Radosław Lach

Interaction of curcumin with lipid monolayers and liposomal bilayers

Curcumin shows huge potential as an anticancer and anti-inflammatory agent. However, to achieve a satisfactory bioavailability and stability of this compound, its liposomal form is preferable. Our detailed studies on the curcumin interaction with lipid membranes are aimed to obtain better understanding of the mechanism and eventually to improve the efficiency of curcumin delivery to cells. Egg yolk phosphatidylcholine (EYPC) one-component monolayers and bilayers, as well as mixed systems containing additionally dihexadecyl phosphate (DHP) and cholesterol, were studied. Curcumin binding constant to EYPC liposomes was determined based on two different methods: UV/Vis absorption and fluorescence measurements to be 4.26×10(4)M(-1) and 3.79×10(4)M(-1), respectively. The fluorescence quenching experiment revealed that curcumin locates in the hydrophobic region of EYPC liposomal bilayer. It was shown that curcumin impacts the size and stability of the liposomal carriers significantly. Loaded into the EYPC/DPH/cholesterol liposomal bilayer curcumin stabilizes the system proportionally to its content, while the EYPC/DPH system is destabilized upon drug loading. The three-component lipid composition of the liposome seems to be the most promising system for curcumin delivery. An interaction of free and liposomal curcumin with EYPC and mixed monolayers was also studied using Langmuir balance measurements. Monolayer systems were treated as a simple model of cell membrane. Condensing effect of curcumin on EYPC and EYPC/DHP monolayers and loosening influence on EYPC/DHP/chol ones were observed. It was also demonstrated that curcumin-loaded EYPC liposomes are more stable upon interaction with the model lipid membrane than the unloaded ones.

Chitosan Derivatives as Novel Potential Heparin Reversal Agents

In emergency cases anticoagulant action of heparin needs to be stopped instantaneously, which is usually achieved by intravenous administration of protamine sulfate (PS). However, PS shows many adverse effects. The objective of the present work was to find out if chitosan (Ch) and a cationically modified chitosan, N-(2-hydroxypropyl)-3-trimethylammonium chitosan chloride (HTCC), may be applied for heparin reversal. For chitosan the efficiency of unfractionated heparin (UFH) binding decreases with increasing pH while for cationically modified chitosan heparin binding is efficient even for high pH values. Complexation of UFH and low-molecular-weight heparin (LMWH) by cationically modified chitosan in the aqueous solution at pH = 7.4 was studied. Complexes of the modified chitosan with UFH are smaller and of lower dispersity than those with PS. Cationically modified chitosan was found to bind both UFH and LMWH. The complex formation capability of cationically modified chitosan is comparable to that of PS.

Cationic derivatives of dextran and hydroxypropylcellulose as novel potential heparin antagonists.

Cationic derivatives of dextran (Dex) and hydroxypropylcellulose (HPC) were studied as potential alternatives of protamine sulfate (PS) used in the reversal of anticoagulant activity of heparin. The modification was performed by the attachment of cationic groups to the Dex main chain or by grafting short side chains of a polycation onto HPC. The cationic derivatives of these polysaccharides were found to bind heparin with the efficiency increasing with growing degree of cationic modification. The degree of cationic modification and consequently the ζ potential of the polymers do not have to be high to achieve effective heparin binding. The size of the complexes of cationic Dex with unfractionated heparin (UFH) is a few micrometers. For complexes of cationic HPC and UFH the size is much below 1 μm, both below and above the lower critical solution temperature of HPC. None of the cationic polysaccharides studied caused hemolysis. The concentrations of the polymers inducing the aggregation of human erythrocytes in vitro were determined.

Ceramizable Composites for Fire Resistant Applications

The paper concerns composite materials made of silicone rubber matrix and ceramic fillers used as flame resistant coverings for electrical cables. Under fire, such materials must be able to form, relatively quickly, compact and stiff protecting coating, strong enough to maintain integrity of electrical circuit, even up to melting temperature of metal core. The residue of fired silicone rubber or silica filled elastomer exhibit a form of white powder. There is no evidence of solidification of silica particles, even after heating at 1100°C. However, the addition of some ceramic phases results in reaction with silica matrix (starting at about 900°C) producing a liquid phase, what facilitates particle binding. At lower firing temperatures (600°C) the problem of binding between the product of pyrolysis (silica) and filler is also present, what results in formation of fragile surface shield. The problem can be overcome by the addition of certain inorganic materials to the silicone rubber matrix. The paper discusses their influence on ability of silicone rubber composites, additionally containing glassy phase, wollastonite, mica, aluminium hydroxide, montmorillonite or calcined caoline, to ceramization.

Consolidation of Aluminium Oxynitride Powders Using Hydrolysis of Aluminium Nitride

One of the materials with high potential for application as a refractory material is aluminum oxynitride with spinel-type structure, γ-alon. Alon materials, single-phase or composites, are characterized by good mechanical properties, high thermal shock resistance and a high corrosion and erosion resistance. Another advantage is possibility of usage of SHS method for producing of relatively good sinterable powders of γ-alon, however, are characterized by poor compressibility. This paper describes a method of compaction of SHS-derived γ-alon powder using the hydrolysis reaction of aluminum nitride, which is one of the products of SHS synthesis. The green bodies made from the powder with addition of 10 mas.% of water after two weeks of storage reach a strength level up to 30 MPa and an open porosity of less than 30%. Pressureless sintering of the such compacts allows to achieve 95% of theoretical density at 1700°C in less than one minute.