Evidence map›Paper›PMID 33076274›Full record

ArticleMolecules (Basel, Switzerland)2020

Mesoporous Silica as a Drug Delivery System for Naproxen: Influence of Surface Functionalization.

Lukáš Žid, Vladimír Zeleňák, Miroslav Almáši, Adriana Zeleňáková, Jaroslava Szücsová, Jozef Bednarčík, Monika Šuleková, Alexander Hudák, Lucia Váhovská

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  3. IR-EcoSpectra: Exploring sustainableJournal of pharmaceutical analysis · 2024
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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

9 authors at 3 institutions in 1 country.

Lukáš ŽidDepartment of Inorganic Chemistry Faculty of Science, P.J. Šafárik University, Moyzesova 11, SK-041 54 Košice, Slovakia.ORCID 0000-0002-4567-2981
Vladimír ZeleňákDepartment of Inorganic Chemistry Faculty of Science, P.J. Šafárik University, Moyzesova 11, SK-041 54 Košice, Slovakia.ORCID 0000-0002-6118-1269
Miroslav AlmášiDepartment of Inorganic Chemistry Faculty of Science, P.J. Šafárik University, Moyzesova 11, SK-041 54 Košice, Slovakia.
Adriana ZeleňákováInstitute of Physics, P. J. Šafárik University, Park Angelinum 9, 04001 Košice, Slovakia.ORCID 0000-0002-8443-9998
Jaroslava SzücsováInstitute of Physics, P. J. Šafárik University, Park Angelinum 9, 04001 Košice, Slovakia.
Jozef BednarčíkInstitute of Physics, P. J. Šafárik University, Park Angelinum 9, 04001 Košice, Slovakia.
Monika ŠulekováDepartment of Chemistry, Biochemistry and Biophysics, Institute of Pharmaceutical Chemistry, The University of Veterinary Medicine and Pharmacy, 04181 Košice, Slovakia.
Alexander HudákDepartment of Chemistry, Biochemistry and Biophysics, Institute of Pharmaceutical Chemistry, The University of Veterinary Medicine and Pharmacy, 04181 Košice, Slovakia.
Lucia VáhovskáDepartment of Chemistry, Biochemistry and Biophysics, Institute of Pharmaceutical Chemistry, The University of Veterinary Medicine and Pharmacy, 04181 Košice, Slovakia.
Institute of Physics of the Slovak Academy of Sciences · SKUniversity of Pavol Jozef Šafárik · SKUniversity of Veterinary Medicine in Košice · SK

Funding

Scientific Grant Agency of the Slovak Republic (VEGA) 1/0745/17The Slovak Research and Development Agency APVV-15-0520
6 · The paper itself

Abstract

In this work we describe the relationship between surface modification of hexagonally ordered mesoporous silica SBA-15 and loading/release characteristics of nonsteroidal anti-inflammatory drug (NSAID) naproxen. Mesoporous silica (MPS) was modified with 3-aminopropyl, phenyl and cyclohexyl groups by grafting method. Naproxen was adsorbed into pores of the prepared MPS from ethanol solution using a solvent evaporation method. The release of the drug was performed in buffer medium at pH 2 and physiological solution at pH 7.4. Parent MPSs as well as naproxen loaded MPSs were characterized using physicochemical techniques such as nitrogen adsorption/desorption, thermogravimetric analysis (TG), Zeta potential analysis, Fourier transform infrared spectroscopy (FT-IR), and elemental analysis. The amount of naproxen released from the MPSs into the medium was determined by high-performance liquid chromatography (HPLC). It was shown that the adsorption and desorption characteristics of naproxen are dependent on the pH of the solution and the surface functionalization of the host.

Indexed as

AdsorptionAnti-Inflammatory Agents, Non-SteroidalDrug Delivery SystemsHumansInflammationNaproxenPorositySilicon DioxideSolventsSurface PropertiesAnti-Inflammatory Agents, Non-SteroidalNaproxenSBA-15Silicon DioxideSolventsdrug delivery systemmesoporous silicananomaterialsnaproxenprolonged release

Identifiers

PMID33076274
PMCPMC7587581
OpenAlexW3092831925

What OpenQuestion holds

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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.