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Updated: Jan 17, 2026

Quantitative and Qualitative Method for Sphingomyelin by LC-MS Using Two Stable Isotopically Labeled Sphingomyelin Species
Published on: May 7, 2018
Correlation between LC-MS/MS and ELISA methods for quantitative analysis of desmosine-containing solutions
Arisa Araki1, Mahiro Takano1, Christian Nanga Chick1
1Department of Materials and Life Sciences, Faculty of Science and Technology, Sophia University, Chiyoda-ku, Japan.
A new ELISA test accurately measures desmosine and isodesmosine, crucial biomarkers for elastin degradation diseases like COPD. This method offers a reliable alternative to LC-MS/MS for in vitro diagnostics.
Area of Science:
- Biochemistry
- Biomarker Discovery
Background:
- Desmosine and isodesmosine are key crosslinking amino acids in elastin.
- Elastin provides elasticity to tissues like lungs and arteries.
- These amino acids are potential biomarkers for elastin degradation diseases, including COPD.
Purpose of the Study:
- To evaluate a newly developed ELISA for desmosine and isodesmosine quantification.
- To compare the accuracy of ELISA with isotope-dilution LC-MS/MS.
Main Methods:
- Analyzed various samples using both ELISA and LC-MS/MS.
- Determined the molar extinction coefficient of synthetic desmosine.
Main Results:
- ELISA and LC-MS/MS showed a high correlation (0.9941).
- ELISA measurements closely matched theoretical values (avg 0.94), while LC-MS/MS deviated significantly (avg 0.87 after recalculation).
- A revised molar extinction coefficient improved LC-MS/MS accuracy.
Conclusions:
- The developed ELISA provides highly accurate desmosine concentration measurements.
- ELISA is a viable and accurate in vitro diagnostic tool for assessing elastin degradation.
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