Evidence map›Paper›PMID 30283149›Full record

ArticleScientific reports2018

Multivalent and multifunctional polysaccharide-based particles for controlled receptor recognition.

Haohao Duan, Mark Donovan, Aude Foucher, Xavier Schultze, Sebastien Lecommandoux

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  3. Article
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  5. Embracing nanomaterials' interactions with the innate immune system.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2021
    Review
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  7. 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

5 authors at 2 institutions in 1 country.

Haohao DuanL'Oréal recherche avancée, 1 avenue Eugène Schueller, 93600, Aulnay-sous-Bois, France.
Mark DonovanL'Oréal recherche avancée, 1 avenue Eugène Schueller, 93600, Aulnay-sous-Bois, France.
Aude FoucherL'Oréal recherche avancée, 1 avenue Eugène Schueller, 93600, Aulnay-sous-Bois, France.
Xavier SchultzeL'Oréal recherche avancée, 1 avenue Eugène Schueller, 93600, Aulnay-sous-Bois, France.
Sebastien LecommandouxLaboratoire de Chimie des Polymères Organiques, CNRS, Université de Bordeaux INP/ENSCBP, 16 avenue Pey Berland, 33600, Pessac, France. lecommandoux@enscbp.fr.ORCID http://orcid.org/0000-0003-0465-8603
L'Oréal (France) · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polysaccharides represent a versatile class of building blocks that are used in macromolecular design. By choosing the appropriate saccharide block, various physico-chemical and biological properties can be introduced both at the level of the polymer chains and the resulting self-assembled nanostructures. Here, we synthetized amphiphilic diblock copolymers combining a hydrophobic and helical poly(γ-benzyl-L-glutamate) PBLG and two polysaccharides, namely hyaluronic acid (HA) and laminarin (LAM). The copolymers could self-assemble to form particles in water by nanoprecipitation. In addition, hybrid particles containing both HA and LAM in different ratios were obtained by co-nanoprecipitation of the two copolymers. By controlling the self-assembly process, five particle samples with different morphologies and compositions were developed. The interaction between the particles and biologically relevant proteins for HA and LAM, namely CD44 and Dectin-1 respectively, was evaluated by surface plasmon resonance (SPR). We demonstrated that the particle-protein interaction could be modulated by the particle structure and composition. It is therefore suggested that this method based on nanoprecipitation is a practical and versatile way to obtain particles with controllable interactions with proteins, hence with the appropriate biological properties for biomedical applications such as drug delivery.

Indexed as

Drug Delivery SystemsDectin-1GlucansHumansHyaluronan ReceptorsHyaluronic AcidHydrophobic and Hydrophilic InteractionsLectins, C-TypePolyglutamic AcidPolysaccharidesSurface Plasmon ResonanceDectin-1GlucansHyaluronan ReceptorsHyaluronic AcidlaminaranLectins, C-Typepoly-gamma-benzyl-L-glutamatePolyglutamic AcidPolysaccharides

Identifiers

PMID30283149
PMCPMC6170371
OpenAlexW2893177956

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.