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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

化学 色谱法 检出限 固相萃取 洗脱 吸附剂 萃取(化学) 柱色谱法 液相色谱-质谱法 质谱法 富集因子 吸附 有机化学
作者
Mohammad Reza Afshar Mogaddam,Elnaz Marzi Khosrowshahi,Mir Ali Farajzadeh,Mahboob Nemati
出处
期刊:Journal of Chromatography B [Elsevier BV]
卷期号:1222: 123692-123692 被引量:1
标识
DOI:10.1016/j.jchromb.2023.123692
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 μL, 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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