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pubmed-article:15246364pubmed:abstractText[125I]-2-iodo-L-phenylalanine, a new radioiodinated phenylalanine analog was evaluated as a potential specific tumor tracer for SPECT. The tracer is obtained with an overall radiochemical yield of at least 98%, a purity of > 99%, and a specific activity of 11 MBq/mmol in one pot Kit conditions using the Cu1+ assisted isotopic exchange. The tracer is evaluated in vitro using R1M rat rabdomyosarcoma cells in HEPES buffer with and without Na+ ions and in MEM buffer. The uptake of [125I]-2-iodo-L-phenylalanine follows a reversible pseudo-first-order reaction which is the same in presence and absence of Na+ ions, but the compound is not incorporated into the cell proteins. The reversible uptake is proven to occur with the same affinity as L-henylalanine by a saturable transport system which is competitively inhibited by BCH, an L transport type selective molecule. Trans-stimulation of the efflux by BCH and typical L transported amino acids shows that the transporter is of the antiport type and fulfils all the properties of the LAT1 heterodimer transport system. [125I]-2-iodo-L-phenylalanine is thus a phenylalanine analog that for the uptake uses for the major part the LAT1 transport system which is known to be over-expressed in tumor cells. This, together with the easy Kit preparation, makes [123I]-2-iodo-L-phenylalanine a promising tumor specific tracer for SPECT.lld:pubmed
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pubmed-article:15246364pubmed:copyrightInfoCopyright 2004 Elsevier Inc.lld:pubmed
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pubmed-article:15246364pubmed:volume31lld:pubmed
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pubmed-article:15246364pubmed:pagination739-46lld:pubmed
pubmed-article:15246364pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:15246364pubmed:articleTitleSynthesis, radiosynthesis, and in vitro characterization of [125I]-2- iodo-L-phenylalanine in a R1M rhabdomyosarcoma cell model as a new potential tumor tracer for SPECT.lld:pubmed
pubmed-article:15246364pubmed:affiliationNuclear Medicine Department/BEFY, Vrije Universiteit Brussel, Belgium. jjmerten@vub.ac.belld:pubmed
pubmed-article:15246364pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15246364pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed