Mariola Samsonowicz

Prof. Mariola Samsonowicz

orcid

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

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

Representative Publications

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4 September 2021 in Nutrients
Verified
Journal Article
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Monika KalinowskaMonika Kalinowska
Monika Kalinowska
EGEwelina Gołębiewska
Ewelina Gołębiewska
Świderski GrzegorzŚwiderski Grzegorz
Świderski Grzegorz
SMSylwia Męczyńska-Wielgosz
Sylwia Męczyńska-Wielgosz
Hanna LewandowskaHanna Lewandowska
Hanna Lewandowska
WLWlodzimierz Lewandowski
Wlodzimierz Lewandowski
Seven derivatives of plant-derived hydroxybenzoic acid (HBA)—including 2,3-dihydroxybenzoic (2,3-DHB, pyrocatechuic), 2,4-dihydroxybenzoic (2,4-DHB, β-resorcylic), 2,5-dihydroxybenzoic (2,5-DHB, gentisic), 2,6-dihydroxybenzoic (2,6-DHB, γ-resorcylic acid), 3,4-dihydroxybenzoic (3,4-DHB, protocatechuic), 3,5-dihydroxybenzoic (3,5-DHB, α-resorcylic), and 3,4,5-trihydroxybenzoic (3,4,5-THB, gallic) acids—were studied for their structural and biological properties. Anti-/pro-oxidant properties were evaluated by using DPPH• (2,2-diphenyl-1-picrylhydrazyl), ABTS•+ (2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid), FRAP (ferric-reducing antioxidant power), CUPRAC (cupric-reducing antioxidant power), and Trolox oxidation assays. Lipophilicity was estimated by means of experimental (HPLC) and theoretical methods. The antimicrobial activity against Escherichia coli (E. coli), Pseudomonas aeruginosa (P. aeruginosa), Staphylococcus aureus (S. aureus), Bacillus subtilis (B. subtilis), Salmonella enteritidis (S. enteritidis), and Candida albicans (C. albicans) was studied. The cytotoxicity of HBAs in MCF-7 and MDA-MB-231 cell lines was estimated. Moreover, the structure of HBAs was studied by means of experimental (FTIR, 1H, and 13C NMR) and quantum chemical DFT methods (the NBO and CHelpG charges, electrostatic potential maps, and electronic parameters based on the energy of HOMO and LUMO orbitals). The aromaticity of HBA was studied based on the calculated geometric and magnetic aromaticity indices (HOMA, Aj, BAC, I6, NICS). The biological activity of hydroxybenzoic acids was discussed in relation to their geometry, the electronic charge distribution in their molecules, their lipophilicity, and their acidity. Principal component analysis (PCA) was used in the statistical analysis of the obtained data and the discussion of the dependency between the structure and activity (SAR: structure–activity relationship) of HBAs. This work provides valuable information on the potential application of hydroxybenzoic acids as bioactive components in dietary supplements, functional foods, or even drugs.

1 April 2019 in Food Chemistry
Verified
Journal Article
Closed access
MSMariola Samsonowicz
Mariola Samsonowicz
EREwa Regulska
Ewa Regulska
DKDanuta Karpowicz
Danuta Karpowicz
Barbara LeśniewskaBarbara Leśniewska
Barbara Leśniewska

1 August 2017 in Chemico-Biological Interactions
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Journal Article
Closed access
MSMariola Samsonowicz
Mariola Samsonowicz
EREwa Regulska
Ewa Regulska
Monika KalinowskaMonika Kalinowska
Monika Kalinowska

1 June 2005 in Journal of Molecular Structure
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Journal Article
Closed access
MSMariola Samsonowicz
Mariola Samsonowicz
THT. Hrynaszkiewicz
T. Hrynaszkiewicz
ŚRŚwisłocka Renata
Świsłocka Renata
ERE. Regulska
E. Regulska
WLWlodzimierz Lewandowski
Wlodzimierz Lewandowski

1 February 2017 in Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
Verified
Journal Article
Closed access
MSMariola Samsonowicz
Mariola Samsonowicz
EREwa Regulska
Ewa Regulska

1 July 2006 in Journal of Molecular Structure
Verified
Journal Article
Closed access
ŚRŚwisłocka Renata
Świsłocka Renata
MSMariola Samsonowicz
Mariola Samsonowicz
ERE. Regulska
E. Regulska
WLWlodzimierz Lewandowski
Wlodzimierz Lewandowski