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用于定量拉曼片剂评估的不同激光照射方法的表征

Characterization of different laser irradiation methods for quantitative Raman tablet assessment.

作者信息

Johansson Jonas, Pettersson Staffan, Folestad Staffan

机构信息

Pharmaceutical and Analytical R and D, AstraZeneca R and D Mölndal, S-431 83 Mölndal, Sweden.

出版信息

J Pharm Biomed Anal. 2005 Sep 15;39(3-4):510-6. doi: 10.1016/j.jpba.2005.04.029.

Abstract

Quantitative Raman spectroscopy of conventional wet granulated pharmaceutical immediate release tablets and subsequent data evaluation was investigated. Different aspects of quantitative assessment of active pharmaceutical ingredient (API) in intact tablets with special focus on sub-sampling issues were addressed. Four different geometric laser irradiance patterns were examined to study the effect of sub-sampling within the tablets. The Raman data was evaluated using both univariate and multivariate techniques. UV absorbance spectroscopy was used as a reference method. The best result in terms of prediction error was attained by irradiating a large area of the tablets. Using multivariate calibration with multiplicative signal correction (MSC) the prediction error was 1.7%. In addition, the effect of tablet density on the Raman assessment was investigated. It was found that quantitative Raman assessment of chemical content can be made insensitive to variations in tablet density corresponding to a manufacturing compression interval of 5-20 kN provided that adequate data treatment is used. A short discussion about sample heating in the context of different irradiation patterns is included with reference to previous work. In conclusion, the present study provides a platform for developing an implementation strategy for quantitative Raman spectroscopy for both laboratory analysis and process analytical technology (PAT) applications.

摘要

研究了传统湿法制粒的药物速释片的定量拉曼光谱及其后续数据评估。探讨了完整片剂中活性药物成分(API)定量评估的不同方面,特别关注子采样问题。研究了四种不同的几何激光辐照模式,以研究片剂内部子采样的影响。使用单变量和多变量技术对拉曼数据进行评估。紫外吸收光谱法用作参考方法。通过大面积照射片剂获得了预测误差方面的最佳结果。使用具有乘法信号校正(MSC)的多变量校准,预测误差为1.7%。此外,还研究了片剂密度对拉曼评估的影响。结果发现,只要采用适当的数据处理方法,在5-20 kN的制造压缩间隔范围内,化学含量的定量拉曼评估对片剂密度的变化可以不敏感。参考先前的工作,对不同辐照模式下的样品加热进行了简短讨论。总之,本研究为开发用于实验室分析和过程分析技术(PAT)应用的定量拉曼光谱实施策略提供了一个平台。

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