| Abstrakt: |
Lecithin, a major phospholipid component of human bile, is instrumental in the formation of mixed micelles in vivo, with implications for the dissolution and absorption of poorly soluble compounds administered orally. Hydrocortisone, a poorly aqueous soluble drug ( S = 1.08 × 10 M), was chosen to compare the rate and mechanism of dissolution in a NaTC/lecithin (mixed micelle) system with its NaTC-only (simple micelle) counterpart. Surface tension, solubility studies, contact angles, rotating disk dissolution rates, and powder dissolution rates were compared for hydrocortisone between solutions containing NaTC/lecithin (4:1) and NaTC-only under conditions representative of the small intestine (0-30 m M NaTC, pH 5.5, 0.1 M NaCl). At all concentrations, the solubility of hydrocortisone in NaTC/lecithin was slightly higher (up to twofold) than in the corresponding NaTC-only solutions. At low NaTC concentrations, initial powder dissolution rates were faster in the NaTC/lecithin solutions than in corresponding NaTC-only solutions. In contrast, at high NaTC concentrations, initial powder dissolution rates in the NaTC-only solutions were faster. Results indicated that in the NaTC-only system wetting effects predominated for dissolution, while in the NaTC/lecithin system, the dissolution rate of hydro-cortisone was enhanced mainly via solubilization. [ABSTRACT FROM AUTHOR] |
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