Evidence map›Paper›PMID 37292468›Full record

ArticleArXiv2023

Dual-ratio approach for detection of point fluorophores in biological tissue.

Giles Blaney, Fernando Ivich, Angelo Sassarolia, Mark Niedre, Sergio Fantini

Abstract readPreprint
In one paragraph

Article in ArXiv, 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

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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

5 · Who and what money

Authors and funding

5 authors.

Giles BlaneyTufts University, Department of Biomedical Engineering, Medford, MA USA, 02155.
Fernando IvichNortheastern University, Department of Bioengineering, Boston, MA USA, 02120.
Angelo SassaroliaTufts University, Department of Biomedical Engineering, Medford, MA USA, 02155.
Mark NiedreNortheastern University, Department of Bioengineering, Boston, MA USA, 02120.
Sergio FantiniTufts University, Department of Biomedical Engineering, Medford, MA USA, 02155.

Funding

Tufts IRACDAK12GM133314 · NIGMS · TUFTS UNIVERSITY BOSTON · PI CLAIRE L MOORE, Jamie Lynn Maguire · 2019 to 2026
$8.4M
Continuous, Non-Invasive Optical Monitoring of Circulating Tumor Cell-Mediated Metastasis in Awake MiceR01CA260202 · NCI · NORTHEASTERN UNIVERSITY · PI Mark Jonathan Niedre · 2022 to 2026
$2.7M
Dual-slope method for enhanced depth sensitivity in frequency-domain near-infrared spectroscopyR01EB029414 · NIBIB · TUFTS UNIVERSITY MEDFORD · PI SERGIO FANTINI · 2021 to 2026
$2.5M
Fluorescence Molecular In Vivo Liquid Biopsy of Circulating Tumor CellsR21CA246413 · NCI · NORTHEASTERN UNIVERSITY · PI NIEDRE, MARK JONATHAN · 2021 to 2022
$389k
NCI NIH HHS R01 CA260202NCI NIH HHS R21 CA246413NIBIB NIH HHS R01 EB029414NIGMS NIH HHS K12 GM133314
6 · The paper itself

Abstract

significanceDiffuse in-vivo Flow Cytometry (DiFC) is an emerging fluorescence sensing method to non-invasively detect labeled circulating cells in-vivo. However, due to Signal-to-Noise Ratio (SNR) constraints largely attributed to background tissue autofluorescence, DiFC's measurement depth is limited. multiplies Aim: The Dual-Ratio (DR) / dual-slope is a new optical measurement method that aims to suppress noise and enhance SNR to deep tissue regions. We aim to investigate the combination of DR and Near-InfraRed (NIR) DiFC to improve circulating cells' maximum detectable depth and SNR. APPROACH: Phantom experiments were used to estimate the key parameters in a diffuse fluorescence excitation and emission model. This model and parameters were implemented in Monte-Carlo to simulate DR DiFC while varying noise and autofluorescence parameters to identify the advantages and limitations of the proposed technique.

resultsTwo key factors must be true to give DR DiFC an advantage over traditional DiFC; first, the fraction of noise that DR methods cannot cancel cannot be above the order of 10% for acceptable SNR. Second, DR DiFC has an advantage, in terms of SNR, if the distribution of tissue autofluorescence contributors is surface-weighted.

conclusionsDR cancelable noise may be designed for (e.g. through the use of source multiplexing), and indications point to the autofluorescence contributors' distribution being truly surface-weighted in-vivo. Successful and worthwhile implementation of DR DiFC depends on these considerations, but results point to DR DiFC having possible advantages over traditional DiFC.

Identifiers

PMID37292468
PMCPMC10246068

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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.