JP5362987B2 - 腫瘍イメージングの方法 - Google Patents
腫瘍イメージングの方法 Download PDFInfo
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- JP5362987B2 JP5362987B2 JP2007523505A JP2007523505A JP5362987B2 JP 5362987 B2 JP5362987 B2 JP 5362987B2 JP 2007523505 A JP2007523505 A JP 2007523505A JP 2007523505 A JP2007523505 A JP 2007523505A JP 5362987 B2 JP5362987 B2 JP 5362987B2
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- Prior art keywords
- pyruvate
- image
- lactate
- tumor
- alanine
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- G01R33/48—NMR imaging systems
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- G01R33/485—NMR imaging systems with selection of signals or spectra from particular regions of the volume, e.g. in vivo spectroscopy based on chemical shift information [CSI] or spectroscopic imaging, e.g. to acquire the spatial distributions of metabolites
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| US20100233096A1 (en) * | 2006-03-29 | 2010-09-16 | Lerche Mathilde H | Method to produce hyperpolarised carboxylates and sulphonates |
| US7202665B1 (en) | 2006-04-19 | 2007-04-10 | Wisconsin Alumni Research Foundation | Magnetic resonance spectroscopy of species with multiple peaks |
| CN101506679B (zh) * | 2006-08-18 | 2013-03-06 | 通用电气医疗集团股份有限公司 | 细胞死亡的13c-mr成像或波谱分析 |
| EP2051739A2 (en) * | 2006-08-18 | 2009-04-29 | GE Healthcare AS | Imaging medium comprising lactate and hyperpolarised 13c-pyruvate |
| KR20140144312A (ko) | 2006-08-30 | 2014-12-18 | 지이 헬스케어 에이에스 | 동적 핵 분극화 방법 및 이러한 방법에서 사용되는 화합물 및 조성물 |
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| US8812076B2 (en) * | 2006-11-21 | 2014-08-19 | General Electric Company | Proton decoupled hyperpolarized magnetic resonance imaging |
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| US7741844B2 (en) * | 2007-05-07 | 2010-06-22 | General Electric Company | Method and system for magnetic resonance imaging using labeled contrast agents |
| CN105054933A (zh) * | 2007-05-17 | 2015-11-18 | 通用电气公司 | 使用包含超极化13c-丙酮酸盐的成像介质使肿瘤分级的mr方法 |
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| WO2009129265A1 (en) | 2008-04-14 | 2009-10-22 | Huntington Medical Research Institutes | Methods and apparatus for pasadena hyperpolarization |
| US8763410B2 (en) * | 2008-04-21 | 2014-07-01 | General Electric Company | Method and apparatus for the dissolution and filtration of a hyperpolarized agent with a neutral dissolution media |
| US20110038802A1 (en) * | 2008-05-02 | 2011-02-17 | Zhong-Min Hu | Method of determining alanine transaminase (alt) activity by 13c-mr detection using hyperpolarised 13c-pyruvate |
| AU2010230330B2 (en) * | 2009-04-02 | 2015-06-25 | Ge Healthcare Limited | Use of a magnetic resonance imaging medium comprising hyperpolarized 13C pyruvate for the detection of inflammation or infection |
| US8968703B2 (en) | 2009-09-10 | 2015-03-03 | Ge Healthcare Limited | 13C-MR detection using hyperpolarised 13C-fructose |
| US9069098B2 (en) * | 2011-09-09 | 2015-06-30 | Schlumberger Technology Corporation | Three or more multiple figure-eight coils for NMR well-logging measurements with azimuthal directional sensitivity |
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| US9874622B2 (en) | 2013-09-27 | 2018-01-23 | General Electric Company | Hyperpolarized media transport vessel |
| DK3058375T3 (en) * | 2013-10-15 | 2019-04-08 | Univ Muenchen Tech | pH Biosensors based on compounds made of pyruvic acid for magnetic resonance imaging and spectroscopy and their applications |
| EP2863229A1 (en) * | 2013-10-15 | 2015-04-22 | Technische Universität München | pH-biosensors based on compounds with pH-sensitive enolic groups for magnetic resonance imaging and spectroscopy and their uses |
| KR101516634B1 (ko) * | 2014-07-09 | 2015-05-06 | 연세대학교 산학협력단 | 13c-자기공명분광영상을 이용한 암 환자의 치료 예후를 예측하는 방법 |
| WO2017147418A1 (en) | 2016-02-24 | 2017-08-31 | Ohio State Innovation Foundation | Methods and devices for contrast agent magnetic resonance imaging |
| CN109477872A (zh) * | 2016-03-10 | 2019-03-15 | 纪念斯隆凯特琳癌症中心 | 超极化微核磁共振系统和方法 |
| RU2634783C1 (ru) * | 2016-07-05 | 2017-11-03 | Федеральное государственное бюджетное учреждение "Национальный медицинский исследовательский центр онкологии имени Н.Н. Петрова" Министерства здравоохранения Российской Федерации | Способ дифференциальной диагностики образований молочной железы и мягких тканей |
| KR101939454B1 (ko) * | 2017-03-21 | 2019-01-16 | 전남대학교산학협력단 | 생체 내 과분극화 c13 피루베이트 자기공명분광법을 이용하여 새로운 정량적 생체지표를 통한 비알코올성 지방간질환 진단 방법 |
| KR102441674B1 (ko) * | 2017-11-21 | 2022-09-08 | 솔벡스 리미티드 라이어빌리티 컴퍼니 | 중수소화된 2-아미노-2-메틸프로피온산 및/또는 2-(n-메틸아미노)-2-메틸프로피온산을 포함하는, 종양성 질환의 자기공명진단을 위한 제제, 및 상기 제제를 이용한 진단방법 |
| RU2741212C1 (ru) * | 2020-03-12 | 2021-01-22 | Государственное автономное учреждение здравоохранения «Республиканский клинический онкологический диспансер Министерства здравоохранения Республики Татарстан» (ГАУЗ «РКОД МЗ РТ») | Способ диагностики злокачественных очаговых образований периферической зоны предстательной железы |
| RU2749126C1 (ru) * | 2020-05-06 | 2021-06-04 | Государственное автономное учреждение здравоохранения «Республиканский клинический онкологический диспансер Министерства здравоохранения Республики Татарстан» (ГАУЗ «РКОД МЗ РТ») | Способ дифференциальной диагностики очаговых образований предстательной железы |
| EP4140505A1 (en) * | 2021-08-26 | 2023-03-01 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. | Purified signal-enhanced contrast agents for magnetic resonance imaging |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01265950A (ja) * | 1988-04-15 | 1989-10-24 | Toshiba Corp | スペクトロスコピックイメージング装置 |
| DE3920433A1 (de) * | 1989-06-22 | 1991-01-03 | Philips Patentverwaltung | Kernresonanzabbildungsverfahren |
| US5323780A (en) * | 1992-08-07 | 1994-06-28 | University Of Florida Research Foundation, Inc. | Artifact-free imaging contrast agent |
| US5671741A (en) * | 1995-08-04 | 1997-09-30 | The Regents Of The University Of California | Magnetic resonance imaging technique for tissue characterization |
| CN1224502A (zh) * | 1996-03-29 | 1999-07-28 | 劳伦斯·伯克利国家实验室 | 利用超极化惰性气体对于核磁共振和磁共振成象质量的提高 |
| FI982069A7 (fi) * | 1996-03-29 | 1998-11-10 | Lawrence Berkeley Nat Laboratory | NMR:n ja MRI:n tehostaminen hyperpolaroitujen jalokaasujen läsnä olles sa |
| US6278893B1 (en) * | 1998-01-05 | 2001-08-21 | Nycomed Imaging As | Method of magnetic resonance imaging of a sample with ex vivo polarization of an MR imaging agent |
| DE102004011874B4 (de) * | 2004-03-11 | 2006-04-20 | Universitätsklinikum Freiburg | Verfahren zur Messung der Magnetresonanz (NMR) mittels Continuously Refocused Multiecho Spectroscopic Imaging |
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Also Published As
| Publication number | Publication date |
|---|---|
| ATE527552T1 (de) | 2011-10-15 |
| HK1107003A1 (en) | 2008-03-28 |
| WO2006011810A2 (en) | 2006-02-02 |
| PL1784227T3 (pl) | 2012-03-30 |
| CN102565735A (zh) | 2012-07-11 |
| EP1784227A2 (en) | 2007-05-16 |
| RU2369406C2 (ru) | 2009-10-10 |
| ES2372058T3 (es) | 2012-01-13 |
| MX2007001033A (es) | 2007-07-25 |
| EP1784227B1 (en) | 2011-10-05 |
| RU2007102845A (ru) | 2008-09-10 |
| AU2005267669B2 (en) | 2011-02-24 |
| CN101031811A (zh) | 2007-09-05 |
| IL180896A (en) | 2013-07-31 |
| KR101126952B1 (ko) | 2012-03-20 |
| CA2576202A1 (en) | 2006-02-02 |
| AU2005267669A1 (en) | 2006-02-02 |
| BRPI0513896A (pt) | 2008-05-20 |
| CN102565735B (zh) | 2016-02-10 |
| IL180896A0 (en) | 2007-07-04 |
| WO2006011810A3 (en) | 2006-04-13 |
| JP2008508023A (ja) | 2008-03-21 |
| ZA200701280B (en) | 2008-09-25 |
| KR20070061806A (ko) | 2007-06-14 |
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