Full Factorial Design, Optimization, In vitro and Ex vivo Studies of Ocular Timolol-Loaded Microsponges
Autor: | Yasser M. Mostafa, Radwa M. A. Abd-Elal, El-Sayed Khafagy, Ghada H. Elosaily, Shadeed Gad |
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Rok vydání: | 2019 |
Předmět: |
chemistry.chemical_classification
Materials science Scanning electron microscope Pharmaceutical Science 02 engineering and technology Polymer Factorial experiment Permeation 021001 nanoscience & nanotechnology 030226 pharmacology & pharmacy Solvent 03 medical and health sciences 0302 clinical medicine Differential scanning calorimetry chemistry Polymer ratio Drug Discovery 0210 nano-technology Thermal analysis Nuclear chemistry |
Zdroj: | Journal of Pharmaceutical Innovation. 15:651-663 |
ISSN: | 1939-8042 1872-5120 |
DOI: | 10.1007/s12247-019-09418-z |
Popis: | Timolol maleate (TMM) is a hydrophilic model drug. The aim of this study was to formulate TMM-loaded microsponges to sustain TMM release and improve its corneal permeability compared with TMM-aqueous solution. The modified quasi-emulsion solvent diffusion technique (water/oil/oil) was used to prepare TMM-loaded microsponges. The impact of the polymer type (X1) and drug:polymer ratio (X2) were studied and optimized, using full factorial design. The production yield (PY) %, entrapment efficiency (EE) %, particles size (PS), and TMM released % after 6 h were selected as dependent variables. Depended on the desirability value by using the Design-Expert® software version 11, the optimized formulation was selected and subjected to further studies, such as scanning electron microscopy (SEM), porosity determination, powder X-ray diffraction (PXRD), differential scanning calorimetry (DSC), ex vivo permeation study, and corneal hydration level. The optimized formulation composed of TMM: EC within the proportion 1:9 exhibited PY of 96.55 ± 4.01%; EE of 72.00 ± 6.08%; PS (d90) of 6283.33 ± 145.71 nm and released 42.12 ± 3.93% of TMM after 6 h. Particles appeared porous with spherical shape. Thermal analysis proved that the drug has been homogeneously dispersed in its amorphous state. The optimized formulation showed higher corneal permeability about 1.45-fold higher than TMM-aqueous solution in a period of 6 h. The modified quasi-emulsion diffusion technique (water/oil/oil) is suitable for improving EE of hydrophilic drug (TMM) and the optimized TMM-loaded microsponge was succeeded to retard the release of TMM and improve its corneal permeability. |
Databáze: | OpenAIRE |
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