Development and Optimization of Osmotically Controlled Asymmetric Membrane Capsules for Delivery of Solid Dispersion of Lycopene
Autor: | Rashmi Sareen, Kanaya Lal Dhar, Nitin Jain, Neeraj Mahindroo |
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Jazyk: | angličtina |
Rok vydání: | 2014 |
Předmět: |
Osmosis
Central composite design Article Subject lcsh:Medicine lcsh:Technology General Biochemistry Genetics and Molecular Biology chemistry.chemical_compound Drug Delivery Systems Lycopene Ethyl cellulose Osmotic pressure Response surface methodology Solubility lcsh:Science Dissolution General Environmental Science Chromatography Chemistry lcsh:T lcsh:R General Medicine Carotenoids Membrane Microscopy Electron Scanning lcsh:Q Research Article |
Zdroj: | The Scientific World Journal The Scientific World Journal, Vol 2014 (2014) |
ISSN: | 2356-6140 |
DOI: | 10.1155/2014/438528 |
Popis: | The aim of the present investigation is to develop and statistically optimize the osmotically controlled asymmetric membrane capsules of solid dispersion of lycopene. Solid dispersions of lycopene withβ-cyclodextrin in different ratios were prepared using solvent evaporation method. Solubility studies showed that the solid dispersion with 1 : 5 (lycopene : β-cyclodextrin) exhibited optimum solubility (56.25 mg/mL) for osmotic controlled delivery. Asymmetric membrane capsules (AMCs) were prepared on glass mold pins via dip coating method. Membrane characterization by scanning electron microscopy showed inner porous region and outer dense region. Central composite design response surface methodology was applied for the optimization of AMCs. The independent variables were ethyl cellulose (X1), glycerol (X2), and NaCl (X3) which were varied at different levels to analyze the effect on dependent variables (percentage of cumulative drug release (Y1) and correlation coefficient of drug release (Y2)). The effect of independent variables on the response was significantly influential. The F18was selected as optimized formulation based on percentage of CDR (cumulative drug release) of 85.63% and correlation coefficient of 0.9994. The optimized formulation was subjected to analyze the effect of osmotic pressure and agitational intensity on percentage of CDR. The drug release was independent of agitational intensity but was dependent on osmotic pressure of dissolution medium. |
Databáze: | OpenAIRE |
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