Abstract |
We developed an HPLC procedure using electrochemical detection for the quantitation of oxycodone and hydrocotarnine in cancer patients serum. An eluent of methanol: acetonitrile:5 mM pH 8 phosphate buffer (2:1:7) was used for the mobile phase. The calibration curve was linear in the range from 10 ng/mL to 100 ng/mL. The recovery of oxycodone and hydrocotarnine was 97.2% and 90.5%, respectively. The relative standard deviations within-runs and between-runs for the assay of oxycodone or hydrocotarnine were less than 4.8%. The method developed here was better than the method reported previously.
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Authors | Hideya Kokubun, Makiko Ouki, Motohiro Matoba, Hiroaki Kubo, Sumio Hoka, Kazuo Yago |
Journal | Analytical sciences : the international journal of the Japan Society for Analytical Chemistry
(Anal Sci)
Vol. 21
Issue 3
Pg. 337-9
(Mar 2005)
ISSN: 0910-6340 [Print] Switzerland |
PMID | 15790123
(Publication Type: Journal Article)
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Chemical References |
- Analgesics, Opioid
- Tetrahydroisoquinolines
- Oxycodone
- hydrocotarnine
|
Topics |
- Analgesics, Opioid
(blood)
- Chromatography, High Pressure Liquid
(methods)
- Electrochemistry
(methods)
- Humans
- Neoplasms
(blood)
- Oxycodone
(blood)
- Tetrahydroisoquinolines
(blood)
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