Bacterial inhibition efficiency of prilocaine and bupivacaine.


Journal

International wound journal
ISSN: 1742-481X
Titre abrégé: Int Wound J
Pays: England
ID NLM: 101230907

Informations de publication

Date de publication:
Oct 2019
Historique:
received: 14 07 2019
revised: 27 07 2019
accepted: 27 07 2019
pubmed: 14 8 2019
medline: 14 3 2020
entrez: 14 8 2019
Statut: ppublish

Résumé

This study aimed to demonstrate the antibacterial effects of bupivacaine and prilocaine on Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa. In our study, the in vitro antimicrobial effects of 20 mg/mL prilocaine and 5 mg/mL bupivacaine were tested against a S. aureus American-type culture collection (ATCC) 29213, P. aeruginosa ATCC 27853, and E. coli ATCC 25922, divided into Group P (Prilocaine) and Group B (Bupivacaine), respectively. S. aureus ATCC 29213, P. aeruginosa ATCC 27853, and E. coli ATCC 25922 were cultured on Mueller Hinton agar (Oxoid, Basingstoke, UK) plates for 18 to 24 hours at 37°C. In terms of inhibition zone diameters, inhibition of S. aureus ATCC 29213 was observed in both groups at the 12th and 24th hours. The 12th- and 24th-hour S. aureus ATCC 29213 value was significantly higher in Group P compared with Group B (P = .008). At the 12th and 24th hours, inhibition of E. coli ATCC 25922 was observed in both groups. The 12th- and 24th-hour E. coli ATCC 25922 value was significantly higher in Group P compared with Group B (P = .008). In our study, it was seen that prilocaine and bupivacaine had an antimicrobial effect on S. aureus and E. coli. In the comparison between these two local anesthetics (LAs), this effect was found to be significantly higher in prilocaine than bupivacaine. Therefore, we are of the opinion that antimicrobial effect potentials should also be taken into account in the selection of an LA agent in order to prevent the complications of an infection that might develop during LA infiltration and might lead to serious morbidity.

Identifiants

pubmed: 31407480
doi: 10.1111/iwj.13180
pmc: PMC7948626
doi:

Substances chimiques

Prilocaine 046O35D44R
Bupivacaine Y8335394RO

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1185-1189

Informations de copyright

© 2019 Medicalhelplines.com Inc and John Wiley & Sons Ltd.

Références

Eur J Clin Microbiol Infect Dis. 2019 Jun;38(6):991-1002
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Int Wound J. 2019 Oct;16(5):1185-1189
pubmed: 31407480
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pubmed: 19157348
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pubmed: 20418532
Eur J Anaesthesiol. 2001 Oct;18(10):687-94
pubmed: 11553246
Br J Anaesth. 1999 Oct;83(4):657-8
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Anesthesiology. 1985 Feb;62(2):178-9
pubmed: 3918482
Int Wound J. 2019 Aug;16(4):1029-1033
pubmed: 31148374
J Dermatolog Treat. 2008;19(6):351-3
pubmed: 18608709
Anaesth Intensive Care. 1986 Nov;14(4):418-20
pubmed: 3105346
Front Chem. 2017 Jul 12;5:51
pubmed: 28748180

Auteurs

Sevgi Kesici (S)

Department of Anesthesiology and Reanimation, Hamidiye Etfal Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.

Mehmet Demirci (M)

Faculty of Medicine, Department of Microbiology, University of Beykent, Istanbul, Turkey.

Ugur Kesici (U)

Faculty of Medicine, Department of General Surgery, University of Beykent, Istanbul, Turkey.

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Classifications MeSH