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一种基于微芯片的荧光偏振免疫分析的治疗药物监测的临床试验。

A clinical trial for therapeutic drug monitoring using microchip-based fluorescence polarization immunoassay.

机构信息

Department of Applied Chemistry, Graduate School of Engineering, Nagoya University, Nagoya 464-8603, Japan.

出版信息

Anal Bioanal Chem. 2011 Oct;401(7):2301-5. doi: 10.1007/s00216-011-5304-9. Epub 2011 Aug 13.

Abstract

Microchip analysis is a promising method for therapeutic drug monitoring. This led us to evaluate a microchip-based fluorescence polarization immunoassay (FPIA) system for point-of-care testing on patients being treated with theophylline. The sera were collected from 20 patients being treated with theophylline. Fluorescence polarization was measured on the microchip and theophylline concentrations in serum were obtained. Regression analysis of the correlations was done between the results given by the microchip-based FPIA and the conventional cloned enzyme donor immunoassay (CEDIA), and between the results given by the microchip-based FPIA and the conventional particle-enhanced turbidimetric inhibition immunoassay (PETINIA). We successfully carried out a quantitative analysis of theophylline in serum at values near its therapeutic range in 65 s. The results obtained by the microchip-based FPIA correlated well with CEDIA and PETINIA results; the correlation coefficients (R(2)) were 0.986 and 0.989, respectively. The FPIA system is a simple and rapid method for point-of-care testing of drugs in serum, and its accuracy is the same as the conventional CEDIA and PETINIA. It is essential to use real samples from patients and to confirm good correlations with conventional methods for a study on the realization of microchip.

摘要

微芯片分析是一种很有前途的治疗药物监测方法。这促使我们评估了一种基于微芯片的荧光偏振免疫分析(FPIA)系统,用于对接受茶碱治疗的患者进行即时检测。从 20 名接受茶碱治疗的患者中采集血清。在微芯片上测量荧光偏振,并获得血清中茶碱的浓度。对微芯片 FPIA 与传统的克隆酶供体免疫测定(CEDIA)之间以及微芯片 FPIA 与传统的颗粒增强浊度抑制免疫测定(PETINIA)之间的相关性结果进行回归分析。我们成功地在 65 秒内对接近治疗范围的血清中茶碱进行了定量分析。微芯片 FPIA 的结果与 CEDIA 和 PETINIA 的结果相关性良好,相关系数(R(2))分别为 0.986 和 0.989。FPIA 系统是一种简单、快速的即时检测血清中药物的方法,其准确性与传统的 CEDIA 和 PETINIA 相同。使用患者的实际样本并与传统方法进行良好的相关性确认对于实现微芯片的研究至关重要。

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