Evidence map›Paper›PMID 40889053›Full record

ArticleDiscover nano2025

Automatic design and optimization of MRI-based neurochemical sensors via reinforcement learning.

Zulaikha Ali, Aaron Asparin, Yunfei Zhang, Hannah Mettee, Diya Taha, Yuna Ha, Deepika Bhanot, Khaldoon Sarwar, Hamzah Kiran, Shuo Wu and 1 more

Abstract read
In one paragraph

Article in Discover nano, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Zulaikha Ali *Department of Chemistry and Biochemistry, California State University Fresno, 2555 E San Ramon Ave, Fresno, CA, 93740, USA.
Aaron Asparin *Department of Chemistry and Biochemistry, California State University Fresno, 2555 E San Ramon Ave, Fresno, CA, 93740, USA.
Yunfei ZhangDepartment of Chemistry and Biochemistry, California State University Fresno, 2555 E San Ramon Ave, Fresno, CA, 93740, USA.
Hannah MetteeDepartment of Chemistry and Biochemistry, California State University Fresno, 2555 E San Ramon Ave, Fresno, CA, 93740, USA.
Diya TahaDepartment of Chemistry and Biochemistry, California State University Fresno, 2555 E San Ramon Ave, Fresno, CA, 93740, USA.
Yuna HaDepartment of Chemistry and Biochemistry, California State University Fresno, 2555 E San Ramon Ave, Fresno, CA, 93740, USA.
Deepika BhanotDepartment of Chemistry and Biochemistry, California State University Fresno, 2555 E San Ramon Ave, Fresno, CA, 93740, USA.
Khaldoon SarwarDepartment of Chemistry and Biochemistry, California State University Fresno, 2555 E San Ramon Ave, Fresno, CA, 93740, USA.
Hamzah KiranDepartment of Chemistry and Biochemistry, California State University Fresno, 2555 E San Ramon Ave, Fresno, CA, 93740, USA.
Shuo WuDepartment of Electrical and Computer Engineering, California State University Fresno, 2320 E San Ramon Ave, Fresno, CA, 93740, USA. shuowu@mail.fresnostate.edu.
He WeiDepartment of Chemistry and Biochemistry, California State University Fresno, 2555 E San Ramon Ave, Fresno, CA, 93740, USA. hewei@mail.fresnostate.edu.ORCID https://orcid.org/0000-0001-7188-8105

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Magnetic resonance imaging (MRI) is a cornerstone of medical imaging, celebrated for its non-invasiveness, high spatial and temporal resolution, and exceptional soft tissue contrast, with over 100 million clinical procedures performed annually worldwide. In this field, MRI-based nanosensors have garnered significant interest in biomedical research due to their tunable sensing mechanisms, high permeability, rapid kinetics, and surface functionality. Extensive studies in the field have reported the use of superparamagnetic iron oxide nanoparticles (SPIONs) and proteins as a proof-of-concept for sensing critical neurochemicals via MRI. However, the signal change ratio and response rate of our SPION-protein-based in vitro dopamine and in vivo calcium sensors need to be further enhanced to detect the subtle and transient fluctuations in neurochemical levels associated with neural activities, starting from in vitro diagnostics. In this paper, we present an advanced reinforcement-learning-based computational model that treats sensor design as an optimal decision-making problem by choosing sensor performance as a weighted reward objective function. The adjustments of the SPION's and protein's three-dimensional configuration and magnetic moment establish a set of actions that can autonomously maximize the cumulative reward in the computational environment. Our new model first elucidates the sensor's conformation alteration behind the increment in T

Identifiers

PMID40889053
PMCPMC12401834

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Registered trials

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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.