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作 者:张志鹏[1] 朱盛山[2] 李苑新[2] 霍务贞[2] 吴燕红[2]
机构地区:[1]湖北科技学院.药学院,湖北咸宁437100 [2]广东药学院中药开发研究所,广东广州510006
出 处:《时珍国医国药》2012年第8期1878-1880,共3页Lishizhen Medicine and Materia Medica Research
基 金:国家"十二五"重大新药创制专项(No.2011ZX09102-011-01);国家自然科学基金(No.30973954);广州市科技局资助项目(No.2008AI-E4101-3)
摘 要:目的建立高效液相色谱(HPLC)法测定大鼠口服中药复方麻黄制剂后血浆中麻黄碱、伪麻黄碱的含量,为研究中药复方麻黄制剂在大鼠体内药动学提供基础。方法采用Synergi 4u Polar-RP 80A(250 mm×4.60 mm,4μm)色谱柱,以甲醇-0.092%磷酸(含0.04%三乙胺、0.02%二正丁胺)为流动相,流速为1.0 ml/min,柱温为25℃,检测波长为207nm。结果麻黄碱在1.43~45.76μg/ml范围内线性关系良好(r=0.999 8),伪麻黄碱在1.35~43.12μg/ml范围内线性关系良好(r=0.999 8),回收率符合生物样品分析,两者日内、日间精密度的RSD<5%。结论建立的高效液相色谱测定方法为动物体内麻黄碱、伪麻黄碱的测定提供了一个可靠的方法。Objective To establish the method for determination of ephedrine and pseudo - ephedrine in rat plasma with high performance liquid chromatography. Methods Ephedrine and pseudo - ephedrine were separated on Synergi 4u Polar - RP 80A column (250 mm × 4.60 mm,4 um) , with mobile phase consisted of methanol - 0.092 % phosphoric acid ( containing 0.04% triethanolamine and 0.02% Di- n -Butyl Amine) at a flow rate of 1.0ml/min, the column temperature was 25℃ ,and the detection wavelength was set at 207 nm. Results The calibration curves of E and PE were linear within the range from 1.43 ug/ml to 45.76 ug/ml ( r = 0. 9998 ) and from 1.35 ug/ml to 43.12 ug/ml ( r = 0.999 8 ), respectively. The RSDs of interday and intraday were all less than 5%. Conclusion The method can be used to determine ephedrine and pseudo - ephedrine in vivo.
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