Evidence map›Paper›PMID 39717514›Full record

ArticleInternational journal of nanomedicine2024

Simulated Gastrointestinal Fluids Impact the Stability of Polymer-Functionalized Selenium Nanoparticles: Physicochemical Aspects.

Atiđa Selmani, Nives Matijaković Mlinarić, Salvatore Fabio Falsone, Ivan Vidaković, Gerd Leitinger, Ida Delač, Borna Radatović, Ivan Nemet, Sanda Rončević, Andreas Bernkop-Schnürch and 4 more

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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

14 authors.

Atiđa SelmaniDepartment of Pharmaceutical Technology and Biopharmacy, Institute of Pharmaceutical Sciences, University of Graz, Graz, 8010, Austria.ORCID 0000-0002-5830-2138
Nives Matijaković MlinarićLaboratory for Precipitation Processes, Division of Material Chemistry, Institute Ruđer Bošković, Zagreb, Croatia.
Salvatore Fabio FalsoneDepartment of Pharmaceutical Technology and Biopharmacy, Institute of Pharmaceutical Sciences, University of Graz, Graz, 8010, Austria.
Ivan VidakovićDivision of Medical Physics and Biophysics, Gottfried Schatz Research Center for Cell Signaling, Metabolism and Aging, Medical University of Graz, Graz, 8010, Austria.
Gerd LeitingerDivision of Cell Biology, Histology and Embryology, Gottfried Schatz Research Center for Cell Signaling, Metabolism and Aging, Medical University of Graz, Graz, 8010, Austria.
Ida DelačCenter for Advanced Laser Techniques, Institute of Physics, Zagreb, 10000, Croatia.ORCID 0000-0002-7481-6542
Borna RadatovićCenter for Advanced Laser Techniques, Institute of Physics, Zagreb, 10000, Croatia.
Ivan NemetDepartment of Chemistry, Faculty of Science, University of Zagreb, Zagreb, 10000, Croatia.
Sanda RončevićDepartment of Chemistry, Faculty of Science, University of Zagreb, Zagreb, 10000, Croatia.
Andreas Bernkop-SchnürchCenter for Chemistry and Biomedicine, Department of Pharmaceutical Technology, Institute of Pharmacy, University of Innsbruck, Innsbruck, 6020, Austria.ORCID 0000-0003-4187-8277
Tomislav VuletićCenter for Advanced Laser Techniques, Institute of Physics, Zagreb, 10000, Croatia.
Karin KornmuellerDivision of Medical Physics and Biophysics, Gottfried Schatz Research Center for Cell Signaling, Metabolism and Aging, Medical University of Graz, Graz, 8010, Austria.
Eva RobleggDepartment of Pharmaceutical Technology and Biopharmacy, Institute of Pharmaceutical Sciences, University of Graz, Graz, 8010, Austria.
Ruth PrasslDivision of Medical Physics and Biophysics, Gottfried Schatz Research Center for Cell Signaling, Metabolism and Aging, Medical University of Graz, Graz, 8010, Austria.ORCID 0000-0002-1010-9494

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Selenium (Se) is a vital micronutrient for maintaining homeostasis in the human body. Selenium nanoparticles (SeNPs) have demonstrated improved bioavailability compared to both inorganic and organic forms of Se. Therefore, supplementing with elemental Se in its nano-form is highly promising for biomedical applications related to Se deficiency. Purpose: The primary objective of this study was to evaluate the impact of the main gastrointestinal proteins on the physicochemical properties and stability of polymer-coated SeNPs. Methods: SeNPs functionalized with thiolated chitosan or hyaluronic acid were characterized based on their composition, morphology, size, and zeta potential. The stability of these particles was evaluated in simulated gastric and intestinal fluids. Additionally, the interaction propensity between major gastric proteins, such as pepsin and pancreatin, and functionalized SeNPs was investigated with FTIR, fluorescence quenching titrations, and in situ adsorption measurements. Results: The composition of the media, including pH and ionic strength, the chemistry of polymers, and the presence of the proteins, influence the size and zeta potential of the SeNPs. The increase in NP size due to the formation of large agglomerates, along with the decrease in zeta potential magnitude, confirmed the formation of a protein corona. Both pepsin and pancreatin showed a strong affinity to the particle surface. Based on the values of the apparent equilibrium dissociation constant this affinity was more pronounced for positively charged thiolated chitosan coated SeNPs compared to those coated with negatively charged hyaluronic acid. The polymer coated SeNPs displayed antioxidative potential, which could be very beneficial for health conditions associated with Se-deficiency. Conclusion: This study highlights the importance of exploring the characteristics of polymer-functionalized SeNPs under gastrointestinal conditions. Such investigations are important for developing nutritional supplements that can gradually release Se from SeNPs, thereby improving selenium absorption, bioavailability, and safety.

Indexed as

ChitosanHyaluronic AcidParticle SizeSeleniumBiological AvailabilityGastric JuiceGastrointestinal TractHumansHydrogen-Ion ConcentrationNanoparticlesPancreatinPepsin APolymersChitosanHyaluronic AcidPancreatinPepsin APolymersSeleniumbio-nano interfacegastrointestinal proteinshyaluronic acidnanoparticlesprotein coronathiolated chitosan

Identifiers

PMID39717514
PMCPMC11663997

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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.