TY - JOUR
T1 - Anti-CEA-functionalized superparamagnetic iron oxide nanoparticles for examining colorectal tumors in vivo
AU - Huang, Kai Wen
AU - Chieh, Jen Jie
AU - Lin, In Tsang
AU - Horng, Herng Er
AU - Yang, Hong Chang
AU - Hong, Chin Yih
N1 - Funding Information:
This work was supported by the National Science Council of Taiwan under grant numbers 102-2112-M-003-017, 102-2923-M-003-001, 102-2120-M-168-001, 102-2112-M-168-001, 102-2221-E-003-008-MY2, and 101–2221-E-003-005; the Department of Health under grant numbers DOH101-TD-N-111-004, DOH100-TD-N-111-008, and DOH100-TD-PB-111-TM022; and the National Taiwan Normal University.
PY - 2013
Y1 - 2013
N2 - 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.
AB - 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.
KW - Carcinoembryonic antigen
KW - Magnetic nanoparticles
KW - Magnetic resonance imaging
KW - Scanning superconducting-quantum-interferencedevice biosusceptometry
UR - http://www.scopus.com/inward/record.url?scp=84887294144&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84887294144&partnerID=8YFLogxK
U2 - 10.1186/1556-276X-8-413
DO - 10.1186/1556-276X-8-413
M3 - Article
AN - SCOPUS:84887294144
SN - 1931-7573
VL - 8
SP - 1
EP - 8
JO - Nanoscale Research Letters
JF - Nanoscale Research Letters
IS - 1
M1 - 413
ER -