Some Items of Interest to Process R&D Chemists and Engineers

Merck scientists shared an example of aligning API process development and product formulation to accelerate the nomination of a robust commercial drug product manufacturing process and to provide early insight into desired API material attributes (Hartmanshenn, C.; et al. J. Pharm. Sci., DOI: 10.1016/j.xphs.2024.11.008). The strategy involved using a diverse range of crystallization conditions and particle size modification technologies to deliberately vary the morphology and density of early API batches along with the particle size distribution ahead of the assessment of their impact on the tensile strength and dissolution of drug product tablets. In the case study described, the very high API loading in the tablets meant that the API material attributes could have an especially large influence on tablet manufacture and performance. The study showed that the API morphology was in fact much less important than the particle size distribution, providing potential flexibility around the API crystallization and how it is described in the marketing authorization application.

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Publication Details

Journal
Organic Process Research & Development
Published
2025-11-12
DOI
https://doi.org/10.1021/acs.oprd.5c00426
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
Field-Weighted Citation Impact
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article

Some Items of Interest to Process R&D Chemists and Engineers

Paul Richardson, David S. B. Daniels, Christopher C. Nawrat, Carlos Mateos et al.
Organic Process Research & Development
Drug Solubulity and Delivery Systems
article

Some Items of Interest to Process R&D Chemists and Engineers

Paul Richardson, David S. B. Daniels, Christopher C. Nawrat, Carlos Mateos, Andrei Zlota, Thomas Verheyen, Alexandre Barthelme, Chad N. Ungarean, Alan Steven, David P. Day, John Knight, Robert B. Kargbo
article en

Abstract

Merck scientists shared an example of aligning API process development and product formulation to accelerate the nomination of a robust commercial drug product manufacturing process and to provide early insight into desired API material attributes (Hartmanshenn, C.; et al. J. Pharm. Sci., DOI: 10.1016/j.xphs.2024.11.008). The strategy involved using a diverse range of crystallization conditions and particle size modification technologies to deliberately vary the morphology and density of early API batches along with the particle size distribution ahead of the assessment of their impact on the tensile strength and dissolution of drug product tablets. In the case study described, the very high API loading in the tablets meant that the API material attributes could have an especially large influence on tablet manufacture and performance. The study showed that the API morphology was in fact much less important than the particle size distribution, providing potential flexibility around the API crystallization and how it is described in the marketing authorization application.

Organic Process Research & DevelopmentVol. 29(11)
Merck & Co., Inc., Rahway, NJ, USA (United States) (US), Institute of Materials, Minerals and Mining (GB), Janssen (Belgium) (BE), University of Dundee (GB), Pfizer (United States) (US), Swedish Orphan Biovitrum (United States) (US), Usona Institute (US), Université Bourgogne Franche-Comté (FR), Eli Lilly (Spain) (ES), Janssen (United States) (US), Swedish Orphan Biovitrum (Switzerland) (CH), Chemopharma (Austria) (AT), Dassault Systèmes (France) (FR), Cardiff University (GB)
Openalex Percentile: Top 72%
Drug Solubulity and Delivery Systems
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