Evidence map›Paper›PMID 41979109›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2026

Quantifying Population Reversibility of Sensor Performance in Multi-Cycle Single-Sensor Recovery Assay.

Geffen Rosenberg, Gili Bisker

Abstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2026. 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

2 authors.

Geffen RosenbergSchool of Biomedical Engineering, Faculty of Engineering, Tel Aviv University, Tel Aviv, Israel.
Gili BiskerSchool of Biomedical Engineering, Faculty of Engineering, Tel Aviv University, Tel Aviv, Israel.ORCID https://orcid.org/0000-0003-2592-7956

Funding

European Research Council NanoNonEq101039127Israel Science Foundation 196/22Israel's Council for Higher EducationMarian Gertner Institute for Medical NanosystemsMinistry of Science, Technology, and Space, Israel 1001818370Ministry of Science, Technology, and Space, Israel 1001944224Naomi Prawer Kadar FoundationNicholas and Elizabeth Slezak Super Center for Cardiac Research and Biomedical EngineeringTel Aviv University Center for AI and Data Science (TAD)Zimin Institute for Engineering Solutions Advancing Better LivesZuckerman STEM Leadership Program
6 · The paper itself

Abstract

Quantitative chemical imaging requires sensors that reliably recover across repeated exposures. While solution-phase bulk measurements provide an averaged response of the sensor population, imaging at the single-sensor level enables mapping of biological processes with spatiotemporal resolution, revealing localized events and interaction sites. To translate such imaging into calibrated measurements, sensor variability across repeated analyte exposures must be analyzed. This work introduces a generic workflow that combines an automated microfluidic flow imaging platform with systematic characterization of the response, recovery, and reversibility of individual nanosensors under multi-cycle challenges. For representative implementation, three near-infrared fluorescent single-walled carbon nanotube (SWCNT) sensor models are tested, each with a distinct functionalization rendering it optically responsive to a corresponding exemplar target: dopamine, thiocholine, or serotonin. While first-cycle responses averaged over the entire field of view recapitulate ensemble calibration, single-sensor analysis uncovers broad heterogeneity in response magnitude, signal recovery, and reversibility across hundreds of individual SWCNTs under repeated exposure and wash cycles. To compare performance across cycles, a standardized Population Reversibility Score based on Kullback-Leibler Divergence is introduced, condensing response distributions into a single cycle- and concentration-dependent, quantitative metric. This framework is generally applicable to other sensor-analyte systems with transient readouts, guiding optimization for spatiotemporal analyte mapping.

Indexed as

fluorescence sensorsnear‐infraredsensor recoverysensor reversibilitysingle‐walled carbon nanotubesspatiotemporal sensors

Identifiers

PMID41979109
PMCPMC13262247

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.