DNA origami nanostructures for controlled therapeutic drug delivery

被引:57
作者
Weiden, Jorieke [1 ]
Bastings, Maartje M. C. [1 ]
机构
[1] Ecole Polytech Fed Lausanne EPFL, Interfac Bioengn Inst IBI, Programmable Biomat Lab PBL, Inst Mat IMX,Sch Engn STI, EPFL STI IMX PBL MXC 340,Stn 12, CH-1015 Lausanne, Switzerland
关键词
Drug delivery; DNA origami; DNA nanomaterials; Nanotechnology; Selective targeting; Controlled release; Translational therapy; Nanomedicine; TRIGGERED RELEASE; NANOPARTICLE SIZE; CELLULAR UPTAKE; CANCER; DOXORUBICIN; DESIGN; ANTHRACYCLINE; MECHANISMS; NANOSYSTEM; PROTECTION;
D O I
10.1016/j.cocis.2020.101411
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
DNA nanostructures are emerging as a versatile platform for controlled drug delivery as a result of recent progress in production yield and strategies to obtain prolonged stability in biological environments. The construction of nanostructures from this unique biomaterial provides unparalleled control over structural and functional parameters. Recent applications of DNA origami-based nanocarriers for therapeutic drug delivery in preclinical phases highlight them as promising alternatives to conventional nanomaterials, as they benefit from the inherent favorable properties of DNA including biocompatibility and precise spatial addressability. By incorporating targeting aptamers and responsive properties into the nanocarrier design, more selective DNA origami-based nanocarriers are successfully prepared. On the other hand, current systems remain poorly understood in terms of biodistribution, final fate, and controlled drug release. As such, advances are needed to translate this material platform in its full potential for therapeutic applications.
引用
收藏
页数:14
相关论文
共 98 条
[1]   Block Copolymer Micellization as a Protection Strategy for DNA Origami [J].
Agarwal, Nayan P. ;
Matthies, Michael ;
Guer, Fatih N. ;
Osada, Kensuke ;
Schmidt, Thorsten L. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2017, 56 (20) :5460-5464
[2]   (Poly)cation-induced protection of conventional and wireframe DNA origami nanostructures [J].
Ahmadi, Yasaman ;
De Llano, Elisa ;
Barisic, Ivan .
NANOSCALE, 2018, 10 (16) :7494-7504
[3]  
Amir Y, 2014, NAT NANOTECHNOL, V9, P353, DOI [10.1038/NNANO.2014.58, 10.1038/nnano.2014.58]
[4]  
[Anonymous], APT CIS RATH TRANSR
[5]  
[Anonymous], THEY OBSERVED ENHANC
[6]  
[Anonymous], DOXORUBICIN PRICES C
[7]  
[Anonymous], USING APTAMERS DIREC
[8]  
[Anonymous], ADDITION CANC CELL T
[9]  
[Anonymous], AUTHORS ARE 1 EXPLOI
[10]  
[Anonymous], THIS WORK PERFORMS D