Abstract:In the present work, the phenolic compounds of Castanea sativa, Filipendula ulmaria and Rosa micrantha flowers from Northeastern Portugal were characterized by HPLC-DAD-ESI/MS. Furthermore, it was performed a screening of their antifungal potential against Candida species (C. albicans, C. glabrata, C. parapsilosis and C. tropicalis).C. sativa sample gave the highest amount of phenolic compounds (18973 ± 40 µg/g, fw)and hydrolysable tannins (14873 ± 110 µg/g). The highest amounts of phenolic acids (569 ± 20 µg/… Show more
“…The extraction, identification and quantification of phenolic compounds from flowers of Castanea sativa, Filipendula ulmaria, Rosa micrantha [24] and Cytisus multiflorus [25], and fresh leaves of Cistus ladanifer [26] were previously described by the authors using a high-performance liquid chromatography-diode array detector/electrospray source mass spectrometer. This work was focused on four different phenolic compounds that seemed more promising against Candida species: one phenolic acid (gallic acid) and three flavonoids (catechin, luteolin and quercetin).…”
Aim: To evaluate the antifungal effect of gallic acid, catechin, luteolin and quercetin, phenolic compounds identified from flowers of North Eastern Portugal, against Candida planktonic and biofilm cells. Materials & methods: The MICs were determined in Candida planktonic cells and the effect of phenolic compounds on Candida biofilms was assessed through quantification of colony-forming units. Results: MIC values demonstrated that gallic acid presented the highest effect against all Candida species. Catechin showed a similar effect against Candida albicans American Type Culture Collection (ATCC) 90028 cells. In addition, gallic acid and quercetin had demonstrated only a minimal effect against Candida species biofilms. Conclusion: Gallic acid affected the growth of the different planktonic Candida species in all concentrations used; still, catechin showed a similar effect against C. albicans ATCC 90028 and Candida glabrata ATCC 2001 cells. In addition, only gallic acid and quercetin demonstrated a slight effect against all Candida species biofilms.
“…The extraction, identification and quantification of phenolic compounds from flowers of Castanea sativa, Filipendula ulmaria, Rosa micrantha [24] and Cytisus multiflorus [25], and fresh leaves of Cistus ladanifer [26] were previously described by the authors using a high-performance liquid chromatography-diode array detector/electrospray source mass spectrometer. This work was focused on four different phenolic compounds that seemed more promising against Candida species: one phenolic acid (gallic acid) and three flavonoids (catechin, luteolin and quercetin).…”
Aim: To evaluate the antifungal effect of gallic acid, catechin, luteolin and quercetin, phenolic compounds identified from flowers of North Eastern Portugal, against Candida planktonic and biofilm cells. Materials & methods: The MICs were determined in Candida planktonic cells and the effect of phenolic compounds on Candida biofilms was assessed through quantification of colony-forming units. Results: MIC values demonstrated that gallic acid presented the highest effect against all Candida species. Catechin showed a similar effect against Candida albicans American Type Culture Collection (ATCC) 90028 cells. In addition, gallic acid and quercetin had demonstrated only a minimal effect against Candida species biofilms. Conclusion: Gallic acid affected the growth of the different planktonic Candida species in all concentrations used; still, catechin showed a similar effect against C. albicans ATCC 90028 and Candida glabrata ATCC 2001 cells. In addition, only gallic acid and quercetin demonstrated a slight effect against all Candida species biofilms.
“…Moreover, the identification of several additional glycosides of quercetin and isorhamnetin is highlighted with two quercetin glycosides derivatives: quercetin-manonylhexoxide (peak 7, m/z 549/551) and quercetin-acetyl hexoside (peak 8, m/z 505), and four compounds that involved isorhamnetin glycosides and derivatives, namely isorhamnetin-O-rhamnose-glucoside (peak 9, m/z 625) isorhamnetin-3-O-glucoside (peak 10, m/z 477/479), isorhamnetin-manonyl hexoside (peak 11, m/z 563/565), and isorhamnetin-acetyl hexoside (peak 12, m/z 519) (Schieber et al 2002, Barros et al 2013 ( Table 3). Other phenolic compounds identified in the pear extracts are phenolic acids, namely quinic acid (peak 1, m/z 191) and caffeoylquinic acid (peak 2, m/z 353); and one procyanidin dimer (peak 3, m/z 577) (Long-Ze and Harnyl, 2007).…”
“…These results will need to be further confirmed with other specific assays for DNA damage. In fact, such a result is surprising considering the fact that the flowers from this plant are known for their rich antioxidants content (Barros et al, 2011;Barros et al, 2013). Nevertheless, those antioxidants might not be enough to avoid DNA damage, as least under the tested in vitro conditions.…”
Section: Effect Of Extract 2 On the Expression Levels Of Proteins Invmentioning
confidence: 98%
“…Filipendula ulmaria (L.) Maxim, commonly known as meadowsweet, is an interesting example of useful plants reported by several ethnobotanical surveys and can be found not only in the Iberian Peninsula, but also in other regions of most of Europe and Western Asia, such as Poland and Russia (Barros et al, 2013). Homemade remedies prepared from this species have been described since the late 16 th and 17 th centuries.…”
Section: Introductionmentioning
confidence: 99%
“…Regarding the phenolic compounds, phenolic acids (caffeic acid derivatives and gallic acid), flavonols (glycosides of quercetin and isorhamnetin) and ellagitannins (digalloylhexahydroxydiphenol-glucose and trigalloyl digalloyl-hexahydroxydiphenol-glucose) have been described (Barros et al, 2013).…”
Filipendula ulmaria (L.) Maxim (meadowsweet) is a popular medicinal species that can be found throughout most Europe and Asia. The plant is known for its rich antioxidants content, having compounds such as flavonoids and ascorbic acid. Therefore, the aim of
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