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在流化床制粒过程中合并实时近红外和过程参数测量以预测颗粒大小。

Merging Real-Time NIR and Process Parameter Measurements in a Fluidized Bed Granulation Process to Predict Particle Size.

作者信息

Jovic Ozren, O'Mahony Marcus, Solomon Samuel, Egan David, O'Callaghan Chris, McCormack Caroline, Jones Ian, Cronin Patrick, Walker Gavin M, Mouras Rabah

机构信息

Pharmaceutical Manufacturing Technology Centre, Bernal Institute, Department of Chemical Sciences, University of Limerick, V94 T9PX Limerick, Ireland.

Dairy Processing Technology Centre, Bernal Institute, Department of Chemical Sciences, University of Limerick, V94 T9PX Limerick, Ireland.

出版信息

Pharmaceutics. 2025 May 29;17(6):720. doi: 10.3390/pharmaceutics17060720.

DOI:10.3390/pharmaceutics17060720
PMID:40574033
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12196058/
Abstract

: Controlling the critical quality attributes (CQAs), such as granule moisture level and particle size distribution, that impact product performance is essential for ensuring product quality in medicine manufacture. Oral solid dosage forms, such as tablets, often require appropriate powder flow for compaction and filling. Spray-dried fluidized bed granulation (FBG) is a key unit operation in the preparation of granulated powders. The determination of particle sizes in FBG using near-infrared spectroscopy (NIR) has been considered in the literature. Herein, for the first time, NIR is combined with process parameters to achieve improved prediction of the particle sizes in FBG. : An inline model for particle size determination using both NIR and FBG process parameters was developed using the partial least square (PLS) method, or 'merged-PLS model'. The particle size was predicted at the end point of the process, i.e., the last 10% of the particle-size data for each batch run. An additional two analyses included a merged-PLS model with 12 batches: (1) where nine batches were training and three batches were a test set; and (2) where 11 batches were training and one was a test batch. : For all considered particle size fractions, Dv10, Dv25, Dv50, Dv75, and Dv90, an improved root-mean-squared error of prediction (RMSEP) is obtained for the merged-PLS model compared to the NIR-only PLS model and compared to the process parameters alone model. Improved RMSEP is also achieved for the additional two analyses. : The improved prediction performance of endpoint particle sizes by the merged-PLS model can help to enhance both the process understanding and the overall control of the FBG process.

摘要

控制影响产品性能的关键质量属性(CQAs),如颗粒水分含量和粒度分布,对于确保药品生产中的产品质量至关重要。口服固体制剂,如片剂,通常需要适当的粉末流动性以进行压片和填充。喷雾干燥流化床制粒(FBG)是制备颗粒粉末的关键单元操作。文献中已考虑使用近红外光谱(NIR)测定FBG中的粒度。在此,首次将NIR与工艺参数相结合,以实现对FBG中粒度的改进预测。

使用偏最小二乘法(PLS)开发了一种同时使用NIR和FBG工艺参数进行粒度测定的在线模型,即“合并PLS模型”。在过程终点预测粒度,即每个批次运行的粒度数据的最后10%。另外两项分析包括一个包含12个批次的合并PLS模型:(1)其中九个批次为训练集,三个批次为测试集;(2)其中11个批次为训练集,一个批次为测试批次。

对于所有考虑的粒度分数,Dv10、Dv25、Dv50、Dv75和Dv90,与仅使用NIR的PLS模型和仅使用工艺参数的模型相比,合并PLS模型获得了改进的预测均方根误差(RMSEP)。另外两项分析也实现了改进的RMSEP。

合并PLS模型对终点粒度的改进预测性能有助于增强对FBG过程的过程理解和整体控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/653053955afd/pharmaceutics-17-00720-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/1d63c52110ba/pharmaceutics-17-00720-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/07c4c6145636/pharmaceutics-17-00720-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/31aca17d4ef9/pharmaceutics-17-00720-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/b0e5427ec0fa/pharmaceutics-17-00720-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/83b2f2623ce3/pharmaceutics-17-00720-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/556665932219/pharmaceutics-17-00720-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/89cf36dc1e47/pharmaceutics-17-00720-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/7487b4393914/pharmaceutics-17-00720-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/653053955afd/pharmaceutics-17-00720-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/1d63c52110ba/pharmaceutics-17-00720-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/07c4c6145636/pharmaceutics-17-00720-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/31aca17d4ef9/pharmaceutics-17-00720-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/b0e5427ec0fa/pharmaceutics-17-00720-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/83b2f2623ce3/pharmaceutics-17-00720-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/556665932219/pharmaceutics-17-00720-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/89cf36dc1e47/pharmaceutics-17-00720-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/7487b4393914/pharmaceutics-17-00720-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1f/12196058/653053955afd/pharmaceutics-17-00720-g009.jpg

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