Curcumin/Carrier Coprecipitation by Supercritical Antisolvent Route

被引:1
|
作者
Mottola, Stefania [1 ,2 ]
De Marco, Iolanda [1 ,2 ]
机构
[1] Univ Salerno, Dept Ind Engn, Via Giovanni Paolo II 132, I-84084 Fisciano, Salerno, Italy
[2] Univ Salerno, Res Ctr Biomat BIONAM, Via Giovanni Paolo II 132, I-84084 Fisciano, Salerno, Italy
关键词
inclusion complexes; coprecipitated microparticles; beta-cyclodextrin; SAS precipitation; fast release; supercritical CO2; BREAST-CANCER; MICROPARTICLES; COMPLEXES; CYCLODEXTRINS; CO2;
D O I
10.3390/pharmaceutics16030352
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this work, polyvinylpyrrolidone (PVP)- and beta-cyclodextrin (beta-CD)-based composite powders containing curcumin (CURC) were obtained through the supercritical antisolvent (SAS) technique. Pressure, total concentration of CURC/carrier in dimethylsulfoxide, and CURC/carrier ratio effects on the morphology and size of the precipitated powders were investigated. Using PVP as the carrier, spherical particles with a mean diameter of 1.72 mu m were obtained at 12.0 MPa, 20 mg/mL, and a CURC/PVP molar ratio equal to 1/2 mol/mol; using beta-CD as the carrier, the optimal operating conditions were 9.0 MPa and 200 mg/mL; well-defined micrometric particles with mean diameters equal to 2.98 and 3.69 mu m were obtained at molar ratios of 1/2 and 1/1 mol/mol, respectively. FT-IR spectra of CURC/ beta-CD inclusion complexes and coprecipitated CURC/PVP powders revealed the presence of some peaks of the active compounds. The stoichiometry of the complexes evaluated through the Job method revealed that beta-CD formed inclusion complexes with CURC at a molar ratio equal to 1/1. Dissolution profiles revealed that in comparison with the curve of the pure ingredient, the SAS-processed powders obtained using both PVP and beta-CD have an improved release rate.
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页数:14
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