4.7 Article

Thermosensitive Injectable Hydrogels for Intra-Articular Delivery of Etanercept for the Treatment of Osteoarthritis

期刊

GELS
卷 8, 期 8, 页码 -

出版社

MDPI
DOI: 10.3390/gels8080488

关键词

osteoarthritis; etanercept; chitosan; Pluronic; thermosensitive hydrogels; intra-articular delivery

资金

  1. European Union [2015-1-NL01-KA 107008639, 777682, 872391, 872860, 807281, 852985, 952520, 861190, 857894, 859908, 860173, 956477]
  2. H2020-MSCA-2020-CARTHAGO [955335]
  3. VIDI personal grant [723.012.110]
  4. Marie Curie Actions (MSCA) [859908, 860173] Funding Source: Marie Curie Actions (MSCA)

向作者/读者索取更多资源

In recent years, there has been significant interest in intra-articular drug administration and modified drugs for the treatment of osteoarthritis. This study successfully prepared injectable-thermosensitive hydrogels for intra-articular administration of Etanercept (ETA) and demonstrated their cytocompatibility and controlled release of ETA. In vivo studies also showed their potential for localized treatment of joints in osteoarthritic mice.
The intra-articular administration of drugs has attracted great interest in recent decades for the treatment of osteoarthritis. The use of modified drugs has also attracted interest in recent years because their intra-articular administration has demonstrated encouraging results. The objective of this work was to prepare injectable-thermosensitive hydrogels for the intra-articular administration of Etanercept (ETA), an inhibitor of tumor necrosis factor-alpha. Hydrogels were prepared from the physical mixture of chitosan and Pluronic F127 with beta-glycerolphosphate (BGP). Adding beta-glycerolphosphate to the system reduced the gelation time and also modified the morphology of the resulting material. In vitro studies were carried out to determine the cytocompatibility of the prepared hydrogels for the human chondrocyte line C28/I2. The in vitro release study showed that the incorporation of BGP into the system markedly modified the release of ETA. In the in vivo studies, it was verified that the hydrogels remained inside the implantation site in the joint until the end of the study. Furthermore, ETA was highly concentrated in the blood of the study mice 48 h after the loaded material was injected. Histological investigation of osteoarthritic knees showed that the material promotes cartilage recovery in osteoarthritic mice. The results demonstrate the potential of ETA-loaded injectable hydrogels for the localized treatment of joints.

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