Preparation and Characterization of Antioxidant Nanoparticles Composed of Chitosan and Fucoidan for Antibiotics Delivery

被引:77
|
作者
Huang, Yi-Cheng [1 ]
Li, Rou-Ying [1 ]
机构
[1] Natl Taiwan Ocean Univ, Coll Life Sci, Dept Food Sci, Keelung 20224, Taiwan
来源
MARINE DRUGS | 2014年 / 12卷 / 08期
关键词
chitosan; fucoidan; nanoparticle; antioxidant; antibiotic; delivery; IN-VITRO CHARACTERIZATION; PULMONARY DRUG-DELIVERY; DRY POWDER; BIODEGRADABLE NANOPARTICLES; SULFATED POLYSACCHARIDES; MICROSPHERES; HEPARIN; RELEASE; CELLS; CYTOTOXICITY;
D O I
10.3390/md12084379
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In this study, we developed novel chitosan/fucoidan nanoparticles (CS/F NPs) using a simple polyelectrolyte self-assembly method and evaluated their potential to be antioxidant carriers. As the CS/F weight ratio was 5/1, the CS/F NPs were spherical and exhibited diameters of approximately 230-250 nm, as demonstrated by TEM. These CS/F NPs maintained compactness and stability for 25 day in phosphate-buffered saline (pH 6.0-7.4). The CS/F NPs exhibited highly potent antioxidant effects by scavenging 1,1-diphenyl-2-picrylhydrazyl (DPPH), reducing the concentration of intracellular reactive oxygen species (ROS) and superoxide anion (O-2(-)) in stimulated macrophages. The DPPH scavenging effect of CS/F NPs primarily derives from fucoidan. Furthermore, these CS/F NPs activated no host immune cells into inflammation-mediated cytotoxic conditions induced by IL-6 production and NO generation. The MTT cell viability assay revealed an absence of toxicity in A549 cells after exposure to the formulations containing 0.375 mg NPs/mL to 3 mg NPs/mL. Gentamicin (GM), an antibiotic, was used as a model drug for an in vitro releasing test. The CS/F NPs controlled the release of GM for up to 72 h, with 99% of release. The antioxidant CS/F NPs prepared in this study could thus be effective in delivering antibiotics to the lungs, particularly for airway inflammatory diseases.
引用
收藏
页码:4379 / 4398
页数:20
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