journal article·2024-06-28Open access

Cross-Link of Telechelic Diacrylate Polyethylene-Glycol in Peptide-Based Fmoc-FF Hydrogel Matrices

Elisabetta Rosa, Paolo Pellegrino, Mariafrancesca Cascione, Rosaria Rinaldi, Eliana Gianolio, Charlotte Edwards-Gayle, Ian W. Hamley, Giancarlo Morelli, Antonella Accardo, Carlo Diaferia

ACS Applied Polymer Materials· Volume 6· Issue 12

Abstract

Hydrogels (HGs) with enhanced structural and mechanical properties can be generated by combining two or more different building blocks in the same matrix. It has been widely demonstrated that the addition of peptides, proteins, sugars, or polymers to the low molecular weight hydrogelator Fmoc-FF [(fluorenyl methyloxycarbonyl)-diphenylalanine] can significantly modify the chemical and structural features of the resulting HGs. In this context, the formulation of multicomponent HGs has been previously described, in which Fmoc-FF is mixed with telechelic diacrylate α-/ω-substituted polyethylene-glycol derivatives (PEGDAs) with a molecular weight of 575 (PEGDA1) or 250 Da (PEGDA2). Here, we investigate the possibility to generate Fmoc-FF-based interpenetrated networks performing the cross-link reaction of PEGDA monomers in supramolecular peptide hydrogels. This approach can allow the modulation of the final properties of the material, in terms of water behavior, topography, and rigidity. The results indicate that the polymerization time, the polymer length, and the Fmoc-FF/PEGDA ratio play a crucial role in the chemistry of the materials and, consequently, of their potential application.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Supramolecular Self-Assembly in Materials · Polydiacetylene-based materials and applications · Hydrogels: synthesis, properties, applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Pharmacy, Research Centre on Bioactive Peptides (CIRPeB), University of Naples “Federico II”, Via T. De Amicis 95, 80145 Naples, Italy

Istituti Clinici Scientifici Maugeri IRCCS of Telese Terme Institute, 82037 Telese Terme, Italy

Institute for Microelectronics and Microsystems (IMM), CNR, Via Monteroni, 73100 Lecce, Italy

Department of Mathematics and Physics “Ennio De Giorgi”, University of Salento, Via Monteroni, 73100 Lecce, Italy

Department of Molecular Biotechnology and Health Sciences, University of Turin, 10126Turin, Italy

School of Chemistry, Pharmacy and Food Biosciences, University of Reading, RG6 6ADBerkshire, United Kingdom

References (56)

Show source-provided references
1. 10.1038/s41557-018-0053-410.1038/s41557-018-0053-4 ↗
2. 10.3389/fbioe.2020.0029510.3389/fbioe.2020.00295 ↗
3. 10.1073/pnas.060321610310.1073/pnas.0603216103 ↗
4. 10.1002/ijch.20190008310.1002/ijch.201900083 ↗
5. 10.1038/s41570-020-0215-y10.1038/s41570-020-0215-y ↗
6. 10.1002/cbic.20220058210.1002/cbic.202200582 ↗
7. 10.1073/pnas.08206589910.1073/pnas.082065899 ↗
8. 10.1021/acs.chemrev.1c0088410.1021/acs.chemrev.1c00884 ↗
9. 10.1560/5MC0-V3DX-KE0B-YF3J10.1560/5MC0-V3DX-KE0B-YF3J ↗
10. 10.1002/chem.20210018210.1002/chem.202100182 ↗
11. 10.1002/chem.20220236810.1002/chem.202202368 ↗
12. 10.1146/annurev-biochem-062917-01254110.1146/annurev-biochem-062917-012541 ↗
13. 10.1002/chem.20160463910.1002/chem.201604639 ↗
14. 10.1039/c3ra40234g10.1039/c3ra40234g ↗
15. 10.3390/biomedicines906067810.3390/biomedicines9060678 ↗
16. 10.1021/acs.langmuir.3c0126910.1021/acs.langmuir.3c01269 ↗
17. 10.1002/adma.20050152210.1002/adma.200501522 ↗
18. 10.1002/adma.20050176510.1002/adma.200501765 ↗
19. 10.1002/adma.20070122110.1002/adma.200701221 ↗
20. 10.3390/ph1509104810.3390/ph15091048 ↗
21. 10.3390/molecules2524603710.3390/molecules25246037 ↗
22. 10.1021/bm900584m10.1021/bm900584m ↗
23. 10.1021/la500589f10.1021/la500589f ↗
24. 10.1039/D0SM00035C10.1039/D0SM00035C ↗
25. 10.1039/c4sm02256d10.1039/c4sm02256d ↗
26. 10.1002/chem.20230066110.1002/chem.202300661 ↗
27. 10.1039/C9TB01043B10.1039/C9TB01043B ↗
28. 10.3390/gels812083110.3390/gels8120831 ↗
29. 10.1002/chem.20160300210.1002/chem.201603002 ↗
30. 10.2144/btn-2018-008310.2144/btn-2018-0083 ↗
31. 10.1006/jmre.1998.153410.1006/jmre.1998.1534 ↗
32. 10.1002/1097-458X(200007)38:7<543::AID-MRC722>3.0.CO;2-#10.1002/1097-458X(200007)38:7<543::AID-MRC722>3.0.CO;2-# ↗
33. 10.1016/S0924-0136(02)00060-210.1016/S0924-0136(02)00060-2 ↗
34. 10.1107/S160057752000996010.1107/S1600577520009960 ↗
35. 10.1107/S160057752001383110.1107/S1600577520013831 ↗
36. Rambo, R. BIOISIS, 2009. http://www.bioisis.net/.
37. 10.1039/c2sm25903f10.1039/c2sm25903f ↗
38. 10.1021/bc800441v10.1021/bc800441v ↗
39. 10.1002/app.4438010.1002/app.44380 ↗
40. 10.1016/S0142-9612(98)00025-810.1016/S0142-9612(98)00025-8 ↗
41. 10.1016/j.ijpharm.2019.04.01410.1016/j.ijpharm.2019.04.014 ↗
42. 10.1002/cphc.20150044610.1002/cphc.201500446 ↗
43. 10.1021/bm900908g10.1021/bm900908g ↗
44. 10.1021/acs.biomac.5b0004110.1021/acs.biomac.5b00041 ↗
45. 10.3389/fchem.2022.109498110.3389/fchem.2022.1094981 ↗
46. 10.1021/ma991206r10.1021/ma991206r ↗
47. 10.1039/C5SM02154E10.1039/C5SM02154E ↗
48. 10.1021/la971334d10.1021/la971334d ↗
49. 10.1021/ma970350e10.1021/ma970350e ↗
50. 10.3390/technologies1102005610.3390/technologies11020056 ↗
51. Hamley I. W. · 202110.1002/9781119768364 ↗
52. 10.3390/proceedings202409705610.3390/proceedings2024097056 ↗
53. 10.1016/j.pmatsci.2021.10091710.1016/j.pmatsci.2021.100917 ↗
54. 10.1002/adma.20221120210.1002/adma.202211202 ↗
55. 10.1021/acsami.9b0746510.1021/acsami.9b07465 ↗
56. 10.1002/admt.20200126310.1002/admt.202001263 ↗