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作 者:李素琴[1]
机构地区:[1]河北省医学科学院实验医学研究所生化研究室,河北石家庄050021
出 处:《色谱》2001年第6期555-557,共3页Chinese Journal of Chromatography
基 金:联邦德国研技部资助项目 (Schoner CHN 115 95 )
摘 要:采用薄层色谱法分离中药蟾酥中内源性哇巴因样物质 ,以三氯甲烷 甲醇 水 (体积比为 75∶2 0∶5 )溶液为展开剂 ,将所获得的活性物用反相高效液相色谱法纯化并经 2 2 0nm及 30 0nm检测后 ,以人红细胞86Rb摄取率试验测定其生物活性 ,得到了匀质的、紫外吸收波长为 2 5 0nm、可明显抑制钠泵活性的一种新的哇巴因样物质。实验结果为薄层色谱 高效液相色谱法用于内源性。An endogenous inhibitor of the sodium pump from the Chinese medication Chansu was purified The dry substance Chansu was extracted with methanol The dry residue dissolved in water and filtered subsequently through membrane filters with the exclusion size of 1000 Da, 3000 Da and 10000 Da in a Filtron Pro Vario 3 System and applied to thin layer chromatographic plate made of Silica gel 60 F 254+366 developed with a mixture of CHCl 3 MeOH H 2O(75∶20∶5, volume ratio) The fractions with R f 0 55 inhibiting the sodium pump were purified on an HPLC C 18 RP column using a linear H 2O methanol gradient with 220 nm and 300 nm DAD detection The bioactivity was measured by 86 Rb uptake into human red blood cells The results showed that a low molecular weight, water soluble compound, which inhibited the sodium pump activity in the red blood cells and had a maximum absorbance at 250 nm was isolated from the Chinese medication Chansu Several mg of the compound in pure state could be obtained from 1 kg Chansu. It was different from ouabain and proscillaridin A in chemical structure, because ouabain and proscillaridin A show a UV maximum absorption at 220 nm and 300 nm, while the new inhibitor at 250 nm
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