Versatile Hyperbranched Poly(β-hydrazide ester) Macromers as Injectable Antioxidative Hydrogels

被引:39
作者
Xu, Qian [1 ]
Venet, Manon [2 ]
Wang, Wei [3 ]
Creagh-Flynn, Jack [1 ]
Wang, Xi [1 ]
Li, Xiaolin [1 ]
Gao, Yongsheng [1 ]
Zhou, Dezhong [1 ]
Zeng, Ming [1 ]
Lara-Saez, Irene [1 ]
Sigen, A. [1 ]
Tai, Hongyun [4 ]
Wang, Wenxin [1 ]
机构
[1] Univ Coll Dublin, Charles Inst Dermatol, Sch Med, Dublin 4, Ireland
[2] Claude Bernard Univ Lyon I, Dept Biol, Mol & Cellular Biol, Specialty Skin Biol, F-69622 Villeurbanne, France
[3] Tianjin Univ, Sch Mat Sci & Engn, Tianjin 300350, Peoples R China
[4] Bangor Univ, Sch Chem, Bangor LL57 2DG, Gwynedd, Wales
基金
爱尔兰科学基金会;
关键词
antioxidant; poly(beta-hydrazide ester); injectable; hydrogel; tissue engineering; POLY(BETA-AMINO ESTER); COMBINATORIAL LIBRARY; DEGRADATION; POLYMERS; DELIVERY; STRESS; DESIGN; OXYGEN; ROS;
D O I
10.1021/acsami.8b15006
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Synthetic reactive oxygen species (ROS)-responsive biomaterials have emerged as a useful platform for regulating critical aspects of ROS-induced pathologies and can improve such hostile microenvironments. Here, we report a series of new hyperbranched poly(beta-hydrazide ester) macromers (HB-PBHEs) with disulfide moieties synthesized via an "A2 + B4" Michael addition approach. The three-dimensional structure of HB-PBHEs with multiacrylate end groups endows the macromers with rapid gelation capabilities to form (1) injectable hydrogels via cross-linking with thiolated hyaluronic acid and (2) robust UV-cross-linked hydrogels. The disulfide-containing macromers and hydrogels exhibit H2O2-responsive degradation compared with the counterparts synthesized by a dihydrazide monomer without disulfide moieties. The cell viability under a high ROS environment can be well-maintained under the protection of the disulfide containing hydrogels.
引用
收藏
页码:39494 / 39504
页数:11
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