用于乳腺癌 HER2 靶向磁共振/近红外成像的 Fe3O4-Cy5.5- 曲妥珠单抗磁性纳米粒子。

IF 3.9 3区 医学 Q2 ENGINEERING, BIOMEDICAL Biomedical materials Pub Date : 2024-04-16 DOI:10.1088/1748-605X/ad3f61
Qiangqiang Yin, Xiaolong Gao, Hao Zhang, Zhicheng Zhang, Xiaoyang Yu, Jialong He, Guangyue Shi, Liguo Hao
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引用次数: 0

摘要

本研究开发了一种具有荧光和磁共振成像功能的探针Fe3O4-Cy5.5-曲妥珠单抗,可靶向HER2高表达的乳腺癌,旨在为早期乳腺癌的诊断提供一种新的理论方法。方法:Fe3O4-Cy5.5-曲妥珠单抗纳米颗粒与Fe3O4结合用于T2成像,与Cy5.5结合用于近红外成像,并与曲妥珠单抗结合用于HER2靶向。我们利用透射电子显微镜、水合粒度、Zeta 电位、紫外光谱和傅立叶变换红外光谱对纳米粒子进行了表征,并研究了其磁性、荧光和弛豫速率相关特性。CCK-8和血液生化分析评估了纳米颗粒的生物安全性和稳定性,并通过体外和体内细胞及动物实验验证了Fe3O4-Cy5.5曲妥珠单抗纳米颗粒的靶向能力。结果表征结果表明,成功合成了直径为 93.72±6.34 nm 的 Fe3O4-Cy5.5 曲妥珠单抗纳米颗粒。纳米颗粒的 T2 弛豫速率为 42.29 mM-1s-1,磁饱和强度为 27.58 emg/g。激光共聚焦和流式细胞仪摄取分析表明,该纳米颗粒能有效靶向乳腺癌细胞表达的 HER2。体外和体内研究表明,Fe3O4-Cy5.5-曲妥珠单抗被特异性摄取并有效聚集到肿瘤区域,具有显著的近红外/红外成像特性。CCK-8、血液生化分析和组织学结果表明,Fe3O4-Cy5.5-曲妥珠单抗对主要器官毒性低,体内生物相容性好。制备的 Fe3O4-Cy5.5-trastuzumab 具有良好的靶向性和近红外/红外成像性能。它有望成为一种安全有效的诊断方法,为有效诊断早期乳腺癌奠定理论基础。结论本研究成功制备了一种具有近红外荧光成像和T2成像特性的纳米颗粒,有望成为乳腺癌早期检测的新理论和新策略。关键词 乳腺癌;HER2;曲妥珠单抗;T2成像特性;近红外荧光成像;早期检测 。
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Fe3O4-Cy5.5-trastuzumab magnetic nanoparticles for magnetic resonance / near-infrared imaging targeting HER2 in breast cancer.
This study developed a probe Fe3O4-Cy5.5-trastuzumab with fluorescence and magnetic resonance imaging functions that can target breast cancer with high HER2 expression, aiming to provide a new theoretical method for the diagnosis of early breast cancer. Methods:Fe3O4-Cy5.5-trastuzumab nanoparticles were combined with Fe3O4 for T2 imaging and Cy5.5 for near-infrared imaging, and coupled with trastuzumab for HER2 targeting. We characterized the nanoparticles used transmission electron microscopy, hydration particle size, Zeta potential, UV and fourier transform infrared spectroscopy, and examined its magnetism, fluorescence, and relaxation rate related properties. CCK-8 and blood biochemistry analysis evaluated the biosafety and stability of the nanoparticles, and validated the targeting ability of Fe3O4-Cy5.5 trastuzumab nanoparticles through in vitro and in vivo cell and animal experiments. Results: Characterization results showed the successful synthesis of Fe3O4-Cy5.5-trastuzumab nanoparticles with a diameter of 93.72±6.34 nm. The nanoparticles showed a T2 relaxation rate 42.29 mM-1s-1, magnetic saturation strength of 27.58 emg/g. Laser confocal and flow cytometry uptake assay showed that the nanoparticles could effectively target HER2 expressed by breast cancer cells. As indicated by in vitro and in vivo studies, Fe3O4-Cy5.5-trastuzumab were specifically taken up and effectively aggregated to tumor regions with prominent NIRF/MR imaging properties. CCK-8, blood biochemical analysis and histological results suggested Fe3O4-Cy5.5-trastuzumab that exhibited low toxicity to major organs and good in vivo biocompatibility. The prepared Fe3O4-Cy5.5-trastuzumab exhibited excellent targeting, NIRF/MR imaging performance. It is expected to serve as a safe and effective diagnostic method that lays a theoretical basis for the effective diagnosis of of early breast cancer. Conclusion: This study successfully prepared a kind of nanoparticles with near-infrared fluorescence imaging and T2 imaging properties, which is expected to serve as a new theory and strategy for early detection of breast cancer. Keywords Breast cancer ; HER2 ;Trastuzumab ;T2 imaging properties; Near infrared fluorescence imaging; Early detection .
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来源期刊
Biomedical materials
Biomedical materials 工程技术-材料科学:生物材料
CiteScore
6.70
自引率
7.50%
发文量
294
审稿时长
3 months
期刊介绍: The goal of the journal is to publish original research findings and critical reviews that contribute to our knowledge about the composition, properties, and performance of materials for all applications relevant to human healthcare. Typical areas of interest include (but are not limited to): -Synthesis/characterization of biomedical materials- Nature-inspired synthesis/biomineralization of biomedical materials- In vitro/in vivo performance of biomedical materials- Biofabrication technologies/applications: 3D bioprinting, bioink development, bioassembly & biopatterning- Microfluidic systems (including disease models): fabrication, testing & translational applications- Tissue engineering/regenerative medicine- Interaction of molecules/cells with materials- Effects of biomaterials on stem cell behaviour- Growth factors/genes/cells incorporated into biomedical materials- Biophysical cues/biocompatibility pathways in biomedical materials performance- Clinical applications of biomedical materials for cell therapies in disease (cancer etc)- Nanomedicine, nanotoxicology and nanopathology- Pharmacokinetic considerations in drug delivery systems- Risks of contrast media in imaging systems- Biosafety aspects of gene delivery agents- Preclinical and clinical performance of implantable biomedical materials- Translational and regulatory matters
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