Evidence map›Paper›PMID 41993629›Full record

ArticleTheranostics2026

Engineering inertial flow patterns for signal amplification in disc-based protein assays.

Hyun-Kyung Woo, Lauren Philp, Dae-Han Jung, Dominique Zarrella, Yein Chung, Yoonjeong Choi, Jueun Jeon, Hyunho Kim, Cesar M Castro, Bo R Rueda and 1 more

Abstract read
In one paragraph

Article in Theranostics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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.

Hyun-Kyung WooCenter for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA 02114, USA.
Lauren PhilpVincent Center for Reproductive Biology, Department of Obstetrics and Gynecology, Massachusetts General Hospital, Boston, MA 02114, USA.
Dae-Han JungCenter for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA 02114, USA.
Dominique ZarrellaVincent Center for Reproductive Biology, Department of Obstetrics and Gynecology, Massachusetts General Hospital, Boston, MA 02114, USA.
Yein ChungCenter for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA 02114, USA.
Yoonjeong ChoiCenter for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA 02114, USA.
Jueun JeonCenter for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA 02114, USA.
Hyunho KimCenter for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA 02114, USA.
Cesar M CastroCenter for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA 02114, USA.
Bo R RuedaVincent Center for Reproductive Biology, Department of Obstetrics and Gynecology, Massachusetts General Hospital, Boston, MA 02114, USA.
Hakho LeeCenter for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA 02114, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Detecting low-abundance proteins is essential in liquid biopsy applications, particularly for extracellular vesicle (EV)-based diagnostics. Here, we introduce RapidEx ( Methods: The device leverages a unique interplay between disc-specific inertial forces (centrifugal and Coriolis) and membrane-filter flow dynamics. Unlike conventional systems, RapidEx utilizes a low-permeability membrane to redirect fluid laterally during rotation, thereby enhancing washing efficiency and signal-to-noise ratio. The performance of the device was validated through numerical simulation and tyramide-mediated amplification assays. This system processed plasma samples from patients with ovarian cancer ( Results: Numerical simulations and experimental validations confirmed that Coriolis-induced lateral flows were found critical to improving labeling and washing efficiency. This synergetic fluidic control with enzymatic chemical reaction enhanced the signal-to-noise ratio, which is >25-fold more sensitive than standard two-step labelling. Applying this platform to clinical samples, protein profiles enabled differentiation between cancer patients and controls and allowed for the identification of platinum therapy resistance in patients prior to chemotherapy treatment. Conclusions: RapidEx could enable rapid and cost-effective protein-based liquid biopsies, with applications in disease detection and monitoring therapeutic responses.

Indexed as

Extracellular VesiclesOvarian NeoplasmsBiomarkers, TumorFemaleHumansSignal-To-Noise RatioBiomarkers, Tumorinertial forcelab-on-a-discovarian cancerprotein assaysignal amplification

Identifiers

PMID41993629
PMCPMC13080452

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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.