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A Novel Metal-Based Imaging Probe for Targeted Dual-Modality SPECT/MR Imaging of Angiogenesis

机译:一种新型的基于金属的成像探针,用于靶向血管生成的双模态SPECT / MR成像

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Superparamagnetic iron oxide nanoparticles with well-integrated multimodality imaging properties have generated increasing research interest in the past decade, especially when it comes to the targeted imaging of tumors. Bevacizumab (BCZM) on the other hand is a well-known and widely applied monoclonal antibody recognizing VEGF-A, which is overexpressed in angiogenesis. The aim of this proof-of-concept study was to develop a dual-modality nanoplatform for in vivo targeted single photon emission tomography (SPET) and magnetic resonance imaging (MRI) of the tumor vascularization. Iron oxide nanoparticles (IONPs) have been coated with dimercaptosuccinic acid (DMSA), for consequent functionalization with the monoclonal antibody BCZM radiolabeled with 99mTc, via well-developed surface engineering. The IONPs were characterized based on their size distribution, hydrodynamic diameter and magnetic properties. In vitro cytotoxicity studies showed that our nanoconstruct does not cause toxic effects in normal and cancer cells. Fe3O4-DMSA-SMCC-BCZM-99mTc were successfully prepared at high radiochemical purity (>92%) and their stability in human serum and in PBS were demonstrated. In vitro cell binding studies showed the ability of the Fe3O4-DMSA-SMCC-BCZM-99mTc to bind to the VEGF-165 isoform overexpressed on M-165 tumor cells. The ex vivo biodistribution studies in M165 tumor-bearing SCID mice showed high uptake in liver, spleen, kidney and lungs. The Fe3O4-DMSA-SMCC-BCZM-99mTc demonstrated quick tumor accumulation starting at 8.9 ± 1.88 %ID/g at 2 h p.i., slightly increasing at 4 h p.i. (16.21 ± 2.56 %ID/g) and then decreasing at 24 h p.i. (6.01 ± 1.69 %ID/g). The tumor-to-blood ratio reached a maximum at 24 h p.i. (~ 7), which is also the case for the tumor-to-muscle ratio (~ 18). Initial pilot imaging studies on an experimental gamma-camera and a clinical MR camera prove our hypothesis and demonstrate the potential of Fe3O4-DMSA-SMCC-BCZM-99mTc for targeted dual-modality imaging. Our findings indicate that Fe3O4-DMSA-SMCC-BCZM-99mTc IONPs could serve as an important diagnostic tool for biomedical imaging as well as a promising candidate for future theranostic applications in cancer.
机译:在过去的十年中,具有良好集成的多峰成像特性的超顺磁性氧化铁纳米粒子引起了越来越多的研究兴趣,尤其是在肿瘤的靶向成像方面。另一方面,贝伐单抗(BCZM)是一种众所周知且广泛应用的单克隆抗体,可识别在血管生成中过表达的VEGF-A。这项概念验证研究的目的是开发一种双模式纳米平台,用于体内靶向肿瘤血管形成的单光子发射断层扫描(SPET)和磁共振成像(MRI)。氧化铁纳米颗粒(IONPs)已被二巯基琥珀酸(DMSA)包覆,从而通过完善的表面工程技术,用99mTc放射性标记的单克隆抗体BCZM进行功能化。根据IONP的尺寸分布,流体动力学直径和磁性能对其进行了表征。体外细胞毒性研究表明,我们的纳米结构不会对正常细胞和癌细胞产生毒性作用。 Fe3O4-DMSA-SMCC-BCZM-99mTc以高放射化学纯度(> 92%)成功制备,并证明了它们在人血清和PBS中的稳定性。体外细胞结合研究表明,Fe3O4-DMSA-SMCC-BCZM-99mTc能够与在M-165肿瘤细胞上过表达的VEGF-165同工型结合。在M165荷瘤SCID小鼠中的离体生物分布研究表明,肝脏,脾脏,肾脏和肺部的摄取量很高。 Fe3O4-DMSA-SMCC-BCZM-99mTc在2 h p.i时以8.9±1.88%ID / g的速度开始出现快速的肿瘤蓄积,在4 h p.i时略有增加。 (16.21±2.56%ID / g),然后在24 h p.i下降。 (6.01±1.69%ID / g)。肿瘤与血液的比例在24 h p.i达到最大值。 (〜7),肿瘤与肌肉的比例也是如此(〜18)。在实验性伽马相机和临床MR相机上进行的初步中试成像研究证明了我们的假设,并证明了Fe3O4-DMSA-SMCC-BCZM-99mTc在靶向双峰成像中的潜力。我们的研究结果表明,Fe3O4-DMSA-SMCC-BCZM-99mTc IONPs可以作为生物医学成像的重要诊断工具,并且可以作为将来在肿瘤治疗中应用的有前途的候选者。

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