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Carbohydr Res ; 488: 107891, 2020 Feb.
Article in English | MEDLINE | ID: mdl-31972437

ABSTRACT

The wide use of chitosan microspheres in pharmaceutical applications, mainly in the controlled release of drugs and as a bactericidal agent, has been widely reported in the literature. However, these important biomaterial applications with multifunctionality is still scarce. In this study, epichlorohydrin-crosslinked chitosan microspheres were prepared and evaluated for Ag+ adsorption and formation of silver nanoparticles. The hybrid material obtained was used to antibacterial activity and controlled drug release. The optimal pH for adsorption of Ag+ ions in aqueous medium was pH 5-7; the best fit was the Langmuir model; the optimal time for maximum adsorption was 10 h. The highest release of the drug occured at neutral pH of the intestinal fluids and remained constant for 6 h. Silver ion microspheres demonstrated activity against E. coli and S. aureus. The concentration of ibuprofen incorporated in the chitosan microspheres was 7.9 × 10-3 mol L-1 and in the microspheres with AgNPs the concentration was 1.8 × 10-2 mol L-1. The microspheres with AgNPs released more drug (77%) than the material without AgNPs.


Subject(s)
Anti-Bacterial Agents/pharmacology , Chitosan/chemistry , Ibuprofen/pharmacology , Silver/chemistry , Adsorption , Anti-Bacterial Agents/chemistry , Delayed-Action Preparations , Epichlorohydrin , Escherichia coli/drug effects , Hydrogen-Ion Concentration , Ibuprofen/chemistry , Metal Nanoparticles , Microbial Sensitivity Tests , Microspheres , Molecular Structure , Silver/pharmacokinetics , Staphylococcus aureus/drug effects
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