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Review
. 2017 Mar;106(3):667-712.
doi: 10.1016/j.xphs.2016.11.011. Epub 2016 Nov 22.

A Review of PAT Strategies in Secondary Solid Oral Dosage Manufacturing of Small Molecules

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Review

A Review of PAT Strategies in Secondary Solid Oral Dosage Manufacturing of Small Molecules

Stephan Laske et al. J Pharm Sci. 2017 Mar.

Abstract

Pharmaceutical solid oral dosage product manufacturing is a well-established, yet revolutionizing area. To this end, process analytical technology (PAT) involves interdisciplinary and multivariate (chemical, physical, microbiological, and mathematical) methods for material (e.g., materials, intermediates, products) and process (e.g., temperature, pressure, throughput, etc.) analysis. This supports rational process modeling and enhanced control strategies for improved product quality and process efficiency. Therefore, it is often difficult to orient and find the relevant, integrated aspects of the current state-of-the-art. Especially, the link between fundamental research, in terms of sensor and control system development, to the application both in laboratory and manufacturing scale, is difficult to comprehend. This review compiles a nonexhaustive overview on current approaches from the recognized academia and industrial practices of PAT, including screening, selection, and final implementations in solid oral dosage manufacturing, through a wide diversity of use cases. Finally, the authors attempt to extract a common consensus toward developing PAT application guidance for different unit operations of drug product manufacturing.

Keywords: Raman spectroscopy; near-infrared spectroscopy; process analytical technology; processing; solid dosage form.

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