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包裹镓的氧化铁纳米探针作为可激活的磁共振成像对比剂。

Gadolinium-encapsulating iron oxide nanoprobe as activatable NMR/MRI contrast agent.

机构信息

Nanoscience Technology Center and Chemistry Department, University of Central Florida, 12424 Research Parkway, Suite 400, Orlando, Florida 32826, USA.

出版信息

ACS Nano. 2012 Aug 28;6(8):7281-94. doi: 10.1021/nn302393e. Epub 2012 Jul 18.

Abstract

Herein we report a novel gadolinium-encapsulating iron oxide nanoparticle-based activatable NMR/MRI nanoprobe. In our design, Gd-DTPA is encapsulated within the poly(acrylic acid) (PAA) polymer coating of a superparamagnetic iron oxide nanoparticle (IO-PAA), yielding a composite magnetic nanoprobe (IO-PAA-Gd-DTPA) with quenched longitudinal spin-lattice magnetic relaxation (T(1)). Upon release of the Gd-DTPA complex from the nanoprobe's polymeric coating in acidic media, an increase in the T(1) relaxation rate (1/T(1)) of the composite magnetic nanoprobe was observed, indicating a dequenching of the nanoprobe with a corresponding increase in the T(1)-weighted MRI signal. When a folate-conjugated nanoprobe was incubated in HeLa cells, a cancer cell line overexpressing folate receptors, an increase in the 1/T(1) signal was observed. This result suggests that, upon receptor-mediated internalization, the composite magnetic nanoprobe degraded within the cell's lysosome acidic (pH 5.0) environment, resulting in an intracellular release of Gd-DTPA complex with subsequent T(1) activation. In addition, when an anticancer drug (Taxol) was coencapsulated with the Gd-DTPA within the folate receptor targeting composite magnetic nanoprobe, the T(1) activation of the probe coincided with the rate of drug release and corresponding cytotoxic effect in cell culture studies. Taken together, these results suggest that our activatable T(1) nanoagent could be of great importance for the detection of acidic tumors and assessment of drug targeting and release by MRI.

摘要

在此,我们报告了一种新型的基于钆包封氧化铁纳米颗粒的可激活磁共振/磁共振纳米探针。在我们的设计中,Gd-DTPA 被包裹在超顺磁性氧化铁纳米颗粒 (IO-PAA) 的聚(丙烯酸) (PAA) 聚合物涂层内,得到一种复合磁性纳米探针 (IO-PAA-Gd-DTPA),其纵向自旋晶格弛豫 (T(1)) 被猝灭。当 Gd-DTPA 复合物从纳米探针的聚合物涂层在酸性介质中释放时,观察到复合磁性纳米探针的 T(1)弛豫率 (1/T(1)) 增加,表明纳米探针去猝灭,相应的 T(1)加权磁共振信号增加。当叶酸偶联的纳米探针在 HeLa 细胞(一种过度表达叶酸受体的癌细胞系)中孵育时,观察到 1/T(1)信号增加。这一结果表明,在受体介导的内化后,复合磁性纳米探针在细胞溶酶体酸性 (pH 5.0) 环境中降解,导致 Gd-DTPA 复合物的细胞内释放,随后 T(1)被激活。此外,当将抗癌药物(紫杉醇)与叶酸受体靶向复合磁性纳米探针内的 Gd-DTPA 共包封时,探针的 T(1)激活与药物释放速率和细胞培养研究中的相应细胞毒性效应一致。总之,这些结果表明,我们的可激活 T(1)纳米剂对于通过磁共振成像检测酸性肿瘤和评估药物靶向和释放可能具有重要意义。

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