Evidence map›Paper›PMID 41744036›Full record

ArticleNano letters2026

Modulation of Peptoid Nanostructure for Antibiofilm Hydrogel Interfaces.

Jae Won Yun, Il-Soo Park, Heewoong Yoon, Jiwon Woo, Dong-Yeong Kim, Woojin Yang, Jieun Choi, Dal-Hee Min, Jung-Hyun Lee, Jiwon Seo and 1 more

Abstract read
In one paragraph

Article in Nano letters, 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

11 authors.

Jae Won YunConvergence Research Center for Solutions to Electromagnetic Interference in Future-mobility, Korea Institute of Science and Technology (KIST), Seoul 02792, Republic of Korea.
Il-Soo ParkElectronic and Hybrid Materials Research Center, Korea Institute of Science and Technology (KIST), Seoul 02792, Republic of Korea.
Heewoong YoonDepartment of Chemistry, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea.ORCID 0009-0003-4851-3390
Jiwon WooDepartment of Chemistry, Seoul National University, Seoul 08826, Republic of Korea.ORCID 0009-0003-6416-301X
Dong-Yeong KimElectronic and Hybrid Materials Research Center, Korea Institute of Science and Technology (KIST), Seoul 02792, Republic of Korea.ORCID 0000-0001-9128-6734
Woojin YangElectronic and Hybrid Materials Research Center, Korea Institute of Science and Technology (KIST), Seoul 02792, Republic of Korea.
Jieun ChoiDepartment of Chemistry, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea.
Dal-Hee MinDepartment of Chemistry, Seoul National University, Seoul 08826, Republic of Korea.ORCID 0000-0001-8623-6716
Jung-Hyun LeeDepartment of Chemical and Biological Engineering, Korea University, Seoul 02841, Republic of Korea.ORCID 0000-0002-9662-1703
Jiwon SeoDepartment of Chemistry, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea.ORCID 0000-0002-5433-5071
Jae Hong KimConvergence Research Center for Solutions to Electromagnetic Interference in Future-mobility, Korea Institute of Science and Technology (KIST), Seoul 02792, Republic of Korea.ORCID 0000-0001-6872-9365

Funding

InnoCORE programKorea governmentNational Research Council of Science & TechnologyNational Research Foundation of Korea
6 · The paper itself

Abstract

Most hospital-acquired infections originate from bacterial biofilms on implantable devices, where the extracellular polymeric substance (EPS) matrix protects microbes and promotes multidrug resistance (MDR). Preventing biofilm initiation, particularly bacterial adhesion and proliferation, offers an effective strategy to combat device-associated infections. However, developing biocompatible materials that combine antimicrobial and antiadhesive functions remains a challenge. Herein, we present a strategy to engineer antibiofilm hydrogels by incorporating antimicrobial peptoids (ampetoids) into a gelatin-based matrix with controlled supramolecular organization. By tuning the stoichiometric ratio between thiol-functionalized ampetoids and norbornene groups in the matrix, we controlled peptoid nanostructure within the hydrogel, where suppression of peptoid self-assembly proved critical for balancing antimicrobial activity, antiadhesive properties, and cytocompatibility. This molecular-level control enabled the hydrogels to inhibit biofilm formation by

Indexed as

Anti-Bacterial AgentsBiofilmsHydrogelsNanostructuresPeptoidsBacterial AdhesionGelatinPseudomonas aeruginosaStaphylococcus aureusAnti-Bacterial AgentsGelatinHydrogelsPeptoidsantiadhesiveantibiofilmantimicrobialhydrogel coatingmultifunctionalpeptoid

Identifiers

PMID41744036
PMCPMC12983360

What OpenQuestion holds

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LicenceCC BY
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.