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作 者:罗学军 田介峰 李冉 李瑞明[1,2] Luo Xuejun;Tian Jiefeng;Li Ran;Li Ruiming(TCM Research Center,Tasly Academy,Tasly Holding Group Co Ltd,Tianjin 300410;State Key Laboratory of Critical Technology in Innovative Chinese Medicine,Tasly Pharmaceutical Group Co Ltd,Tianjin300410;TianjinUniversity of Traditional Chinese Medicine,Tianjin301617)
机构地区:[1]天士力控股集团有限公司天士力研究院,天津300410 [2]天士力医药集团股份有限公司创新中药关键技术国家重点实验室,天津300410 [3]天津中医药大学,天津301617
出 处:《天津药学》2021年第5期6-11,共6页Tianjin Pharmacy
基 金:科学技术部国家“重大新药创制”科技重大专项(No.2008ZX09401-006)。
摘 要:目的:制备满足复方丹参滴丸申报FDA过程中产品质量研究及检测所需的对照品。方法:采用柱层析法从三七中提取分离并纯化得到3个单体化合物三七皂苷R_(1)、人参皂苷Rg_(1)和人参皂苷Re,采用紫外、红外光谱、质谱、核磁对其进行结构鉴定,以质量守恒法计算相对纯度,分装得到自制对照品,并对其进行长期稳定性考查。结果:制备得到三七皂苷R_(1)、人参皂苷Rg_(1)和人参皂苷Re,相对纯度分别为94.39%、97.39%和95.00%,长期稳定性研究表明所有对照品24个月稳定性良好,未见降解。结论:通过提取纯化得到3个自制对照品候选物,并通过均一化、结构鉴定、纯度定值,分装成为对照品,满足FDA申报需求。Objective:To prepare a reference substance for quality study and detection of compound salvia miltiorrhizae dropping pills in the process of FDA application.Methods:Three monomer compounds,notoginsenoside R_(1),ginsenoside Rg_(1),and ginsenoside Re,were isolated and purified from Panax notoginseng by column chromatography.These structures were identified by UV,IR,MS,NMR spectra,and the relative purity was calculated by the mass conservation method.The self-made reference substance was obtained by packing,and the long-term stability was tested.Results:Panax notoginsenoside R_(1),ginsenoside Rg_(1),and ginsenoside Re were prepared with relative purity of 94.39%,97.39%,and 95.00%,respectively.The long-term stability study showed that all the reference substances had good stability after 24 months without degradation.Conclusion:Three self-made reference substances candidates were obtained through identification,value determination,and stability study,meeting the requirements of FDA application.
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