Evidence map›Paper›PMID 39468876›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2025

Squeezable Hydrogel Microparticles for Single Extracellular Vesicle Protein Profiling.

Yoon Ho Roh, Renee-Tyler T Morales, Emily Huynh, Uday Chintapula, David E Reynolds, Renis J Agosto-Nieves, Daniel Oh, Akari J Seiner, Jianhua Lim, Christopher B Rodell and 1 more

Abstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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.

Yoon Ho RohDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Renee-Tyler T MoralesDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Emily HuynhDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Uday ChintapulaDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.
David E ReynoldsDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Renis J Agosto-NievesDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Daniel OhDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Akari J SeinerSchool of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, 19104, USA.
Jianhua LimDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Christopher B RodellSchool of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, 19104, USA.
Jina KoDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.ORCID 0000-0002-4941-4234

Funding

Droplet-based Spatially Encoded Live Cell Digital ExtractionDP2GM154018 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI JINA KO · 2023 to 2026
$2.5M
Designing supramolecular delivery strategies to understand and exploit synergies in immunoregenerative medicineR35GM147184 · NIGMS · DREXEL UNIVERSITY · PI Christopher B Rodell · 2022 to 2026
$2.0M
Mapping Single Extracellular Vesicles to Parent Cells for Immunotherapy MonitoringR00CA256353 · NCI · UNIVERSITY OF PENNSYLVANIA · PI KO, JINA · 2022 to 2024
$741k
American Heart Association 23CDA1054367National Science Foundation GRFPNCI NIH HHS R00 CA256353NIGMS NIH HHS DP2 GM154018NIGMS NIH HHS R35 GM147184NIH HHS R35GM147184PennPREP ScholarshipU.S. Department of Education pre-doctoral GAANN fellowship
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are promising for molecular diagnostics, but current analyses are limited by the rarity and compositional heterogeneity of EV protein expression. Therefore, single EV profiling methods require high sensitivity, multiplexing, and throughput to address these issues. Here a single EV analysis technique that utilizes squeezable methacrylated hyaluronic acid hydrogel microparticles (MHPs) is described as a scaffold to immobilize EVs and perform an integrated rolling circle amplification (RCA) assay for an ultra-sensitive and multiplex analysis of single EV proteins. EVs are prepared into MHPs in a high-throughput manner with droplet microfluidics and optimally labeled with antibody-oligonucleotide conjugates in MHPs without steric limitations. By designing MHPs with high compressibility, single EV protein signals are amplified as RCA products that can be aligned on the same plane by physically squeezing MHPs and visualized with low magnification. This method provides a simple and scalable single EV imaging analysis pipeline for identifying multiplex marker expression patterns from single EVs. For validation, the single EV heterogeneity of highly expressed cancer cell markers is profiled across different cancer cell lines. These findings exemplify squeezable MHPs as a robust platform with high sensitivity, multiplexing, and scalability for resolving single EV heterogeneity and advancing molecular assay technologies.

Indexed as

Extracellular VesiclesHydrogelsCell Line, TumorHumansHyaluronic AcidProteinsHyaluronic AcidHydrogelsProteinsdigital assaysextracellular vesiclesmultiplexingrolling circle amplificationsqueezable hydrogel

Identifiers

PMID39468876
PMCPMC11707585

What OpenQuestion holds

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LicenceCC BY
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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.