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一种用于测定从桦褐孔菌中分离得到的氧化三萜二醇的新型生物分析方法及其在药代动力学研究中的应用。

A Novel Bioanalytical Method for Determination of Inotodiol Isolated from Inonotus Obliquus and Its Application to Pharmacokinetic Study.

作者信息

Kim Jin Hyeok, Gao Dan, Cho Chong Woon, Hwang Inkyu, Kim Hyung Min, Kang Jong Seong

机构信息

College of Pharmacy, Chungnam National University, Daejeon 34134, Korea.

出版信息

Plants (Basel). 2021 Aug 9;10(8):1631. doi: 10.3390/plants10081631.

Abstract

In this study, we developed a bioanalytical method using liquid chromatography coupled to triple quadrupole tandem mass spectrometry (LC-MS/MS) to apply to a pharmacokinetic study of inotodiol, which is known for its anti-cancer activity. Plasma samples were prepared with alkaline hydrolysis, liquid-liquid extraction, and solid-phase extraction. Inotodiol was detected in positive mode with atmospheric pressure chemical ionization by multiple-reaction monitoring mode using LC-MS/MS. The developed method was validated with linearity, accuracy, and precision. Accuracy ranged from 97.8% to 111.9%, and the coefficient of variation for precision was 1.8% to 4.4%. The developed method was applied for pharmacokinetic study, and the mean pharmacokinetic parameters administration were calculated as follows: λ 0.016 min; T 49.35 min; C 2582 ng/mL; Cl 0.004 ng/min; AUC 109,500 ng×min/mL; MRT 32.30 min; Vd 0.281 mL after intravenous administration at dose of 2 mg/kg and λ 0.005 min; T 138.6 min; T 40 min; C 49.56 ng/mL; AUC 6176 ng×in/mL; MRT 103.7 min after oral administration. The absolute oral bioavailability of inotodiol was 0.45%, similar to nonpolar phytosterols. Collectively, this is the first bioanalytical method and pharmacokinetic study for inotodiol.

摘要

在本研究中,我们开发了一种使用液相色谱-三重四极杆串联质谱联用仪(LC-MS/MS)的生物分析方法,用于进行以抗癌活性闻名的肌醇二醇的药代动力学研究。血浆样本通过碱性水解、液-液萃取和固相萃取进行制备。使用LC-MS/MS通过多反应监测模式在大气压化学电离正模式下检测肌醇二醇。所开发的方法通过线性、准确度和精密度进行了验证。准确度范围为97.8%至111.9%,精密度的变异系数为1.8%至4.4%。所开发的方法应用于药代动力学研究,静脉注射给药剂量为2mg/kg后的平均药代动力学参数计算如下:λ为0.016分钟;T为49.35分钟;C为2582ng/mL;Cl为0.004ng/分钟;AUC为109,500ng×分钟/mL;MRT为32.30分钟;Vd为0.281mL;口服给药后λ为0.005分钟;T为138.6分钟;T为40分钟;C为49.56ng/mL;AUC为6176ng×分钟/mL;MRT为103.7分钟。肌醇二醇的绝对口服生物利用度为0.45%,与非极性植物甾醇相似。总体而言,这是首次针对肌醇二醇的生物分析方法和药代动力学研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f57/8401913/99337df14a08/plants-10-01631-g001.jpg

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