Evidence map›Paper›PMID 26450165›Full record

ArticleScientific reports2015

Characterization of Pressure Transients Generated by Nanosecond Electrical Pulse (nsEP) Exposure.

Caleb C Roth, Ronald A Barnes, Bennett L Ibey, Hope T Beier, L Christopher Mimun, Saher M Maswadi, Mehdi Shadaram, Randolph D Glickman

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

8 authors.

Caleb C RothSchool of Medicine, Dept. of Radiological Sciences, University of Texas Health Science Center San Antonio, 7703 Floyd Curl Drive, San Antonio, Texas, USA 78229.
Ronald A BarnesDept. of Electrical Engineering, University of Texas San Antonio, 1 UTSA Circle, San Antonio, Texas, USA 78249.
Bennett L IbeyRadio Frequency Bioeffects Branch, Bioeffects Division, Human Effectiveness Directorate, 711th Human Performance Wing, Air Force Research Laboratory, 4141 Petroleum Road, JBSA Fort Sam Houston, Texas, USA 78234.
Hope T BeierOptical Radiation Bioeffects Branch, Bioeffects Division, Human Effectiveness Directorate, 711th Human Performance Wing, Air Force Research Laboratory, 4141 Petroleum Road, JBSA Fort Sam Houston, Texas, USA 78234.
L Christopher MimunDept. of Physics, University of Texas San Antonio, 1 UTSA Circle, San Antonio, Texas, USA 78249.
Saher M MaswadiDept. of Electrical Engineering, University of Texas San Antonio, 1 UTSA Circle, San Antonio, Texas, USA 78249.
Mehdi ShadaramDept. of Electrical Engineering, University of Texas San Antonio, 1 UTSA Circle, San Antonio, Texas, USA 78249.
Randolph D GlickmanSchool of Medicine, Dept. of Ophthalmology, University of Texas Health Science Center San Antonio, 7703 Floyd Curl Drive, San Antonio, Texas, USA 78229.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mechanism(s) responsible for the breakdown (nanoporation) of cell plasma membranes after nanosecond pulse (nsEP) exposure remains poorly understood. Current theories focus exclusively on the electrical field, citing electrostriction, water dipole alignment and/or electrodeformation as the primary mechanisms for pore formation. However, the delivery of a high-voltage nsEP to cells by tungsten electrodes creates a multitude of biophysical phenomena, including electrohydraulic cavitation, electrochemical interactions, thermoelastic expansion, and others. To date, very limited research has investigated non-electric phenomena occurring during nsEP exposures and their potential effect on cell nanoporation. Of primary interest is the production of acoustic shock waves during nsEP exposure, as it is known that acoustic shock waves can cause membrane poration (sonoporation). Based on these observations, our group characterized the acoustic pressure transients generated by nsEP and determined if such transients played any role in nanoporation. In this paper, we show that nsEP exposures, equivalent to those used in cellular studies, are capable of generating high-frequency (2.5 MHz), high-intensity (>13 kPa) pressure transients. Using confocal microscopy to measure cell uptake of YO-PRO®-1 (indicator of nanoporation of the plasma membrane) and changing the electrode geometry, we determined that acoustic waves alone are not responsible for poration of the membrane.

Indexed as

Cell Membrane PermeabilityAnimalsBenzoxazolesCell MembraneCHO CellsCricetinaeCricetulusElectricityElectroporationFluorescent DyesFourier AnalysisMicroscopy, ConfocalPorosityPressureQuinolinium CompoundsTime FactorsBenzoxazolesFluorescent DyesQuinolinium CompoundsYO-PRO 1

Identifiers

PMID26450165
PMCPMC4598730

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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.