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机构地区:[1]广东药科大学中药学院,广州510006 [2]广东药科大学药学院,广州510006 [3]广东省药品检验所,广州510018
出 处:《中国实验方剂学杂志》2017年第20期56-60,共5页Chinese Journal of Experimental Traditional Medical Formulae
基 金:上海市药物(中药)代谢产物研究重点实验室开放课题(2015SHDX1001)
摘 要:目的:采用超高效液相色谱法(UPLC)同时测定补肾强身片中原儿茶酸、绿原酸、金丝桃苷、特女贞苷、朝藿定C和淫羊藿苷的含量。方法:以Agilent SB-C18色谱柱(4.6 mm×100 mm,2.7μm),乙腈-0.1%磷酸水溶液为流动相进行梯度洗脱,流速0.5 m L·min^(-1),柱温40℃,检测波长260,325,360,224,270 nm。结果:6个成分的检测范围分别为原儿茶酸0.78~201.00 mg·L^(-1)(r=0.999 9),绿原酸0.79~202.60 mg·L^(-1)(r=0.999 7),金丝桃苷0.93~238.39 mg·L^(-1)(r=0.999 9),特女贞苷0.66~169.62 mg·L^(-1)(r=0.999 9),朝藿定C 0.81~206.85 mg·L^(-1)(r=0.999 9),淫羊藿苷0.74~190.85 mg·L^(-1)(r=0.999 9)。平均回收率分别为97.6%(RSD 1.0%),99.6%(RSD 1.5%),99.7%(RSD 1.5%),97.2%(RSD 0.8%),95.5%(RSD 0.4%),96.3%(RSD 0.9%)。结论:该方法简便可靠,可用于补肾强身片的质量控制。Objective: To simultaneously determinate the contents of protocatechuic acid,chlorogenic acid,hyperoside,specnuezhenide,epmedin C and icariin in Bushen Qiangshen pills( BQP) by developing an Ultra high performance liquid method( UPLC). Method: The UPLC separation was performed on an Agilent SBC18 reversed-phase column( 4. 6 mm × 100 mm,2. 7 μm) with acetonitrile-0. 1% phosphoric acid solution as the mobile phase for gradient elution. The detective wavelength was set at 260,325,360,224,270 nm. Result: The calibration curve was linear when amount was within 0. 78-201. 00 mg·L^(-1) for protocatechuic acid( r = 0. 999 9);0. 79-202. 60 mg·L^(-1) for chlorogenic acid( r = 0. 999 7); 0. 93-238. 39 mg·L^(-1) for hyperoside( r = 0. 999 9);0. 66^(-1)69. 62 mg·L^(-1) for specnuezhenide( r = 0. 999 9); 0. 81-206. 85 mg·L^(-1) for epmedin C( r = 0. 999 9);and 0. 74^(-1)90. 85 mg·L^(-1) for icariin( r = 0. 999 9). The recoveries were 97. 6%,99. 6%,99. 7%,97. 2%,95. 5%,96. 3% with RSDs of 1. 0%,1. 5%,1. 5%,0. 8%,0. 4% and 0. 9%,respectively. Conclusion: This simple and reliable method can be used for the quality control of BQP.
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