Evidence map›Paper›PMID 41205280›Full record

ArticleBiomaterials2026

Antimicrobial coated intracortical probes reduce invading microbe abundance and subsequent neuroinflammation.

G Burkhart, S E Grabinski, J J Wang, G Glusauskas, A Thompson, A Lee, Z Zhu, C J Donskey, H A von Recum, L L Zhang and 3 more

Abstract read
In one paragraph

Article in Biomaterials, 2026. 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
–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

1 citing paper in PubMed.

  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

13 authors.

G BurkhartDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA; Advanced Platform Technology Center, Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, OH, 44106, USA.
S E GrabinskiDepartment of Population and Quantitative Health Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH, 44106, USA.
J J WangDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA; Advanced Platform Technology Center, Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, OH, 44106, USA.
G GlusauskasDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA; Advanced Platform Technology Center, Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, OH, 44106, USA.
A ThompsonDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA; Advanced Platform Technology Center, Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, OH, 44106, USA.
A LeeDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA; Advanced Platform Technology Center, Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, OH, 44106, USA.
Z ZhuDepartment of Population and Quantitative Health Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH, 44106, USA.
C J DonskeyAdvanced Platform Technology Center, Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, OH, 44106, USA.
H A von RecumDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA; Advanced Platform Technology Center, Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, OH, 44106, USA.
L L ZhangDepartment of Population and Quantitative Health Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH, 44106, USA.
A Hess-DunningDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA; Advanced Platform Technology Center, Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, OH, 44106, USA.
H Amani HamedaniDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA; Department of Materials Science and Engineering, Case Western Reserve University, Cleveland, OH, USA. Electronic address: hxa260@case.edu.
J R CapadonaDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA; Advanced Platform Technology Center, Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, OH, 44106, USA. Electronic address: jrc35@case.edu.

Funding

TUMOR METABOLISM PROGRAMP30CA043703 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI Amar Desai · 1987 to 2026
$142.3M
Integrated Neural Engineering and Rehabilitation Training ProgramT32EB004314 · NIBIB · CASE WESTERN RESERVE UNIVERSITY · PI Jeffrey R Capadona, Robert F. Kirsch · 2004 to 2026
$6.1M
Characterizing and Mitigating the Role of Oxidative Damage in Microelectrode FailureR01NS110823 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI CAPADONA, JEFFREY R, PANCRAZIO, JOSEPH J. · 2019 to 2023
$3.3M
Deploying Intracortical Electrode Arrays to Record and Stimulate in a Tissue VolumeR01NS131502 · NINDS · TEXAS A&M UNIVERSITY · PI Taylor H Ware · 2023 to 2026
$1.9M
NCI NIH HHS P30 CA043703NIBIB NIH HHS T32 EB004314NINDS NIH HHS R01 NS110823NINDS NIH HHS R01 NS131502RRD VA I01 RX002611RRD VA I21 RX004895RRD VA IK6 RX003077
6 · The paper itself

Abstract

Intracortical microelectrodes allow for the recording of neural signals in the brain but show decreased recording performance over time. This failure is due primarily to the neuroinflammatory response triggered by microelectrode implantation. We have shown that one consequence of the disruption of the blood-brain barrier following microelectrode probe implantation is the invasion of non-native bacteria to the implant site, which exacerbates the neuroinflammatory response. This study investigates the effects of coating non-functional silicon intracortical microelectrodes with an antimicrobial titania nanotube array (TNA) to reduce the relative abundance of invasive microbes and the resulting neuroinflammatory response. TNA-coated probes were implanted into mice for either 4 weeks (N = 4) or 12 weeks (N = 4) and compared to uncoated probes at both time points. We found that the TNA coatings reduce microbe relative abundance at both acute and chronic time points, correlating with fewer significantly expressed neuroinflammatory markers. Coating probes with TNAs allows for the beneficial effects of the antimicrobial coating to persist to chronic time points, in contrast to the detrimental effects of chronic systemic antibiotic administration reported previously. This study establishes antimicrobial TNA coatings as a platform for controlling the microbial environment, reducing invasive bacteria and neuroinflammation at the implant site. By mitigating the neuroinflammatory response, TNA-coated probes address one of the key contributors to intracortical microelectrode failure, thereby providing a strong platform that may support improved chronic recording performance in future functional intracortical microelectrode applications.

Indexed as

Anti-Infective AgentsCoated Materials, BiocompatibleElectrodes, ImplantedNeuroinflammatory DiseasesAnimalsAnti-Bacterial AgentsInflammationMaleMiceMice, Inbred C57BLMicroelectrodesNanotubesTitaniumAnti-Bacterial AgentsAnti-Infective AgentsCoated Materials, BiocompatibleTitaniumtitanium dioxide

Identifiers

PMID41205280
PMCPMC13479818

What Socratic 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 Socratic graph.