Tumor-targeted nanomedicines for cancer theranostics

被引:189
作者
Arranja, Alexandra G. [1 ,2 ]
Pathak, Vertika [3 ]
Lammers, Twan [2 ,3 ,4 ]
Shi, Yang [3 ]
机构
[1] Delft Univ Technol, Dept Chem Engn, NL-2629 HZ Delft, Netherlands
[2] Univ Utrecht, Utrecht Inst Pharmaceut Sci UIPS, Dept Pharmaceut, NL-3584 CG Utrecht, Netherlands
[3] RWTH Aachen Univ Clin, Inst Expt Mol Imaging ExMI, Dept Nanomed & Theranost, D-52074 Aachen, Germany
[4] Univ Twente, MIRA Inst Biomed Technol & Tech Med, Dept Targeted Therapeut, NL-7500 AE Enschede, Netherlands
基金
欧洲研究理事会;
关键词
Nanomedicine; Tumor targeting; Imaging; Theranostics; Clinical translation; GUIDED DRUG-DELIVERY; PEGYLATED LIPOSOMAL DOXORUBICIN; TEMPERATURE-SENSITIVE LIPOSOMES; IN-VIVO; POLYMERIC MICELLES; MACROMOLECULAR THERAPEUTICS; VASCULAR-PERMEABILITY; LOADED NANOPARTICLES; SOLID TUMORS; PHASE-III;
D O I
10.1016/j.phrs.2016.11.014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chemotherapeutic drugs have multiple drawbacks, including severe side effects and suboptimal therapeutic efficacy. Nanomedicines assist in improving the biodistribution and target accumulation of chemotherapeutic drugs, and are therefore able to enhance the balance between efficacy and toxicity. Multiple types of nanomedicines have been evaluated over the years, including liposomes, polymer-drug conjugates and polymeric micelles, which rely on strategies such as passive targeting, active targeting and triggered release for improved tumor-directed drug delivery. Based on the notion that tumors and metastases are highly heterogeneous, it is important to integrate imaging properties in nanomedicine formulations in order to enable non-invasive and" quantitative assessment of targeting efficiency. By allowing for patient pre-selection, such next generation nanotheranostics are useful for facilitating clinical translation and personalizing nanomedicine treatments. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:87 / 95
页数:9
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