Evidence map›Paper›PMID 42164312›Full record

ArticleSensors and actuators. B, Chemical2025

A Dual-Function Micropatterned Gold Platform for Cell Patterning and Optical Imaging Applications.

Swati Tanwar, Lintong Wu, Matthew Pittman, Linika Goel, Le Liang, Yun Chen, Ishan Barman

Abstract read
In one paragraph

Article in Sensors and actuators. B, Chemical, 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

7 authors.

Swati TanwarDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, Maryland, 21218, USA.ORCID 0000-0002-0430-1922
Lintong WuDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, Maryland, 21218, USA.ORCID 0000-0003-2534-0768
Matthew PittmanDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, Maryland, 21218, USA.
Linika GoelDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland 21218, USA.
Le LiangThe Institute for Advanced Studies, Wuhan University, Wuhan, 430072, China.
Yun ChenDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, Maryland, 21218, USA.
Ishan BarmanDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, Maryland, 21218, USA.ORCID 0000-0003-0800-0825

Funding

Wide-Field Short-Wave Infrared (SWIR) multiphoton (MP) tissue imagingP41EB015871 · NIBIB · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SO, PETER T. · 2012 to 2021
$11.3M
Determination of functional and molecular biomarkers of treatment resistance with multimodal optical spectroscopyR01CA238025 · NCI · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI RAJARAM, NARASIMHAN · 2019 to 2024
$2.0M
Next-generation optical nanoprobes: From quantum biosensing to cellular monitoringR35GM149272 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI ISHAN BARMAN · 2023 to 2026
$1.6M
High-Throughput, Multiplexing-Ready Intracellular Pressure ProbesR21GM146105 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI CHEN, YUN, LIN, CHENXIANG · 2022 to 2023
$465k
Genetically Encoded Magnetometer for Intracellular Dynamic MeasurementR21GM154219 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI CHEN, YUN · 2024 to 2025
$414k
NCI NIH HHS R01 CA238025NIBIB NIH HHS P41 EB015871NIGMS NIH HHS R21 GM146105NIGMS NIH HHS R21 GM154219NIGMS NIH HHS R35 GM149272
6 · The paper itself

Abstract

How can we reliably study cellular interactions and molecular responses in well-defined microenvironments while maintaining compatibility with high-sensitivity optical imaging techniques? Addressing this question is critical for understanding tissue development, disease progression, and cellular heterogeneity. Despite the promise of Raman spectroscopy for label-free molecular analysis, a major bottleneck lies in the lack of platforms that combine precise spatial control of cell placement with seamless integration into optical workflows. Here, we present CELLPAC a high-throughput, biocompatible cell-patterning platform that integrates micropatterned gold substrates, self-assembled PEG monolayers, and c-RGD peptides to create microscale adhesive domains for controlled cell confinement. CELLPAC enables the localization and co-localization of single or multiple human keratinocytes into tailored geometric patterns, supporting detailed studies of intercellular communication and migration. Crucially, the platform's gold component supports surface-enhanced Raman spectroscopy (SERS), and our measurements reveal ~3-fold signal enhancement for intrinsic cellular biomolecules. This dual functionality allows CELLPAC to not only direct cell behavior with high spatial fidelity but also to probe associated molecular processes. With its modular design and optical compatibility, CELLPAC provides a versatile foundation for studying curvature-guided migration, biochemical signaling, and other microenvironment-dependent cell responses advancing biomedical research in areas such as tissue engineering, drug screening, and biosensing.

Indexed as

Cell patterningfabricationoptical imagingProtein and lipid sensingSurface enhanced Raman spectroscopy

Identifiers

PMID42164312
PMCPMC13185076

What OpenQuestion holds

Textmetadata
LicenceTDM
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.