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出 处:《药学学报》1998年第2期138-142,共5页Acta Pharmaceutica Sinica
基 金:国家自然科学基金
摘 要:建立了选择性测定血浆中普罗帕酮对映异构体的柱前衍生化反相HPLC法。用S(+)1(1萘基)乙基异氰酸酯为衍生化试剂,与血浆中提取出的普罗帕酮反应生成非对映立体异构体,以HPLCUV检测法(220nm)定量。采用此法成功地测试了10名健康受试者单剂量口服300mg盐酸普罗帕酮片后对映异构体的药代动力学曲线。此法灵敏度高(75ng·ml-1),操作简便,重现性好。A reversed phase HPLC method to stereoselectively determine enantiomers of propafenone in human plasma has been developed. After extraction of 1 ml plasma with 3 ml of nC6H14∶CH2Cl2∶2C3H7OH (100∶50∶5, v/v) and dried under N2, the enantiomers of propafenone were allowed to react with homochiral S(+)1(1naphthyl) ethyl isocyanate (566 μg in 60 μl CH2Cl2) at RT for 30 min, to give the diastereomeric derivatives. Their separation was achieved using HPLC with a C18column and UVdetection (220 nm) and the enantiomeric ratios were measured. The concentrations of each enantiomer were then calculated using the enantiomeric ratios and the racemic propafenone concentrations previously measured. This method after validation procedures has been applied to the multisample analyses of a human pharmacokinetic study with 10 healthy volunteers after an oral dose of 300 mg propafenone hydrochloride. The method was shown to be sensitive (75 ng·ml-1), convenient and reproducible.
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