Results 191 to 200 of about 1,392 (217)
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Isolation of actinium-225 for medical purposes
Radiochemistry, 2015A procedure is described for isolation and purification of 225Ac as a 229Th daughter decay product using ion exchange. The process includes the following steps: separation of 229Th from a mixture of 225Ac and 225Ra (225Ac precursor) using an anion-exchange resin; separation of 225Ac and 225Ra using a cation-exchange resin; purification of 225Ac to ...
A. A. Kotovskii +6 more
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Production of actinium-225 for alpha particle mediated radioimmunotherapy
Applied Radiation and Isotopes, 2005The initial clinical trials for treatment of acute myeloid leukemia have demonstrated the effectiveness of the alpha emitter (213)Bi in killing cancer cells. Bismuth-213 is obtained from a radionuclide generator system from decay of 10-days (225)Ac parent.
Rose A, Boll +2 more
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Improved in Vivo Stability of Actinium-225 Macrocyclic Complexes
Journal of Medicinal Chemistry, 1999The favorable nuclear properties of actinium-225 ((225)Ac) have led to proposal of this isotope for use in radioimmunotherapy. In an effort to reduce the toxicity of free (225)Ac, a series of ligands were evaluated for stability in vivo. Loss of (225)Ac from acyclic chelating agents resulted in high liver uptake and poor whole body clearance.
K A, Deal +4 more
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Actinium-225 Prostate-specific Membrane Antigen Theranostics: Will α Beat β?
European Urology, 2021Optimisation of prostate-specific membrane antigen (PSMA) based radioligand therapy (RLT) requires a focus on prospective trials.
Nattakorn Dhiantravan +2 more
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Carboxylate-derived calixarenes with high selectivity for actinium-225
Chemical Communications, 1998The binding properties of two ligands, 5,11,17,23-tetra-tert-butyl-25,26,27,28-tetrakis(carboxymethoxy)calix[4]arene 1 and 5,11,17,23,29,35-hexa-tert-butyl-37,38,39,40,41,42- hexakiscarboxymethoxy)calix[6]arene 2, which show high selectivity for 225Ac3+ (an α-emitter with t1/2 = 10 days) over Na+, K+, Mg2+, Ca2+ and Zn2+ are described.
Xiaoyuan Chen +4 more
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NorthStar Perspectives for Actinium-225 Production at Commercial Scale
Current Radiopharmaceuticals, 2018Actinium-225, and its daughter Bismuth-213, have great promise in Alpha Immuno Therapy (AIT) for treatment of various disease modalities. Unfortunately, current production levels of actinium-225 do not support broad use of either actinium-225 or bismuth-213 in development or use for disease treatment.
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Actinium-225 Conjugates of MAb CC49 and Humanized ΔCH2CC49
Cancer Biotherapy and Radiopharmaceuticals, 2002Radioisotopes with moderate half-lives are essential for conventional radioimmunotherapy using tumor-selective MAbs which require days for localization. Actinium-225, with a half-life of 10 days and a yield of 4 alpha particles in its decay chain, may be an ideal choice for tumor-targeted radioimmunotherapy.
Stephen J, Kennel +4 more
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Growth and decay tables for radium-225 and actinium-225
Journal of Radioanalytical Chemistry, 1970To facilitate the use of225Ra as a yield tracer in radiochemical assays of226Ra and228Ra, growth and decay tables for225Ra, and its daughter225Ac, have been computed.
K. A. Smith, B. O. Bartlett
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Targeted alpha therapy with bismuth‐213 and actinium‐225: Meeting future demand
Journal of Labelled Compounds and Radiopharmaceuticals, 2019Targeted alpha therapy (TAT) is a promising approach for the treatment of cancer. The use of alpha emitters for cancer therapy has two distinct advantages over conventional therapies. The short range of alpha radiation in human tissue (less than 0.1 mm), corresponding to only a few cell diameters, allows selective killing of targeted cancer cells while
Frank Bruchertseifer +3 more
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ChemInform Abstract: Carboxylate‐Derived Calixarenes with High Selectivity for Actinium‐225.
ChemInform, 1998AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
X. CHEN, M. JI, D. R. FISHER, C. M. WAI
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