𝔖 Bobbio Scriptorium
✦   LIBER   ✦

New preparation of [123I]PE2I: investigation of the oxidation and purification steps

✍ Scribed by E. Berthommier; C. Loc'h; S. Chalon; C. Olivier; P. Emond; H. Dao Boulanger; M.A. Lelait; L. Mauclaire


Publisher
John Wiley and Sons
Year
2002
Tongue
French
Weight
105 KB
Volume
45
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

In order to simplify preparation of [^123^I]PE2I, iodogen and hydrogen peroxide were examined as oxidants for the preparation of radioiodinated PE2I, e.g. (E)‐N‐(3‐iodoprop‐2‐enyl)‐2__β__‐carbomethoxy‐3__β__‐(4′‐tolyl) nortropane). Among the oxidizing compounds assayed, iodogen appears to afford the best results for this purpose (high radiochemical yield, high chemical purity and a reasonable reaction time). A simplified and efficient method is described here for the preparation of [^123^I]PE2I based on the exchange of a ^123^I tributyl tin analogue in oxidative conditions followed by purification by solid phase extraction (SPE). Using this method, [^123^I]PE2I was obtained with a radio‐pharmaceutical yield over 60%, with chemical and radiochemical purities higher than 95% without the addition of a carrier (Na^127^I) (2G Bq/nmol) or with a specific activity adjusted to 85–90 MBq/nmol in the presence of the carrier. Copyright © 2002 John Wiley & Sons, Ltd.


📜 SIMILAR VOLUMES


Preparation and a simple one-step purifi
✍ Janos Gardi; James M. Krueger; Robert C. Speth 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 French ⚖ 144 KB

## Abstract A one‐step purification of [His^1^‐mono‐^125^I‐Tyr^10^,Nle^27^]‐hGHRH(1‐32)‐NH~2~, prepared using chloramine‐T, by HPLC with isocratic elution is described. The labeled GHRH analog was suitable for GHRH receptor binding assays. Copyright © 2002 John Wiley & Sons, Ltd.

The preparation and purification of 3–(4
✍ A. Bobik; E. A. Woodcock; C. I. Johnston; W. J. Funder 📂 Article 📅 1977 🏛 John Wiley and Sons 🌐 French ⚖ 250 KB

## 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

SN2 or Electron Transfer?? A new techniq
✍ De-Ling Zhou; Peristera Walder; Rolf Scheffold; Lorenz Walder 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 German ⚖ 921 KB

The following abbreviations are used: Cbl = cobalamin [le]; for convenience, we use 'Cby' instead of Cby(MeO), for heptamethyl cobyrinate (cf Cby = cobyric acid [le]), [Co(oep)] = (2,3,7,8,12,13,17,18-octaethy1porphyrinato)cobalt [If], [Co(tpp)] = (5,10,15,20-tetraphenylporphyrinato)cobalt [If]; [Co

The preparation and purification of labe
✍ J. Burns 📂 Article 📅 1970 🏛 John Wiley and Sons 🌐 French ⚖ 444 KB 👁 1 views

The preparation of 1"-propranolol hydrochloride from l-naphthol-I-14C is described. Several preparations of the compound have been carried out with overall radiochemical yields of 17 %-21 %. Specific activities of 3.51 pCilmg, 8.8 pCilmg, and 23.2 pCilmg have been obtained. Propranolol has also bee