Yousef Ijjeh , Nowar Alsarayreh , Alaa Rifai , Hiba Abdelnabi , Sara Al-Mahamid , Dana A. Alqudah , Hamdi Nsairat , Zainab Lafi , Mohamad Ak Mousa , Yusuf Al-Hiari , Walhan Alshaer
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QbDD enables smart digital simulations and predictive analytics to improve nanoparticles with precise bio-physicochemical properties, thereby enhancing batch reproducibility while reducing reliance on resource-intensive physical experiments, lowering costs, and minimizing environmental impact. This digital infrastructure not only optimizes nanoparticle design and efficacy but also ensures compliance with regulatory standards. This review examines the fundamentals of nano-informatics and its integration with QbDD in nanomedicine, focusing on AI-powered molecular simulations and in silico screening to pre-select nanoparticle candidates, thereby reducing dependence on labor-intensive experimental validation. Furthermore, it discusses digital innovations in nanopharmaceuticals, including real-time monitoring systems and digital twins for process verification, highlighting how these advancements enhance nanoparticle synthesis, making it more efficient, cost-effective, and sustainable.</div></div>","PeriodicalId":12018,"journal":{"name":"European Journal of Pharmaceutical Sciences","volume":"213 ","pages":"Article 107239"},"PeriodicalIF":4.7000,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Quality by digital design for accelerated sustainable nanomedicine development\",\"authors\":\"Yousef Ijjeh , Nowar Alsarayreh , Alaa Rifai , Hiba Abdelnabi , Sara Al-Mahamid , Dana A. 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QbDD enables smart digital simulations and predictive analytics to improve nanoparticles with precise bio-physicochemical properties, thereby enhancing batch reproducibility while reducing reliance on resource-intensive physical experiments, lowering costs, and minimizing environmental impact. This digital infrastructure not only optimizes nanoparticle design and efficacy but also ensures compliance with regulatory standards. This review examines the fundamentals of nano-informatics and its integration with QbDD in nanomedicine, focusing on AI-powered molecular simulations and in silico screening to pre-select nanoparticle candidates, thereby reducing dependence on labor-intensive experimental validation. 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Quality by digital design for accelerated sustainable nanomedicine development
Drug delivery systems, diagnostics, and treatments are all being revolutionized by nanomedicine, greatly improving contemporary healthcare. However, traditional nanomedicine development relies on extensive experimental testing, which is costly, time-consuming, and environmentally harmful. To address these challenges, the Quality by Digital Design (QbDD) concept and framework have been developed, integrating digital technologies such as substantial data analytics, Artificial Intelligence (AI), Machine Learning (ML), and computational modeling to transform nanoparticle design. QbDD enables smart digital simulations and predictive analytics to improve nanoparticles with precise bio-physicochemical properties, thereby enhancing batch reproducibility while reducing reliance on resource-intensive physical experiments, lowering costs, and minimizing environmental impact. This digital infrastructure not only optimizes nanoparticle design and efficacy but also ensures compliance with regulatory standards. This review examines the fundamentals of nano-informatics and its integration with QbDD in nanomedicine, focusing on AI-powered molecular simulations and in silico screening to pre-select nanoparticle candidates, thereby reducing dependence on labor-intensive experimental validation. Furthermore, it discusses digital innovations in nanopharmaceuticals, including real-time monitoring systems and digital twins for process verification, highlighting how these advancements enhance nanoparticle synthesis, making it more efficient, cost-effective, and sustainable.
期刊介绍:
The journal publishes research articles, review articles and scientific commentaries on all aspects of the pharmaceutical sciences with emphasis on conceptual novelty and scientific quality. The Editors welcome articles in this multidisciplinary field, with a focus on topics relevant for drug discovery and development.
More specifically, the Journal publishes reports on medicinal chemistry, pharmacology, drug absorption and metabolism, pharmacokinetics and pharmacodynamics, pharmaceutical and biomedical analysis, drug delivery (including gene delivery), drug targeting, pharmaceutical technology, pharmaceutical biotechnology and clinical drug evaluation. The journal will typically not give priority to manuscripts focusing primarily on organic synthesis, natural products, adaptation of analytical approaches, or discussions pertaining to drug policy making.
Scientific commentaries and review articles are generally by invitation only or by consent of the Editors. Proceedings of scientific meetings may be published as special issues or supplements to the Journal.