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Imaging Sessions (imaging + session)
Selected AbstractsTumor imaging in small animals with a combined micro-CT/micro-DSA system using iodinated conventional and blood pool contrast agentsCONTRAST MEDIA & MOLECULAR IMAGING, Issue 4 2006Cristian T. Badea Abstract X-ray based micro-computed tomography (CT) and micro-digital subtraction angiography (DSA) are important non-invasive imaging modalities for following tumorogenesis in small animals. To exploit these imaging capabilities further, the two modalities were combined into a single system to provide both morphological and functional data from the same tumor in a single imaging session. The system is described and examples are given of imaging implanted fibrosarcoma tumors in rats using two types of contrast media: (a) a new generation of blood pool contrast agent containing iodine with a concentration of 130,mg/mL (FenestraÔ VC, Alerion Biomedical, San Diego, CA, USA) for micro-CT and (b) a conventional iodinated contrast agent (Isovue®-370,mg/mL iodine, trademark of Bracco Diagnostics, Princeton, NJ, USA) for micro-DSA. With the blood pool contrast agent, the 3D vascular architecture is revealed in exquisite detail at 100,µm resolution. Micro-DSA images, in perfect registration with the 3D micro-CT datasets, provide complementary functional information such as mean transit times and relative blood flow through the tumor. This imaging approach could be used to understand tumor angiogenesis better and be the basis for evaluating anti-angiogenic therapies. Copyright © 2006 John Wiley & Sons Ltd. [source] Effect of molecular weight and end capping on poly(lactic- co -glycolic acid) ultrasound contrast agentsPOLYMER ENGINEERING & SCIENCE, Issue 9 2008J.R. Eisenbrey Ultrasound contrast agents (CA) consist of stabilized gas bubbles that, when injected intravenously, provide an acoustic impedance mismatch, producing additional contrast to a diagnostic ultrasound scan. These agents must be smaller than 8 ,m in order to pass safely through the capillaries, contain gas for an impedance mismatch and should be stable enough to survive the duration of the imaging session. A double emulsion technique has previously been optimized within our laboratory to create CA with 50:50 poly (lactic- co -glycolic acid) (PLGA). Although a great deal of research has focused on the effects of molecular weight and end capping on solid PLGA particles, very little has been done to examine the effects of these parameters on hollow CAs formed in a double emulsion. Non-end capped PLGA was found to provide maximum enhancement at a molecular weight of 66.0 kDa, giving an ultrasound enhancement of roughly 18.5 dB. The enhancement demonstrated by CA formed using the end-capped PLGA rose to a maximum enhancement of 19 dB at the highest commercially available molecular weight of 82.4 kDa. A strong correlation was seen between ultrasound enhancement, stability under ultrasonic conditions, surface morphology and zeta potential. This study shows the influence of polymer characteristics on the resulting properties of CA and the ability to tailor CAs to particular applications by varying the polymer choice. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers [source] Signal fluctuations induced by non-T1 -related confounds in variable TR fMRI experimentsJOURNAL OF MAGNETIC RESONANCE IMAGING, Issue 5 2009Shuowen Hu BS Abstract Purpose To assess and model signal fluctuations induced by non-T1 -related confounds in variable repetition time (TR) functional magnetic resonance imaging (fMRI) and to develop a compensation procedure to correct for the non-T1 -related artifacts. Materials and Methods Radiofrequency disabled volume gradient sequences were effected at variable offsets between actual image acquisitions, enabling perturbation of the measurement system without perturbing longitudinal magnetization, allowing the study of non-T1 -related confounds that may arise in variable TR experiments. Three imaging sessions utilizing a daily quality assurance (DQA) phantom were conducted to assess the signal fluctuations, which were then modeled as a second-order system. A modified projection procedure was implemented to correct for signal fluctuations arising from non-T1 -related confounds, and statistical analysis was performed to assess the significance of the artifacts with and without compensation. Results Assessment using phantom data reveals that the signal fluctuations induced by non-T1 -related confounds was consistent in shape across the phantom and well-modeled by a second-order system. The phantom exhibited significant spurious detections (at P < 0.01) almost uniformly across the central slices of the phantom. Conclusion Second-order system modeling and compensation of non-T1 -related confounds achieves significant reduction of spurious detection of fMRI activity in a phantom. J. Magn. Reson. Imaging 2009;29:1234,1239. © 2009 Wiley-Liss, Inc. [source] A quantitative study of factors affecting in vivo bioluminescence imagingLUMINESCENCE: THE JOURNAL OF BIOLOGICAL AND CHEMICAL LUMINESCENCE, Issue 5 2008Kemi Cui Abstract In vivo bioluminescence imaging (BLI) has the advantages of high sensitivity and low background. By counting the number of photons emitted from a specimen, BLI can quantify biological events such as tumour growth, gene expression and drug response. The intensities and kinetics of the BL signal are affected by many factors and may confound the quantitative results acquired from consecutive imaging sessions or different specimens. We used three different mouse models of tumours to examine whether anaesthetics, positioning and tumour growth may affect the consistency of the BL signal. The results showed that BLI signal could be affected by different anaesthetics and repetitive positioning. Using the same anaesthetics produced consistent peak times, while other factors were held constant. However, as the tumours grew the peak times shifted and the time course of BL signals had different shapes, depending on the positioning of the mice. The data indicate that a carefully designed BLI experiment is required to generate optimal and consistent results. Copyright © 2008 John Wiley & Sons, Ltd. [source] Fast mapping of myocardial blood flow with MR first-pass perfusion imagingMAGNETIC RESONANCE IN MEDICINE, Issue 6 2008Thomas A. Goldstein Abstract Accurate and fast quantification of myocardial blood flow (MBF) with MR first-pass perfusion imaging techniques on a pixel-by-pixel basis remains difficult due to relatively long calculation times and noise-sensitive algorithms. In this study, Zierler's central volume principle was used to develop an algorithm for the calculation of MBF with few assumptions on the shapes of residue curves. Simulation was performed to evaluate the accuracy of this algorithm in the determination of MBF. To examine our algorithm in vivo, studies were performed in nine normal dogs. Two first-pass perfusion imaging sessions were performed with the administration of the intravascular contrast agent Gadomer at rest and during dipyridamole-induced vasodilation. Radiolabeled microspheres were injected to measure MBF at the same time. MBF measurements in dogs using MR methods correlated well with the microsphere measurements (R2 = 0.96, slope = 0.9), demonstrating a fair accuracy in the perfusion measurements at rest and during the vasodilation stress. In addition to its accuracy, this method can also be optimized to run relatively fast, providing potential for fast and accurate myocardial perfusion mapping in a clinical setting. Magn Reson Med, 2008. © 2008 Wiley-Liss, Inc. [source] Improvement of quantification of myocardial first-pass perfusion mapping: A temporal and spatial wavelet denoising methodMAGNETIC RESONANCE IN MEDICINE, Issue 2 2006Thomas A. Goldstein Abstract Mapping of myocardial blood flow (MBF) with first-pass perfusion imaging is becoming an important tool in the study of coronary artery disease. In this study a wavelet-based denoising method was developed to improve the accuracy of pixel-by-pixel MBF maps. We performed an in vivo study in five stenotic dogs with 70% stenosis in the left coronary arteries. First-pass perfusion imaging sessions were performed by administering the intravascular contrast agent Gadomer at rest and during dipyridamole-induced vasodilation. Color microspheres (MS) were injected into the dogs to measure MBF at the same time. After denoising was performed, the signal-to-noise ratio (SNR) of the first-pass perfusion image improved by approximately 180%, whereas spatial variation of MBF maps decreased 38%. It was also found that the correlation of MBFs measured by MRI with the MS method indicates a significant improvement with the denoising method (R2 increased from 0.24 to 0.78, P < .001). This suggests that the wavelet denoising method may be an effective way to increase the accuracy of pixel-by-pixel MBF quantification and reduce spatial variation, and may be applicable to other forms of noise-sensitive image analysis. Magn Reson Med, 2006. © 2006 Wiley-Liss, Inc. [source] Progressive brain changes in schizophrenia: a 1-year follow-up study of diffusion tensor imagingACTA NEUROPSYCHIATRICA, Issue 6 2009Miho Ota Objective: Recent cross-sectional studies suggest that brain changes in schizophrenia are progressive during the course of the disorder. However, it remains unknown whether this is a global process or whether some brain areas are affected to a greater degree. The aim of this study was to examine the longitudinal brain changes in patients with chronic older schizophrenia by magnetic resonance imaging (MRI). Methods: Three-dimensional (3D) T1-weighted and diffusion tensor (DT) MRI were performed twice on each of 16 chronic older schizophrenia patients (mean age = 58.1 ± 6.7 years ) with an interval of 1 year between imaging sessions. To clarify the longitudinal morphological and white matter changes, volume data and normalised diffusion tensor imaging (DTI) metrics were compared between the first and follow-up studies using a paired t -test. Results: Focal cortical volume loss was observed in the left prefrontal lobe and anterior cingulate on volumetric study. In addition, DTI metrics changed significantly at the bilateral posterior superior temporal lobes, left insula, genu of the corpus callosum and anterior cingulate. Conclusion: There are ongoing changes in the brains of schizophrenic patients during the course of the illness. Discrepancies between volume data and DTI metrics may indicate that the pattern of progressive brain changes varies according to brain region. 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