Mass spectrometric determination of eicosapentaenoic acid and docosahexaenoic acid
US-9696325-B2 · Jul 4, 2017 · US
US2018024151A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2018024151-A1 |
| Application number | US-201715635509-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jun 28, 2017 |
| Priority date | Sep 16, 2010 |
| Publication date | Jan 25, 2018 |
| Grant date | — |
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The invention relates to the detection of DHA and EPA. In a particular aspect, the invention relates to methods for detecting DHA and EPA by mass spectrometry and kits for carrying out such methods.
Opening claim text (preview).
That which is claimed is: 1 . A method for determining the amount of one or more omega-3 fatty acids in a sample by mass spectrometry, the method comprising: (i) ionizing said one or more omega-3 fatty acids from the sample to generate one or more ions detectable by mass spectrometry; (ii) determining the amount of said one or more omega-3 fatty acids ions by mass spectrometry; and (iii) relating the amount of DHA ions to the amount of one or more omega-3 fatty acids in the sample, wherein said one or more omega-3 fatty acids comprises docosahexaenoic acid (DHA) and/or eicosapentaenoic acid (EPA). 2 . The method of claim 1 , wherein said ionizing comprises atmospheric pressure chemical ionization (APCI). 3 . The method of claim 2 , wherein said APCI is in negative ionization mode. 4 . The method of claim 1 , wherein said ionizing comprises electrospray ionization (ESI). 5 . The method of claim 1 , wherein mass spectrometry comprises tandem mass spectrometry. 6 . The method of claim 1 , wherein said one or more ions comprise an ion with a mass to charge ratio (m/z) of 327.2±0.5. 7 . The method of claim 1 , wherein said one or more ions comprise an ion with a mass to charge ratio (m/z) of 301.2±0.5. 8 . The method of claim 1 , wherein said sample comprises human serum or plasma. 9 . The method of claim 1 , wherein said sample is subjected to a hydrolyzing agent prior to ionization. 10 . The method of claim 8 , wherein said hydrolyzing agent is an acid. 11 . The method of claim 1 , wherein said one or more omega-3 fatty acids is subjected to liquid/liquid extraction prior to ionization. 12 . The method of claim 1 , wherein said one or more omega-3 fatty acids is purified by liquid chromatography prior to ionization. 13 . The method of claim 12 , wherein said liquid chromatography comprises high performance liquid chromatography (HPLC). 14 . The method of claim 1 , wherein said method comprises determining the amount of an internal standard. 15 . The method of claim 14 , wherein said internal standard is a deuterated omega-3 fatty acid. 16 . The method of claim 15 , wherein said deuterated omega-3 fatty acid is DHA- 2 H 5 . 17 . The method of claim 15 , wherein said deuterated omega-3 fatty acid is EPA- 2 H 5 .
Liberation or purification of sample or separation of material from a sample [e.g., filtering, centrifuging, etc.] · CPC title
using chemical ionisation · CPC title
Lipid, cholesterol, or triglyceride standard or control · CPC title
Step by step routines describing the use of the apparatus (H01J49/0081 takes precedence) · CPC title
by electric field, e.g. electrospray · CPC title
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