Evidence map›Paper›PMID 28052769›Full record

ArticleJournal of nanobiotechnology2017

Elasto-inertial microfluidics for bacteria separation from whole blood for sepsis diagnostics.

Muhammad Asim Faridi, Harisha Ramachandraiah, Indradumna Banerjee, Sahar Ardabili, Sergey Zelenin, Aman Russom

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Review
  2. Review
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  4. Isolation Techniques of Micro/Nano-Scaled Species for Biomedical Applications.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Exploitation of elasto-inertial fluid flow for the separation of nano-sized particles: Simulating the isolation of extracellular vesicles.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Multi-Modal Microfluidics (MMicromachines · 2022
    Article
  16. Review
  17. Length-based separation ofMicrosystems & nanoengineering · 2022
    Article
  18. Review
  19. Review
  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

6 authors.

Muhammad Asim FaridiDivision of Proteomics & Nano-biotechnology, School of Biotechnology, Royal Institute of Technology KTH, SciLifeLab Tomtebodavägen 23, 17165, Solna, Sweden.
Harisha RamachandraiahDivision of Proteomics & Nano-biotechnology, School of Biotechnology, Royal Institute of Technology KTH, SciLifeLab Tomtebodavägen 23, 17165, Solna, Sweden.
Indradumna BanerjeeDivision of Proteomics & Nano-biotechnology, School of Biotechnology, Royal Institute of Technology KTH, SciLifeLab Tomtebodavägen 23, 17165, Solna, Sweden.
Sahar ArdabiliDivision of Proteomics & Nano-biotechnology, School of Biotechnology, Royal Institute of Technology KTH, SciLifeLab Tomtebodavägen 23, 17165, Solna, Sweden.
Sergey ZeleninDivision of Proteomics & Nano-biotechnology, School of Biotechnology, Royal Institute of Technology KTH, SciLifeLab Tomtebodavägen 23, 17165, Solna, Sweden.
Aman RussomDivision of Proteomics & Nano-biotechnology, School of Biotechnology, Royal Institute of Technology KTH, SciLifeLab Tomtebodavägen 23, 17165, Solna, Sweden. aman.russom@scilifelab.se.ORCID http://orcid.org/0000-0002-0242-358X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBloodstream infections (BSI) remain a major challenge with high mortality rate, with an incidence that is increasing worldwide. Early treatment with appropriate therapy can reduce BSI-related morbidity and mortality. However, despite recent progress in molecular based assays, complex sample preparation steps have become critical roadblock for a greater expansion of molecular assays. Here, we report a size based, label-free, bacteria separation from whole blood using elasto-inertial microfluidics.

resultsIn elasto-inertial microfluidics, the viscoelastic flow enables size based migration of blood cells into a non-Newtonian solution, while smaller bacteria remain in the streamline of the blood sample entrance and can be separated. We first optimized the flow conditions using particles, and show continuous separation of 5 μm particles from 2 μm at a yield of 95% for 5 µm particle and 93% for 2 µm particles at respective outlets. Next, bacteria were continuously separated at an efficiency of 76% from undiluted whole blood sample.

conclusionWe demonstrate separation of bacteria from undiluted while blood using elasto-inertial microfluidics. The label-free, passive bacteria preparation method has a great potential for downstream phenotypic and molecular analysis of bacteria.

Indexed as

BacteriaBlood CellsElasticityEscherichia coliFluorescent DyesHumansMicrofluidicsParticle SizeSepsisFluorescent DyesElasto-inertial microfluidicsMicro particle separationSample preparationSepsis

Identifiers

PMID28052769
PMCPMC5210221

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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.