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总有机碳TOC分析在制药设备清洁验证中的应用 被引量:16

Application of total organic carbon analysis in production equipment cleaning validation for tobramycin
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摘要 目的:中国2010年版GMP要求制药企业对生产设备进行清洁验证,总有机碳TOC(Total Organic Carbon)分析是适用于清洁验证的分析方法。方法:对妥布霉素的生产设备,建立了淋洗法与擦拭法结合的清洁规程,用TOC分析仪检测清洁验证的样品。结果:TOC分析妥布霉素,得到良好的线性、回收率及精确度。建立的清洁验证规程可行,对实际的清洁验证样品检测,TOC数据重现性良好,低于设立的允许残留限值。结论:TOC方法适用于制药设备的清洁验证。TOC表征所有的有机物污染程度,为设备清洁验证提供了有力的安全性和可靠性。 Objective:To do cleaning validation (CV) for production equipment according to China new GMP 2010 requirement for pharmaceutical manufacturers, by total organic carbon (TOC) analysis which is suitable for CV. Methods:For the production equipment of tobramycin, the CV SOP was established with combination of rinse and swab sampling methods, and the CV samples were analyzed with TOC analyzer. Results:A satisfactory linearity was obtained, so were recovery and precision when measuring tobramycin with TOC analyzer, which revealed that the es- tablished CV SOP was feasible. CV samples were measured through this SOP and the TOC result represented a good reproducibility which was lower than allowable residue levels. Conclusion:TOC is a good analysis method for CV of pharmaceutical equipment. TOC indicates contamination of all kinds of organics. It guarantees safety and reliability of CV procedure.
出处 《药物分析杂志》 CAS CSCD 北大核心 2013年第3期478-485,共8页 Chinese Journal of Pharmaceutical Analysis
关键词 总有机碳 TOC 清洁验证 CV 妥布霉素 淋洗水法 棉签擦拭 GMP 生产设备验证 total organic carbon TOC cleaning validation CV tobramycin rinse water method swabing method GMP produotion equipment validation
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  • 1Ministry of Health of the People's Republic of China (中华人民共和国卫生部),Good Manufacturing Practice (2010 Revision) (药品生产质量管理规范(2010年修订).2011,Item 143 (第一百四十三条),P26.
  • 221 CFR 211.67-Equipment Cleaning and Maintenance (21 美国联邦法规CFR 211.67 – 设备清洁与维护),2008,http://cfr.vlex.com/vid/211-67-equipment-cleaning-maintenance-19708254.
  • 3ChP(中国药典).2010.Appendix Ⅷ R TOC Method for Pharmaceutical Water (附录 Ⅷ R 制药用水中总有机碳测定法);Purified Water (纯化水),Water for Injection (注射用水).
  • 4China Food and Drug Administration (国家食品药品监督管理局).Guide to Drug Production Validation (药品生产验证指南),Chapter 3 Test method and cleaning validation (第三篇检验方法和清洁验证).Beijing(北京):Chemical Industry Press (化学工业出版社),2003.205.
  • 5U.S.Food and Drug Administration,FDA(美国食品药品监督管理局FDA).Guide to Inspection of Cleaning Validation (清洁验证检查指南),1993.
  • 6China State Food and Drug Administration,Certification and Administration Center (国家食品药品监督管理局药品认证管理中心).Guidance of Good Manufacturing Practices for Drug (药品GMP指南),Oral Solid Dosage Forms (口服固体制剂).2011.181.
  • 7GE Analytical Instruments (GE公司分析仪器).GE Sievers 820 TOC Analyzer Operation and Maintenance Manual (GE Sievers 820 总有机碳TOC操作与维护手册).2002.
  • 8.ChP(中国药典)WaterforInjection(注射用水).,2010.
  • 9.ChP(中国药典)PurifiedWater(纯化水).,2010.

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