Presence Of Amphiphilic Copolymer Research Articles

Calcein release from DPPC liposomes by phospholipase A2 activity: Effect of cholesterol and amphipathic copolymers

In this study, we evaluated the impact of incorporating diblock and triblock amphiphilic copolymers, as well as cholesterol into DPPC liposomes on the release of a model molecule, calcein, mediated by exogenous phospholipase A2 activity. Our findings show that calcein release slows down in the presence of copolymers at low concentration, while at high concentration, the calcein release profile resembles that of the DPPC control. Additionally, calcein release mediated by exogenous PLA2 decreases as the amount of solubilized cholesterol increases, with a maximum between 18 mol% and 20 mol%. At concentrations higher than 24 mol%, no calcein release was observed. Studies conducted on HEK-293 and HeLa cells revealed that DPPC liposomes reduced viability by only 5% and 12%, respectively, after 3 hours of incubation, while DPPC liposome in presence of 33 mol% of Cholesterol reduced viability by approximately 11% and 23%, respectively, during the same incubation period. For formulations containing copolymers at low and high concentrations, cell viability decreased by approximately 20% and 40%, respectively, after 3 hours of incubation. Based on these preliminary results, we can conclude that the presence of amphiphilic copolymers at low concentration can be used in the design of new DPPC liposomes, and together with cholesterol, they can modulate liposome stabilization. The new formulations showed low cytotoxicity in HEK-293 cells, and it was observed that calcein release depended entirely on PLA2 activity and the presence of calcium ions.

New polymer materials with controlled nanoporous structure based on N-vinylpyrrolidone

The polymer networks with nanoporous structure were obtained by the crosslinking free-radical copolymerization of N-vinylpyrrolidone with triethylene glycol dimethacrylate in bulk in the presence of amphiphilic copolymer and its fractions as templates. The templating agents consisted of copolymer or their fragments with similar monomer units and different molecular weight. Macromolecular templates were shown to be removed from the polymer composite by PriOH leaving the pores. The values of the specific surface areas, the total pore volumes, pore size, and pore size distribution were measured by the method of low-temperature nitrogen absorption. The maximum value of the specific surface area was calculated to be ~26 m2 g–1. The value was significantly higher than that for the usual copolymer network. The relationship between specific surface area, parameters of pores, and macromolecular structure of template has been established. It is shown by Brunauer—Emmett—Teller method that the macromolecules having a branched architecture are more effective for the preparation of the polymer network with more developed specific surface area and narrow pore size distribution.

Effect of SBA-15 on the energy absorption characteristics of epoxy resin for blast mitigation applications

The energy absorption characteristics of silica-filled epoxy composites, for potential application as a blast mitigating retrofitting polymer coating has been explored. Mesoporous silica (SBA-15) with controlled pore size of 5.4 nm was synthesized by the hydrolysis of tetraethyl orthosilicate in the presence of amphiphilic copolymer (PEO-PPO-PEO) which was characterized by nitrogen physisorption studies at 77 K. The porous siliceous rods were homogeneously dispersed in the epoxy resin by ultrasonication (0.5–7 wt%) and subsequently cured using triethylene tetra-amine hardener to prepare silica reinforced composites. Structural, thermal and mechanical properties of the composites were evaluated under dynamic as well as quasi-static conditions which revealed that introduction of SBA-15 at low loadings (1 wt%) led to an increase in the toughness of the base resin but macroporous silica led to deterioration in the properties. The results clearly revealed that the mesoporous nature of silica plays a major role towards improving the dispersion of the filler which in turn resulted in improved properties. Neat epoxy samples fractured in a brittle fashion, but in the presence of SBA-15, the sample exhibited ductile failure, which was explained on the basis of a crack pinning mechanism. High strain rate studies (~103 s−1) of selected compositions were performed on a Split Hopkinson pressure bar and the effect of addition of mesoporous silica on the energy absorption characteristics were established. Finite element analysis was used to predict the behavior of concrete slabs on exposure to dynamic loadings resulting from TNT explosions, both in the presence and absence of the epoxy layer, which revealed the role of the retrofit as a fragment arrestor.

Reverse self-assemblies based on amphiphilic polyphosphazenes for encapsulation ofwater-soluble molecules

A novel series of amphiphilic polyphosphazenes (PNIPAm/AA-PPP) containing hydrophilicoligo-(N-isopropylacrylamide) (oligo-NIPAm) and various hydrophobic aliphatic amines asco-substitutes was synthesized via a two-step substitution reaction. The extraction andsolubilization of water-soluble substances such as fluorescein sodium and trypan blue froman aqueous phase into the chloroform phase were supposed to result from theformation of polyphosphazene reverse self-assemblies in the organic phase. Afield emission scanning electronic microscope was adopted to characterize themorphology of reverse assemblies in chloroform. Additionally, a significant improvementof encapsulation and release profiles of water-soluble substances was found forpoly(lactic-co-glycolic acid) (PLGA) microparticles in the presence of amphiphilic copolymers, which wasassociated with the chemical structure of copolymers as well as the content of copolymer inthe microparticles.

The formation of hydrophobic inorganic nanoparticles in the presence of amphiphilic copolymers

The presented paper describes a novel procedure for the preparation of inorganic nanoparticles and their surface functionalization in situ dedicated to an application in technical polymers. Using an inverse emulsion technique and amphiphilic block or statistical copolymers as stabilizers, a broad variety of nanoparticles such as ZnO, CdS, MgCO3, Ni, or Cu can be prepared. The amphiphilic polymers serve not only as surface active compounds in the emulsion but also to hydrophobize the inorganic particles as they remain adsorbed on the surface after the precipitation. As a consequence of the high degree of surface coverage by polymer chains, organic solvents are able to redisperse these particles in the aggregate free manner. The utilization of the block copolymers instead of statistical copolymers resulted in the formation of the particles, which were larger in size and possessed a much broader size distribution. The chemical nature of the adsorbed polymer layer on the particle surface is crucial to the preparation of polymer nanocomposites. The primary goal of this contribution is to demonstrate the universality of such a one-pot synthetic procedure, which was found to be relevant for industrial use.