New protein/peptide conjugates from novel PN ligands
AbstractAbstract
[en] Central to the production of new antibody-conjugated radioisotopes for diagnostic or therapeutic use is the development of fundamental main-group and inorganic chemistry. In this respect, 109Pd is an attractive isotope for radioimmunotherapy. It has a suitable half-life (13.1 hr) and suitable physical properties (β=1.02 MeV, 100%). It decays to a 40 sec half-life 109Ag which emits an 88 keV γ, making it suitable for imaging. The authors' approach to this endeavor involves the application of functionalized phosphorus hydrazides which form kinetically robust complexes with transition metals/metallic radioisotopes. The -COOH functionality in the bifunctional chelate after activation can be used to conjugate onto peptides/proteins to generate a new genre of metal-conjugated biomolecules for applications in nuclear medicine. The synthesis, spectroscopic and X-ray crystallographic analysis of bifunctional chelates are discussed
Source
Anon; 1905 p; 1993; p. 890, Paper NUCL 154; American Chemical Society; Washington, DC (United States); 206. American Chemical Society (ACS) national meeting; Chicago, IL (United States); 22-27 Aug 1993; American Chemical Society, 1155 16th St., NW, Washington, DC 20036-4899 (United States)
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Book
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Conference
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Descriptors (DEC)
BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, DRUGS, EVEN-ODD NUCLEI, HOURS LIVING RADIOISOTOPES, IMMUNOTHERAPY, INTERMEDIATE MASS NUCLEI, INTERNAL CONVERSION RADIOISOTOPES, ISOMERIC TRANSITION ISOTOPES, ISOTOPES, LABELLED COMPOUNDS, MATERIALS, MEDICINE, MINUTES LIVING RADIOISOTOPES, NUCLEI, ODD-EVEN NUCLEI, ORGANIC COMPOUNDS, ORGANIC NITROGEN COMPOUNDS, PALLADIUM ISOTOPES, RADIOACTIVE MATERIALS, RADIOISOTOPES, RADIOTHERAPY, SECONDS LIVING RADIOISOTOPES, SILVER ISOTOPES, STABLE ISOTOPES, SYNTHESIS, THERAPY
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