Surface Modification of Polysaccharide-Based Nanoparticles with PEG and Dextran and the Effects on Immune Cell Binding and Stimulatory Characteristics

被引:43
作者
Bamberger, Denise [1 ]
Hobernik, Dominika [2 ]
Konhaeuser, Matthias [1 ]
Bros, Matthias [2 ]
Wich, Peter R. [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Dept Pharm & Biochem, Staudingerweg 5, D-55128 Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Dermatol, Obere Zahlbacher Str 63, D-55131 Mainz, Germany
关键词
nanoparticles; acetalated dextran; PEGylation; DEXylation; immune cells; macrophages; dendritic cells; DRUG-DELIVERY SYSTEMS; SCAVENGER RECEPTORS; ACETALATED DEXTRAN; POLYMERIC NANOPARTICLES; POLY(ETHYLENE GLYCOL); HYALURONIC-ACID; PROTEIN CORONA; CLASS-A; CANCER; IMMUNOTHERAPY;
D O I
10.1021/acs.molpharmaceut.7b00507
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Surface modifications of nanoparticles can alter their physical and biological properties significantly. They effect particle aggregation, circulation times, and cellular uptake. This is particularly critical for the interaction with primary immune cells due to their important role in particle processing. We can show that the introduction of a hydrophilic PEG layer on the surface of the polysaccharide-based nanoparticles prevents unwanted aggregation under physiological conditions and decreases unspecific cell uptake in different primary immune cell types. The opposite effect can be observed with a parallel-performed introduction of a layer of low molecular weight dextran. (3.5 and 5 kDa) on the particle surface (DEXylation) that encourages the nanoparticle uptake by antigen-presenting cells like macrophages and dendritic cells. Binding of DEXylated particles to these immune cells results in an upregulation of surface maturation markers and elevated production of proinflammatory cytokines, reflecting cell activation. Hence, DEXylated particles can potentially be used for passive targeting of antigen presenting cells with inherent adjuvant function for future immunotherapeutic applications.
引用
收藏
页码:4403 / 4416
页数:14
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