药代动力学
化学
生物利用度
电喷雾电离
色谱法
儿茶素
没食子酸表没食子酸酯
选择性反应监测
药理学
口服
没食子酸
质谱法
串联质谱法
生物化学
抗氧化剂
多酚
医学
核化学
作者
Lei Chwen Lin,Meng Nan Wang,Ting Yu Tseng,Jung Sung Sung,Tung Hu Tsai
摘要
A liquid chromatography technique coupled with tandem mass spectrometry (LC-MS/MS) electrospray ionization was used to measure (−)-epigallocatechin-3-gallate (EGCG) in rat plasma. This method was applied to investigate the pharmacokinetics of EGCG in a conscious and freely moving rat by an automated blood sampling device. Multiple reaction monitoring (MRM) was used to monitor the transition of the deprotonated molecule m/z of 457 [M − H]- to the product ion 169 for EGCG and the m/z of 187 to 164 for the internal standard. The limit of quantification (LOQ) of EGCG in rat plasma was determined to be 5 ng/mL, and the linear range was 5−5000 ng/mL. The protein binding of EGCG in rat plasma was 92.4 ± 2.5%. The brain distribution result indicated that EGCG may potentially penetrate through the blood−brain barrier at a lower rate. The disposition of EGCG in the rat blood was fitted well by the two-compartmental model after intravenous administration (10 mg/kg, iv). The elimination half-life of EGCG was 62 ± 11 and 48 ± 13 min for intravenous (10 mg/kg) and oral (100 mg/kg) administration, respectively. The pharmacokinetic data indicate that the oral bioavailability of EGCG in a conscious and freely moving rat was about 4.95%. Keywords: Camellia sinensis; catechin; (−)-epigallocatechin-3-gallate; freely moving rat; pharmacokinetics; tandem mass spectrometry
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