ZHANG Jun-ying, YU Shuang, ZHANG Lei, et al. Preparation of Curcumin-Loaded Pluronic F127 Micelles and NMR Analysis of Its Micellization Behavior[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(24): 1-4.
DOI:
ZHANG Jun-ying, YU Shuang, ZHANG Lei, et al. Preparation of Curcumin-Loaded Pluronic F127 Micelles and NMR Analysis of Its Micellization Behavior[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(24): 1-4. DOI: 10.11653/syfj2013240001.
Preparation of Curcumin-Loaded Pluronic F127 Micelles and NMR Analysis of Its Micellization Behavior
Objective: To prepare curcumin-loaded Pluronic F127 micelles and clarify micellization behavior of Pluronic F127 in water. Method: The content of curcumin was determined by HPLC with mobile phase of 0.1% formic acid solution-methanol(30:70) and detection wavelength of 420 nm.Curcumin-loaded Pluronic F127 micelles were prepared by thin-film hydration method and effects of curcumin-Pluronic F127 mass ratio
aqueous phase amount
pH of aqueous phase and hydration time on drug-loading coefficient and entrapment efficiency were investigated by orthogonal design.Particle size of micelles was determined by dynamic light scattering method. In vitro release profile of curcumin in micelles was investigated by dynamic dialysis method.1H-NMR was performed to study micellization behavior of Pluronic F127 in water. Result: Optimized formulation process was as follows:curcumin-Pluronic F127(1:15)
aqueous phase amount 10 mL
pH of aqueous phase 5.0 and hydration time 1.0 h. Average size of curcumin-loaded Pluronic F127 micelles was about 30 nm with average entrapment efficiency of 64.5% and average drug-loading coefficient of 4.1%. In vitro release data fitted well to Higuchi equation.1H-NMR results demonstrated that chemical shift of Pluronic F127 upshifted and signals broadened with increasing of the concentration. Conclusion: Pluronic F127 has been formed hydrophobic micelles core for drug-loaded in water
thus showing excellent drug-loaded and release capability.
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