Xyloglucan-block-Poly(ε-Caprolactone) Copolymer Nanoparticles Coated with Chitosan as Biocompatible Mucoadhesive Drug Delivery System

被引:31
|
作者
Mazzarino, Leticia [1 ]
Otsuka, Issei [2 ]
Halila, Sami [2 ]
Bubniak, Lorena dos Santos [3 ]
Mazzucco, Suelen [3 ]
Santos-Silva, Maria C. [3 ]
Lemos-Senna, Elenara [1 ]
Borsali, Redouane [2 ]
机构
[1] Univ Fed Santa Catarina, Dept Ciencias Farmaceut, Ctr Ciencias Saude, BR-88040900 Florianopolis, SC, Brazil
[2] Univ Grenoble Alpes, Ctr Rech Macromol Vegetales CERMAV, UPR CNRS 5301, F-38041 Grenoble 9, France
[3] Univ Fed Santa Catarina, Dept Anal Clin, Ctr Ciencias Saude, BR-88040900 Florianopolis, SC, Brazil
关键词
block copolymer nanoparticles; chitosan-coated nanoparticles; curcumin; cytotoxicity; mucoadhesive nanoparticles; polysaccharide coating; DIBLOCK COPOLYMERS; IN-VITRO; CURCUMIN; PROLIFERATION; MELANOMA; CELLS; PARTICLES; POLYMER; MUCIN;
D O I
10.1002/mabi.201300465
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The development of novel xyloglucan-block-poly(e-caprolactone) (XGO-b-PCL) nanoparticles coated with the mucoadhesive polysaccharide chitosan is described. XGO-b-PCL nanoparticles show monodisperse size distribution (R-h = 50 nm). Curcumin is successfully encapsulated within the PCL core within drug to polymer ratio of 1:5 (w/w). The coating of nanoparticles with chitosan results in an increased particle size and positive surface charge due to the polycation nature of the chitosan. Mucoadhesive properties of chitosan-coated nanoparticles are demonstrated by its exceptional ability to interact with mucin through electrostatic forces. Finally, in vitro studies show that curcumin-loaded nanoparticles exhibit higher cytotoxic effects against B16F10 melanoma cells than L929 fibroblast cells.
引用
收藏
页码:709 / 719
页数:11
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