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Saudi Medical Journal. 2009; 30 (9): 1138-1143
in English | IMEMR | ID: emr-102301

ABSTRACT

To improve a new high performance liquid chromatography [HPLC] method for coenzyme Q10 [CoQ10] measurement in human plasma. We conducted this study in the Chemistry and Biochemistry Department, College of Medicine, Al-Nahrain University, Baghdad, Iraq from September 2004 to July 2005. Sixty healthy volunteers aged 28. 51 +/- 7. 30 years were participated in this study. All participants were non-smokers and under no any treatment for the last 3 days and fast for 12 hours before analysis. Coenzyme Q10 levels were measured by improved isocratic reversed phase HPLC technique after one-step ice-cold 1-propanol extraction step. The ultra violet [UV] detection, developed HPLC method gives a good linearity range between 0.1-4.0 mg/L. The coefficients of variations [CVs%] of within-day precision for CoQ10 in human plasma were 0.2-3.90%. Analytical recoveries were 95.5-101.30%, whereas the average CV% of CoQ10 reproducibility was 0.959%. A new improved rapid, precise, and sensitive HPLC method for the quantitation of CoQ10 is suitable for analysis of blood plasma samples


Subject(s)
Humans , Chromatography, High Pressure Liquid/methods , Ubiquinone/analogs & derivatives , Ubiquinone/blood , Spectrophotometry, Ultraviolet , Reproducibility of Results , Reference Values , Calibration
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