Genetically Engineered Liposome-like Nanovesicles as Active Targeted Transport Platform

© 2017 The Authors. Published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 30(2018), 7 vom: 30. Feb.
1. Verfasser: Zhang, Pengfei (VerfasserIn)
Weitere Verfasser: Zhang, Long, Qin, Zainen, Hua, Suhang, Guo, Zhide, Chu, Chengchao, Lin, Huirong, Zhang, Yang, Li, Wengang, Zhang, Xianzhong, Chen, Xiaoyuan, Liu, Gang
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2018
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article biofunctionalized nanovesicles biomimetic synthesis exosomes ligand-targeted delivery theranostics Ligands Liposomes Peptides Doxorubicin 80168379AG
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520 |a © 2017 The Authors. Published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. 
520 |a Ligand-targeted delivery of drug molecules to various types of tumor cells remains a major challenge in precision medicine. Inspired by the secretion process and natural cargo delivery functions of natural exosomes, biomimetic synthetic strategies are exploited to prepare biofunctionalized liposome-like nanovesicles (BLNs) that can artificially display a wide variety of targeting protein/peptide ligands and directly encapsulate medical agents for enhanced drug delivery. Here, as a proof of concept, genetically engineered BLNs, which display human epidermal growth factor (hEGF) or anti-HER2 Affibody as targeting moieties, are developed to, respectively, target two types of tumor cells. Notably, in comparison to synthetic liposomes covalently coupled with hEGF, it is demonstrated in this work that biosynthetically displayed hEGF ligands on BLNs possess higher biological activities and targeting capabilities. Additionally, treatments with doxorubicin-loaded BLNs displaying Affibody ligands exhibit much better antitumor therapeutic outcomes than clinically approved liposomal doxorubicin (Doxil) in HER2-overexpressing BT474 tumor xenograft models. These data suggest that BLN is suitable as a potent surrogate for conventional proteoliposomes or immunoliposomes as a result of excellent targeting capacities and facile production of BLNs 
650 4 |a Journal Article 
650 4 |a biofunctionalized nanovesicles 
650 4 |a biomimetic synthesis 
650 4 |a exosomes 
650 4 |a ligand-targeted delivery 
650 4 |a theranostics 
650 7 |a Ligands  |2 NLM 
650 7 |a Liposomes  |2 NLM 
650 7 |a Peptides  |2 NLM 
650 7 |a Doxorubicin  |2 NLM 
650 7 |a 80168379AG  |2 NLM 
700 1 |a Zhang, Long  |e verfasserin  |4 aut 
700 1 |a Qin, Zainen  |e verfasserin  |4 aut 
700 1 |a Hua, Suhang  |e verfasserin  |4 aut 
700 1 |a Guo, Zhide  |e verfasserin  |4 aut 
700 1 |a Chu, Chengchao  |e verfasserin  |4 aut 
700 1 |a Lin, Huirong  |e verfasserin  |4 aut 
700 1 |a Zhang, Yang  |e verfasserin  |4 aut 
700 1 |a Li, Wengang  |e verfasserin  |4 aut 
700 1 |a Zhang, Xianzhong  |e verfasserin  |4 aut 
700 1 |a Chen, Xiaoyuan  |e verfasserin  |4 aut 
700 1 |a Liu, Gang  |e verfasserin  |4 aut 
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773 1 8 |g volume:30  |g year:2018  |g number:7  |g day:30  |g month:02 
856 4 0 |u http://dx.doi.org/10.1002/adma.201705350  |3 Volltext 
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