Evidence map›Paper›PMID 31324294›Full record

ArticleJournal of food and drug analysis2019

An ultra-rapid drug screening method for acetaminophen in blood serum based on probe electrospray ionization-tandem mass spectrometry.

Kiyotaka Usui, Haruka Kobayashi, Yuji Fujita, Eito Kubota, Tomoki Hanazawa, Tomohiro Yoshizawa, Yoshito Kamijo, Masato Funayama

Open access · hybridAbstract read
In one paragraph

Article in Journal of food and drug analysis, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 35% of its field
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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
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

8 authors at 3 institutions in 1 country.

Kiyotaka UsuiDivision of Forensic Medicine, Tohoku University Graduate School of Medicine, Sendai, 980-8575, Japan.
Haruka KobayashiDivision of Forensic Medicine, Tohoku University Graduate School of Medicine, Sendai, 980-8575, Japan.
Yuji FujitaDivision of Emergency Medicine, Iwate Medical University, Morioka, 020-8505, Japan.
Eito KubotaDivision of Forensic Medicine, Tohoku University Graduate School of Medicine, Sendai, 980-8575, Japan.
Tomoki HanazawaEmergency Medical Center and Poison Center, Saitama Medical University Hospital, Saitama, 350-0495, Japan.
Tomohiro YoshizawaEmergency Medical Center and Poison Center, Saitama Medical University Hospital, Saitama, 350-0495, Japan.
Yoshito KamijoEmergency Medical Center and Poison Center, Saitama Medical University Hospital, Saitama, 350-0495, Japan.
Masato FunayamaDivision of Forensic Medicine, Tohoku University Graduate School of Medicine, Sendai, 980-8575, Japan.
Tohoku University · JPSaitama Medical University Hospital · JPIwate Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Poisoning incidents caused by drugs, accidental ingestion of poisons, attempted suicide, homicide, and exposure to toxic compounds occur frequently every year across the globe. This raises the need to rapidly identify toxic agents in poisoned patients in a clinical emergency setting. In addition, determining drug/poison concentration is undoubtedly necessary to arrive at a toxicological treatment plan. The purpose of this study was to develop an ultra-rapid drug screening method for the clinical treatment of poisoning. Probe electrospray ionization (PESI), one of the ambient ionization techniques, is able to detect compounds from various biological materials almost directly. We applied the PESI technique to the rapid detection of acetaminophen (APAP). Blood serum samples were diluted 100-fold with 10 mM ammonium formate/ethanol (1:1 v/v) solution including deuterium-labeled internal standards (IS; APAP-d4). Only 10 μL of the diluted sample was used for measurement. The tandem mass spectrometer (MS/MS) equipped with a PESI was used in selected reaction monitoring mode for the quantitation of APAP; the measurement time was only 18 s. Transitions were set at 152 > 110 for quantitation, 152 > 65 for qualifier, and 156 > 114 for IS (APAP-d4). All measurements were conducted in positive mode. The calibration curve (1/x

Indexed as

AcetaminophenAnalgesics, Non-NarcoticDrug Evaluation, PreclinicalHumansMolecular StructureSpectrometry, Mass, Electrospray IonizationTandem Mass SpectrometryAcetaminophenAnalgesics, Non-NarcoticAcetaminophenBlood serumProbe electrospray ionizationRapid drug screeningTandem mass spectrometry

Identifiers

PMID31324294
PMCPMC9307038
OpenAlexW2915870510

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.