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Injectable Thermosensitive Hydrogels for a Sustained Release of Iron Nanochelatorsoa mark
  • Park, Seung Hun ;
  • Kim, Richard S. ;
  • Stiles, Wesley R. ;
  • Jo, Minjoo ;
  • Zeng, Lingxue ;
  • Rho, Sunghoon ;
  • Baek, Yoonji ;
  • Kim, Jonghan ;
  • Kim, Moon Suk ;
  • Kang, Homan ;
  • Choi, Hak Soo
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Publication Year
2022-05-01
Publisher
John Wiley and Sons Inc
Citation
Advanced Science, Vol.9
Keyword
chelation therapydeferoxaminehydrogeliron chelatorsustained release
Mesh Keyword
Chelating agentChelation therapyDeferoxamineHalf livesInjectable hydrogelsInjectablesIron overloadsIron-chelatorSustained releaseThermo-sensitive hydrogelDelayed-Action PreparationsHumansHydrogelsIronIron OverloadPoloxamer
All Science Classification Codes (ASJC)
Medicine (miscellaneous)Chemical Engineering (all)Materials Science (all)Biochemistry, Genetics and Molecular Biology (miscellaneous)Engineering (all)Physics and Astronomy (all)
Abstract
Deferoxamine (DFO) is an FDA-approved iron-chelating agent which shows good therapeutic efficacy, however, its short blood half-life presents challenges such as the need for repeated injections or continuous infusions. Considering the lifelong need of chelating agents for iron overload patients, a sustained-release formulation that can reduce the number of chelator administrations is essential. Here, injectable hydrogel formulations prepared by integrating crosslinked hyaluronic acid into Pluronic F127 for an extended release of DFO nanochelators are reported. The subcutaneously injected hydrogel shows a thermosensitive sol–gel transition at physiological body temperature and provides a prolonged release of renal clearable nanochelators over 2 weeks, resulting in a half-life 47-fold longer than that of the nanochelator alone. In addition, no chronic toxicity of the nanochelator-loaded hydrogel is confirmed by biochemical and histological analyses. This injectable hydrogel formulation with DFO nanochelators has the potential to be a promising formulation for the treatment of iron overload disorders.
ISSN
2198-3844
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/32622
DOI
https://doi.org/10.1002/advs.202200872
Type
Article
Funding
This study was supported by NIH/NHLBI #R01HL143020, the Creative Materials Discovery Program through the National Research Foundation of Korea (2019M3D1A1078938), and the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (H19C1343). The content expressed is solely the responsibility of the authors and does not necessarily represent the official views of the NIH. Figure 1 was illustrated from BioRender.com.
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