首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Raman spectroscopy of coated pharmaceutical tablets and physical models for multivariate calibration to tablet coating thickness
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Raman spectroscopy of coated pharmaceutical tablets and physical models for multivariate calibration to tablet coating thickness

机译:包衣片剂的拉曼光谱和物理模型可对片剂包衣厚度进行多元校准

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摘要

Raman spectra of a set of coated pharmaceutical tablets were analyzed for the purpose of calibrating the spectra to tablet coating thickness. Acetaminophen tablets were coated with a hydroxypropylmethylcellulose/polyethylene glycol film coating whose thickness was varied from 0 to 6% weight gain. Coatings were also prepared with two concentrations of TO_2 at several film thicknesses. The resulting spectral data set was analyzed using several different multivariate calibration procedures. The procedures examined in this study included spectral correction followed by target factor analysis, spectral correction with baseline subtraction followed by principal component regression, and first derivative computation followed by principal component regression. The results demonstrate that target factor analysis is a viable method for calibration of Raman spectra to tablet coating thickness. Calibration based on derivative spectra resulted in linear correlation that was equal to that of the results of target factor analysis for coatings without TiO_2. However, target factor analysis was found to be superior to other methods when TiO_2 was present in the tablet coatings. The effect of sample fluorescence on each of these chemometric methods was also examined. It was found that when photobleaching of fluorescent impurities due to exposure to the Raman excitation source was controlled, the tablet coating thickness could be calibrated to the intensity of the fluorescence signal. The results also demonstrate that for the samples examined here, calibration by target factor analysis is insensitive to variation in fluorescent intensity when the tablet coating emission spectrum is included in the matrix of target vectors.
机译:分析一组包衣药物片剂的拉曼光谱,以将光谱校准至片剂包衣厚度。对乙酰氨基酚片剂用羟丙基甲基纤维素/聚乙二醇薄膜衣包衣,其厚度在0至6%的重量增加之间变化。还制备了具有几种浓度的两种浓度的TO_2的涂层。使用几种不同的多元校准程序分析所得的光谱数据集。本研究中检查的程序包括:光谱校正,然后进行目标因子分析;光谱校正,进行基线减法,然后进行主成分回归;以及一阶导数计算,然后进行主成分回归。结果表明,目标因子分析是一种将拉曼光谱校正至片剂包衣厚度的可行方法。基于导数光谱的校准产生的线性相关性与不含TiO_2的涂层的目标因子分析结果相同。但是,当片剂包衣中存在TiO_2时,发现目标因子分析优于其他方法。还检查了样品荧光对每种化学计量方法的影响。已经发现,当控制由于暴露于拉曼激发源而引起的荧光杂质的光漂白时,可以将片剂包衣的厚度校准为荧光信号的强度。结果还表明,对于此处检查的样品,当片剂包衣发射光谱包含在目标载体的基质中时,通过目标因子分析进行的校准对荧光强度的变化不敏感。

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