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利用叶酸受体实现癌症纳米治疗药物的主动靶向

Utilizing the folate receptor for active targeting of cancer nanotherapeutics.

作者信息

Zwicke Grant L, Mansoori G Ali, Jeffery Constance J

机构信息

Department of Biological Sciences, University of Illinois at Chicago, Chicago, IL, USA.

出版信息

Nano Rev. 2012;3. doi: 10.3402/nano.v3i0.18496. Epub 2012 Dec 7.


DOI:10.3402/nano.v3i0.18496
PMID:23240070
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3521101/
Abstract

The development of specialized nanoparticles for use in the detection and treatment of cancer is increasing. Methods are being proposed and tested that could target treatments more directly to cancer cells, which could lead to higher efficacy and reduced toxicity, possibly even eliminating the adverse effects of damage to the immune system and the loss of quick replicating cells. In this mini-review we focus on recent studies that employ folate nanoconjugates to target the folate receptor. Folate receptors are highly overexpressed on the surface of many tumor types. This expression can be exploited to target imaging molecules and therapeutic compounds directly to cancerous tissues.

摘要

用于癌症检测和治疗的专用纳米颗粒的研发正在增加。人们正在提出并测试一些方法,这些方法可以使治疗更直接地靶向癌细胞,这可能会提高疗效并降低毒性,甚至有可能消除对免疫系统的损害以及快速复制细胞损失所带来的不良影响。在本综述中,我们重点关注了最近使用叶酸纳米共轭物靶向叶酸受体的研究。叶酸受体在许多肿瘤类型的表面高度过表达。这种表达可被用于将成像分子和治疗化合物直接靶向癌组织。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6175/3521101/67ff6592b4e2/NANO-3-18496-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6175/3521101/1b16361e3785/NANO-3-18496-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6175/3521101/b8f0e4457015/NANO-3-18496-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6175/3521101/b4d693e16ee9/NANO-3-18496-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6175/3521101/4157d0931548/NANO-3-18496-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6175/3521101/bca3286d9bf4/NANO-3-18496-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6175/3521101/7a2de17fce5f/NANO-3-18496-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6175/3521101/67ff6592b4e2/NANO-3-18496-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6175/3521101/1b16361e3785/NANO-3-18496-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6175/3521101/b8f0e4457015/NANO-3-18496-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6175/3521101/b4d693e16ee9/NANO-3-18496-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6175/3521101/4157d0931548/NANO-3-18496-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6175/3521101/bca3286d9bf4/NANO-3-18496-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6175/3521101/7a2de17fce5f/NANO-3-18496-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6175/3521101/67ff6592b4e2/NANO-3-18496-g007.jpg

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本文引用的文献

[1]
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Small. 2012-4-17

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J Phys Condens Matter. 2012-3-30

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Cancer Res. 2012-3-6

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