Chemoselective Ligation in the Functionalization of Polysaccharide-Based Particles

被引:51
作者
Beaudette, Tristan T. [1 ]
Cohen, Joel A. [1 ]
Bachelder, Eric M. [1 ]
Broaders, Kyle E. [1 ]
Cohen, Jessica L. [1 ]
Engleman, Edgar G. [2 ]
Frechet, Jean M. J. [1 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Stanford Univ, Dept Pathol, Sch Med, Palo Alto, CA 94304 USA
基金
美国国家卫生研究院;
关键词
NANOPARTICLES; DELIVERY; DEXTRAN; CELLS; OXIME; PEPTIDES; VACCINES;
D O I
10.1021/ja903984s
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Despite the promise of precisely targeted or otherwise functionalized polymeric particulate drug delivery vehicles, typical biocompatible particles are generally not amenable to facile and selective surface modification. Herein, we report the development of a simple, mild, and chemoselective strategy for the conjugation of biologically active molecules to the surface of dextran-based microparticles. Alkoxyamine-bearing reagents were used to form stable oxime conjugates with latent aldehyde functionality present in reducing carbohydrate chain ends. We demonstrate the functionalization of dextran-based microparticles with a fluorophore as well, as a cell-penetrating peptide sequence, which facilitated the delivery of cargo to nonphagocytic cells leading to a 60-fold increase in the expression of a reporter gene when plasmid DNA-loaded particles were used.
引用
收藏
页码:10360 / +
页数:3
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