Evidence map›Paper›PMID 40822889›Full record

ArticleJournal of applied electrochemistry2023

Field‑use device for the electrochemical quantification of carbamazepine levels in a background of human saliva.

Lael Wentland, Jacob M Cook, Jade Minzlaff, Stephen A Ramsey, Matthew L Johnston, Elain Fu

Abstract read
In one paragraph

Article in Journal of applied electrochemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Lael WentlandSchool of Chemical, Biological, and Environmental Engineering, Oregon State University, Corvallis, OR 97331, USA.
Jacob M CookSchool of Electrical Engineering and Computer Science, Oregon State University, Corvallis, OR 97331, USA.
Jade MinzlaffSchool of Chemical, Biological, and Environmental Engineering, Oregon State University, Corvallis, OR 97331, USA.
Stephen A RamseySchool of Electrical Engineering and Computer Science, Oregon State University, Corvallis, OR 97331, USA.
Matthew L JohnstonSchool of Electrical Engineering and Computer Science, Oregon State University, Corvallis, OR 97331, USA.
Elain FuSchool of Chemical, Biological, and Environmental Engineering, Oregon State University, Corvallis, OR 97331, USA.

Funding

Development of an intraoral device for therapeutic drug monitoring of anti-epileptic drugsR21DE031101 · NIDCR · OREGON STATE UNIVERSITY · PI FU, ELAIN, JOHNSTON, MATTHEW L · 2022 to 2023
$372k
NIDCR NIH HHS R21 DE031101
6 · The paper itself

Abstract

Microfluidic devices are well suited for use in field applications, including for point-of-care (POC) diagnosis and therapy monitoring. Advantages of the use of microfluidics include small sample volumes, rapid sample to answer times, and disposable test cards combined with minimal portable instrumentation. A continuing challenge is detection from a complex sample, like saliva, which often requires extensive manual preprocessing to reduce background from interferents and for which analytes are often at lower concentrations than in blood. Further, coupling electrochemical detection to microfluidic devices has shown promise for multiple applications, but most often has been demonstrated with benchtop potentiostats rather than POC-compatible instrumentation. In the current report, we demonstrate a disposable microfluidic flow cell paired with a portable, miniature potentiostat for electrochemical measurement of the anticonvulsant drug carbamazepine in a background of human saliva. Specific highlights of the device include the small input volume of 12 μL of saliva, the absence of any manual preprocessing of the saliva sample, and carbamazepine quantification using an inexpensive polymeric laminate flow cell with stencil-printed electrodes and miniature potentiostat. With this system, accurate and robust quantification of carbamazepine drug level was achieved at therapeutically relevant concentrations of 2.5 μM to 15 μM carbamazepine in saliva. Further, functional dry storage of the microfluidic flow cells was demonstrated over 90 days.

Indexed as

Carbamazepine detectionElectrochemical sensingMicrofluidicsPoint-of-care devices

Identifiers

PMID40822889
PMCPMC12356398

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.