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用环状 RGD 肽对小型刚性平台进行功能化,以靶向过度表达 αvβ3-整合素的肿瘤。

Functionalization of small rigid platforms with cyclic RGD peptides for targeting tumors overexpressing αvβ3-integrins.

机构信息

Laboratoire de Physico-Chimie des Matériaux Luminescents, UMR 5620 CNRS - Université Claude Bernard Lyon 1, 69622 Villeurbanne Cedex, France.

出版信息

Bioconjug Chem. 2013 Sep 18;24(9):1584-97. doi: 10.1021/bc4002097. Epub 2013 Sep 9.

Abstract

Gadolinium based Small Rigid Plaforms (SRPs) have previously demonstrated their efficiency for multimodal imaging and radiosensitization. Since the RGD sequence is well-known to be highly selective for αvβ3 integrins, a cyclic pentapeptide containing the RGD motif (cRGDfK) has been grafted onto the SRP surface. An appropriate protocol led to the grafting of two targeting ligands per nano-object. The resulting nanoparticles have demonstrated a strong association with αvβ3 integrins in comparison with cRADfK grafted SRPs as negative control. Flow cytometry and fluorescence microscopy have also been used to highlight the ability of the nanoparticles to target efficiently HEK293(β3) and U87MG cells. Finally the grafted radiosensitizing nanoparticles were intravenously injected into Nude mice bearing subcutaneous U87MG tumors and the signal observed by optical imaging was twice as high for SRP-cRGDfK compared to their negative analogue.

摘要

基于钆的小分子刚性平台(SRP)先前已被证明在多模态成像和放射增敏方面的有效性。由于 RGD 序列对 αvβ3 整合素具有高度选择性,因此将含有 RGD 基序的环状五肽(cRGDfK)接枝到 SRP 表面。一个合适的方案导致每个纳米物体上接枝了两个靶向配体。与作为阴性对照的接枝 cRADfK 的 SRP 相比,所得纳米颗粒与 αvβ3 整合素表现出强烈的关联。流式细胞术和荧光显微镜也被用于突出纳米颗粒有效靶向 HEK293(β3)和 U87MG 细胞的能力。最后,将接枝的放射增敏纳米颗粒静脉注射到荷有皮下 U87MG 肿瘤的裸鼠中,并且与它们的阴性类似物相比,SRP-cRGDfK 的光学成像信号高两倍。

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