Integrin Targeted Delivery of Chemotherapeutics

被引:183
作者
Chen, Kai [2 ]
Chen, Xiaoyuan [1 ]
机构
[1] NIBIB, Lab Mol Imaging & Nanomed, NIH, Bethesda, MD 20892 USA
[2] Univ So Calif, Keck Sch Med, Dept Radiol, Mol Imaging Ctr, Los Angeles, CA 90033 USA
来源
THERANOSTICS | 2011年 / 1卷
基金
美国国家卫生研究院;
关键词
Integrin; Targeted delivery; Chemotherapeutics; RGD; Bioconjugation; TUMOR-NECROSIS-FACTOR; ARG-GLY-ASP; STERICALLY STABILIZED LIPOSOMES; PEPTIDE-PACLITAXEL CONJUGATE; IMPROVED ANTITUMOR EFFICACY; RGD-BASED STRATEGIES; FACTOR-ALPHA; CELL-ADHESION; ENDOTHELIAL-CELLS; DRUG-DELIVERY;
D O I
10.7150/thno/v01p0189
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Targeted delivery of chemotherapeutics is defined in the sense, that is, to maximize the therapeutic index of a chemotherapeutic agent by strictly localizing its pharmacological activity to the site or tissue of action. Integrins are a family of heterodimeric transmembrane glycoproteins involved in a wide range of cell-to-extracellular matrix (ECM) and cell-to-cell interactions. As cell surface receptors, integrins readily interact with extracellular ligands and play a vital role in angiogenesis, leukocytes function and tumor development, which sets up integrins as an excellent target for chemotherapy treatment. The peptide ligands containing the arginine-glycine-aspartic acid (RGD), which displays a strong binding affinity and selectivity to integrins, particularly to integrin alpha v beta 3, have been developed to conjugate with various conventional chemotherapeutic agents, such as small molecules, peptides and proteins, and nanoparticle-carried drugs for integtrin targeted therapeutic studies. This review highlights the recent advances in integrin targeted delivery of chemotherapeutic agents with emphasis on target of integrin alpha v beta 3, and describes the considerations for the design of the diverse RGD peptide-chemotherapeutics conjugates and their major applications.
引用
收藏
页码:189 / 200
页数:12
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