The landscape of nanomedicines: An expert perspective
The field of nanotechnology is at the forefront of a scientific revolution, where the term "nano" transcends mere size and opens the door to enormous possibilities. In the context of drug development, the selection of a suitable drug delivery system (corresponding to a certain active pharm...
Ausführliche Beschreibung
Autor*in: |
Nikolić Ines [verfasserIn] Filipić Brankica [verfasserIn] Petrović Marija [verfasserIn] Jordan Olivier [verfasserIn] Savić Snežana [verfasserIn] Borchard Gerrit [verfasserIn] |
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2023 |
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Übergeordnetes Werk: |
In: Arhiv za farmaciju - Pharmaceutical Association of Serbia, Belgrade, Serbia, 2018, 73(2023), 5, Seite 390-403 |
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Übergeordnetes Werk: |
volume:73 ; year:2023 ; number:5 ; pages:390-403 |
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Link aufrufen |
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DOI / URN: |
10.5937/arhfarm73-46686 |
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DOAJ099418371 |
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10.5937/arhfarm73-46686 doi (DE-627)DOAJ099418371 (DE-599)DOAJ9f518f6a5835435db58f8c14d2af54f0 DE-627 ger DE-627 rakwb srp RS1-441 Nikolić Ines verfasserin aut The landscape of nanomedicines: An expert perspective 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The field of nanotechnology is at the forefront of a scientific revolution, where the term "nano" transcends mere size and opens the door to enormous possibilities. In the context of drug development, the selection of a suitable drug delivery system (corresponding to a certain active pharmaceutical ingredient) is a pivotal decision. Accordingly, nanosystems have emerged as a promising avenue, offering innovative solutions, and gaining recognition for addressing healthcare issues. While these products hold immense promise, they have faced certain complexities in their translation from the preclinical to the clinical setting, reflected in the lack of proper assessment protocols for quality and safety aspects and, consequently, an insufficiently defined regulatory environment. Since the groundbreaking US Food and Drug Administration (FDA) approval of liposomal doxorubicin in 1995, approximately 80 nanomedicine products have received regulatory approval so far. Recent attention has gravitated toward lipid-based nanomedicines, particularly in the development of mRNA vaccines during the COVID-19 pandemic, further highlighting their significance. However, the relatively modest number of approved nanomedicines compared to the extensive research efforts raises important questions and underscores areas of uncertainty. This article provides an overview of the challenges in defining nanomedicines, their properties, the complexities of regulatory frameworks, and the imperative for standardized characterization protocols. nanomedicines nanoparticles characterization protocols regulation of nanomedicines Pharmacy and materia medica Filipić Brankica verfasserin aut Petrović Marija verfasserin aut Jordan Olivier verfasserin aut Savić Snežana verfasserin aut Borchard Gerrit verfasserin aut In Arhiv za farmaciju Pharmaceutical Association of Serbia, Belgrade, Serbia, 2018 73(2023), 5, Seite 390-403 (DE-627)1692190660 22178767 nnns volume:73 year:2023 number:5 pages:390-403 https://doi.org/10.5937/arhfarm73-46686 kostenfrei https://doaj.org/article/9f518f6a5835435db58f8c14d2af54f0 kostenfrei https://scindeks-clanci.ceon.rs/data/pdf/0004-1963/2023/0004-19632305390N.pdf kostenfrei https://doaj.org/toc/0004-1963 Journal toc kostenfrei https://doaj.org/toc/2217-8767 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ AR 73 2023 5 390-403 |
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The landscape of nanomedicines: An expert perspective |
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The field of nanotechnology is at the forefront of a scientific revolution, where the term "nano" transcends mere size and opens the door to enormous possibilities. In the context of drug development, the selection of a suitable drug delivery system (corresponding to a certain active pharmaceutical ingredient) is a pivotal decision. Accordingly, nanosystems have emerged as a promising avenue, offering innovative solutions, and gaining recognition for addressing healthcare issues. While these products hold immense promise, they have faced certain complexities in their translation from the preclinical to the clinical setting, reflected in the lack of proper assessment protocols for quality and safety aspects and, consequently, an insufficiently defined regulatory environment. Since the groundbreaking US Food and Drug Administration (FDA) approval of liposomal doxorubicin in 1995, approximately 80 nanomedicine products have received regulatory approval so far. Recent attention has gravitated toward lipid-based nanomedicines, particularly in the development of mRNA vaccines during the COVID-19 pandemic, further highlighting their significance. However, the relatively modest number of approved nanomedicines compared to the extensive research efforts raises important questions and underscores areas of uncertainty. This article provides an overview of the challenges in defining nanomedicines, their properties, the complexities of regulatory frameworks, and the imperative for standardized characterization protocols. |
abstractGer |
The field of nanotechnology is at the forefront of a scientific revolution, where the term "nano" transcends mere size and opens the door to enormous possibilities. In the context of drug development, the selection of a suitable drug delivery system (corresponding to a certain active pharmaceutical ingredient) is a pivotal decision. Accordingly, nanosystems have emerged as a promising avenue, offering innovative solutions, and gaining recognition for addressing healthcare issues. While these products hold immense promise, they have faced certain complexities in their translation from the preclinical to the clinical setting, reflected in the lack of proper assessment protocols for quality and safety aspects and, consequently, an insufficiently defined regulatory environment. Since the groundbreaking US Food and Drug Administration (FDA) approval of liposomal doxorubicin in 1995, approximately 80 nanomedicine products have received regulatory approval so far. Recent attention has gravitated toward lipid-based nanomedicines, particularly in the development of mRNA vaccines during the COVID-19 pandemic, further highlighting their significance. However, the relatively modest number of approved nanomedicines compared to the extensive research efforts raises important questions and underscores areas of uncertainty. This article provides an overview of the challenges in defining nanomedicines, their properties, the complexities of regulatory frameworks, and the imperative for standardized characterization protocols. |
abstract_unstemmed |
The field of nanotechnology is at the forefront of a scientific revolution, where the term "nano" transcends mere size and opens the door to enormous possibilities. In the context of drug development, the selection of a suitable drug delivery system (corresponding to a certain active pharmaceutical ingredient) is a pivotal decision. Accordingly, nanosystems have emerged as a promising avenue, offering innovative solutions, and gaining recognition for addressing healthcare issues. While these products hold immense promise, they have faced certain complexities in their translation from the preclinical to the clinical setting, reflected in the lack of proper assessment protocols for quality and safety aspects and, consequently, an insufficiently defined regulatory environment. Since the groundbreaking US Food and Drug Administration (FDA) approval of liposomal doxorubicin in 1995, approximately 80 nanomedicine products have received regulatory approval so far. Recent attention has gravitated toward lipid-based nanomedicines, particularly in the development of mRNA vaccines during the COVID-19 pandemic, further highlighting their significance. However, the relatively modest number of approved nanomedicines compared to the extensive research efforts raises important questions and underscores areas of uncertainty. This article provides an overview of the challenges in defining nanomedicines, their properties, the complexities of regulatory frameworks, and the imperative for standardized characterization protocols. |
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