Discerning Amyloid-β and Tau Pathologies with Learning-Based Quantum Sensing

Photon entanglement, a key feature of quantum correlations, provides a level of coherence absent in classical correlations, potentially offering new information when interacting with biological matter. One promising application is using entanglement decoherence to distinguish between healthy and diseased samples. However, achieving this requires efficient entangled photon sources capable of surviving through biological samples for reliable detection. In this work, we show the applicability of a polarization-entangled photon source as a label-free diagnostic tool for distinguishing between transgenic mouse models of amyloidosis and tauopathy and their respective control strains. We investigated cortical and hippocampal regions of these models, and our findings revealed greater preservation of entanglement in the transgenic samples compared to controls. To further enhance classification accuracy, we employed a supervised machine learning approach, achieving reliable distinctions between disease and control groups in unseen test samples. The quantum-based results were further validated through confocal imaging of the transgenic and control samples. These findings suggest that quantum sensing could serve as a label-free approach for distinguishing biological samples, with potential applications in the study of neurodegenerative disorders.

Authors

Publication Details

Journal
Open Access CRIS of the University of Bern
Published
2025-09-25
DOI
https://doi.org/10.48620/93040
Primary Topic
Biofield Effects and Biophysics
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Discerning Amyloid-β and Tau Pathologies with Learning-Based Quantum Sensing

M. V. Jabir, Lukas Glandorf, Daniel Razansky, Shruti Sundar et al.
Open Access CRIS of the University of Bern
Biofield Effects and Biophysics
article

Discerning Amyloid-β and Tau Pathologies with Learning-Based Quantum Sensing

M. V. Jabir, Lukas Glandorf, Daniel Razansky, Shruti Sundar, Ruiqing Ni, Michael Reiss
article en

Abstract

Photon entanglement, a key feature of quantum correlations, provides a level of coherence absent in classical correlations, potentially offering new information when interacting with biological matter. One promising application is using entanglement decoherence to distinguish between healthy and diseased samples. However, achieving this requires efficient entangled photon sources capable of surviving through biological samples for reliable detection. In this work, we show the applicability of a polarization-entangled photon source as a label-free diagnostic tool for distinguishing between transgenic mouse models of amyloidosis and tauopathy and their respective control strains. We investigated cortical and hippocampal regions of these models, and our findings revealed greater preservation of entanglement in the transgenic samples compared to controls. To further enhance classification accuracy, we employed a supervised machine learning approach, achieving reliable distinctions between disease and control groups in unseen test samples. The quantum-based results were further validated through confocal imaging of the transgenic and control samples. These findings suggest that quantum sensing could serve as a label-free approach for distinguishing biological samples, with potential applications in the study of neurodegenerative disorders.

Open Access CRIS of the University of Bern
Openalex Percentile: Top 30%
Biofield Effects and Biophysics
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.