Ewa Oledzka

Prof. Dr. Ewa Oledzka

Faculty of Pharmacy, Department of Analytical Chemistry and Biomaterials, Medical University of Warsaw, Warsaw, Mazowieckie, Poland
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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1 June 2020 in International Journal of Nanomedicine
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Journal Article
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AKAdam Kasiński
Adam Kasiński
Monika Zielińska-PisklakMonika Zielińska-Pisklak
Monika Zielińska-Pisklak
EOEwa Oledzka
Ewa Oledzka
Marcin SobczakMarcin Sobczak
Marcin Sobczak
Among modern drug formulations, stimuli-responsive hydrogels also called “smart hydrogels” deserve a special attention. The basic feature of this system is the ability to change their mechanical properties, swelling ability, hydrophilicity, bioactive molecules permeability, etc., influenced by various stimuli, such as temperature, pH, electromagnetic radiation, magnetic field and biological factors. Therefore, stimuli-responsive matrices can be potentially used in tissue engineering, cell cultures and technology of innovative drug delivery systems (DDSs), releasing the active substances under the control of internal or external stimuli. Moreover, smart hydrogels can be used as injectable DDSs, due to gel–sol transition connected with in situ cross-linking process. Innovative smart hydrogel DDSs can be utilized as matrices for targeted therapy, which enhances the effectiveness of tumor chemotherapy and subsequently limits systemic toxicity. External stimulus sensitivity allows remote control over the drug release profile and gel formation. On the other hand, internal factors provide drg accumulation in tumor tissue and reduce the concentration of active drug form in healthy tissue. In this report, we summarise the basic knowledge and chemical strategies for the synthetic smart hydrogel DDSs applied in antitumor therapy.

28 June 2017 in Chemical Biology & Drug Design
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Journal Article
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Urszula Helena PiotrowskaUrszula Helena Piotrowska
Urszula Helena Piotrowska
Marcin SobczakMarcin Sobczak
Marcin Sobczak
EOEwa Oledzka
Ewa Oledzka

14 November 2013 in Molecules
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Journal Article
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Marcin SobczakMarcin Sobczak
Marcin Sobczak
CDCezary Dębek
Cezary Dębek
EOEwa Oledzka
Ewa Oledzka
RKRyszard Kozłowski
Ryszard Kozłowski
The past decade has seen growing interest in the investigation of peptides with antimicrobial activity (AMPs). One approach utilized in infection control is incorporation of antimicrobial agents conjugated with the polymers. This review presents the recent developments on polymeric AMP carriers and their potential applications in the biomedical and pharmaceutical fields.

1 June 2014 in Materials Science and Engineering: C
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Journal Article
Closed access
Joanna KolmasJoanna Kolmas
Joanna Kolmas
EOEwa Oledzka
Ewa Oledzka
Marcin SobczakMarcin Sobczak
Marcin Sobczak
GNGrzegorz Nałęcz-Jawecki
Grzegorz Nałęcz-Jawecki

Verified
Journal Article
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MBMaria Bialik
Maria Bialik
MKMarzena Kuras
Marzena Kuras
Marcin SobczakMarcin Sobczak
Marcin Sobczak
EOEwa Oledzka
Ewa Oledzka
Rectal drug delivery is an effective alternative to oral and parenteral treatments. This route allows for both local and systemic drug therapy. Traditional rectal dosage formulations have historically been used for localised treatments, including laxatives, hemorrhoid therapy and antipyretics. However, this form of drug dosage often feels alien and uncomfortable to a patient, encouraging refusal. The limitations of conventional solid suppositories can be overcome by creating a thermosensitive liquid suppository. Unfortunately, there are currently only a few studies describing their use in therapy. However, recent trends indicate an increase in the development of this modern therapeutic system. This review introduces a novel rectal drug delivery system with the goal of summarising recent developments in thermosensitive liquid suppositories for analgesic, anticancer, antiemetic, antihypertensive, psychiatric, antiallergic, anaesthetic, antimalarial drugs and insulin. The report also presents the impact of various types of components and their concentration on the properties of this rectal dosage form. Further research into such formulations is certainly needed in order to meet the high demand for modern, efficient rectal gelling systems. Continued research and development in this field would undoubtedly further reveal the hidden potential of rectal drug delivery systems.

9 February 2015 in Molecules
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Journal Article
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KŻKarolina Żółtowska
Karolina Żółtowska
Marcin SobczakMarcin Sobczak
Marcin Sobczak
EOEwa Oledzka
Ewa Oledzka
Polycaprolactone (PCL) is a biodegradable synthetic polymer that is currently widely used in many pharmaceutical and medical applications. In this paper we describe the coordination ring-opening polymerization of ε-caprolactone in the presence of two newly synthesized catalytic systems: diethylzinc/gallic acid and diethylzinc/propyl gallate. The chemical structures of the obtained PCLs were characterized by 1H- or 13C-NMR, FTIR spectroscopy and MALDI TOF mass spectrometry. The average molecular weight of the resulting polyesters was analysed by gel permeation chromatography and a viscosity method. The effects of temperature, reaction time and type of catalytic system on the polymerization process were examined. Linear PCLs with defined average molecular weight were successfully obtained. Importantly, in some cases the presence of macrocyclic products was not observed during the polymerization process. This study provides an effective method for the synthesis of biodegradable polyesters for medical and pharmaceutical applications due to the fact that gallic acid/propyl gallate are commonly used in the pharmaceutical industry.