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大鼠血浆中甲基泼尼松龙、琥珀酸甲基泼尼松龙和内源性皮质酮的同步分析。

Simultaneous analysis of methylprednisolone, methylprednisolone succinate, and endogenous corticosterone in rat plasma.

作者信息

Mehvar R, Dann R O, Hoganson D A

机构信息

School of Pharmacy, Texas Tech University Health Sciences Center, Anmarillo 79106, USA.

出版信息

J Pharm Biomed Anal. 2000 Jul;22(6):1015-22. doi: 10.1016/s0731-7085(00)00253-3.

Abstract

A reversed-phase HPLC method is reported for simultaneous quantitation of methylprednisolone (MP), MP succinate (MPS), and endogenous corticosterone (CST) in plasma of rats. Additionally, the 11-keto metabolite of MP (methylprednisone, MPN) is resolved from the other analytes. After addition of internal standard (triamcinolone acetonide: IS) and an initial clean up step, the analytes of interest are extracted into methylene chloride. The steroids are then resolved on a reversed-phase polymer column using a mobile phase of 0.1 M acetate buffer (pH 5.7): acetonitrile (77:23) which is pumped at a flow rate of 1.5 ml min-1. Sample detection was accomplished using an UV detector at a wavelength of 250 nm. All the five components (MPS, MP, MPN, CST and IS) were baseline resolved from each other and other components of plasma. Linear relationships were found between the steroids: IS peak area ratios and plasma concentrations in the range of 0.1-4 mircog ml-1 for MP and MPS and 0.1-1.0 microg ml-1 for MPN and CST. The assay is accurate as intra- and inter-run error values were < +/- 8% for all the components. Further, the intra- and inter-run CVs of the assay were < 16% at all the concentrations and for all the components. The application of the assay was demonstrated after the injection of a single 5 mg kg-1 (MP equivalent) dose of MPS or a macromolecular prodrug of MP to rats.

摘要

本文报道了一种反相高效液相色谱法,用于同时定量大鼠血浆中的甲基泼尼松龙(MP)、琥珀酸甲泼尼龙(MPS)和内源性皮质酮(CST)。此外,还可将MP的11-酮代谢物(甲基泼尼松,MPN)与其他分析物分离。加入内标(曲安奈德:IS)并经过初步净化步骤后,将目标分析物萃取到二氯甲烷中。然后,使用0.1 M醋酸盐缓冲液(pH 5.7):乙腈(77:23)作为流动相,以1.5 ml min-1的流速泵入,在反相聚合物柱上分离类固醇。使用紫外检测器在250 nm波长下完成样品检测。所有五种成分(MPS、MP、MPN、CST和IS)在基线处相互分离,且与血浆中的其他成分分离。在0.1 - 4 mircog ml-1范围内,MP和MPS的类固醇:IS峰面积比与血浆浓度之间存在线性关系;在0.1 - 1.0 microg ml-1范围内,MPN和CST的类固醇:IS峰面积比与血浆浓度之间存在线性关系。该测定方法准确,所有成分的批内和批间误差值均<±8%。此外,该测定方法在所有浓度下和所有成分的批内和批间CV均<16%。在给大鼠注射单次5 mg kg-1(MP当量)剂量的MPS或MP的大分子前药后,证明了该测定方法的应用。

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