The main metabolite of prostaglandin E, (PGE2) 13,14-dihydro-Sketo-PGE, readily dehydrates and can subsequently form a cyclic derivative. This problem can be overcome by the immediate formation of oximes of the 9 and 15 ketones in aqueous solution followed by subsequent extraction, methylation and t
Enzymatic and chemical labelling of prostaglandin E1 and 13,14-dihydro-15-keto-prostaglandin E1
✍ Scribed by Dimitrios Tsikas; Stefan Bracht; Dirk Stichtenoth; Jürgen C. Frölich
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- French
- Weight
- 447 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
Chemical and enzymatic tools were employed to synthesize [1,1‐^18^O~2~]‐prostaglandin (PG) E1, [1,1‐^18^O~2~]‐13,14‐dihydro‐15‐keto‐PGE~1~ and [5,6‐^3^H~2~]‐13,14‐dihydro‐15‐keto‐PGE~1~ starting from the corresponding unlabelled compounds adn [5,6‐^3^H~2~]‐PGE~1~, respectively. Reaction products were purified by high‐performance liquid chromatography and their isotopic purity was determined by gas chromatographymass spectrometry (GC‐MS). The utility of [1,1‐^18^O~2~]‐PGE~1~ and [1,1‐^18^O~2~]‐13,14‐dihydro‐15‐keto‐PGE~1~ as internal standards for GC‐MS analysis of the corresponding endogenous compounds in biological fluids is demonstrated. [5,6‐^3^H~2~]‐13,14‐dihydro‐15‐keto‐PGE~1~ was found to be useful in developing extraction and purification procedures for the quantitation of endogenous 13,14‐dihydro‐15‐keto‐PGE~1~ in human plasma by GC‐tandem MS.
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