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      Polymer hydrogel from carboxymethyl guar gum and carbon nanotube for sustained trans-dermal release of diclofenac sodium.

      International Journal of Biological Macromolecules
      Administration, Cutaneous, Animals, Anti-Inflammatory Agents, Non-Steroidal, chemistry, metabolism, pharmacology, Chemistry, Pharmaceutical, methods, Delayed-Action Preparations, chemical synthesis, Diclofenac, Diffusion Chambers, Culture, Drug Carriers, Drug Compounding, Galactans, Humans, Hydrogels, Hydrogen-Ion Concentration, Inflammation, drug therapy, Kinetics, Magnetic Resonance Spectroscopy, Mannans, Nanotubes, Carbon, Plant Gums, Polymers, Solubility, Spectroscopy, Fourier Transform Infrared, Viscosity

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          Abstract

          Novel carboxymethyl guar gum (CMG)-chemically modified multiwalled carbon nanotube (MCNT) hybrid hydrogels were synthesized at different MCNT levels as potential device for sustained trans-dermal release of diclofenac sodium. Spectroscopy together with morphology, thermogravimetry, and rheological studies proved relatively strong CMG-MCNT interaction at 0.5 and 1 wt% levels of MCNT whereas de-wetting was increased with higher MCNT concentration. Drug encapsulation tendency increased with addition of MCNT; maximum entrapment was noticed at 1 wt% MCNT level. Hydrogels containing 0.5, 1 and 3 wt% MCNT exhibited slower trans-dermal release than neat CMG due to slightly higher gel viscosity and more drug entrapment. Slowest but steady release was obtained from 1 wt% MCNT loaded hydrogel due to highest viscous resistance among all other hybrid nanocomposites. Copyright © 2011 Elsevier B.V. All rights reserved.

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