Phase gradient imaging for positive contrast generation to superparamagnetic iron oxide nanoparticle-labeled targets in magnetic resonance imaging

被引:12
作者
Zhu, Haitao [1 ]
Demachi, Kazuyuki [1 ]
Sekino, Masaki [2 ]
机构
[1] Univ Tokyo, Dept Nucl Engn, Tokyo 1130032, Japan
[2] Univ Tokyo, Dept Elect Engn & Informat Syst, Tokyo 1130033, Japan
关键词
Positive contrast; Phase gradient mapping; SPIO; Unwrapping; Truncation artifact; STEM-CELLS; VISUALIZATION; AGENTS;
D O I
10.1016/j.mri.2011.04.011
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Positive contrast imaging methods produce enhanced signal at large magnetic field gradient in magnetic resonance imaging. Several postprocessing algorithms, such as susceptibility gradient mapping and phase gradient mapping methods, have been applied for positive contrast generation to detect the cells targeted by superparamagnetic iron oxide nanoparticles. In the phase gradient mapping methods, smoothness condition has to be satisfied to keep the phase gradient unwrapped. Moreover, there has been no discussion about the truncation artifact associated with the algorithm of differentiation that is performed in k-space by the multiplication with frequency value. In this work, phase gradient methods are discussed by considering the wrapping problem when the smoothness condition is not satisfied. A region-growing unwrapping algorithm is used in the phase gradient image to solve the problem. In order to reduce the truncation artifact, a cosine function is multiplied in the k-space to eliminate the abrupt change at the boundaries. Simulation, phantom and in vivo experimental results demonstrate that the modified phase gradient mapping methods may produce improved positive contrast effects by reducing truncation or wrapping artifacts. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:891 / 898
页数:8
相关论文
共 24 条
[1]   Noninvasive MR imaging of magnetically labeled stem cells to directly identify neovasculature in a glioma model [J].
Anderson, SA ;
Glod, J ;
Arbab, AS ;
Noel, M ;
Ashari, P ;
Fine, HA ;
Frank, JA .
BLOOD, 2005, 105 (01) :420-425
[2]   Efficient magnetic cell labeling with protamine sulfate complexed to ferumoxides for cellular MRI [J].
Arbab, AS ;
Yocum, GT ;
Kalish, H ;
Jordan, EK ;
Anderson, SA ;
Khakoo, AY ;
Read, EJ ;
Frank, JA .
BLOOD, 2004, 104 (04) :1217-1223
[3]   Phase gradient mapping as an aid in the analysis of object-induced and system-related phase perturbations in MRI [J].
Bakker, Chris J. G. ;
de Leeuw, Hendrik ;
Vincken, Koen L. ;
Vonken, Evert-Jan ;
Hendrikse, Jeroen .
PHYSICS IN MEDICINE AND BIOLOGY, 2008, 53 (18) :N349-N358
[4]   Self-Refocused Spatial-Spectral Pulse for Positive Contrast Imaging of Cells Labeled with SPIO Nanoparticles [J].
Balchandani, Priti ;
Yamada, Mayumi ;
Pauly, John ;
Yang, Phillip ;
Spielman, Daniel .
MAGNETIC RESONANCE IN MEDICINE, 2009, 62 (01) :183-192
[5]   Iron oxide MR contrast agents for molecular and cellular imaging [J].
Bulte, JWM ;
Kraitchman, DL .
NMR IN BIOMEDICINE, 2004, 17 (07) :484-499
[6]   POsitive contrast magnetic resonance imaging of cells labeled with magnetic nanoparticles [J].
Cunningham, CH ;
Arai, T ;
Yang, PC ;
McConnell, MV ;
Pauly, JM ;
Conolly, SM .
MAGNETIC RESONANCE IN MEDICINE, 2005, 53 (05) :999-1005
[7]   Susceptibility gradient mapping (SGM): A new postprocessing method for positive contrast generation applied to superparamagnetic iron oxide particle (SPIO)-labeled cells [J].
Dahnke, Hannes ;
Liu, Wei ;
Herzka, Daniel ;
Frank, Joseph A. ;
Schaeffter, Tobias .
MAGNETIC RESONANCE IN MEDICINE, 2008, 60 (03) :595-603
[8]  
Girard OM, 2010, P 18 ANN M ISMRM STO
[9]   Susceptibility weighted imaging (SWI) [J].
Haacke, EM ;
Xu, YB ;
Cheng, YCN ;
Reichenbach, JR .
MAGNETIC RESONANCE IN MEDICINE, 2004, 52 (03) :612-618
[10]   Phase-derivative analysis in MR angiography: Reduced V-enc dependency and improved vessel wall detection in laminar and disturbed flow [J].
Hoogeveen, RM ;
Bakker, CJG ;
Viergever, MA .
JMRI-JOURNAL OF MAGNETIC RESONANCE IMAGING, 1997, 7 (02) :321-330