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pHLIP 肽将纳米金颗粒靶向肿瘤。

pHLIP peptide targets nanogold particles to tumors.

机构信息

Physics Department, University of Rhode Island, Kingston, RI 02881, USA.

出版信息

Proc Natl Acad Sci U S A. 2013 Jan 8;110(2):465-70. doi: 10.1073/pnas.1219665110. Epub 2012 Dec 24.


DOI:10.1073/pnas.1219665110
PMID:23267062
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3545779/
Abstract

Progress in nanomedicine depends on the development of nanomaterials and targeted delivery methods. In this work, we describe a method for the preferential targeting of gold nanoparticles to a tumor in a mouse model. The method is based on the use of the pH Low Insertion Peptide (pHLIP), which targets various imaging agents to acidic tumors. We compare tumor targeting by nonfunctionalized nanogold particles with nanogold-pHLIP conjugates, where nanogold is covalently attached to the N terminus of pHLIP. Our most important finding is that both intratumoral and i.v. administration demonstrated a significant enhancement of tumor uptake of gold nanoparticles conjugated with pHLIP. Statistically significant reduction of gold accumulation was observed in acidic tumors and kidney when pH-insensitive K-pHLIP was used as a vehicle, suggesting an important role of pH in the pHLIP-mediated targeting of gold nanoparticles. The pHLIP technology can substantially improve the delivery of gold nanoparticles to tumors by providing specificity of targeting, enhancing local concentration in tumors, and distributing nanoparticles throughout the entire tumor mass where they remain for an extended period (several days), which is beneficial for radiation oncology and imaging.

摘要

纳米医学的进展依赖于纳米材料和靶向递送方法的发展。在这项工作中,我们描述了一种将金纳米粒子优先靶向小鼠模型中肿瘤的方法。该方法基于使用 pH 低插入肽(pHLIP),将各种成像剂靶向到酸性肿瘤。我们比较了非功能化纳米金颗粒与纳米金-pHLIP 缀合物的肿瘤靶向性,其中纳米金通过共价键连接到 pHLIP 的 N 端。我们最重要的发现是,无论是瘤内还是静脉内给药,与未缀合的金纳米颗粒相比,pHLIP 缀合的金纳米颗粒在肿瘤中的摄取均显著增强。当使用 pH 不敏感的 K-pHLIP 作为载体时,在酸性肿瘤和肾脏中观察到金积累的统计学显著减少,这表明 pH 在 pHLIP 介导的金纳米颗粒靶向中起重要作用。pHLIP 技术可以通过提供靶向特异性、增强肿瘤内的局部浓度以及将纳米颗粒分布在整个肿瘤质量中(持续数天)来显著改善金纳米颗粒向肿瘤的递送,这对放射肿瘤学和成像有益。

相似文献

[1]
pHLIP peptide targets nanogold particles to tumors.

Proc Natl Acad Sci U S A. 2012-12-24

[2]
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[3]
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[4]
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[5]
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Acta Biomater. 2017-3-29

[6]
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[7]
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[8]
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[9]
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[10]
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[3]
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[4]
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[5]
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[6]
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[7]
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J Chem Theory Comput. 2022-11-8

[8]
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[9]
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[10]
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本文引用的文献

[1]
In vivo pH imaging with (99m)Tc-pHLIP.

Mol Imaging Biol. 2012-12

[2]
pH-controlled delivery of luminescent europium coated nanoparticles into platelets.

Proc Natl Acad Sci U S A. 2012-1-20

[3]
Plasmonic circular dichroism of Peptide-functionalized gold nanoparticles.

Nano Lett. 2011-1-5

[4]
Measuring tumor aggressiveness and targeting metastatic lesions with fluorescent pHLIP.

Mol Imaging Biol. 2011-12

[5]
Noninvasive radiofrequency field destruction of pancreatic adenocarcinoma xenografts treated with targeted gold nanoparticles.

Clin Cancer Res. 2010-12-1

[6]
Micro-CT enables microlocalisation and quantification of Her2-targeted gold nanoparticles within tumour regions.

Br J Radiol. 2010-11-16

[7]
pH-sensitive membrane peptides (pHLIPs) as a novel class of delivery agents.

Mol Membr Biol. 2010-10

[8]
New insights into the physiological role of carbonic anhydrase IX in tumour pH regulation.

Oncogene. 2010-10-4

[9]
A reexamination of active and passive tumor targeting by using rod-shaped gold nanocrystals and covalently conjugated peptide ligands.

ACS Nano. 2010-10-26

[10]
Gold nanoframes: very high surface plasmon fields and excellent near-infrared sensors.

J Am Chem Soc. 2010-9-15

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