Evidence map›Paper›PMID 42154178›Full record

ArticleDiscover nano2026

Enhancement in Ct-DNA binding affinity and antimicrobial activity of ZnO nanoparticles via Ag-doping.

Sultan Saad Almadhhi, Anuj Kumar, Mohd Ubaidullah, Abdullah M Al-Enizi

Abstract read
In one paragraph

Article in Discover nano, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Sultan Saad AlmadhhiDepartment of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh, 11451, Saudi Arabia.
Anuj KumarNano-Technology Research Laboratory, Department of Chemistry, GLA University, Mathura, 281406, Uttar Pradesh, India. anuj.kumar@gla.ac.in.
Mohd UbaidullahDepartment of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh, 11451, Saudi Arabia.ORCID http://orcid.org/0000-0002-0484-0299
Abdullah M Al-EniziDepartment of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh, 11451, Saudi Arabia. amenizi@ksu.edu.sa.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Developing multifunctional nanomaterials with improved antibacterial properties and reliable biocompatibility is an essential issue in biomedical research to address the increasing concern of antibiotic resistance. Ag-doped zinc oxide nanoparticles (ZnO NPs) were synthesized using a green and eco-friendly route using hibiscus flower extract as a reducing and stabilizing agent. The nanoparticles were synthesized successfully and characterized through FT-IR, TEM, EDX, and UV-Vis analysis. The bactericidal action potential was tested against E. coli, S. aureus, B. subtilis, Lactobacillus, and C. albicans pathogens using the Kirby-Bauer disk diffusion method. Ag-doped ZnO NPs were observed to have superior inhibition action against E. coli compared to pristine ZnO NPs. The interactions of ZnO and Ag-ZnO NPs towards calf thymus DNA (ct-DNA) were examined spectroscopically using absorption and fluorescence studies. It was observed that Ag-doped ZnO NPs showed a greater interaction with ct-DNA than pristine ZnO NPs. Thus, we conclude that biosynthesized Ag-ZnO NPs are multifunctional nanomaterials with good antibacterial action, an improved ability to bind to DNA, and better biocompatibility for future biomedical applications.

Indexed as

Antimicrobial activityDNA binding affinityFluorescence quenchingZnO nanoparticles

Identifiers

PMID42154178
PMCPMC13187099

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.