Control of Mesh Size and Modulus by Kinetically Dependent Cross‐Linking in Hydrogels
Source abstract
Abstract
Kinetically controlled cross-linking processes produce mechanically distinguishable hydrogels using identical precursor chemistry. The oxime ligation demonstrates tunable reaction kinetics with pH and buffer strength, which induce changes in the structural features of hydrogels and determine their mechanical properties. Small-angle neutron scattering and swelling studies provide an insight into how structural properties correlate with mechanical properties for this hydrogel system. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Hydrogels: synthesis, properties, applications · Supramolecular Self-Assembly in Materials · Polymer Surface Interaction Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Polymer Science The University of Akron Akron, OH 44325 USA
Department of Polymer Engineering The University of Akron Akron OH 44325 USA
Funding
RESBIO “Integrated Technology Resource for Polymeric Biomaterials” · National Science Foundation
References (38)
Show source-provided references
1. 10.1002/adma.20080210610.1002/adma.200802106 ↗
2. 10.1002/(SICI)1097-4636(200008)51:2<164::AID-JBM4>3.0.CO;2-W10.1002/(SICI)1097-4636(200008)51:2<164::AID-JBM4>3.0.CO;2-W ↗
3. 10.1002/1097-4636(20000905)51:3<343::AID-JBM7>3.0.CO;2-D10.1002/1097-4636(20000905)51:3<343::AID-JBM7>3.0.CO;2-D ↗
4. 10.1016/0079-6700(95)00011-410.1016/0079-6700(95)00011-4 ↗
5. 10.1016/j.biomaterials.2008.11.02310.1016/j.biomaterials.2008.11.023 ↗
6. 10.1016/j.biomaterials.2010.06.00110.1016/j.biomaterials.2010.06.001 ↗
7. 10.1016/j.biomaterials.2009.01.03410.1016/j.biomaterials.2009.01.034 ↗
8. 10.1016/j.cell.2006.06.04410.1016/j.cell.2006.06.044 ↗
9. 10.1126/science.119103510.1126/science.1191035 ↗
10. 10.1016/j.actbio.2011.12.03210.1016/j.actbio.2011.12.032 ↗
11. 10.1016/j.ceb.2014.09.00610.1016/j.ceb.2014.09.006 ↗
12. 10.1038/nmat358610.1038/nmat3586 ↗
13. 10.1038/nmat393710.1038/nmat3937 ↗
14. 10.1242/jcs.09559610.1242/jcs.095596 ↗
15. 10.1016/j.biomaterials.2013.07.10310.1016/j.biomaterials.2013.07.103 ↗
16. 10.1021/bm401482710.1021/bm4014827 ↗
17. 10.1021/bm400418g10.1021/bm400418g ↗
18. 10.1016/j.biomaterials.2009.01.03410.1016/j.biomaterials.2009.01.034 ↗
19. 10.1021/bm070052h10.1021/bm070052h ↗
20. 10.1021/bm100137q10.1021/bm100137q ↗
21. 10.1021/cm101391y10.1021/cm101391y ↗
22. 10.1021/ma961870x10.1021/ma961870x ↗
23. 10.1021/ma302520p10.1021/ma302520p ↗
24. 10.1021/ma901900910.1021/ma9019009 ↗
25. 10.1021/ma302270a10.1021/ma302270a ↗
26. 10.1021/bm401133r10.1021/bm401133r ↗
27. 10.1021/bm025744e10.1021/bm025744e ↗
28. 10.1002/adma.20120523410.1002/adma.201205234 ↗
29. 10.1021/bm301346e10.1021/bm301346e ↗
30. 10.1021/ja01235a03010.1021/ja01235a030 ↗
31. 10.1021/ja01511a05310.1021/ja01511a053 ↗
32. Clayden J. · 2001
33. Flory P. J. · 1953
34. 10.1107/S002188980603505910.1107/S0021889806035059 ↗
35. 10.1107/S002188989701702010.1107/S0021889897017020 ↗
36. B.Hammouda Probing Nanoscale Structures – The SANS Toolbox http://www.ncnr.nist.gov/staff/hammouda/the_SANS_toolbox.pdf(accessed: February2015).
37. 10.1021/ma00188a02610.1021/ma00188a026 ↗
38. 10.1021/ma00046a02110.1021/ma00046a021 ↗