Biopolymer-based microparticles for encapsulation of all-trans-retinoic acid

被引:0
|
作者
Silva, Leticia A. [1 ]
Dambros, Roberta [1 ]
Leonardi, Gislaine R. [2 ]
Perrechil, Fabiana [1 ]
机构
[1] Univ Fed Sao Paulo UNIFESP, Dept Engn Quim, Diadema, SP, Brazil
[2] Univ Estadual Campinas, Fac Pharmaceut Sci, Campinas, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
biopolymers and renewable polymers; drug delivery systems; microscopy; polysaccharides; proteins; SOLID LIPID NANOPARTICLES; COMPLEX COACERVATION; PROTEIN ISOLATE; IN-VIVO; GELATIN; FABRICATION; DELIVERY; CHITOSAN; GUM; MICROENCAPSULATION;
D O I
10.1002/app.51335
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This work aims to investigate the potential of complex coacervation technique to encapsulate and protect all-trans retinoic acid (RA). Gelatin and kappa-carrageenan were used as wall material and pequi oil was employed as a hydrophobic phase. Three formulations with different protein: polysaccharide ratio and pH were defined to produce the microparticles based on the zeta potential and turbidity analysis: (F1) ratio 3:1 and pH 3.5, (F2) ratio 8:1 and pH 3.5, and (F3) ratio 8:1 and pH 5.0. Microparticles were evaluated regarding their morphology, yield, encapsulation efficiency (EE), and stability. The properties of microparticles were mainly affected by the protein: polysaccharide ratio and the turbidity of the mixtures, which is directly related to the protein-polysaccharide interaction. Formulation 1 showed the optimal values of yield (75.6%), EE (100.2%), and stability (85% of the encapsulated RA remained in the particle). The results demonstrated the high potential of this innovative technique to encapsulate RA for a future application in topical formulations.
引用
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页数:8
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