Size-switchable polymer-based nanomedicines in the advanced therapy of rheumatoid arthritis
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
36403682
DOI
10.1016/j.jconrel.2022.11.027
PII: S0168-3659(22)00772-6
Knihovny.cz E-zdroje
- Klíčová slova
- Collagen II-induced arthritis, Dexamethasone, Drug delivery, HPMA, Inflammation, Passive targeting, Polymer conjugate,
- MeSH
- antiflogistika terapeutické užití MeSH
- artritida experimentální * diagnostické zobrazování farmakoterapie MeSH
- myši MeSH
- nanomedicína MeSH
- polymery terapeutické užití MeSH
- rentgenová mikrotomografie MeSH
- revmatoidní artritida * diagnostické zobrazování farmakoterapie MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antiflogistika MeSH
- polymery MeSH
Chronic inflammatory diseases such as rheumatoid arthritis represent a substantial socio-economic impact and have a high prevalence in the modern world. Nano-sized polymer therapeutics have shown suitable characteristics for becoming the next generation of anti-inflammatory nanomedicines. Here, we present biocompatible and stimuli-sensitive N-(2-hydroxypropyl)methacrylamide based polymer conjugates with the anti-inflammatory drug dexamethasone (DEX), which has been tailored for prolonged blood circulation, enhanced inflammatory site accumulation, site-specific drug release and subsequent elimination of the carrier via urine excretion. The hydrodynamic size of novel polymer-DEX nanomedicine was adjusted to prolong its blood circulation whilst maintaining the renal excretability of the polymer carrier after drug release in inflamed tissue. The therapeutic efficacy of the studied polymer nanomedicines was evaluated in a model of dissipated chronic arthritis, i.e. collagen II-induced arthritis, in mice. The pH-sensitive drug attachment enabled enhanced blood circulation with minimal systemic drug release, as well as rapid drug activation in affected joints. Importantly, unlike free DEX, the polymer nanomedicines were able to diminish joint inflammation and arthritis-induced bone damage - even at a reduced dosing regimen - as evaluated by micro computed tomography (micro-CT).
Institut Cochin Université de Paris INSERM CNRS 75014 Paris France
Institute of Macromolecular Chemistry Czech Academy of Sciences 162 06 Prague Czech Republic
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