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采用高效液相色谱-荧光检测法分析人血浆中的唑吡坦:在单剂量药代动力学研究中的应用。

Analysis of zolpidem in human plasma by high-performance liquid chromatography with fluorescence detection: application to single-dose pharmacokinetic studies.

作者信息

Durol A L, Greenblatt D J

机构信息

Department of Pharmacology and Experimental Therapeutics, Tufts University School of Medicine, Boston, MA 02111, USA.

出版信息

J Anal Toxicol. 1997 Sep;21(5):388-92. doi: 10.1093/jat/21.5.388.

Abstract

Zolpidem, an imidazopyradine hypnotic agent, can be quantitated by high-performance liquid chromatography (HPLC) with fluorescence detection. After the addition of a structurally related internal standard (propyl-zolpidem), plasma samples were double-extracted at neutral pH with toluene-isoamyl alcohol or benzene-isoamyl alcohol. The organic extracts were evaporated to dryness, reconstituted with mobile phase, and analyzed by HPLC using a C-18 reversed-phase column, a mobile phase of acetonitrile-50mM potassium dihydrogen phosphate (50:50), and fluorescence detection with excitation and emission wavelengths of 254 and 390 nm, respectively. The lower limit of reliable quantitation was in the range of 1-2.5 ng/mL. The method is applicable to single-dose pharmacokinetic studies of zolpidem in humans.

摘要

唑吡坦是一种咪唑并吡啶类催眠药,可通过高效液相色谱(HPLC)结合荧光检测进行定量分析。加入结构相关的内标(丙基唑吡坦)后,血浆样品在中性pH条件下用甲苯 - 异戊醇或苯 - 异戊醇进行两次萃取。有机萃取物蒸发至干,用流动相复溶,然后使用C - 18反相柱、乙腈 - 50mM磷酸二氢钾(50:50)的流动相进行HPLC分析,并分别在激发波长和发射波长为254和390nm处进行荧光检测。可靠定量的下限在1 - 2.5 ng/mL范围内。该方法适用于唑吡坦在人体的单剂量药代动力学研究。

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