| Literature DB >> 34921569 |
Dize Li1, Kaiwen Chen2, Han Tang1, Shanshan Hu1, Liangjing Xin1, Xuan Jing1, Qingqing He1, Si Wang1, Jinlin Song1, Li Mei1,3, Richard D Cannon3, Ping Ji1, Huanan Wang2, Tao Chen1.
Abstract
The regeneration of diabetic bone defects remains challenging as the innate healing process is impaired by glucose fluctuation, reactive oxygen species (ROS), and overexpression of proteinases (such as matrix metalloproteinases, MMPs). A "diagnostic" and therapeutic dual-logic-based hydrogel for diabetic bone regeneration is therefore developed through the design of a double-network hydrogel consisting of phenylboronic-acid-crosslinked poly(vinyl alcohol) and gelatin colloids. It exhibits a "diagnostic" logic to interpret pathological cues (glucose fluctuation, ROS, MMPs) and determines when to release drug in a diabetic microenvironment and a therapeutic logic to program different cargo release to match immune-osteo cascade for better tissue regeneration. The hydrogel is also shown to be mechanically adaptable to the local complexity at the bone defect. Furthermore, the underlying therapeutic mechanism is elucidated, whereby the logic-based cargo release enables the regulation of macrophage polarization by remodeling the mitochondria-related antioxidative system, resulting in enhanced osteogenesis in diabetic bone defects. This study provides critical insight into the design and biological mechanism of dual-logic-based tissue-engineering strategies for diabetic bone regeneration.Entities:
Keywords: BMP-2; IL-10; controlled release; diabetes mellitus; hydrogels; osteoimmunomodulation
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Year: 2022 PMID: 34921569 DOI: 10.1002/adma.202108430
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849