Folic Acid-Conjugated Fe-Au-Based Nanoparticles for Dual Detection of Breast Cancer Cells by Magnetic Resonance Imaging and Computed Tomography

Q3 Health Professions
Nasim Jamshidi, A. Tarighatnia, Mona Fazel Ghaziyani, Fakhrossadat Sajadian, Maryam Olad-Ghaffari, Nader D. Nader
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引用次数: 0

Abstract

Purpose: We synthesized folic acid-conjugated Fe3O4/Au-pralidoxime chloride Nanoparticles (Fe2O3/Au@PAM NPs) for use as dual-modal contrast agents for Magnetic Resonance Imaging (MRI) and Computed Tomography (CT) in the diagnosis of breast cancer. Materials and Methods: Fe2O3/Au@PAM NPs labeled or not to folic acid were synthesized and analyzed by dynamic light scattering, transmission electron microscopy, and vibrating sample magnetometry. The ability of these NPs to create image contrast was also investigated in silico and in vitro (in MCF-7 breast cancer cells and A549 lung cancer cells) with CT and MRI. Results: Dynamic light scattering and transmission electron microscopy revealed that the Fe2O3/Au@PAM NPs were nearly spherical. The average diameter of Fe2O3/Au NPs increased from 11.6 nm to 98 nm after folic acid conjugation. The saturation magnetization values of Fe2O3/Au@PAM NPs with and without folic acid conjugation were 25.56 and 32.6 emu/g, respectively. Conjugation of folic acid to NPs greatly improved their uptake by cancer cells. The additional coating of NPs with FA reduced the T2 relaxation time and signal intensity for MRI. Folic acid-labeled MCF-7 cells had a radiodensity measurement of 208 Hunsfield Units (HU) compared to 95 HU for A549 cells. For breast cancer cells, NPs labeled with folic acid significantly improved the X-ray absorption coefficient as a sign of active cellular uptake compared to NPs without labeling. Conclusion: Folic acid-labeled Fe2O3/Au@PAM NPs can serve as dual CT/MRI contrast agents and improve the sensitivities of both modalities for the detection of cancer cells.
通过磁共振成像和计算机断层扫描双重检测乳腺癌细胞的叶酸共轭铁-金基纳米粒子
目的:我们合成了叶酸共轭的 Fe3O4/Au-pralidoxime chloride 纳米粒子(Fe2O3/Au@PAM NPs),可用作诊断乳腺癌的磁共振成像(MRI)和计算机断层扫描(CT)双模式造影剂。 材料与方法:合成了叶酸标记或未标记的 Fe2O3/Au@PAM NPs,并通过动态光散射、透射电子显微镜和振动样品磁强计进行了分析。还利用 CT 和 MRI 对这些 NPs 形成图像对比的能力进行了硅学和体外(MCF-7 乳腺癌细胞和 A549 肺癌细胞)研究。 研究结果动态光散射和透射电子显微镜显示,Fe2O3/Au@PAM NPs 几乎呈球形。叶酸共轭后,Fe2O3/Au NPs 的平均直径从 11.6 nm 增加到 98 nm。叶酸共轭和未共轭的 Fe2O3/Au@PAM NPs 饱和磁化值分别为 25.56 和 32.6 emu/g。叶酸与 NPs 的共轭大大提高了癌细胞对它们的吸收。在 NPs 上额外包覆 FA 可减少核磁共振成像的 T2 松弛时间和信号强度。叶酸标记的 MCF-7 细胞的放射密度测定值为 208 亨斯菲尔德单位(HU),而 A549 细胞为 95 HU。对于乳腺癌细胞,与未标记的 NPs 相比,标记叶酸的 NPs 显著提高了 X 射线吸收系数,这是细胞主动吸收的标志。 结论叶酸标记的 Fe2O3/Au@PAM NPs 可作为 CT/MRI 双重造影剂,提高了这两种成像模式检测癌细胞的灵敏度。
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来源期刊
Frontiers in Biomedical Technologies
Frontiers in Biomedical Technologies Health Professions-Medical Laboratory Technology
CiteScore
0.80
自引率
0.00%
发文量
34
审稿时长
12 weeks
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