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In vitro synthesis of fluorescein monoglucuronide
1Department of Pharmacology, University of Illinois College of Medicine, Chicago.
Pharmacology
|January 1, 1988
Abstract:
A simple, economical method for the in vitro synthesis of milligram amounts of fluorescein monoglucuronide is presented. The compound can be synthesized in 1 day, and 2 chromatographic steps result in complete purification. The synthetic fluorescein monoglucuronide was found to be identical to biosynthetic fluorescein monoglucuronide by spectrophotometric and fluorometric criteria.