Evidence map›Paper›PMID 40391170›Full record

ArticleCyborg and bionic systems (Washington, D.C.)2025

ODEP-Based Robotic System for Micromanipulation and In-Flow Analysis of Primary Cells.

Joanna Filippi, Paola Casti, Valentina Lacconi, Gianni Antonelli, Michele D'Orazio, Giorgia Curci, Carlo Ticconi, Rocco Rago, Massimiliano De Luca, Alessandro Pecora and 4 more

Abstract read
In one paragraph

Article in Cyborg and bionic systems (Washington, D.C.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
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

14 authors.

Joanna FilippiDepartment of Electronic Engineering, University of Rome Tor Vergata, 00133 Rome, Italy.
Paola CastiDepartment of Electronic Engineering, University of Rome Tor Vergata, 00133 Rome, Italy.
Valentina LacconiDepartment of Biomedicine and Prevention, Tor Vergata University, 00133 Rome, Italy.
Gianni AntonelliDepartment of Electronic Engineering, University of Rome Tor Vergata, 00133 Rome, Italy.
Michele D'OrazioDepartment of Electronic Engineering, University of Rome Tor Vergata, 00133 Rome, Italy.
Giorgia CurciDepartment of Electronic Engineering, University of Rome Tor Vergata, 00133 Rome, Italy.
Carlo TicconiDepartment of Surgical Sciences, Section of Gynecology and Obstetrics, University of Rome Tor Vergata, Rome, Italy.
Rocco RagoDepartment of Gender, Parenting, Child and Adolescent Medicine, Physiopathology of Reproduction and Andrology Unit, Sandro Pertini Hospital, Rome, Italy.
Massimiliano De LucaItalian Nation Research Council (CNR), Rome, Italy.
Alessandro PecoraItalian Nation Research Council (CNR), Rome, Italy.
Arianna MencattiniDepartment of Electronic Engineering, University of Rome Tor Vergata, 00133 Rome, Italy.
Steven L NealeJames Watt School of Engineering, University of Glasgow, Glasgow, UK.
Luisa CampagnoloDepartment of Biomedicine and Prevention, Tor Vergata University, 00133 Rome, Italy.
Eugenio MartinelliDepartment of Electronic Engineering, University of Rome Tor Vergata, 00133 Rome, Italy.ORCID https://orcid.org/0000-0002-6673-2066

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The presence of cellular defects of multifactorial nature can be hard to characterize accurately and early due to the complex interplay of genetic, environmental, and lifestyle factors. With this study, by bridging optically-induced dielectrophoresis (ODEP), microfluidics, live-cell imaging, and machine learning, we provide the ground for devising a robotic micromanipulation and analysis system for single-cell phenotyping. Cells under the influence of nonuniform electric fields generated via ODEP can be recorded and measured. The induced responses obtained under time-variant ODEP stimulation reflect the cells' chemical, morphological, and structural characteristics in an automated, flexible, and label-free manner. By complementing the electrokinetic fingerprint of the cell centroid motion with data on the dynamics of electro-deformation and orientation, we show that subtle differences at the single-cell level can be elucidated. Specifically, here, we demonstrate, for the first time, the ability of the combined ODEP-based robotic and automatic analysis platform to discriminate between primary endometrial stromal cells obtained from fertile patients and patients with disrupted receptivity/selectivity equilibrium. When multiple cells were considered at the patient level, the performance achieved an average accuracy of 98%. Single-cell micro-operation and analysis systems may find a more general application in the clinical diagnosis and management of patients with pathological alterations at the cellular level.

Identifiers

PMID40391170
PMCPMC12087799

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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.