Evidence map›Paper›PMID 27299468›Full record

ArticleBiomedical microdevices2016

Dynamic monitoring of single cell lysis in an impedance-based microfluidic device.

Ying Zhou, Srinjan Basu, Ernest D Laue, Ashwin A Seshia

Abstract read
In one paragraph

Article in Biomedical microdevices, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. 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

4 authors.

Ying ZhouDepartment of Engineering, Nanoscience Centre, University of Cambridge, 11 JJ Thomson Avenue, Cambridge, CB3 0FF, UK.
Srinjan BasuDepartment of Biochemistry, University of Cambridge, 80 Tennis Court Road, Cambridge, CB2 1GA, UK.
Ernest D LaueDepartment of Biochemistry, University of Cambridge, 80 Tennis Court Road, Cambridge, CB2 1GA, UK.
Ashwin A SeshiaDepartment of Engineering, Nanoscience Centre, University of Cambridge, 11 JJ Thomson Avenue, Cambridge, CB3 0FF, UK. aas41@cam.ac.uk.

Funding

Biotechnology and Biological Sciences Research Council BB/K013726/1
6 · The paper itself

Abstract

A microfluidic device that is capable of trapping and sensing dynamic variations in the electrical properties of individual cells is demonstrated. The device is applied to the real-time recording of impedance measurements of mouse embryonic stem cells (mESCs) during the process of membrane lysis, with the resulting changes in the electrical properties of cells during this process being quantitatively tracked over time. It is observed that the impedance magnitude decreases dramatically after cell membrane lysis. A significant shift in the phase spectrum is also observed during the time course of this process. By fitting experimental data to physical models, the electrical parameters of cells can be extracted and parameter variations quantified during the process. In the cell lysis experiments, the equivalent conductivity of the cell membrane is found to increase significantly due to pore formation in the membrane during lysis. An increase in the specific capacitance of the membrane is also observed. On the other hand, the conductivity of the cytoplasm is observed to decrease, which may be explained the fact that excess water enters the cell through the gradual permeabilization of the membrane during lysis. Cells can be trapped in the device for periods up to several days, and their electrical response can be monitored by real-time impedance measurements in a label-free and non-invasive manner. Furthermore, due to the highly efficient single cell trapping capacity of the device, a number of cells can be trapped and held in separate wells for concurrent parallel experiments, allowing for the possibility of stepped parametric experiments and studying cell heterogeneity by combining measurements across the array.

Indexed as

Electric ImpedanceLab-On-A-Chip DevicesSingle-Cell AnalysisAnimalsCell MembraneDimethylpolysiloxanesElectric CapacitanceEmbryonic Stem CellsEquipment DesignEvaluation Studies as TopicMiceMicrofluidic Analytical TechniquesModels, TheoreticalbaysilonDimethylpolysiloxanesImpedance spectroscopyMicrofluidicsReal-time measurementsSingle cell trappingStem cells

Identifiers

PMID27299468
PMCPMC4908161

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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.