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A HFCF-UF method to directly analyze the total concentration of protein-binding drugs

机译:HFCF-UF方法直接分析蛋白质结合药物的总浓度

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摘要

In the present study, a direct injection hollow fiber centrifugal ultrafiltration (HFCF-UF) method was developed for therapeutic drug monitoring (TDM) for the total concentration of liposoluble protein binding drugs. We used carbamazepine (CBZ) and phenobarbital (PB) as model drugs and proposed a HFCF-UF method to analyze the total concentration of liposoluble protein binding drugs without the use of traditional biological sample preparations. Our results demonstrate that acetone acts as a liposoluble desorption agent and can make the target compounds release from the protein-drug complexes and then re-dissolve the released compounds. The absolute recovery is excellent at approximately 100%, which is higher than when traditional biological sample preparations have to be used. Calibration curves can be established in a plasma-free standard solution instead of using spiked human plasma. The HFCF-UF method offers the advantages of highly satisfactory performance and simple and fast pretreatment, consistent with the practical requirements of TDM.
机译:在本研究中,开发了一种直接注射中空纤维离心超滤(HFCF-UF)方法用于脂溶性蛋白结合药物总浓度的治疗药物监测(TDM)。我们使用卡马西平(CBZ)和苯巴比妥(PB)作为模型药物,并提出了HFCF-UF方法来分析脂溶性蛋白结合药物的总浓度,而无需使用传统的生物样品制备方法。我们的结果表明,丙酮充当脂溶性解吸剂,可以使目标化合物从蛋白质-药物复合物中释放出来,然后重新溶解释放的化合物。绝对回收率极佳,约为100%,这比必须使用传统的生物样品制剂时要高。可以在无血浆的标准溶液中建立校准曲线,而无需使用加标的人体血浆。 HFCF-UF方法具有非常令人满意的性能以及简单快速的预处理方法,符合TDM的实际要求。

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