Marcelina Jaworska

Mr. Marcelina Jaworska

orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

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

Representative Publications

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2 August 2020 in Journal of Clinical Medicine
Verified
Journal Article
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KHKatarzyna Hampelska
Katarzyna Hampelska
MJMarcelina Jaworska
Marcelina Jaworska
ZBZuzanna Łucja Babalska
Zuzanna Łucja Babalska
Tomasz M. KarpinskiTomasz M. Karpinski
Tomasz M. Karpinski
Halitosis is a common ailment concerning 15% to 60% of the human population. Halitosis can be divided into extra-oral halitosis (EOH) and intra-oral halitosis (IOH). The IOH is formed by volatile compounds, which are produced mainly by anaerobic bacteria. To these odorous substances belong volatile sulfur compounds (VSCs), aromatic compounds, amines, short-chain fatty or organic acids, alcohols, aliphatic compounds, aldehydes, and ketones. The most important VSCs are hydrogen sulfide, dimethyl sulfide, dimethyl disulfide, and methyl mercaptan. VSCs can be toxic for human cells even at low concentrations. The oral bacteria most related to halitosis are Actinomyces spp., Bacteroides spp., Dialister spp., Eubacterium spp., Fusobacterium spp., Leptotrichia spp., Peptostreptococcus spp., Porphyromonas spp., Prevotella spp., Selenomonas spp., Solobacterium spp., Tannerella forsythia, and Veillonella spp. Most bacteria that cause halitosis are responsible for periodontitis, but they can also affect the development of oral and digestive tract cancers. Malodorous agents responsible for carcinogenesis are hydrogen sulfide and acetaldehyde.

1 April 2019 in European Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
KPKrystian Pyta
Krystian Pyta
AJAnna Janas
Anna Janas
MSMonika Szukowska
Monika Szukowska
PPPaulina Pecyna
Paulina Pecyna
MJMarcelina Jaworska
Marcelina Jaworska
PPPiotr Przybylski
Piotr Przybylski

19 August 2016 in Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
KKKatarzyna Klich
Katarzyna Klich
KPKrystian Pyta
Krystian Pyta
MJMarcelina Jaworska
Marcelina Jaworska
Piotr RuszkowskiPiotr Ruszkowski
Piotr Ruszkowski
LCLech Celewicz
Lech Celewicz
PPPiotr Przybylski
Piotr Przybylski

1 June 2016 in Herba Polonica
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MKMałgorzata Kikowska
Małgorzata Kikowska
JDJolanta Długaszewska
Jolanta Długaszewska
MJMarcelina Jaworska
Marcelina Jaworska
IKIzabela Kędziora
Izabela Kędziora
JBJaromir Budzianowski
Jaromir Budzianowski
BTBarbara Thiem
Barbara Thiem
Summary: Introduction: Due to increasing resistance against antibiotics and antifungal agents, crude plant extracts, fractions, and isolated pure compounds became a new interest as antimicrobial agents. Objectives: The antimicrobial activity of methanolic extracts and fractions of Eryngium planum L., E. campestre L., and E. maritimum L. was evaluated against selected bacteria, yeast and mould, and compared in tested Eryngium species and in their organs. Methods: The antimicrobial activity was studied with use of broth microdilution method. The antibacterial (Staphylococcus aureus, Pseudomonas aeruginosa) and antifungal (Candida albicans, Aspergillus niger) activity of selected extracts and fractions compared with the reference substance was expressed by Minimal Inhibitory Concentration (MIC) and Minimal Bactericidal/Fungicidal Concentration (MBC/MFC). The extract and fraction compounds were identified on the basis of TLC examination. Results: The saponin-phenolic acid fractions of E. maritimum and E. planum and a saponin fraction of E. planum showed the highest activity against S. aureus (MIC = 1–2.5 mg·ml−1). The growth of C. albicans was inhibited by methanolic extract of E. planum cell suspension culture (MIC = 7.8 mg·ml−1). Conclusion: The antimicrobial activity depends on the Eryngium species, tested biomass, and microorganism.

1 June 2016 in European Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
DCDominika Czerwonka
Dominika Czerwonka
JDJoanna Domagalska
Joanna Domagalska
KPKrystian Pyta
Krystian Pyta
MJMarcelina Jaworska
Marcelina Jaworska
PPPaulina Pecyna
Paulina Pecyna
PPPiotr Przybylski
Piotr Przybylski

25 March 2015 in Materials
Verified
Journal Article
Open access
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KJKarolina Jurczyk
Karolina Jurczyk
GAGrzegorz Adamek
Grzegorz Adamek
MJMarcelina Jaworska
Marcelina Jaworska
Jarosław JakubowiczJarosław Jakubowicz
Jarosław Jakubowicz
Mieczyslawa U. JurczykMieczyslawa U. Jurczyk
Mieczyslawa U. Jurczyk
The article presents an investigation on the effectiveness of nanostructured titanium-10 wt% 45S5 Bioglass-1 wt% Ag composite foams as a novel class of antibacterial materials for medical applications. The Ti-based composite foams were prepared by the combination of mechanical alloying and a “space-holder” sintering process. In the first step, the Ti-10 wt% 45S5 Bioglass-1 wt% Ag powder synthesized by mechanical alloying and annealing mixed with 1.0 mm diameter of saccharose crystals was finally compacted in the form of pellets. In the next step, the saccharose crystals were dissolved in water, leaving open spaces surrounded by metallic-bioceramic scaffold. The sintering of the scaffold leads to foam formation. It was found that 1:1 Ti-10 wt% 45S5 Bioglass-1 wt% Ag/sugar ratio leads to porosities of about 70% with pore diameter of about 0.3–1.1 mm. The microstructure, corrosion resistance in Ringer’s solution of the produced foams were investigated. The value of the compression strength for the Ti-10 wt% 45S5 Bioglass-1 wt% Ag foam with 70% porosity was 1.5 MPa and the Young’s modulus was 34 MPa. Silver modified Ti-10 wt% 45S5 Bioglass composites possess excellent antibacterial activities against Staphylococcus aureus. Porous Ti-10 wt% 45S5 Bioglass-1 wt% foam could be a possible candidate for medical implants applications.