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《中药、天然药物稳定性研究技术指导原则(2006年)》由会员上传分享,免费在线阅读,更多相关内容在行业资料-天天文库。
1、中药、天然药物稳定性研究技术指导原则目录一、概述··················································1二、稳定性研究实验设计····································2(一)样品的批次和规模··································2(二)包装及放置条件····································2(三)考察时间点···································
2、·····2(四)考察项目··········································3(五)分析方法··········································3三、稳定性研究实验方法···································3(一)影响因素试验······································31、高温试验·············································32、高湿试验
3、·············································43、光照试验·············································4(二)加速试验··········································4(三)长期试验··········································5(四)药品上市后的稳定性研究····························5四、稳定性研究要求与结果评价····
4、·························5(一)稳定性研究要求····································51、新药················································52、已有国家标准药品····································63、其他················································6(二)稳定性研究结果评价·····················
5、···········721、贮存条件的确定·······································72、包装材料/容器的确定··································73、有效期的确定·········································7五、名词解释·············································8六、参考文献··········································
6、···8七、著者·················································8八、附录·················································8稳定性研究报告的一般内容3一、概述中药、天然药物的稳定性是指中药、天然药物(原料或制剂)的化学、物理及生物学特性发生变化的程度。通过稳定性试验,考察中药、天然药物在不同环境条件(如温度、湿度、光线等)下药品特性随时间变化的规律,以认识和预测药品的稳定趋势,为药品生产、包装、贮存、运输条件的确定
7、和有效期的建立提供科学依据。稳定性研究是评价药品质量的主要内容之一,在药品的研究、开发和注册管理中占有重要地位。为此起草了中药、天然药物稳定性研究技术指导原则。根据研究目的和条件的不同,稳定性研究内容可分为影响因素试验、加速试验和长期试验等。影响因素试验是在剧烈条件下探讨药物的稳定性、了解影响其稳定性的因素及所含成份的变化情况。为制剂处方设计、工艺筛选、包装材料和容器的选择、贮存条件的确定、有关物质的控制提供依据。并为加速试验和长期试验应采用的温度和湿度等条件提供参考。加速试验是在加速条件下进行的稳定性试验,其目
8、的是在较短的时间内,了解原料或制剂的化学、物理和生物学方面的变化,为制剂设计、质量评价和包装、运输、贮存条件等提供试验依据,并初步预测样品的稳定性。长期试验是在接近药品的实际贮存条件下进行的稳定性试验,为制订药物的有效期提供依据。此外,有些药物制剂还应考察使用过程中的稳定性。稳定性研究具有阶段性特点,不同阶段具有不同的目的。一般始于药品的临床前研究,贯穿药品研究与开发的全
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