Evidence map›Paper›PMID 36321680›Full record

ArticleRapid communications in mass spectrometry : RCM2023

Matrix-assisted laser desorption/ionization-Fourier-transform ion cyclotron resonance-mass spectrometry analysis of exosomal lipids from human serum.

Iqbal Jalaludin, Huu-Quang Nguyen, Kyoung-Soon Jang, Jaebeom Lee, David M Lubman, Jeongkwon Kim

Open access · bronzeAbstract read
In one paragraph

Article in Rapid communications in mass spectrometry : RCM, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Exosome enrichment from human serum using polyethylene glycol precipitation.Journal of analytical science and technology · 2025
    Article
  4. Quantitative mass spectrometry imaging: therapeutics & biomolecules.Chemical communications (Cambridge, England) · 2024
    Review
  5. Size-exclusion chromatography for the characterization of urinary extracellular vesicles.Journal of chromatography. B, Analytical technologies in the biomedical and life sciences · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Iqbal JalaludinDepartment of Chemistry, Chungnam National University, Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0001-9117-2489
Huu-Quang NguyenDepartment of Chemistry, Chungnam National University, Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0002-8609-3038
Kyoung-Soon JangBiomedical Omics Center, Korea Basic Science Institute, Cheongju, Republic of Korea.
Jaebeom LeeDepartment of Chemistry, Chungnam National University, Daejeon, Republic of Korea.
David M LubmanDepartment of Surgery, University of Michigan Medical Center, Ann Arbor, Michigan.
Jeongkwon KimDepartment of Chemistry, Chungnam National University, Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0002-0087-1151
Chungnam National University · KRKorea Basic Science Institute · KRUniversity of Michigan · US

Funding

Universal Internal Standard for Reproducible Accurate Quantification of Exosome Protein MarkersR01CA258240 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI David M. Lubman, Tujin Shi · 2022 to 2026
$2.3M
Basic Science Research Capacity Enhancement Project through the Korea Basic Science Institute 2019R1A6C1010030Basic Science Research Program through the National Research Foundation of Korea (NRF) 2016R1D1A1B02008854Korea Basic Science Institute C230430NCI NIH HHS 1R01 CA258240NCI NIH HHS R01 CA258240
6 · The paper itself

Abstract

rationaleExosomes contain biomarkers such as proteins and lipids that help in understanding normal physiology and diseases. Lipids, in particular, are infrequently studied using matrix-assisted laser desorption/ionization (MALDI) mass spectrometry (MS) for biomarker discovery. In this study, MALDI was equipped with a high-resolution MS to investigate exosomal lipids from human serum.

methodsExosomal lipids were profiled using MALDI with Fourier-transform ion cyclotron resonance (FTICR)-MS. Four matrices (i.e., α-cyano-4-hydroxycinnamic acid [CHCA], 2,5-dihydroxybenzoic acid, sinapinic acid, and graphene oxide [GO]) and three sample preparation methods (i.e., dried droplet, thin layer, and two layer) were compared for the number of lipid species detected and the relative abundance of each lipid from human serum and human serum exosomes.

resultsIn sum, 172 and 89 lipid species were identified from human serum and human serum exosomes, respectively, using all the methods. The highest number of exosome lipid species, 69, was detected using the CHCA matrix, whereas only 8 exosome lipid species were identified using the GO matrix. Among the identified lipid species, phosphatidylcholine was identified most frequently, probably due to the use of a positive ion mode.

conclusionsExosomes and human serum showed comparable lipid profiles as determined using MALDI-FTICR-MS. These findings provide a new perspective on exosomal lipidomics analysis and may serve as a foundation for future lipidomics-based biomarker research using MALDI-FTICR-MS.

Indexed as

LipidsProteinsGraphiteHumansLasersSpectrometry, Mass, Matrix-Assisted Laser Desorption-Ionizationgraphene oxideGraphiteLipidsProteins

Identifiers

PMID36321680
PMCPMC9757854
OpenAlexW4307967060

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Registered trials

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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.