TY - JOUR
T1 - SPIO-PICsome
T2 - Development of a highly sensitive and stealth-capable MRI nano-agent for tumor detection using SPIO-loaded unilamellar polyion complex vesicles (PICsomes)
AU - Kokuryo, Daisuke
AU - Anraku, Yasutaka
AU - Kishimura, Akihiro
AU - Tanaka, Sayaka
AU - Kano, Mitsunobu R.
AU - Kershaw, Jeff
AU - Nishiyama, Nobuhiro
AU - Saga, Tsuneo
AU - Aoki, Ichio
AU - Kataoka, Kazunori
N1 - Funding Information:
The authors thank Sayaka Shibata and Aiko Sekita (NIRS) for helping with the animal experiments. This research was supported by the Japan Society for the Promotion of Science through the Funding Program for World-Leading Innovation R&D on Science and Technology (FIRST program) . We are grateful to Dr. S. Fukuda at the University of Tokyo Hospital, and the staff of the Research Hub for Advanced Nano Characterization, The University of Tokyo, which is supported by MEXT of Japan, for their valuable support while performing the TEM measurements.
PY - 2013
Y1 - 2013
N2 - Size controllable polyion complex vesicles (PICsomes), composed of biocompatible poly(ethylene glycol) (PEG) and poly(amino acid)s, have an extremely prolonged lifetime in the bloodstream that enables them to accumulate effectively in tumors via the enhanced permeability and retention (EPR) effect. The purpose of this study was to use PICsomes to synthesize a highly sensitive MRI contrast agent for more precise tumor detection. We synthesized SPIO-Cy5-PICsomes (superparamagnetic iron oxide nanoparticle-loaded Cy5-cross-linked Nano-PICsomes) and characterized them using dynamic light scattering and transmission electron microscopy in vitro and evaluated their ability to detect subcutaneously grafted tumors in vivo with MRI. The transverse relaxivity (r2) of the SPIO-Cy5-PICsomes (r2 = 663 ± 28 mM-1 s-1) was 2.54 times higher than that of bare clinically-used SPIO. In in vivo MRI experiments on mice subcutaneously grafted with colon-26 tumor cells, the tumor signal was significantly altered at 3 h after SPIO-Cy5-PICsome administration and persisted for at least 24 h. Small and early-stage in vivo tumors (3 days after grafting, approximately 4 mm3) were also clearly detected with MRI. SPIO-loaded PICsomes are sensitive MRI contrast agents that can act as a powerful nanocarrier to detect small tumors for early diagnosis.
AB - Size controllable polyion complex vesicles (PICsomes), composed of biocompatible poly(ethylene glycol) (PEG) and poly(amino acid)s, have an extremely prolonged lifetime in the bloodstream that enables them to accumulate effectively in tumors via the enhanced permeability and retention (EPR) effect. The purpose of this study was to use PICsomes to synthesize a highly sensitive MRI contrast agent for more precise tumor detection. We synthesized SPIO-Cy5-PICsomes (superparamagnetic iron oxide nanoparticle-loaded Cy5-cross-linked Nano-PICsomes) and characterized them using dynamic light scattering and transmission electron microscopy in vitro and evaluated their ability to detect subcutaneously grafted tumors in vivo with MRI. The transverse relaxivity (r2) of the SPIO-Cy5-PICsomes (r2 = 663 ± 28 mM-1 s-1) was 2.54 times higher than that of bare clinically-used SPIO. In in vivo MRI experiments on mice subcutaneously grafted with colon-26 tumor cells, the tumor signal was significantly altered at 3 h after SPIO-Cy5-PICsome administration and persisted for at least 24 h. Small and early-stage in vivo tumors (3 days after grafting, approximately 4 mm3) were also clearly detected with MRI. SPIO-loaded PICsomes are sensitive MRI contrast agents that can act as a powerful nanocarrier to detect small tumors for early diagnosis.
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U2 - 10.1016/j.jconrel.2013.03.016
DO - 10.1016/j.jconrel.2013.03.016
M3 - Article
C2 - 23542239
AN - SCOPUS:84885171684
SN - 0168-3659
VL - 169
SP - 220
EP - 227
JO - Journal of Controlled Release
JF - Journal of Controlled Release
IS - 3
ER -