机构地区:[1]School of Dentistry, Federal University of Amazonas, Manaus, AM, Brazil [2]Federal University of Paraíba, Health Sciences Center, Department of Clinical and Social Dentistry, Joã o Pessoa, PB, Brazil [3]Faculty of Pharmaceutical Sciences, Federal University of Amazonas, Manaus, AM, Brazil [4]Manaus Municipal Health Department, SEMSA, Manaus, AM, Brazil
出 处:《Advances in Microbiology》2020年第9期434-442,共9页微生物学(英文)
摘 要:This study aimed to evaluate the antimicrobial activity of the extract of <i>Libidibia ferrea</i> L. (228.022-INPA) and a mouthwash formulation against microorganisms of the dental biofilm. The extract of <i>Libidibia ferrea</i> L. was prepared and formulated with an alcohol-free mouthwash. The Minimum Inhibitory Concentration—MIC was determined by microdilution and cell viability was evaluated through fluorescence. The MICs for the extract were 4.375 μg/mL (<i>Streptococcus mutans</i>), 3.750 μg/mL (<i>Streptococcus oralis</i>), 4.375 μg/mL (<i>Lactobacillus casei</i>). In contrast, for the mouthwash, the MICs were 6.000 μg/mL (bacteriostatic against <i>Streptococcus mutans</i> and bactericidal against <i>Streptococcus oralis</i>). In 1.250 μg/mL of the extract, the number of viable cells measured by fluorescence tests was 16.47% and 14.12% for <i>Streptococcus mutans</i> and <i>Lactobacillus casei</i>, respectively. For the mouthwash (1.000 μg/mL), 20.60% of viable cells for <i>Streptococcus mutans</i>, and 9.60% for <i>Lactobacillus casei</i> were observed. It can be concluded that the extract and its mouthwash containig <i>Libidibia ferrea</i> L. showed antibacterial activity against microorganisms from the dental biofilm.This study aimed to evaluate the antimicrobial activity of the extract of <i>Libidibia ferrea</i> L. (228.022-INPA) and a mouthwash formulation against microorganisms of the dental biofilm. The extract of <i>Libidibia ferrea</i> L. was prepared and formulated with an alcohol-free mouthwash. The Minimum Inhibitory Concentration—MIC was determined by microdilution and cell viability was evaluated through fluorescence. The MICs for the extract were 4.375 μg/mL (<i>Streptococcus mutans</i>), 3.750 μg/mL (<i>Streptococcus oralis</i>), 4.375 μg/mL (<i>Lactobacillus casei</i>). In contrast, for the mouthwash, the MICs were 6.000 μg/mL (bacteriostatic against <i>Streptococcus mutans</i> and bactericidal against <i>Streptococcus oralis</i>). In 1.250 μg/mL of the extract, the number of viable cells measured by fluorescence tests was 16.47% and 14.12% for <i>Streptococcus mutans</i> and <i>Lactobacillus casei</i>, respectively. For the mouthwash (1.000 μg/mL), 20.60% of viable cells for <i>Streptococcus mutans</i>, and 9.60% for <i>Lactobacillus casei</i> were observed. It can be concluded that the extract and its mouthwash containig <i>Libidibia ferrea</i> L. showed antibacterial activity against microorganisms from the dental biofilm.
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