Blanco M, Alcalá M
Department of Chemistry, Analytical Chemistry Unity, Faculty of Sciences, Autonomous University of Barcelona, E-08193 Bellaterra, Barcelona, Spain.
Eur J Pharm Sci. 2006 Feb;27(2-3):280-6. doi: 10.1016/j.ejps.2005.10.008. Epub 2005 Dec 13.
A near infrared spectroscopic method for the simultaneous determination of the active principles paracetamol, ascorbic acid, dextrometorphan hydrobromide, caffeine and chlorpheniramine maleate in a pharmaceutical preparation was developed. The five active principles are quantified using a partial least-squares regression method (PLS1). The proposed method is applicable over a wide analyte concentration range (0.04-6.50 wt.%), so it requires careful selection of the calibration set. Also, there is the difficulty of ensuring thorough homogenization of the product. The method was validated in accordance with the ICH standard and the EMEA validation guidelines for NIR spectroscopy by determining its selectivity, linearity, accuracy, precision and robustness. Based on the results, it is an effective alternative to existing choices (HPLC and redox titrimetry) for the same purpose.
开发了一种近红外光谱法,用于同时测定药物制剂中的活性成分对乙酰氨基酚、抗坏血酸、氢溴酸右美沙芬、咖啡因和马来酸氯苯那敏。使用偏最小二乘回归法(PLS1)对这五种活性成分进行定量。所提出的方法适用于较宽的分析物浓度范围(0.04-6.50 wt.%),因此需要仔细选择校准集。此外,确保产品充分均匀化也存在困难。该方法按照ICH标准和欧洲药品管理局(EMEA)近红外光谱验证指南进行了验证,通过测定其选择性、线性、准确性、精密度和稳健性。基于这些结果,对于相同目的而言,它是现有方法(高效液相色谱法和氧化还原滴定法)的有效替代方法。