PET-CENTRETS ÅRSRAPPORT 2008 - Aarhus Universitetshospital
PET-CENTRETS ÅRSRAPPORT 2008 - Aarhus Universitetshospital
PET-CENTRETS ÅRSRAPPORT 2008 - Aarhus Universitetshospital
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Sukker stofskifte og<br />
sukker transport<br />
Sporstof<br />
[ 18 F]fluorodeoxyglucose, [ 11 C]glucose, [ 18 F]-fluorogalactose,<br />
3-O-[ 11 C]methylglucose<br />
Gennemblødning [ 15 O]water, [ 13 N]ammonia, [ 15 O]butanol<br />
Ilt stofskifte [ 15 O]oxygen, [ 11 C]acetate<br />
Blod volumen [ 15 O]carbon monoxide, [ 11 C]carbon monoxide<br />
Amino syre [ 18 F]6-fluoroDOPA, [ 11 C]methionine, [ 11 C]-methyl-alpha-isobutyric<br />
acid (MeAIB),a-[18F]fluoro-b-alanine<br />
[ 11 C]asparagine, [ 11 C]2,4-diaminobutyric acid, [ 11 C]aspartic<br />
acid<br />
Transportør ligander DAT: [ 11 C] b-CIT-FE, [ 11 C]NS 2214<br />
SERT: [ 11 C]DASB, [ 11 C]NS9531, [ 11 C]NS9762, [11C]NS<br />
6417, [ 11 C]NS 2495, [ 11 C]NS 4194, [ 11 C]NS 2456, [ 11 C]NS<br />
2381, [ 11 C]venlafaxine, [ 11 C]nefopam, [ 11 C]nitroquipazine<br />
NET: [ 11 C]-SS-MeNER<br />
Receptor ligander [ 11 C]Raclopride (D2,3 antagonist), [ 11 C]-WAY 100,635 (5-<br />
HT1A antagonist), [ 11 C]PK 11195 (peripheral benzodiazepine<br />
receptor ligand), [ 11 C]mirtazapine (adrenoceptors),<br />
[ 11 C]MDL100,907 (5-HT2A antagonist, [ 11 C]Yohimbine<br />
(adrenoceptors), [ 11 C]FLB 457 (D2 antagonist), [ 11 C]mianserin<br />
(adrenoceptors), [ 11 C]NMSP (5-HT and D2 antagonist),<br />
[ 11 C]SCH23390 (D1 antagonist), [ 11 C]NNC112 (D1 antagonist),<br />
[ 11 C]SKF 75670 (D1 agonist), [ 11 C]SKF 82957 (D1<br />
agonist), [ 11 C]NPA (D2 agonist), [ 11 C]CP 643,051 (NK1 antagonist),<br />
[ 11 C]GR 205171 (NK1 antagonist), [ 11 C]SB 207145 (5-<br />
HT4 antagonist), [ 11 C]melatonin (MT receptor ligand), [ 11 C]NS<br />
3957(nicotinergic system), [ 11 C]methylamantadine (NMDA<br />
antagonist), [ 11 C]Flumazenil (dibenzodiazepine receptor<br />
ligand).<br />
Hypoxi markør [ 18 F]fluoromisonidazole, [ 18 F]-FAZA<br />
Forskellige [ 18 F]fluoride (bone metabolism), [ 11 C]harmine (MAO inhibitor),<br />
[ 11 C]rolipram (PDE IV inhibitor), [ 11 C]PIB (bamyloid<br />
plaque labeling), [ 11 C Tarceva (EPG-ligand),<br />
[ 11 C]methamphetamine and [ 11 C] b,b-difluoromethamphetamine,<br />
[ 11 C]Ral1 (PDEV ligand).<br />
Tabel: Sporstoffer til rådighed ved Århus Sygehusets <strong>PET</strong> centret (sporstoffer godkendt<br />
til human brug i kursiv).<br />
Forskningsaktiviteter<br />
Ved siden af varetagelse af rutineopgaver deltog <strong>PET</strong>-centrets kemikere også i <strong>2008</strong> meget<br />
aktiv i <strong>PET</strong>-centrets forskningsaktiviteter, både iht. egne mere radiokemisk relaterede<br />
<strong>PET</strong>-centret i Århus | Årsrapport <strong>2008</strong>