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作 者:黄瑞雪[1] 黎翊君 茅玉炜 刘乐环 王渐鸿 余家齐 戴俊东[1]
出 处:《中国药师》2017年第4期664-667,共4页China Pharmacist
基 金:北京中医药大学自主选题项目(编号:2016-JYB-XS072)
摘 要:目的:建立HPLC法测定姜黄素-槲皮素复方自微乳(CUR-QUE-SMEDDS)的载药量和包封率。方法:采用离心法分离游离药物,HPLC法测定药物含量。色谱柱:Purospher STAR LP C18柱(250 mm×4.6 mm,5μm),流动相:乙腈-4%冰醋酸(50∶50),流速:1.0 ml·min^(-1),检测波长:370 nm,柱温:30℃,进样量:10μl。结果:姜黄素和槲皮素的线性范围分别为10.728~96.552μg·ml^(-1)(r=0.999 8)和1.08~9.72μg·ml^(-1)(r=0.999 9),平均回收率分别为99.98%(RSD=1.46%,n=9)和100.34%(RSD=1.06%,n=9)。CUR-QUE-SMEDDS中姜黄素和槲皮素的包封率分别为(95.97#0.50)%和(95.91#2.52)%,载药量分别为(25.82#0.15)mg·g^(-1)和(1.80#0.05)mg·g^(-1)。结论:该法准确可靠,快速简便,适用于测定CURQUE-SMEDDS的载药量和包封率。Objective: To establish an HPLC method to determine the entrapment efficiency (EE) and drug loading (DL) of curcumin (CUR)and quereetin (QUE)loaded self-mieroemulsifying drug delivery system. Methods: A centrifugation method was used to isolate the free drug. The eontent of drug was determined by HPLC. The analytical column was a Purospher STAR LP C18 column (250 mm×4.6 mm, 5 μm) and the column temperature was 30℃. The mobile phase was acetonitrile-4% acetic acid (50:50) and the flow rate was 1.0 ml· min^-1. The UV detection wavelength was set at 370 nm and the injection volume was 10μl. Results: CUR and QUE were linear within the range of 10.728-96. 552μg·ml^- 1( r = 0.999 8 ) and 1.08-9.72 μg · ml^ - 1 ( r = 0. 999 9 ) , respectively. The average recovery was 99.98% ( RSD = 1.46% , n = 9 ) and 100.34% ( RSD = 1.06% , n = 9 ), respectively. In CUR-QUESMEDDS, the EE of curcumin and quercetin was (95.97 · 0.50) % and (95.91 ·2.52) %, and the DL was (25.82·0.15) mg · g^ - 1 and (1.80±0.05) mg · g^-1, respectively. Conclusion: The method is accurate, rapid and simple, and suitable for the determination of DL and EE in CUR-QUE-SMEDDS.
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