Evidence map›Paper›PMID 25859852›Full record

ArticlePloS one2015

Carvacrol codrugs: a new approach in the antimicrobial plan.

Ivana Cacciatore, Mara Di Giulio, Erika Fornasari, Antonio Di Stefano, Laura Serafina Cerasa, Lisa Marinelli, Hasan Turkez, Emanuela Di Campli, Soraya Di Bartolomeo, Iole Robuffo and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
7.2field-weighted citation impact, top 3% 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

25 citing papers in PubMed, 65 citations in OpenAlex.

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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

11 authors at 2 institutions in 2 countries.

Ivana CacciatoreDepartment of Pharmacy, University "G. d'Annunzio" Chieti-Pescara, Chieti, Italy.
Mara Di GiulioDepartment of Pharmacy, University "G. d'Annunzio" Chieti-Pescara, Chieti, Italy.
Erika FornasariDepartment of Pharmacy, University "G. d'Annunzio" Chieti-Pescara, Chieti, Italy.
Antonio Di StefanoDepartment of Pharmacy, University "G. d'Annunzio" Chieti-Pescara, Chieti, Italy.
Laura Serafina CerasaDepartment of Pharmacy, University "G. d'Annunzio" Chieti-Pescara, Chieti, Italy.
Lisa MarinelliDepartment of Pharmacy, University "G. d'Annunzio" Chieti-Pescara, Chieti, Italy.
Hasan TurkezDepartment of Pharmacy, University "G. d'Annunzio" Chieti-Pescara, Chieti, Italy; Department of Molecular Biology and Genetics, Faculty of Science, Erzurum Technical University, Erzurum, Turkey.
Emanuela Di CampliDepartment of Pharmacy, University "G. d'Annunzio" Chieti-Pescara, Chieti, Italy.
Soraya Di BartolomeoDepartment of Pharmacy, University "G. d'Annunzio" Chieti-Pescara, Chieti, Italy.
Iole RobuffoInstitute of Molecular Genetics, National Research Council (CNR) section of Chieti, Chieti, Italy.
Luigina CelliniDepartment of Pharmacy, University "G. d'Annunzio" Chieti-Pescara, Chieti, Italy.
University of Chieti-Pescara · ITNational Research Council · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe increasing prevalence of antibiotic-resistant bacterial infections led to identify alternative strategies for a novel therapeutic approach. In this study, we synthesized ten carvacrol codrugs - obtained linking the carvacrol hydroxyl group to the carboxyl moiety of sulphur-containing amino acids via an ester bond - to develop novel compounds with improved antimicrobial and antibiofilm activities and reduced toxicity respect to carvacrol alone.

methodAll carvacrol codrugs were screened against a representative panel of Gram positive (S. aureus and S. epidermidis), Gram negative (E. coli and P. aeruginosa) bacterial strains and C. albicans, using broth microdilution assays.

findingsResults showed that carvacrol codrug 4 possesses the most notable enhancement in the anti-bacterial activity displaying MIC and MBC values equal to 2.5 mg/mL for all bacterial strains, except for P. aeruginosa ATCC 9027 (MIC and MBC values equal to 5 mg/mL and 10 mg/mL, respectively). All carvacrol codrugs 1-10 revealed good antifungal activity against C. albicans ATCC 10231. The cytotoxicity assay showed that the novel carvacrol codrugs did not produce human blood hemolysis at their MIC values except for codrugs 8 and 9. In particular, deepened experiments performed on carvacrol codrug 4 showed an interesting antimicrobial effect on the mature biofilm produced by E. coli ATCC 8739, respect to the carvacrol alone. The antimicrobial effects of carvacrol codrug 4 were also analyzed by TEM evidencing morphological modifications in S. aureus, E. coli, and C. albicans.

conclusionThe current study presents an insight into the use of codrug strategy for developing carvacrol derivatives with antibacterial and antibiofilm potentials, and reduced cytotoxicity.

Indexed as

AnimalsAnti-Infective AgentsBiofilmsCandida albicansCymenesErythrocytesGram-Negative BacteriaGram-Positive BacteriaHemolysisHumansMicrobial Sensitivity TestsMicroscopy, Electron, TransmissionMonoterpenesRatsAnti-Infective AgentscarvacrolCymenesMonoterpenes

Identifiers

PMID25859852
PMCPMC4393269
OpenAlexW1964944721

What OpenQuestion holds

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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.