Preparation and stability of a radioiodinated pentamidine isethionate analog
β Scribed by Philip J. Blower; Claire M. Smith; Raymond J. Smith; Gareth E. Moores; Michael J. O'Doherty
- Book ID
- 103922916
- Publisher
- Elsevier Science
- Year
- 1992
- Weight
- 512 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0883-2889
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β¦ Synopsis
Iodopentamidine isethionate was heated for 70 min with [I-123]- or [I-125]-sodium iodide and ammonium sulphate in the absence of solvent at 140 degrees C. The product, [I-123]- or [I-125]-iodopentamidine isethionate, was purified by ion exchange chromatography. It was stable at room temperature in aqueous solution over several days, in human blood in vitro for at least 24 h (showing no binding to either cells or proteins), in urine over at least 15 h, and during nebulization in both ultrasonic and jet nebulizers.
π SIMILAR VOLUMES
## Abstract A simple procedure is described for preparing^125^Iβlabelled alginic acid. The reducing terminal of alginic acid is derivatized with tyramine through the formation of Schiff base which is subsequently reduced with sodium cyanoborohydride. By radioiodination of the aromatic ring introduc