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

机译:液-液微萃取后生物样品中波生坦的光谱分析

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Introduction Microextraction processes with UV-Vis measurement have been developed and validated for analysis of bosentan in biological samples. Methods In this work, liquida??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 1.0a??5.0 ??g.mLa??1, with coefficient of determination (R2) of & 0.998. The limit of detection (LOD) was 0.07 mg.La??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.
机译:引言已经开发了利用UV-Vis测量的微萃取工艺,并经过验证可用于分析生物样品中的波生坦。方法在这项工作中,采用液态液相微萃取程序(DLLME& USAEME)进行纯化,预浓缩和通过270 nm的UV-Vis光谱法测定生物样品中的波生坦。该方法经过验证,可用于测定加标血清,呼出气冷凝物和尿液样品中的波生坦。结果研究了各种实验因素,包括萃取类型和分散溶剂,其体积,pH,超声处理时间和离心时间。在最佳条件下,该方法在1.0a≤5.0≤g·mLa≤1范围内是线性的,测定系数(R2)≥1。 0.998。检出限(LOD)为0.07mg.La△1。生物样品中目标分析物的回收率为106.2%。该方法可轻松用于更高浓度的波生坦,并需要更大的改进才能用于需要更敏感方法的药代动力学研究中。结论建立了一种简单,低成本,精确,准确的分光光度法测定生物样品中波生坦的分光光度法,并已用于常规分析。

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