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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Calibration transfer from powder mixtures to intact tablets: A new use in pharmaceutical analysis for a known tool
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Calibration transfer from powder mixtures to intact tablets: A new use in pharmaceutical analysis for a known tool

机译:从粉末混合物到完整片剂的校准转移:已知工具在药物分析中的新用途

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Calibration transfer is commonly used for spectra obtained in different spectrometers or other conditions. This paper proposed the use of calibration transfer between spectra recorded for the same samples in different physical forms. A new method was developed for the direct determination of nevirapine in solid pharmaceutical formulations based on diffuse reflectance near infrared spectroscopy (NIRS) and partial least squares (PLS). This method was developed with 50 powder mixtures and then, successfully extended to the quantification in intact tablets by using calibration transfer with double window piecewise direct standardization (DWPDS). This chemometric strategy provided good results with a small number of tablet transfer samples, only seven, prepared out of the narrow range of active principle ingredients (API) content around the nominal value of the formulation (100%). The method was fully validated in the working range of 83.0-113.9% of nevirapine and the use of DWPDS allowed to significantly decreasing the root mean square error of prediction (RMSEP) from 4.8% (tablets predicted by a model built with only powder samples) to 2.6%. The range of relative errors decreased from -5.1/8.7% to -4.6/3.3%. Considering that the amount of raw materials demanded for preparing tablets is up to ten times higher than for powder mixtures, this type of application is of particular interest in pharmaceutical analysis. In the context of process analytical technology (PAT), the use of the same multivariate model in different steps of the production is very advantageous, saving time and labor. (C) 2015 Elsevier B.V. All rights reserved.
机译:校准转移通常用于在不同光谱仪或其他条件下获得的光谱。本文提出了在不同物理形式的相同样品记录的光谱之间使用校准转移的方法。开发了一种基于漫反射近红外光谱(NIRS)和偏最小二乘(PLS)直接测定固体药物制剂中奈韦拉平的新方法。该方法是用50种粉末混合物开发的,然后通过使用带有双窗口分段直接标准化(DWPDS)的标定传递成功地扩展到完整片剂中的定量分析。这种化学计量策略使用少量的片剂转移样品(仅七个),从大约标称值(100%)的有效成分(API)含量的狭窄范围中制备出了良好的结果。该方法在奈韦拉平的83.0-113.9%的工作范围内得到了充分验证,并且DWPDS的使用可将预测的均方根误差(RMSEP)从4.8%显着降低(仅使用粉末样品构建的模型预测的片剂)到2.6%。相对误差范围从-5.1 / 8.7%降低到-4.6 / 3.3%。考虑到制备片剂所需的原料量是粉末混合物的十倍之多,因此这种类型的应用在药物分析中尤为重要。在过程分析技术(PAT)的背景下,在生产的不同步骤中使用相同的多变量模型非常有利,可以节省时间和劳动力。 (C)2015 Elsevier B.V.保留所有权利。

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