Phagocytic uptake by mouse peritoneal macrophages of microspheres coated with phosphocholine or polyethylene glycol phosphate-derived perfluoroalkylated surfactants
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Keywords:
Phosphocholine
Protein Adsorption
Phosphocholine
Protein Adsorption
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The enrichment of poly(ethylene glycol) (PEG) segments on the surface of polyethylene/poly(ethylene gly-col) blends (PE/PEG) was investigated using FTIR-ATR and SEM. It has been found that the selective aggregation of the PEG on the surface of PE/PEG blends is mainly affected by the size and the size distribution of the segregated domains of PEG. If the compatibilzer is added to the blends, the size of PEG segregated domains can be reduced and the selective aggregation of PEG on the surface can be enhanced. It was believed that a proper amount of compatibilzer in the blends is useful for controlling the surface selectivity of PEG component.
Morphology
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The use of poly(ethylene glycol) in the purification of plasma and cellular protein is somewhat complicated by the difficulty of removing it from the protein product. The method presented here, quickly and efficiently removes over 95% of the PEG by the simple addition of salts to induce an aqueous two-phase separation with the PEG in the upper phase and greater than 90% of the protein in the lower phase.
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Polyethylene glycol (PEG) grafted poly (γ-benzyl L-glutamate) (PBLG) was synthesized by the substitution reaction of PBLG and PEG having primary amino groups at both ends. PEG-g-PBLG films containing hydroxyl group were also prepared by the substitution reaction of PEG-g-PBLG film and ethanolamine (EA). Adhesion of platelets and activation of plasma proteins on the copolypeptide films were studied. The results showed that platelets are less adhered and activated on the PEG-g-PBLG than on other polypeptides and plasma recalcification time (PRT) on the PEG-g-PBLG was longer than that on other polypeptides. These results were consistent with those of blood clotting time and thrombus formation on the polypeptides. As a results, PEG-g-PBLG surfaces showed better blood compatibility than PBLG or PEG-g-PBLG-EA surfaces.
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Polyethylene glycol (PEG) grafted poly γ-benzyl L-glutamate (PBLG) were prepared from esterification or substitution reaction of PBLG with PEG having hydroxyl group at one end or primary amino groups at both ends. The viscosity of these polymer solution was decreased with decrease of polymer concentration. But in more dilute solution the viscosity was increased with decrease of polymer concentration. PEG-grafted PBLG polymers showed smaller water contact angles than PBLG homopolymer, and the water contact angles of the surface of PEG-grafted PBLG polymers were largely dropped by reacting with aminoethanol, resulting in hydrogel surfaces.
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Microparticulate carrier systems have significant potential for antigen delivery. The authors studied how microspheres coated with the polycationic copolymer poly(L-lysine)-graft-poly(ethylene glycol) (PLL-g-PEG) can be protected against unspecific phagocytosis by antigen presenting cells, a prerequisite for selective targeting of phagocytic receptors. For this aim the authors explored the influence of PLL-g-PEG architecture on recognition of coated microspheres by antigen presenting cells with regard to both grafting ratio and molecular weight of the grafted PEG chains. Carboxylated polystyrene microspheres (5 μm) were coated with a small library of PLL-g-PEG polymers with PLL backbones of 20 kDa, grafting ratios from 2 to 20, and PEG side chains of 1–5 kDa. The coated microspheres were characterized by their ζ-potential and resistance to IgG adsorption. Phagocytosis of these microspheres by human monocyte derived dendritic cells (DCs) and macrophages (MΦ) was quantified by phase contrast microscopy and by analysis of the cells’ side scattering in a flow cytometer. Generally, increasing grafting ratios impaired the protein resistance of coated microspheres, leading to higher phagocytosis rates. For DC, long PEG chains of 5 kDa decreased the phagocytosis of coated microspheres even in the case of considerable IgG adsorption. In addition, preferential adsorption of dysopsonins is discussed as another factor for decreased phagocytosis rates. For comparison, the authors studied the cellular adhesion of DC and Mζ to PLL-g-PEG coated microscopy slides. Remarkably, DC and Mζ were found to adhere to relatively protein-resistant PLL-g-PEG adlayers, whereas phagocytosis of microspheres coated with the same copolymers was inefficient. Overall, PLL(20)-[3.5]-PEG(2) was identified as the optimal copolymer to ensure resistance to both phagocytosis and cell adhesion. Finally, the authors studied coatings made from binary mixtures of PLL-g-PEG type copolymers that led to microspheres with combined properties. This enables future studies on cell targeting with ligand modified copolymers.
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Tuning the amphiphilicity of (aza)phthalocyanine hydrophobic cores by introducing multiple polyethylene glycol (PEG) moieties with controlled orientations of their (non)peripheral positions is an innovative approach to fabricating water-soluble macrocyclic materials. Although many water-soluble PEGylated macrocycles have been produced in this way, the ability to generate substances with PEG tails oriented outward from the macrocyclic plane in order to obtain non-aggregated, water soluble forms remains a challenge. In this study, we resolved this issue by developing a methods for the synthesis of four new dual directional PEG containing Zn(II)/Mg(II) amphiphiles (ZnPc-PEG, MgPc-PEG, ZnAzaPc-PEG and MgAzaPc-PEG). In addition, the non-aggregating behaviour, and photophysical and photochemical properties of these PEG-complexes were elucidated.
Water soluble
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Exogenous surfactant administration in patients with the acute re-spiratory distress syndrome is currently being evaluated, although resource limitations and the potential expense are existing concerns. Previous in vitro and in vivo studies have shown that substances such as polyethylene glycol (PEG) added to exogenous surfactant improved the function of the surfactant. Based on these data, we hypothesized that PEG would augment surfactant function in an adult rabbit model of lung injury induced by lung lavage and mechanical ventilation, and that this would be accomplished by altering surfactant metabolism. Contrary to our hypothesis, however, mean PaO2 , PaCO2 , and peak inspiratory pressures values 3 h after treatment were significantly worse in the surfactant + PEG treatment groups compared with the surfactant alone groups. These effects were observed for two different doses of surfactant tested. Lavage analyses after sacrifice showed that animals given PEG with their surfactant had significantly lower total and large aggregate surfactant pool sizes compared with animals given surfactant alone. We conclude that in this lung injury model, PEG attenuated surfactant responses, suggesting that further preclinical studies are required before testing this approach in humans.
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The use of poly(ethylene glycol) in the purification of plasma and cellular protein is somewhat complicated by the difficulty of removing it from the protein product. The method presented here, quickly and efficiently removes over 95% of the PEG by the simple addition of salts to induce an aqueous two-phase separation with the PEG in the upper phase and greater than 90% of the protein in the lower phase.
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Polyethylene glycol(PEG) brush can form a highly hydrophilic layer on the material surfaces to prevent the non-selective adsorption of proteins and reduce the adhesion of bacterium and microbes for its repulsive penetration.The anti-fouling applications of poly(ethylene glycol) brush on polymers,siliceous materials and metal surfaces are reviewed and the possible application on metal surface for anticorrosion is covered.
Polymer brush
Penetration (warfare)
Protein Adsorption
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