Coassembly Generates Peptide Hydrogel with Wound Dressing Material Properties
Author(s) -
Chaitanya Kumar Thota,
A. Berger,
Laura Elomaa,
Chaunxiong Nie,
Christoph Böttcher,
Beate Koksch
Publication year - 2020
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.9b04371
Subject(s) - self healing hydrogels , biocompatibility , materials science , peptide , biomedical engineering , transmission electron microscopy , rheology , nanotechnology , wound healing , chemistry , biophysics , composite material , polymer chemistry , surgery , biochemistry , medicine , biology , metallurgy
Multicomponent self-assembly of peptides is a powerful strategy to fabricate novel functional materials with synergetic properties that can be used for several nanobiotechnological applications. In the present study, we used a coassembly strategy to generate an injectable ultrashort bioactive peptide hydrogel formed by mixing a dipeptide hydrogelator with a macrophage attracting short chemotactic peptide ligand. Coassembly does not impede hydrogelation as shown by cryo-transmission electron microscopy (cryo-TEM), scanning electron microscopy, and rheology. Biocompatibility was shown by cytotoxicity assays and confocal microscopy. The hydrogels release the entrapped skin antibiotic ciprofloxacin, among others, in a slow and continuous manner. Such bioinspired advanced functional materials can find applications as wound dressing materials to treat chronic wound conditions like diabetic foot ulcer.
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