2015
DOI: 10.3390/molecules201018685
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Antimicrobial Activity of Rhoeo discolor Phenolic Rich Extracts Determined by Flow Cytometry

Abstract: Abstract:Traditional medicine has led to the discovery of important active substances used in several health-related areas. Phytochemicals in Rhoeo discolor extracts have proven to have important antimicrobial activity. In the present study, our group determined the antimicrobial effects of extracts of Rhoeo discolor, a plant commonly used in Mexico for both medicinal and ornamental purposes. We evaluated the in vitro activity of phenolic rich extracts against specifically chosen microorganisms of human health… Show more

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Cited by 17 publications
(4 citation statements)
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“…According to the literature, extracts of T. spathacea leaves can be obtained by distinct methods, such as decoction 36 and by Soxhlet, 37 however, the overall extraction yields (2.8, 8.4% and 3.4%, respectively) were reported to be lower than those found in our study. Moreover, DTTS values of phenolic compounds and flavonoids were higher than others previously reported: TPC of 2.3 mg/g, 7 8.5 mg/g, 38 TFC of 0.7 mg/g, 7 and 10.8 mg/g. 4 …”
Section: Discussioncontrasting
confidence: 76%
“…According to the literature, extracts of T. spathacea leaves can be obtained by distinct methods, such as decoction 36 and by Soxhlet, 37 however, the overall extraction yields (2.8, 8.4% and 3.4%, respectively) were reported to be lower than those found in our study. Moreover, DTTS values of phenolic compounds and flavonoids were higher than others previously reported: TPC of 2.3 mg/g, 7 8.5 mg/g, 38 TFC of 0.7 mg/g, 7 and 10.8 mg/g. 4 …”
Section: Discussioncontrasting
confidence: 76%
“…leaves is purple. This distinct coloration is attributed to the presence of anthocyanins, which are known for their potential to confer resistance to microbes (García-Varela et al, 2015). The appearance of the Zebrina pendula Schinzl plant is shown in Fig.…”
Section: Resultsmentioning
confidence: 99%
“…The flow cytofluorometric method is capable to discriminate three distinct subpopulations (dead, viable and injured cells), allowing one to evaluate the antifungal activity of the plant extract on the tested microorganism. Fungal spores suspension is mixed with an equal volume of plant extract and shook for the desired time, usually 25 °C for 24 h [ 224 ] or 10 min at room temperature [ 225 ]. Then, the cells are pelleted, resuspended in PI solution (25 µg/mL in phosphate-buffered saline) and incubated in the dark for 30 min at 32 °C.…”
Section: Most Common Techniques For the Validation Of Antifungal Amentioning
confidence: 99%