| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 599111 | Colloids and Surfaces B: Biointerfaces | 2016 | 7 Pages |
•Colloidal carriers for Angelica gigas Nakai (AGN) ethanol extract were developed.•Omega-3 (ω-3)/Labrasol/TPGS/water-based oil-in-water microemulsion (ME) was prepared.•MEs provided the enhanced release of decursin and decursinol angelate.•Oral bioavailability of decursinol from ME group was higher than suspension group.
Omega-3 (ω-3) fish oil-enriched colloidal systems were developed for the oral delivery of Angelica gigas Nakai (AGN) extract (ext). By constructing a pseudo-ternary phase diagram, the composition of oil-in-water (o/w) microemulsion (ME) systems based on ω-3 (oil), Labrasol (surfactant), and water was determined. AGN ext was dissolved into the ME system and d-α-tocopherol polyethylene glycol 1000 succinate (TPGS) was added to the ME formulation in order to enhance the mucosal absorption of the pharmacologically active ingredients in the AGN ext. The droplet size of AGN-loaded MEs was 205–277 nm and their morphology was spherical. The release of major components of AGN, decursin (D) and decursinol angelate (DA), from ME formulations in pH 1.2 and 6.8 buffers was significantly greater (P < 0.05) than that from the AGN suspension group. The pharmacokinetic properties of AGN-loaded MEs in rats were evaluated by measuring decursinol (DOH) concentrations in plasma after oral administration. TPGS-included ME (F2) resulted in significantly greater (P < 0.05) systemic exposure of DOH than that with ME without TPGS (F1), AGN ext + TPGS, and AGN in suspension. Severe toxicity of F1 and F2 on the intestinal epithelium was not observed by histological staining. The colloidal carriers described herein are promising delivery systems for oral administration of AGN ext.
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