Evidence map›Paper›PMID 34454520›Full record

ArticleJournal of nanobiotechnology2021

The role of the electrokinetic charge of neurotrophis-based nanocarriers: protein distribution, toxicity, and oxidative stress in in vitro setting.

Maria Dąbkowska, Zofia Ulańczyk, Karolina Łuczkowska, Dorota Rogińska, Anna Sobuś, Monika Wasilewska, Maria Olszewska, Katarzyna Jakubowska, Bogusław Machaliński

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2021. 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
–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

6 citing papers in PubMed.

  1. Article
  2. Review
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  6. 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

9 authors.

Maria DąbkowskaDepartment of Medical Chemistry, Pomeranian Medical University, Rybacka 1, 70-204, Szczecin, Poland. maria.dabkowska@pum.edu.pl.ORCID http://orcid.org/0000-0003-0190-1292
Zofia UlańczykDepartment of General Pathology, Pomeranian Medical University, Rybacka 1, 70-204, Szczecin, Poland.
Karolina ŁuczkowskaDepartment of General Pathology, Pomeranian Medical University, Rybacka 1, 70-204, Szczecin, Poland.
Dorota RogińskaDepartment of General Pathology, Pomeranian Medical University, Rybacka 1, 70-204, Szczecin, Poland.
Anna SobuśDepartment of General Pathology, Pomeranian Medical University, Rybacka 1, 70-204, Szczecin, Poland.
Monika WasilewskaJerzy Haber Institute of Catalysis and Surface Chemistry Polish Academy of Sciences, Niezapominajek 8, 30-239, Cracow, Poland.
Maria OlszewskaDepartment of Medical Chemistry, Pomeranian Medical University, Rybacka 1, 70-204, Szczecin, Poland.
Katarzyna JakubowskaDepartment of Biochemistry, Pomeranian Medical University, Rybacka 1, 70-204, Szczecin, Poland.
Bogusław MachalińskiDepartment of General Pathology, Pomeranian Medical University, Rybacka 1, 70-204, Szczecin, Poland.

Funding

Narodowe Centrum Badań i Rozwoju STRATEGMED1/234261/2NCBR/2014
6 · The paper itself

Abstract

backgroundThe rational chemical design of nanoparticles can be readily controlled and optimized by quantitatively studying protein adsorption at variously charged polymer carriers, determining their fate in biological fluids. We manufactured brain-derived neurotrophic factor (BDNF) -based electrostatic nanocomplexes with a different type of dendrimer core (anionic or cationic), encapsulated or not in polyethylene glycol (PEG), and studied their physicochemical properties and behavior in a biological setting. We investigated whether the electrokinetic charge of dendrimer core influences BDNF loading and desorption from the nanoparticle and serves as a determinant of nanoparticles' behavior in in vitro setting, influencing mitochondrial dysfunction, lipid peroxidation, and general nanoparticles' cellular toxicity.

resultsWe found that the electrokinetic charge of the dendrimer core influences nanoparticles in terms of BDNF release profile from their surfaces and their effect on cell viability, mitochondrial membrane potential, cell phenotype, and induction of oxidative stress. The electrostatic interaction of positively charged core of nanoparticles with cell membranes increases their cytotoxicity, as well as serious phenotype alterations compared to negatively charged nanoparticles core in neuron-like differentiated human neuroblastoma cells. Moreover, PEG adsorption at nanoparticles with negatively charged core presents a distinct decrease in metabolic cell activity. On the contrary, charge neutralization due to PEG adsorption on the surface of nanoparticles with positively charged core does not reduce their cytotoxicity, makes them less biocompatible with differentiated cells, and presumably shows non-specific toxicity.

conclusionsThe surface charge transformation after adsorption of protein or polyelectrolyte during nanocarriers formulation has an important role not only in designing nanomaterials with potent neuroprotective and neuroregenerative properties but also in applying them in a cellular environment.

Indexed as

Oxidative StressAdsorptionHumansIonsNanoparticlesOxidopaminePolyethylene GlycolsPolymersProteinsStatic ElectricitySurface PropertiesIonsOxidopaminePolyethylene GlycolsPolymersProteins

Identifiers

PMID34454520
PMCPMC8399784

What Socratic 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 Socratic graph.