Evidence map›Paper›PMID 42040452›Full record

ArticleACS omega2026

Geometry-Dependent Pitch Variation Controls Platelet Adhesion on FluidFM-Fabricated Residual-Layer-Free Micro/Nanostructures.

Marcus Soter, Dikshita Madkatte, Doris Heinrich, Thi-Huong Nguyen

Abstract read
In one paragraph

Article in ACS omega, 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.

Marcus SoterInstitute for Bioprocessing and Analytical Measurement Techniques (iba), Heilbad Heiligenstadt 37308, Germany.ORCID https://orcid.org/0009-0004-5653-0489
Dikshita MadkatteInstitute for Bioprocessing and Analytical Measurement Techniques (iba), Heilbad Heiligenstadt 37308, Germany.
Doris HeinrichInstitute for Bioprocessing and Analytical Measurement Techniques (iba), Heilbad Heiligenstadt 37308, Germany.
Thi-Huong NguyenInstitute for Bioprocessing and Analytical Measurement Techniques (iba), Heilbad Heiligenstadt 37308, Germany.ORCID https://orcid.org/0000-0002-9237-3482

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Platelet storage remains a critical challenge in transfusion medicine, with current WHO and FDA guidelines limiting storage to just 72 h due to the risk of platelet dysfunction and bacterial contamination. This study examines how platelet adhesion is influenced by the interstructured distance of various microstructured geometries printed by mask-free nanoimprinting fluid force microscopy (FluidFM) technology. Microstructures of multiple geometries (circles, Pacman, lines, grids, and triangles) were printed on glass surfaces using the commercial Loctite AA3491, composed of multiple acrylate monomers, at three different peak-to-peak distances: 10 μm, 5 μm, and 2 μm. Atomic force microscopy (AFM) was employed to characterize the topography and printing precision of these structures. All structures exhibited nanoscale heights and demonstrated high fidelity to the designed patterns. Adhered platelets on the structured surfaces were quantified using confocal laser scanning microscopy. Results demonstrated that platelet attachment is significantly affected by both structural geometry and peak-to-peak distance. Circular and Pacman-like structures consistently showed reduced platelet adhesion, particularly at the largest peak-to-peak distance of 10 μm. Platelet attachment generally increased with decreasing peak-to-peak distance between the microstructures, yet all structured surfaces showed reduced adhesion compared to unstructured glass and nonpatterned Loctite, indicating that microtopographical modifications can effectively inhibit platelet attachment. Our results provide insights into designing antifouling surfaces for medical applications, demonstrating the potential of FluidFM technology in fabricating precision microstructures to mitigate platelet attachment as a mechanistic model to study geometry-dependent platelet-surface interactions.

Identifiers

PMID42040452
PMCPMC13103838

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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.