文章摘要
段晓杰,魏利娜,邵安良,陈亮,徐丽明.神经系统接触类器械的生物学评价要点和神经细胞培养技术简介[J].中国药事,2018,32(9):1251-1256
神经系统接触类器械的生物学评价要点和神经细胞培养技术简介
The Key Items of Biological Evaluation of Medical Devices Contacted with Nerverous System and Introduction of Nerve Cell Culture Techniques
投稿时间:2018-06-24  
DOI:10.16153/j.1002-7777.2018.09.016
中文关键词: 植入类医疗器械  神经系统  神经毒性  神经毒性评价要点  安全性评价  质量控制
英文关键词: implantable medical devices  nervous system  neurotoxicity  keypoints of neurotoxicity evaluation  safety evaluation  quality control
基金项目:科技部重点研发计划"生物源性材料及产品的检测与评价关键技术和标准化研究"(编号2016YFC1103203)
作者单位E-mail
段晓杰 中国食品药品检定研究院, 北京 102629  
魏利娜 中国食品药品检定研究院, 北京 102629  
邵安良 中国食品药品检定研究院, 北京 102629  
陈亮 中国食品药品检定研究院, 北京 102629 cc539@aliyun.com 
徐丽明 中国食品药品检定研究院, 北京 102629 xuliming@nifdc.org.cn 
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中文摘要:
      目前,有关与人体神经系统直接或者间接接触的植入类医疗器械越来越多。这些植入类医疗器械可能会引起神经系统结构和/或功能的不利反应,导致广泛的副作用,这些副作用则被称为医疗器械产品的神经毒性。由于神经系统有限的修复能力,因此增加了临床前评价神经毒性的重要性。目前,还没有特定的标准或指南来规范医疗器械产品的神经毒性评价要求。本文结合国内外最新的相关标准和参考文献,给出植入类医疗器械神经毒性评价的要点,为相关产品的临床前安全性评价、质量控制及注册前技术审评提供技术参考。
英文摘要:
      Currently, there are more and more implantable medical devices which directly or indirectly make contact with the human nervous system. These implantable medical devices may cause adverse reactions to the structure and/or function of the nervous system, leading to extensive side effects, which are known as neurotoxicity of medical device products. Due to the limited repair capacity of the nervous system, preclinical evaluation of neurotoxicity becomes important. At present, there are no distinct standards or guidelines to regulate the neurotoxicity evaluation for medical devices. In this paper, based on the latest relevant standards and references at home and abroad, the keypoints of neurotoxicity evaluation for implantable medical devices were introduced, and relevant nervous cells culture techniques were demonstrated in order to provide technical references for preclinical safety assessment, quality control and technical review of related products before registration.
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