نتایج جستجو برای: dnp pet

تعداد نتایج: 55700  

Objective(s): It is difficult to investigate the whole-body distribution of an orally administered drug by means of positron emission tomography (PET), owing to the short physical half-life of radionuclides, especially when 11C-labeled compounds are tested. Therefore, we aimed to examine the whole-body distribution of donepezil (DNP) as an acetylcholinesterase inhibitor by means of 11C-DNP PET ...

Journal: :asia oceania journal of nuclear medicine and biology 0
ikuko mochida department of nuclear medicine and tracer kinetics, osaka university graduate school of medicine osaka university graduate school of medicine immunology frontier research center eku shimosegawa department of molcular imaging in medicine, osaka university graduate school of medicine department of molcular imaging in medicine, osaka university graduate school of medicine yasukazu kanai department of nuclear medicine and tracer kinetics, osaka university graduate school of medicine department of molcular imaging in medicine, osaka university graduate school of medicine sadahiro naka department of nuclear medicine and tracer kinetics, osaka university graduate school of medicine osaka university hospital jun hatazawa department of nuclear medicine and tracer kinetics, osaka university graduate school of medicine osaka university graduate school of medicine immunology frontier research center keiko matsunaga department of nuclear medicine and tracer kinetics, osaka university graduate school of medicine osaka university graduate school of medicine immunology frontier research center

objective(s): it is difficult to investigate the whole-body distribution of an orally administered drug by means of positron emission tomography (pet), owing to the short physical half-life of radionuclides, especially when 11c-labeled compounds are tested. therefore, we aimed to examine the whole-body distribution of donepezil (dnp) as an acetylcholinesterase inhibitor by means of 11c-dnp pet ...

2017
Ikuko Mochida Eku Shimosegawa Yasukazu Kanai Sadahiro Naka Keiko Matsunaga Kayako Isohashi Genki Horitsugi Tadashi Watabe Hiroki Kato Jun Hatazawa

OBJECTIVES It is difficult to investigate the whole-body distribution of an orally administered drug by means of positron emission tomography (PET), owing to the short physical half-life of radionuclides, especially when 11C-labeled compounds are tested. Therefore, we aimed to examine the whole-body distribution of donepezil (DNP) as an acetylcholinesterase inhibitor by means of 11C-DNP PET ima...

Journal: :Circulation research 2013
Maulik D Majmudar Jeongsoo Yoo Edmund J Keliher Jessica J Truelove Yoshiko Iwamoto Brena Sena Partha Dutta Anna Borodovsky Kevin Fitzgerald Marcelo F Di Carli Peter Libby Daniel G Anderson Filip K Swirski Ralph Weissleder Matthias Nahrendorf

RATIONALE Myeloid cell content in atherosclerotic plaques associates with rupture and thrombosis. Thus, imaging of lesional monocytes and macrophages could serve as a biomarker of disease progression and therapeutic intervention. OBJECTIVE To noninvasively assess plaque inflammation with dextran nanoparticle (DNP)-facilitated hybrid positron emission tomography/magnetic resonance imaging (PET...

2014
Tadashi Watabe Sadahiro Naka Hayato Ikeda Genki Horitsugi Yasukazu Kanai Kayako Isohashi Mana Ishibashi Hiroki Kato Eku Shimosegawa Hiroshi Watabe Jun Hatazawa Israel Silman

PURPOSE Acetylcholinesterase (AChE) inhibitors have been used for patients with Alzheimer's disease. However, its pharmacokinetics in non-target organs other than the brain has not been clarified yet. The purpose of this study was to evaluate the relationship between the whole-body distribution of intravenously administered (11)C-Donepezil (DNP) and the AChE activity in the normal rat, with spe...

Journal: :Journal of nuclear medicine : official publication, Society of Nuclear Medicine 2014
Bernadette V Marquez Oluwatayo F Ikotun Jesse J Parry Buck E Rogers Claude F Meares Suzanne E Lapi

UNLABELLED Imaging agents based on peptide probes have desirable pharmacokinetic properties provided that they have high affinities for their target in vivo. An approach to improve a peptide ligand's affinity for its target is to make this interaction covalent and irreversible. For this purpose, we evaluated a (64)Cu-labeled affinity peptide tag, (64)Cu-L19K-(5-fluoro-2,4-dinitrobenzene) ((64)C...

2014
David A. Nathanson Amanda L. Armijo Michelle Tom Zheng Li Elizabeth Dimitrova Wayne R. Austin Julian Nomme Dean O. Campbell Lisa Ta Thuc M. Le Jason T. Lee Ryan Darvish Ari Gordin Liu Wei Hsiang-I Liao Moses Wilks Colette Martin Saman Sadeghi Jennifer M. Murphy Nidal Boulos Michael E. Phelps Kym F. Faull Harvey R. Herschman Michael E. Jung Johannes Czernin Arnon Lavie Caius G. Radu

Pharmacological targeting of metabolic processes in cancer must overcome redundancy in biosynthetic pathways. Deoxycytidine (dC) triphosphate (dCTP) can be produced both by the de novo pathway (DNP) and by the nucleoside salvage pathway (NSP). However, the role of the NSP in dCTP production and DNA synthesis in cancer cells is currently not well understood. We show that acute lymphoblastic leuk...

ژورنال: سلامت و محیط زیست 2017

Background and Objective:  Nitrophenols are among the most common and toxic compounds in industrial effluents that 2, 4 dinitrophenol (2, 4-DNP) is the most toxic compound in this group. The object of this study was to optimize the removal of 2, 4-DNP by thermally activated persulfate using a central composite design. Materials and Methods: This study was performed on a batch thermal reactor w...

2014
Gigin Lin Yuen-Li Chung

Cancer is known to have unique metabolic features such as Warburg effect. Current cancer therapy has moved forward from cytotoxic treatment to personalized, targeted therapies, with some that could lead to specific metabolic changes, potentially monitored by imaging methods. In this paper we addressed the important aspects to study cancer metabolism by using image techniques, focusing on opport...

Journal: :The Journal of Experimental Medicine 1974
Michael H. Julius Leonard A. Herzenberg

Cells binding DNP groups conjugated to fluoresceinated mouse gamma globulin ((F)DNP-MGG) were isolated from spleens of unprimed mice using a fluorescence-activated cell sorter (FACS). The isolated cells were specifically enriched at least 100-fold for anti-DNP precursor activity in an adoptive transfer assay as compared to unfractionated spleen. The fraction depleted of binding cells, although ...

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