Formation, microstructure, biodistribution and absence of toxicity of polymeric micelles formed by N-octyl-N,O-carboxymethyl chitosan

被引:38
作者
Huo, Meirong [1 ]
Zhang, Yong [1 ]
Zhou, Jianping [1 ]
Zou, Aifeng [1 ]
Li, Jing [1 ]
机构
[1] China Pharmaceut Univ, Dept Pharmaceut, Nanjing 210009, Peoples R China
关键词
Amphiphilic chitosan derivatives; Microstructure; Biodistribution; Biocompatibility; SELF-ASSEMBLED NANOPARTICLES; ACID-MODIFIED CHITOSAN; O-SULFATE CHITOSAN; IN-VIVO EVALUATION; STEARIC-ACID; GENE DELIVERY; PHYSICOCHEMICAL CHARACTERISTICS; OLIGOSACCHARIDE MICELLES; ANTITUMOR-ACTIVITY; CELLULAR UPTAKE;
D O I
10.1016/j.carbpol.2010.10.073
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In this study, N-octyl-N,O-carboxymethyl chitosans (octyl-CM-Chitosan) with different molecular weights and degrees of alkylation were synthesized. The critical micelle concentration of octyl-CM-Chitosan was in the range of 7.5-30.4 mg/L, depending on their chemical compositions. Micelles formed by octyl-CM-Chitosan were spherical, with a particle size of <200 nm and high negative zeta potentials of similar to 30 mV. Additionally, multi-core microstructure of octyl-CM-Chitosan micelle was confirmed by using fluorescence quenching technique. With the decrease of molecular weight and increase of alkylation, both of the hydrophobicity of inner-core and aggregation number of alkyl chains per microdomain increased. Fluorescein-labeled octyl-CM-Chitosan micelles could easily avoid the mononuclear phagocyte system (MPS) clearance and had the potential for passive targeting to non-MPS tissues. The absence of toxicity of octyl-CM-Chitosan micelles as intravenous materials was confirmed by hemolysis, cell viability assays and histopathological evaluations. These results suggest that octyl-CM-Chitosans are promising materials for intravenous administration. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1959 / 1969
页数:11
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