Factors determining self-assembly of hyaluronan
Language English Country Great Britain, England Media print-electronic
Document type Journal Article
PubMed
33357873
DOI
10.1016/j.carbpol.2020.117307
PII: S0144-8617(20)31480-6
Knihovny.cz E-resources
- Keywords
- Aggregates, Atomic force microscopy, Hyaluronan, Network, Polysaccharides,
- MeSH
- Hydrophobic and Hydrophilic Interactions MeSH
- Saline Solution, Hypertonic chemistry MeSH
- Hyaluronic Acid chemistry MeSH
- Microscopy, Atomic Force methods MeSH
- Molecular Structure MeSH
- Molecular Weight MeSH
- Polymers chemistry MeSH
- Surface Properties MeSH
- Solubility MeSH
- Aluminum Silicates chemistry MeSH
- Drug Storage MeSH
- Water chemistry MeSH
- Hydrogen Bonding MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Saline Solution, Hypertonic MeSH
- Hyaluronic Acid MeSH
- mica MeSH Browser
- Polymers MeSH
- Aluminum Silicates MeSH
- Water MeSH
The conditions determining network-forming and aggregation properties of hyaluronan on the mica surface were studied. The hyaluronan was deposited on the surface from aqueous and saline solutions and attached by a bivalent cation. The morphology of the immobilized assemblies was characterized by atomic force microscopy. The experimental results show that the morphology and size of the aggregates as well as the density of the interconnecting fibrillar network, both made of hyaluronan, at the liquid-solid phase interface are determined not only by its molecular weight or concentration in solution, but also by the dissolution conditions and storage time. These findings extend the current state of knowledge about the conformational variability of this biologically important polymer. Understanding the conformational variability is of great importance, as it governs the physiological functions of hyaluronan, as well as its processability and formulations. That in turn determines its usability in different pharmacological and biomaterial applications.
References provided by Crossref.org
Controlled Structuring of Hyaluronan Films by Phase Separation and Inversion