Evidence map›Paper›PMID 35625185›Full record

ArticleAntibiotics (Basel, Switzerland)2022

Validation and Application of an HPLC-UV Method for Routine Therapeutic Drug Monitoring of Dalbavancin.

Ute Chiriac, Heike Rau, Otto R Frey, Anka C Röhr, Sabrina Klein, Anna L Meyer, Benedict Morath

Open access · goldAbstract read
In one paragraph

Article in Antibiotics (Basel, Switzerland), 2022. 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
3.8field-weighted citation impact, top 7% 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, 24 citations in OpenAlex.

  1. Article
  2. Review
  3. Quantitative analysis of related substances in acetaminophen tablets using pre-column derivatization coupled with HPLC-ICP-MS.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. 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

7 authors at 1 institution in 1 country.

Ute ChiriacDepartment of Pharmacy, Heidelberg University Hospital, 69120 Heidelberg, Germany.ORCID 0000-0002-4288-1745
Heike RauDepartment of Pharmacy, General Hospital of Heidenheim, 89522 Heidenheim, Germany.
Otto R FreyDepartment of Pharmacy, General Hospital of Heidenheim, 89522 Heidenheim, Germany.ORCID 0000-0001-9482-5094
Anka C RöhrDepartment of Pharmacy, General Hospital of Heidenheim, 89522 Heidenheim, Germany.
Sabrina KleinDepartment of Infectious Diseases, Medical Microbiology and Hospital Hygiene, Heidelberg University Hospital, 69120 Heidelberg, Germany.
Anna L MeyerDepartment of Cardiac Surgery, Heidelberg University Hospital, 69120 Heidelberg, Germany.
Benedict MorathDepartment of Pharmacy, Heidelberg University Hospital, 69120 Heidelberg, Germany.ORCID 0000-0003-1926-0585
Heidelberg University · DE

Funding

Correvio FC81A543-5FE5-4B8F-9C75-0F2C788BF031
6 · The paper itself

Abstract

Dalbavancin is emerging as a promising alternative in the ambulant treatment of gram-positive infections that require long-term antibiotic treatment such as osteomyelitis, prosthetic joint infections, and endocarditis. The aim of the current study was to develop and validate a simple, rapid, and cost-effective high-performance liquid chromatography-ultraviolet spectrometry (HPLC-UV) method for the quantification of dalbavancin. Sample clean-up included a protein precipitation protocol, followed by chromatographic separation on a reverse phase HPLC column (C-18) with gradient elution of the mobile phase. Quantification was performed with the internal standard (caffeine) method. Linear relationships between peak area responses and drug concentrations were obtained in the range of 12.5-400 mg/L. The variation coefficient of precision and the bias of accuracy (both inter- and intraday) were less than 10%. The limit of quantification (LOQ) was 12.5 mg/L. The simple and reliable HPLC-UV assay described is a powerful tool for routine therapeutic drug monitoring (TDM) of dalbavancin in human serum in clinical laboratories. With a total process time of approximately 20 min, it allows for accurate and selective quantification up to the expected pharmacokinetic peak concentrations. The method was successfully used to analyze subsequent serum samples of three patients and showed good performance in monitoring serum levels.

Indexed as

dalbavancinhigh performance liquid chromatography–ultraviolet spectrometry (HPLC–UV)pharmacokinetic/pharmacodynamics (PK/PD)therapeutic drug monitoring (TDM)

Identifiers

PMID35625185
PMCPMC9137512
OpenAlexW4224234570

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.