Chitosan (CH) was used as a biocompatible and bioadhesive polymer material to prepare solid dispersions as well as hydrogelsloaded with dexamethasone sodium phosphate (DSP), a steroidal anti-inflammatory agent clinically used for treatment ofdifferent mouth diseases.Binary solid dispersions at various drug-to-polymer weight ratios were prepared by freeze-drying; their direct compressiongave tablets which were characterized for the swelling behaviour and drug release in vitro. Similarly, DSP-loaded hydrogelscomposed of CH and glycerine were prepared and characterized.CH and DSP showed a good physical compatibility. A slow and prolonged release of the drug was observed in vitro fromboth kinds of systems. The swelling properties of the polymer seemed to be the main parameter affecting the drug releaseprofile from both tablets and hydrogels at the pH value of mouth.In vivo buccal application of both the systems allowed to obtain a prolonged release of DSP, as compared with a glycerinesolution of the drug. From the in vitro swelling studies and in vivo test, the 2:1 CH-DSP solid dispersion in particular can bedesignated for further investigation.
Dexamethasone sodium phosphate-loaded Chitosan based delivery systems for buccal application
PIGNATELLO, Rosario;PUGLISI, Giovanni
2007-01-01
Abstract
Chitosan (CH) was used as a biocompatible and bioadhesive polymer material to prepare solid dispersions as well as hydrogelsloaded with dexamethasone sodium phosphate (DSP), a steroidal anti-inflammatory agent clinically used for treatment ofdifferent mouth diseases.Binary solid dispersions at various drug-to-polymer weight ratios were prepared by freeze-drying; their direct compressiongave tablets which were characterized for the swelling behaviour and drug release in vitro. Similarly, DSP-loaded hydrogelscomposed of CH and glycerine were prepared and characterized.CH and DSP showed a good physical compatibility. A slow and prolonged release of the drug was observed in vitro fromboth kinds of systems. The swelling properties of the polymer seemed to be the main parameter affecting the drug releaseprofile from both tablets and hydrogels at the pH value of mouth.In vivo buccal application of both the systems allowed to obtain a prolonged release of DSP, as compared with a glycerinesolution of the drug. From the in vitro swelling studies and in vivo test, the 2:1 CH-DSP solid dispersion in particular can bedesignated for further investigation.File | Dimensione | Formato | |
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