Supercritical carbon dioxide-assisted nanonization of dihydromyricetin for anticancer and bacterial biofilm inhibition efficacies

被引:20
|
作者
Xu, Pei-Yao [1 ]
Fu, Chao-Ping [2 ,3 ]
Kankala, Ranjith Kumar [1 ,2 ,3 ]
Wang, Shi-Bin [2 ,3 ]
Chen, Ai-Zheng [1 ,2 ,3 ]
机构
[1] Huaqiao Univ, Coll Chem Engn, Xiamen 361021, Peoples R China
[2] Huaqiao Univ, Inst Biomat & Tissue Engn, Xiamen 361021, Peoples R China
[3] Huaqiao Univ, Fujian Prov Key Lab Biochem Technol, Xiamen 361021, Peoples R China
基金
中国国家自然科学基金;
关键词
Dihydromyricetin; Supercritical carbon dioxide; Nanoparticles; Anticancer; Antibiotic; SOLUTION-ENHANCED DISPERSION; COPRECIPITATION; PRECIPITATION; CO2; 2R; 3R-DIHYDROMYRICETIN; SOLUBILITY; RESISTANCE; CURCUMIN;
D O I
10.1016/j.supflu.2020.104840
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Owing to its poor solubility, the applicability of dihydromyricetin (DMY) is limited in various biomedical applications. To overcome this issue, nano-sized DMY particles (DMY NPs) were fabricated using the supercritical antisolvent (SAS) approach for improving the bioavailability of DMY. Initially, the experimental conditions were optimized such as temperature of 45 degrees C, pressure of 8 MPa, and DMY solution flow rate of 0.5 mL/min, resulting in the DMY particles at a mean particle size of 169.1 +/- 23.7 nm. Further, the physicochemical characteristics of the resultant DMY NPs were evaluated using various characterization techniques. The DMY NPs with reduced particle size and improved dissolution rate resulted in improved anticancer, antibacterial, and biofilm inhibition efficacies, comparable to that of unprocessed DMY. Together, the designed DMY NPs using the SAS process have great potential in food and pharmaceutical industries. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页数:10
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