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北京中医药大学 中药学院,北京 102488
毕嘉谣,在读硕士,从事中药新剂型与新技术研究,Tel:024-52818899,E-mail:15641300076@163.com
* 杜守颖,博士,教授,从事中药新剂型与新技术研究,Tel:010-84738615,E-mail:dushouying@263.net;
* 白洁,博士,副教授,从事中药新剂型与新技术研究,Tel:010-84738657,E-mail:baijie22811@163.com
收稿日期:2020-11-24,
网络出版日期:2021-01-12,
纸质出版日期:2021-08-20
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毕嘉谣,田湾湾,张翼等.经典名方易黄汤物质基准的量值传递分析[J].中国实验方剂学杂志,2021,27(16):24-31.
BI Jia-yao,TIAN Wan-wan,ZHANG Yi,et al.Analysis on Quality Transmitting of Substance Benchmarks of Yihuangtang[J].Chinese Journal of Experimental Traditional Medical Formulae,2021,27(16):24-31.
毕嘉谣,田湾湾,张翼等.经典名方易黄汤物质基准的量值传递分析[J].中国实验方剂学杂志,2021,27(16):24-31. DOI: 10.13422/j.cnki.syfjx.20210488.
BI Jia-yao,TIAN Wan-wan,ZHANG Yi,et al.Analysis on Quality Transmitting of Substance Benchmarks of Yihuangtang[J].Chinese Journal of Experimental Traditional Medical Formulae,2021,27(16):24-31. DOI: 10.13422/j.cnki.syfjx.20210488.
目的
2
以指纹图谱、指标成分含量及出膏率为评价指标探索饮片-物质基准的量值传递关系,考察15批易黄汤物质基准的关键质量属性,初步建立其物质基准的质量标准。
方法
2
制备15批易黄汤物质基准冻干粉样品,采用高效液相色谱法(HPLC)对15批饮片和物质基准进行指纹图谱、指标成分含量测定,流动相选择乙腈(A)-0.1%磷酸水溶液(B)梯度洗脱(0~6 min,97%B;6~12 min,97%~92%B;12~25 min,92%~90%B;25~35 min,90%~89%B;35~50 min,89%~82%B;50~75 min,82%~72%B;75~85 min,72%~35%B),检测波长230 nm,结合出膏率明确特征峰的归属及其与对照图谱的相似度范围,京尼平苷酸、盐酸小檗碱的含量范围及转移率范围,物质基准的出膏率范围及变化幅度等。
结果
2
建立的HPLC指纹图谱检测方法精密度、重复性和稳定性均良好,能同时适用于饮片、物质基准指纹图谱的检测。15批易黄汤物质基准指纹图谱与对照指纹图谱的相似度均>0.99;共归属15个特征峰,经对照品比对后指认了8个特征峰信息,其中6个来自盐黄柏,1个来自酒车前子,1个来自炒山药。15批易黄汤物质基准中京尼平苷酸、盐酸小檗碱质量分数范围分别为0.10%~0.16%,0.63%~1.05%,转移率范围分别为20.91%~32.65%,19.60%~29.59%;物质基准出膏率范围8.45%~9.92%。
结论
2
采用指纹图谱、出膏率及指标成分含量测定相结合的模式,对经典名方易黄汤物质基准的量值传递过程进行分析,可初步拟定易黄汤物质基准的质量标准,可为该经典名方的质量控制及相关制剂开发提供依据。
Objective
2
To explore the quality transmitting relationship between decoction pieces and substance benchmarks with the fingerprint, index component content and dry extract rate as evaluation indexes, and investigate the key quality attributes of 15 batches of substance benchmarks of Yihuangtang, and establish the quality standard of this substance benchmarks.
Method
2
Fifteen batches of Yihuangtang substance benchmarks freeze-dried powder samples were prepared, the fingerprint and index component content of 15 batches of decoction pieces and substance benchmarks were determined by high performance liquid chromatography (HPLC), the mobile phase was acetonitrile (A)-0.1% phosphoric acid aqueous solution (B) for gradient elution (0-6 min, 97%B; 6-12 min, 97%-92%B; 12-25 min, 92%-90%B; 25-35 min, 90%-89%B; 35-50 min, 89%-82%B; 50-75 min, 82%-72%B; 75-85 min, 72%-35%B), the detection wavelength was set at 230 nm, combined the dry extract rate to clarify the attribution of characteristic peaks and the range of similarity with the control chromatogram, the content range and transfer rate range of geniposidic acid and berberine hydrochloride, the dry extract rate range and the variation range of the substance benchmarks.
Result
2
The established HPLC fingerprint had good precision, repeatability and stability, and could be used for the simultaneous determination of decoction pieces and substance benchmarks of Yihuangtang. The similarities between the control chromatogram and fingerprint of substance benchmarks were >0.99. A total of 15 characteristic peaks were assigned, and 8 characteristic peaks were identified by the reference substances, of which 6 were from Phellodendri Chinensis Cortex processed with salt, 1 was from Plantaginis Semen processed with wine, and 1 was from stir-fried Dioscoreae Rhizoma. The content ranges of geniposidic acid and berberine hydrochloride in 15 batches of substance benchmarks of Yihuangtang were 0.10%-0.16% and 0.63%-1.05%, the transfer rate ranges of them were 20.91%-32.65% and 19.60%-29.59%, respectively. The dry extract rate range of the substance benchmarks was 8.45%-9.92%.
Conclusion
2
The quality standard of Yihuangtang substance benchmarks can be preliminarily formulated by the combination of fingerprint, dry extract rate and determination of index component, which can provide the basis for the quality control of Yihuangtang and the development of related preparations.
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