Bioactive glass with antimicrobial agents : in vitro evaluation.
Nenhuma Miniatura disponível
Data
2014
Título da Revista
ISSN da Revista
Título de Volume
Editor
Resumo
Bioactive glass is biocompatible and has the ability to stimulate bone formation. The aim of the
present study was to evaluate the efficiency of bioactive glass in releasing tetracycline and/or
hydrocortisone through an in vitro growth inhibition study involving microorganisms commonly
found in the oral cavity: Staphylococcus aureus (ATCC 27664), Enterococcus faecalis (ATCC 12399)
and Streptococcus mutans (ATCC 70069). The bioactive glass was prepared using the sol-gel
method and had a molar composition of 80% SiO2, 4% P2O5 and 16% CaO. Four groups were
formed: a drug-free control group (CG); a hydrocortisone group (HG) with 2% (in weight) of the drug
incorporated into the bioactive glass; a tetracycline group (TG) containing 2% (in weight) of the drug;
and a hydrocortisone-tetracycline group (HTG) containing 2% of each drug. Test specimens were
distributed in Petri dishes containing agar previously inoculated with the microorganisms and
incubated for 24 hours. Statistical analysis involved the Kruskal-Wallis and Mann-Whitney tests. The
CG and HG proved ineffective in inhibiting the growth of the microorganisms. The TG exhibited
inhibition zones on all microorganisms tested. The HTG had the largest inhibition zones for
Staphylococcus aureus (ATCC 27664) and Enterococcus faecalis (ATCC 12399), with statistically
significant differences in comparison to the other groups (p < 0.001). The present study
demonstrates that bioactive glass is able to release tetracycline for effective antibiotic action.
Descrição
Palavras-chave
Bioactive glass, Tetracycline, Hydrocortisone
Citação
CARVALHO, M. F. F. de. Bioactive glass with antimicrobial agents: in vitro evaluation. Journal of Medicine and Medical Sciences, JMMS, v. 5, p. 109, 2014. Disponível em: <https://www.interesjournals.org/abstract/bioactive-glass-with-antimicrobial-agents-in-vitro-evaluation-17082.html>. Acesso em: 20 abr. 2017.