Evidence map›Paper›PMID 37957480›Full record

ArticleMolecular biotechnology2024

Superior Performance of Iron-Coated Silver Nanoparticles and Cefoxitin as an Antibiotic Composite Against Methicillin-Resistant  Staphylococcus aureus (MRSA): A Population Study.

Nahal Hadi, Sedigheh Nakhaeitazreji, Farshad Kakian, Zahra Hashemizadeh, Alireza Ebrahiminezhad, Jun Wei Roy Chong, Aydin Berenjian, Pau Loke Show

Abstract read
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Article in Molecular biotechnology, 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
0.4field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

8 authors at 4 institutions in 4 countries.

Nahal HadiDepartment of Bacteriology & Virology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Sedigheh NakhaeitazrejiDepartment of Bacteriology and Virology, School of Medicine, Students Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
Farshad KakianDepartment of Bacteriology and Virology, School of Medicine, Students Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
Zahra HashemizadehDepartment of Bacteriology and Virology, School of Medicine, Students Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
Alireza EbrahiminezhadBiotechnology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. a_ebrahimi@sums.ac.ir.
Jun Wei Roy ChongFaculty of Science and Engineering, Department of Chemical and Environmental Engineering, University of Nottingham Malaysia, Jalan Broga, 43500, Semenyih, Selangor Darul Ehsan, Malaysia.
Aydin BerenjianDepartment of Chemical and Biological Engineering, Colorado State University, Fort Collins, CO, 80523, USA. aydin.berenjian@colostate.edu.ORCID http://orcid.org/0000-0003-4957-3582
Pau Loke ShowDepartment of Chemical Engineering, Khalifa University, P.O. Box 127788, Abu Dhabi, United Arab Emirates.
Shiraz University of Medical Sciences · IRColorado State University · USKhalifa University of Science and Technology · AEUniversity of Nottingham Malaysia Campus · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The synergistic effects of antimicrobial nanostructures with antibiotics present a promising solution for overcoming resistance in methicillin-resistant Staphylococcus aureus (MRSA). Previous studies have introduced iron as a novel coating for silver nanoparticles (AgNPs) to enhance both economic efficiency and potency against S. aureus. However, there are currently no available data on the potential of these novel nanostructures to reverse MRSA resistance. To address this gap, a population study was conducted within the MRSA community, collecting a total of 48 S. aureus isolates from skin lesions. Among these, 21 isolates (43.75%) exhibited cefoxitin resistance as determined by agar disk diffusion assay. Subsequently, a PCR test confirmed the presence of the mecA gene in 20 isolates, verifying them as MRSA. These results highlight the cefoxitin disk diffusion susceptibility test as an accurate screening method for predicting mecA-mediated resistance in MRSA. Synergy tests were performed on cefoxitin, serving as a marker antibiotic, and iron-coated AgNPs (Fe@AgNPs) in a combination study using the checkerboard assay. The average minimal inhibitory concentration (MIC) and fractional inhibitory concentration (FIC) of cefoxitin were calculated as 11.55 mg/mL and 3.61 mg/mL, respectively. The findings indicated a synergistic effect (FIC index < 0.5) between Fe@AgNPs and cefoxitin against 90% of MRSA infections, while an additive effect (0.5 ≤ FIC index ≤ 1) could be expected in 10% of infections. These results suggest that Fe@AgNPs could serve as an economically viable candidate for co-administration with antibiotics to reverse resistance in MRSA infections within skin lesions. Such findings may pave the way for the development of future treatment strategies against MRSA infections.

Indexed as

Anti-Bacterial AgentsCefoxitinIronMetal NanoparticlesMethicillin-Resistant Staphylococcus aureusSilverCupressusHumansMicrobial Sensitivity TestsParticle SizeSpectrophotometry, UltravioletSpectroscopy, Fourier Transform InfraredX-Ray DiffractionAnti-Bacterial AgentsCefoxitinIronSilverAntimicrobial nanoparticlesDrug resistanceMetal nanoparticlesSkin infectionsSusceptibility

Identifiers

PMID37957480
OpenAlexW4388627733

What OpenQuestion holds

Textmetadata
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.