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首页> 外文期刊>Applied Spectroscopy: Society for Applied Spectroscopy >Discerning Some Tylenol Brands Using Attenuated Total Reflection Fourier Transform Infrared Data and Multivariate Analysis Techniques
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Discerning Some Tylenol Brands Using Attenuated Total Reflection Fourier Transform Infrared Data and Multivariate Analysis Techniques

机译:使用衰减全反射傅立叶变换红外数据和多元分析技术识别一些泰诺品牌

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摘要

Principal component analysis (PCA) and partial least squares discriminant analysis (PLS-DA) were used to classify acetaminophen-containing medicines using their attenuated total reflection Fourier transform infrared (ATR-FT-IR) spectra. Four formulations of Tylenol (Arthritis Pain Relief, Extra Strength Pain Relief, 8 Hour Pain Relief, and Extra Strength Pain Relief Rapid Release) along with 98percent pure acetaminophen were selected for this study because of the similarity of their spectral features, with correlation coefficients ranging from 0.9857 to 0.9988. Before acquiring spectra for the predictor matrix, the effects on spectral precision with respect to sample particle size (determined by sieve size opening), force gauge of the ATR accessory, sample reloading, and between-tablet variation were examined. Spectra were baseline corrected and normalized to unity before multivariate analysis. Analysis of variance (ANOVA) was used to study spectral precision. The large particles (35 mesh) showed large variance between spectra, while fine particles (120 mesh) indicated good spectral precision based on the F-test. Force gauge setting did not significantly affect precision. Sample reloading using the fine particle size and a constant force gauge setting of 50 units also did not compromise precision. Based on these observations, data acquisition for the predictor matrix was carried out with the fine particles (sieve size opening of 120 mesh) at a constant force gauge setting of 50 units. After removing outliers, PCA successfully classified the five samples in the first and second components, accounting for 45.0percent and 24.5percent of the variances, respectively. The four-component PLS-DA model (R~(2)(velence)0.925 and Q~(2)(velence)0.906) gave good test spectra predictions with an overall average of 0.961 +- 7.1percent RSD versus the expected 1.0 prediction for the 20 test spectra used.
机译:主成分分析(PCA)和偏最小二乘判别分析(PLS-DA)用于通过衰减全反射傅立叶变换红外光谱(ATR-FT-IR)对含对乙酰氨基酚的药物进行分类。本研究选择了泰诺酚的四种制剂(关节炎止痛,特效止痛,8小时止痛和特效止痛快速释放)以及98%的对乙酰氨基酚,因为它们的光谱特征相似,相关系数范围为从0.9857到0.9988。在获取预测矩阵的光谱之前,检查了光谱精度对样品粒度(由筛孔尺寸决定),ATR附件的测力规,样品重新装填和片剂间变化的影响。在多变量分析之前,对光谱进行基线校正并归一化为单位。方差分析(ANOVA)用于研究光谱精度。基于F检验,大颗粒(35目)在光谱之间显示出很大的差异,而细颗粒(120目)显示出良好的光谱精度。测力计的设置不会显着影响精度。使用细粒度和50单位的恒定测力计设置的样品重载也不会影响精度。基于这些观察结果,以50个单位的恒定测力计设置的细颗粒(筛孔尺寸为120目筛)进行了预测矩阵的数据采集。除去异常值后,PCA成功地将五个样本分为第一部分和第二部分,分别占方差的45.0%和24.5%。四成分PLS-DA模型(R〜(2)(velence)0.925和Q〜(2)(velence)0.906)给出了良好的测试光谱预测,相对于预期的1.0预测,总体平均RSD为0.961 +-7.1%对于使用的20个测试光谱。

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