Versatile Hyperbranched Poly(β-Hydrazide Ester) Macromers as Injectable Antioxidative Hydrogels
Allbwn ymchwil: Cyfraniad at gyfnodolyn › Erthygl › adolygiad gan gymheiriaid
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Yn: ACS Applied materials and interfaces, Cyfrol 10, Rhif 46, 30.10.2018, t. 39494-39504.
Allbwn ymchwil: Cyfraniad at gyfnodolyn › Erthygl › adolygiad gan gymheiriaid
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T1 - Versatile Hyperbranched Poly(β-Hydrazide Ester) Macromers as Injectable Antioxidative Hydrogels
AU - Xu, Qian
AU - Venet, Manon
AU - WAng, Wei
AU - Creagh-Flynn, Jack
AU - Wang, Xi
AU - Li, Xiaolin
AU - Gao, Yongshenng
AU - Zhou, Dezhong
AU - Zeng, Ming
AU - Lara-Saez, Irene
AU - A, Sigen
AU - Tai, Hongyun
AU - Wang, Wenxin
PY - 2018/10/30
Y1 - 2018/10/30
N2 - Synthetic reactive oxygen species (ROS)-responsive biomaterials have emerged as a useful platform for regu-lating critical aspects of ROS-induced pathologies and can improve such hostile microenvironments. Here, we report a se-ries of new hyperbranched poly(β-hydrazide ester) macromers (HB-PBHEs) with disulfide moieties synthesized via an “A2+B4” Michael addition approach. The three-dimensional structure of HB-PBHEs with multi-acrylate end groups endows the macromers with rapid gelation capabilities to form (1) injectable hydrogels via crosslinking with thiolated hyaluronic acid, and (2) robust UV-crosslinked hydrogels. The disulfide containing macromers and hydrogels exhibit H2O2-responsive degradation compared to the counterparts synthesized by a dihydrazide monomer without disulfide moieties. The cell via-bility under a high ROS environment can be well-maintained under the protection of the disulfide containing hydrogels.
AB - Synthetic reactive oxygen species (ROS)-responsive biomaterials have emerged as a useful platform for regu-lating critical aspects of ROS-induced pathologies and can improve such hostile microenvironments. Here, we report a se-ries of new hyperbranched poly(β-hydrazide ester) macromers (HB-PBHEs) with disulfide moieties synthesized via an “A2+B4” Michael addition approach. The three-dimensional structure of HB-PBHEs with multi-acrylate end groups endows the macromers with rapid gelation capabilities to form (1) injectable hydrogels via crosslinking with thiolated hyaluronic acid, and (2) robust UV-crosslinked hydrogels. The disulfide containing macromers and hydrogels exhibit H2O2-responsive degradation compared to the counterparts synthesized by a dihydrazide monomer without disulfide moieties. The cell via-bility under a high ROS environment can be well-maintained under the protection of the disulfide containing hydrogels.
U2 - 10.1021/acsami.8b15006
DO - 10.1021/acsami.8b15006
M3 - Article
VL - 10
SP - 39494
EP - 39504
JO - ACS Applied materials and interfaces
JF - ACS Applied materials and interfaces
SN - 1944-8244
IS - 46
ER -