Automated synthesis of radiopharmaceuticals for positron emission tomography: an apparatus for labelling with [11C] methyl iodide (MIASA)

Author:

Cork D. G.12,Yamato H.13,Yajima K.1,Hayashi N.14,Sugawara T.5,Kato S.5

Affiliation:

1. Institute for Biofunctional Research, c/o National Cardiovascular Center, Fujishirodai, Suita, Osaka 565, Japan

2. Molecular Chemistry Laboratory, Takeda Chemical Industries Ltd, Yodogawa-ku, Osaka 532, Japan

3. Medical Chemistry Discovery Research, Yoshitomi Pharmaceutical Industries Ltd, 955 Koiwai, Yoshitomi-cho Chikuhjo-gun, Fukuoka 871, Japan

4. Ogiwaradai-nishi 3-chome 184, Hyogo, Kawanishi 666, Japan

5. Molecular Chemistry Laboratory, Takeda Chemical Industries Ltd, Todogawa-ku, Osaka 532, Japan

Abstract

A fully automated apparatus for the routine synthesis and formulation of short-lived11C (t1/2=20min) labelled radiopharmaceuticals for positron emission tomography (PET) has been developed. [11C]Carbon dioxide is converted to [11C]methyl iodide, which can be used to label a wide variety of substrates by methylation at C, N, O, or S electron rich centres. The apparatus, MIASA (methyl iodide automated synthesis apparatus), was designed to operate as part of an automated labelling system in a shielded ‘hot’ laboratory. The apparatus was designed without the size constraints of typical instrumentation used in hot cells, although it is compact where necessary. Ample use of indicators and sensors, together with compact design of the reaction flasks for small dead space and efficient evaporation, led to good reliability and performance. The design of the hardware and software is described in this paper, together with a preparation of 3-N-[11C]methylspiperone as a sterile injectable solution in physiological saline.

Funder

Japan Health Science Foundation

Publisher

Hindawi Limited

Subject

Clinical Biochemistry

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