Evidence map›Paper›PMID 42178770›Full record

ReviewChemical record (New York, N.Y.)2026

Redox Cycling-Based Signal Amplification in Electrochemical Immunosensors: A Personal Account.

Md Rajibul Akanda

Abstract readReview
In one paragraph

Review in Chemical record (New York, N.Y.), 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

1 author.

Md Rajibul AkandaDepartment of Chemistry, Jagannath University, Dhaka, Bangladesh.ORCID 0000-0002-9529-0578

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Electrochemical immunosensors are powerful tools for sensitive biomolecular detection but are often limited by low signal intensity at ultralow analyte concentrations. This personal account presents our systematic development of redox cycling-based amplification strategies to overcome this challenge. Starting with enzyme-amplified electrochemical-chemical cycling, we progressed to chemical-chemical and EC-chemical systems, enabling repeated utilization of enzymatically generated electroactive species. Mechanistic insights into electron-transfer pathways (i.e. inner sphere-philic and outer sphere- philic nature) guided the rational selection of enzyme substrates, redox mediators, and oxidant-reductant pairs. Integrating alkaline phosphatase-catalyzed reactions with multistep redox cycling substantially enhanced signal-to-background ratios and detection limits without complex electrode modification. Hydroquinone diphosphate-based systems offered superior performance due to favorable redox properties and stability. Besides, with enzyme mediated electrochemical-enzymatic cycling, we progressed to EC-enzymtic systems, enzyme itself is redox active. These approaches enabled ultrasensitive detection of protein biomarkers at femtogram-per-milliliter levels and reliable quantification of pathogenic bacteria. The account also addresses challenges in background suppression, reagent stability, and assay reproducibility, providing general design principles for robust, scalable, and sustainable electrochemical biosensors.

Indexed as

Biosensing TechniquesElectrochemical TechniquesAlkaline PhosphataseHumansImmunoassayOxidation-ReductionAlkaline Phosphataseelectrochemical immunosensorsenzyme‐mediated detectionredox cyclingsignal amplificationultrasensitive biosensing

Identifiers

PMID42178770
PMCPMC13480492

What OpenQuestion holds

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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.