Anti-CEA-functionalized superparamagnetic iron oxide nanoparticles for examining colorectal tumors in vivo

被引:0
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作者
Kai-Wen Huang
Jen-Jie Chieh
In-Tsang Lin
Herng-Er Horng
Hong-Chang Yang
Chin-Yih Hong
机构
[1] National Taiwan University Hospital,Department of Surgery and Hepatitis Research Center
[2] National Taiwan University,Graduate Institute of Clinical Medicine
[3] National Taiwan Normal University,Institute of Electro
[4] Xiamen University,optical Science and Technology
[5] National Taiwan University,Center for Molecular Imaging and Translational Medicine
[6] Kun Shan University,Graduate Institute of Electronics Engineering
[7] National Chung Hsing University,Department of Electro
来源
Nanoscale Research Letters | / 8卷
关键词
Carcinoembryonic antigen; Magnetic nanoparticles; Scanning superconducting-quantum-interference-device biosusceptometry; Magnetic resonance imaging;
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摘要
Although the biomarker carcinoembryonic antigen (CEA) is expressed in colorectal tumors, the utility of an anti-CEA-functionalized image medium is powerful for in vivo positioning of colorectal tumors. With a risk of superparamagnetic iron oxide nanoparticles (SPIONPs) that is lower for animals than other material carriers, anti-CEA-functionalized SPIONPs were synthesized in this study for labeling colorectal tumors by conducting different preoperatively and intraoperatively in vivo examinations. In magnetic resonance imaging (MRI), the image variation of colorectal tumors reached the maximum at approximately 24 h. However, because MRI requires a nonmetal environment, it was limited to preoperative imaging. With the potentiality of in vivo screening and intraoperative positioning during surgery, the scanning superconducting-quantum-interference-device biosusceptometry (SSB) was adopted, showing the favorable agreement of time-varied intensity with MRI. Furthermore, biological methodologies of different tissue staining methods and inductively coupled plasma (ICP) yielded consistent results, proving that the obtained in vivo results occurred because of targeted anti-CEA SPIONPs. This indicates that developed anti-CEA SPIONPs owe the utilities as an image medium of these in vivo methodologies.
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