Preparation of [125I]-3H2-iopiperidol-A by exchange radioiodination
✍ Scribed by Marc Ogan; Frank Tomasella; Jan-I Tu
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- French
- Weight
- 325 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Preparation of radiolabeled [^125^I]‐N,N′‐bis(2,3‐dihydroxypropyl)‐5‐(3‐hydroxy‐2‐oxo‐1‐piperidinyl)‐2,4,6‐ triiodo‐1,3‐benzenedicarboxamide, ([^125^I]‐3H2‐iopiperidol‐A), a nonionic radiographic contrast agent, was achieved by HAuCl~4~ mediated exchange radioiodination. [^125^I]‐Iopiperidol‐A was isolated by reversed‐ phase HPLC in 83% radiochemical yield. The radiochemical purity of isolated [^125^I]‐3H2‐iopiperidol‐A was 98.7% and the specific activity was 6.6 mCi/μmol. The role of HAuCl~4~ in facilitating exchange radioiodination of 3H2‐iopiperidol‐A, however, appears to be a complex process not limited to the production of electrophilic iodine ion.
📜 SIMILAR VOLUMES
Pteroylglutamic acid was labeled with deuterium by trifluoroacetic acid-catalyzed exchange with deuterium oxide. The product, pteroylglutamic acid-3',5'-H2, was selectively labeled with deuterium in the 4-aminobenzoyl portion of the molecule; there was no evidence for isotope incorporation at C or
## Abstract No‐carrier‐added 2‐(4‐[^131^I]iodophenyl)‐ and 8‐[^131^I]iodo‐2‐phenylpyrazolo[4,3‐c]quinolin‐3(5H)‐one were prepared in isolated radiochemical yields of 11.6 and 5.4%, respectively, by acid decomposition of aryl triazenes in acetonitrile. A modified triazene method involving solid‐phas
## Abstract The preparation of an iodine‐125 labelled beta adrenergic ligand, 3–(4‐iodophenoxy)‐1‐isopropylamino‐2‐propanol, suitable for β‐adrenergic receptor membrane binding studies is described. Several preparations have been carried out with radiochemical yields of 20–30%. Specific activities