Search Results (3)

The highly inert surface of polyester micro- and nano- drug carriers is a challenging substrate for further modification. The presence of surface moieties suitable for macromolecule coupling is crucial in the development of targeted drug delivery systems. Among available methods of surface activation, those based on adsorption of charged macromolecules may be carried out in mild conditions. In this work, alendronate-loaded microcores of three polyesters: poly-ε-caprolactone (PCL), poly(l-lactide-co-ε-caprolactone) (PLA-co-PCL) and poly(lactic-co-glycolic acid) (PLGA) were coated with three polyelectrolyte shells composed of chitosan/heparin (CHIT/HEP), polyallylamine/heparin (PAH/HEP), and polyethyleneimine/heparin (PEI/HEP) via the layer-by-layer method. Subsequently, the feasibility of model protein immobilization on obtained shells was assessed. Electrokinetic potential measurements confirmed the possibility of deposition of all investigated coating variants, and a positive correlation between initial core ζ potential and intensity of charge alterations after deposition of subsequent layers was identified. PEI/HEP assembly was stable in physiological-like conditions, while PAH/HEP multilayers disassembled in presence of phosphate ions, and CHIT/HEP shell showed limited stability in pH 7.4. Fluorescence assays of fluorescein tagged lysozyme surface coupled via ethylcarbodiimide hydrochloride/N-Hydroxysuccinimide (EDC/NHS) click reaction with all shell variants indicated satisfying reaction efficiency. Poly-ε-caprolactone cores coated with CHIT/HEP tetralayer were selected as suitable for model IgG surface immobilization. Antibodies immobilized on the shell surface exhibited a moderate degree of affinity to fluorescent IgG binding protein. Full article

Magnetic microparticles (MMPs) have been notably used as platforms in biosensing. Due to their magnetic behavior, they simplify purification and separation procedures, reducing time of analysis. They also allow sample preconcentration, minimizing matrix effects, which is of key relevance for applications using real samples. Even though there is a great number of commercially available MMPs, their performance is not always reliable. In this work, we propose the synthesis of novel polymeric MMPs for their use as electrochemical immunosensing platforms. Initially, magnetic nanoparticles of a diameter of 12 ± 2 nm and a saturation magnetization of 70 emu/g were synthesized and characterized. Then, they were encapsulated in a polymeric matrix of poly (lactic-co-glycolic) acid (PLGA), generating MMPs with a diameter of 90 ± 18 nm. Later, MMPs were functionalized with polyethyleneimine (PEI) as an intermediate step for the immobilization of affinity proteins or antibodies, necessary in electrochemical immunosensing. This would allow the obtaining of MMPs comparable to the commercially available ones but possessing higher saturation magnetization. The use of such MMPs could facilitate the detection of analytes of interest in diagnostics, among other applications. Full article

In recent years, gene therapy has become a promising technology to enhance endothelialization of artificial vascular grafts. The ideal gene therapy requires a gene carrier with low cytotoxicity and high transfection efficiency. In this paper, we prepared a biodegradable cationic copolymer poly(d,l-lactide-co-glycolide)-graft-PEI (PLGA-g-PEI), grafted Cys-Ala-Gly-Trp (CAGW) peptide onto this copolymer via the thiol-ene Click-reaction, and then prepared micelles by a self-assembly method. pEGFP-ZNF580 plasmids (pDNA) were condensed by these micelles via electrostatic interaction to form gene complexes. The CAGW peptide enables these gene complexes with special recognition for endothelial cells, which could enhance their transfection. As a gene carrier system, the PLGA-g-PEI-g-CAGW/pDNA gene complexes were evaluated and the results showed that they had suitable diameter and zeta potential for cellular uptake, and exhibited low cytotoxicity and high transfection efficiency for EA.hy926 cells. Full article