## Abstract Carcinoembryonic antigen /CEA/ was labelled with iodine‐125 using lactoperoxidase. The radiochemical yield of /^125^I/CEA was about 25% at the specific activity of about 30μCi/μg /1.1MBq/μg/. The percentage binding of /^125^I/CEA with specific anti‐CEA serum was determined in lyophilize
Fluorine-18- and iodine-125-labelling of spiegelmers
✍ Scribed by B. Kuhnast; S. Klussmann; F. Hinnen; R. Boisgard; B. Rousseau; J. P. Fürste; B. Tavitian; F. Dollé
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- French
- Weight
- 155 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0022-2135
- DOI
- 10.1002/jlcr.781
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Spiegelmers are high‐affinity l‐enantiomeric oligonucleotide ligands (aptamers) that display high resistance to enzymatic degradation compared to d‐oligonucleotides. Spiegelmers belong to the third generation of aptamers, and are currently extensively investigated as potential therapeutic agents. We have previously developed an original method to label natural oligonucleotides with radiohalogens and particularly with fluorine‐18, the most widely used positron‐emitter, t~1/2~: 109.8 min. Using the same strategy, we herein report the labelling of Spiegelmers, both with fluorine‐18 for positron emission tomography imaging and iodine‐125 for high resolution autoradiography. Three 25‐mer l‐oligonucleotides have been used, differing (a) by the position of the terminal phosphorothioate monoester group (3′‐ or 5′‐end, and therefore differing by the position of the labelling on the macromolecule) and (b) by the nature of the backbone sugar moiety (2′‐OH or 2′‐H, therefore covering the RNA and DNA series, respectively). N‐(4‐[^18^F]fluorobenzyl)‐2‐bromoacetamide was synthesized in three radiochemical steps from 4‐cyano‐N,N,N‐trimethylanilinium trifluoromethanesulfonate and HPLC‐purified in 90 min (typical production: 2.2–2.4 GBq starting from a batch of 22–24 GBq of [^18^F]fluoride). N‐(4‐[^125^I]iodobenzyl)‐2‐bromoacetamide was synthesized from the corresponding trimethylsilyl derivative (one pot, two radiochemical steps) and HPLC‐purified in 60 min (typical production: 24 MBq starting from 37 MBq of Na[^125^I]I). Coupling of the Spiegelmers with the appropriate HPLC‐purified [radiolabelled]‐halobenzyl‐2‐bromoacetamide (MeOH/PBS (0.1 M, pH 8), 10 min, 120°C) gave the corresponding labelled conjugated Spiegelmers after RP‐HPLC purification. For fluorine‐18, the whole synthetic procedure yields up to 1.1 GBq of pure labelled Spiegelmers in 160 min with a specific radioactivity of 37–74 GBq/μmol at the end of synthesis starting from 22–24 GBq of [^18^F]fluoride. For iodine‐125, the whole synthetic procedure allows producing up to 7.4 MBq of pure labelled Spiegelmers in 100 min with a specific radioactivity of 11–37 GBq/μmol starting from 37 MBq of Na[^125^I]I. Copyright © 2003 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
## Abstract The carrier‐free synthesis of 4‐(5′,6′,7′,8′‐tetrahydro‐4′‐[^125^I]iodo‐5′,5′,8′,8′‐tetramethyl‐2′‐anthracenyl)benzoic acid (4′‐[^125^I]TTAB) is described. Site specific radioiodination was accomplished by electrophilic destannylation of the tri(__n__‐butyl)tin analog of the retinoid wi
## Abstract Iodine‐125 labelled vinyl and aryl iodides are formed via the reaction of sodium iodide‐125 with vinyl‐ and arylboronic acids. Good yields of isomerically pure products are obtained.
d e r i v a t i v e s of 2 and 2 were req u i r e d f o r b i o d i s t r i b u t i o n s t u d i e s . U t i l i z i n g a new exchange p r o c e d u r e t h e s e r a d i o i o d i n a t e d a n a l o g u e s were s y n t h e s i z e d w i t h r a d i o c h e m i c a l y i e l d s r a n g i n g fr
w-[ 1251]Iodoundecyl choleeteryl ether has been synthesized via a hydroboration-iodination sequence. The syntheses can be used to prepare high specific activity (no-carrier-added) reagents.