NMPA Key Laboratory for Quality Analysis of Chemical Drug Preparations, Shanghai, 201203, China; Shanghai Institute for Food and Drug Control, Shanghai, 201203, China.
NMPA Key Laboratory for Quality Analysis of Chemical Drug Preparations, Shanghai, 201203, China; Shanghai Institute for Food and Drug Control, Shanghai, 201203, China.
J Pharm Biomed Anal. 2021 Feb 5;194:113766. doi: 10.1016/j.jpba.2020.113766. Epub 2020 Nov 27.
Backscattering NIR, Raman (BSR) and transmission Raman spectroscopy (TRS) coupled with chemometrics have shown to be rapid and non-invasive tools for the quantification of active pharmaceutical ingredient (API) content in tablets. However, the developed models are generally specifically related to the measurement conditions and sample characteristics. In this study, a number of calibration transfer methods, including DS, PDS, DWPDS, GLSW and SST, were evaluated for the spectra correction between modelled tablets produced in the laboratory and commercial samples. Results showed that the NIR and BSR spectra of commercial tablet corrected by DWPDS and PDS, respectively, enabled accurate API predictions with the high ratio of prediction error to deviation (RPD) values of 2.33 and 3.03. The most successfully approach was achieved with DS corrected TRS data and SiPLS modelling (161 variables) and yielded RMSE of 0.72 %, R of 0.946 and RPD of 4.35. The proposed calibration transfer strategy offers the opportunities to analyse samples produced in different conditions; in the future, its implication will find extensively process control and quality assurance applications and benefit all possible users in the entire pharmaceutical industry.
近红外背散射(BSR)、拉曼(Raman)和传输拉曼光谱(TRS)与化学计量学相结合,已被证明是快速、非侵入式的工具,可用于定量片剂中的活性药物成分(API)含量。然而,开发的模型通常与测量条件和样品特征有关。在这项研究中,评估了几种校准传递方法,包括 DS、PDS、DWPDS、GLSW 和 SST,用于在实验室中制造的模型片剂和商业样品之间的光谱校正。结果表明,分别通过 DWPDS 和 PDS 校正的商业片剂的近红外和 BSR 光谱,可以通过高预测误差与偏差比(RPD)值 2.33 和 3.03 进行准确的 API 预测。最成功的方法是使用 DS 校正的 TRS 数据和 SiPLS 建模(161 个变量),得到的 RMSE 为 0.72%、R 为 0.946 和 RPD 为 4.35。所提出的校准传递策略为分析在不同条件下生产的样品提供了机会;在未来,它的应用将广泛应用于过程控制和质量保证,并使整个制药行业的所有可能用户受益。