完整後設資料紀錄
DC 欄位語言
dc.contributor.authorHsieh, YZen_US
dc.contributor.authorHuang, HYen_US
dc.date.accessioned2019-04-02T06:00:31Z-
dc.date.available2019-04-02T06:00:31Z-
dc.date.issued1997-01-24en_US
dc.identifier.issn0021-9673en_US
dc.identifier.urihttp://dx.doi.org/10.1016/S0021-9673(96)00768-6en_US
dc.identifier.urihttp://hdl.handle.net/11536/149437-
dc.description.abstractIn this study, we examine the feasibility of determining saikosaponins a, b1, b2, c and d, i.e., the bioactive components in Bupleuri Radix, using the micellar electrokinetic capillary chromatography technique. Results obtained from using different anion surfactants, bile salt or sodium dodecyl sulfate (SDS), are also compared. By using bile salt as a pseudostationary phase, the baseline separation of saikosaponins is observed; however, the detection limit is unfavorable. Whereas the baseline resolution of saikosaponins is achieved after adding gamma-cyclodextrin in the SDS running buffer. In addition, another separating method is developed with the mixed micellar system of SDS and Brij 35 containing gamma-cyclodextrin. The contents of saikosaponins in traditional Chinese medicinal prescriptions, such as Sheau Chair Hwu Tang, Bupleuri Radix plant and Chair Hwu San are analyzed by one of the above methods. The entire separation can be completed within 9 min by these methods. The R.S.D. values of the migration times are all below 1%. Moreover, the detection limits of saikosaponins vary from 7 to 33 mu g/ml.en_US
dc.language.isoen_USen_US
dc.subjectbuffer compositionen_US
dc.subjectpharmaceutical analysisen_US
dc.subjectsaikosaponinsen_US
dc.subjectsaponinsen_US
dc.titleDetermination of saikosaponins by micellar electrokinetic capillary chromatographyen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/S0021-9673(96)00768-6en_US
dc.identifier.journalJOURNAL OF CHROMATOGRAPHY Aen_US
dc.citation.volume759en_US
dc.citation.spage193en_US
dc.citation.epage201en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:A1997WH31200019en_US
dc.citation.woscount23en_US
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