Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5157048 | Carbohydrate Polymers | 2017 | 29 Pages |
Abstract
Hyaluronic acid (HA) containing CC double bond in positions 4 and 5 of N-acetyl-glucosamine ring (ÎHA) is an unique material, which could be used for biomedical applications and cosmetics. The main advantage of the CC double bond is its ability to react with a wide range of oxidation agents. Location of the CC double bond directly on the glucopyranose ring allows to change the chemical capabilities and simultaneously to mimic the intrinsic physical properties of HA without introduction of linkers or other substances. The synthesis, structural analysis and basic chemical and biological characteristics of this novel biopolymer are described in details. In vitro cytotoxicity assays showed selective activity of ÎHA against cancer cell lines in comparison with standard human fibroblasts so this material has great potential in the field of anticancer drugs.
Keywords
DPPH4-dimethylaminopyridineHSQCIPAGlcNAcDMAPTMEDANBSNHDFGlcAN-bromosuccinimideSEC-MALLSPBS3T3standard fibroblast cell linenuclear magnetic resonance2,2-diphenyl-1-picrylhydrazyl3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acidAPsMTTUV/Visw/vAntioxidationGlucuronic acidUltraviolet and visible spectroscopyOxidationTroloxtriethylamineNMRChemical shiftDiffusion Ordered SpectroscopYDegree of substitutionHourAnticancercorrelation spectroscopyAdditionDOSYPhosphate buffered salineHuman dermal fibroblastsN-acetylglucosamineHyaluronanweight per volumeMolecular weightammonium persulfateTEACOSYheteronuclear single quantum coherence
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Radovan Buffa, Petra Å edová, Ivana Basarabová, TomáÅ¡ Bobula, PavlÃna Procházková, Hana Vágnerová, Iva DoleÄková, SoÅa MoravÄÃková, Lenka Hejlová, VladimÃr Velebný,