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Determination of pipemidic acid in plasma by normal-phase high-pressure liquid chromatography.

机译:正相高压液相色谱法测定血浆中的哌啶酸。

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摘要

An improved high-pressure liquid chromatography procedure for determining the concentration of pipemidic acid in human plasma was developed, which uses a normal-phase silica gel column and aqueous mobile solvent system similar to that used in reverse-phase chromatography. Precolumn derivatization of pipemidic acid was achieved by a methylation reaction with boron trifluoride in methanol after extraction from plasma with chloroform containing 4% ethanol. The percent recovery of pipemidic acid was 88.3 +/- 7.7, the variation of which became negligible when quinacrine was used as an internal standard for the determination. High-pressure liquid chromatography analysis was performed by conventional silica gel and mobile solvent mixtures containing 3% of 0.14% HClO4 solution, 19% methanol, and 78% chloroform. The UV detector was set at 265 nm. The detection limit of pipemidic acid methyl ester was as low as 10 ng of the injection amounts or 0.5 micrograms of the plasma per ml, with 0.01 absorbance units (full scale) and a signal-to-noise ratio of 3.
机译:开发了一种改进的高压液相色谱法,用于测定人血浆中的哌啶酸浓度,该方法使用了与反相色谱法相似的正相硅胶柱和水性流动溶剂系统。在用含有4%乙醇的氯仿从血浆中萃取后,通过与三氟化硼在甲醇中的甲基化反应,实现哌啶酸的柱前衍生。哌啶酸的回收百分率为88.3 +/- 7.7,当将喹那林用作测定的内标时,其变化可忽略不计。用常规硅胶和流动溶剂混合物进行高压液相色谱分析,该混合物包含3%的0.14%HClO4溶液,19%的甲醇和78%的氯仿。紫外线检测器设置在265 nm。哌啶甲酯的检出限低至每毫升10 ng进样量或0.5微克血浆,吸光度单位为0.01(满量程),信噪比为3。

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