Engineered Nanoparticles for Drug Delivery in Cancer Therapy

被引:1825
作者
Sun, Tianmeng [1 ,2 ]
Zhang, Yu Shrike [1 ,2 ]
Pang, Bo [1 ,2 ]
Hyun, Dong Choon [1 ,2 ]
Yang, Miaoxin [3 ]
Xia, Younan [1 ,2 ,3 ]
机构
[1] Georgia Inst Technol, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30332 USA
[2] Emory Univ, Atlanta, GA 30332 USA
[3] Georgia Inst Technol, Sch Chem & Biochem, Atlanta, GA 30332 USA
关键词
cancer therapy; controlled release; drug delivery; nanomedicine; nanoparticles; MESOPOROUS SILICA NANOPARTICLES; PEGYLATED LIPOSOMAL DOXORUBICIN; IRON-OXIDE NANOPARTICLES; ON-DEMAND DRUG; LONG-CIRCULATING NANOPARTICLES; OVERCOME MULTIDRUG-RESISTANCE; RECEPTOR-MEDIATED ENDOCYTOSIS; POLYMERIC MICELLE FORMULATION; WALLED CARBON NANOTUBES; TRAIL-INDUCED APOPTOSIS;
D O I
10.1002/anie.201403036
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In medicine, nanotechnology has sparked a rapidly growing interest as it promises to solve a number of issues associated with conventional therapeutic agents, including their poor water solubility (at least, for most anticancer drugs), lack of targeting capability, nonspecific distribution, systemic toxicity, and low therapeutic index. Over the past several decades, remarkable progress has been made in the development and application of engineered nanoparticles to treat cancer more effectively. For example, therapeutic agents have been integrated with nanoparticles engineered with optimal sizes, shapes, and surface properties to increase their solubility, prolong their circulation half-life, improve their biodistribution, and reduce their immunogenicity. Nanoparticles and their payloads have also been favorably delivered into tumors by taking advantage of the pathophysiological conditions, such as the enhanced permeability and retention effect, and the spatial variations in the pHvalue. Additionally, targeting ligands (e.g., small organic molecules, peptides, antibodies, and nucleic acids) have been added to the surface of nanoparticles to specifically target cancerous cells through selective binding to the receptors overexpressed on their surface. Furthermore, it has been demonstrated that multiple types of therapeutic drugs and/or diagnostic agents (e.g., contrast agents) could be delivered through the same carrier to enable combination therapy with a potential to overcome multidrug resistance, and real-time readout on the treatment efficacy. It is anticipated that precisely engineered nanoparticles will emerge as the next-generation platform for cancer therapy and many other biomedical applications.
引用
收藏
页码:12320 / 12364
页数:45
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