Evidence map›Paper›PMID 26826485›Full record

ArticleGene therapy2016

Mapping of bionic array electric field focusing in plasmid DNA-based gene electrotransfer.

C J Browne, J L Pinyon, D M Housley, E N Crawford, N H Lovell, M Klugmann, G D Housley

Open access · hybridAbstract read
In one paragraph

Article in Gene therapy, 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
2.4field-weighted citation impact, top 13% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  4. Review
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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

7 authors at 1 institution in 1 country.

C J BrowneTranslational Neuroscience Facility and Department of Physiology, School of Medical Sciences, UNSW Australia, Sydney, New South Wales, Australia.
J L PinyonTranslational Neuroscience Facility and Department of Physiology, School of Medical Sciences, UNSW Australia, Sydney, New South Wales, Australia.
D M HousleyTranslational Neuroscience Facility and Department of Physiology, School of Medical Sciences, UNSW Australia, Sydney, New South Wales, Australia.
E N CrawfordTranslational Neuroscience Facility and Department of Physiology, School of Medical Sciences, UNSW Australia, Sydney, New South Wales, Australia.
N H LovellGraduate School of Biomedical Engineering, UNSW Australia, Sydney, New South Wales, Australia.
M KlugmannTranslational Neuroscience Facility and Department of Physiology, School of Medical Sciences, UNSW Australia, Sydney, New South Wales, Australia.ORCID http://orcid.org/0000-0003-0574-612X
G D HousleyTranslational Neuroscience Facility and Department of Physiology, School of Medical Sciences, UNSW Australia, Sydney, New South Wales, Australia.
UNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular medicine through gene therapy is challenged to achieve targeted action. This is now possible utilizing bionic electrode arrays for focal delivery of naked (plasmid) DNA via gene electrotransfer. Here, we establish the properties of array-based electroporation affecting targeted gene delivery. An array with eight 300 μm platinum ring electrodes configured as a cochlear implant bionic interface was used to transduce HEK293 cell monolayers with a plasmid-DNA green fluorescent protein (GFP) reporter gene construct. Electroporation parameters were pulse intensity, number, duration, separation and electrode configuration. The latter determined the shape of the electric fields, which were mapped using a voltage probe. Electrode array-based electroporation was found to require ~100 × lower applied voltages for cell transduction than conventional electroporation. This was found to be due to compression of the field lines orthogonal to the array. A circular area of GFP-positive cells was created when the electrodes were ganged together as four adjacent anodes and four cathodes, whereas alternating electrode polarity created a linear area of GFP-positive cells. The refinement of gene delivery parameters was validated in vivo in the guinea pig cochlea. These findings have significant clinical ramifications, where spatiotemporal control of gene expression can be predicted by manipulation of the electric field via current steering at a cellular level.

Indexed as

Gene Transfer TechniquesAnimalsBionicsElectrodesElectroporationGene ExpressionGenetic TherapyGuinea PigsHEK293 CellsHumansPlasmids

Identifiers

PMID26826485
PMCPMC4827009
OpenAlexW2313946441

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.