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. 2017:2017:7194075.
doi: 10.1155/2017/7194075. Epub 2017 Jun 1.

Determination of Epimedin B in Rat Plasma and Tissue by LC-MS/MS: Application in Pharmacokinetic and Tissue Distribution Studies

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Determination of Epimedin B in Rat Plasma and Tissue by LC-MS/MS: Application in Pharmacokinetic and Tissue Distribution Studies

Qianru Feng et al. J Anal Methods Chem. 2017.

Abstract

A simple, sensitive, and specific liquid chromatography tandem mass-spectrometric method was developed and validated for the determination of epimedin B in rat plasma and tissue samples. After being processed with a protein precipitation method, these samples were separated on an Agilent Eclipse XDB-C18 column with an isocratic mobile phase consisting of acetonitrile and 0.1% formic acid aqueous solution (32 : 68, v/v). The calibration curve of epimedin B was linear over the concentration range from 1 to 500 ng/mL in plasma and tissue homogenate. The method was then applied to pharmacokinetic and tissue distribution studies after a single oral administration of Herba Epimedii extract to SD rats. Results showed that epimedin B reached the plasma peak concentration at 0.4 h and the terminal elimination half-life was 1.6 h in rat plasma, and the plasma area under the curve from time zero to infinity (AUC0- ) was 14.35 μg/L·h. The concentration distribution of epimedin B in rat tissue was in the following order: liver > ovary > womb > lung > kidney > spleen > heart > brain, indicating that the compound could be widely distributed in rat, and the reproductive system may be the principal target of epimedin B for female rat.

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Figures

Figure 1
Figure 1
Chemical structure of epimedin B and genistein (internal standard).
Figure 2
Figure 2
(1) Full-scan mass spectrum of epimedin B (A1) and internal standard (genistein, B1). (2) Product ion spectrum of epimedin B (A2) and internal standard (genistein, B2).
Figure 3
Figure 3
Representative MRM chromatograms: (A1) blank plasma, (A2) blank plasma spiked with epimedin B at LOQ, (A3) rat plasma sample obtained at 0.5 h after administration, (A4) blank plasma spiked with IS, (B1) blank liver, (B2) blank liver spiked with epimedin B at LOQ, (B3) rat liver sample obtained at 0.5 h after administration, and (B4) blank liver spiked with IS.
Figure 4
Figure 4
Mean plasma concentration-time profile and tissue distribution of epimedin B in female rats after a single oral dose of Herba Epimedii extract (containing 15 mg/g epimedin B).

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