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采用高效液相色谱-荧光检测法研究大鼠口服和静脉注射补骨脂素后的药代动力学、生物利用度及排泄情况。

The pharmacokinetics, bioavailability and excretion of bergapten after oral and intravenous administration in rats using high performance liquid chromatography with fluorescence detection.

作者信息

Yu Xie-An, Azietaku John Teye, Li Jin, An Mingrui, He Jun, Hao Jia, Cao Jun, Chang Yan-Xu

机构信息

Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, 300193 China.

Department of Surgery, University of Michigan, Ann Arbor, MI 48109 USA.

出版信息

Chem Cent J. 2016 Oct 14;10:62. doi: 10.1186/s13065-016-0212-x. eCollection 2016.

Abstract

A sensitive, specific, reproducible and optimized high performance liquid chromatography with fluorescence detection (HPLC-FLD) method for the determination of bergapten in rat plasma was established and applied to the pharmacokinetic and bioavailability study in rat after oral and intravenous administration of bergapten. The method was also successfully applied to the excretion study of bergapten after an oral administration of bergapten at a dose of 15 mg kg to rats. The sample preparation was achieved using liquid-liquid extraction. Isoimperatorin was used as the internal standard (IS). The analytes were detected by using fluorescence detection at an excitation and emission wavelength of 288 and 478 nm, respectively. Using aqueous formic acid (0.1 %, v/v) and acetonitrile as the mobile phase, the chromatographic separation was achieved on a Hedera™ ODS column at a flow rate of 1 mL min. The lower limit of quantitation (LLOQ) of bergapten was 2 ng mL. The HPLC-FLD method was successfully applied to the pharmacokinetic, bioavailability and excretion study of bergapten in rats.Graphical abstractAn high performance liquid chromatography with fluorescence detection (HPLC-FLD) method for the pharmacokinetic and bioavailability study in rat after administration of bergapten.

摘要

建立了一种灵敏、特异、可重复且优化的高效液相色谱-荧光检测法(HPLC-FLD),用于测定大鼠血浆中的补骨脂素,并将其应用于大鼠口服和静脉注射补骨脂素后的药代动力学和生物利用度研究。该方法还成功应用于以15 mg/kg剂量给大鼠口服补骨脂素后的排泄研究。采用液-液萃取法进行样品制备。异欧前胡素用作内标(IS)。分别在激发波长288 nm和发射波长478 nm处采用荧光检测法检测分析物。以甲酸水溶液(0.1%,v/v)和乙腈为流动相,在Hedera™ ODS柱上以1 mL/min的流速实现色谱分离。补骨脂素的定量下限(LLOQ)为2 ng/mL。HPLC-FLD法成功应用于大鼠补骨脂素的药代动力学、生物利用度和排泄研究。

图形摘要

一种用于补骨脂素给药后大鼠药代动力学和生物利用度研究的高效液相色谱-荧光检测法(HPLC-FLD)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b7c/5064970/343e4c523853/13065_2016_212_Figa_HTML.jpg

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