Evidence map›Paper›PMID 27561639›Full record

ArticleThe Journal of membrane biology2017

Exploring the Applicability of Nano-Poration for Remote Control in Smart Drug Delivery Systems.

Agnese Denzi, Elena Della Valle, Francesca Apollonio, Marie Breton, Lluis M Mir, Micaela Liberti

Abstract read
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In one paragraph

Article in The Journal of membrane biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Stimuli-Responsive Drug Release from Smart Polymers.Journal of functional biomaterials · 2019
    Review
  4. Article
  5. Article
  6. 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

6 authors.

Agnese DenziCenter for Life Nano Science at Sapienza, Istituto Italiano di Tecnologia, 00161, Rome, Italy.
Elena Della ValleItalian Inter-University Centre of Electromagnetic Fields and Bio-Systems (ICEmB)@Department of Information Engineering, Electronics and Telecommunication (DIET), University of Rome "La Sapienza", 00184, Rome, Italy.
Francesca ApollonioItalian Inter-University Centre of Electromagnetic Fields and Bio-Systems (ICEmB)@Department of Information Engineering, Electronics and Telecommunication (DIET), University of Rome "La Sapienza", 00184, Rome, Italy.
Marie BretonVectorology and Antitumor Therapies, UMR 8203, CNRS, Univ. Paris-Sud, Université Paris-Saclay, Gustave Roussy, Villejuif, 94805, France.
Lluis M MirVectorology and Antitumor Therapies, UMR 8203, CNRS, Univ. Paris-Sud, Université Paris-Saclay, Gustave Roussy, Villejuif, 94805, France.
Micaela LibertiItalian Inter-University Centre of Electromagnetic Fields and Bio-Systems (ICEmB)@Department of Information Engineering, Electronics and Telecommunication (DIET), University of Rome "La Sapienza", 00184, Rome, Italy. liberti@die.uniroma1.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Smart drug delivery systems represent an interesting tool to significantly improve the efficiency and the precision in the treatment of a broad category of diseases. In this context, a drug delivery mediated by nanosecond pulsed electric fields seems a promising technique, allowing for a controlled release and uptake of drugs by the synergy between the electropulsation and nanocarriers with encapsulated drugs. The main concern about the use of electroporation for drug delivery applications is the difference in dimension between the liposome (nanometer range) and the cell (micrometer range). The choice of liposome dimension is not trivial. Liposomes larger than 500 nm of diameter could be recognized as pathogen agents by the immune system, while liposomes of smaller size would require external electric field of high amplitudes for the membrane electroporation that could compromise the cell viability. The aim of this work is to theoretically study the possibility of a simultaneous cell and liposomes electroporation. The numerical simulations reported the possibility to electroporate the cell and a significant percentage of liposomes with comparable values of external electric field, when a 12 nsPEF is used.

Indexed as

Drug Delivery SystemsElectroporationCell Membrane PermeabilityHumansLiposomesModels, TheoreticalMuscle Fibers, SkeletalLiposomesDrug deliveryElectroporationLiposomesMicrodosimetryNanosecond pulsed electric fields

Identifiers

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.