Evidence map›Paper›PMID 33693976›Full record

ArticleAnalytical and bioanalytical chemistry2021

Targeted LC-MS/MS platform for the comprehensive determination of peptides in the kallikrein-kinin system.

Tanja Gangnus, Bjoern B Burckhardt

Open access · hybridAbstract readValidation Study
In one paragraph

Article in Analytical and bioanalytical chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. The journal of allergy and clinical immunology. Global · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Bradykinin - An elusive peptide in measuring and understanding.Research and practice in thrombosis and haemostasis · 2022
    Article
  8. Reliable measurement of plasma kinin peptides: Importance of preanalytical variables.Research and practice in thrombosis and haemostasis · 2022
    Article
  9. Article
  10. The des-ArgFrontiers in physiology · 2022
    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

2 authors at 1 institution in 1 country.

Tanja GangnusInstitute of Clinical Pharmacy and Pharmacotherapy, Heinrich Heine University, 40225, Dusseldorf, Germany.
Bjoern B BurckhardtInstitute of Clinical Pharmacy and Pharmacotherapy, Heinrich Heine University, 40225, Dusseldorf, Germany. bjoern.burckhardt@hhu.de.ORCID http://orcid.org/0000-0002-1782-9937
Heinrich Heine University Düsseldorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The kallikrein-kinin system (KKS) is involved in many physiological and pathophysiological processes and is assumed to be connected to the development of clinical symptoms of angioedema or COVID-19, among other diseases. However, despite its diverse role in the regulation of physiological and pathophysiological functions, knowledge about the KKS in vivo remains limited. The short half-lives of kinins, their low abundance and structural similarities and the artificial generation of the kinin bradykinin greatly hinder reliable and accurate determination of kinin levels in plasma. To address these issues, a sensitive LC-MS/MS platform for the comprehensive and simultaneous determination of the four active kinins bradykinin, kallidin, des-Arg(9)-bradykinin and des-Arg(10)-kallidin and their major metabolites bradykinin 2-9, bradykinin 1-7 and bradykinin 1-5 was developed. This platform was validated according to the bioanalytical guideline of the US Food and Drug Administration regarding linearity, accuracy, precision, sensitivity, carry-over, recovery, parallelism, matrix effects and stability in plasma of healthy volunteers. The validated platform encompassed a broad calibration curve range from 2.0-15.3 pg/mL (depending on the kinin) up to 1000 pg/mL, covering the expected concentrations in disease states. No source-dependent matrix effects were identified, and suitable stability of the analytes in plasma was observed. The applicability of the developed platform was proven by the determination of endogenous levels in healthy volunteers, whose plasma kinin levels were successfully detected in the low pg/mL range. The established platform facilitates the investigation of kinin-mediated diseases (e.g. angioedema, COVID-19) and enables the assessment of the impact of altered enzyme activities on the formation or degradation of kinins.

Indexed as

Kallikrein-Kinin SystemBradykininChromatography, LiquidCOVID-19HumansKallidinLimit of DetectionPeptide FragmentsTandem Mass SpectrometryBradykininbradykinin (1-5)bradykinin (2-9)bradykinin, des-Arg(9)-Kallidinkallidin, des-Arg(10)-Peptide FragmentsAngioedemaBradykininCOVID-19Kallikrein-kinin systemLC-MS/MSPlasma

Identifiers

PMID33693976
PMCPMC7946403
OpenAlexW3133668063

What OpenQuestion holds

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LicenceCC BY
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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.