Evidence map›Paper›PMID 29184110›Full record

ArticleScientific reports2017

Differential effects on membrane permeability and viability of human keratinocyte cells undergoing very low intensity megasonic fields.

F Domenici, F Brasili, S Giantulli, B Cerroni, A Bedini, C Giliberti, R Palomba, I Silvestri, S Morrone, G Paradossi and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  5. Review
  6. Article
  7. Evaluation of supercritical COThe Science of the total environment · 2021
    Article
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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

12 authors at 4 institutions in 1 country.

F DomeniciDipartimento di Scienze e Tecnologie Chimiche, Università degli Studi di Roma "Tor Vergata", Rome, Italy. fabio.domenici@uniroma2.it.ORCID 0000-0001-6776-2737
F BrasiliDipartimento di Fisica, Università degli Studi di Roma "Sapienza", Rome, Italy.
S GiantulliDipartimento di Fisica, Università degli Studi di Roma "Sapienza", Rome, Italy.
B CerroniDipartimento di Scienze e Tecnologie Chimiche, Università degli Studi di Roma "Tor Vergata", Rome, Italy.
A BediniDipartimento Innovazioni Tecnologiche e Sicurezza degli Impianti, Prodotti e Insediamenti Antropici (DIT), INAIL, Monteporzio Catone, Rome, Italy.
C GilibertiDipartimento Innovazioni Tecnologiche e Sicurezza degli Impianti, Prodotti e Insediamenti Antropici (DIT), INAIL, Monteporzio Catone, Rome, Italy.
R PalombaDipartimento Innovazioni Tecnologiche e Sicurezza degli Impianti, Prodotti e Insediamenti Antropici (DIT), INAIL, Monteporzio Catone, Rome, Italy.
I SilvestriDipartimento di Medicina Molecolare, Università degli Studi di Roma "Sapienza", Rome, Italy.
S MorroneDipartimento di Medicina Sperimentale, Università degli Studi di Roma "Sapienza", Rome, Italy.
G ParadossiDipartimento di Scienze e Tecnologie Chimiche, Università degli Studi di Roma "Tor Vergata", Rome, Italy.
M MatteiCentro Servizi Interdipartimentale - Stazione Tecnologia Animale and Dipartimento di Biologia, Università degli Studi di Roma "Tor Vergata", Rome, Italy.
F BordiDipartimento di Fisica, Università degli Studi di Roma "Sapienza", Rome, Italy.
Sapienza University of Rome · ITUniversity of Rome Tor Vergata · ITIstituto Nazionale per l'Assicurazione Contro gli Infortuni sul Lavoro · ITInstitute for Complex Systems · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Among different therapeutic applications of Ultrasound (US), transient membrane sonoporation (SP) - a temporary, non-lethal porosity, mechanically induced in cell membranes through US exposure - represents a compelling opportunity towards an efficient and safe drug delivery. Nevertheless, progresses in this field have been limited by an insufficient understanding of the potential cytotoxic effects of US related to the failure of the cellular repair and to the possible activation of inflammatory pathway. In this framework we studied the in vitro effects of very low-intensity US on a human keratinocyte cell line, which represents an ideal model system of skin protective barrier cells which are the first to be involved during medical US treatments. Bioeffects linked to US application at 1 MHz varying the exposure parameters were investigated by fluorescence microscopy and fluorescence activated cell sorting. Our results indicate that keratinocytes undergoing low US doses can uptake drug model molecules with size and efficiency which depend on exposure parameters. According to sub-cavitation SP models, we have identified the range of doses triggering transient membrane SP, actually with negligible biological damage. By increasing US doses we observed a reduced cells viability and an inflammatory gene overexpression enlightening novel healthy relevant strategies.

Indexed as

Ultrasonic WavesAnimalsApoptosisBiomarkersCell LineCell MembraneCell Membrane PermeabilityCell SurvivalFlow CytometryHumansKeratinocytesMiceMicroscopy, FluorescenceSonicationTime FactorsBiomarkers

Identifiers

PMID29184110
PMCPMC5705699
OpenAlexW2770822081

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.