Versatile Hyperbranched Poly(β-hydrazide ester) Macromers as Injectable Antioxidative Hydrogels
Source abstract
Abstract
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(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 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.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Dendrimers and Hyperbranched Polymers · Polymer Surface Interaction Studies · Advanced Polymer Synthesis and Characterization
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Charles Institute of Dermatology, School of Medicine, University College Dublin, Belfield, Dublin 4, Ireland
Molecular and Cellular Biology, Specialty Skin Biology, Department of Biology, Claude Bernard University Lyon I, 69622, France
School of Materials Science and Engineering, Tianjin University, Tianjin 300350, China
School of Chemistry, Bangor University, Bangor, Gwynedd LL57 2DG, U.K.
Funding
Science Foundation Ireland · Irish Research Council · Health Research Board
References (34)
Show source-provided references
1. 10.1146/annurev.pharmtox.47.120505.10512210.1146/annurev.pharmtox.47.120505.105122 ↗
2. 10.1073/pnas.150852211210.1073/pnas.1508522112 ↗
3. 10.1002/mabi.20150044010.1002/mabi.201500440 ↗
4. 10.1038/nchembio.8510.1038/nchembio.85 ↗
5. 10.1039/c5bm00542f10.1039/c5bm00542f ↗
6. 10.1039/c3py01192e10.1039/c3py01192e ↗
7. 10.1039/c4py00938j10.1039/c4py00938j ↗
8. 10.1039/c2py20021j10.1039/c2py20021j ↗
9. 10.1007/s10753-017-0526-410.1007/s10753-017-0526-4 ↗
10. 10.1021/jacs.7b1202510.1021/jacs.7b12025 ↗
11. 10.1016/j.carbpol.2008.05.01810.1016/j.carbpol.2008.05.018 ↗
12. 10.1016/j.biomaterials.2015.08.01810.1016/j.biomaterials.2015.08.018 ↗
13. 10.1016/j.jep.2016.05.03210.1016/j.jep.2016.05.032 ↗
14. 10.1016/j.ijbiomac.2015.10.05710.1016/j.ijbiomac.2015.10.057 ↗
15. 10.1126/science.aaf362710.1126/science.aaf3627 ↗
16. 10.1002/adma.20060052910.1002/adma.200600529 ↗
17. 10.1021/ja001538810.1021/ja0015388 ↗
18. 10.1038/nbt140210.1038/nbt1402 ↗
19. 10.1073/pnas.090543210610.1073/pnas.0905432106 ↗
20. 10.1126/sciadv.160010210.1126/sciadv.1600102 ↗
21. 10.1016/j.polymer.2017.01.05710.1016/j.polymer.2017.01.057 ↗
22. 10.1021/mz500277j10.1021/mz500277j ↗
23. 10.1039/c7sc03913a10.1039/c7sc03913a ↗
24. 10.1016/j.jvs.2008.11.04910.1016/j.jvs.2008.11.049 ↗
25. 10.1111/j.1365-2133.2010.09804.x10.1111/j.1365-2133.2010.09804.x ↗
26. 10.1038/nbt117110.1038/nbt1171 ↗
27. 10.1021/acsami.6b1500510.1021/acsami.6b15005 ↗
28. 10.1021/acs.biomac.5b0096610.1021/acs.biomac.5b00966 ↗
29. 10.1016/j.jconrel.2016.06.01410.1016/j.jconrel.2016.06.014 ↗
30. 10.1016/j.actbio.2017.12.03010.1016/j.actbio.2017.12.030 ↗
31. 10.1002/marc.20100015410.1002/marc.201000154 ↗
32. 10.1039/c6ce00290k10.1039/c6ce00290k ↗
33. 10.1271/bbb.66.64110.1271/bbb.66.641 ↗
34. 10.1126/scitranslmed.aan368210.1126/scitranslmed.aan3682 ↗