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在流化床包衣过程中对药物丸片的薄膜厚度进行在线近红外定量分析。

In line NIR quantification of film thickness on pharmaceutical pellets during a fluid bed coating process.

机构信息

Department of Smart Foods & Drugs, Inje University, Gimhae, Gyeongnam, South Korea.

出版信息

Int J Pharm. 2011 Jan 17;403(1-2):66-72. doi: 10.1016/j.ijpharm.2010.10.022. Epub 2010 Oct 28.

Abstract

Along with the risk-based approach, process analytical technology (PAT) has emerged as one of the key elements to fully implement QbD (quality-by-design). Near-infrared (NIR) spectroscopy has been extensively applied as an in-line/on-line analytical tool in biomedical and chemical industries. In this study, the film thickness on pharmaceutical pellets was examined for quantification using in-line NIR spectroscopy during a fluid-bed coating process. A precise monitoring of coating thickness and its prediction with a suitable control strategy is crucial to the quality assurance of solid dosage forms including dissolution characteristics. Pellets of a test formulation were manufactured and coated in a fluid-bed by spraying a hydroxypropyl methylcellulose (HPMC) coating solution. NIR spectra were acquired via a fiber-optic probe during the coating process, followed by multivariate analysis utilizing partial least squares (PLS) calibration models. The actual coating thickness of pellets was measured by two separate methods, confocal laser scanning microscopy (CLSM) and laser diffraction particle size analysis (LD-PSA). Both characterization methods gave superb correlation results, and all determination coefficient (R(2)) values exceeded 0.995. In addition, a prediction coating experiment for 70min demonstrated that the end-point can be accurately designated via NIR in-line monitoring with appropriate calibration models. In conclusion, our approach combining in-line NIR monitoring with CLSM and LD-PSA can be applied as an effective PAT tool for fluid-bed pellet coating processes.

摘要

随着基于风险的方法的出现,过程分析技术(PAT)已成为全面实施质量源于设计(QbD)的关键要素之一。近红外(NIR)光谱已广泛应用于生物医学和化学工业中的在线/在线分析工具。在这项研究中,在流化床包衣过程中使用在线 NIR 光谱法检查了药物丸剂的薄膜厚度,以便进行定量分析。精确监测涂层厚度并采用合适的控制策略对包括溶出特性在内的固体制剂的质量保证至关重要。通过喷涂羟丙基甲基纤维素(HPMC)包衣溶液在流化床中制造和包衣测试配方的丸剂。在包衣过程中通过光纤探头采集 NIR 光谱,然后利用偏最小二乘(PLS)校准模型进行多元分析。通过两种独立的方法(共聚焦激光扫描显微镜(CLSM)和激光衍射粒度分析(LD-PSA))测量丸剂的实际涂层厚度。这两种表征方法均得出了极好的相关结果,所有决定系数(R(2))值均超过 0.995。此外,70 分钟的预测涂层实验表明,通过适当的校准模型进行在线 NIR 监测可以准确指定终点。总之,我们将在线 NIR 监测与 CLSM 和 LD-PSA 相结合的方法可作为流化床丸剂包衣过程的有效 PAT 工具。

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