Evidence map›Paper›PMID 42307820›Full record

ArticleBiomedical microdevices2026

Reversibly-sealable microfluidic platform for multi-molecule gradient delivery to large adherent cell cultures.

Julia Radzio, Łukasz Suprewicz, Da Kuang, Alexander Karpowicz, Paul A Janmey, Jai-Yoon Sul, David A Issadore, James H Eberwine, Paulo E Arratia

Abstract read
In one paragraph

Article in Biomedical microdevices, 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

9 authors.

Julia RadzioDepartment of Mechanical Engineering and Applied Mechanics, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, PA, USA.
Łukasz SuprewiczDepartment of Physiology and Institute for Medicine and Engineering, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Da KuangDepartment of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Alexander KarpowiczDepartment of Mechanical Engineering and Applied Mechanics, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, PA, USA.
Paul A JanmeyDepartment of Physiology and Institute for Medicine and Engineering, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Jai-Yoon SulDepartment of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
David A IssadoreDepartment of Bioengineering, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, PA, USA.
James H EberwineDepartment of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Paulo E ArratiaDepartment of Mechanical Engineering and Applied Mechanics, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, PA, USA. parratia@seas.upenn.edu.

Funding

The Secret Lives of RNA: The In Vivo 3D-Structural Logic of Single Neuron RNA MetabolismDP1AA028409 · NIAAA · UNIVERSITY OF PENNSYLVANIA · PI EBERWINE, JAMES H · 2019 to 2023
$5.7M
NIAAA NIH HHS DP1 AA028409NIH HHS DP1AA028409
6 · The paper itself

Abstract

Spatial manipulation of flow gradients and chemical microenvironments is essential for understanding fundamental biological mechanisms and investigating therapeutic responses in adherent cells. Convection-dominated gradient generators in microfluidic devices enable tunable chemical and shear stress gradients across large cell culture areas. However, most concentration generators are irreversibly sealed and operate in a narrow range of shear stresses, which restricts access to the cells after treatment and the physiological relevance of the flow conditions. Here, we present a reversibly sealable microfluidic platform that enables spatiotemporally controlled delivery of multiple small molecules to mammalian cells grown on large glass coverslips. Our device generates a relatively wide range of shear stresses and robust, spatially predictable chemical gradients across centimeter-scale areas and provides optical access compatible with live-cell imaging; it operates in the Stokes and laminar flow regimes. A mechanical sandwich clamp enables leak-free perfusion into the cell culture chamber and access to the cells after treatment. We experimentally and numerically demonstrate the ability to modulate the amount of mixing between co-flowing streams of small molecules. We verify the uptake of fluorophores across a monolayer of cells and assess their viability after perfusion and removal from the device. This platform provides a versatile and reusable approach for studying cellular responses to microenvironmental gradients in varied physiologically relevant shear stress conditions.

Indexed as

Cell Culture TechniquesLab-On-A-Chip DevicesAnimalsCell AdhesionEquipment DesignHumansAdherent cellsGradient generationMicrofluidicsReversibly-sealable

Identifiers

PMID42307820
PMCPMC13275633

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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.