نتایج جستجو برای: radiochemical

تعداد نتایج: 1803  

Journal: :Dalton transactions 2014
Trevor J Ferris Putthiporn Charoenphun Levente K Meszaros Gregory E D Mullen Philip J Blower Michael J Went

The increasing availability of the long half-life positron emitter Zr-89 (half life 78.4 h) suggests that it is a strong candidate for cell labelling and hence cell tracking using positron emission tomography. The aim was to produce a range of neutral ZrL4 lipophilic complexes for cell labelling which could be prepared under radiopharmaceutical conditions. This was achieved when the ligand was ...

Journal: :Organic & biomolecular chemistry 2015
Mathieu André Sophie Besse Jean-Michel Chezal Emmanuelle Mounetou

In the development of our melanoma-selective delivery approach, three preselected conjugates of 5-iodo-2'-deoxyuridine (IUdR) to the ICF01012 melanoma-carrier were radiolabelled with iodine-125, and their in vivo distribution profile was determined. A radioiodination method for the conjugate 1a and its PEGylated derivatives 1b-c was developed via electrophilic iododestannylation in good radioch...

Journal: :Radioisotopes 1984
H Saji A Tanaka Y Magata K Enoki T Tokui Y Nishihara M Senda Y Yonekura A Yokoyama K Torizuka

Biological significance of 11C-glucose purity has been a controversial matter. In order to understand the contribution of impurities contained in the photosynthetic 11C-glucose, its analysis and biodistribution in mice was studied. Studies indicated the interference of impurities, particularly 11C-fructose in the injectate, with the quantitative evaluation of glucose metabolic rate in brain. Fu...

Journal: :Bioorganic & medicinal chemistry letters 2013
Alessandra Monaco Vincent Zoete Gian Carlo Alghisi Curzio Rüegg Olivier Michelin John Prior Leonardo Scapozza Yann Seimbille

The development of RGD-based antagonist of αvβ3 integrin receptor has enhanced the interest in PET probes to image this receptor for the early detection of cancer, to monitor the disease progression and the response to therapy. In this work, a novel prosthetic group (N-(4-fluorophenyl)pent-4-ynamide or FPPA) for the (18)F-labeling of an αvβ3 selective RGD-peptide was successfully prepared. [(18...

2016
Elise Verger Pierre Drion Geneviève Meffre Claire Bernard Luc Duwez Nicolas Lepareur Olivier Couturier François Hindré Roland Hustinx Franck Lacoeuille

PURPOSE This work aims to develop, validate and optimize the radiolabeling of Starch-Based Microparticles (SBMP) by 188Re and 68Ga in the form of ready-to-use radiolabeling kits, the ultimate goal being to obtain a unique theranostic vector for the treatment of Hepatocellular Carcinoma. METHODS Optimal labeling conditions and composition of freeze-dried kits were defined by monitoring the rad...

Keyvan Sadri, Mohammad Hossein Babaei Mostafa Gandomkar Reza Najafi Seyed Esmaeil Sadat Ebrahimi Seyed Rasoul Zakavi,

  Introduction: Radioimmunotherapy (RIT) is a very promising new therapy for the treatment of recurrent B-Cell non-Hodgkin's lymphoma (NHL). Iodine-131 is the most frequently used nuclide in clinical RIT, but its usefulness has been limited by dehalogenation of monoclonal antibodies labeled via conventional methods. To circumvent this problem, we have synthesized a tr...

A.R. Jalilian, F. Bolourinovin, F. Mirazizi, H. Nazem, H. Sadeghpour, J. Garousi,

Background: In order to diagnose the site of thrombi, radiolabeled streptokinase can be prepared. The radiolabeled compound can be used in imaging of thrombi in many cardiovascular diseases. Materials and Methods: Streptokinase was successively labeled with [67Ga]-gallium chloride using cyclic DTPA-dianhydride. The conjugation with DTPA was optimized for concentration, time and temperature foll...

Journal: :Nucleation and Atmospheric Aerosols 2021

Cancer is the second leading cause of death globally and increasing every year, including in Indonesia. Promethium-149 (149Pm) one beta-emitting (Eβ-max 1.07 MeV T1/2 2.21 days) radiolanthanides that can be used for therapeutic application. Radioisotope 149Pm produced with high specific activity was suitable labeling biomolecule as a targeted radiopharmaceutical cancer therapy. Radiochemical se...

Journal: :Journal of Radioanalytical and Nuclear Chemistry 1999

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