Evidence map›Paper›PMID 29063498›Full record

ArticleDrug delivery and translational research2018

Inhibiting influenza virus replication and inducing protection against lethal influenza virus challenge through chitosan nanoparticles loaded by siRNA.

Abbas Jamali, Fatemeh Mottaghitalab, Asghar Abdoli, Meshkat Dinarvand, Aida Esmailie, Masoumeh Tavassoti Kheiri, Fatemeh Atyabi

Abstract read
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In one paragraph

Article in Drug delivery and translational research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

24 citing papers in PubMed, 44 citations in OpenAlex.

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  14. Nanomedicine based approaches for combating viral infections.Journal of controlled release : official journal of the Controlled Release Society · 2021
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  18. Antiviral therapies: advances and perspectives.Fundamental & clinical pharmacology · 2021
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  20. Chitosan-Based Nanoparticles Against Viral Infections.Frontiers in cellular and infection microbiology · 2021
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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 2 institutions in 1 country.

Abbas JamaliDepartment of Influenza Research and Other Respiratory Viruses, Pasteur Institute of Iran, Tehran, Iran.
Fatemeh MottaghitalabNanotechnology Research Centre, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, P.O. Box 17141, Iran.
Asghar AbdoliDepartment of Hepatitis and AIDS, Pasteur Institute of Iran, Tehran, Iran.
Meshkat DinarvandNanotechnology Research Centre, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, P.O. Box 17141, Iran.
Aida EsmailieNanotechnology Research Centre, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, P.O. Box 17141, Iran.
Masoumeh Tavassoti KheiriDepartment of Influenza Research and Other Respiratory Viruses, Pasteur Institute of Iran, Tehran, Iran. mtkheiri@pasteur.ac.ir.
Fatemeh AtyabiNanotechnology Research Centre, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, P.O. Box 17141, Iran. atyabifa@tums.ac.ir.
Tehran University of Medical Sciences · IRPasteur Institute of Iran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Influenza virus causes a highly contagious viral respiratory tract infection with potentially fatal outcomes in humans and animals. There is now widespread influenza virus resistance to commercial drugs due to the genetic diversity of virus. Therefore, new therapeutic formulation needs to be developed. Chitosan/siRNA nanoparticles were generated as a new therapeutic approach against influenza virus infections both in vitro and in vivo. Designed siRNA against influenza nucleoprotein was formulated in chitosan polymer as siRNA/chitosan nanoparticle complex. Particle size and zeta potential of the nanoparticles were measured by dynamic light scattering. The uptake of labeled siRNA into Vero cells was visualized using fluorescence microscopy. Nanoparticle-mediated knockdown of enhanced green fluorescent protein (EGFP) was analyzed and quantified by flow cytometry in Vero cells. Results of the in vitro study showed that chitosan/siRNA nanoparticle was efficiently uptaken by Vero cells, leading to inhibition of influenza virus replication. Furthermore, nasal delivery of siRNA by chitosan nanoparticle complex has antiviral effects and significantly protected BALB/c mice from a lethal influenza challenge. These findings suggest that chitosan nanoparticle equipped with siRNA is a promising system for controlling influenza virus infection.

Indexed as

AnimalsChitosanChlorocebus aethiopsFemaleGreen Fluorescent ProteinsHumansInfluenza A Virus, H1N1 SubtypeMice, Inbred BALB CNanoparticlesNucleoproteinsOrthomyxoviridae InfectionsRNA, Small InterferingVero CellsViral Core ProteinsVirus ReplicationChitosanenhanced green fluorescent proteinGreen Fluorescent ProteinsNucleoproteinsRNA, Small InterferingViral Core ProteinsChitosanInfluenza virusNanoparticlesNasal deliverysiRNA

Identifiers

PMID29063498
OpenAlexW2765559662

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.