Academic literature on the topic 'DOTA-Gd'
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Journal articles on the topic "DOTA-Gd"
LE MIGNON, MARIE-MADELEINE, CATHERINE CHAMBON, STEVE WARRINGTON, ROGER DAVIES, and BRUNO BONNEMAIN. "Gd-DOTA." Investigative Radiology 25, no. 8 (August 1990): 933–37. http://dx.doi.org/10.1097/00004424-199008000-00010.
Full textZhan, Youyang, Rong Xue, Mengchao Zhang, Chuanling Wan, Xiaojing Li, Fengkui Pei, Changjiang Sun, and Lin Liu. "Synthesis and Evaluation of a Biocompatible Macromolecular Gadolinium Compound as a Liver-Specific Contrast Agent for MRI." Australian Journal of Chemistry 70, no. 3 (2017): 307. http://dx.doi.org/10.1071/ch16347.
Full textDemine, Stéphane, Alexander Balhuizen, Vinciane Debaille, Lieke Joosten, Maïté Fereau, Satya Chilla, Isabelle Millard, et al. "Imaging of Human Insulin Secreting Cells with Gd-DOTA-P88, a Paramagnetic Contrast Agent Targeting the Beta Cell Biomarker FXYD2γa." Molecules 23, no. 9 (August 21, 2018): 2100. http://dx.doi.org/10.3390/molecules23092100.
Full textHodler, J., J. Orellano, S. Thurnher, B. Marincek, and G. von Schulthess. "Gd-DOTA bei muskuloskelettalen Erkrankungen." RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren 153, no. 11 (November 1990): 535–39. http://dx.doi.org/10.1055/s-2008-1033433.
Full textGazzi, Thais P., Luiz A. Basso, Diógenes S. Santos, and Pablo Machado. "A greener approach toward gadolinium-based contrast agents." RSC Adv. 4, no. 19 (2014): 9880–84. http://dx.doi.org/10.1039/c4ra00272e.
Full textGranata, Vincenza, Marco Cascella, Roberta Fusco, Nicoletta dell’Aprovitola, Orlando Catalano, Salvatore Filice, Vincenzo Schiavone, Francesco Izzo, Arturo Cuomo, and Antonella Petrillo. "Immediate Adverse Reactions to Gadolinium-Based MR Contrast Media: A Retrospective Analysis on 10,608 Examinations." BioMed Research International 2016 (2016): 1–6. http://dx.doi.org/10.1155/2016/3918292.
Full textKe, Xian-Sheng, Juan Tang, Zi-Shu Yang, and Jun-Long Zhang. "β-conjugation of gadolinium(III) DOTA complexes to zinc(II) porpholactol as potential multimodal imaging contrast agents." Journal of Porphyrins and Phthalocyanines 18, no. 10n11 (October 2014): 950–59. http://dx.doi.org/10.1142/s1088424614500758.
Full textBeaumont, Marine, Benjamin Lemasson, Régine Farion, Christoph Segebarth, Chantal Rémy, and Emmanuel L. Barbier. "Characterization of Tumor Angiogenesis in Rat Brain Using Iron-Based Vessel Size Index MRI in Combination with Gadolinium-Based Dynamic Contrast-Enhanced MRI." Journal of Cerebral Blood Flow & Metabolism 29, no. 10 (July 8, 2009): 1714–26. http://dx.doi.org/10.1038/jcbfm.2009.86.
Full textRandolph, Lyndsay M., Clare L. M. LeGuyader, Michael E. Hahn, Christopher M. Andolina, Joseph P. Patterson, Robert F. Mattrey, Jill E. Millstone, Mauro Botta, Miriam Scadeng, and Nathan C. Gianneschi. "Polymeric Gd-DOTA amphiphiles form spherical and fibril-shaped nanoparticle MRI contrast agents." Chemical Science 7, no. 7 (2016): 4230–36. http://dx.doi.org/10.1039/c6sc00342g.
Full textBourrinet, Philippe, Eric Martel, Abdel I. El Amrani, Pascal Champeroux, Serge Richard, Nicolas Fauchou, Franck Le Coz, Milo Drici, Bruno Bonnemain, and Sophie Gaillard. "Cardiovascular Safety of Gadoterate Meglumine (Gd-DOTA)." Investigative Radiology 42, no. 2 (February 2007): 63–77. http://dx.doi.org/10.1097/01.rli.0000251565.61487.1a.
Full textDissertations / Theses on the topic "DOTA-Gd"
Kaufels, Nicola. "MRT-Myokarduntersuchungen zur Vitalität und Perfusion mit P792 im Vergleich zu Gd-DOTA an Schweinen nach Induktion eines akuten Herzinfarktes /." Berlin : Mensch-und-Buch-Verl, 2005. http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&doc_number=014780625&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA.
Full textKaufels, Nicola [Verfasser]. "MRT-Myokarduntersuchungen zur Vitalität und Perfusion mit P792 im Vergleich zu Gd-DOTA an Schweinen nach Induktion eines akuten Herzinfarktes / vorgelegt von Nicola Kaufels." Berlin : Mensch-und-Buch-Verl, 2006. http://d-nb.info/979208319/34.
Full textPerrat, Emilie. "Impacts environnementaux des agents de contraste à base de Gadolinium : situation locale, approche cellulaire et in vivo." Thesis, Université de Lorraine, 2017. http://www.theses.fr/2017LORR0370/document.
Full textThe increasing use of Gadolinium-based Contrast Agents (Gd-CA) for Magnetic Resonance Imaging (MRI) results in their rejection in Waste Water Treatment Plants (WWTPs). Due to the lack of specific recycling process in European WWTPs, these pharmaceutical produces enter the aquatic environment from river to tap water. The effects of Gd-CA in aquatic media have been not studied yet. The lack of knowledge about these effects highlighted the need to study their environmental impacts on aquatic organisms. In this context, we decided to measure anthropogenic concentrations of Gd in the aquatic environment in the Lorraine region (France) closed to WWTPs outputs and catchment areas used for drinking water. Our measurements underlined the presence of anthropogenic Gd on all the collected samples at concentrations ranging from few ng/L to several dozen of µg/L. In this research we focused on the effects of the most frequently used Gd-CA, the gadoteric acid (Gd-DOTA - Dotarem®) which is also the most stable one. Several representative species of aquatic environment were selected for ecotoxicological assays: i.e. unicellular green microalgae (Chlorella vulgaris and Pseudokirchneriella subcapitata), microcrustacean (Daphnia magna) and aquatic vertebrate (Danio rerio). Assays were conducted in laboratory under controlled conditions as well as in situ. Gd-DOTA accumulation was measured in the tissues of the different organisms. Environmental realistic concentrations of Gd-CA were used to assess their effects at the individual level by means of growth, reproduction and mortality measurements. The Gd-DOTA accumulation was also measured in bivalves’ tissues (Corbicula fluminea and Dresseina rostriformis bugensis) and compared to Gd ones in situ in these organisms. Physiological responses were assessed based on a battery of 11 complementary biomarkers measured in the digestive gland and in the gills of both bivalve species. At cellular level, the effects of Gd-DOTA were studied in vitro on D. rerio fibroblasts (ZF4 – ATCC-2050). Indirect ecotoxicological effects of Gd-CA and of Gd-DOTA especially have been highlighted at all biological levels. Accumulation of Gd-DOTA was observed in bivalves only, but defense systems were mobilized in all organisms to limit toxicity. Our results demonstrated that following both research on ecotoxicological effects of the Gd-CA and evolution of their concentrations in aquatic ecosystem are necessary to assess more precisely their environmental risk and to propose solutions for their environmental management
Schürholz, Hellmut Andreas [Verfasser], and Arno [Akademischer Betreuer] Bücker. "Vergleich der experimentellen Kontrastmittel P792 und P846 gegenüber Gd-DOTA hinsichtlich Kontrastmittelanreicherung und Kontrast-zu-Rausch-Verhältnis bei experimentell erzeugten Hirngliomen in Ratten mittels MRT bei 3T / Hellmut Andreas Schürholz. Betreuer: Arno Bücker." Saarbrücken : Saarländische Universitäts- und Landesbibliothek, 2011. http://d-nb.info/1051434513/34.
Full textAit, Sarkouh Rafik. "Synthèse de conjugués avec la toxine de Shiga pour des thérapies anticancéreuses ciblées et la détection de tumeurs par IRM." Thesis, Paris 5, 2012. http://www.theses.fr/2012PA05P641.
Full textPas de résumé en anglais
Lei, Iok-Sun, and 李毓璇. "Synthesis of DOTA-OIA and Physicochemical Characterization of Its Gd(III) Complex." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/03589625003821062214.
Full text高雄醫學大學
醫藥暨應用化學研究所
98
This research is focusing on developing the Gd ligands which have potential to targeting contrast agent. The carboxylic acid terminal of 5-(1-bromoacatamido)-2,3-dihydro-1-oxo-1H-indene-2-acetic acid can be modified with appropriate peptide or other target specific residue to develop target specific MRI contrast agent for potential application in tumor imaging. This research is to develop a ligand which has the character of optimal lipophilicity. The calculated value obtained for [Gd(DOTA-OIA)] (miLogP = -4.147) is similar to that of MS-325 (-4.575) which is clinically used blood pool MRI contrast agent. Together with the help of 1H-NMR、and the identification of LC-MS. I have successfully synthesized 5-(1-bromoacatamido) -2,3- dihydro-1- oxo-1H-indene-2-acetic acid. With the result of identification of LC-MS, its molecule weight is 327.93 which meets the expectation value. The synthesis of [Gd(DOTA-OIA)] is still in progress and expected to complete soon. The synthesis of [Gd(DOTA-OIA)] will be completed and get the spectral of last step. By using 20MHz relaxometor to measure the relaxivity.
Wang, Yan-Syun, and 王彥勛. "Synthesis and Characterization of [Gd(DOTA-iRGD)] as a Tumor Specific MRI Contrast Agent." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/09960076364742716921.
Full text國立交通大學
生物科技學系
99
The MRI contrast agents bearing peptides as target moiety can be used to differentiate tumor tissue with normal one, the contrast of MR imaging will evaluate by specific binding to tumor tissue. iRGD is a cyclic peptide sequence compose of nine amino acid , with ability of brining material to αv integrin over expression or angiogenic endothelial cells and be uptake by cell. iRGD bearing MR contrast agent [Gd(DOTA-iRGD)] is designed and synthesized, expect it will evaluate the contrast of MR imaging by cell internalize and discuss it chemical and physical property. Relaxivity (r1) of [Gd(DOTA- iRGD)] under 20 MHz, 37.0 ± 0.1 ℃ is 4.91 ± 0.03 mM-1s-1. In cytotoxicity assay, [Gd(DOTA-iRGD)] induce apoptosis of PC-3, an αv integrin over expression cell line, but has no significant effect to lower expression HT-1080 cell line even at high concentration. In vitro MR imaging show that PC-3 cell line can evaluate more contrast than αv integrin lower expression HT-1080 cell line.
Fontes, André Filipe Gomes Soares. "DOTA-based Ga(III) and Gd(III) chelates for medical imaging (PET, SPECT and MRI)." Doctoral thesis, 2015. http://hdl.handle.net/1822/38710.
Full textThe work developed aimed at the design, synthesis and characterization of new Gd(III) and Ga(III) chelates with potential application as imaging probes. The initial part of the work is focused on the synthesis of new DOTA-based bifunctional ligands. The chelator DOTA-AHA (1,4,7,10-tetraazacyclododecane-1-[(6-amino)hexanoic]- 4,7,10-triacetic acid) was successfully synthesized and characterized. This ligand was the starting point for the development of three sets of molecular constructs, which include dimeric ligands, PEGylated chelators and c(RGDWK) peptide bioconjugates. The Gd(III) chelates of DOTA-AHA, dimeric ligands and DOTA-AHA PEGylated ligands were obtained. All Gd(III) chelates were studied by variable temperature 1H NMRD (nuclear magnetic relaxation dispersion) and 17O NMR (nuclear magnetic resonance) spectroscopy in order to measure the relaxivity and the parameters that govern it. Gd(DOTA-AHA) and the binuclear chelates form weakly bound aggregates and even if the aggregates contain only 10 to 15% of the total amount of Gd(III) ions a marked increase in relaxivity between 30 and 100 MHz is observed. PEGylation did not show to be a very efficient process for relaxivity improvement. Despite the moderate water exchange rates of the PEGylated Gd(III) chelates and the high global rotational correlation times, these chelates present lower relaxivity values than the binuclear chelates. The distance between the two Gd(III) centers in the binuclear compounds has been determined by double electron-electron resonance (DEER) experiments and by molecular modelling studies giving comparable distances. 1H NMR spectra of paramagnetic lanthanide chelates of DOTA-A(PEG750)HA were recorded at different temperatures. The data obtained gave information on the structure and dynamics of the chelates in solution. In vitro studies with 67Ga-radiolabeled DOTA-AHA and DOTA-A(PEG750)HA showed that both chelates are extremely hydrophilic. The lack of biospecificity of 67Ga(DOTA-AHA) and [67Ga(DOTA-A(PEG750)HA)]- is revealed by their biodistribution profiles, which show that both radiolabeled chelates have significant uptake in major tissues.
O trabalho desenvolvido teve como objectivo o desenho, síntese e caracterização de novos quelatos de Gd(III) e Ga(III) com potencial aplicação como agentes de imagem. A parte inicial do trabalho focou-se na síntese de novos ligandos funcionais do tipo DOTA. O ligando DOTA-AHA (ácido 1,4,7,10-tetraazaciclododecano-1-[(6- amino)hexanóico]-4,7,10-triacético) foi sintetizado e caracterizado com sucesso. Este ligando foi o ponto de partida para o desenvolvimento de ligandos diméricos, ligandos PEGuilados e bioconjugados com o péptido c(RGDWK). Preparam-se os quelatos de Gd(III) do ligando DOTA-AHA, dos ligandos diméricos e dos ligandos PEGuilados. Todos os quelatos de Gd(III) foram estudados por DRMN (dispersão de relaxação magnética nuclear) e RMN (ressonância magnética nuclear) de 17O, de modo a obter os valores de relaxividade e os parâmetros que a afectam. O quelato Gd(DOTA-AHA) e os quelatos binucleares formam agregados fracamente ligados e apesar de os agregados só conterem 10 a 15% da quantidade total de iões Gd(III) verifica-se um aumento acentuado na relaxividade para frequências entre 30 e 100 MHz. A PEGuilação mostrou ser um processo pouco eficiente para melhorar a relaxividade. Apesar das constantes de troca de água dos respectivos complexos de Gd(III) se mostrarem consideráveis e dos seus elevados tempos de correlação rotacional globais, estes quelatos apresentam valores de relaxividade inferiores à dos quelatos binucleares. A distância entre os dois centros de Gd(III) nos compostos binucleares foi determinada por ressonância dupla electrão-electrão (RDEE) e por estudos de modelação molecular, tendo sido obtidos resultados comparáveis. Estudos de 1H RMN dos quelatos de DOTA-A(PEG750)HA com lantanídeos paramagnéticos foram efectuados a diferentes temperaturas. Os dados recolhidos forneceram informação sobre a estrutura e dinâmica destes quelatos em solução. Estudos in vitro com os ligandos DOTA-AHA e DOTA-A(PEG750)HA marcados com 67Ga mostraram que ambos os quelatos são extremamente hidrofílicos. A falta de bioespecificidade de 67Ga(DOTA-AHA) e [67Ga(DOTA-A(PEG750)HA)]- é evidenciada através dos perfis de biodistribuição destes radiocomplexos.
Fundação para a Ciência e Tecnologia PhD grant SFRH /BD/63676/2009.
Liu, Wan-Chun, and 劉婉淳. "The synthetic and characteristic study of 19F MRI contrast agent [Gd(DOTA-CF3)] to detect H2S." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/69612816342192588141.
Full text國立交通大學
生物資訊及系統生物研究所
103
H2S, an important small molecule in the body, performs an indispensable role in many biological activities. H2S detection using MRI in human body plays a crucial role in Molecular Imaging clinical trial with potential outcome. In this study, we designed a Gadolinium complex [Gd(DOTA-CF3)] containing a hydrophilic ligand with fluorine as the functional site to detect the H2S. Upon reaction with biothiols the PRE effect in complex enhances the paramagnetism between Gadolinium and fluorine and this helps to shorten 19F MRI signals which can be detected easily using 19F-NMR. Results showed that [Gd(DOTA-CF3)] selectively detects H2S among the biothiols .
Reinländer, Claudia [Verfasser]. "MRT-Kontrastmittel für das Knochenmark : vergleichende experimentelle Untersuchungen von USPIO, SPIO und Gd-DOTA / vorgelegt von Claudia Reinländer." 2003. http://d-nb.info/969510896/34.
Full textBook chapters on the topic "DOTA-Gd"
Kravtzoff, Roger, Eric Urvoase, Catherine Chambon, and Claude Ropars. "Gd-DOTA Loaded into Red Blood Cells, a New Magnetic Resonance Imaging Contrast Agents for Vascular System." In The Use of Resealed Erythrocytes as Carriers and Bioreactors, 347–54. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3030-5_42.
Full textParizel, P. M., H. R. Degryse, J. Gheuens, J. J. Martin, M. Van Vyve, C. De la Porte, P. Selosse, P. Van de Heyning, and A. M. De Schepper. "Initial Clinical Results with the Paramagnetic MR Contrast Agent Gd-DOTA in the Diagnosis of Central Nervous System Lesions." In Imaging of Brain Metabolism Spine and Cord Interventional Neuroradiology Free Communications, 559–62. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74337-5_159.
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