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藥物食品檢驗局調查研究年報

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篇名 Determination of Polar Constituents of Scrophulariae Radix in Bai-He-Gu-Jin-Tang by Micellar Electrokinetic Capillary Chromatography
卷期 17
作者 顧祐瑞周鳳琴溫國慶林哲輝廖俊亨
頁次 251-259
關鍵字 Pharmaceutical analysisScrophulariae RadixBai-He-Gu-Jin-TangHarpagosideMEKCTSCI
出刊日期 199909

中文摘要

英文摘要

A micellar electrokinetic capillary chromatographic method was established for the determination of 2-(3-hydroxy-4-methoxyphenyl)ethyI l-0-[a-L-arabi-nopyranosyl(l—>6)]-feruIoyI(l—>4)-a-L-rhamnopyranosyl(l-^3)-P-D-glucopyra noside (SN-A), harpagoside (SN-B) and cinnamic acid (SN-C) in the traditional Chinese medicinal prescription, Bai-He-Gu-Jin-Tang, which contains Scrophulariae Radix. This chromatographic technique was carried out using a buffer composed of 20 mM sodium tetraborate and sodium dihydrogen phosphate containing 120 mM sodium cholate and 12 % methanol at pH 7.5. 2-(4-Hy-droxyphenyl)-ethylammonium chloride was used as an internal standard and detected at 280 nm. The linear calibration ranges for SN-A, B and C were 11.76-188.16 |lg/mL (r = 0.9998), 8.16-130.56 [ig/mL (r = 0.9992) and 4.48-71.68 ^ig/mL (r = 0.9991), respectively. The recoveries of the markers listed above were SN-A: 104.3 ±2.8 %, SN-B: 98.1 ±2.2 % and SN-C: 98.2 ±1.4 The relative standard deviations of the three marker substances for intraday and interday analyses ranged from 0.85 to 2.87 % and from 1.42 to 4.14 %, respectively.

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