低并生成了戊二酸。我们发现GA可通过细胞色素P450氧化,而细胞色素P450是S9的主要代谢因子。我们发现,尽管GA可能是动物源生物材料生物相容性评价阳性反应的原因,但由于包括S9系统在内的各种解毒机制的存在,它可能并不代表人体中实际发生的情况。总体而言,为了在风险管理和实际应用之间实现总体平衡,必须考虑基于综合分析的合理决策。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fba5/7748443/6853c15442b7/rbaa041f1.jpg

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