Evidence map›Paper›PMID 33829340›Full record

ArticlePharmaceutical research2021

Characterization of Biological Material Adsorption to the Surface of Nanoparticles without a Prior Separation Step: a Case Study of Glioblastoma-Targeting Peptide and Lipid Nanocapsules.

Claire Gazaille, Marion Sicot, Marthe Akiki, Nolwenn Lautram, Aurélien Dupont, Patrick Saulnier, Joël Eyer, Guillaume Bastiat

Abstract read
In one paragraph

Article in Pharmaceutical research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

8 authors.

Claire GazailleUniversity of Angers, Inserm, CNRS, MINT, SFR ICAT, F-49000, Angers, France.
Marion SicotUniversity of Angers, Inserm, CNRS, MINT, SFR ICAT, F-49000, Angers, France.
Marthe AkikiUniversity of Angers, Inserm, CNRS, MINT, SFR ICAT, F-49000, Angers, France.
Nolwenn LautramUniversity of Angers, Inserm, CNRS, MINT, SFR ICAT, F-49000, Angers, France.
Aurélien DupontUniversity of Rennes, CNRS, Inserm, BIOSIT, UMS 3480, US_S 018, F-35000, Rennes, France.
Patrick SaulnierUniversity of Angers, Inserm, CNRS, MINT, SFR ICAT, F-49000, Angers, France.
Joël EyerUniversity of Angers, Inserm, CNRS, MINT, SFR ICAT, F-49000, Angers, France.
Guillaume BastiatUniversity of Angers, Inserm, CNRS, MINT, SFR ICAT, F-49000, Angers, France. guillaume.bastiat@univ-angers.fr.ORCID http://orcid.org/0000-0001-6495-6747

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCurrent preclinical therapeutic strategies involving nanomedicine require increasingly sophisticated nanosystems and the characterization of the complexity of such nanoassemblies is becoming a major issue. Accurate characterization is often the factor that can accelerate the translational approaches of nanomedicines and their pharmaceutical development to reach the clinic faster. We conducted a case study involving the adsorption of the NFL-TBS.40-63 (NFL) peptide (derived from neurofilaments) to the surface of lipid nanocapsules (LNCs) (a combined nanosystem used to target glioblastoma cells) to develop an analytical approach combining the separation and the quantification in a single step, leading to the characterization of the proportion of free peptide and thus the proportion of peptide adsorbed to the lipid nanocapsule surface.

methodsLNC suspensions, NFL peptide solution and LNC/NFL peptide mixtures were characterized using a Size-Exclusion Chromatography method (with a chromatographic apparatus). In addition, this method was compared to centrifugal-filtration devices, currently used in literature for this case study.

resultsCombining the steps for separation and characterization in one single sequence improved the accuracy and robustness of the data and led to reproducible results. Moreover the data deviation observed for the centrifugal-filtration devices demonstrated the limits for this increasingly used characterization approach, explained by the poor separation quality and highlighting the importance for the method optimization. The high potential of the technique was shown, proving that H-bond and/or electrostatic interactions mediate adsorption of the NFL peptide to the surface of LNCs.

conclusionsUsed only as a characterization tool, the process using chromatographic apparatus is less time and solvent consuming than classical Size-Exclusion Chromatography columns only used for separation. It could be a promising tool for the scientific community for characterizing the interactions of other combinations of nanosystems and active biological agents.

Indexed as

AdsorptionBrain NeoplasmsCell Line, TumorChemistry, PharmaceuticalDrug CarriersGlioblastomaHumansLipidsNanocapsulesNeurofilament ProteinsPeptide FragmentsDrug CarriersLipidsNanocapsulesNeurofilament ProteinsNFL-TBS.40-63 peptidePeptide Fragmentsadsorptioncentrifugal-filtration deviceslipid nanocapsulespeptidesize-exclusion chromatography

Identifiers

PMID33829340
PMCPMC8026175

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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.