Quantification of Flavonoids, Naphthopyranones and Xanthones in Eriocaulaceae Species by LC-PDA

Abstract

The linearity, stability, accuracy and inter-day precisions of the assay method were evaluated in methanolic aerial-part extracts of Paepalanthus giganteus and Syngontnhus nitens from the Eriocaulaceae family. Their small capitulae hinder morphological analysis, and thus complicate taxonomic studies of these species, which present anti-ulcer, antimutagenic and antioxidant activities. Taxonomic studies of these plants revealed that the Paepalanthus genus presents flavonols and naphthopyranones while the Syngontnhus genus has flavone and xanthone as majority compounds. The prepared samples were analyzed quantitatively by High Performance Liquid Chromatography with PDA detection for the presence of quercetin, luteolin, 3,6-dimethoxy-1,5,7-tri-hydroxyxanthone and paepalantine. The substances were recovered from these samples at rates from 98.01% to 99.99%. The coefficient of variation in the quantitative analysis of the sample compounds was under 5%. The linearity of the method was determined by linear regression. The analysis of the samples spiked with known amounts of analyte demonstrated that the response was proportional to the concentrations of the samples with respective determination coefficients of r 2 = 0.9999 (luteolin and 3,6-dimethoxy-1,5,7-tri-hydroxyxanthone) and r 2 = 0.9998 (quercetin and paepalantine) for the linear range of the analytical calibration curves of the samples. The detection limits were 0.07 µg·mL -1 for quercetin and luteolin, 0.06 µg·mL -1 for 3,6-dimethoxy-1,5,7-tri-hydroxyxanthone and 0.10 µg·mL -1 for paepalantine. The quantification limits were 0.23 µg·mL -1 for quercetin and luteolin, 0.20 µg·mL -1 for 3,6-dimethoxy-1,5,7-tri-hydroxyxanthone and 0.33 µg·mL -1 for paepalantine by LC. The method was considered sen-sitive for quantification of the quercetin, luteolin, 3,6-dimethoxy-1,5,7-tri-hydroxyxanthone and paepalantine in plant samples.

Characterization of Flavonoids and Naphthopyranones in Methanol Extracts of Paepalanthus chiquitensis Herzog by HPLC-ESI-IT-MSn and Their Mutagenic Activity

“…It can be seen therefore that most of the compounds in the methanolic extracts of capitulae and scapes of P. chiquitensis were basically flavonoids (quercetin derivatives) and naphthopyranones (paepalantine derivatives), illustrated in Figure 3 . The contents of quercetin and paepalantine derivatives were determined in µg/100 mg of capitulae extract (335 ± 2.4 and 455 ± 3.3) and scapes (391 ± 1.1 and 431 ± 1.4) respectively [ 31 ].…”

Review on Compounds Isolated from Eriocaulaceae Family and Evaluation of Biological Activities by Machine Learning

“…Flavonoids were quantified in methanolic aerial part extracts of Paepalanthus giganteus and Syngonanthus nitens by LC-PDA with co-injection experiments. Quercetin ( 3 ) was identified in capitula and scapes of P. giganteus and luteolin ( 12 ) in capitula and scapes of S. nitens [ 33 ].…”

“…Paepalantine was found in capitula and scape of Paepalanthus giganteus [ 33 ] and also in P. speciosus and P. microphyllus [ 22 ]. Additionally, Vilegas et al isolated glycoside paepalantine-9- O -β-D-glucopyranoside ( 132 ) and paepalantine-9- O -β-D-allopyranosyl(1→6)glucopyranoside ( 133 ) for the first time in 1998 in ethanolic extract from capitula of P. bromelioides [ 74 ].…”

“…None of the isolated compounds showed mutagenicity against the Salmonella typhimurium TA100, TA98, TA97a, and TA102 strains but all of them showed antimutagenic potential [ 63 ]. Xanthone 199 , 1,5,7-trihydroxy-3,6-dimethoxyxanthone, was identified in methanol extract of S. nitens capitula by performing co-injection experiments in HPLC-PDA [ 33 ].…”