Evidence map›Paper›PMID 25053808›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Stationary nanoliter droplet array with a substrate of choice for single adherent/nonadherent cell incubation and analysis.

Jonathan Shemesh, Tom Ben Arye, Jonathan Avesar, Joo H Kang, Amir Fine, Michael Super, Amit Meller, Donald E Ingber, Shulamit Levenberg

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Modular microfluidics for life sciences.Journal of nanobiotechnology · 2023
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Microfluidic chambers using fluid walls for cell biology.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  16. Article
  17. Article
  18. Article
  19. Rapid phenotypic antimicrobial susceptibility testing using nanoliter arrays.Proceedings of the National Academy of Sciences of the United States of America · 2017
    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

9 authors.

Jonathan ShemeshDepartment of Biomedical Engineering andRussell Berrie Nanotechnology Institute, Technion-Israel Institute of Technology, Haifa 32000, Israel;
Tom Ben AryeDepartment of Biomedical Engineering andRussell Berrie Nanotechnology Institute, Technion-Israel Institute of Technology, Haifa 32000, Israel;
Jonathan AvesarDepartment of Biomedical Engineering and.
Joo H KangWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115;Harvard School of Engineering and Applied Sciences, Cambridge, MA 02139; and.
Amir FineDepartment of Biomedical Engineering and.
Michael SuperWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115;
Amit MellerDepartment of Biomedical Engineering andRussell Berrie Nanotechnology Institute, Technion-Israel Institute of Technology, Haifa 32000, Israel;
Donald E IngberWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115;Harvard School of Engineering and Applied Sciences, Cambridge, MA 02139; andVascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, MA 02115.
Shulamit LevenbergDepartment of Biomedical Engineering andRussell Berrie Nanotechnology Institute, Technion-Israel Institute of Technology, Haifa 32000, Israel; shulamit@bm.technion.ac.il.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microfluidic water-in-oil droplets that serve as separate, chemically isolated compartments can be applied for single-cell analysis; however, to investigate encapsulated cells effectively over prolonged time periods, an array of droplets must remain stationary on a versatile substrate for optimal cell compatibility. We present here a platform of unique geometry and substrate versatility that generates a stationary nanodroplet array by using wells branching off a main microfluidic channel. These droplets are confined by multiple sides of a nanowell and are in direct contact with a biocompatible substrate of choice. The device is operated by a unique and reversed loading procedure that eliminates the need for fine pressure control or external tubing. Fluorocarbon oil isolates the droplets and provides soluble oxygen for the cells. By using this approach, the metabolic activity of single adherent cells was monitored continuously over time, and the concentration of viable pathogens in blood-derived samples was determined directly by measuring the number of colony-formed droplets. The method is simple to operate, requires a few microliters of reagent volume, is portable, is reusable, and allows for cell retrieval. This technology may be particularly useful for multiplexed assays for which prolonged and simultaneous visual inspection of many isolated single adherent or nonadherent cells is required.

Indexed as

AnimalsCell AdhesionCell Line, TumorCell ProliferationCell SurvivalColony Count, MicrobialFibroblastsHumansLeukemiaMiceMicrofluidic Analytical TechniquesSingle-Cell AnalysisStaphylococcus aureusdiagnosticsnanoliter arraysingle cell

Identifiers

PMID25053808
PMCPMC4128147

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.