Chitosan/Poly(2-ethyl-2-oxazoline) films with ciprofloxacin for application in vaginal drug delivery

Chitosan (CHI) and chitosan/poly(2-ethyl-2-oxazoline) (CHI/POZ)-based films were prepared by casting from aqueous solutions of polymer blends with different compositions. Ciprofloxacin was used as a model drug in these formulations. The weight, thickness, folding endurance and transparency of blend films were measured and characterised. All films had a uniform thickness (0.06 ± 0.01 mm) and exhibited sufficient flexibility. The surface pHs of films ranged from 3.76 ± 0.49 to 4.14 ± 0.32, which is within the pH range suitable for vaginal applications. The cumulative release of the drug from the films in experiments in vitro was found to be 42 ± 2% and 56 ± 1% for pure CHI and CHI/POZ (40:60) films, respectively. Drug-free chitosan/poly(2-ethyl-2-oxazoline) films showed weak antimicrobial activity against Escherichia coli. Drug-loaded CHI and CHI/POZ films showed good antimicrobial properties against both Gram-positive Staphylococcus aureus and Gram-negative bacteria Escherichia coli. Mucoadhesive properties of these films with respect to freshly excised sheep vaginal mucosa were evaluated using a tensile method. It was established that all films were mucoadhesive, but an increase in POZ content in the blend resulted in a gradual reduction of their ability to stick to vaginal mucosa. These films could potentially find applications in vaginal drug delivery

Polymer protected gold nanoparticles: synthesis, characterization and application in catalysis

This review discusses the stabilization of gold nanoparticles (AuNPs) by nonionic, anionic, cationic and amphoteric polymers. The protocols used for synthesis of AuNPs in aqueous and organic solvents are described. Size, shape and morphology of AuNPs are characterized by various physicochemical methods. Application aspects of polymer-protected AuNPs in catalysis are outlined

Synthesis of fluorescently-labelled poly(2-ethyl-2-oxazoline)-protected gold nanoparticles

Gold nanoparticles (GNPs) protected by poly(2-ethyl-2-oxazoline) (POZ) of different molecular weights (Mw = 5, 50, 200 and 500 kDa) were synthesised and characterised by dynamic light scattering, nanoparticle tracking analysis, zeta potential measurement and transmission electron microscopy. It was established that the use of POZ with 50 kDa resulted in formation of GNPs with low polydispersity while POZ with greater molecular weights led to formation of more polydisperse GNPs. Fluorescent labelling of these nanoparticles was achieved through their reaction with polyethyleneglycol dithiol (8-12 kDa) as a linker molecule with subsequent reaction with 6-(iodoacetamido) fluorescein. The fluorescent nature of obtained GNPs was confirmed by the appearance of the fluorescence peak at 510 nm that is typical for fluorescein molecules and glowing of the aqueous solution under the UV irradiaton. The fluorescently-labelled GNPs are promising tool in biomedical application to monitor the biological systems using fluorescent microscopy

Application of Interpolymer Complexes of Novel Poly(ampholyteelectrolyte) as Soil Structuring Agents and for Extraction of Radioactive Strontium

Novel linear copolymer exhibiting poly(ampholyte-electrolyte) behavior was involved into complexation reaction with anionic, cationic and nonionic polymers. Interpolymer complexes were prepared by mixing of aqueous solutions of individual polymers with concentration varying from 10-1-10-4 mol⋅L-1. The formed interpolymer complexes showed the soil structuring effect and the ability to extract the radioactive strontium from the polluted topsoil of Semipalatinsk Test Site. The mechanism of soil stabilization or aggregation was explained by the fact that the soil particles bearing negative charges interact with positively charged "loops" of interpolymer complexes resulting in the formation of so called "cobweb" (or protective crust) on the soil surface. The effective capturing of radioactive strontium by interpolymer complexes may be connected with formation of more stable ternary polymer-metal complexes. It was demonstrated that: I) interpolymer complexes are the most effective soil structuring agents than that of individual components; II) the optimal concentration of interpolymer complexes for soil aggregation is 10-2 mol⋅L-1; III) pouring of soil surface by interpolymer complexes is more effective than the splashing; IV) the treatment of the soil by already pre-existing interpolymer complexes is most effective than the successive treatment of the soil by individual components; V) the best soil structuring properties were shown for interpolymer complexes stabilized by H–bonds and intra salt bonds

The use of Lewis acid AlCl3 as a promoter in the Pd-complex catalytic system of the cyclohexene hydroethoxycarbonylation reaction

This paper presents the results of detailed studies of the possibility of using Lewis acid AlCl3 as a promoter of the catalytic three-component system PdCl2(PPh3)2–PPh3–AlCl3 in the hydroethoxycarbonylation reaction of cyclohexene at low carbon monoxide pressures (2.5 MPa). As a result a high catalytic activity of the three-component system was established and the reaction proceeds regioselectively with the formation of ethyl ether of cyclohexanecarboxylic acid. The optimal conditions of the process have been elaborated (molar ratio of the starting reagents [Cyclohexene]:[Ethanol] = 1:1; molar ratio of the components of the catalytic system = = [PdCl2(PPh3)2]:[PPh3]:[AlCl3] = 1:6:9; carbon monoxide pressure PCO = 2.5 MPa; process temperature T = 120 °C and reaction time τ = 5 h) at which the target product yield reaches 80.7 %. To identify the obtained ethyl ester of cyclohexane carboxylic acid gas chromatographic analysis and mass- and IR- spectra were carried out. Based on the data obtained, a possible mechanism of the reaction route of cyclohexene carbonylation with carbon monoxide and ethanol in the presence of the three-component system PdCl2(PPh3)2–PPh3–AlCl3 is proposed and discussed

Protein adsorption on preadsorbed polyampholytic monolayers

The adsorption behaviour of five different globular proteins on pure silicon substrates and on preadsorbed polyampholytic monolayers has been investigated as a function of protein concentration. The prelayers were prepared by adsorption of the ampholytic diblock copolymer poly(methacrylic acid)-block-poly ((dimethylamino)ethyl methacrylate) (PMAA-b-PDMAEMA). This polyampholyte adsorbs in densely packed micelles directly from aqueous solution. Ellipsometry was used to determine the amount of adsorbed polyampholyte and protein. While ATR-IR spectroscopy gives information about the adsorption and desorption behaviour of the preadsorbed polyampholytic layer, the lateral structures of the dried films were investigated by scanning force microscopy (SFM). The amount of protein adsorbed was found to be strongly influenced by the preadsorbed polyampholyte compared to the adsorption on the pure silicon substrates. No displacement of the polyampholyte by the proteins was detected. In most cases the protein adsorption was reduced by the preadsorbed polyampholytic layer. The observed trends are explained by the change in electrostatic and hydrophilic characteristics of the substrates. Furthermore, the entropy of adsorption has to be taken into account.Peer reviewe

Nonthrombogenic, Biodegradable Elastomeric Polyurethanes with Variable Sulfobetaine Content

For applications where degradable polymers are likely to have extended blood contact, it is often important for these materials to exhibit high levels of thromboresistance. This can be achieved with surface modification approaches, but such modifications may be transient with degradation. Alternatively, polymer design can be altered such that the bulk polymer is thromboresistant and this is maintained with degradation. Toward this end a series of biodegradable, elastic polyurethanes (PESBUUs) containing different zwitterionic sulfobetaine (SB) content were synthesized from a polycaprolactone-diol (PCL-diol):SB-diol mixture (100:0, 75:25, 50:50, 25:75 and 0:100) reacted with diisocyanatobutane and chain extended with putrescine. The chemical structure, tensile mechanical properties, thermal properties, hydrophilicity, biodegradability, fibrinogen adsorption and thrombogenicity of the resulting polymers was characterized. With increased SB content some weakening in tensile properties occurred in wet conditions and enzymatic degradation also decreased. However, at higher zwitterionic molar ratios (50% and 75%) wet tensile strength exceeded 15 MPa and breaking strain was >500%. Markedly reduced thrombotic deposition was observed both before and after substantial degradation for both of these PESBUUs and they could be processed by electrospinning into a vascular conduit format with appropriate compliance properties. The mechanical and degradation properties as well as the acute in vitro thrombogenicity assessment suggest that these tunable polyurethanes could provide options appropriate for use in blood contacting applications where a degradable, elastomeric component with enduring thromboresistance is desired