A novel freeze-dried storage and preparation method for the determination of mycophenolic acid in plasma by high-performance liquid chromatography

被引:2
|
作者
Wang, Lei [1 ,2 ]
Qiang, Wei [2 ]
Li, Ying [3 ]
Cheng, Zeneng [2 ]
Xie, Mengmeng [2 ]
机构
[1] Cent S Univ, Sch Life Sci, Changsha, Hunan, Peoples R China
[2] Cent S Univ, Sch Pharmaceut Sci, Res Inst Drug Metab & Pharmacokinet, Changsha, Hunan, Peoples R China
[3] Guiyang Coll, Sch Food & Pharmaceut Engn, Guiyang, Guizhou, Peoples R China
基金
中国国家自然科学基金;
关键词
freeze-dry; HPLC-UV; mycophenolic acid; sample storage; TANDEM MASS-SPECTROMETRY; SOLID-PHASE EXTRACTION; BLOOD SPOTS; LC-MS/MS; QUANTIFICATION; MOFETIL; PHARMACOKINETICS; GLUCURONIDE; RECIPIENTS;
D O I
10.1002/bmc.3958
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Plasma samples were conventionally stored at freezing conditions until the time of detection. Such a technique, when carried out over an extended period, is energy consuming; in addition, preparation and transportation of stored samples is inconvenient. In this study, a freeze-dried storage and preparation method was proposed to determine the presence of mycophenolic acid (MPA) in plasma. Fresh plasma samples were freeze-dried using a device, and then stored at ambient temperature. After the stored samples were soaked with methanol spiked with the internal standard, high-performance liquid chromatography was conducted to detect MPA. The proposed method was demonstrated to be precise and accurate over the linear range of 0.5-50 mu g mL(-1), with both intra- and inter-day precision being <7% and biases <10%. The freeze-dried samples were stable at ambient temperature for at least 40 days. This method was also successfully applied to the pharmacokinetic study of MPA in healthy volunteers. Pharmacokinetic parameters, such as maximum plasma concentration, time point of maximum plasma concentration and elimination half-life, among others, were consistent with the results in the published study. This proposed technique was proved to be simple, reproducible and energy saving. This approach could also simplify the storage and analysis of samples in clinical and scientific drug research.
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页数:8
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