TY - JOUR
T1 - Off-resonance saturation MRI of superparamagnetic nanoprobes
T2 - Theoretical models and experimental validations
AU - Khemtong, Chalermchai
AU - Togao, Osamu
AU - Ren, Jimin
AU - Kessinger, Chase W.
AU - Takahashi, Masaya
AU - Sherry, A. Dean
AU - Gao, Jinming
N1 - Funding Information:
We thank the financial support from the following agencies: National Institutes of Health (R21 EB005394 and R01 CA129011 to JG, NIH CA15531 to ADS) and Robert A. Welch Foundation (AT-584 to ADS). C. Khemtong was supported by a Department of Defense Breast Cancer Research Program Multidisciplinary Postdoctoral Award (W81XWH-06-1-0751).
PY - 2011/3
Y1 - 2011/3
N2 - Off-resonance saturation (ORS) is a new magnetic resonance imaging (MRI) method that has shown greatly improved contrast sensitivity for the detection of cancer-specific biomarkers by superparamagnetic nanoprobes in vivo. However, quantitative understanding of the ORS contrast mechanism and its dependence on the structural parameters of superparamagnetic nanoprobes are still lacking. Here we propose a quantitative model of ORS contrast and its experimental validation by superparamagnetic polymeric micelles (SPPM) with precisely controlled structural properties. Size selected, monodisperse Fe 3O4 nanoparticles (6.1 ± 0.2 nm) were used to form a series of SPPM nanoprobes with specifically controlled corona thickness using 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-methoxypoly(ethylene glycol) (DSPE-PEG) with different PEG molecular weights. Transmission electron microscopy and dynamic light scattering showed that SPPM were uniform in size. The average hydrodynamic diameters of SPPM with PEG lengths of 0.55, 1, 2, and 5 kD were 16.6 ± 2.8, 18.4 ± 2.9, 24.1 ± 3.4, and 28.9 ± 3.4 nm, respectively. MRI experiments at 7T determined that r 2 values of SPPM with 0.55, 1, 2, and 5 kD PEG as corona were 201 ± 3, 136 ± 8, 107 ± 5, and 108 ± 8 Fe mM -1 s-1, respectively. ORS intensity from Z-spectra of SPPM showed a significant correlation with the inverse of T2 relaxation rates (1/T2, s-1) of the SPPM nanoprobes regardless of the PEG corona thickness. These data provide the fundamental understanding of the structure-property relationships between the SPPM nanostructures and ORS sensitivity, which offers useful mechanistic insights for the future improvement of SPPM nanoprobes in cancer molecular imaging applications.
AB - Off-resonance saturation (ORS) is a new magnetic resonance imaging (MRI) method that has shown greatly improved contrast sensitivity for the detection of cancer-specific biomarkers by superparamagnetic nanoprobes in vivo. However, quantitative understanding of the ORS contrast mechanism and its dependence on the structural parameters of superparamagnetic nanoprobes are still lacking. Here we propose a quantitative model of ORS contrast and its experimental validation by superparamagnetic polymeric micelles (SPPM) with precisely controlled structural properties. Size selected, monodisperse Fe 3O4 nanoparticles (6.1 ± 0.2 nm) were used to form a series of SPPM nanoprobes with specifically controlled corona thickness using 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-methoxypoly(ethylene glycol) (DSPE-PEG) with different PEG molecular weights. Transmission electron microscopy and dynamic light scattering showed that SPPM were uniform in size. The average hydrodynamic diameters of SPPM with PEG lengths of 0.55, 1, 2, and 5 kD were 16.6 ± 2.8, 18.4 ± 2.9, 24.1 ± 3.4, and 28.9 ± 3.4 nm, respectively. MRI experiments at 7T determined that r 2 values of SPPM with 0.55, 1, 2, and 5 kD PEG as corona were 201 ± 3, 136 ± 8, 107 ± 5, and 108 ± 8 Fe mM -1 s-1, respectively. ORS intensity from Z-spectra of SPPM showed a significant correlation with the inverse of T2 relaxation rates (1/T2, s-1) of the SPPM nanoprobes regardless of the PEG corona thickness. These data provide the fundamental understanding of the structure-property relationships between the SPPM nanostructures and ORS sensitivity, which offers useful mechanistic insights for the future improvement of SPPM nanoprobes in cancer molecular imaging applications.
UR - http://www.scopus.com/inward/record.url?scp=79951679938&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79951679938&partnerID=8YFLogxK
U2 - 10.1016/j.jmr.2010.12.013
DO - 10.1016/j.jmr.2010.12.013
M3 - Article
C2 - 21277813
AN - SCOPUS:79951679938
SN - 1090-7807
VL - 209
SP - 53
EP - 60
JO - Journal of Magnetic Resonance
JF - Journal of Magnetic Resonance
IS - 1
ER -