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Establishment of norvancomycin fluorescence polarization immunoassay for therapeutic drug monitoring

机译:去甲万古霉素荧光偏振免疫分析法在治疗药物监测中的建立

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To establish a rapid and simple fluorescence polarization immunoassay method for determination of norvancomycin serum concentration, we collected 300 serum samples from the patients receiving norvancomycin in the hospitals localized in Shanghai, China. The drug concentrations were measured by the established HPLC method and FPIA with vancomycin kit. A FPIA algorithm for the determination of norvancomycin concentration was established according to the correlation between the FPIA and HPLC results. The methods and algorithm were validated in another 70 clinical samples. HPLC determination showed a good linear correlation within the range of 0.5-100 mgl -1 of norvancomycin concentrations. The method was validated via extraction recovery, intra- and inter-day methodological recovery and stability of norvancomycin in serum. Correlation analysis between the measurements of HPLC and FPIA in 300 serum samples gave the linear regression equation: (concentration by HPLC)0.760 × (concentration by FPIA)-0.577 (P0.001, R 2 0.982). An algorithm was derived from this correlation for measuring the serum norvancomycin concentrations with FPIA. When it was validated in additional 70 serum samples from patients, FPIA algorithm showed good accuracy versus HPLC: FPIA algorithm0.93 (HPLC)0.63, R 2 0.962, and 94.3% of the results from FPIA algorithm fell within the range of 20%/20% of HPLC. This algorithm developed in this study can be easily used for determination of norvancomycin using TDx analyzer with vancomycin kit indirectly. It may also be useful for norvancomycin therapeutic drug monitoring.
机译:为了建立快速,简单的荧光偏振免疫测定法测定去甲万古霉素的血清浓度,我们在中国上海的医院从接受去甲万古霉素的患者中收集了300份血清样品。通过建立的HPLC方法和带万古霉素试剂盒的FPIA测量药物浓度。根据FPIA和HPLC结果之间的相关性,建立了测定去甲万古霉素浓度的FPIA算法。该方法和算法已在另外70个临床样本中得到验证。 HPLC测定显示在0.5-100 mgl -1的正古霉素浓度范围内具有良好的线性相关性。该方法已通过提取回收率,日内和日间方法学回收率以及去甲万古霉素在血清中的稳定性进行了验证。在300个血清样品中HPLC和FPIA的测量值之间的相关性分析得出线性回归方程:(HPLC浓度)0.760×(FPIA浓度)-0.577(P <0.001,R 2 0.982)。从这种相关性中得出了一种算法,用于使用FPIA测量血清降血糖药的浓度。当在另外70个患者血清样品中进行验证时,FPIA算法与HPLC相比显示出良好的准确性:FPIA算法0.93(HPLC)0.63,R 2 0.962和FPIA算法结果的94.3%落在20%/ HPLC的20%。使用带有万古霉素试剂盒的TDx分析仪,可以轻松地将本研究中开发的算法轻松用于测定万古霉素。它对于去甲万古霉素治疗药物的监测也可能有用。

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