Spectroscopic analysis of bosentan in biological samples after a liquid-liquid microextraction

Sanaz SAJEDI-AMIN, Karim Assadpour-Zeynali, Vahid Panahi-Azar, A. Kebriaeezadeh, M. Khoubnasabjafari, K. Ansarin, V. Jouyban-Gharamaleki, A. Jouyban
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引用次数: 9

Abstract

Introduction:Microextraction processes with UV-Vis measurement have been developed and validated for analysis of bosentan in biological samples. Methods:In this work, liquid–liquid microextraction procedures (DLLME & USAEME) were employed for cleanup, pre-concentration, and determination of bosentan in biological samples by UV-Vis spectroscopy at 270 nm. The method was validated and applied to the determination of bosentan in spiked serum, exhaled breath condensate and urine samples. Results:Various experimental factors including type of extraction and dispersive solvents and their volumes, pH, sonication time and centrifuging time were investigated. Under the optimum conditions, the method was linear in the range of 1.0–5.0 μg.mL-1, with coefficient of determination (R2) of > 0.998. The limit of detection (LOD) was 0.07 mg.L-1. Recovery of the target analyte in biological samples was 106.2%. The method could be easily applied for higher concentration of bosentan and needs more improvement for application in the pharmacokinetic investigations where more sensitive methods are required. Conclusion:A simple, low cost, precise and accurate spectrophotometric analysis of bosentan in biological samples after liquid-liquid microextraction were developed and validated for routine analyses.
液-液微萃取后生物样品中波生坦的光谱分析
微萃取工艺与紫外可见测量已经开发和验证了分析生物样品中的波生坦。方法:采用液液微萃取法(DLLME和USAEME)对生物样品中的波生坦进行清洗、预富集和270 nm紫外可见光谱测定。验证了该方法的有效性,并将其应用于加标血清、呼出液和尿液样品中波生坦的测定。结果:考察了萃取溶剂和分散溶剂的种类及其体积、pH、超声时间和离心时间等因素。在最佳条件下,该方法在1.0 ~ 5.0 μg范围内呈线性关系。mL-1,决定系数(R2) > 0.998。检出限为0.07 mg.L-1。目标分析物在生物样品中的回收率为106.2%。该方法可方便地用于较高浓度的波生坦,但在需要更灵敏方法的药代动力学研究中仍需进一步改进。结论:建立了一种简单、低成本、精确、准确的液液微萃取分光光度法分析生物样品中波生坦的方法,可用于常规分析。
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