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作 者:彭芳[1] 黄颖[1] 李帅[1] 胡本容[1] 王嘉陵[1] 向继洲[1]
机构地区:[1]华中科技大学同济医学院药理系,湖北武汉430030
出 处:《中国医院药学杂志》2007年第6期762-764,共3页Chinese Journal of Hospital Pharmacy
摘 要:目的:建立测定大鼠血浆和肝脏匀浆中甲基莲心碱浓度的高效液相色谱法。方法:大鼠血浆和肝脏匀浆样品经乙醚萃取,进样分析。采用HypersilBDSC18(4.0mm×250mm,5μm)柱分离。以甲醇-磷酸二氢钾缓冲液-三乙胺(71∶29∶0.002)为流动相,检测波长为282nm。结果:血浆中甲基莲心碱的线性范围为31.25μg·L-1~2.00mg·L-1;日内和日间RSD分别为小于8.0%和5.0%,绝对回收率为77.45%~89.23%。其在肝脏匀浆中的线性范围为62.5μg·L-1~16.0mg·L-1,日内和日间RSD均小于3.0%,绝对回收率为73.53%~88.43%。结论:该方法符合生物样品的检测要求,可应用于大鼠血浆和肝脏匀浆中甲基莲心碱浓度的测定。OBJECTIVE To develop an HPLC method for the determination of Neferine(NEF) in rat plasma and liver. METHODS The samples were separated on a reversed phase column ( Hypersil BDS C18, particle size 5 μm, 4. 0 mm × 250 mm) after extracting by ether. The mobile phase consisted of methanol phosphate buffered saline triethylamine (71 : 29 : 0. 002), and the UV detection wavelength was 282 nm. RESULTS The linear range was 31.25 μg·L^-1 - 2. 00 mg·L^-1 in plasma, and 62. 5 μg·L^-1- 16.0 mg·L^-1 in liver. The absolute recovery rate was between 77. 45% and 89. 23% in plasma, and between 73. 53% and 88. 43% in liver. It showed good reproducibility that the precision was within 8. 0% in plasma, and within 3. 0% in liver. CONCLUSION This method accorded with the standard of drug analysis in biological specimen and was successfully applied to determining the concentration of NEF in rat plasma and liver.
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