Julia Bogusz
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Julia Bogusz has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
- Irena Macias
Department of Pharmaceutical Biology, Faculty of Pharmacy, Medical University of Warsaw, 1 Banacha St., 02-097 Warsaw, Poland
1 shared publication - Joanna Jabłońska
Medical University of Warsaw
1 shared publication - Katarzyna Sykłowska-Baranek
Department of Pharmaceutical Biology, Faculty of Pharmacy, Medical University of Warsaw, 1 Banacha St., 02-097 Warsaw, Poland
1 shared publication - Maciej ObręBski
Microbiota Lab, Department of Pharmaceutical Microbiology and Bioanalysis, Medical University of Warsaw
1 shared publication - Rafał M. Kiełkiewicz
Department of Pharmaceutical Biology, Faculty of Pharmacy, Medical University of Warsaw, 1 Banacha St., 02-097 Warsaw, Poland
1 shared publication - Weronika Skowrońska
Department of Pharmaceutical Biology, Faculty of Pharmacy, Medical University of Warsaw, Banacha 1, 02-097 Warsaw, Poland
1 shared publication
Latest Publications
- Open Access
Antioxidant and Anti-Aging Activity of Helichrysum arenarium (L.) Moench: Comparative Evaluation of Extracts from Shoots, Inflorescences, Plantlets and Callus Tissue
Helichrysum arenarium (L.) Moench is a European native species typically associated with dry, sunny, sandy, and nutrient-poor habitats. In European herbal practice, preparations from H. arenarium inflorescences are traditionally used for the symptomatic relief of digestive complaints. Polyphenolic constituents, particularly flavonoid and chalcone derivatives, are among the most characteristic compounds detected in the inflorescences. Intensive harvesting and degradation of natural habitats have increased pressure on wild populations. Since H. arenarium is legally protected in many countries, biotechnological approaches for plant biomass production represent a promising alternative. In the present study, shoot and callus cultures were established, and detailed extract profiling was performed using ultra-high-performance liquid chromatography coupled with diode-array detection and electrospray ionization multistage mass spectrometry (UHPLC-DAD-ESI-MS3). Cytotoxic, antioxidant, anti-inflammatory, wound-healing, anti-collagenase, and anti-hyaluronidase activities were also evaluated. In vitro-derived materials were compared with inflorescences and shoots of the maternal plant. The analyzed materials showed pronounced tissue-dependent metabolic differentiation. The highest callus growth rate was observed for the Ha-C-1 line, which also accumulated the highest levels of chlorogenic acid (25.80 ± 3.09 mg/g dry extract) and isochlorogenic acid A (55.83 ± 13.78 mg/g dry extract). Apigenin was detected in the inflorescence extract, reaching 3.55 ± 1.42 mg/g dry extract. The extracts did not markedly affect HaCaT viability at 15.63–500 µg/mL, while the strongest bioactivities were observed for inflorescence and maternal plant extracts.
Open AccessAntioxidant and Anti-Aging Activity of Helichrysum arenarium (L.) Moench: Comparative Evaluation of Extracts from Shoots, Inflorescences, Plantlets and Callus Tissue
Helichrysum arenarium (L.) Moench is a European native species typically associated with dry, sunny, sandy, and nutrient-poor habitats. In European herbal practice, preparations from H. arenarium inflorescences are traditionally used for the symptomatic relief of digestive complaints. Polyphenolic constituents, particularly flavonoid and chalcone derivatives, are among the most characteristic compounds detected in the inflorescences. Intensive harvesting and degradation of natural habitats have increased pressure on wild populations. Since H. arenarium is legally protected in many countries, biotechnological approaches for plant biomass production represent a promising alternative. In the present study, shoot and callus cultures were established, and detailed extract profiling was performed using ultra-high-performance liquid chromatography coupled with diode-array detection and electrospray ionization multistage mass spectrometry (UHPLC-DAD-ESI-MS3). Cytotoxic, antioxidant, anti-inflammatory, wound-healing, anti-collagenase, and anti-hyaluronidase activities were also evaluated. In vitro-derived materials were compared with inflorescences and shoots of the maternal plant. The analyzed materials showed pronounced tissue-dependent metabolic differentiation. The highest callus growth rate was observed for the Ha-C-1 line, which also accumulated the highest levels of chlorogenic acid (25.80 ± 3.09 mg/g dry extract) and isochlorogenic acid A (55.83 ± 13.78 mg/g dry extract). Apigenin was detected in the inflorescence extract, reaching 3.55 ± 1.42 mg/g dry extract. The extracts did not markedly affect HaCaT viability at 15.63–500 µg/mL, while the strongest bioactivities were observed for inflorescence and maternal plant extracts.