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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.
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