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Comparison of Differential Pulse Voltammetry (DPV)-a new method of carbamazepine analysis-with Fluorescence Polarization Immunoassay (FPIA)

机译:差分脉冲伏安法(DpV)的比较 - 卡马西平分析的新方法 - 荧光偏振免疫分析(FpIa)

摘要

Carbamazepine is a widely used anti-epileptic drug with narrow therapeutic range. Many methods have been developed for monitoring the serum drug level. Differential pulse voltammetry (DPV), an electrochemical method advantaged by simple, inexpensive, and relatively short analysis time, has recently been developed for carbamazepine detection. We used a newly developed DPV method with glassy carbon as a working electrode to determine the carbamazepine level. The performance of DPV is compared with the widely used fluorescence polarization immunoassay (FPIA) technique in precision, accuracy, linearity and detection limit. The precision, linearity and accuracy of the DPV and FPIA techniques were comparable at most clinical used levels. The detection limit was 1 mu g/mL for the DPV technique and 0.5 mu g/mL for the FPIA technique. The performance of the DPV technique was within the FDA guidelines for bioanalytical methods, which ensures the clinical applicability of the DPV technique. The DPV technique may have the potential to be a good alternative for carbamazepine analysis.
机译:卡马西平是一种广泛使用的抗癫痫药,治疗范围狭窄。已经开发了许多用于监测血清药物水平的方法。近年来,差动脉冲伏安法(DPV)是一种电化学方法,具有简单,便宜且分析时间短等优点,已被用于卡马西平的检测。我们使用了一种新开发的DPV方法,其中使用玻璃碳作为工作电极来测定卡马西平的含量。将DPV的性能与广泛使用的荧光偏振免疫测定(FPIA)技术进行了比较,其准确性,准确性,线性度和检测极限均得到了验证。 DPV和FPIA技术的精度,线性和准确性在大多数临床使用水平上都是可比的。 DPV技术的检出限为1μg / mL,FPIA技术的检出限为0.5μg / mL。 DPV技术的性能在FDA的生物分析方法指南之内,从而确保了DPV技术的临床适用性。 DPV技术可能会成为卡马西平分析的良好替代方法。

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