Evidence map›Paper›PMID 27080572›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2016

Mechanisms allowing protein delivery in nasal mucosa using NPL nanoparticles.

B Bernocchi, R Carpentier, I Lantier, C Ducournau, I Dimier-Poisson, D Betbeder

Open access · hybridAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

34 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
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  10. Human T-cell activation withLife science alliance · 2024
    Article
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  12. Review
  13. Article
  14. Article
  15. Nasal vaccination of six squirrel monkeys (International journal for parasitology. Parasites and wildlife · 2023
    Article
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  18. 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

6 authors at 2 institutions in 1 country.

B BernocchiInserm, LIRIC-UMR 995, F-59000 Lille, France; Université de Lille, LIRIC-UMR 995, F-59000 Lille, France; CHRU de Lille, LIRIC-UMR 995, F-59000 Lille, France.
R CarpentierInserm, LIRIC-UMR 995, F-59000 Lille, France; Université de Lille, LIRIC-UMR 995, F-59000 Lille, France; CHRU de Lille, LIRIC-UMR 995, F-59000 Lille, France. Electronic address: rodolphe.carpentier@univ-lille2.fr.
I LantierINRA, UMR1282 Infectiologie et Santé Publique, F-37380 Nouzilly, France. Laboratoire d'Expertise en Infection Animale; Université François-Rabelais de Tours, UMR1282 Infectiologie et Santé Publique, F-37000 Tours, France. Immunologie Parasitaire et Vaccinologie, Biothérapies Anti-Infectieuses.
C DucournauUniversité François-Rabelais de Tours, UMR1282 Infectiologie et Santé Publique, F-37000 Tours, France. Immunologie Parasitaire et Vaccinologie, Biothérapies Anti-Infectieuses; INRA, UMR1282 Infectiologie et Santé Publique, F-37380 Nouzilly, France. Laboratoire d'Expertise en Infection Animale.
I Dimier-PoissonUniversité François-Rabelais de Tours, UMR1282 Infectiologie et Santé Publique, F-37000 Tours, France. Immunologie Parasitaire et Vaccinologie, Biothérapies Anti-Infectieuses; INRA, UMR1282 Infectiologie et Santé Publique, F-37380 Nouzilly, France. Laboratoire d'Expertise en Infection Animale.
D BetbederInserm, LIRIC-UMR 995, F-59000 Lille, France; Université de Lille, LIRIC-UMR 995, F-59000 Lille, France; CHRU de Lille, LIRIC-UMR 995, F-59000 Lille, France; University of Artois, 62000 Arras, France.
Inserm · FRUniversité de Tours · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The intranasal administration of proteins using nanoparticles is a promising approach for several applications, especially for mucosal vaccines. Delivery of protein within the epithelial barrier is a key point to elicit an immune response and nano-carrier has to show no toxicity. The aim of this work was to elucidate the interactions of cationic porous nanoparticles loaded with protein delivery for antigen delivery in the nose. We investigated the loading, the cellular delivery and the epithelial transcytosis of proteins associated to these nanoparticles containing an anionic lipid in their core (NPL). NPL were highly endocytosed by airway epithelial cells and significantly improved the protein delivery into the cell. In vitro transcytosis studies showed that NPL did not modify the in vitro epithelial permeability suggesting no toxicity of these carriers. Moreover protein and NPL did not translocate the epithelial barrier. In vivo studies demonstrated that NPL prolonged the nasal residence time of the protein and no NPL were found beyond the epithelial barrier in vivo, precluding a negative side effect. All together these results establish the NPL as a bio-eliminable and optimal vaccine carrier.

Indexed as

Administration, IntranasalAnimalsAntigensDrug CarriersEndocytosisEpichlorohydrinEpoxy CompoundsMiceNanoparticlesNasal MucosaOvalbuminPermeabilityPolysaccharidesQuaternary Ammonium CompoundsAntigensDrug CarriersEpichlorohydrinEpoxy Compoundsglycidyl trimethylammoniummaltodextrinOvalbuminPolysaccharidesQuaternary Ammonium CompoundsBiodistributionIntranasal drug deliveryNanoparticleProtein deliveryTranscytosisVaccine

Identifiers

PMID27080572
PMCPMC4907310
OpenAlexW2333733391

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.