Method to Assay Coenzzyme Q10 in Blood Plasma or Blood Serum
Abstract
A method is described for determining CoQ 10 concentrations in plasma samples. CoQ 10 in the plasma sample is oxidized by treating the sample with an oxidizing agent having a redox potential higher than the redox potential of COQ 10 , such as, for example, para-benzoquinone. Following oxidation of the COQ 10 , the CoQ 10 in the plasma sample is extracted with an alcohol, such as, for example, 1-propanol. The alcohol extract is analyzed using direct injection into the HPLC apparatus. This method achieves a rapid, accurate analysis of plasma CoQ 10 levels, which can be used for monitoring the bioavailability of orally administered CoQ 10 used as a food supplement or as an adjunctive therapy.
Claims
exact text as granted — not AI-modified1 . A method for determining the total concentration of CoQ 10 in blood plasma or blood serum, comprising the steps of:
(a) obtaining a sample of blood plasma or blood serum from a human; (b) treating the sample with an oxidizing agent having a redox potential than the redox potential of the ubiquinone/ubiquinol couple (c) extracting the ubiquinone-10 from the sample using an alcohol; and (d) following extraction of the ubiquinone-10, analyzing the alcohol extract using High Pressure Liquid Chromatography to determine the concentration of of ubiquinone-10, in the alcohol extract.
2 . (canceled)
3 . The method of claim 1 , wherein the alcohol is selected from the group consisting of n-propanol, butanol and pentanol.
4 . The method of claim 1 , wherein the alcohol is 1-propanol.
5 . (canceled)
6 . A method for determining the total concentration of CoQ 10 in blood plasma or blood serum, comprising the steps of:
(a) obtaining a sample of blood plasma or blood serum from a human; (b) depositing an aliquot of the sample in a container; (c) adding to the sample in the container a sufficient volume of an oxidizing agent having a redox potential higher than the redox potential of ubiquinone/ubiquinol couple to oxidize ubiquinol-10 in the sample; (d) vortexing the sample containing the oxidizing agent; (e) allowing the vortexed sample containing the oxidizing agent to stand for a sufficient period of time for the oxidizing agent to oxidize ubiquinol-10 contained in the sample; (f) adding an alcohol to the sample containing the oxidizing agent to extract ubiquinone-10 from the sample; (g) vortexing the sample containing the alcohol; (b) centrifuging the sample containing the alcohol to spin down the protein precipitate; (i) removing an aliquot of the supernatant from the centrifuged sample and analyzing the aliquot of supernatant using High Pressure Liquid Chromatography to determine the concentration of ubiquinone-10 in the sample.
7 . (canceled)
8 . The method of claim 6 , wherein the alcohol is selected from the group consisting of n-propanol, butanol and pentanol.
9 . The method of claim 6 , wherein the alcohol is 1-propanol.
10 . (canceled)
11 . (canceled)Join the waitlist — get patent alerts
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