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可激活的水溶性探针通过响应pH失调并呈现高肿瘤与肝脏荧光发射对比度来增强肿瘤成像。

Activatable Water-Soluble Probes Enhance Tumor Imaging by Responding to Dysregulated pH and Exhibiting High Tumor-to-Liver Fluorescence Emission Contrast.

作者信息

Xiong Hu, Kos Petra, Yan Yunfeng, Zhou Kejin, Miller Jason B, Elkassih Sussana, Siegwart Daniel J

机构信息

Simmons Comprehensive Cancer Center, Department of Biochemistry, The University of Texas Southwestern Medical Center , Dallas, Texas 75390, United States.

出版信息

Bioconjug Chem. 2016 Jul 20;27(7):1737-44. doi: 10.1021/acs.bioconjchem.6b00242. Epub 2016 Jun 20.

DOI:10.1021/acs.bioconjchem.6b00242
PMID:27285307
Abstract

Dysregulated pH has been recognized as a universal tumor microenvironment signature that can delineate tumors from normal tissues. Existing fluorescent probes that activate in response to pH are hindered by either fast clearance (in the case of small molecules) or high liver background emission (in the case of large particles). There remains a need to design water-soluble, long circulating, pH-responsive nanoprobes with high tumor-to-liver contrast. Herein, we report a modular chemical strategy to create acidic pH-sensitive and water-soluble fluorescent probes for high in vivo tumor detection and minimal liver activation. A combination of a modified Knoevenagel reaction and PEGylation yielded a series of NIR BODIPY fluorophores with tunable pKas, high quantum yield, and optimal orbital energies to enable photoinduced electron transfer (PeT) activation in response to pH. After intravenous administration, Probe 5c localized to tumors and provided excellent tumor-to-liver contrast (apparent T/L = 3) because it minimally activates in the liver. This phenomenon was further confirmed by direct ex vivo imaging experiments on harvested organs. Because no targeting ligands were required, we believe that this report introduces a versatile strategy to directly synthesize soluble probes with broad potential utility including fluorescence-based image-guided surgery, cancer diagnosis, and theranostic nanomedicine.

摘要

pH失调已被公认为一种普遍的肿瘤微环境特征,可用于区分肿瘤组织与正常组织。现有的对pH响应而激活的荧光探针,小分子存在快速清除问题,大颗粒则存在肝脏背景发射高的问题。仍然需要设计具有高肿瘤与肝脏对比度的水溶性、长循环、pH响应性纳米探针。在此,我们报告一种模块化化学策略,用于创建对酸性pH敏感的水溶性荧光探针,以实现高体内肿瘤检测和最小的肝脏激活。改良的Knoevenagel反应和聚乙二醇化相结合,产生了一系列具有可调pKa、高量子产率和最佳轨道能量的近红外BODIPY荧光团,以实现对pH响应的光诱导电子转移(PeT)激活。静脉注射后,探针5c定位于肿瘤部位,并提供了出色的肿瘤与肝脏对比度(表观T/L = 3),因为它在肝脏中的激活最小。对收获器官进行的直接离体成像实验进一步证实了这一现象。由于不需要靶向配体,我们相信本报告介绍了一种通用策略,可直接合成具有广泛潜在用途的可溶性探针,包括基于荧光的图像引导手术、癌症诊断和治疗诊断纳米医学。

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