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  3. Drug delivery in intervertebral disc degeneration and osteoarthritis: Selecting the optimal platform for the delivery of disease-modifying agents.
 

Drug delivery in intervertebral disc degeneration and osteoarthritis: Selecting the optimal platform for the delivery of disease-modifying agents.

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BORIS DOI
10.48350/149049
Date of Publication
December 10, 2020
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Author
Colella, Fabio
Garcia, João Pedro
Sorbona, Marco
Lolli, Andrea
Antunes, Bernardo
D'Atri, Domenico
Barré, Florian P Y
Oieni, Jacopo
Vainieri, Maria Letizia
Zerrillo, Luana
Capar, Serdar
Häckel, Sonjaorcid-logo
Universitätsklinik für Orthopädische Chirurgie und Traumatologie
Cai, Yunpeng
Creemers, Laura B
Subject(s)

600 - Technology::610...

Series
Journal of controlled release
ISSN or ISBN (if monograph)
0168-3659
Publisher
Elsevier
Language
English
Publisher DOI
10.1016/j.jconrel.2020.08.041
PubMed ID
32860929
Description
Osteoarthritis (OA) and intervertebral disc degeneration (IVDD) as major cause of chronic low back pain represent the most common degenerative joint pathologies and are leading causes of pain and disability in adults. Articular cartilage (AC) and intervertebral discs are cartilaginous tissues with a similar biochemical composition and pathophysiological aspects of degeneration. Although treatments directed at reversing these conditions are yet to be developed, many promising disease-modifying drug candidates are currently under investigation. Given the localized nature of these chronic diseases, drug delivery systems have the potential to enhance therapeutic outcomes by providing controlled and targeted release of bioactives, minimizing the number of injections needed and increasing drug concentration in the affected areas. This review provides a comprehensive overview of the currently most promising disease-modifying drugs as well as potential drug delivery systems for OA and IVDD therapy.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/38451
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FileFile TypeFormatSizeLicensePublisher/Copright statementContent
1-s2.0-S016836592030482X-main.pdfAdobe PDF2.86 MBpublishedOpen
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