Evidence map›Paper›PMID 25584111›Full record

ArticleBiomicrofluidics2014

Integration of programmable microfluidics and on-chip fluorescence detection for biosensing applications.

J W Parks, M A Olson, J Kim, D Ozcelik, H Cai, R Carrion, J L Patterson, R A Mathies, A R Hawkins, H Schmidt

Abstract read
In one paragraph

Article in Biomicrofluidics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Optofluidic multiplex detection of single SARS-CoV-2 and influenza A antigens using a novel bright fluorescent probe assay.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Optofluidic bioanalysis: fundamentals and applications.Nanophotonics (Berlin, Germany) · 2017
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
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

10 authors.

J W ParksSchool of Engineering, University of California Santa Cruz , Santa Cruz, California 95064, USA.
M A OlsonDepartment of Electrical and Computer Engineering, Brigham Young University , Provo, Utah 84602, USA.
J Kim
D OzcelikSchool of Engineering, University of California Santa Cruz , Santa Cruz, California 95064, USA.
H CaiSchool of Engineering, University of California Santa Cruz , Santa Cruz, California 95064, USA.
R CarrionDepartment of Virology and Immunology, Texas Biomedical Research Institute , 7620 NW Loop 410, San Antonio, Texas 78227, USA.
J L PattersonDepartment of Virology and Immunology, Texas Biomedical Research Institute , 7620 NW Loop 410, San Antonio, Texas 78227, USA.
R A MathiesDepartment of Chemistry, University of California Berkeley , Berkeley, California 94720, USA.
A R HawkinsDepartment of Electrical and Computer Engineering, Brigham Young University , Provo, Utah 84602, USA.
H SchmidtSchool of Engineering, University of California Santa Cruz , Santa Cruz, California 95064, USA.

Funding

Hybrid integrated molecular analysis (HIMAS) for point-of-care diagnosticsR33AI100229 · NIAID · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI SCHMIDT, HOLGER · 2014 to 2016
$1.7M
Hybrid integrated molecular analysis (HIMAS) for point-of-care diagnosticsR21AI100229 · NIAID · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI SCHMIDT, HOLGER · 2012 to 2013
$448k
EXTRAMURAL RESEARCH FACILITIES CONSTRUCTIONC06RR012087 · NCRR · SOUTHWEST FOUNDATION FOR BIOMEDICAL RES · PI VANDEBERG, JOHN L · 1996 to 1996
–
NCRR NIH HHS C06 RR012087NIAID NIH HHS R21 AI100229NIAID NIH HHS R33 AI100229
6 · The paper itself

Abstract

We describe the integration of an actively controlled programmable microfluidic sample processor with on-chip optical fluorescence detection to create a single, hybrid sensor system. An array of lifting gate microvalves (automaton) is fabricated with soft lithography, which is reconfigurably joined to a liquid-core, anti-resonant reflecting optical waveguide (ARROW) silicon chip fabricated with conventional microfabrication. In the automaton, various sample handling steps such as mixing, transporting, splitting, isolating, and storing are achieved rapidly and precisely to detect viral nucleic acid targets, while the optofluidic chip provides single particle detection sensitivity using integrated optics. Specifically, an assay for detection of viral nucleic acid targets is implemented. Labeled target nucleic acids are first captured and isolated on magnetic microbeads in the automaton, followed by optical detection of single beads on the ARROW chip. The combination of automated microfluidic sample preparation and highly sensitive optical detection opens possibilities for portable instruments for point-of-use analysis of minute, low concentration biological samples.

Identifiers

PMID25584111
PMCPMC4290670

What OpenQuestion holds

Textmetadata
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.