8 results on '"Muradian, I."'
Search Results
2. Large production system for hyperpolarized 129Xe for human lung imaging studies.
- Author
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Hersman FW, Ruset IC, Ketel S, Muradian I, Covrig SD, Distelbrink J, Porter W, Watt D, Ketel J, Brackett J, Hope A, Patz S, Hersman, F William, Ruset, Iulian C, Ketel, Stephen, Muradian, Iga, Covrig, Silviu D, Distelbrink, Jan, Porter, Walter, and Watt, David
- Abstract
Rationale and Objectives: Hyperpolarized gases such as (129)Xe and (3)He have high potential as imaging agents for functional lung magnetic resonance imaging (MRI). We present new technology offering (129)Xe production rates with order-of-magnitude improvement over existing systems, to liter per hour at 50% polarization. Human lung imaging studies with xenon, initially limited by the modest quantity and quality of hyperpolarized gas available, can now be performed with multiliter quantities several times daily.Materials and Methods: The polarizer is a continuous-flow system capable of producing large quantities of highly-polarized (129)Xe through rubidium spin-exchange optical pumping. The low-pressure, high-velocity operating regime takes advantage of the enhancement in the spin exchange rate provided by van der Waals molecules dominating the atomic interactions. The long polarizing column moves the flow of the gas opposite to the laser direction, allowing efficient extraction of the laser light. Separate sections of the system assure full rubidium vapor saturation and removal.Results: The system is capable of producing 64% polarization at 0.3 L/hour Xe production rate. Increasing xenon flow reduces output polarization. Xenon polarization was studied as a function of different system operating parameters. A novel xenon trapping design was demonstrated to allow full recovery of the xenon polarization after the freeze-thaw cycle. Delivery methods of the gas to an offsite MRI facility were demonstrated in both frozen and gas states.Conclusions: We demonstrated a new concept for producing large quantities of highly polarized xenon. The system is operating in an MRI facility producing liters of hyperpolarized gas for human lung imaging studies. [ABSTRACT FROM AUTHOR]- Published
- 2008
- Full Text
- View/download PDF
3. A system for open-access 3He human lung imaging at very low field.
- Author
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Ruset, I.C., Tsai, L.L., Mair, R.W., Patz, S., Hrovat, M.I., Rosen, M.S., Muradian, I., Ng, J., Topulos, G.P., Butler, J.P., Walsworth, R.L., and Hersman, F.W.
- Published
- 2006
- Full Text
- View/download PDF
4. Toward 13C hyperpolarized biomarkers produced by thermal mixing with hyperpolarized 129Xe.
- Author
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Lisitza N, Muradian I, Frederick E, Patz S, Hatabu H, and Chekmenev EY
- Subjects
- Magnetic Resonance Spectroscopy methods, Temperature, Biomarkers, Carbon Isotopes, Xenon Isotopes chemistry
- Abstract
The (13)C NMR signal of acetic acid 1-(13)C-AcH is enhanced by polarization transfer from hyperpolarized (129)Xe using a thermal mixing procedure. 1-(13)C-AcH acid and hyperpolarized (129)Xe are mixed as gases to disperse (129)Xe in the acetic acid. The mixture is frozen with liquid N(2) at 0.5 T. The magnetic field is then momentarily dropped to allow for exchange of spin polarization between (13)C and (129)Xe. After polarization exchange the magnetic field is raised to its original value and the mixture is thawed, resulting in a solution of polarization enhanced 1-(13)C-AcH. A (13)C nuclear spin polarization enhancement of 10 is observed compared to its thermal polarization at 4.7 T. This polarization enhancement is approximately three orders of magnitude lower than that predicted by theory. The discrepancy is attributed to the formation of either an inhomogeneous solid matrix and/or spin dynamics during polarization transfer. Despite the low polarization enhancement, this is the first report of polarization transfer from (129)Xe to (13)C nuclear spins achieved by thermal mixing for a proton-containing molecule of biomedical importance. If future work can increase the enhancement, this method will be useful in hyperpolarizing a wide range of (13)C enriched compounds important in biomedical and biophysical research.
- Published
- 2009
- Full Text
- View/download PDF
5. Human pulmonary imaging and spectroscopy with hyperpolarized 129Xe at 0.2T.
- Author
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Patz S, Muradian I, Hrovat MI, Ruset IC, Topulos G, Covrig SD, Frederick E, Hatabu H, Hersman FW, and Butler JP
- Subjects
- Administration, Inhalation, Adult, Humans, Image Enhancement methods, Pulmonary Diffusing Capacity physiology, Diffusion Magnetic Resonance Imaging methods, Lung physiology, Xenon Isotopes chemistry
- Abstract
Rationale and Objectives: Using a novel (129)Xe polarizer with high throughput (1-2 L/hour) and high polarization (approximately 55%), our objective was to demonstrate and characterize human pulmonary applications at 0.2T. Specifically, we investigated the ability of (129)Xe to measure the alveolar surface area per unit volume of gas, S(A)/V(gas)., Materials and Methods: Variable spin echo time (TE) gradient and radiofrequency (RF) echoes were used to obtain estimates of the lung's contribution to both T(2)* and T(2). Standard multislice ventilation images were obtained and signal-to-noise ratio (SNR) determined. Whole-lung, time-dependent measurements of (129)Xe diffusion from gas to septal tissue were obtained with a chemical shift saturation recovery (CSSR) method. Four healthy subjects were studied, and the Butler et al CSSR formalism (J Phys Condensed Matter 2002; 14:L297-L304) was used to calculate S(A)/V(gas). A single-breath version of the xenon transfer contrast (SB-XTC) method was implemented and used to image (129)Xe diffusion between alveolar gas and septal tissue. A direct comparison of CSSR and SB-XTC was performed., Results: T(2)*=135+/-29 ms amd T(2)=326.2+/-9.5 ms. Maximum SNR=36 for ventilation images from inhalation of 1L 86% (129)Xe and voxel volume =0.225 mL. CSSR analysis showed S(A)/V(gas) decreased with increasing lung volume in a manner very similar to that observed from histology measurements; however, the absolute value of S(A)/V(gas) was approximately 40% smaller than histology values. SB-XTC images in different postures demonstrate gravitationally dependent values. Initial comparison of CSSR with XTC showed fairly good agreement with expected ratios., Conclusions: Hyperpolarized (129)Xe human imaging and spectroscopy are very promising methods to provide functional information about the lung.
- Published
- 2008
- Full Text
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6. Hyperpolarized (129)Xe MRI: a viable functional lung imaging modality?
- Author
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Patz S, Hersman FW, Muradian I, Hrovat MI, Ruset IC, Ketel S, Jacobson F, Topulos GP, Hatabu H, and Butler JP
- Subjects
- Administration, Inhalation, Animals, Equipment Design, Humans, Lasers, Magnetic Resonance Imaging instrumentation, Oxygen blood, Oxygen Consumption physiology, Partial Pressure, Pulmonary Alveoli anatomy & histology, Pulmonary Diffusing Capacity physiology, Rubidium chemistry, Safety, Technology, Radiologic instrumentation, Ventilation-Perfusion Ratio physiology, Contrast Media, Image Enhancement methods, Lung physiology, Magnetic Resonance Imaging methods, Xenon Isotopes chemistry
- Abstract
The majority of researchers investigating hyperpolarized gas MRI as a candidate functional lung imaging modality have used (3)He as their imaging agent of choice rather than (129)Xe. This preference has been predominantly due to, (3)He providing stronger signals due to higher levels of polarization and higher gyromagnetic ratio, as well as its being easily available to more researchers due to availability of polarizers (USA) or ease of gas transport (Europe). Most researchers agree, however, that hyperpolarized (129)Xe will ultimately emerge as the imaging agent of choice due to its unlimited supply in nature and its falling cost. Our recent polarizer technology delivers vast improvements in hyperpolarized (129)Xe output. Using this polarizer, we have demonstrated the unique property of xenon to measure alveolar surface area noninvasively. In this article, we describe our human protocols and their safety, and our results for the measurement of the partial pressure of pulmonary oxygen (pO(2)) by observation of (129)Xe signal decay. We note that the measurement of pO(2) by observation of (129)Xe signal decay is more complex than that for (3)He because of an additional signal loss mechanism due to interphase diffusion of (129)Xe from alveolar gas spaces to septal tissue. This results in measurements of an equivalent pO(2) that accounts for both traditional T(1) decay from pO(2) and that from interphase diffusion. We also provide an update on new technological advancements that form the foundation for an improved compact design polarizer as well as improvements that provide another order-of-magnitude scale-up in xenon polarizer output.
- Published
- 2007
- Full Text
- View/download PDF
7. A System for Open-Access He Human Lung Imaging at Very Low Field.
- Author
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Ruset IC, Tsai LL, Mair RW, Patz S, Hrovat MI, Rosen MS, Muradian I, Ng J, Topulos GP, Butler JP, Walsworth RL, and Hersman FW
- Abstract
We describe a prototype system built to allow open-access very-low-field MRI of human lungs using laser-polarized (3)He gas. The system employs an open four-coil electromagnet with an operational B(0) field of 4 mT, and planar gradient coils that generate gradient fields up to 0.18 G/cm in the x and y direction and 0.41 G/cm in the z direction. This system was used to obtain (1)H and (3)He phantom images and supine and upright (3)He images of human lungs. We include discussion on challenges unique to imaging at 50 -200 kHz, including noise filtering and compensation for narrow-bandwidth coils.
- Published
- 2006
- Full Text
- View/download PDF
8. [Rare clinical syndromes in ischemic cerebral infarction].
- Author
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Virozub EI, Evtushenko SK, Muradian IZ, and Zykova IA
- Subjects
- Adult, Aged, Aphasia diagnosis, Female, Humans, Hypotension, Orthostatic diagnosis, Male, Middle Aged, Paralysis diagnosis, Aphasia etiology, Arm innervation, Brain Ischemia complications, Cerebral Infarction complications, Hypotension, Orthostatic etiology, Leg innervation, Paralysis etiology
- Published
- 1990
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