Evidence map›Paper›PMID 40947852›Full record

ArticleBioanalysis2025

Correlation between LC-MS/MS and ELISA methods for quantitative analysis of desmosine-containing solutions.

Arisa Araki, Mahiro Takano, Christian Nanga Chick, Takumi Yamazaki, Jun Nojima, Toyonobu Usuki

Abstract read
In one paragraph

Article in Bioanalysis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Arisa ArakiDepartment of Materials and Life Sciences, Faculty of Science and Technology, Sophia University, Chiyoda-ku, Japan.
Mahiro TakanoDepartment of Materials and Life Sciences, Faculty of Science and Technology, Sophia University, Chiyoda-ku, Japan.
Christian Nanga ChickDepartment of Materials and Life Sciences, Faculty of Science and Technology, Sophia University, Chiyoda-ku, Japan.
Takumi YamazakiDepartment of Materials and Life Sciences, Faculty of Science and Technology, Sophia University, Chiyoda-ku, Japan.
Jun NojimaDepartment of Materials and Life Sciences, Faculty of Science and Technology, Sophia University, Chiyoda-ku, Japan.
Toyonobu UsukiDepartment of Materials and Life Sciences, Faculty of Science and Technology, Sophia University, Chiyoda-ku, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDesmosine and isodesmosine are crosslinking amino acids found in extracellular matrix protein elastin, which imparts elasticity to tissues such as those of the lungs and arteries. These compounds are promising biomarkers for diseases involving elastin degradation, such as chronic obstructive pulmonary disease. RESEARCH DESIGN AND

methodThis study examined the correlation between isotope-dilution LC-MS/MS and a newly established ELISA for in vitro diagnosis using a variety of samples.

resultsResults of ELISA and LC-MS/MS analyses exhibited a high correlation coefficient (0.9941). However, whereas the LC-MS/MS measurements deviated approximately 2-fold from the theoretical values, the ELISA measurements ranged from 0.83 to 1.06 (avg 0.94) times the theoretical values. Precise measurement of the absorbance of synthetic desmosine revealed a molar extinction coefficient of 2403, which differed markedly from the previously reported value of 4900 in 1963. Using this value to recalculate the amount of added desmosine, the LC-MS/MS measurements were 0.68 to 0.99 (avg 0.87) times the theoretical values.

conclusionThus, the developed ELISA enables highly accurate determination of desmosine concentrations, comparable to LC-MS/MS, suggesting that ELISA is a potentially useful in vitro diagnostic tool.

Indexed as

DesmosineTandem Mass SpectrometryChromatography, LiquidEnzyme-Linked Immunosorbent AssayHumansLiquid Chromatography-Mass SpectrometrySolutionsDesmosineSolutionsCOPDDesmosineELISALC-MS/MSquantitative analysis

Identifiers

PMID40947852
PMCPMC12536777

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.