Erythrocyte-Platelet Hybrid Membrane Coating for Enhanced Nanoparticle Functionalization

被引:648
作者
Dehaini, Diana [1 ,2 ]
Wei, Xiaoli [1 ,2 ]
Fang, Ronnie H. [1 ,2 ]
Masson, Sarah [1 ,2 ]
Angsantikul, Pavimol [1 ,2 ]
Luk, Brian T. [1 ,2 ]
Zhang, Yue [1 ,2 ]
Ying, Man [1 ,2 ]
Jiang, Yao [1 ,2 ]
Kroll, Ashley V. [1 ,2 ]
Gao, Weiwei [1 ,2 ]
Zhang, Liangfang [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Nanoengn, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
DRUG-DELIVERY; COATED NANOPARTICLES; BIOMIMETIC NANOPARTICLES; BIOMEDICAL APPLICATIONS; SELF; VACCINATION; CLEARANCE; THERAPY; SYSTEMS; MARKER;
D O I
10.1002/adma.201606209
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cell-membrane-coated nanoparticles have recently been studied extensively for their biological compatibility, retention of cellular properties, and adaptability to a variety of therapeutic and imaging applications. This class of nanoparticles, which has been fabricated with a variety of cell membrane coatings, including those derived from red blood cells (RBCs), platelets, white blood cells, cancer cells, and bacteria, exhibit properties that are characteristic of the source cell. In this study, a new type of biological coating is created by fusing membrane material from two different cells, providing a facile method for further enhancing nanoparticle functionality. As a proof of concept, the development of dual-membrane-coated nanoparticles from the fused RBC membrane and platelet membrane is demonstrated. The resulting particles, termed RBC-platelet hybrid membrane-coated nanoparticles ([RBC-P] NPs), are thoroughly characterized, and it is shown that they carry properties of both source cells. Further, the [RBC-P] NP platform exhibits long circulation and suitability for further in vivo exploration. The reported strategy opens the door for the creation of biocompatible, custom-tailored biomimetic nanoparticles with varying hybrid functionalities, which may be used to overcome the limitations of current nanoparticle-based therapeutic and imaging platforms.
引用
收藏
页数:8
相关论文
共 39 条
[1]   Liposomal drug delivery systems: From concept to clinical applications [J].
Allen, Theresa M. ;
Cullis, Pieter R. .
ADVANCED DRUG DELIVERY REVIEWS, 2013, 65 (01) :36-48
[2]   Biomimetic Delivery with Micro- and Nanoparticles [J].
Balmert, Stephen C. ;
Little, Steven R. .
ADVANCED MATERIALS, 2012, 24 (28) :3757-3778
[3]   Nanoparticle and targeted systems for cancer therapy [J].
Brannon-Peppas, L ;
Blanchette, JO .
ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (11) :1649-1659
[4]   Clearance of pathological antibodies using biomimetic nanoparticles [J].
Copp, Jonathan A. ;
Fang, Ronnie H. ;
Luk, Brian T. ;
Hu, Che-Ming J. ;
Gao, Weiwei ;
Zhang, Kang ;
Zhang, Liangfang .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (37) :13481-13486
[5]   Biomimetic strategies for targeted nanoparticle delivery [J].
Dehaini, Diana ;
Fang, Ronnie H. ;
Zhang, Liangfang .
BIOENGINEERING & TRANSLATIONAL MEDICINE, 2016, 1 (01) :30-46
[6]   Cancer Cell Membrane-Coated Nanoparticles for Anticancer Vaccination and Drug Delivery [J].
Fang, Ronnie H. ;
Hu, Che-Ming J. ;
Luk, Brian T. ;
Gao, Weiwei ;
Copp, Jonathan A. ;
Tai, Yiyin ;
O'Connor, Derek E. ;
Zhang, Liangfang .
NANO LETTERS, 2014, 14 (04) :2181-2188
[7]   Lipid-insertion enables targeting functionalization of erythrocyte membrane-cloaked nanoparticles [J].
Fang, Ronnie H. ;
Hu, Che-Ming J. ;
Chen, Kevin N. H. ;
Luk, Brian T. ;
Carpenter, Cody W. ;
Gao, Weiwei ;
Li, Shulin ;
Zhang, Dong-Er ;
Lu, Weiyue ;
Zhang, Liangfang .
NANOSCALE, 2013, 5 (19) :8884-8888
[8]   Quick Synthesis of Lipid-Polymer Hybrid Nanoparticles with Low Polydispersity Using a Single-Step Sonication Method [J].
Fang, Ronnie H. ;
Aryal, Santosh ;
Hu, Che-Ming Jack ;
Zhang, Liangfang .
LANGMUIR, 2010, 26 (22) :16958-16962
[9]   Impact of Nanotechnology on Drug Delivery [J].
Farokhzad, Omid C. ;
Langer, Robert .
ACS NANO, 2009, 3 (01) :16-20
[10]   Evolutionary considerations in relating oligosaccharide diversity to biological function [J].
Gagneux, P ;
Varki, A .
GLYCOBIOLOGY, 1999, 9 (08) :747-755