Evidence map›Paper›PMID 39841926›Full record

ArticleACS applied materials & interfaces2025

Carboxylate-Terminated Electrode Surfaces Improve the Performance of Electrochemical Aptamer-Based Sensors.

Rose Mery Bakestani, Yuyang Wu, Bettina Glahn-Martínez, Tod E Kippin, Kevin W Plaxco, Ruben W Kolkman

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

6 authors.

Rose Mery BakestaniDepartment of Chemistry and Biochemistry, University of California Santa Barbara, Santa Barbara, California 93106, United States.ORCID 0009-0004-3185-281X
Yuyang WuDepartment of Chemistry and Biochemistry, University of California Santa Barbara, Santa Barbara, California 93106, United States.
Bettina Glahn-MartínezDepartment of Chemistry and Biochemistry, University of California Santa Barbara, Santa Barbara, California 93106, United States.ORCID 0000-0003-0128-3113
Tod E KippinDepartment of Psychological and Brain Sciences, University of California Santa Barbara, Santa Barbara, California 93106, United States.
Kevin W PlaxcoDepartment of Chemistry and Biochemistry, University of California Santa Barbara, Santa Barbara, California 93106, United States.ORCID 0000-0003-4772-8771
Ruben W KolkmanDepartment of Chemistry and Biochemistry, University of California Santa Barbara, Santa Barbara, California 93106, United States.ORCID 0000-0002-2050-0876

Funding

Bio-electrochemical detectors for in vivo continuous monitoringR01EB022015 · NIBIB · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI KIPPIN, TOD EDWARD, PLAXCO, KEVIN W · 2017 to 2025
$4.6M
Continuous Therapeutic Drug Monitoring of Antibiotics in CRRTR01DK126739 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MOHAN, SUMIT · 2021 to 2024
$2.8M
NIBIB NIH HHS R01 EB022015NIDDK NIH HHS R01 DK126739
6 · The paper itself

Abstract

Electrochemical aptamer-based (EAB) sensors are a molecular measurement platform that enables the continuous, real-time measurement of a wide range of drugs and biomarkers in situ in the living body. EAB sensors are fabricated by depositing a thiol-modified, target-binding aptamer on the surface of a gold electrode, followed by backfilling with an alkanethiol to form a self-assembled monolayer. And while the majority of previously described EAB sensors have employed hydroxyl-terminated monolayers, a handful of studies have shown that altering the monolayer headgroup can strongly affect sensor performance. Here, using 4 different EAB sensors, we show that the mixed monolayers composed of mixtures of 6-carbon hydroxyl-terminated thiols and varying amounts of either 6- or 8-carbon, carboxylate-terminated thiols lead to improved EAB sensor performance. Specifically, the use of such mixed monolayers enhances the signal gain (the relative change in the signal seen upon target addition) for all tested sensors, often by several fold, both in buffer and whole blood at room temperature or physiological temperatures. Moreover, these improvements in gain are achieved without significant changes in the aptamer affinity or the stability of the resulting sensors. In addition to proving a ready means of improving EAB sensor performance, these results suggest that exploration of the chemistry of the electrode surface employed in such sensors could prove to be a fruitful means of advancing this unique in vivo sensing technology.

Indexed as

Aptamers, NucleotideBiosensing TechniquesCarboxylic AcidsElectrochemical TechniquesElectrodesGoldHumansSulfhydryl CompoundsSurface PropertiesAptamers, NucleotideCarboxylic AcidsGoldSulfhydryl Compoundselectrochemical aptamer-based sensorselectrochemical biosensingself-assembled monolayersquare-wave voltammetrysurface chemistry

Identifiers

PMID39841926
PMCPMC11803614

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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.