Thermally reversible xyloglucan gels as vehicles for nasal drug delivery

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Abstract

The aim of this study was to investigate the potential application of thermosensitive gels formed by a xyloglucan polysaccharide derived from tamarind seed for nasal drug delivery. Xyloglucan that had been partially degraded by β-galactosidase to eliminate 45% of galactose residues formed gels at concentrations of 2.5% w/w at gelation temperatures decreasing over the range 2728°C. The in vitro release of ondansetron hydrochloride from the enzyme-degraded xyloglucan gels followed higuchi kinetics over a period of 5h at 34°C by anomalous transport mechanism. The ex vivo permeation of ondansetron hydrochloride from the gels was sustained. Histological examination of nasal mucosa following a single administration of the gels showed no evidence of mucosal damage. Finally, the bioavailability study in rabbits revealed that the absolute bioavailability of ondansetron hydrochloride was significantly increased from 28.64% in the case of the oral drug solution to 52.79% in the case of the nasal in situ gel. The results of this study suggest the potential of the enzyme-degraded xyloglucan gels as vehicles for nasal delivery of drugs. © 2012 Informa Healthcare USA, Inc.

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APA

Mahajan, H. S., Tyagi, V., Lohiya, G., & Nerkar, P. (2012). Thermally reversible xyloglucan gels as vehicles for nasal drug delivery. Drug Delivery, 19(5), 270–276. https://doi.org/10.3109/10717544.2012.704095

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