Quantitative Structural and Compositional Elucidation of Real-World Pharmaceutical Tablet Using Large Field-of-View, Correlative Microscopy-Tomography Techniques and AI-Enabled Image Analysis.

IF 3.5 3区 医学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pharmaceutical Research Pub Date : 2025-01-01 Epub Date: 2025-01-08 DOI:10.1007/s11095-024-03812-0
Yinshan Chen, Sruthika Baviriseaty, Prajwal Thool, Jonah Gautreau, Phillip D Yawman, Kellie Sluga, Jonathan Hau, Shawn Zhang, Chen Mao
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Abstract

Purpose: The purpose of this study is to present a correlative microscopy-tomography approach in conjunction with machine learning-based image segmentation techniques, with the goal of enabling quantitative structural and compositional elucidation of real-world pharmaceutical tablets.

Methods: Specifically, the approach involves three sequential steps: 1) user-oriented tablet constituent identification and characterization using correlative mosaic field-of-view SEM and energy dispersive X-ray spectroscopy techniques, 2) phase contrast synchrotron X-ray micro-computed tomography (SyncCT) characterization of a large, representative volume of the tablet, and 3) constituent segmentation and quantification of the imaging data through user-guided, iterative supervised machine learning and deep learning.

Results: This approach was implemented on a real-world tablet containing 15% API and multiple common excipients. A representative volumetric tablet image was obtained using SyncCT at a 0.36-µm resolution, from which constituent particles and pores were fully segmented and quantified. As validation, the derived tablet formulation composition and porosity agreed with the experimental values, despite the micrometer-scale particle and pore sizes. The approach also revealed the formation of ordered mixture inside the tablet. Notably, the image-derived size distributions of both the agglomerated microcrystalline cellulose and its primary particulate units matched the laser diffraction-based measurements of the as-is material. Key pore attributes including the pore size distribution, spatial anisotropy, and pore interconnectivity were also qualified.

Conclusion: Overall, this study demonstrated that the correlative microscopy-tomography approach, by leveraging phase contrast SyncCT and AI-based image analysis, can deliver new, practically-useful structural and compositional information and facilitate more efficient formulation and process development of tablets.

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使用大视场、相关显微镜断层扫描技术和人工智能支持的图像分析对真实世界的药物片剂进行定量结构和成分分析。
目的:本研究的目的是提出一种相关的显微镜断层扫描方法,结合基于机器学习的图像分割技术,目的是实现真实世界药物片剂的定量结构和成分阐明。具体而言,该方法包括三个连续步骤:1)利用相关的拼接视场扫描电镜(SEM)和能量色散x射线光谱学技术对面向用户的片剂成分进行识别和表征;2)利用相衬同步加速器x射线微计算机断层扫描(SyncCT)对大量具有代表性的片剂进行表征;3)通过用户引导、迭代监督的机器学习和深度学习对成像数据进行成分分割和量化。结果:该方法在含有15%原料药和多种常用赋形剂的实际片剂上实现。在0.36-µm分辨率下,使用SyncCT获得了具有代表性的体积片图像,并从中对组成颗粒和孔隙进行了充分的分割和定量。作为验证,推导出的片剂组成和孔隙度与实验值一致,尽管颗粒和孔隙尺寸为微米级。该方法还揭示了药片内部有序混合物的形成。值得注意的是,凝聚微晶纤维素及其主要颗粒单元的图像衍生尺寸分布与基于激光衍射的原始材料测量结果相匹配。关键孔隙属性包括孔径分布、空间各向异性和孔隙连通性。结论:总体而言,本研究表明,通过相衬SyncCT和基于人工智能的图像分析,相关显微断层扫描方法可以提供新的、实用的结构和成分信息,促进更有效的片剂处方和工艺开发。
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来源期刊
Pharmaceutical Research
Pharmaceutical Research 医学-化学综合
CiteScore
6.60
自引率
5.40%
发文量
276
审稿时长
3.4 months
期刊介绍: Pharmaceutical Research, an official journal of the American Association of Pharmaceutical Scientists, is committed to publishing novel research that is mechanism-based, hypothesis-driven and addresses significant issues in drug discovery, development and regulation. Current areas of interest include, but are not limited to: -(pre)formulation engineering and processing- computational biopharmaceutics- drug delivery and targeting- molecular biopharmaceutics and drug disposition (including cellular and molecular pharmacology)- pharmacokinetics, pharmacodynamics and pharmacogenetics. Research may involve nonclinical and clinical studies, and utilize both in vitro and in vivo approaches. Studies on small drug molecules, pharmaceutical solid materials (including biomaterials, polymers and nanoparticles) biotechnology products (including genes, peptides, proteins and vaccines), and genetically engineered cells are welcome.
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