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Merck
CN
  • Physicochemical properties and controlled drug release of microcapsules prepared by simple coacervation.

Physicochemical properties and controlled drug release of microcapsules prepared by simple coacervation.

Colloids and surfaces. B, Biointerfaces (2013-01-10)
Ken-ichi Shimokawa, Katsuhiko Saegusa, Yuko Wada, Fumiyoshi Ishii
摘要

Ternary phase diagrams of gelatin-water-methanol, gelatin-water-ethanol, and gelatin-water-propanol systems were prepared to evaluate optimal coacervation. The results of their evaluation suggested that the optimal coacervation region expands with the hydrophobicity of the added poor solvent (methanol, ethanol, 1-propanol, and 2-propanol). Microcapsules prepared based on the optimal coacervation region differed in controlled drug release among poor solvents used even when the concentration of gelatin, a membrane component, is the same. Compared with microcapsules prepared using the gelatin-water-ethanol system, those prepared using the gelatin-water-propanol system showed a 34% decrease in the drug release rate 24h after the initiation of the drug release test. These results suggested that microcapsules prepared using gelatin-water-various lower alcohol systems can readily control drug release and can be a useful drug delivery system (DDS).

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Sigma-Aldrich
1-丙醇, suitable for HPLC, ≥99.9%
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1-丙醇, ACS reagent, ≥99.5%
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1-丙醇, ≥99%, FG
Sigma-Aldrich
1-丙醇, anhydrous, 99.7%
Supelco
1-丙醇, analytical standard
Sigma-Aldrich
1-丙醇, natural, ≥98%, FG