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使用偏最小二乘多元校准法对药物制剂中的乙酰水杨酸和咖啡因进行固相荧光光谱测定。

Solid-phase spectrofluorimetric determination of acetylsalicylic acid and caffeine in pharmaceutical preparations using partial least-squares multivariate calibration.

作者信息

Moreira Altair B, Dias Iara L T, Neto Graciliano O, Zagatto Elias A G, Ferreira Márcia M C, Kubota Lauro T

机构信息

Instituto de Química, Universidade Estadual de Campinas, Campinas SP, Brazil.

出版信息

Talanta. 2005 Jul 15;67(1):65-9. doi: 10.1016/j.talanta.2005.02.004. Epub 2005 Feb 24.

Abstract

PLS-1, a variant of the partial least-squares algorithm was used for the solid-phase spectrofluorimetric determination of acetylsalicylic acid (ASA) and caffeine (CF) in pharmaceutical formulations. The method allows the simultaneous quantification of the analytes, as the closely overlapping spectral bands are efficiently solved. Sample preparation prior to analysis is not required. The calibration set consisted of 83 samples with 50-170mgg(-1) ASA plus 5-20mgg(-1) CF; another set of 25 samples was used for external validation. Agreement between predicted and experimental concentrations was fair (r=0.987 and 0.974 for ASA and CF models). For both models, the prediction performance was evaluated in terms of the coefficient of variability (CV), relative predictive determination (RPD), and ratio error range (RER). The final PLS-1 models were used for the determination of ASA and CF in pharmaceutical formulations.

摘要

偏最小二乘法(PLS - 1)的一种变体被用于药物制剂中乙酰水杨酸(ASA)和咖啡因(CF)的固相荧光光谱测定。该方法能够同时对分析物进行定量,因为能有效解决紧密重叠的光谱带问题。分析前无需进行样品制备。校准集由83个样品组成,其中ASA含量为50 - 170mg g⁻¹,CF含量为5 - 20mg g⁻¹;另一组25个样品用于外部验证。预测浓度与实验浓度之间的一致性良好(ASA和CF模型的r分别为0.987和0.974)。对于这两个模型,均根据变异系数(CV)、相对预测决定系数(RPD)和比率误差范围(RER)来评估预测性能。最终的PLS - 1模型用于药物制剂中ASA和CF的测定。

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