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作 者:顾小燕[1] 朱全刚[1] 张若曦[1] 袁松涛[1]
机构地区:[1]上海中医药大学附属岳阳中西医结合医院药剂科,上海200437
出 处:《中医药导报》2016年第12期51-53,共3页Guiding Journal of Traditional Chinese Medicine and Pharmacy
基 金:上海中医药大学预算内项目(2013JW51);上海市科委中医重点项目(No.13401902002);上海市卫计委进一步加快中医药事业发展三年行动计划(2014年-2016年)项目(ZY3-JSFC-2-3006)
摘 要:目的:通过梯度洗脱的方法,建立了金黄凝胶中芦荟大黄素、大黄酸、姜黄素、大黄素、大黄酚的含量测定方法。方法:采用ZORBAX SB-C18色谱柱(4.6×250 mm,5μm),以乙腈-4%冰醋酸为流动相梯度洗脱,柱温:30℃,检测波长:430 nm,流速:1.0 m L·min^(-1)。结果:在此条件下5种成分能够得到很好的分离,芦荟大黄素、大黄酸、姜黄素、大黄素、大黄酚的线性范围分别为0.316~6.32μg·mL^(-1)(r=1.0000,n=5),0.536~10.72μg·mL^(-1)(r=0.9999,n=5),0.325~6.50μg·mL^(-1)(r=1.0000,n=5),0.57~11.40μg·mL^(-1)(r=1.0000,n=5),0.491~9.82μg·mL^(-1)(r=1.0000,n=5)。平均加样回收率(n=6)分别为99.7%,98.8%,99.2%,97.4%,99.9%,RSD%分别为2.47%,2.55%,2.64%,1.50%,2.54%。结论:该方法简便、快速、准确,重复性好,可用于控制金黄凝胶的质量。Objective: To establish a HPLC method for quantitative determination of aloe / emodin, rhein, curcumin,emodin and chrysophanol in Jinhuang gel (金黄凝胶) using gradient elution method. Methods: HPLC method was used, with ZORBAX SB-C18 column, acetonitrile-4% acetic acid, linear gradient elution, column temperature was maintained at 30℃, as mobile phase with a flow rate of 1.0 mL·min-1, and detecting wave-length 430 nm. Results: In the chromatographic condition, the five components were completely separated. The calibration curves of aloe emodin, rhein, curcumin, emodin and chrysophanol were linear in the range of 0.3166.32μg·mL-1(r=1.0000,n=5),0.53610.72μg·mL-1(r=0.9999,n=5),0.3256.50μg·mL-1(r=1.0000,n=5),0.5711.40μg·mL-1(r=1.0000,n=5),0.4919.82μg·mL-1(r=1.0000,n=5), respectively. The average recoveries (n=6) were 99.7%, 98.8%, 99.2%, 97.4%, 99.9%, respectively, and RSD was 2.47%, 2.55%, 2.64%, 1.50%, 2.54%. Conclusion: The method is simple and repeatable, which can be applied to determine five ingredients at the same test condition in Jinhuang gel.
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