Optimization and characterization of curcumin-piperine dual drug loaded self-microemulsifying drug delivery system by simplex lattice design.
- Author:
Qiu-Ping LI
;
Jun-Dong DAI
;
Wen-Wen ZHAI
;
Qiao-Li JIANG
- Publication Type:Journal Article
- MeSH:
Alkaloids;
chemistry;
Benzodioxoles;
chemistry;
Chemistry, Pharmaceutical;
methods;
Curcumin;
chemistry;
Drug Carriers;
chemistry;
Drug Combinations;
Drug Delivery Systems;
Drugs, Chinese Herbal;
chemistry;
Emulsions;
chemistry;
Methylmethacrylates;
chemistry;
Particle Size;
Piperidines;
chemistry;
Polystyrenes;
chemistry;
Polyunsaturated Alkamides;
chemistry
- From:
China Journal of Chinese Materia Medica
2014;39(20):3936-3944
- CountryChina
- Language:Chinese
-
Abstract:
The objective of the study was to prepare and evaluate the quality of curcumin-piperinedual drug loaded self-microemulsifying drug delivery system(Cur-PIP-SMEDDS). Simplex lattice design was constructed using optimal oil phase, surfactant and co-surfactant concentration as independent variables, and the curcumin and piperine were used as model drugs to optimize Cur-PIP-SMEDDS formulation. In the present study, the drug loadings of curcumin and piperine, mean particle size of Cur-PIP-SMEDDS were made as indicators, and the experiment design, model building and response surface analysis were established using Design Expert 8. 06 software to optimize and verify the composition of SMEDDS formulation. The quality of Cur-PIP-SMEDDS was evaluated by observing the appearance status, transmission electron microscope micrographs and determining particle diameter, electric potential, drug entrapment efficiency and drug loading of it. As a result, the optimal formulation of SMEDDS was CapryoL 90-Cremophor RH40-TranscutoL HP (10:60:30). The appearance of Cur-PIP-SMEDDS remained clarified and transparent, and the microemulsion droplets appeared spherical without aggregation with uniform particle size distribution. The mean size of microemulsion droplet formed from Cur-PIP-SMEDDS was 15.33 nm, the drug loading of SMEDDS for Cur and PIP were 40.90 mg · g(-1) and 0.97 mg · g(-1), respectively, the drug entrapment efficiency were 94.98% and 90.96%, respectively. The results show that Cur-PIP-SMEDDS can increase the solubility and stability of curcumin significantly, in the expectation of enhancing the bioavailability of it. Taken together, these findings can provide the reference to a preferable choice of the Cur formulation and contribute to therapeutic application in clinical research.
