Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Process Analytical Technology (PAT) has revolutionized pharmaceutical manufacturing by providing real-time monitoring and control capabilities throughout the production process. This review paper comprehensively examines the application of PAT methodologies specifically in the production of solid active pharmaceutical ingredients (APIs). Beginning with an overview of PAT principles and objectives, the paper explores the integration of advanced analytical techniques such as spectroscopy, imaging modalities and others into solid API substance production processes. Novel developments in in-line monitoring at academic level are also discussed. Emphasis is placed on the role of PAT in ensuring product quality, consistency, and compliance with regulatory requirements. Examples from existing literature illustrate the practical implementation of PAT in solid API substance production, including work-up, crystallization, filtration, and drying processes. The review addresses the quality and reliability of the measurement technologies, aspects of process implementation and handling, the integration of data treatment algorithms and current challenges. Overall, this review provides valuable insights into the transformative impact of PAT on enhancing pharmaceutical manufacturing processes for solid API substances.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ijpharm.2024.124412DOI Listing

Publication Analysis

Top Keywords

solid api
12
process analytical
8
analytical technology
8
pharmaceutical manufacturing
8
api substance
8
substance production
8
pat
6
process
4
technology downstream-processing
4
downstream-processing drug
4

Similar Publications

Novel development of lipid-based formulations: Improved wettability and homogeneous API solid dispersion visualised via near-infrared hyperspectral imaging.

Eur J Pharm Biopharm

September 2025

Research Center Pharmaceutical Engineering GmbH, Inffeldgasse 13, 8010 Graz, Austria; University of Graz, Institute of Pharmaceutical Sciences, Department of Pharmaceutical, Technology and Biopharmacy, Graz, Austria. Electronic address:

Lipid-based formulations have been successfully applied to improve the aqueous solubility of active pharmaceutical ingredients (APIs), however, with the bottleneck of limited wettability of the system. In this study, a lipid-based system was developed using polyglycerol ester of fatty acids (PGFA) as the main component and hexaglycerol (PG6) as a wetting agent. Felodipine, a BCS class II compound was selected as a model API.

View Article and Find Full Text PDF

Dexamethasone (Dexa) is widely used for the prophylaxis of chemotherapy-induced nausea and vomiting. In pediatric patients, individual dosing often requires the manipulation of commercial tablets, leading to dose inaccuracies, higher treatment complexity and poor acceptance due to Dexa's intensely bitter taste. This study aimed to develop 3D-printed chewable Dexa tablets with effective taste masking for pediatric oncology.

View Article and Find Full Text PDF

Revealing slip behavior in organic molecular crystals: AFM nanoindentation of acetaminophen.

J Pharm Sci

August 2025

Agricultural and Biological Engineering, Purdue University, West Lafayette, IN 47907, USA. Electronic address:

Molecular crystals are subjected to mechanical stress that can alter their slip planes which are structural features that play a critical role in governing mechanical behaviors such as milling, that requires fundamental insight for the successful manufacturing and performance of solid oral dosage forms. Milling is a critical unit operation in the manufacturing of pharmaceutical dosage forms. During this process, slip planes may become disrupted and dislocations can form, potentially inducing plastic deformation and significantly altering the physicochemical properties of active pharmaceutical ingredients (API).

View Article and Find Full Text PDF

The aim of this study is to propose a novel method for quantifying the crystallinity of active pharmaceutical ingredients (APIs) in solid dispersion (SD)-based pharmaceuticals. The key technology employed for this quantitative method is time-domain NMR (TD-NMR) T relaxometry. Model SDs were prepared using indomethacin (IMC) and polyvinylpyrrolidone (PVP).

View Article and Find Full Text PDF

: is an artificial intelligence-based platform designed to predict the Beyond Use Dates (BUDs) of compounded oral solid dosage forms. The study aims to develop a decision-support tool for pharmacists by integrating molecular, formulation, and environmental parameters to assist in optimizing the stability of extemporaneous preparations. : A tree ensemble regression model was trained using a curated dataset of 55 experimental BUD values collected from the Stabilis database.

View Article and Find Full Text PDF