Merck
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  • Cloaking nanoparticles with protein corona shield for targeted drug delivery.

Cloaking nanoparticles with protein corona shield for targeted drug delivery.

Nature communications (2018-11-02)
Jun Yong Oh, Han Sol Kim, L Palanikumar, Eun Min Go, Batakrishna Jana, Soo Ah Park, Ho Young Kim, Kibeom Kim, Jeong Kon Seo, Sang Kyu Kwak, Chaekyu Kim, Sebyung Kang, Ja-Hyoung Ryu
摘要

Targeted drug delivery using nanoparticles can minimize the side effects of conventional pharmaceutical agents and enhance their efficacy. However, translating nanoparticle-based agents into clinical applications still remains a challenge due to the difficulty in regulating interactions on the interfaces between nanoparticles and biological systems. Here, we present a targeting strategy for nanoparticles incorporated with a supramolecularly pre-coated recombinant fusion protein in which HER2-binding affibody combines with glutathione-S-transferase. Once thermodynamically stabilized in preferred orientations on the nanoparticles, the adsorbed fusion proteins as a corona minimize interactions with serum proteins to prevent the clearance of nanoparticles by macrophages, while ensuring systematic targeting functions in vitro and in vivo. This study provides insight into the use of the supramolecularly built protein corona shield as a targeting agent through regulating the interfaces between nanoparticles and biological systems.

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Sigma-Aldrich
(3-氨基丙基)三甲氧基硅烷, 97%
Sigma-Aldrich
辛二酸双(N-羟基琥珀酰亚胺酯), ≥95%, powder
Sigma-Aldrich
3-(三甲氧基甲硅基)丙烯酸丙酯, 92%, contains 100 ppm BHT as inhibitor