Evidence map›Paper›PMID 37056621›Full record

ArticleNanoscale advances2023

Identification of fluorescently-barcoded nanoparticles using machine learning.

Ana Ortiz-Perez, Cristina Izquierdo-Lozano, Rens Meijers, Francesca Grisoni, Lorenzo Albertazzi

Abstract read
In one paragraph

Article in Nanoscale advances, 2023. 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

5 authors.

Ana Ortiz-PerezInstitute for Complex Molecular Systems (ICMS), Eindhoven University of Technology PO Box 513 5600 MB Eindhoven The Netherlands l.albertazzi@tue.nl.ORCID https://orcid.org/0000-0003-0023-9444
Cristina Izquierdo-LozanoInstitute for Complex Molecular Systems (ICMS), Eindhoven University of Technology PO Box 513 5600 MB Eindhoven The Netherlands l.albertazzi@tue.nl.ORCID https://orcid.org/0000-0003-0917-8860
Rens MeijersInstitute for Complex Molecular Systems (ICMS), Eindhoven University of Technology PO Box 513 5600 MB Eindhoven The Netherlands l.albertazzi@tue.nl.
Francesca GrisoniInstitute for Complex Molecular Systems (ICMS), Eindhoven University of Technology PO Box 513 5600 MB Eindhoven The Netherlands l.albertazzi@tue.nl.ORCID https://orcid.org/0000-0001-8552-6615
Lorenzo AlbertazziInstitute for Complex Molecular Systems (ICMS), Eindhoven University of Technology PO Box 513 5600 MB Eindhoven The Netherlands l.albertazzi@tue.nl.ORCID https://orcid.org/0000-0002-6837-0812

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Barcoding of nano- and micro-particles allows distinguishing multiple targets at the same time within a complex mixture and is emerging as a powerful tool to increase the throughput of many assays. Fluorescent barcoding is one of the most used strategies, where microparticles are labeled with dyes and classified based on fluorescence color, intensity, or other features. Microparticles are ideal targets due to their relative ease of detection, manufacturing, and higher homogeneity. Barcoding is considerably more challenging in the case of nanoparticles (NPs), where their small size results in a lower signal and greater heterogeneity. This is a significant limitation since many bioassays require the use of nano-sized carriers. In this study, we introduce a machine-learning-assisted workflow to write, read, and classify barcoded PLGA-PEG NPs at a single-particle level. This procedure is based on the encapsulation of fluorescent markers without modifying their physicochemical properties (writing), the optimization of their confocal imaging (reading), and the implementation of a machine learning-based barcode reader (classification). We found nanoparticle heterogeneity as one of the main factors that challenges barcode separation, and that information extracted from the dyes' nanoscale confinement effects (such as Förster Resonance Energy Transfer, FRET) can aid barcode identification. Moreover, we provide a guide to reaching the optimal trade-off between the number of simultaneous barcodes and classification accuracy supporting the use of this workflow for a variety of bioassays.

Identifiers

PMID37056621
PMCPMC10089084

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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.