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J Mater Sci Mater Med ; 21(4): 1175-81, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20069345

ABSTRACT

We have characterized the relative efficacies of a number of protein crosslinking agents that have the potential for use in the crosslinking of proteinaceous matrices both in vitro and in vivo. The crosslinkers tested were; L: -threose (LT), Genipin (GP), Methylglyoxal (MG), 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC), proanthrocyanidin (PA) and glutaraldehyde (GA). The relative effectiveness of the crosslinkers with regard to their saturating concentrations was: GA > PA > EDC > MG = GP >> LT. Most of the crosslinkers displayed a pH dependence and were more effective at more alkaline pH. At optimal pH and saturating conditions, the relative reaction rates of the crosslinkers were: PA = GA > EDC > GP > MG >> LT.


Subject(s)
Cross-Linking Reagents/pharmacokinetics , Proteins/metabolism , Animals , Carbodiimides/chemistry , Carbodiimides/pharmacokinetics , Carbodiimides/pharmacology , Cattle , Cross-Linking Reagents/chemistry , Cross-Linking Reagents/pharmacology , Extracellular Matrix Proteins/chemistry , Extracellular Matrix Proteins/metabolism , Glutaral/chemistry , Glutaral/pharmacokinetics , Glutaral/pharmacology , Hydrogen-Ion Concentration , Iridoid Glycosides , Iridoids/chemistry , Iridoids/pharmacokinetics , Iridoids/pharmacology , Kinetics , Osmolar Concentration , Proanthocyanidins/chemistry , Proanthocyanidins/pharmacokinetics , Proanthocyanidins/pharmacology , Protein Processing, Post-Translational/drug effects , Proteins/chemistry , Pyruvaldehyde/chemistry , Pyruvaldehyde/pharmacokinetics , Pyruvaldehyde/pharmacology , Solubility , Tetroses/chemistry , Tetroses/pharmacokinetics , Tetroses/pharmacology , Thermodynamics
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