Evidence map›Paper›PMID 34049630›Full record

ArticleAnalytica chimica acta2021

Rapid separation of blood plasma exosomes from low-density lipoproteins via a hydrophobic interaction chromatography method on a polyester capillary-channeled polymer fiber phase.

Sisi Huang, Xiaohui Ji, Kaylan K Jackson, David M Lubman, Mary B Ard, Terri F Bruce, R Kenneth Marcus

Abstract read
In one paragraph

Article in Analytica chimica acta, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
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

26 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Exosome-Based Therapeutics in Dermatology.Biomaterials research · 2025
    Review
  7. Review
  8. Article
  9. Bladder cancer: non-coding RNAs and exosomal non-coding RNAs.Functional & integrative genomics · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

7 authors.

Sisi HuangDepartment of Chemistry, Biosystems Research Complex, Clemson University, Clemson, SC, 29634, USA.
Xiaohui JiDepartment of Surgery, Medical Science Research Building I, University of Michigan, Ann Arbor, MI, 48109, USA.
Kaylan K JacksonDepartment of Chemistry, Biosystems Research Complex, Clemson University, Clemson, SC, 29634, USA.
David M LubmanDepartment of Surgery, Medical Science Research Building I, University of Michigan, Ann Arbor, MI, 48109, USA.
Mary B ArdGeorgia Electron Microscopy Core Facility, University of Georgia Athens, GA, 30602, USA.
Terri F BruceDepartment of Bioengineering, Life Sciences Facility, Clemson University, Clemson, SC, 29634, USA.
R Kenneth MarcusDepartment of Chemistry, Biosystems Research Complex, Clemson University, Clemson, SC, 29634, USA. Electronic address: marcusr@clemson.edu.

Funding

Supplemental for Detection of Glycopeptides of MCI in Patient SerumR01CA160254 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI David M. Lubman · 2012 to 2026
$5.4M
NCI NIH HHS R01 CA160254
6 · The paper itself

Abstract

Exosomes are membrane-bound, cell-secreted vesicles, with sizes ranging from 30 to 150 nm. Exosomes in blood plasma have become proposed targets as measurable indicators of disease conditions. Current methods for plasma-based exosome isolation are time-consuming, complex, and have high operational costs. One of the most commonly reported shortcomings of current isolation protocols is the co-extraction of lipoproteins (e.g. low-density lipoproteins, LDLs) with the target exosomes. This report describes the use of a rapid, single-operation hydrophobic interaction chromatography (HIC) procedure on a polyester (PET) capillary-channeled polymer (C-CP) fiber column, demonstrating the ability to efficiently purify exosomes. The method has previously been demonstrated for isolation of exosomes from diverse biological matrices, but questions were raised about the potential co-elution of LDLs. In the method described herein, a step-gradient procedure sequentially elutes spiked lipoproteins and blood plasma-originating exosomes in 10 min, with the LDLs excluded from the desired exosome fraction. Mass spectrometry (MS) was used to characterize an impurity in the primary LDL material, identifying the presence of exosomal material. Transmission electron microscopy (TEM) and an enzyme-linked immunosorbent assay (ELISA) were used to identify the various elution components. The method serves both as a rapid means of high purity exosome isolation as well as a screening tool for the purity of LDL samples with respect to extracellular vesicles.

Indexed as

ExosomesChromatographyHumansHydrophobic and Hydrophilic InteractionsLipoproteins, LDLPlasmaPolyestersPolymersLipoproteins, LDLPolyestersPolymersCapillary-channeled polymer (C-CP)Enzyme-linked immunosorbent assay (ELISA)ExosomesExtracellular vesicles (EVs)FibersHydrophobic interaction chromatographyLow-density lipoprotein (LDL)ProteomicsTransmission electron microscopy (TEM)

Identifiers

PMID34049630
PMCPMC8164660

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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.