Evidence map›Paper›PMID 22958145›Full record

ArticleAnalytical chemistry2012

Multiparameter cell affinity chromatography: separation and analysis in a single microfluidic channel.

Peng Li, Yan Gao, Dimitri Pappas

Open access · greenAbstract read
In one paragraph

Article in Analytical chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Affinity chromatography: A review of trends and developments over the past 50 years.Journal of chromatography. B, Analytical technologies in the biomedical and life sciences · 2020
    Review
  5. Review
  6. Article
  7. Single Cell Isolation and Analysis.Frontiers in cell and developmental biology · 2016
    Review
  8. Article
  9. Review
  10. Microfluidic blood cell sorting: now and beyond.Small (Weinheim an der Bergstrasse, Germany) · 2014
    Review
  11. Review
  12. Review
  13. 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

3 authors at 1 institution in 1 country.

Peng LiDepartment of Chemistry and Biochemistry, Texas Tech University, Lubbock, Texas 79409, USA.
Yan Gao
Dimitri Pappas
Texas Tech University · US

Funding

Rapid Single Molecule Detection System for Intracellular Protease ActivityR21RR025782 · NCRR · TEXAS TECH UNIVERSITY · PI PAPPAS, DIMITRI · 2010 to 2011
$346k
Rapid Single Molecule Detection System for Intracellular Protease ActivityR21GM103550 · NIGMS · TEXAS TECH UNIVERSITY · PI PAPPAS, DIMITRI · 2012 to 2012
$172k
NCRR NIH HHS R21 RR025782NCRR NIH HHS RR025782NIGMS NIH HHS GM103550NIGMS NIH HHS R21 GM103550
6 · The paper itself

Abstract

The ability to sort and capture more than one cell type from a complex sample will enable a wide variety of studies of cell proliferation and death and the analysis of disease states. In this work, we integrated a pneumatic actuated control layer to an affinity separation layer to create different antibody-coating regions on the same fluidic channel. The comparison of different antibody capture capabilities to the same cell line was demonstrated by flowing Ramos cells through anti-CD19- and anti-CD71-coated regions in the same channel. It was determined that the cell capture density on the anti-CD19 region was 2.44 ± 0.13 times higher than that on the anti-CD71-coated region. This approach can be used to test different affinity molecules for selectivity and capture efficiency using a single cell line in one separation. Selective capture of Ramos and HuT 78 cells from a mixture was also demonstrated using two antibody regions in the same channel. Greater than 90% purity was obtained on both capture areas in both continuous flow and stop flow separation modes. A four-region antibody-coated device was then fabricated to study the simultaneous, serial capture of three different cell lines. In this case the device showed effective capture of cells in a single separation channel, opening up the possibility of multiple cell sorting. Multiparameter sequential blood sample analysis was also demonstrated with high capture specificity (>97% for both CD19+ and CD4+ leukocytes). The chip can also be used to selectively treat cells after affinity separation.

Indexed as

Microfluidic Analytical TechniquesCells, CulturedCell SeparationChromatography, AffinityHumans

Identifiers

PMID22958145
PMCPMC3483040
OpenAlexW2094511893

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.