Please use this identifier to cite or link to this item: https://doi.org/10.48548/pubdata-117
Resource TypeJournal Article
TitleDesigning greener active pharmaceutical ingredients: Insights from pharmaceutical industry into drug discovery and development
DOI10.48548/pubdata-117
Handle20.500.14123/137
CreatorPuhlmann, Neele  0000-0002-9397-2540 (Institut für Nachhaltige Chemie (INSC), Leuphana Universität Lüneburg  02w2y2t16)
Vidaurre, Rodrigo (Ecologic Institute, Berlin  04ejkkg63)
Kümmerer, Klaus  0000-0003-2027-6488 (Institut für Nachhaltige Chemie (INSC), Leuphana Universität Lüneburg  02w2y2t16)
AbstractActive pharmaceutical ingredients (APIs), their metabolites and transformation products (TPs) are found as pollutants in the environment. They can impact human and environmental health. To address this issue, an efficient, long-term prevention strategy could be the design of APIs that have less impact on the natural environment, i.e. the design of greener APIs, by the implementation of environmental parameters into the drug discovery and development process (also abbreviated R&D for ‘research and development’). Our study aimed to evaluate the feasibility of the design of greener APIs based on insights from drug design experts working in large, research-based pharmaceutical companies. The feasibility evaluation also identified needs and incentives for process modification. For this purpose, 30 R&D and environmental experts from seven globally active pharmaceutical companies were interviewed along a structured questionnaire. Main findings are that the interviewed experts saw manifold opportunities to include properties rendering APIs greener in different stages along the R&D process. This implementation would be favoured by the fact that the pharmaceutical R&D process is very flexible and relies on balancing multiple parameters. Furthermore, some API properties that reduce environmental risks were considered compatible with common desirable properties for application. Environmental properties should be considered early during R&D, i.e. when molecules are screened and optimized. It has been found that availability of suitable in silico models and in vitro assays is crucial for this environmental consideration. Their attributes, e.g. throughput and costs, determine at which process stage they can be successfully applied. An intensified exchange between R&D and environmental experts within and outside companies would push the industrial application of the benign by design approach for APIs forward. Collaboration across pharmaceutical companies, authorities, and academia is seen as highly promising in this respect. Financial, social, and regulatory incentives would support future design of greener APIs.
LanguageEnglish
KeywordsActive pharmaceutical ingredients; API; Sustainable; Environment; Feasibility; Interview; Experts
Year of Publication in PubData2024
Publishing TypeParallel publication
Publication versionPublished Version
Date issued2023-11-01
Creation ContextResearch
Published byMedien- und Informationszentrum, Leuphana Universität Lüneburg
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FieldValue
Resource typeJournal
Title of the resource typeEuropean Journal of Pharmaceutical Sciences
IdentifierDOI: 10.1016/j.ejps.2023.106614
Publication year2024
Volume192
Number106614
Number typeArticle
PublisherElsevier
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