Institute of Chemistry, State University of Campinas-UNICAMP, PO Box 6154, 13083-970 Campinas, SP, Brazil.
Spectrochim Acta A Mol Biomol Spectrosc. 2013 Feb 15;103:311-8. doi: 10.1016/j.saa.2012.10.074. Epub 2012 Nov 7.
This paper reports the application of piecewise direct standardization (PDS) for matrix correction in front face fluorescence spectroscopy of solids when different excipients are used in a pharmaceutical preparation based on a mixture of acetylsalicylic acid (ASA), paracetamol (acetaminophen) and caffeine. As verified in earlier studies, the use of different excipients and their ratio can cause a displacement, change in fluorescence intensity or band profile. To overcome this important drawback, a standardization strategy was adopted to convert all the excitation-emission fluorescence spectra into those used for model development. An excitation-emission matrix (EEM) for which excitation and emission wavelengths ranging from 265 to 405 nm and 300 to 480 nm, respectively, was used. Excellent results were obtained using unfolded partial least squares (U-PLS), with RMSEP values of 8.2 mg/g, 10.9 mg/g and 2.7 mg/g for ASA, paracetamol and caffeine, respectively, and with relative errors lesser than 5% for the three analytes.
本文报告了分段直接标准化(PDS)在基于乙酰水杨酸(ASA)、对乙酰氨基酚(acetaminophen)和咖啡因混合物的药物制剂中使用不同赋形剂时的固体前向荧光光谱的矩阵校正中的应用。正如早期研究所验证的,使用不同的赋形剂及其比例会导致位移、荧光强度或带型变化。为了克服这一重要缺点,采用了一种标准化策略,将所有激发-发射荧光光谱转换为用于模型开发的光谱。使用激发和发射波长分别为 265 至 405nm 和 300 至 480nm 的激发-发射矩阵(EEM)。采用非折叠偏最小二乘法(U-PLS)获得了优异的结果,对于 ASA、对乙酰氨基酚和咖啡因,RMSEP 值分别为 8.2mg/g、10.9mg/g 和 2.7mg/g,并且对于三种分析物的相对误差均小于 5%。