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Polyphenolic QTOF-ESI MS characterization and the antioxidant and cytotoxic activities of Prunus domestica.

dc.creatorNavarro Hoyos, Mirtha
dc.creatorArnáez Serrano, Elizabeth
dc.creatorQuesada Mora, Silvia
dc.creatorAzofeifa Cordero, Gabriela
dc.creatorWilhelm Romero, Krissia
dc.creatorQuirós Fallas, María isabel
dc.creatorAlvarado Corella, Luis Diego
dc.creatorVargas Huertas, Luis Felipe
dc.creatorSánchez Kopper, Andrés
dc.date.accessioned2022-11-10T21:36:22Z
dc.date.available2022-11-10T21:36:22Z
dc.date.issued2021
dc.description.abstractThere is an increased interest in plum research because of their metabolites’ potential bioactivities. In this study, the phenolic profiles of Prunus domestica commercial cultivars (Methley, Pisardii and Satsuma) in Costa Rica were determined by Ultra Performance Liquid Chromatogra phy coupled with High Resolution Mass Spectrometry using a quadrupole-time-of-flight analyzer (UPLC-ESI-QTOF MS) on enriched phenolic extracts obtained through Pressurized Liquid Extraction (PLE) under acidic and neutral extraction conditions. In total, 41 different phenolic compounds were identified in the skin and flesh extracts, comprising 11 flavan-3-ols, 14 flavonoids and 16 hydrox ycinnamic acids and derivatives. Neutral extractions for the skins and flesh from all of the cultivars yielded a larger number of compounds, and were particularly rich in the number of procyanidin trimers and tetramers when compared to the acid extractions. The total phenolic content (TPC) and antioxidant potential using the DPPH and ORAC methods exhibited better results for neutral extracts with Satsuma skins and Methley flesh, which showed the best values (685.0 and 801.6 mg GAE/g extract; IC50 = 4.85 and 4.39 µg/mL; and 12.55 and 12.22 mmol TE/g extract, respectively). A Two-Way ANOVA for cytotoxicity towards AGS gastric adenocarcinoma and SW620 colon adenocar cinoma indicated a significant difference (p < 0.05) for PLE conditions, with better results for neutral extractions, with Satsuma skin delivering the best results (IC50 = 60.7 and 46.7 µg/mL respectively) along with Methley flesh (IC50 = 76.3 and 60.9 µg/mL, respectively). In addition, a significant positive correlation was found between TPC and ORAC (r = 0.929, p < 0.05), as well as a significant negative correlation (p < 0.05) between TPC and cytotoxicity towards AGS and SW620 cell lines (r = −0.776, and −0.751, respectively). A particularly high, significant, negative correlation (p < 0.05) was found between the number of procyanidins and cytotoxicity against the AGS (r = −0.868) and SW620 (r = −0.855) cell lines. Finally, the PCA clearly corroborated that neutral extracts are a more homogenous group exhibiting higher antioxidant and cytotoxic results regardless of the part or cultivar; therefore, our findings suggest that PLE extracts under neutral conditions would be of interest for further studies on their potential health benefits.es_ES
dc.description.procedenceUCR::Vicerrectoría de Docencia::Salud::Facultad de Medicina::Escuela de Medicinaes_ES
dc.description.procedenceUCR::Vicerrectoría de Docencia::Ciencias Básicas::Facultad de Ciencias::Escuela de Químicaes_ES
dc.description.sponsorshipUniversidad de Costa Ricaes_ES
dc.identifier.citationhttps://www.mdpi.com/1420-3049/26/21/6493es_ES
dc.identifier.codproyecto115-B2-657
dc.identifier.codproyectoED-3239
dc.identifier.codproyecto115-B0-047
dc.identifier.codproyectoED-2033
dc.identifier.doi10.3390/molecules26216493
dc.identifier.issn1420-3049
dc.identifier.urihttps://hdl.handle.net/10669/87679
dc.language.isoenges_ES
dc.rightsacceso embargado
dc.sourceMolecules, 26(21).es_ES
dc.subjectPrunus domesticaes_ES
dc.subjectplumes_ES
dc.subjectUPLCes_ES
dc.subjectmass spectrometryes_ES
dc.subjectQTOF ESI-MSes_ES
dc.subjectpolyphenolses_ES
dc.subjectprocyanidinses_ES
dc.subjectflavonoidses_ES
dc.subjectantioxidantes_ES
dc.subjectantitumorales_ES
dc.subjectCHEMICAL ANALYSISes_ES
dc.subjectCOSTA RICAes_ES
dc.subjectMETABOLISMes_ES
dc.titlePolyphenolic QTOF-ESI MS characterization and the antioxidant and cytotoxic activities of Prunus domestica.es_ES
dc.typeartículo originales_ES

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