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Injectable click-crosslinked hydrogel containing resveratrol to improve the therapeutic effect in triple negative breast canceroa mark
  • Shin, Gi Ru ;
  • Kim, Hee Eun ;
  • Ju, Hyeon Jin ;
  • Kim, Jae Ho ;
  • Choi, Sangdun ;
  • Choi, Hak Soo ;
  • Kim, Moon Suk
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Publication Year
2022-12-01
Publisher
Elsevier B.V.
Citation
Materials Today Bio, Vol.16
Keyword
Click-crosslinkingInjectable hydrogelIntratumoral injectionResveratrolTriple-negative breast cancer
Mesh Keyword
Cancer patientsClick-crosslinkingCross-linked hydrogelsCrosslinkedInhibitory effectInjectable hydrogelsInjectablesIntratumoral injectionTherapeutic effectsTriple-negative breast cancers
All Science Classification Codes (ASJC)
BiotechnologyBioengineeringBiomaterialsBiomedical EngineeringMolecular BiologyCell Biology
Abstract
Triple-negative breast cancer (TNBC) patients are considered intractable, as this disease has few effective treatments and a very poor prognosis even in its early stages. Here, intratumoral therapy with resveratrol (Res), which has anticancer and metastasis inhibitory effects, was proposed for the effective treatment of TNBC. An injectable Res-loaded click-crosslinked hyaluronic acid (Res-Cx-HA) hydrogel was designed and intratumorally injected to generate a Res-Cx-HA depot inside the tumor. The Res-Cx-HA formulation exhibited good injectability into the tumor tissue, quick depot formation inside the tumor, and the depot remained inside the injected tumor for extended periods. In vivo formed Res-Cx-HA depots sustained Res inside the tumor for extended periods. More importantly, the bioavailability and therapeutic efficacy of Res remained almost exclusively within the tumor and not in other organs. Intratumoral injection of Res-Cx-HA in animal models resulted in significant negative tumor growth rates (i.e., the tumor volume decreased over time) coupled with large apoptotic cells and limited angiogenesis in tumors. Therefore, Res-Cx-HA intratumoral injection is a promising way to treat TNBC patients with high efficacy and minimal adverse effects.
ISSN
2590-0064
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/32849
DOI
https://doi.org/10.1016/j.mtbio.2022.100386
Fulltext

Type
Article
Funding
This study was supported by the National Research Foundation of Korea (NRF) grants, Creative Materials Discovery Program ( 2019M3D1A1078938 ) and Priority Research Centers Program ( 2019R1A6A1A11051471 ).
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Kim, Moon Suk김문석
Department of Applied Chemistry & Biological Engineering
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