Solution and microwave assisted synthesis of ß-Cyclodextrin grafted polyacrylamide: Water treatment and In-vitro drug release study.

The present article reports the application of ß-cyclodextrin grafted polyacrylamides synthesized through solution and microwave assisted polymerization techniques as flocculants and then the employment of partially hydrolyzed products of best grade of each technique in-vitro drug release study of diclofenac sodium. Five different grades of ß-cyclodextrin grafted polyacrylamides by each of solution and microwave assisted polymerization techniques have been synthesized, by varying the monomer concentration. The synthesized polymers have been well characterized and their flocculation performances have been evaluated in kaolin suspension through settling and jar test methods Then the best performing grades of both the techniques have been partially hydrolyzed to prepare three different grades each technique by varying the concentration aqueous NaOH solution. Flocculation efficiencies of these polymers have been investigated in kaolin suspension. Thus best grades of partially hydrolyzed grafted polymers of each technique have been chosen for further study of drug delivery. In-vitro drug release study has been done using diclofenac sodium loaded microbeads prepared by ionic gelation method with two partially hydrolyzed grafted polymers (one from each technique) in phosphate buffer solution (PBS) at 37±0.5 ○C and pH 7.4. The drug load and release have been analyzed by UV-vis spectroscopy.

Synthesis, characterization and cyclic voltammetric study of copper(II) and nickel(II) polymer chelates.

Graft copolymers based on dextran (Dx) and 2-acrylamido-2-methyl-1-propane sulphonic acid (AMPS) were synthesized by free radical initiated solution polymerization technique using ceric ammonium nitrate as initiator. These graft copolymers were used to prepare Cu(II) and Ni(II) chelates by reactions with Cu(II) and Ni(II) metal ions respectively. Graft copolymer and metal chelates were characterized by elemental analysis, intrinsic viscosity, FT-IR, scanning electron microscopy (SEM), atomic force microscopy (AFM), thermogravimetric analysis (TGA) and powder X-ray diffraction (XRD). Elemental analysis, intrinsic viscosity and FT-IR studies revealed the incorporation of metal ions to form metal chelates. SEM studies showed the change in morphology due to metal incorporation. From AFM studies it was observed that there was increase in Root mean square (RMS) roughness values in case of metal complexes. Metal chelates were observed to be thermally more stable than graft copolymer from TGA. UV-vis spectroscopy study revealed increase in absorbance values and cyclic voltammetric (CV) studies showed more than tenfold increase in redox current due to formation of Cu(II) and Ni(II) metal chelates. The binding constants of each complex determined by using UV-visible spectroscopy revealed that Cu(II) has more binding ability than Ni(II).