Injectable nanomaterials for drug delivery: Carriers, targeting moieties, and therapeutics

被引:101
|
作者
Webster, David M.
Sundaram, Padma
Byrne, Mark E. [1 ]
机构
[1] Auburn Univ, Dept Chem Engn, Auburn, AL 36849 USA
关键词
Nanocarriers; Therapeutics; Targeting moieties; Injectable nanoparticles; Drug delivery carriers; WALLED CARBON NANOTUBES; GOLD NANOPARTICLES; CYCLODEXTRIN CORE; CELLULAR UPTAKE; GENE DELIVERY; IN-VITRO; POLYMERSOMES; LIPOSOMES; CELLS; SIRNA;
D O I
10.1016/j.ejpb.2012.12.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Therapeutics such as nucleic acids, proteins/peptides, vaccines, anti-cancer, and other drugs have disadvantages of low bio-availability, rapid clearance, and high toxicity. Thus, there is a significant need for the development of efficient delivery methods and carriers. Injectable nanocarriers have received much attention due to their vast range of structures and ability to contain multiple functional groups, both within the bulk material and on the surface of the particles. Nanocarriers may be tailored to control drug release and/or increase selective cell targeting, cellular uptake, drug solubility, and circulation time, all of which lead to a more efficacious delivery and action of therapeutics. The focus of this review is injectable, targeted nanoparticle drug delivery carriers highlighting the diversity of nanoparticle materials and structures as well as highlighting current therapeutics and targeting moieties. Structures and materials discussed include liposomes, polymersomes, dendrimers, cyclodextrin-containing polymers (CDPs), carbon nanotubes (CNTs), and gold nanoparticles. Additionally, current clinical trial information and details such as trial phase, treatment, active drug, carrier sponsor, and clinical trial identifier for different materials and structures are presented and discussed. (C) 2012 Elsevier B.V. All rights reserved.
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页码:1 / 20
页数:20
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