Evidence map›Paper›PMID 33739124›Full record

ArticleBone & joint research2021

Influence of ceftriaxone on human bone cell viability and in vitro mineralization potential is concentration- and time-dependent.

Matthias Guido Wiesli, Jean-Pierre Kaiser, Emanuel Gautier, Peter Wick, Katharina Maniura-Weber, Markus Rottmar, Peter Wahl

Open access · goldAbstract read
In one paragraph

Article in Bone & joint research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Gentamicin fails to eradicateJournal of bone and joint infection · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. 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 3 institutions in 1 country.

Matthias Guido WiesliLaboratory for Biointerfaces, Empa - Swiss Federal Laboratories for Materials Science and Technology, St. Gallen, Switzerland.ORCID https://orcid.org/0000-0002-7422-5777
Jean-Pierre KaiserLaboratory for Particles-Biology Interactions, Empa - Swiss Federal Laboratories for Materials Science and Technology, St. Gallen, Switzerland.
Emanuel GautierDepartment of Orthopaedics, HFR Fribourg - Cantonal Hospital, Fribourg, Switzerland.
Peter WickLaboratory for Particles-Biology Interactions, Empa - Swiss Federal Laboratories for Materials Science and Technology, St. Gallen, Switzerland.ORCID https://orcid.org/0000-0002-0079-4344
Katharina Maniura-WeberLaboratory for Biointerfaces, Empa - Swiss Federal Laboratories for Materials Science and Technology, St. Gallen, Switzerland.ORCID https://orcid.org/0000-0001-7895-3563
Markus RottmarLaboratory for Biointerfaces, Empa - Swiss Federal Laboratories for Materials Science and Technology, St. Gallen, Switzerland.ORCID https://orcid.org/0000-0001-7636-428X
Peter WahlDivision of Orthopaedics and Traumatology, Cantonal Hospital Winterthur, Winterthur, Switzerland.ORCID https://orcid.org/0000-0002-8895-8621
Swiss Federal Laboratories for Materials Science and Technology · CHFribourg Development Agency · CHKantonsspital Winterthur · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsIn orthopaedic and trauma surgery, implant-associated infections are increasingly treated with local application of antibiotics, which allows a high local drug concentration to be reached without eliciting systematic adverse effects. While ceftriaxone is a widely used antibiotic agent that has been shown to be effective against musculoskeletal infections, high local concentrations may harm the surrounding tissue. This study investigates the acute and subacute cytotoxicity of increasing ceftriaxone concentrations as well as their influence on the osteogenic differentiation of human bone progenitor cells.

methodsHuman preosteoblasts were cultured in presence of different concentrations of ceftriaxone for up to 28 days and potential cytotoxic effects, cell death, metabolic activity, cell proliferation, and osteogenic differentiation were studied.

resultsCeftriaxone showed a cytotoxic effect on human bone progenitor cells at 24 h and 48 h at concentrations above 15,000 mg/l. With a longer incubation time of ten days, subtoxic effects could be observed at concentrations above 500 mg/l. Gene and protein expression of collagen, as well as mineralization levels of human bone progenitor cells, showed a continuous decrease with increasing ceftriaxone concentrations by days 14 and 28, respectively. Notably, mineralization was negatively affected already at concentrations above 250 mg/l.

conclusionThis study demonstrates a concentration-dependent influence of ceftriaxone on the viability and mineralization potential of primary human bone progenitor cells. While local application of ceftriaxone is highly established in orthopaedic and trauma surgery, a therapeutic threshold of 250 mg/l or lower should diminish the risk of reduced osseointegration of prosthetic implants. Cite this article:

Indexed as

CeftriaxoneCytotoxicityHuman bone progenitor cellsOsteogenic differentiation

Identifiers

PMID33739124
PMCPMC7998344
OpenAlexW3138887470

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.