Malonylchitosan Microspheres as a Matrix for Oral Enrofloxacin Delivery |
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Authors: | Saléte Valgas Vanessa Lima Gonçalves Mauro C. M. Laranjeira Valfredo T. Fávere Rozangela Curi Pedrosa |
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Affiliation: | 1. Departament of Chemistry, Federal University of Santa Catarina, Florianópolis 88040-900, Santa Catarina, Brasil;2. Departament of Biochemistry, Federal University of Santa Catarina, Florianópolis 88040-900, Santa Catarina, Brasil |
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Abstract: | Summary: The purpose of this study was to produce malonylchitosan microspheres to be used as a pH sensitive matrix for the controlled delivery of drugs. Chitosan microspheres were obtained by the coacervation–phase separation method. The microspheres were then treated with malonic acid to obtain amidified chitosan microspheres. The resulting malonylchitosan microspheres were characterized by means of elemental analysis (CHN), infrared spectroscopy, conductometric titration and scanning electron microscopy (SEM). The data obtained from infrared spectroscopy, elemental analysis and conductometric titration of amino groups were consistent with the N-substitution of malonyl groups in the chitosan microspheres. In vivo studies for controlled delivery of enrofloxacin were performed in male Wistar rats and the results indicated increase and prolonged blood levels with delayed peak and improved bioavailability for malonylchitosan microspheres compared to commercial tablets. |
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Keywords: | biopolymers drug delivery systems enrofloxacin in vivo studies malonylchitosan |
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