Verma N, Singh S K, Gupta R C
Pharmacokinetics and Metabolism Division, Central Drug Research Institute, Lucknow, India.
J Chromatogr B Biomed Sci Appl. 1998 Apr 24;708(1-2):243-8. doi: 10.1016/s0378-4347(97)00626-9.
Simultaneous separation of E- and Z-guggulsterone, which is the main ingredient of 'Guggulip', an ayurvedic drug, was accomplished by HPLC on a C18 column using methanol, acetonitrile, buffer and tetrahydrofuran as a mobile phase. The compounds were monitored at 248 nm on a photodiode array detector. The assay method was used for the simultaneous determination of stereoisomers (E and Z) of guggulsterone in spiked serum and dosed (50 mg/kg, p.o.) rats. The recoveries of E- and Z-isomers from serum samples were always greater than 90%. The calibration graph was linear over the range of 25-2500 ng/ml for Z- and E-isomers. Lowest quantitation limit of Z- and E-guggulsterones was 25 ng/ml.
通过在C18柱上使用甲醇、乙腈、缓冲液和四氢呋喃作为流动相的高效液相色谱法(HPLC),实现了对阿育吠陀药物“古古勒普”(Guggulip)的主要成分E-和Z-古古勒甾酮的同时分离。在光电二极管阵列检测器上于248 nm处监测这些化合物。该测定方法用于同时测定加标血清和给药(50 mg/kg,口服)大鼠中古古勒甾酮的立体异构体(E和Z)。血清样品中E-和Z-异构体的回收率始终大于90%。Z-和E-异构体的校准曲线在25 - 2500 ng/ml范围内呈线性。Z-和E-古古勒甾酮的最低定量限为25 ng/ml。