Phenol Biodegradation by Two Xenobiotics-Tolerant Bacteria Immobilized in Polyethylene Oxide Cryogels

Biofilms were formed on poly(ethylene oxide) (PEO) cryogels by using bacteria cultured from xenobiotics polluted environments and their phenol biodegrading capability was studied. PEO cryogels were synthesized via UV irradiation cross linking of moderately frozen aqueous system. Two xenobiotics tolerant bacterial isolates KCM R5 and KCM RG5 were used to construct the biofilms on the cryogels. Obtained PEO-biofilms were assessed for their ability to remove phenol at concentrations 300, 400, 600 and 1000 mg L-1 for 28 days. The biofilm PEO-KCM RG5 removed phenol up to 600mg L-1/24 h, whereas the biofilm PEO-KCM R5 was able to degrade up to 1000 mg L-1/24 h. The high content of free-water in the cryogels allowed reproduction of the used bacteria. The high content of free-water in the cryogels allowed reproduction of the used bacteria. Short initial adaptation of the PEO-bio�lms with 100 mg L-1/24 h phenol was crucial for protecting the bacterial cells from dead. The obtained results showed that the liquid debit through the bio�lms on the 28th day of the experiments was lower than at the beginning. The cryogels demonstrated non-toxicity, high biocompatibility with bacteria and excellent mechanical characteristics. After aggressive phenol treatment the PEO-biofilms remained compact, porous and elastic. The investigated new biological materials demonstrate potential for application in the industrial wastewater treatment technologies

Stabilized micelles as delivery vehicles for paclitaxel

Paclitaxel is an antineoplastic drug used against a variety of tumors, but its low aqueous solubility and active removal caused by P-glycoprotein in the intestinal cells hinder its oral administration. In our study, new type of stabilized Pluronic micelles were developed and evaluated as carriers for paclitaxel delivery via oral or intravenous route. The pre-stabilized micelles were loaded with paclitaxel by simple solvent/evaporation technique achieving high encapsulation efficiency of approximately 70%. Gastrointestinal transit of the developed micelles was evaluated by oral administration of rhodamine-labeled micelles in rats. Our results showed prolonged gastrointestinal residence of the marker encapsulated into micelles, compared to a solution containing free marker. Further, the oral administration of micelles in mice showed high area under curve of micellar paclitaxel (similar to the area of i.v. Taxol®), longer mean residence time (9-times longer than i.v. Taxol®) and high distribution volume (2-fold higher than i.v. Taxol®) indicating an efficient oral absorption of paclitaxel delivered by micelles. Intravenous administration of micelles also showed a significant improvement of pharmacokinetic parameters of micellar paclitaxel vs. Taxol®, in particular higher area under curve (1.2-fold), 5-times longer mean residence time and lower clearance, indicating longer systemic circulation of the micelles

Thermoresponsive Polyoxazolines as Vectors for Transfection of Nucleic Acids

Poly(2-oxazoline)s (POx) are an attractive platform for the development of non-viral gene delivery systems. The combination of POx moieties, exhibiting excellent biocompatibility, with DNA-binding polyethyleneimine (PEI) moieties into a single copolymer chain is a promising approach to balance toxicity and transfection efficiency. The versatility of POx in terms of type of substituent, copolymer composition, degree of polymerization, degree of hydrolysis, and chain architecture, as well as the introduction of stimuli-responsive properties, provides opportunities to finely tune the copolymer characteristics and physicochemical properties of the polyplexes to increase the biological performance. An overview of the current state of research in the POx–PEI-based gene delivery systems focusing particularly on thermosensitive POx is presented in this paper

Partially hydrolyzed poly(n-propyl-2-oxazoline) : synthesis, aqueous solution properties, and preparation of gene delivery systems

Random copolymers of n-propyl-2-oxazoline and ethylenimine (PPrOx-PEI) were prepared by partial acidic hydrolysis of poly(n-propyl-2-oxazoline) (PPrOx). Dynamic and electrophoretic light scattering and diffusion ordered NMR spectroscopy were utilized to investigate aqueous solution properties of the copolymers. Above a specific cloud point temperature, well-defined nanoparticles were formed. The latter consisted of a core composed predominantly of PPrOx and a thin positively charged shell from PEI moieties that mediated formation of polyplexes with DNA. The polyplexes were prepared at 65 degrees C at varying N/P (amine-to-phosphate groups) ratios. They underwent structural changes upon temperature variations 65-25-37 degrees C depending on N/P. At N/P = 2 resulting in large swollen microgel particles were overcome by coating of the polyplex particles with a cross-linked polymeric shell. The shell retained the colloidal stability and preserved the physicochemical parameters of the initial polyplex particles while it reduced the high surface potential values. Progressive loss of cytotoxicity upon complexation with DNA and coating of polyplex particles was displayed