Isabel Borrás-Linares

Dr. Isabel Borrás-Linares

Research and Development of Functional Food Centre (CIDAF), Health Science Technological Park Avda. del Conocimiento s/n, BioRegion Building, 18016 Granada, Spain
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Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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Isabel Borrás-LinaresIsabel Borrás-Linares
Isabel Borrás-Linares
Zorica S. StojanovićZorica S. Stojanović
Zorica S. Stojanović
RQRosa Quirantes-Piné
Rosa Quirantes-Piné
David Arraez-RomanDavid Arraez-Roman
David Arraez-Roman
Jaroslava Švarc-GajićJaroslava Švarc-Gajić
Jaroslava Švarc-Gajić
Antonio Segura-CarreteroAntonio Segura-Carretero
Antonio Segura-Carretero
In an extensive search for bioactive compounds from plant sources, the composition of different extracts of rosemary leaves collected from different geographical zones of Serbia was studied. The qualitative and quantitative characterization of 20 rosemary (Rosmarinus officinalis) samples, obtained by microwave-assisted extraction (MAE), was determined by high performance liquid chromatography coupled to electrospray quadrupole-time of flight mass spectrometry (HPLC–ESI-QTOF-MS). The high mass accuracy and true isotopic pattern in both MS and MS/MS spectra provided by the QTOF-MS analyzer enabled the characterization of a wide range of phenolic compounds in the extracts, including flavonoids, phenolic diterpenes and abietan-type triterpenoids, among others. According to the data compiled, rosemary samples from Sokobanja presented the highest levels in flavonoids and other compounds such as carnosol, rosmaridiphenol, rosmadial, rosmarinic acid, and carnosic acid. On the other hand, higher contents in triterpenes were found in the extracts of rosemary from Gložan (Vojvodina).

1 July 2018 in Journal of Pharmaceutical and Biomedical Analysis
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SPSandra Pimentel-Moral
Sandra Pimentel-Moral
Isabel Borrás-LinaresIsabel Borrás-Linares
Isabel Borrás-Linares
JSJesus Lozano Sanchez
Jesus Lozano Sanchez
David Arraez-RomanDavid Arraez-Roman
David Arraez-Roman
AMAntonio Martinez-Ferez
Antonio Martinez-Ferez
Antonio Segura-CarreteroAntonio Segura-Carretero
Antonio Segura-Carretero

1 March 2018 in Food Research International
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JFJorge G. Figueroa
Jorge G. Figueroa
Isabel Borrás-LinaresIsabel Borrás-Linares
Isabel Borrás-Linares
JSJesus Lozano Sanchez
Jesus Lozano Sanchez
Antonio Segura-CarreteroAntonio Segura-Carretero
Antonio Segura-Carretero


27 August 2019 in Molecules
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IPInés Cea Pavez
Inés Cea Pavez
JSJesus Lozano Sanchez
Jesus Lozano Sanchez
Isabel Borrás-LinaresIsabel Borrás-Linares
Isabel Borrás-Linares
HNHugo Nuñez
Hugo Nuñez
PRPaz Robert
Paz Robert
Antonio Segura-CarreteroAntonio Segura-Carretero
Antonio Segura-Carretero
The olive oil industry produces large volumes of wastes, which are also potential sources of bioactive compounds by developing healthy and/or functional foods. Extraction of phenolic compounds from the residues of the olive oil is mainly carried out with solvents. However, there is currently a growing public awareness about the use of organic solvents in food processing, which has pointed out the need for the application of clean technologies such as pressurized liquid extraction (PLE). Therefore, the aim of this research was to optimize the phenolic compound extraction from olive pomace by PLE, establishing the qualitative and quantitative phenolic profile by HPLC-ESI-TOF/MS. The extraction design to recover phenolics from olive pomace demonstrates a great compositional variability of PLE extracts obtained under different experimental conditions. Indeed, quantitative results have pointed out the selectivity of PLE extraction when this technique is applied to the treatment of olive pomace. PLE-optimized conditions showed higher total phenolic compound content than conventional extraction (1659 mg/kg d.w. and 281.7 mg/kg d.w., respectively). Among these phenolics, the quantity of secoiridoids and flavonoids in the optimized PLE extract was three and four times higher than in conventional extracts. Furthermore, optimal PLE conditions allowed to obtain an enriched hydroxytyrosol extract which was not detected in the conventional one.

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María de la Luz Cádiz-GurreaMaría de la Luz Cádiz-Gurrea
María de la Luz Cádiz-Gurrea
Isabel Borrás-LinaresIsabel Borrás-Linares
Isabel Borrás-Linares
JSJesus Lozano Sanchez
Jesus Lozano Sanchez
Jorge JovenJorge Joven
Jorge Joven
SFSalvador Fernández-Arroyo
Salvador Fernández-Arroyo
Antonio Segura-CarreteroAntonio Segura-Carretero
Antonio Segura-Carretero
Phenolic compounds, which are secondary plant metabolites, are considered an integral part of the human diet. Physiological properties of dietary polyphenols have come to the attention in recent years. Especially, proanthocyanidins (ranging from dimers to decamers) have demonstrated potential interactions with biological systems, such as antiviral, antibacterial, molluscicidal, enzyme-inhibiting, antioxidant, and radical-scavenging properties. Agroindustry produces a considerable amount of phenolic-rich sources, and the ability of polyphenolic structures to interacts with other molecules in living organisms confers their beneficial properties. Cocoa wastes and grape seeds and skin byproducts are a source of several phenolic compounds, particularly mono-, oligo-, and polymeric proanthocyanidins. The aim of this work is to compare the phenolic composition of Theobroma cacao and Vitis vinifera grape seed extracts by high pressure liquid chromatography coupled to a quadrupole time-of-flight mass spectrometer and equipped with an electrospray ionization interface (HPLC-ESI-QTOF-MS) and its phenolic quantitation in order to evaluate the proanthocyanidin profile. The antioxidant capacity was measured by different methods, including electron transfer and hydrogen atom transfer-based mechanisms, and total phenolic and flavan-3-ol contents were carried out by Folin–Ciocalteu and Vanillin assays. In addition, to assess the anti-inflammatory capacity, the expression of MCP-1 in human umbilical vein endothelial cells was measured.