
Phd Magdalena Zaremba-Czogalla
assistant professor
Department of Lipids and Liposomes
Dean's representative for studies in English
Faculty of Biotechnology
ul. F. Joliot-Curie 14a
magdalena.zaremba-czogalla@uwr.edu.pl
tel. +48 71 375 62 03, +48 71 375 62 04
Interested
- cancer
- biochemistry molecular biology
- pancreatic cancer
- natural compounds
- naturally derived compounds
- plga
- hemolysis
- terpenoids
- nanoemulsion
- ursolic acid
Scientific discipline
- medical sciences
- biomedical engineering
Latest publications
- Azacarbazole n-3 and n-6 polyunsaturated fatty acids ethyl esters nanoemulsion with enhanced efficacy against Plasmodium falciparum
- The conjugates of indolo[2,3-b]quinoline as anti-pancreatic cancer agents: design, synthesis, molecular docking and biological evaluations
- Evaluation of the in vitro cytotoxic activity of caffeic acid derivatives and liposomal formulation against pancreatic cancer cell lines.
- Novel Liposomal Formulation of Baicalein for the Treatment of Pancreatic Ductal Adenocarcinoma: Design, Characterization, and Evaluation
- Nanoencapsulation of a ruthenium(II) complex with triazolopyrimidine in liposomes as a tool for improving its anticancer activity against melanoma cell lines.
- Evaluation of the In Vitro Cytotoxic Activity of Ursolic Acid PLGA Nanoparticles against Pancreatic Ductal Adenocarcinoma Cell Lines
- Design and Development of a New Type of Hybrid PLGA/Lipid Nanoparticle as an Ursolic Acid Delivery System against Pancreatic Ductal Adenocarcinoma Cells
- Multi- and unilamellar liposomal encapsulation of ciprofloxacin as ways to modify its phototoxicity and photodegradation.
- Dual Role of Vitamin C-Encapsulated Liposomal Berberine in Effective Colon Anticancer Immunotherapy
- The conjugates of 5′-deoxy-5-fluorocytidine and hydroxycinnamic acids – synthesis, anti-pancreatic cancer activity and molecular docking studies
- Efficient one-pot synthesis of novel caffeic acid derivatives as potential antimalarials
- A novel regulatory function of CDKN1A/p21 in TNFα-induced matrix metalloproteinase 9-dependent migration and invasion of triple-negative breast cancer cells