Evidence map›Paper›PMID 39598659›Full record

ArticleMolecules (Basel, Switzerland)2024

Multiplex Evaluation of Biointerface-Targeting Abilities and Affinity of Synthetized Nanoparticles-A Step Towards Improved Nanoplatforms for Biomedical Applications.

Mélanie Romain, Céline Elie-Caille, Dorra Ben Elkadhi, Olivier Heintz, Michaële Herbst, Lionel Maurizi, Wilfrid Boireau, Nadine Millot

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

8 authors.

Mélanie RomainLaboratoire Interdisciplinaire Carnot de Bourgogne, UMR 6303 CNRS-Université de Bourgogne, 21078 Dijon, France.ORCID 0000-0003-3355-8257
Céline Elie-CailleInstitut FEMTO-ST, UMR 6174 CNRS-Université de Franche-Comté, 25030 Besançon, France.
Dorra Ben ElkadhiLaboratoire Interdisciplinaire Carnot de Bourgogne, UMR 6303 CNRS-Université de Bourgogne, 21078 Dijon, France.
Olivier HeintzLaboratoire Interdisciplinaire Carnot de Bourgogne, UMR 6303 CNRS-Université de Bourgogne, 21078 Dijon, France.
Michaële HerbstLaboratoire Interdisciplinaire Carnot de Bourgogne, UMR 6303 CNRS-Université de Bourgogne, 21078 Dijon, France.ORCID 0009-0004-9750-4228
Lionel MauriziLaboratoire Interdisciplinaire Carnot de Bourgogne, UMR 6303 CNRS-Université de Bourgogne, 21078 Dijon, France.ORCID 0000-0002-6346-7623
Wilfrid BoireauInstitut FEMTO-ST, UMR 6174 CNRS-Université de Franche-Comté, 25030 Besançon, France.
Nadine MillotLaboratoire Interdisciplinaire Carnot de Bourgogne, UMR 6303 CNRS-Université de Bourgogne, 21078 Dijon, France.ORCID 0000-0002-0127-3858

Funding

EIPHI Graduate School ANR-17-EURE-0002
6 · The paper itself

Abstract

To obtain versatile nanoplatforms comparable for various bio-applications, synthesis and functionalization of two inorganic nanoparticles (NPs), i.e., gold (AuNPs) and iron oxide (SPIONs), are described for different NP diameters. Chosen ligands have adapted chemical function to graft to the surfaces of the NPs (thiols and phosphonates, respectively) and the identical frequently used external carboxyl group for comparison of the NPs' material effect on their final behavior. To further evaluate molecular length effect, AuNPs are functionalized by different ligands. Numerous characterizations highlight the colloidal stability when grafting organic molecules on NPs. The potentiality of the functionalized NPs to react efficiently with a protein monolayer is finally evaluated by grafting them on a protein covered chip, characterized by atomic force microscopy. Comparison of the NPs' surface densities and measured heights enable observation of different NPs' reactivity and infer the influence of the inorganic core material, as well as the NPs' size and ligand length. AuNPs have higher affinities to biomolecules, especially when covered by shorter ligands. NP ligands should be chosen not only based on their length but also on their chemical chain, which affects proteic layer interactions. This original multiplex comparison method using AFM is of great interest to screen the effects of used NP materials and functionalization when developing theranostic nanoplatforms.

Indexed as

GoldMetal NanoparticlesFerric CompoundsLigandsMicroscopy, Atomic ForceParticle SizeSurface PropertiesFerric Compoundsferric oxideGoldLigandsAFMbiofunctionalizationfunctionalizationgold nanoparticlesmercaptohexanoic acidPEGphosphonoacetic acidSPIONssynthesistheranosticsthioglycolic acid

Identifiers

PMID39598659
PMCPMC11596608

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.