Hydrogel Patches on Live Cells through Surface-Mediated Polymerization

被引:15
|
作者
Wu, Pei-Jung [1 ]
Lilly, Jacob L. [1 ]
Arreaza, Roberto [1 ]
Berron, Brad J. [1 ]
机构
[1] Univ Kentucky, Chem & Mat Engn, 153 FPAT, Lexington, KY 40506 USA
基金
美国国家科学基金会;
关键词
POLY(ETHYLENE GLYCOL) DIACRYLATE; TARGETED DRUG-DELIVERY; COATINGS; PHOTOPOLYMERIZATION; NANOPARTICLES;
D O I
10.1021/acs.langmuir.7b01139
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Many naturally occurring cells possess an intrinsic ability to cross biological barriers that block conventional drug delivery, and these cells offer a possible mode of active transport across the bloodbrain barrier or into the core of tumor masses. While many technologies for the formation of complete, nanoparticle-loaded coatings on cells exist, a complete coating on the cell surface would disrupt the interaction of cells with their environments. To address this issue, cell surface patches that partially cover cell surfaces might provide a superior approach for cell-mediated therapeutic delivery. The goal of this study is to establish a simplified approach to producing polymeric patches of arbitrary shapes on a live cell via surface-mediated photopolymerization. Cell surfaces were nonspecifically labeled with eosin, and polyethylene (glycol) diacrylate (PEGDA) coatings were directed to specific sites using 530 nm irradiation through a chrome-coated photomask. These coatings may entrap drug-loaded or imaging particles. The extent of nonspecific formation of PEGDA hydrogel coatings increased with irradiation time, light intensity, and initiating species; 40 mW/cm(2) irradiation for 5 min delivered high-resolution patterns on the surface of A549 cells, and these cells remained viable for 48 h postpatterning with fluorescent nanoparticle-loaded coatings. This work first demonstrated the feasibility of photopatterning polymer patches directly on the surface of cells.
引用
收藏
页码:6778 / 6784
页数:7
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