Salting-out liquid-liquid microextraction to the determination of mycophenolic acid in plasma samples

被引:7
作者
Niknafs, Maryam [1 ,2 ]
Kaviani, Raha [3 ]
Gharekhani, Afshin [4 ]
Jouyban, Abolghasem [5 ,6 ,7 ]
Shayanfar, Ali [5 ,6 ]
机构
[1] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz, Iran
[2] Tabriz Univ Med Sci, Student Res Comm, Tabriz, Iran
[3] Tabriz Univ Med Sci, Biotechnol Res Ctr, Tabriz, Iran
[4] Tabriz Univ Med Sci, Sina Hosp, Fac Pharm, Dept Clin Pharm Pharmacotherapy, Tabriz, Iran
[5] Tabriz Univ Med Sci, Pharmaceut Anal Res Ctr, Tabriz, Iran
[6] Tabriz Univ Med Sci, Fac Pharm, Tabriz, Iran
[7] Univ Tehran Med Sci, Digest Dis Res Inst, Tehran, Iran
来源
CHEMICAL PAPERS | 2020年 / 74卷 / 05期
关键词
Mycophenolic acid; Human plasma; Salting-out liquid-liquid microextraction; Fluorescent complex; SOLID-PHASE EXTRACTION; GLUCURONIDE; CHROMATOGRAPHY; QUANTIFICATION; METABOLITES; SERUM;
D O I
10.1007/s11696-019-01018-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study aimed to develop a determination method of mycophenolic acid (MPA) in biological samples using salting-out liquid-liquid microextraction from human plasma samples based on the formation of a fluorescent complex with terbium ion and its application in quantification of the MPA in clinical samples. MPA extracted from plasma samples by salting-out liquid-liquid microextraction after protein precipitation by acetonitrile. Then, the fluorescence intensity was measured at 545 nm using an excitation wavelength of 347 nm after optimization of extraction parameters. Under the optimum conditions for the developed method, it provided a linear range between 0.5 and 5.0 mu g/mL with a correlation coefficient (R-2) of 0.998, and then, the validation was performed according to the FDA guideline and the developed method could quantify MPA concentration in real plasma samples. The results showed that linearity, accuracy, and precision of the developed analysis method were suitable for the determination of the MPA in plasma samples.
引用
收藏
页码:1663 / 1668
页数:6
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