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采用高选择性近红外偏最小二乘法同时测定还原型谷胱甘肽片的杂质和径向拉伸强度。

Simultaneous determination of the impurity and radial tensile strength of reduced glutathione tablets by a high selective NIR-PLS method.

机构信息

School of Pharmacy, Chongqing Medical University, Chongqing 400016, China.

Enterprise Technology Center, Chongqing Yaoyou Pharmaceutical Co., Ltd, Chongqing 401121, China.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2014 May 5;125:278-84. doi: 10.1016/j.saa.2014.01.097. Epub 2014 Feb 4.

Abstract

This paper establishes a high-throughput and high selective method to determine the impurity named oxidized glutathione (GSSG) and radial tensile strength (RTS) of reduced glutathione (GSH) tablets based on near infrared (NIR) spectroscopy and partial least squares (PLS). In order to build and evaluate the calibration models, the NIR diffuse reflectance spectra (DRS) and transmittance spectra (TS) for 330 GSH tablets were accurately measured by using the optimized parameter values. For analyzing GSSG or RTS of GSH tablets, the NIR-DRS or NIR-TS were selected, subdivided reasonably into calibration and prediction sets, and processed appropriately with chemometric techniques. After selecting spectral sub-ranges and neglecting spectrum outliers, the PLS calibration models were built and the factor numbers were optimized. Then, the PLS models were evaluated by the root mean square errors of calibration (RMSEC), cross-validation (RMSECV) and prediction (RMSEP), and by the correlation coefficients of calibration (R(c)) and prediction (R(p)). The results indicate that the proposed models have good performances. It is thus clear that the NIR-PLS can simultaneously, selectively, nondestructively and rapidly analyze the GSSG and RTS of GSH tablets, although the contents of GSSG impurity were quite low while those of GSH active pharmaceutical ingredient (API) quite high. This strategy can be an important complement to the common NIR methods used in the on-line analysis of API in pharmaceutical preparations. And this work expands the NIR applications in the high-throughput and extraordinarily selective analysis.

摘要

本文建立了一种基于近红外(NIR)光谱和偏最小二乘法(PLS)的高通量和高选择性方法,用于测定名为氧化型谷胱甘肽(GSSG)和还原型谷胱甘肽(GSH)片剂的径向拉伸强度(RTS)。为了建立和评估校准模型,通过使用优化的参数值,准确测量了 330 片 GSH 的 NIR 漫反射光谱(DRS)和透射光谱(TS)。为了分析 GSH 片剂中的 GSSG 或 RTS,选择了 NIR-DRS 或 NIR-TS,将其合理地细分为校准集和预测集,并使用化学计量技术进行适当处理。在选择光谱子范围和忽略光谱异常值之后,建立了 PLS 校准模型,并优化了因子数量。然后,通过校准(RMSEC)、交叉验证(RMSECV)和预测(RMSEP)的均方根误差、校准(R(c))和预测(R(p))的相关系数来评估 PLS 模型。结果表明,所提出的模型具有良好的性能。因此,很明显,NIR-PLS 可以同时、选择性、非破坏性和快速地分析 GSH 片剂中的 GSSG 和 RTS,尽管 GSSG 杂质的含量相当低,而 GSH 活性药物成分(API)的含量相当高。该策略可以成为药物制剂中 API 在线分析中常用的常见 NIR 方法的重要补充。这项工作扩展了 NIR 在高通量和极高选择性分析中的应用。

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