Publications by authors named "I Grozdova"

Article Synopsis
  • A new method for creating mixed polymer micelles using amorphous poly-D,L-lactide-block-polyethyleneglycol and crystalline amino-terminated poly-L-lactide significantly reduces the preparation time from several days to just 15-20 minutes through ultrasonication.
  • The resulting micelles, approximately 150 nm in size, exhibit low cytotoxicity, high stability in various conditions, and have an average molecular weight of 2.1 × 10 with an aggregation number of 6000.
  • They show potential as drug delivery vehicles, effectively encapsulating the antitumor drug paclitaxel with a lethal concentration similar to that found in commercial formulations.
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Here we report formation of gold nanoparticles (GNPs) in micelles of polytyrosine-PEG copolymers that combine the properties of a reducer and a stabilizer. The size and properties of the GNPs were tailored by the excess chloroaurate over the copolymer. The latter quickly formed non-covalent complexes with HAuCl4 and then slowly reduced it to form GNPs.

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We report here the first evidence for the interaction of poly(ethylene glycol) (PEG) with hyaluronan (HA) in aqueous solutions. PEG-HA complexes ( = 45,000 ± 8000 M) contained about 3.3 ± 0.

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Many natural substances exhibit anti-inflammatory activity and considerable potential in prophylaxis and treatment of allergies. Knowing exact molecular targets, which is required for developing these as medicinal products, is often challenging for multicomponent compositions. In the present study we examined novel polyphenolic substance, a water-soluble fraction of wood lignin (laboratory code BP-Cx-1).

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Positively charged linear chitosan molecules were cross-linked with sulfate-anions to form chitosan nanoparticles which were used as a scaffold of negatively charged cardiolipin/egg lecithin liposomes loaded with doxorubicin (DOX). Thus formed multi-liposomal complexes (MLCs) containing 55 liposomes/chitosan and bearing a slight positive net charge effectively transmitted DOX into the cytoplasm of cells in culture. The efficiency of DOX delivery increased 4-5-fold upon drug incorporation in MLCs.

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