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作 者:隋鑫[1] 毕开顺[1] 房丽娜[1] 冯静[1] 陈晓辉[1]
出 处:《中南药学》2009年第6期422-424,共3页Central South Pharmacy
摘 要:目的建立HPLC方法同时测定大鼠肠灌流液中L-肌肽和酚红的质量浓度。方法采用KromasilNH2色谱柱(200mm×4.6mm,5μm),流动相为乙腈-磷酸盐缓冲液(1mmol.L^-1磷酸二氢钾,0.2mmol.L^-1磷酸氢二钾)(体积比50:50),流速1.0mL·min^-1,柱温35℃,检测波长210nm,进样量20μL。结果L-肌肽和酚红分别在质量浓度22.6~158mg·L^-1(r=0.9998)、14.2~99.4mg·L^-1(r=0.9991)与峰面积线性关系良好,2种成分回收率分别为99.1%、98.8%,RSD均〈3%。结论所用方法准确、简便、专属性好,可准确快速测定大鼠肠灌流液中L-肌肽和酚红的含量;L-肌肽的摄取过程依赖于H^+电位梯度。Objective To establish an HPLC method for the simultaneous determination of L-carnosine and phenolsul- fonphthalein in rat single pass intestinal perfusion solution. Methods The separation was performed on a Kromasil NH2 column (200 mm × 4.6 mm, 5 μm) with the mobile phase of acetonitrile and phosphate buffer solution (1 mmol·L^-1 of potassium dihydrogen phosphate and 0.2 mmol·L^-1 of dipotassium hydrogen phosphate) (50 : 50). The flow rate was 1.0 mL·min^-1. The column temperature was 35℃. The UV detector was 210 nrlL Results The linear ranges of L-carnosine and phenolsulfonphthalein were 22.6-158 mg· L^-1 (r=0. 999 8) and 14. 2-99.4 mg·L^-1 (r=0. 999 1), respectively. The average recovery of L-carnosine and phenolsulfonphthalein was 99.1% and 98. 8%. Conclusion The method is simple, accurate and rapid for the simultaneous determination of L-carnosine and phenolsul- fonphthalein in rat single pass intestinal perfusion solution. L-carnosine uptake process depends on the H^+ potential gradient.
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