Apostolis Angelis

Dr. Apostolis Angelis

Pharmacy, National and Kapodistrian University of Athens, Athens, Attikí, Greece
orcid

Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

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

Representative Publications

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1 May 2020 in Journal of Ethnopharmacology
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Journal Article
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Vasiliki K. PachiVasiliki K. Pachi
Vasiliki K. Pachi
EMEleni V. Mikropoulou
Eleni V. Mikropoulou
PGPetros Gkiouvetidis
Petros Gkiouvetidis
KSKonstantinos Siafakas
Konstantinos Siafakas
AAAikaterini Argyropoulou
Aikaterini Argyropoulou
MHMaria Halabalaki
Maria Halabalaki

20 July 2017 in International Journal of Molecular Medicine
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Journal Article
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PKParaskevi Kouka
Paraskevi Kouka
APAlexandros Priftis
Alexandros Priftis
DSDimitrios Stagos
Dimitrios Stagos
AAApostolis Angelis
Apostolis Angelis
PSPanagiotis Stathopoulos
Panagiotis Stathopoulos
Dimitrios KouretasDimitrios Kouretas
Dimitrios Kouretas
Olive oil (OO) constitutes the basis of the Mediterranean diet, and it seems that its biophenols, such as hydroxytyrosol (HT) may scavenge free radicals, attracting distinct attention due to their beneficial effects in many pathological conditions, such as cancer. To the best of our knowedge, this is the first study in which the functional properties of an OO total polyphenolic fraction (TPF) and pure HT were examined in order to determine their antioxidant effects at a cellular level in endothelial cells and myoblasts. The test compounds were isolated using a green gradient‑elution centrifugal partition chromatography‑based method that allows the isolation of large volumes of OO in a continuous extraction procedure and with extremely low solvent consumption. For the isolation of HT, a combination of two chromatographic techniques was used, which is effective for the recovery of pure compounds from complex natural extracts. Moreover, TPF and HT exhibited potent free radical scavenging activity in vitro. The cells were treated with non‑cytotoxic concentrations and their redox status [in terms of glutathione (GSH) and reactive oxygen species (ROS) levels] was assessed. TPF extract was less cytotoxic than HT, and the observed differences between the two cell lines used suggest a tissue‑specific activity. Finally, flow cytometric analysis revealed that both TPF and HT improved the redox status by increasing the levels of GSH, one of the most important antioxidant molecules, in both endothelial cells and myoblasts, while the ROS levels were not significantly affected.

2 March 2012 in PLOS ONE
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CSChrysoula Spanou
Chrysoula Spanou
AVAristidis S Veskoukis
Aristidis S Veskoukis
TKThalia Kerasioti
Thalia Kerasioti
MKMaria Kontou
Maria Kontou
AAApostolis Angelis
Apostolis Angelis
Dimitrios KouretasDimitrios Kouretas
Dimitrios Kouretas
Legumes and the polyphenolic compounds present in them have gained a lot of interest due to their beneficial health implications. Dietary polyphenolic compounds, especially flavonoids, exert antioxidant properties and are potent inhibitors of xanthine oxidase (XO) activity. XO is the main contributor of free radicals during exercise but it is also involved in pathogenesis of several diseases such as vascular disorders, cancer and gout. In order to discover new natural, dietary XO inhibitors, some polyphenolic fractions and pure compounds isolated from two legume plant extracts were tested for their effects on XO activity. The fractions isolated from both Vicia faba and Lotus edulis plant extracts were potent inhibitors of XO with IC50 values range from 40–135 µg/mL and 55–260 µg/mL, respectively. All the pure polyphenolic compounds inhibited XO and their Ki values ranged from 13–767 µM. Ten of the compounds followed the non competitive inhibitory model whereas one of them was a competitive inhibitor. These findings indicate that flavonoid isolates from legume plant extracts are novel, natural XO inhibitors. Their mode of action is under investigation in order to examine their potential in drug design for diseases related to overwhelming XO action.

1 March 2017 in Journal of Chromatography A
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Journal Article
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AAApostolis Angelis
Apostolis Angelis
MHMahmoud Hamzaoui
Mahmoud Hamzaoui
NANektarios Aligiannis
Nektarios Aligiannis
TNTheodora Nikou
Theodora Nikou
DMDimitris Michailidis
Dimitris Michailidis
LSLeandros Skaltsounis
Leandros Skaltsounis

21 November 2016 in Molecules
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AAApostolis Angelis
Apostolis Angelis
JHJane Hubert
Jane Hubert
NANektarios Aligiannis
Nektarios Aligiannis
RMROZALIA MICHALEA
ROZALIA MICHALEA
AAAmin Abedini
Amin Abedini
JRJean-Hugues Renault
Jean-Hugues Renault
Common spruce (Picea abies L.) is a fast-growing coniferous tree, widely used in several countries for the production of sawn wood, timber and pulp. During this industrial exploitation, large quantities of barks are generated as waste materials. The aim of this study was the bio-guided investigation and the effective recovery of methanol-soluble metabolites of common spruce bark for the development of new dermo-cosmetic agents. The active methanol extract was initially fractionated by Centrifugal Partition Chromatography (CPC) using a triphasic solvent system in a step-gradient elution mode. All resulting fractions were evaluated for their antibacterial activity, antioxidant activity and their capability to inhibit tyrosinase, elastase and collagenase activity. In parallel, the chemical composition of each fraction was established by combining a 13C-NMR dereplication approach and 2D-NMR analyses. As a result, fourteen secondary metabolites corresponding to stilbene, flavonoid and phenolic acid derivatives were directly identified in the CPC fractions. A high amount (0.93 g) of E-astringin was recovered from 3 g of crude extract in a single 125 min run. E-Astringin significantly induced the tyrosinase activity while E-piceid, taxifolin, and taxifolin-3′-O-glucopyranoside exhibited significant anti-tyrosinase activity. The above compounds showed important anti-collagenase and antimicrobial activities, thus providing new perspectives for potential applications as cosmetic ingredients.

28 June 2016 in Planta Medica
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Journal Article
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JHJane Hubert
Jane Hubert
AAApostolis Angelis
Apostolis Angelis
NANektarios Aligiannis
Nektarios Aligiannis
MRMichalea Rosalia
Michalea Rosalia
AAAmin Abedini
Amin Abedini
JRJean-Hugues Renault
Jean-Hugues Renault
Wood residues produced from forestry activities represent an interesting source of biologically active, high value-added secondary metabolites. In this study, 30 extracts from 10 barks of deciduous and coniferous tree species were investigated for their potential dermo-cosmetic use. The extracts were obtained from Fagus sylvatica, Quercus robur, Alnus glutinosa, Prunus avium, Acer pseudoplatanus, Fraxinus excelsior, Populus robusta, Larix decidua, Picea abies, and Populus tremula after three successive solid/liquid extractions of the barks with n-heptane, methanol, and methanol/water. All extracts were evaluated for their radical scavenging capacity, for their elastase, collagenase, and tyrosinase inhibitory activities, as well as for their antibacterial activity against gram-positive Staphylococcus aureus. In parallel, the global metabolite profiles of all extracts were established by 1D and 2D NMR and related to their biological activity. The results showed that the methanol extracts of Q. robur, A. glutinosa, L. decidua, and P. abies barks exhibit particularly high activities on most bioassays, suggesting their promising use as active ingredients in the dermo-cosmetic industry.