摘要
目的:运用反相高效液相法(RP-HPLC)比较不同超微粉碎条件下中药复方麻杏石甘汤样品中的麻黄碱(ephedrine)与伪麻黄碱(d-pseudo-ephedrine)的溶出率变化趋势。方法:YMC ODS-C18柱(4.6 mm×150 mm,4μm);流动相水-乙腈-十二烷基硫酸钠(SDS)-磷酸(650∶350∶5∶1);柱温50℃;检测波长210 nm;流速1.5 mL.min-1。结果:超微粉碎前后样品溶出率差异显著。结论:证明对于麻杏石甘汤复方,经过超微粉碎技术处理后的样品,其麻黄碱与伪麻黄碱的溶出速度比未经超微粉碎处理之复方加快,且溶出率增加。
Objective: To compare the solubilities of ephedrine and d-pseudo-ephdrine in the compound of traditional Chinese drugs--Maxing Shigan decoction with and without ultramicro-pulverizations using a RP-HPLC procedure. Method: The analytical column was a YMC ODS-C18 (4.6 mm × 150mm, 4 μm) . A mixture of water-acetonitrile-sodium dodecyl sulfate-phosphorous acid (650: 350:5:1 ) was used as the mobile phase at flow rate of 1.5 mL·min^-1 The column temperature was 50℃ and the wavelength was 210 nm. Results: In this way, ephedrine and d-pseudo-ephedrine of the compound samples can be separated well and showed significant differences before and after the ultramicro-pulverizations. Conclusion: For the Maxing Shigan decoction, the dissolution rates and solubilites of ephedrine and d-pseudoephedrine ultramicro-pulverization were greatly improved.
出处
《中国中药杂志》
CAS
CSCD
北大核心
2006年第11期884-886,共3页
China Journal of Chinese Materia Medica
关键词
反相高效液相法
超微粉碎
麻黄碱
伪麻黄碱
溶出率
RP-HPLC
ultramicro-pulverization
ephedrine, d-pseudo-ephedrine
solubilities