Evidence map›Paper›PMID 35233729›Full record

ArticlePharmaceutical research2022

Defining Endocytic Pathways of Fucoidan-Coated PIBCA Nanoparticles from the Design of their Surface Architecture.

M C B Lira-Nogueira, V P Gibson, V Nicolas, N S Santos-Magalhães, C Vauthier

Open access · bronzeAbstract read
In one paragraph

Article in Pharmaceutical research, 2022. 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
4.0field-weighted citation impact, top 7% 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

6 citing papers in PubMed, 19 citations in OpenAlex.

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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

5 authors at 3 institutions in 2 countries.

M C B Lira-NogueiraCentro Acadêmico de Vitória, Universidade Federal de Pernambuco, Vitória de Santo Antão, Brazil.
V P GibsonLaboratório de Immunopatologia Keizo-Asami, Universidade Federal de Pernambuco Recife, Recife, Brazil.
V NicolasPlateforme d'Imagerie Cellulaire MIPSIT, UMS-IPSIT, Inserm, CNRS, Ingénierie et Plateformes au Service de l'Innovation Thérapeutique, Université Paris-Saclay, CNRS, UMR 8612, Université Paris-Sud, 5 Rue J.B. Clément, 92296, Châtenay, Malabry Cedex, France.
N S Santos-MagalhãesLaboratório de Immunopatologia Keizo-Asami, Universidade Federal de Pernambuco Recife, Recife, Brazil.
C VauthierCNRS, Institut Galien Paris-Saclay, Université Paris-Saclay, 92296, Châtenay, Malabry, France. christine.vauthier@universite-paris-saclay.fr.ORCID http://orcid.org/0000-0003-3963-0045
Centre National de la Recherche Scientifique · FRUniversidade Federal de Pernambuco · BRUniversité Paris-Sud · FR

Funding

CAPES PRINTS PRINT 2761/2018cNPQ 249904/2013-06cNPQ Auxílio Pesquisador 065880/2020-93cNPQ Qualis A 23076.054228/2020-29cNPQ Universal 427243/2016-5COFECUB-CAPES CAPES-COFECUB 721/11COFECUB-CAPES COFECUB-CAPES 721/11
6 · The paper itself

Abstract

purposeThis work investigated the endocytic pathways taken by poly(isobutylcyanoacrylate) (PIBCA) nanoparticles differing in their surface composition and architecture, assuming that this might determine their efficiency of intracellular drug delivery.

methodsNanoparticles (A0, A25, A100, R0, R25 ) were prepared by anionic or redox radical emulsion polymerization using mixtures of dextran and fucoidan (0, 25, 100 % in fucoidan). Cell uptake was evaluated by incubating J774A.1 macrophages with nanoparticles. Endocytic pathways were studied by incubating cells with endocytic pathway inhibitors (chlorpromazine, genistein, cytochalasin D, methyl-ß-cyclodextrin and nocodazole) and nanoparticle uptake was evaluated by flow cytometry and confocal microscopy.

resultsThe fucoidan-coated PIBCA nanoparticles A

conclusionInternalization pathways of PIBCA nanoparticles by J774A.1 macrophages could be determined by nanoparticle fucoidan surface composition and architecture. In turn, this influenced the extent of internalization and localization of accumulated nanoparticles within cells. The results are of interest for rationalizing the design of nanoparticles for potential cytoplamic drug delivery by controlling the nature of the nanoparticle surface.

Indexed as

NanoparticlesDrug Delivery SystemsEmulsionsPolysaccharidesEmulsionsfucoidanPolysaccharidescellular uptakeendocytic pathwayfucoidannanoparticlesPIBCA

Identifiers

PMID35233729
PMCPMC8887940
OpenAlexW4214810151

What OpenQuestion holds

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Registered trials

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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.