Rapid electrophoretic monitoring of the anaesthetic ketamine and its metabolite norketamine in rat blood using a contactless conductivity detector to study the pharmacokinetics
Language English Country Germany Media print-electronic
Document type Journal Article
Grant support
17-12648S
Czech Science Foundation
- Keywords
- acetonitrile stacking, capillary electrophoresis, contactless conductivity detection, ketamine, pharmacokinetics,
- MeSH
- Anesthetics blood pharmacokinetics MeSH
- Electric Conductivity MeSH
- Ketamine analogs & derivatives blood metabolism pharmacokinetics MeSH
- Rats MeSH
- Limit of Detection MeSH
- Rats, Wistar MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Anesthetics MeSH
- Ketamine MeSH
- norketamine MeSH Browser
A method of capillary electrophoresis with contactless conductivity detection has been developed for non-enantioselective monitoring the anaesthetic ketamine and its main metabolite norketamine. The separation is performed in a 15 μm capillary with an overall length of 31.5 cm and length to detector of 18 cm; inner surface of the capillary is covered with a commercial coating solution to reduce the electroosmotic flow. In an optimised background electrolyte with composition 2 M acetic acid + 1% v/v coating solution under application of a high voltage of 30 kV, the migration time is 97.1 s for ketamine and 95.8 s for norketamine, with an electrophoretic resolution of 1.2. The attained detection limit was 83 ng/mL (0.3 μmol/L) for ketamine and 75 ng/mL (0.3 μmol/L) for norketamine; the number of theoretic plates for separation of an equimolar model mixture with a concentration of 2 μg/mL was 683 500 plates/m for ketamine and 695 400 plates/m for norketamine. Laboratory preparation of rat blood plasma is based on mixing 10 μL of plasma with 30 μL of acidified acetonitrile, followed by centrifugation. A pharmacokinetic study demonstrated an exponential decrease in the plasma concentration of ketamine after intravenous application and much slower kinetics for intraperitoneal application.
Department of Hygiene 3rd Faculty of Medicine Charles University Prague Czechia
Department of Physiology 3rd Faculty of Medicine Charles University Prague Czechia
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