Controlling the Surface Chemistry of a Hydrogel for Spatially Defined Cell Adhesion
Source abstract
Abstract
A two-step synthesis is described for activating the surface of a fully hydrated hydrogel that is of interest as a possible scaffold for neural regeneration devices. The first step exploits the water content of the hydrogel and the hydrophobicity of the reaction solvent to create a thin oxide layer on the hydrogel surface using a common titanium or zirconium alkoxide. This layer serves as a reactive interface that enables rapid transformation of the hydrophilic, cell-nonadhesive hydrogel into either a highly hydrophobic surface by reaction with an alkylphosphonic acid, or into a cell-adhesive one using a (α,ω-diphosphono)alkane. Physically imprinting a mask ("debossing") into the hydrogel, followed by a two-step surface modification with a phosphonate, allows for patterning its surface to create spatially defined, cell-adhesive regions.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: 3D Printing in Biomedical Research · Neuroscience and Neural Engineering · Hydrogels: synthesis, properties, applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (50)
Show source-provided references
1. 10.1038/nmeth.383910.1038/nmeth.3839 ↗
2. 10.1021/acsbiomaterials.6b0023310.1021/acsbiomaterials.6b00233 ↗
3. 10.1007/s10856-010-4094-510.1007/s10856-010-4094-5 ↗
4. 10.1021/acsami.6b0092910.1021/acsami.6b00929 ↗
5. 10.1016/j.biomaterials.2009.04.01810.1016/j.biomaterials.2009.04.018 ↗
6. 10.1163/156856208x38638110.1163/156856208x386381 ↗
7. 10.1089/scd.2012.061610.1089/scd.2012.0616 ↗
8. 10.1016/j.msec.2015.01.08910.1016/j.msec.2015.01.089 ↗
9. 10.1016/j.actbio.2011.12.03110.1016/j.actbio.2011.12.031 ↗
10. 10.4103/1673-5374.15696610.4103/1673-5374.156966 ↗
11. 10.1155/2015/94804010.1155/2015/948040 ↗
12. 10.1016/j.biomaterials.2007.12.03010.1016/j.biomaterials.2007.12.030 ↗
13. 10.1021/bm100699q10.1021/bm100699q ↗
14. 10.1002/term.243110.1002/term.2431 ↗
15. 10.1089/ten.tea.2015.001910.1089/ten.tea.2015.0019 ↗
16. 10.1016/s0142-9612(03)00340-510.1016/s0142-9612(03)00340-5 ↗
17. 10.1021/bm200083n10.1021/bm200083n ↗
18. 10.1177/088532820708699310.1177/0885328207086993 ↗
19. 10.1007/s10856-008-3625-910.1007/s10856-008-3625-9 ↗
20. 10.1007/s13233-012-0058-610.1007/s13233-012-0058-6 ↗
21. 10.1039/c3sm50587a10.1039/c3sm50587a ↗
22. 10.1002/mabi.20120004210.1002/mabi.201200042 ↗
23. 10.1039/c0sm00508h10.1039/c0sm00508h ↗
24. 10.1016/j.actbio.2011.10.02710.1016/j.actbio.2011.10.027 ↗
25. 10.1021/bm201802w10.1021/bm201802w ↗
26. 10.1016/j.jiec.2008.08.00110.1016/j.jiec.2008.08.001 ↗
27. 10.1016/j.biomaterials.2010.07.01410.1016/j.biomaterials.2010.07.014 ↗
28. 10.4028/www.scientific.net/msf.567-568.26510.4028/www.scientific.net/msf.567-568.265 ↗
29. 10.1021/ja065217t10.1021/ja065217t ↗
30. 10.1021/am900494610.1021/am9004946 ↗
31. 10.1021/ja810075c10.1021/ja810075c ↗
32. 10.1039/b714947f10.1039/b714947f ↗
33. 10.1039/c3tb21864c10.1039/c3tb21864c ↗
34. 10.1021/acs.jpcc.5b1052910.1021/acs.jpcc.5b10529 ↗
35. 10.1021/bm100048q10.1021/bm100048q ↗
36. 10.1021/cm00045a01310.1021/cm00045a013 ↗
37. 10.1021/la010649x10.1021/la010649x ↗
38. 10.1016/s0928-4931(02)00310-710.1016/s0928-4931(02)00310-7 ↗
39. 10.1021/la960762110.1021/la9607621 ↗
40. Kitaigorodskii, A. I. Organic Chemical Crystallography; Consultants Bureau: New York, 1961; p 541.
41. Dennes, T. J., III. Spatially-Controlled Surface Activation of Preformed Polymers. Ph.D. Dissertation, Princeton University, Ann Arbor, 2008.
42. 10.1021/acs.chemmater.5b0444510.1021/acs.chemmater.5b04445 ↗
43. 10.1002/adma.20160156810.1002/adma.201601568 ↗
44. 10.1039/c3tb20565g10.1039/c3tb20565g ↗
45. 10.1016/j.matbio.2016.08.01110.1016/j.matbio.2016.08.011 ↗
46. 10.1021/la036084h10.1021/la036084h ↗
47. 10.1002/jbm.a.3165110.1002/jbm.a.31651 ↗
48. Taylor S. E. · 2013
49. 10.1017/s1740925x0600010x10.1017/s1740925x0600010x ↗
50. 10.1021/acsbiomaterials.7b0033910.1021/acsbiomaterials.7b00339 ↗