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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2011-4-12
pubmed:abstractText
We have recently reported a new N-methylaminooxy-based prosthetic group for the site-selective introduction of ¹?F-fluorine under mild acidic aqueous conditions into model peptides functionalized with a Michael acceptor moiety. To further investigate the utility of this methodology, the radiosynthesis of two cyclic RGD peptides was carried out, and in vivo biodistribution and microPET studies were performed in tumor-bearing mice. A cyclic RGD peptide was functionalized with the Michael acceptors trans-?-nitrostyrene carboxylic acid and 3-vinylsulfonylpropionic acid. Radiolabeling was then performed with the prosthetic group O-(2-(2-[¹?F]fluoroethoxy)ethyl)-N-methylhydroxylamine (¹?F-FENMA) yielding the ¹?F-conjugates in moderate yields (8.5-12%). Biodistribution, blocking, and microPET imaging studies were performed in a mouse xenograft model. The vinylsulfonyl-modified conjugate demonstrated good in vitro plasma stability. Biodistribution and microPET studies revealed excellent tumor uptake with low background in key organs and renal elimination as the predominant route of excretion. Blocking studies with coinjected nonlabeled RGD peptide confirmed the in vivo specificity for the integrin ?(v)??. On the other hand, ¹?F-FENMA-nitrostyrene-RGD, although stable at conjugation pH 5, was found to rapidly degrade at physiological pH through loss of the ¹?F-prosthetic group.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1520-4812
pubmed:author
pubmed:issnType
Electronic
pubmed:day
15
pubmed:volume
21
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2297-304
pubmed:meshHeading
pubmed-meshheading:21070000-Animals, pubmed-meshheading:21070000-Carboxylic Acids, pubmed-meshheading:21070000-Diagnostic Imaging, pubmed-meshheading:21070000-Drug Stability, pubmed-meshheading:21070000-Fluorine Radioisotopes, pubmed-meshheading:21070000-Halogenation, pubmed-meshheading:21070000-Hydroxylamines, pubmed-meshheading:21070000-Integrin alphaVbeta3, pubmed-meshheading:21070000-Isotope Labeling, pubmed-meshheading:21070000-Mice, pubmed-meshheading:21070000-Mice, Inbred BALB C, pubmed-meshheading:21070000-Mice, Nude, pubmed-meshheading:21070000-Neoplasm Transplantation, pubmed-meshheading:21070000-Osteosarcoma, pubmed-meshheading:21070000-Peptides, Cyclic, pubmed-meshheading:21070000-Positron-Emission Tomography, pubmed-meshheading:21070000-Propionic Acids, pubmed-meshheading:21070000-Radiopharmaceuticals, pubmed-meshheading:21070000-Styrenes, pubmed-meshheading:21070000-Tissue Distribution, pubmed-meshheading:21070000-Transplantation, Heterologous
pubmed:year
2010
pubmed:articleTitle
Radiosynthesis and biodistribution of a prosthetic group (¹?F-FENMA) conjugated to cyclic RGD peptides.
pubmed:affiliation
Department of Pharmaceutics & Biopharmaceutics, University of Tromsø, Norway.
pubmed:publicationType
Journal Article