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1
Division of Pediatric Neurology, The Childrens Hospital Medical Center, 3333 Burnet Ave., Cincinnati, OH 45229-3039.
2
Department of Pathology and Laboratory Medicine, College
of Medicine, University of Cincinnati, 231 Bethesda Ave., Cincinnati,
OH 45267-0559.
a Address correspondence to this author at: Clinical Neuropharmacology Laboratory, Division of Pediatric Neurology, The Childrens Hospital Medical Center, 3333 Burnet Ave., Cincinnati, OH 45229-3039. Fax 513-636-6359; e-mail Tangp0{at}chmcc.org.
Background: The percentage of reduced coenzyme Q10 (CoQ10H2) in total coenzyme Q10 (TQ10) is decreased in plasma of patients with prematurity, hyperlipidemia, and liver disease. CoQ10H2 is, however, easily oxidized and difficult to measure, and therefore reliable quantification of plasma CoQ10H2 is of clinical importance.
Methods: Venous blood was collected into evacuated tubes containing heparin, which were immediately placed on ice and promptly centrifuged at 4 °C. The plasma was harvested and stored in screw-top polypropylene tubes at -80 °C until analysis. After extraction with 1-propanol and centrifugation, the supernatant was injected directly into an HPLC system with coulometric detection.
Results: The in-line reduction procedure permitted
transformation of CoQ10 into
CoQ10H2 and avoided artifactual oxidation of
CoQ10H2. The electrochemical reduction yielded
99% CoQ10H2. Only 100 µL of plasma was
required to simultaneously measure CoQ10H2 and
CoQ10 over an analytical range of 10 µg/L to 4 mg/L.
Intra- and interassay CVs for CoQ10 in human plasma were
1.24.9% across this range. Analytical recoveries were
95.8101.0%. The percentage of
CoQ10H2 in TQ10 was
96% in
apparently healthy individuals. The method allowed analysis of up to 40
samples within an 8-h period.
Conclusions: This optimized method for CoQ10H2 analysis provides rapid and precise results with the potential for high throughput. This method is specific and sufficiently sensitive for use in both clinical and research laboratories.
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