...
【24h】

Quantitative determination of diclofenac sodium in solid dosage forms by FT-Raman spectroscopy.

机译:FT-拉曼光谱法定量测定固体剂型中双氯芬酸钠。

获取原文
获取原文并翻译 | 示例
           

摘要

The FT-Raman quantification of diclofenac sodium in tablets and capsules was performed with the help of the partial least squares (PLS), principal component regression (PCR) and counter-propagation artificial neural networks (CP-ANN) methods. For the analysed tablets, calibration models were built using unnormalised spectra and spectra normalised by the intensity of a selected band of an internal standard. Different pre-processing methods were applied for the capsules. To compare the predictive ability of the models, the relative standard errors of prediction (RSEP) were calculated. The 5 x 5 CP-ANN and PLS methods gave models of comparable quality, which were usually more efficient than the PCR ones. The RSEP error values for the tablets were in the range of 2.4-3.8% for the calibration and 2.6-3.5% for the validation data sets and for the three procedures applied. For capsules, the RSEP errors were in the range of 0.8-1.9% and 1.4-1.7% for the calibration and validation samples, respectively. Five commercial products containing 25, 50 or 75 mg of diclofenac sodium per tablet/capsule were quantified. Concentrations found from the Raman data analysis agree with the results of the reference analysis and correlate strongly with the declared values with the recovery of 99.5-101.3%, 99.7-102.0% and 99.9-101.2% for the PLS, PCR and CP-ANN methods, respectively. The proposed procedure can be a fast and convenient alternative to the standard pharmacopoeial methods of diclofenac sodium quantification in solid dosage forms.
机译:借助偏最小二乘(PLS),主成分回归(PCR)和反向传播人工神经网络(CP-ANN)方法对片剂和胶囊中双氯芬酸钠的FT-拉曼定量分析。对于分析的药片,使用未归一化的光谱和通过内标选定谱带的强度归一化的光谱建立校正模型。将不同的预处理方法应用于胶囊。为了比较模型的预测能力,计算了相对标准预测误差(RSEP)。 5 x 5 CP-ANN和PLS方法提供的模型质量相当,通常比PCR模型更有效。片剂的RSEP误差值在校准范围内为2.4-3.8%,在验证数据集和所应用的三个步骤中,为2.6-3.5%。对于胶囊,校准和验证样品的RSEP误差分别在0.8-1.9%和1.4-1.7%的范围内。定量每片/胶囊含有25、50或75 mg双氯芬酸钠的五种商品。从拉曼数据分析中发现的浓度与参考分析的结果一致,并且与声明的值高度相关,PLS,PCR和CP-ANN方法的回收率分别为99.5-101.3%,99.7-102.0%和99.9-101.2% , 分别。所提出的方法可以作为固体剂型中双氯芬酸钠定量的标准药典方法的一种快速便捷的替代方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号