Search results for "solvent"
showing 10 items of 1395 documents
Tomographic and Topographic Investigation of Poly-D,L-Lactide-Co-Glycolide Microspheres Loaded with Prostaglandine E<sub>2</sub> for Exte…
2010
Polymeric, biodegradable microspheres represent a good reliable system to investigate the release of bioactive substances in both in vitro and in vivo applications. Common biomaterials for the synthesis of these microspheres are aliphatic polyesters of the poly(α-hydroxy)acids, especially poly-L-lactides (PLA) and polyglycolides (PGA) or their copolymers poly-D,L-lactide-co-glycolides (PLGA). In our own previous studies we have developed PLGA microspheres with integrated PGE2 as model substance for a wide range of biomedical applications, especially in angiogenesis, fracture healing and cartilage repair. The synthesis is based on a binary solvent in water emulsion approach, where two differ…
Expanded micro-particles by supercritical antisolvent precipitation: Interpretation of results
2008
Abstract Supercritical antisolvent (SAS) micronization has been used to obtain nanoparticles and micro-particles of several kinds of materials. Sometimes hollow expanded micro-particles have also been obtained. This work is focused on the analysis of this last morphology. We organized literature data and our previous experiments and we added new experiments on previously tested compounds and on compounds never tested before. As a result, expanded micro-particles using several compounds belonging to different categories and precipitated from different solvents in laboratory and pilot scale plants were obtained with diameters between about 10 and 180 μm. They also showed different sub-structu…
Structured Nanoparticles from the Self-Assembly of Polymer Blends through Rapid Solvent Exchange
2017
Molecular dynamics simulations were performed to study systematically the rapid mixing of a polymer blend in solution with a miscible nonsolvent. In agreement with experiments, we observe that polymers self-assemble into complex nanoparticles, such as Janus and core-shell particles, when the good solvent is displaced by the poor solvent. The emerging structures can be predicted on the basis of the surface tensions between the polymers as well as between the polymers and the surrounding liquid. Furthermore, the size of the nanoparticles can be independently tuned through the mixing rate and the polymer concentration in the feed stream; meanwhile, the composition of the nanoparticles can be c…
On the Stability of Polymeric Nanoparticles Fabricated through Rapid Solvent Mixing.
2018
We study the stability of polymeric nanoparticles fabricated through the rapid mixing of polymers in a good solvent with a poor solvent that is miscible with the good solvent. In previous experiments where water was used as the poor solvent, a negative surface charge was measured on the precipitated nanoparticles, which led to the long-time stability of the dispersion. It was argued that these charges originate presumably from either water or hydroxide adsorption at the hydrophobic nanoparticle surface or from impurities in the feed streams that preferentially adsorb on the precipitated nanoparticles. To elucidate the origin of this stabilization mechanism, we performed experiments wherein …
Pearl-necklace structures of molecular brushes with rigid backbone under poor solvent conditions: A simulation study
2010
Bottle-brush polymers, where flexible side chains containing N=20 to 50 effective monomers are grafted to a rigid backbone, are studied by molecular dynamics simulations, varying the grafting density σ and the solvent quality. Whereas for poor solvents and large enough σ the molecular brush is a cylindrical object, homogeneous in axial direction, for intermediate values of σ an axially inhomogeneous structure of "pearl-necklace" type is formed. The "pearls," however, have a strongly nonspherical ellipsoidal shape, due to the fact that several side chains cluster together in one pearl, qualitatively consistent with predictions of Sheiko et al. [Eur. Phys. J. E 13, 125 (2004)] We analyze the …
PLLA/PLA scaffolds prepared via Thermally Induced Phase Separation (TIPS): tuning of properties and biodegradability
2008
Foams for tissue engineering applications were prepared via thermally induced phase separation (TIPS). Poly-L-Lactic Acid (PLLA) and blends of PLLA with PLA in different proportions were used (100/0, 90/10, 75/25, 50/50, 0/100 PLLA/PLA wt/wt) starting from ternary systems where dioxane was the solvent and water the non-solvent. Morphology was evaluated by Scanning Electron Microscopy (average pore size and interconnection) and the void fraction was measured by means of Hg porosimetry. Foams apparent density was also evaluated (porosity ranges from 87% to 92%). Biodegradability was estimated in a body mimicking fluid. Results show that structure and morphology (in terms of average pore size …
The mechanism of polymer permeation through polymer gel membranes
2007
Polymer gels are capable of producing separation effects on polymers. Applications for fractionation and for osmotic measurements are possible. Investigations are reported concerning the separation properties of polystyrene layers grafted onto a supporting cellulose basis. The permeation for pure solvents and the separating molecular limit for different solvents are tested. Their size depends uniquely on the interaction between the grafted polystyrene and the solvent.
Relative strength of H-bonding groups on biodegradable polymer-based blends in solution
2006
The intermolecular hydrogen bonding interactions between poly(3-hydroxybutyrate) and poly(styrene-co-vinyl phenol) copolymers with mutual solvent epichlorohydrin were thoroughly investigated by steady-state fluorescence and viscosity techniques. Fluorescence spectroscopy along with viscosity technique was used to asses the intermolecular hydrogen bonding between poly-(3-hydroxybutyrate) and its blends with five copolymer samples of styrene–vinyl phenol, containing different proportions of vinyl phenol but similar average molecular weight and polydispersity index. In the case of very low OH contents (2–4 mol %), as expected, both components of poly(3-hydroxybutyrate) and poly(styrene-co-4-vi…
Modelling the hydrogen-bonding interactions in a copolymer/biodegradable homopolymer blend through excess functions
2008
A recent theoretical approach based on the coupling of both the Flory-Huggins (FH) and the Association Equilibria thermodynamic (AET) theories was modified and adapted to study the miscibility properties of a multi- component system formed by two polymers (a proton-donor and a proton-acceptor) and a proton-acceptor solvent, named copolymer(A)/solvent(B)/polymer(C). Compatibility between polymers was mainly attained by hydrogen- bonding between the hydroxyl group on the phenol unit of the poly(styrene-co-vinyl phenol) (PSVPh) and the car- bonyl group of the biodegradable and environmentally friendly poly(3-hydroxybutyrate) (PHB). However, the self- association of PSVPh and specific interacti…
Polymer-polymer interaction parameters in solvent/polymer/polymer ternary systems
1981
Abstract Empirical equations defining the relationships between b23 and χ23 interaction parameters for the ternary systems toluene (1)/poly(dimethylsiloxane), PDMS, (2)/polystyrene, PS, (3) and benzene (1)/PDMS(2)/PS(3) have been determined. The dependences of both interaction parameters on the mean molecular weights of the macromolecular components have also been studied. A single dependence of b23 (or χ23) upon the mean molecular weight is found when both polymeric components have intermediate to high molecular weights. However, that single dependence is not found when the molecular size of polymer (2) is low.