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In vitro enzyme inhibitory properties, antioxidant activities, and phytochemical profile of Potentilla thuringiaca
Scopus
Toplam 432 atıf DOI
The genus Potentilla is interesting for the pharmaceutical field due to its valuable medicinal properties, which have been observed in complementary and alternative medicine. In recent years, studies conducted to estimate the biological activity of several of the Potentilla species have shown a wide spectrum of therapeutic properties. In particular, in the present paper, different extracts obtained from the herb P. thuringiaca were analysed for antioxidant and enzyme inhibitory activities. The UHPLC-DAD-MS3 hyphenated techniques reported herein allow for the identification of phytoconstituents. The analyses showed the presence of flavonoids and ellagitannins as major components. Furthermore, the data demonstrated that the analysed extracts revealed a high total antioxidant capacity in the phosphomolybdenum assay. The free radical scavenging activity of the extracts was evaluated using DPPH and ABTS assays. The reducing power activity of P. thuringiaca was also determined by FRAP and CUPRAC assays, as well as metal chelating activity. In addition, the total extracts and the different fractions of P. thuringiaca revealed potent inhibitory activities against α-amylase and α-glucosidase, AChE, tyrosinase and lipase. Surprisingly, no activity against BChE was shown. P. thuringiaca could be a valuable natural source of antioxidants with interesting inhibitory actions against the key enzymes involved in several human diseases, and could represent a valid starting point for the development of new treatment and management strategies, including its use as a food supplement.
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Atıf Yapan Yayın
Connecting chemical and biological properties to identify new functional materials: A study on Trifolium nigrescens extracts
Scopus
Havuzumuzda Open Access 3 atıf almış
In this study, extracts of the plant species Trifolium nigrescens collected in Turkey were examined. The extracts were obtained by maceration as a conventional method for the extraction of bioactive metabolites, using solvents of different polarity (ethyl acetate, ethanol, 70 % ethanol and water). The antioxidant, enzyme inhibitory and anti-biofilm potential was investigated using in vitro assays, as well as chemical profiles. Ellagic acid was the dominant phenolic acid (4115.87 mg/kg), delphinidin-3-galactoside was the most abundant anthocyanin (24789.25 mg/kg), while hyperoside as flavonoid was identified in the highest concentration (42450.94 mg/kg). Ethanol and 70 % ethanol were the most effective extracts in the radical scavenging and reducing power assays. However, the metal chelating abilities of the ethyl acetate (14.80 mg EDTAE/g) and 70 % ethanol (14.13 mg EDTAE/g) extracts were close to each other. In terms of AChE and tyrosinase inhibition, 70 % ethanol was the most active with these values of 2.34 mg GALAE/g and 48.97 mg KAE/g, respectively. Based on the microbiological aspects, the extracts were able to inhibit the mature biofilm or act on the metabolism of their sessile cells, with the percentage of inhibition reaching almost 60 %. In some cases, such as in the evaluation of anti-biofilm activity against Acinetobacter baumannii, the presence of water in the extract buffer had a positive effect on the inhibition of mature biofilm. Furthermore, molecular docking and 100-ns molecular dynamics simulations were conducted to assess the interaction of selected compounds with both microbial proteins and all five standard enzymes. The correlation analysis identified some polyphenols, including phenolic acids and flavonoids, which were most involved in enhancing or attenuating the antibiofilm effect of the extracts.
Atıf Yapan Makale Bilgileri
Kurumlar (8)
Harran Üniversitesi
Sanliurfa, Turkey
Istituto di Scienze dell'Alimentazione
Avellino, Italy
Marmara Üniversitesi
Istanbul, Turkey
Selçuk Üniversitesi
Selçuklu, Turkey
Università degli Studi di Camerino
Camerino, Italy
Università degli Studi di Napoli Federico II
Naples, Italy
Universitatea de Medicina si Farmacie Iuliu Hatieganu din Cluj-Napoca
Cluj Napoca, Romania
University of Novi Sad
Novi Sad, Serbia