In the present research program, polymer nanocomposites have been used as the drug carrier for delivery systems of anticancer drug. Chitosan (Cs) and Polyvinyl Alcohol (PVA) with different ratios were blended with dif...In the present research program, polymer nanocomposites have been used as the drug carrier for delivery systems of anticancer drug. Chitosan (Cs) and Polyvinyl Alcohol (PVA) with different ratios were blended with different wt% of Cloisite 30B solution by solvent casting method. Glutaraldehyde with different wt% was added to the blended solution as a crosslinking agent. Cloisite 30B was incorporated in the formulation as a matrix material component which also plays the role of a co-emulsifier in the nanocomposite preparation. Curcumin with different concentrations were loaded with CS-PVA/ C 30B nanocomposites for studying the in-vitro drug delivery systems. Morphology and structure characterization of nanocomposites were investigated by fourier transmission infra red spectroscopy (FTIR), scanning electron microscope (SEM), tensile strength and water uptake capacity. The drug release was studied by changing time, pH and drug concentrations. The kinetics of the drug release was studied in order to ascertain the type of release mechanism. Based on the diffusion as well as the kinetics, the mechanism of the drug release from the composite matrix has been reported.展开更多
In the present research program, cost effective and environment friendly gold nanoparticless were synthesized using the onion (Allium cepa) extract as the reducing agent. The nanoparticless were characterized using UV...In the present research program, cost effective and environment friendly gold nanoparticless were synthesized using the onion (Allium cepa) extract as the reducing agent. The nanoparticless were characterized using UV-visble, XRD, and SEM, TEM methods. The absorption peak at 540 nm was found to be broaden with increase in time indicating the polydispersity nature of the nanoparticles. The XRD results suggested that the crystallization of the bio-organic phase occurs on the surface of the gold nanoparticles or vice versa. The broadening of peaks in the XRD patterns was attributed to particle size effects. The internalization of nanoparticles within cells could occur via processes including phagocytosis, fluid-phase endocytosis and receptor mediated endocytosis.展开更多
文摘In the present research program, polymer nanocomposites have been used as the drug carrier for delivery systems of anticancer drug. Chitosan (Cs) and Polyvinyl Alcohol (PVA) with different ratios were blended with different wt% of Cloisite 30B solution by solvent casting method. Glutaraldehyde with different wt% was added to the blended solution as a crosslinking agent. Cloisite 30B was incorporated in the formulation as a matrix material component which also plays the role of a co-emulsifier in the nanocomposite preparation. Curcumin with different concentrations were loaded with CS-PVA/ C 30B nanocomposites for studying the in-vitro drug delivery systems. Morphology and structure characterization of nanocomposites were investigated by fourier transmission infra red spectroscopy (FTIR), scanning electron microscope (SEM), tensile strength and water uptake capacity. The drug release was studied by changing time, pH and drug concentrations. The kinetics of the drug release was studied in order to ascertain the type of release mechanism. Based on the diffusion as well as the kinetics, the mechanism of the drug release from the composite matrix has been reported.
文摘In the present research program, cost effective and environment friendly gold nanoparticless were synthesized using the onion (Allium cepa) extract as the reducing agent. The nanoparticless were characterized using UV-visble, XRD, and SEM, TEM methods. The absorption peak at 540 nm was found to be broaden with increase in time indicating the polydispersity nature of the nanoparticles. The XRD results suggested that the crystallization of the bio-organic phase occurs on the surface of the gold nanoparticles or vice versa. The broadening of peaks in the XRD patterns was attributed to particle size effects. The internalization of nanoparticles within cells could occur via processes including phagocytosis, fluid-phase endocytosis and receptor mediated endocytosis.
