Biofunctionalization of PEGylated Microcapsules for Exclusive Binding to Protein Substrates

被引:18
作者
Deo, Devendra I. [1 ]
Gautrot, Julien E. [1 ]
Sukhorukov, Gleb B. [1 ]
Wang, Wen [1 ]
机构
[1] Queen Mary Univ London, Inst Bioengn, London E1 4NS, England
基金
英国工程与自然科学研究理事会;
关键词
SURFACE-PLASMON RESONANCE; POLYELECTROLYTE MICROCAPSULES; CONTROLLED-RELEASE; ACOUSTIC-WAVE; LAYER; DELIVERY; NANOPARTICLES; MULTILAYERS; FABRICATION; ADSORPTION;
D O I
10.1021/bm500412d
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Targeted delivery of drugs to specific diseased sites in the body is an area of research that has attracted many studies, particularly in drug deliveries that utilize microparticles. By achieving targeted delivery of a drug, one can increase the efficacy of the treatment, thus, reducing unwanted side effects. This study aims to synthesize microcapsules that are able to target and adsorb to specific proteins (i.e., collagen type IV and fibronectin) through antibody antigen interactions, while simultaneously suppressing any unspecific binding, a characteristic that is commonly observed in polyelectrolyte microcapsule protein interactions. This is accomplished by creating an antibody-functionalized poly(ethylene glycol) (PEG) assembly within the microcapsule structure. Site-specific adsorption of these microcapsules is tested using protein micropatterns. Results show that significant adsorption is achieved on the target protein, with unspecific adsorptions being heavily suppressed on control proteins. In conclusion, we have successfully manufactured microcapsules that specifically and exclusively bind to their complementary target area. This paves the way for future in vivo experiments using microcapsules as targeted drug carriers.
引用
收藏
页码:2555 / 2562
页数:8
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