Ramón Pamies

Temperature-induced formation and contraction of micelle-like aggregates in aqueous solutions of thermoresponsive short-chain copolymers.

A combination of turbidity, light scattering, and steady shear viscosity experiments has revealed that aqueous solutions of an amphiphilic diblock copolymer or a negatively charged triblock copolymer, both containing poly(N-isopropylacrylamide), can undergo a temperature-induced transition from loose intermicellar clusters to collapsed core-shell nanostructures. Turbidity, light scattering, and viscosity results of these short-chain copolymers disclose transition peaks at intermediate temperatures. At high temperatures, the compact core-shell particles from the diblock copolymer aggregate, whereas no renewed interpolymer association is observed for the triblock copolymer or for the solution of the diblock copolymer with added sodium dodecyl sulfate because the electrostatic repulsive interactions suppress the tendency of forming interpolymer clusters. The temperature-induced building up of intermicellar structures and the formation of large aggregates at high temperature in the solution of the diblock copolymer is significantly reduced under the influence of high shear rates.

Temperature-induced intermicellization of "hairy" and "crew-cut" micelles in an aqueous solution of a thermoresponsive copolymer.

Temperature-induced intermicellar structures in aqueous solutions of the thermoresponsive methoxypoly(ethylene glycol)-block-poly(N-isopropylacrylamide) (MPEGn-b-NIPAAM71) copolymer that exhibit a lower critical solution temperature were studied by means of turbidimetry, dynamic light scattering (DLS), shear viscosity, and rheo small-angle light scattering (rheo-SALS) methods. The length of the hydrophilic chains (MPEG) of the copolymer varies from n=0 to n=114. It is shown that this change has a major impact on the temperature-induced association behavior of the polymer in solution. The turbidity results at quiescent conditions revealed a transition peak in the turbidity curve at intermediate temperatures, and this peak as well as the cloud point is shifted toward higher temperatures with increasing length of the hydrophilic chains of the copolymer. The DLS measurements disclosed a fast and a slow relaxation mode, which both are diffusive. From the fast and slow relaxation times the sizes of unimers/micelles and intermicellar clusters, respectively, can be determined. The temperature-induced aggregation is less pronounced in solutions of copolymers with long hydrophilic chains, and the intermicellar structures exhibit an interesting transition at intermediate temperatures. In the shear viscosity measurements large association complexes are formed at high temperatures and at low shear flow for the polymers with short hydrophilic chains, whereas at high shear rates breakup of interaggregate chains was observed. For the copolymer with the highest number of hydrophilic chains (n=114), a novel transition peak was found in the viscosity data. The rheo-SALS results divulged shear-induced structural changes of the association complexes at elevated temperatures. For copolymers with short hydrophilic chains, shear-induced disruption of association complexes was found at higher temperatures, whereas for hairy micelles augmented shear flow promoted the growth of complexes.

Characterization of polyelectrolyte features in polysaccharide systems and mucin.

This review elucidates several aspects on the behavior of charged polysaccharides and mucin. Viscosification of dilute aqueous solutions of hyaluronan (HA) occurs in the course of time at low shear flow, whereas shear thinning as time evolves is found at moderate shear rates. Hydrogen bonds and electrostatic interaction play an important role for the emergence of these features. No time effect of the viscosity is observed for semidilute HA solutions. A degradation of HA is observed at low and high pH and this effect continues over long times, and it is only in the approximate interval 5<pH<10 that HA is stable. Small angle neutron scattering (SANS) measurements on semidilute aqueous solutions of mucin at pH=7 reveal a fractal dimension of 1.4, and the effect of temperature is insignificant on the fractal structure. This suggests that the mucin chains on a semi-local dimensional scale are rod-like. From various experimental methods on solutions of mucin it was found that at pH values around 2 (uncharged polymer), the intensive hydrophobic interactions lead to large association complexes, whereas at pH>>2 the negative charges suppress the tendency of forming associations. At pH<2, the mucin chains are compressed and they are decorated by some positive charges. In the semidilute regime, a fragmented network is developed. The intense association in semidilute solutions of mucin at pH=2 is further supported by the results from rheo-small angle light scattering measurements. Effects of ionic strength on the radius of gyration (R(g)) for dilute solutions of HA (pH=7) and positively charged hydroxyethylcellulose (HEC(+)) are studied with the aid of Monte Carlo simulations, and essential features of the polyelectrolyte effect on R(g) are captured in the computer simulation. Strong interactions are observed in aqueous mixtures of an anionic polysaccharide (HEC(-)) and an oppositely charged surfactant (cetyltrimethylammonium bromide; CTAB); this gives rise to extensive associations and macroscopic phase separation is approached. The massive association complexes are disclosed in the SANS experiments by a pronounced upturn in the scattered intensity at low values of the wave vector.

Temperature-induced intermicellization and contraction in aqueous mixtures of sodium dodecyl sulfate and an amphiphilic diblock copolymer.

Aqueous solutions of a thermoresponsive amphiphilic diblock copolymer, containing poly(N-isopropylacrylamide), in the presence of the anionic sodium dodecyl sulfate (SDS) surfactant can undergo a temperature-induced transition from loose intermicellar clusters to collapsed core-shell nanostructures. The polymer-surfactant mixtures have been characterized with the aid of turbidity, small-angle neutron scattering (SANS), intensity light scattering (ILS), dynamic light scattering (DLS), shear viscosity, and rheo-small angle light scattering (rheo-SALS). In the absence of SDS, compressed intermicellar structures are formed at intermediate temperatures, and at higher temperatures further aggregation is detected. The SANS results disclose a structure peak in the scattered intensity profile at the highest measured temperature. This peak is ascribed to the formation of ordered structures (crystallites). In the presence of a low amount of SDS, a strong collapse of the intermicellar clusters is observed at moderate temperatures, and only a slight renewed interpolymer association is found at higher temperatures because of repulsive electrostatic interactions. Finally, at moderate surfactant concentrations, temperature-induced loose intermicellar clusters are detected but no shrinking was registered in the considered temperature range. At a high level of SDS addition, large polymer-surfactant complexes appear at low temperatures, and these species are compressed at elevated temperatures. The rheo-SALS results show that the transition structures are rather fragile under the influence of shear flow.

Effect of polyethylene glycol (PEG) length on the association properties of temperature-sensitive amphiphilic triblock copolymers (PNIPAAMm-b-PEGn-b-PNIPAAMm) in aqueous solution

Effects of temperature on the association behavior in aqueous solutions of a series of thermosensitive poly(N-isopropylacrylamide)-block-poly(ethylene glycol)-block-poly(N-isopropylacrylamide) triblock copolymers (PNIPAAMm-b-PEGn-b-PNIPAAMm) with the length of the PNIPAAM block fixed (m ≈ 67) and with different lengths of the PEG block (n = 23, 34, 77, and 165) have been studied with the aid of turbidity, dynamic light scattering (DLS), and Monte Carlo simulations. The turbidity results show that the sharp transition to high turbidity values is shifted to higher temperatures when the length of the PEG spacer is increased from 23 to 77, whereas no transition is observed for the longest PEG block. These findings are consistent with the DLS results, which suggest the formation of large association structures at temperatures well above the cloud point. The simulation results indicate that a long PEG-block portion separating the PNIPAAM blocks in the triblock copolymer reduces the tendency of the polymer forming interchain associations at elevated temperatures. Simulation shows that for a long PEG spacer, the copolymer moiety is rather extended even at high temperatures, whereas for copolymers with a short PEG length the thermoresponsive block copolymer undergoes a transition from an extended to a compact conformation.

Single-Molecule Behavior of Asymmetric Thermoresponsive Amphiphilic Copolymers in Dilute Solution

A bead-and-spring model has been used to simulate the behavior of thermoresponsive asymmetric diblock amphiphilic copolymers with aid of Monte Carlo simulations. The alteration of the thermodynamic conditions was mimicked by using a Lennard-Jones potential, which was related to the measured temperatures by comparison with experimental data for aqueous solutions of two sets of diblock copolymers, namely methoxypoly(ethylene glycol)-block-poly(N-isopropylacrylamide), one with different lengths of the hydrophilic block (MPEG(n)-b-PNIPAAM(71)) and one with varying lengths of the hydrophobic block (MPEG(57)-b-PNIPAAM(m)). The influence of the length of both the thermoresponsive and the hydrophilic block on the size and conformation of single molecules at various temperatures was studied by means of simulations. The temperature-induced contraction of the copolymer (MPEG(n)-b-PNIPAAM(71)) entities is only modestly affected by changing the length of the hydrophilic block, whereas for the MPEG(57)-b-PNIPAAM(m) copolymer both the transition temperature and the magnitude of the compression of the molecules are strongly influenced by the length of the thermosensitive block. When the MPEG chain fully covers the hydrophobic core, the copolymer moieties are stabilized, whereas poorly covered cores can promote interchain aggregation at elevated temperatures.

Aggregation behaviour of gold nanoparticles in presence of chitosan

Chitosan (CS) is a biocompatible polysaccharide with positive charge that is widely used as a coating agent for negatively charged nanoparticles. However, the types of structures that emerge by combining CS and nanoparticles as well as their behaviour are still poorly understood. In this work, we characterize the nanocomposites formed by gold nanoparticles (AuNPs) and CS and study the influence of CS in the expected aggregation process that should experience those nanoparticles under the favourable conditions of low pH and high ionic strength. Thus, at the working CS concentration, we observe the existence of CS structures that quickly trap the AuNPs and avoid the formation of nanoparticle aggregates in environmental conditions that, otherwise, would lead to such an aggregation.

Adsorption of cationic hydroxyethylcellulose derivatives onto planar and curved gold surfaces.

The adsorption of two positively charged hydroxyethylcellulose derivatives with 7 and 60 mol % positively charged groups and a cationic, hydrophobically modified hydroxyethylcellulose containing 1 mol % hydrophobic groups and 7 mol % charged groups onto flat and spherical citrate-coated gold surfaces of different sizes has been investigated. The planar surfaces were studied by means of the quartz crystal microbalance with dissipation monitoring, whereas nanoparticle suspensions were examined using dynamic light scattering and UV-vis spectroscopy. Two different driving forces for adsorption have been evaluated: the electrostatic interaction between the positive charges on the polymers and the negatively charged gold surfaces and the affinity of the polymers for gold due to hydrophobic interactions. The comparison between the data obtained from curved and planar surfaces suggests a strong correlation between surface curvature and adlayer conformation in the formation of the hybrid polymer-gold nanoparticles. The influence of particle size on the amount of adsorbed polymer has been evaluated for the different polymers. The impact of the ionic strength on polymer adsorption has been explored, and the adsorbed polymer layer has been found to protect the gold nanoparticles from aggregation when salt is added to the solution. The addition of salt to a mixture of gold particles and a charged polymer can induce a thicker adsorbed layer at low salinity, and desorption was found at high levels of salt addition.

Characterization of low molecular mass thermosensitive diblock copolymers and their self-assembly by means of analytical ultracentrifugation

The characterization of a series of four poly(N-isopropylacrylamide)-based copolymers with a hydrophilic block of poly(ethylene glycol) with a variable length (MPEGn-b-PNIPAAM71) has been performed by means of analytical ultracentrifugation. Molecular mass, partial specific volume, sedimentation coefficient (s), and hydrodynamic radius (Rh) have been determined and successfully compared with other techniques. In addition, the self-assembly process of these four copolymers has been evaluated, finding multimeric species at temperatures lower than low critical solution temperature in the case of the longest copolymer.