Evidence map›Paper›PMID 41594553›Full record

ArticleBiomolecules2025

Correction of Background in Fluorescence Correlation Spectroscopy for Accurate Determination of Particle Number.

Elisa Longo, Greta Paternò, Elisabetta Di Franco, Paolo Bianchini, Marco Castello, Alberto Diaspro, Giuseppe Vicidomini, Elena Bruno, Paolo Musumeci, Maria Josè Lo Faro and 2 more

Abstract read
In one paragraph

Article in Biomolecules, 2025. 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

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

12 authors.

Elisa LongoDepartment of Physics and Astronomy "Ettore Majorana", University of Catania, 95123 Catania, Italy.ORCID 0009-0001-9159-7871
Greta PaternòDepartment of Physics and Astronomy "Ettore Majorana", University of Catania, 95123 Catania, Italy.ORCID 0000-0002-5568-8872
Elisabetta Di FrancoDepartment of Physics and Astronomy "Ettore Majorana", University of Catania, 95123 Catania, Italy.
Paolo BianchiniNanoscopy, CHT Erzelli, Istituto Italiano di Tecnologia, 16163 Genoa, Italy.ORCID 0000-0001-6457-751X
Marco CastelloR&D Department, Genoa Instruments S.r.l., Via E. Melen 83, 16152 Genova, Italy.
Alberto DiasproNanoscopy, CHT Erzelli, Istituto Italiano di Tecnologia, 16163 Genoa, Italy.ORCID 0000-0002-4916-5928
Giuseppe VicidominiMolecular Microscopy and Spectroscopy, CHT Erzelli, Istituto Italiano di Tecnologia, 16163 Genoa, Italy.
Elena BrunoDepartment of Physics and Astronomy "Ettore Majorana", University of Catania, 95123 Catania, Italy.ORCID 0000-0002-1935-586X
Paolo MusumeciDepartment of Physics and Astronomy "Ettore Majorana", University of Catania, 95123 Catania, Italy.ORCID 0000-0002-5160-1522
Maria Josè Lo FaroDepartment of Physics and Astronomy "Ettore Majorana", University of Catania, 95123 Catania, Italy.ORCID 0000-0002-2067-1608
Nunzio TuccittoDepartment of Chemical Sciences, University of Catania, 95125 Catania, Italy.ORCID 0000-0003-4129-0406
Luca LanzanòDepartment of Physics and Astronomy "Ettore Majorana", University of Catania, 95123 Catania, Italy.ORCID 0000-0001-6539-394X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since the early development of Fluorescence Correlation Spectroscopy (FCS), it has been recognized that background intensity can lead to artifacts in the amplitude of the autocorrelation function (ACF) and, consequently, to inaccurate estimates of particle numbers. Here, we present a protocol for quantitative background evaluation and amplitude correction in FCS experiments, applicable to different sources of background such as detector noise, autofluorescence, and light scattering. We demonstrate the performance of our approach through three representative case studies: (i) FCS measurements of a bright fluorophore at low concentration, (ii) FCS of dim nanoparticles affected by solvent Raman scattering, and (iii) FCS performed using a confocal setup equipped with a SPAD array, where background originates from detector hot pixels. These examples represent typical experimental conditions in which background signals compromise quantitative interpretation, illustrating how our protocol restores accuracy and reproducibility in FCS analysis. By systematically identifying and correcting these effects, the proposed protocol addresses a long-standing limitation of FCS and provides a robust framework for improving the accuracy and reproducibility of quantitative fluorescence measurements.

Indexed as

NanoparticlesFluorescent DyesMicroscopy, ConfocalReproducibility of ResultsSpectrometry, FluorescenceFluorescent Dyescarbon dotsconfocal microscopeFCSSPAD arrayuncorrelated background

Identifiers

PMID41594553
PMCPMC12838558

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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.