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Extracellularly activated nanocarriers: a new paradigm of tumor targeted drug delivery.

作者信息

Gullotti Emily, Yeo Yoon

机构信息

Weldon School of Biomedical Engineering, Purdue University, 206 South Martin Jischke Drive, West Lafayette, Indiana 47907, USA.

出版信息

Mol Pharm. 2009 Jul-Aug;6(4):1041-51. doi: 10.1021/mp900090z.


DOI:10.1021/mp900090z
PMID:19366234
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2743941/
Abstract

One of the main goals of nanomedicine is to develop a nanocarrier that can selectively deliver anticancer drugs to the targeted tumors. Extensive efforts have resulted in several tumor-targeted nanocarriers, some of which are approved for clinical use. Most nanocarriers achieve tumor-selective accumulation through the enhanced permeability and retention effect. Targeting molecules such as antibodies, peptides, ligands, or nucleic acids attached to the nanocarriers further enhance their recognition and internalization by the target tissues. While both the stealth and targeting features are important for effective and selective drug delivery to the tumors, achieving both features simultaneously is often found to be difficult. Some of the recent targeting strategies have the potential to overcome this challenge. These strategies utilize the unique extracellular environment of tumors to change the long-circulating nanocarriers to release the drug or interact with cells in a tumor-specific manner. This review discusses the new targeting strategies with recent examples, which utilize the environmental stimuli to activate the nanocarriers. Traditional strategies for tumor-targeted nanocarriers are briefly discussed with an emphasis on their achievements and challenges.

摘要

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本文引用的文献

[1]
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Clin Cancer Res. 2009-3-15

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