QBD-based systematic development of Bosentan SNEDDS: Formulation, characterization and pharmacokinetic assessment
Autor: | Goutam Kumar Jena, Ch. Niranjan Patra, Kahnu Charan Panigrahi, Jayashree Jena, M. E. Bhanoji Rao |
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Rok vydání: | 2018 |
Předmět: |
Chromatography
Central composite design Chemistry technology industry and agriculture Cmax Pharmaceutical Science 02 engineering and technology 021001 nanoscience & nanotechnology 030226 pharmacology & pharmacy Bosentan Bioavailability 03 medical and health sciences 0302 clinical medicine Pulmonary surfactant Pharmacokinetics PEG ratio Drug delivery medicine 0210 nano-technology medicine.drug |
Zdroj: | Journal of Drug Delivery Science and Technology. 47:31-42 |
ISSN: | 1773-2247 |
DOI: | 10.1016/j.jddst.2018.06.021 |
Popis: | The aim of this study was to develop self-nanoemulsifying drug delivery system (SNEDDS) of bosentan using quality by design (QBD) approach with better bioavailability. The major component of the formulation vis-a-vis lipid (Capmul MCM), surfactant (LABRASOL) and co-surfactant (PEG 600) were selected on the basis of saturation solubility. Mixture of LABRASOL and PEG 600 in the ratio of 1:1 showed better nano emulsifying region as depicted by pseudo ternary phase diagram. The optimum mixture of Capmul MCM, LABRASOL and PEG 600 were selected by using response surface method (RSM) with central composite design (CCD). Pharmacokinetic study was conducted to determine various critical parameters. The optimized formulation showed 98.5% drug release in 15 min, globule size of 62.5 nm, emulsification time of 12 s and PDI of 0.146. TEM study revealed the drug entrapment within the oil globules of nano size range. Pharmacokinetic study of optimized formulation indicated faster dissolution and absorption which was evidenced from significantly higher Cmax, larger AUC and lower Tmax than pure drug bosentan. Thus the present study confirms potential of SNEDDS in enhancing the oral bioavailability of bosentan. |
Databáze: | OpenAIRE |
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