首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Simple and ultra-fast recognition and quantitation of compounded monoclonal antibodies: Application to flow injection analysis combined to UV spectroscopy and matching method
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Simple and ultra-fast recognition and quantitation of compounded monoclonal antibodies: Application to flow injection analysis combined to UV spectroscopy and matching method

机译:复合单克隆抗体的简单和超快速识别和定量:流动注射分析的应用组合于UV光谱和匹配方法

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摘要

Compounding of monoclonal antibody (mAbs) constantly increases in hospital. Quality control (QC) of the compounded mAbs based on quantification and identification is required to prevent potential errors and fast method is needed to manage outpatient chemotherapy administration. A simple and ultra-fast (less than 30 s) method using flow injection analysis associated to least square matching method issued from the analyzer software was performed and evaluated for the routine hospital QC of three compounded mAbs: bevacizumab, infliximab and rituximab. The method was evaluated through qualitative and quantitative parameters. Preliminary analysis of the UV absorption and second derivative spectra of the mAbs allowed us to adapt analytical conditions according to the therapeutic range of the mAbs. In terms of quantitative QC, linearity, accuracy and precision were assessed as specified in ICH guidelines. Very satisfactory recovery was achieved and the RSD (%) of the intermediate precision were less than 1.1%. Qualitative analytical parameters were also evaluated in terms of specificity, sensitivity and global precision through a matrix of confusion. Results showed to be concentration and mAbs dependant and excellent (100%) specificity and sensitivity were reached within specific concentration range. Finally, routine application on "real life" samples (n = 209) from different batch of the three mAbs complied with the specifications of the quality control i.e. excellent identification (100%) and +/- 15% of targeting concentration belonging to the calibration range. The successful use of the combination of second derivative spectroscopy and partial least square matching method demonstrated the interest of FIA for the ultra-fast QC of mAbs after compounding using matching method.
机译:单克隆抗体(单克隆抗体)的复利不断增加医院。根据定性和定量的复合单克隆抗体的质量控制(QC)是为了防止潜在的错误,并且需要快速的方法来管理门诊化疗管理。进行相关联,以从分析仪软件发出最小二乘匹配方法的简单和超快速(小于30秒),使用方法流动注射分析并评价三个配混的mAb例程医院QC:贝伐单抗,英夫利昔单抗和利妥希玛。该方法通过定性和定量的参数进行评价。所述单克隆抗体的UV吸收和二阶导数光谱的初步分析使我们能够根据mAb的治疗范围适应的分析条件。在定量QC,线性,准确性和精度方面如在ICH指南规定进行了评估。非常令人满意的回收达到和的中间精密度的RSD(%)均小于1.1%。定性分析参数也通过混淆矩阵评价在特异性,灵敏度和全球精确的术语。结果表明是浓度和单克隆抗体依赖性和优异的(100%)的特异性和灵敏度被特定的浓度范围内达到。最后,对来自不同批次的质量控制,即优异的标识(100%)的规格符合的三种mAb的“现实生活”样本(N = 209)和+/-靶向浓度属于校准的15%常规应用范围。成功使用二阶导数光谱和偏最小二乘匹配方法的组合的证实FIA用于mAb的超快速QC使用匹配方法配混后的兴趣。

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