Evidence map›Paper›PMID 40137635›Full record

ArticleNanomaterials (Basel, Switzerland)2025

Investigating Simulated Cellular Interactions on Nanostructured Surfaces with Antibacterial Properties: Insights from Force Curve Simulations.

Jonathan Wood, Dennis Palms, Quan Trong Luu, Krasimir Vasilev, Richard Bright

Abstract read
In one paragraph

Article in Nanomaterials (Basel, Switzerland), 2025. 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

5 authors.

Jonathan WoodAcademic Unit of STEM, University of South Australia, Adelaide, SA 5095, Australia.
Dennis PalmsCollege of Medicine and Public Health, Flinders University, Adelaide, SA 5042, Australia.
Quan Trong LuuCollege of Medicine and Public Health, Flinders University, Adelaide, SA 5042, Australia.
Krasimir VasilevCollege of Medicine and Public Health, Flinders University, Adelaide, SA 5042, Australia.ORCID 0000-0003-3534-4754
Richard BrightCollege of Medicine and Public Health, Flinders University, Adelaide, SA 5042, Australia.ORCID 0000-0003-1988-0725

Funding

ARC DP220103543Flinders Foundation Seed FundingNHMRC GNT1194466
6 · The paper itself

Abstract

This study investigates the simulation of interactions between cells and antibacterial nanostructured surfaces. Understanding the physical interaction forces between cells and nanostructured surfaces is crucial for developing antibacterial materials, yet existing physical models are limited. Force simulation studies can simplify analysis by focusing on mechanical interactions while disregarding factors such as bacterial deformation and complex biochemical signals. To simulate these interactions, Atomic Force Microscopy (AFM) was employed to generate force curves, allowing precise monitoring of the interaction between a 5 µm spherical cantilever tip and titanium alloy (Ti6Al4V) surfaces. AFM uniquely enables customized approaches and retraction cycles, providing detailed insights into attractive-repulsive forces across different surface morphologies. Two nanostructured surfaces, created via hydrothermal etching using KOH and NaOH, were compared to a Ti6Al4V control surface. Results demonstrated significant changes in nanomechanical properties due to surface chemistry and morphology. The Ti6Al4V control surface exhibited a 44 ± 5 N/m stiffness, which decreased to 20 ± 3 N/m on KOH-etched nanostructured (NS) surfaces and 29 ± 4 N/m on NaOH-etched NS surfaces. Additionally, surface energy decreased by magnitude on nanostructured surfaces compared to the control. The nature of interaction forces also varied: short-range forces were predominant on KOH-etched surfaces, while NaOH-etched surfaces exhibited stronger long-range forces. These findings provide valuable insights into how nanostructure patterning influences cell-like interactions, offering potential applications in antibacterial surface design. By tailoring nanomechanical properties through specific etching techniques, biomaterial performance can be optimized for clinical applications, enhancing antibacterial efficacy and reducing microbial adhesion.

Indexed as

antibacterialatomic force microscopyforce curvenanomechanicalnanostructurevan der Waals

Identifiers

PMID40137635
PMCPMC11944641

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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.