Cell membrane-coated nanoparticles for tumor-targeted drug delivery

被引:39
作者
Chai, Zhilan [1 ]
Hu, Xuefeng [1 ]
Lu, Weiyue [1 ]
机构
[1] Fudan Univ, Sch Pharm, Dept Pharmaceut, Key Lab Smart Drug Delivery, Shanghai 201203, Peoples R China
基金
中国国家自然科学基金;
关键词
cellmembrane; biomimetic nanoparticle; tumor-targeting; drug delivery; ERYTHROCYTE-MEMBRANE; IN-VIVO; POLYMERIC NANOPARTICLES; PHOTOTHERMAL THERAPY; CANCER-THERAPY; RBC MEMBRANES; CO-DELIVERY; LIPOSOMES; METASTASIS; PLATELETS;
D O I
10.1007/s40843-016-5163-4
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Nanoparticles can be enriched at tumor site and improve the therapeutic efficacy of many chemotherapy drugs with the well-known enhanced permeability and retention (EPR) effect. While conventional preparations of materials for nanoscale drug delivery system mainly focused on chemical synthesis, recently the combination of synthetic carrier and natural biomimetic carrier has gained more and more attention. As a new generation of biomimetic nanoparticles, cell membrane-coated nanoparticles combine the complex biological functions of natural membranes and the physicochemical properties of synthetic nanomaterials for a more effective drug delivery. Herein, we briefly review the recent advances on cell membrane-coated nanoparticles for tumor-targeted drug delivery via the prolonging systemic circulation lifetime and the active targeting effect. Since the preferential accumulation of cell membrane-coated nanoparticles in tumor site, they are able to improve the therapeutic efficacy of conventional chemotherapy drugs in antitumor treatment as well as to reduce the systemic toxicity. We also introduce a systematic targeted strategy for the promising application of this platform on brain tumors.
引用
收藏
页码:504 / 510
页数:7
相关论文
共 66 条
[1]  
Aryal S, 2013, NANOMEDICINE-UK, V8, P1271, DOI [10.2217/NNM.12.153, 10.2217/nnm.12.153]
[2]   Heparin and cancer revisited: Mechanistic connections involving platelets, P-selectin, carcinoma mucins, and tumor metastasis [J].
Borsig, L ;
Wong, R ;
Feramisco, J ;
Nadeau, DR ;
Varki, NM ;
Varki, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (06) :3352-3357
[3]   LEUKOCYTE-ENDOTHELIAL CELL RECOGNITION - 3 (OR MORE) STEPS TO SPECIFICITY AND DIVERSITY [J].
BUTCHER, EC .
CELL, 1991, 67 (06) :1033-1036
[4]   A Perspective on Cancer Cell Metastasis [J].
Chaffer, Christine L. ;
Weinberg, Robert A. .
SCIENCE, 2011, 331 (6024) :1559-1564
[5]   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
[6]   Increased intracellular targeting to airway cells using octaarginine-coated liposomes: In vitro assessment of their suitability for inhalation [J].
Cryan, Sally-Ann ;
Devocelle, Marc ;
Moran, Padraig J. ;
Hickey, Anthony J. ;
Kelly, John G. .
MOLECULAR PHARMACEUTICS, 2006, 3 (02) :104-112
[7]   The blood-brain barrier in health and disease [J].
Daneman, Richard .
ANNALS OF NEUROLOGY, 2012, 72 (05) :648-672
[8]   Nanoparticle therapeutics: an emerging treatment modality for cancer [J].
Davis, Mark E. ;
Chen, Zhuo ;
Shin, Dong M. .
NATURE REVIEWS DRUG DISCOVERY, 2008, 7 (09) :771-782
[9]   Synthesis and grafting of thioctic acid-PEG-folate conjugates onto Au nanoparticles for selective targeting of folate receptor-positive tumor cells [J].
Dixit, Vivechana ;
Van den Bossche, Jeroen ;
Sherman, Debra M. ;
Thompson, David H. ;
Andres, Ronald P. .
BIOCONJUGATE CHEMISTRY, 2006, 17 (03) :603-609
[10]   Red blood cell-mimicking synthetic biomaterial particles [J].
Doshi, Nishit ;
Zahr, Alisar S. ;
Bhaskar, Srijanani ;
Lahann, Joerg ;
Mitragotri, Samir .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (51) :21495-21499