The effect of hydrazide linkers on hyaluronan hydrazone hydrogels
Language English Country Great Britain, England Media print-electronic
Document type Journal Article
PubMed
31047083
DOI
10.1016/j.carbpol.2019.04.011
PII: S0144-8617(19)30395-9
Knihovny.cz E-resources
- Keywords
- Schiff base, acylation, hyaluronan, hydrazone, hydrogel,
- MeSH
- Acylation MeSH
- Biocompatible Materials chemical synthesis chemistry toxicity MeSH
- Swiss 3T3 Cells MeSH
- Hydrazines chemical synthesis chemistry toxicity MeSH
- Hydrazones chemical synthesis chemistry toxicity MeSH
- Hydrogels chemical synthesis chemistry toxicity MeSH
- Kinetics MeSH
- Hydrogen-Ion Concentration MeSH
- Hyaluronic Acid analogs & derivatives chemical synthesis toxicity MeSH
- Elastic Modulus MeSH
- Mice MeSH
- Cross-Linking Reagents chemical synthesis chemistry toxicity MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Biocompatible Materials MeSH
- Hydrazines MeSH
- Hydrazones MeSH
- Hydrogels MeSH
- Hyaluronic Acid MeSH
- Cross-Linking Reagents MeSH
The effect of hydrazide linkers on the formation and mechanical properties of hyaluronan hydrogels was intensively evaluated. The reaction kinetics of hydrazone formation was monitored by NMR spectroscopy under physiological conditions where polyaldehyde hyaluronan (unsaturated: ΔHA-CHO, saturated: HA-CHO) was reacted with various hydrazides to form hydrogels. Linear (adipic, oxalic dihydrazide) and branched (N,N´,N´´-tris(hexanoylhydrazide-6-yl)phosphoric triamide and 4-arm-PEG hydrazide) hydrazides were compared as crosslinking agents. The mechanical properties of hydrogels were also modified by attaching a hydrophobic chain to HA-CHO; however, it was found that this modification did not lead to an increase in hydrogel stiffness. Cytotoxicity tests showed that all tested hydrazide crosslinkers reduced the viability of cells only slightly, and that the final hyaluronan hydrogels were non-toxic materials.
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