CuBTC metal organic framework-based dispersive solid phase extraction of cyclosporine and tacrolimus from plasma samples prior to determination by high performance liquid chromatography-tandem mass spectrometry

被引:3
|
作者
Mogaddam, Mohammad Reza Afshar [1 ,2 ]
Khosrowshahi, Elnaz Marzi [1 ]
Farajzadeh, Mir Ali [3 ,4 ]
Nemati, Mahboob [1 ,5 ]
机构
[1] Tabriz Univ Med Sci, Food & Drug Safety Res Ctr, Tabriz, Iran
[2] Tabriz Univ Med Sci, Pharmaceut Anal Res Ctr, Tabriz, Iran
[3] Tabriz Univ, Fac Chem, Dept Analyt Chem, Tabriz, Iran
[4] Near East Univ, Engn Fac, Mersin 10, TR-99138 Nicosia, North Cyprus, Turkiye
[5] Tabriz Univ Med Sci, Fac Pharm, Pharmaceut & Food Control Dept, Tabriz, Iran
关键词
Metal organic framework; Dispersive solid phase extraction; Plasma; High performance liquid chromatography; tandem mass spectrometry; Immunosuppressive drugs; WHOLE-BLOOD; SIROLIMUS; IMMUNOSUPPRESSANTS; ASSAY;
D O I
10.1016/j.jchromb.2023.123692
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Immunosuppressive drugs are prescribed to reduce the immune system of persons who are undergoing organ transplants. The concentration of these drugs in blood and plasma samples must be accurately and precisely determined during immunosuppressive therapy due to their significant side effects. In this study, a metal organic framework-based dispersive solid phase extraction method was developed for the extraction of tacrolimus and cyclosporine from plasma samples before their determination by high performance liquid chromatography-tandem mass spectrometry. For this purpose, CuBTC metal organic framework nanoparticles were prepared by a hydrothermal approach and they were used as the sorbent in the extraction procedure. The adsorbed analytes were eluted by a suitable organic solvent and then more concentrated by evaporation of the eluate. All of the effective parameters of the method including sorbent amount, adsorption time, eluent type, desorption time, eluent volume, and sample solution pH were studied and optimized. They were obtained 5 mg, 5 min, acetone, 5 min, 300 mu L, and 5, respectively. Under optimal conditions, the developed method was validated and the data showed that the linear range, the limit of detection, the limit of quantification, the coefficient of determination, the enrichment factor, and relative standard deviation values were 1-1000 ng mL-1, 0.30 ng mL-1, 0.5 ng mL-1, 0.99, 15.6, and 5.8 % for tacrolimus and 0.8-500 ng mL-1, 0.25 ng mL-1, 0.4 ng mL-1, 0.99, 17, and 5.6 % for cyclosporine, respectively. Finally, the method was successfully used in the determination of the studied drugs in plasma samples.
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页数:8
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