Injectable polymeric nanoparticle hydrogel system for long-term anti-inflammatory effect to treat osteoarthritis

Authors
Seo, Bo-BaeYoungjoong KwonJun KimKi Hyun HongKim, S.-E.Song, H.-R.Kim, Young MinSong, Soo Chang
Issue Date
2022-01
Publisher
Elsevier
Citation
Bioactive Materials, v.7, pp.14 - 25
Abstract
Treatment of osteoarthritis (OA) by administration of corticosteroids is a commonly used method in clinics using anti-inflammatory medicine. Oral administration or intra-articular injection of corticosteroids can reduce the pain and progress of cartilage degeneration, but they are usually insufficient to show local and long-term anti-inflammatory effects because of their fast clearance in the body. In this study, we suggest an injectable anti-OA drug depot system for sustained drug release that provides long-term effective therapeutic advantages. Amphiphilic poly(organophosphazene), which has temperature-dependent nanoparticle forming and sol-gel transition behaviors when dissolved in aqueous solution, was synthesized for triamcinolone acetonide (TCA) delivery. Because hydrophobic parts of the polymer can interact with hydrophobic parts of the TCA, the TCA was encapsulated into the self-assembled polymeric nanoparticles. The TCA-encapsulated polymeric nanoparticles (TePNs) were well dispersed in an aqueous solution below room temperature so that they can be easily injected as a sol state into an intra-articular region. However, the TePNs solution transforms immediately to a viscose 3D hydrogel like a synovial fluid in the intra-articular region via the conducted body temperature. An in vitro TCA release study showed sustained TCA release for six weeks. One-time injection of the TePN hydrogel system in an early stage of OA-induced rat model showed a great inhibition effect against further OA progression. The OA-induced knees completely recovered as a healthy cartilage without any abnormal symptoms. ? 2021 The Authors
Keywords
polymerization; RNA isolation; corticosteroid; dichlorophosphazene; Hexachlorocyclotriphosphazene; hyaluronic acid; hydrogel; hydroxyproline; inorganic compound; levofloxacin; macrogol; molecular scaffold; stromelysin; triamcinolone; triamcinolone acetonide; tumor necrosis factor; unclassified drug; animal experiment; animal tissue; antiinflammatory activity; Article; biocompatibility; biodegradability; biodegradation; body temperature; cartilage degeneration; cell viability; chondrocyte; controlled study; cytokine release; cytotoxicity; dispersity; drug stability; encapsulation; flow kinetics; gene expression; genetic transcription; inflammation; male; mouse; mutagenicity; nonhuman; osteoarthritis; polymerase chain reaction; Osteoarthritis; Polymer nanoparticle; Sustained release; Thermosensitive hydrogel; Triamcinolone acetonide
ISSN
2452-199X
URI
https://pubs.kist.re.kr/handle/201004/115917
DOI
10.1016/j.bioactmat.2021.05.028
Appears in Collections:
KIST Article > 2022
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