Published 1991 | Version v1
Book

Captive solvent methods for fast, simple carbon-11 radioalkylations

  • 1. Univ. of Michigan Medical School, Ann Arbor (United States)
  • 2. Univ. of Iowa, Iowa City (United States)

Description

Carbon-11 labeled radiopharmaceuticals for receptor studies usually require final purification by high performance liquid chromatography (HPLC). A significant simplification of the apparatus is possible if the radiolabeling reaction can be done directly in the HPLC injection circuit. Captive solvent methods in which the reaction is done in a small volume of solvent absorbed in a porous solid matrix are a general approach to this problem. For N-methylations with [11C] methyl iodide, a basic catalyst may be incorporated in the polymeric or alumina solid phase. Reaction volumes are from 20 to 100 ML. Often no heating or cooling of the reaction column is necessary. The syntheses of [11C]PK11195 and [11C] flumazenil are described to illustrate some of the advantages and limitations of captive solvent methods

Part of:
New trends in radiopharmaceutical synthesis, quality assurance, and regulatory control

Additional details

Publishing Information

Publisher
Plenum Press.
Imprint Place
New York, NY (United States)
Imprint Title
New trends in radiopharmaceutical synthesis, quality assurance, and regulatory control
Imprint Pagination
529 p.
Journal Page Range
p. 387-391.

Conference

Title
200. American Chemical Society (ACS) national meeting.
Dates
26-31 Aug 1990.
Place
Washington, DC (United States).

Optional Information

Secondary number(s)
CONF-900802--.