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At least 19 recordsLinked to original sources

Molecular sieving by polymer solutions: dependence on particle and polymer size, independence of polymer entanglement.

The previous postulate of collision and displacement mechanisms of molecular sieving based on a biphasic plot of retardation coefficient vs particle radius ("R-plot") was extended and modified in four ways: i) A wider size range of particles and polymers confirmed the biphasic nature of the R-plot and, in addition, revealed a third mechanistic phase in the largest size range of particles and polymers which exhibits a positive slope in plots of retardation coefficient vs log (particle or polymer size), presumably denoting a collision mechanism. ii) Peaks of retardation in polyethyleneglycol (PEG) solutions were found with a particle M(r) of 10(7) independently of the M(r) of PEG, and with a PEG M(r) of 4 x 10(5) independently of particle M(r), showing that the retardation mechanism is not qualitatively a function of the particle/polymer size ratio as postulated previously, although quantitatively retardation is directly related to the size of particle and polymer. iii) Items i) and ii) were confirmed using band width in lieu of mobility measurement. iv) The entanglement threshold, c*, was found to decrease monotonically across the entire polymer size range in which the triphasic retardation takes place. Thus c* cannot be the sole cause for a non-monotonic change of retardation or normalized relative bandwidth with polymer size and particle size. Moreover, Ferguson plots across c* do not reflect it in any way.

Electrophoresis, Capillary↗

Influence of polymer architecture and polymer-wall interaction on the adsorption of polymers into a slit-pore.

The effects of molecular topology and polymer-surface interaction on the properties of isolated polymer chains trapped in a slit were investigated using off-lattice Monte Carlo simulations. Various methods were implemented to allow efficient simulation of molecular structure, confinement force, and free energy for a chain interacting with such "sticky" surfaces. The simulations were performed in the canonical ensemble, and the free energy was sampled via virtual slit-separation moves. Six different chain architectures were studied: linear, star-branched, dendritic, cyclic, two-node (i.e., containing two tetrafunctional intramolecular crosslinks), and six-node molecules. The first three topologies entail increasing degrees of branching, and the last three topologies entail increasing degrees of intramolecular bonding. The confinement force, monomer density profile, and conformational properties for all these systems were compared (for identical molecular weight N) and analyzed as a function of adsorption strength. The compensation point where the wall attraction counterbalances the polymer-slit exclusion effects was the focus of our study. It was found that the attractive energy at the compensation point, epsilon(c), is a weak increasing function of the chain length for excluded-volume chains. The value of epsilon(c) differs significantly for different topologies, and smaller values are associated with better-adsorbing molecules. Due to their globular shape and numerous chain ends, branched molecules (e.g., stars and dendrimers) experience a relatively small entropic penalty for adsorption at low adsorption force and moderate confinement. However, as the adsorption force increases, the more flexible linear chains reach the compensation point at a weaker attractive energy because of the ease with which monomers can be packed near the walls. In moderate to weak confinement, molecules with intramolecular cross-links, such as cyclic, two-node, and six-node molecules, always adsorb better than the other chains (with the same N). Especially at strong adsorption, two-node and six node molecules are highly localized in the region near the walls. Under strong confinement conditions, chain rigidity becomes the dominating factor and the more flexible linear chain adsorbs the best at all adsorption strengths. These results provide useful insights for controlling confinement and depletion forces of polymers with different molecular architectures in the presence of attractive polymer-surface interactions.

Adsorption↗

Polymer-solvent interaction parameters in polymer solutions at high polymer concentrations.

Molecular mass and temperature dependences of the polymer-solvent interaction parameter have been investigated in the extreme interval of high polymer concentration using inverse gas chromatography (IGC). The observed molecular mass dependence has been compared with the predictions of a theoretical model, which emphasises the role of intramolecular contacts in the polymer chain. The model reproduces reasonably well the molecular mass dependence. However, enthalpic and entropic contributions of the interaction parameter, obtained from IGC measurements at different temperatures, exhibit behaviours difficult to explain in the framework of the current models.

Chromatography, Gas↗

Assessment of polymer-polymer interactions in blends of HPMC and film forming polymers by modulated temperature differential scanning calorimetry.

PURPOSE: To assess the miscibility and phase behavior of binary blends of hydroxypropylmethyl cellulose (HPMC) with hydroxypropyl cellulose (HPC), methylcellulose (MC), and polyvinylpyrrolidone (PVP). METHODS: Polymer-polymer miscibility was assessed by measurement of the glass transition temperature (Tg) and the width of the glass transition temperature (W-Tg), using modulated temperature differential scanning calorimetry (MTDSC). RESULTS: HPMC K4M/PVP and HPMC E5/MC blends were miscible as evidenced by a single, composition dependent, Tg throughout the entire composition range. HPMC/HPC blends were immiscible at all compositions. For the miscible blends, the variation in Tg with blend composition was compared to the values predicted by the Fox and Couchman-Karasz equations. At intermediate blend compositions, HPMC K4M/PVP blends exhibited negative deviations from ideal behavior. The Tg of the HPMC E5/MC blends was found to follow the Fox equation. The W-Tg measurements of the miscible blends gave evidence of phase separation at certain compositions. CONCLUSIONS: MTDSC was shown to be a useful technique in characterizing the interactions between some commonly used pharmaceutical polymers.

Calorimetry, Differential Scanning↗

Controlling cell attachment selectively onto biological polymer-colloid templates using polymer-on-polymer stamping.

A new patterning approach using polymer-on-polymer stamping (POPS) has been developed to fabricate polymer-colloid templates for controlling selective cell attachment. In this paper, a polyamine surface patterned onto a poly(acrylic acid)/poly(allylamine hydrochloride) (PAA/PAH) cell resistant multilayer platform serves as a template for the deposition of close- or loose-packed colloidal particles. Peptides containing the RGD adhesion sequence were used to modify the PAH/colloid surface for specific cell attachment. Cell behavior was studied by varying colloidal packing array density, pattern geometry, and surface chemistry. It was found that loose-packed RGD-modified colloidal arrays enhance cell adhesion, as observed through the development of focal adhesion contacts and orientation of actin stress fibers, but close-packed colloidal arrays induce a rounded and nonadhesive cell morphology and yield a smaller number of attached cells. On loose-packed arrays, cells adjust their shapes to the pattern geometry when the stripe width is smaller than 50 microm and increase their extent of attachment when the concentration of surface RGD peptides is increased. This new biomaterials system allows the examination of cell behavior as a function of RGD surface distribution on the molecular to micrometer scale and reveals cellular response to different surface roughnesses.

Acrylic Resins↗

In situ compatibilizer-reinforced interface between a flexible polymer (a functionalized polypropylene) and a rodlike polymer (a thermotropic liquid crystalline polymer).

We present an investigation of the interfacial reinforcement between a flexible folded-chain polymer (functionalized polypropylene-maleic anhydride-grafted polypropylene, MAPP) and a rodlike polymer (a themotropic liquid crystalline polymer, TCLP - poly(ester amide)). Fracture toughness was measured using an asymmetric double-cantilever beam test (ADCB). High fracture toughness at the bonding temperature of 200 degrees C indicates that a chemical reaction has occurred at the interface to provide a strong interaction between MAPP and TLCP. Despite the higher modulus of TLCP, the fracture was propagated in the TLCP phase because of inherent TLCP domain structure. An analysis on the locus of failure revealed that at constant bonding temperature the fracture toughness between MAPP and TLCP was influenced not only by the bonding temperature but also by the bonding time. The fracture toughness increased with the bonding temperature until 200 degrees C was reached and then decreased at higher bonding temperature. The fracture toughness increased with annealing time until it reached a plateau value. We ascribe the dependence of the fracture toughness on the bonding time to the progressive occurrence of two different failure mechanisms, adhesive failure and cohesive failure. The adhesive strength increased with bonding temperature whereas the cohesive strength decreased because of weaker adhesion between TLCP crystalline domains. The dependence of fracture toughness on bonding time was explained in terms of the TLCP crystalline domain structure.

Journal Article↗

The swelling phenomenon of acrylic resin polymer teeth at the interface with denture base polymers.

PURPOSE: This study examined the interface between acrylic resin polymer teeth and denture base polymers. MATERIAL AND METHODS: An autopolymerized denture base polymer was cured either at 30 degrees C, 50 degrees C, or 70 degrees C, and a heat-cured denture base polymer was cured at 100 degrees C in contact with acrylic resin polymer teeth. The specimens were ground wet and polished to a thickness of 0.21 mm for the examination of the interface with a light microscope. The surface of the specimens was then treated with the solvent tetrahydrofuran, and the specimens were examined with a scanning electron microscope (SEM). RESULTS: As a result of grinding, the inner parts of the beads at the interface of the teeth were exposed to the denture base polymer. The inner part in these polymer beads of the polymer teeth swelled to a depth of 3 microns when the autopolymerized polymer was cured at 30 degrees C. When cured at 70 degrees C, the thickness of the swelled layer was 21 microns (p < 0.001). Microscopically, the interface between the heat-cured denture base polymer and the polymer teeth appeared diffuse in the region of the interpenetrating polymer networks (IPN) and the matrix. The IPN appeared as a separate zone in the outer parts of the beads of the teeth, both with the light microscope and with the SEM. CONCLUSIONS: The results suggest that by increasing the polymerization temperature, the monomers of the denture base polymers diffused more effectively into acrylic resin polymer teeth. This increases the bond strength between the polymer teeth and the denture base polymer.

Acrylic Resins↗

Purification of protein and recycling of polymers in a new aqueous two-phase system using two thermoseparating polymers.

In this study we present a new aqueous two-phase system where both polymers are thermoseparating. In this system it is possible to recycle both polymers by temperature induced phase separation, which is an improvement of the aqueous two-phase system previously reported where one of the polymers was thermoseparating and the other polymer was dextran or a starch derivative. The polymers used in this work are EO50PO50, a random copolymer of 50% ethylene oxide (EO) and 50% propylene oxide (PO), and a hydrophobically modified random copolymer of EO and PO with aliphatic C14H29-groups coupled to each end of the polymer (HM-EOPO). In water solution both polymers will phase separate above a critical temperature (cloud point for EO50PO50 50 degrees C, HM-EOPO, 14 degrees C) and this will for both polymers lead to formation of an upper water phase and a lower polymer enriched phase. When EO50PO50 and HM-EOPO are mixed in water, the solution will separate in two phases above a certain concentration i.e. an aqueous two-phase system is formed analogous to poly(ethylene glycol) (PEG)/dextran system. The partitioning of three proteins, bovine serum albumin, lysozyme and apolipoprotein A-1, has been studied in the EO50PO50/HM-EOPO system and how the partitioning is affected by salt additions. Protein partitioning is affected by salts in similar way as in traditional PEG/dextran system. Recombinant apolipoprotein A-1 has been purified from a cell free E. coli fermentation solution. Protein concentrations of 20 and 63 mg/ml were used, and the target protein could be concentrated in the HM-EOPO phase with purification factors of 6.6 and 7.3 giving the yields 66 and 45%, respectively. Recycling of both copolymers by thermoseparation was investigated. In protein free systems 73 and 97.5% of the EO50PO50 and HM-EOPO polymer could be recycled respectively. Both polymers were recycled after aqueous two-phase extraction of apolipoprotein A-1 from a cell free E. coli fermentation solution. Apolipoprotein A-1 was extracted to the HM-EOPO phase with contaminating proteins in the EO50PO50 phase. The yield (78%) and purification factor (5.5) of apolipoprotein A-1 was constant during three polymer recyclings. This new phase system based on two thermoseparating polymers is of great interest in large scale extractions where polymer recycling is of increasing importance.

Apolipoprotein A-I↗

Small changes in the polymer structure influence the adsorption behavior of fibrinogen on polymer surfaces: validation of a new rapid screening technique.

Numerous studies conclude that the selective adsorption of plasma proteins on materials contacting blood or tissue affects all subsequent interactions related to the biocompatibility of artificial surfaces. However, there are only a few studies available, which clearly demonstrate that there is a correlation between surface chemistry and selective protein adsorption. Detailed knowledge of such correlations would facilitate the design of biocompatible materials. In this study, a rapid, fluorescence-based, screening technique using a 384-well format for polymer-protein interactions was developed. The screening assay was used to measure the adsorption of human fibrinogen on 46 test polymers (44 polyarylates selected from a combinatorial library of tyrosine-derived polyarylates, and two lactide-based polymers). In this library of polyarylates, structural changes are generated by variations in either the polymer backbone or the polymer pendent chain. Although no overall trend between polymer hydrophobicity and fibrinogen adsorption could be identified using the entire set of test polymers (R(2) = 0.43), fibrinogen adsorption was clearly correlated with variations in the pendent chain structure. Thus, when the test polymers were grouped by backbone composition, increased hydrophobicity of the pendent chain was significantly correlated with reduced fibrinogen adsorption. The following R(2) coefficients within the polymer backbone groups were determined: 0.87 (diglycolates); 0.98 (glutarates); 0.73 (adipates); 0.87 (suberates); 0.67 (3-methyl-adipates). Our results demonstrate that it is possible to screen for protein-material interactions in a cost-effective fashion using a miniaturized immunofluorescence technique. Further, we demonstrate that small changes in chemical composition can significantly influence the adsorption of human fibrinogen on polymer surfaces. The lactide-based polymers were among those polymers exhibiting the highest tendency to adsorb fibrinogen. This information may be useful when polymers have to be selected for specific biomaterial applications.

Adsorption↗

Shear bond strength of denture reline polymers to denture base polymers.

PURPOSE: This study was undertaken to characterize the shear bond strength established between four denture base polymers and four denture reline polymers. MATERIALS AND METHODS: Cylindric columns of denture reline polymers were bonded to columns of denture base polymers. Specimens were immersed in water for 4 months and then thermocycled. The strength at which the bond failed under shear stress was recorded. RESULTS: Significant differences in bond strength existed among the specimens because of the denture base polymer variable, the denture reline polymer variable, and their interaction (P < .05). A light-activated denture base polymer (Triad) bonded adequately with a light-activated reline polymer (Triad) but less well with the other reline polymers tested. The bond strength established between some denture base polymers and a different light-activated reline polymer (Rebaron LC) was relatively low. CONCLUSION: The type of denture base polymer and denture reline polymer affected the shear bond strength between them.

Acrylic Resins↗

Preparation of blood-compatible hollow fibers from a polymer alloy composed of polysulfone and 2-methacryloyloxyethyl phosphorylcholine polymer.

Blood-compatible hollow fibers were successfully prepared from a polymer alloy composed of polysulfone (PSf) and the 2-methacryloyloxyethyl phosphorylcholine (MPC) polymer. To improve the hydrophilicity, fouling-resistance characteristics, and blood compatibility of the PSf hollow fiber in a hemodialyzer, an MPC polymer that can be blended with PSf was synthesized in order to prepare the polymer alloy (PSf/MPC polymer). The contents of the MPC polymer blended in the PSf were 7 and 15 wt%. The PSf/MPC polymer hollow fiber could be prepared by both wet and dry-wet processing methods. The hollow fiber took an asymmetric structure, that is, the hollow-fiber membrane had a dense skin layer on the porous sponge-like structure. The mechanical strength was higher than that of conventional PSf hollow fibers for hemodialysis. The surface characterization of the PSf/MPC polymer hollow fiber by x-ray photoelectron spectroscopy revealed that the MPC units were concentrated at the surface. The permeability for solutes through the PSf/MPC polymer hollow fibers was measured for 4 h. The permeabilities of both a low-molecular-weight compound and protein were greater than those of the PSf hollow fibers. The amount of adsorbed protein was lower on the PSf/MPC polymer hollow fiber when compared to that of the PSf hollow fiber. Moreover, platelet adhesion was also effectively inhibited on the PSf/MPC polymer hollow fiber. Based on these results, the addition of the MPC polymer to the PSf is a very useful method to improve the functions and blood compatibility of the hollow fiber.

Biocompatible Materials↗

Bioadhesive polymers as platforms for oral controlled drug delivery II: synthesis and evaluation of some swelling, water-insoluble bioadhesive polymers.

A series of cross-linked, swellable polymers was sythesized from monomers such as acrylic acid, methacrylic acid, and others with various cross-linking agents to produce a range of polymers differing in charge densities and hydrophobicity. The densities, rate, and extent of hydration of the polymers were determined. An increase in the number of hydrophobic groups in the polymer structure reduced hydration whereas the density of the polymer was unaffected. A sensitive in vitro method for measuring adhesion of polymer to tissue from the rabbit stomach was developed. Polymers of acrylic acid loosely cross-linked (0.3%, w/w) with three different agents, divinyl glycol, 2,5-dimethyl-1,5-hexadiene, and divinylbenzene, showed the same degree of bioadhesion while poly(methacrylic acid-divinylbenzene) showed reduced bioadhesion. The small percent of cross-linking agent, irrespective of physicochemical properties, did not contribute substantially to bioadhesion, whereas the starting monomer had a large effect. The effect of pH on the bioadhesion of poly(acrylic acid-divinyl glycol) was studied at constant temperature, ionic strength, and osmolality. The polymer showed maximum adhesion at pH 5 and 6 and a minimum at pH 7. Gastrointestinal transit studies of cross-linked polymers in rats were studied. Poly(acrylic acid-divinyl glycol) and poly(methacrylic acid-divinylbenzene) were shown to have substantially longer GI transit times than the control, Amberlite 200 resin beads. The delay in transit time was due to bioadhesion of the polymer to the mucin-epithelial cell surface which was clearly observable on animal autopsy. The acrylic acid polymer showed a longer GI transit time than the methacrylic acid polymer, and this in vivo GI transit result is consistent with in vitro bioadhesion test results.

Acrylic Resins↗

Hydrodynamic theories for mixtures of polymers and rodlike liquid crystalline polymers.

We develop a hydrodynamic theory for flows of incompressible blends of flexible polymers and rodlike nematic polymers (RNPs) or rodlike nematic liquid crystal polymers (RNLCPs) extending the thermodynamical theory of Muratov and E [J. Chem. Phys. 116, 4723 (2002)] for phase separation kinetics of the blend. We model the flexible polymer molecules in the polymer matrix as Rouse chains and assume the translational diffusion of the molecules is predominantly through the volume fraction of the flexible polymer and the molecules of rodlike nematic liquid crystal polymers. We then (i) derive the translational flux for the rodlike nematic liquid crystal polymers to ensure the incompressibility constraint; (ii) derive the elastic stress tensor, accounting for the contribution from both the rodlike nematic polymer and the flexible polymer matrix, as well as the extra elastic body force due to the nonlocal intermolecular potential for long range molecular interaction; (iii) show that the theory obeys positive entropy production and thereby satisfies the second law of thermodynamics. By applying the gradient expansion technique on the number density function of RNLCPs, we present an approximate, weakly nonlocal theory in differential form in which the intermolecular potential is given by gradients of the number density function of the RNLCP and the volume fraction of the flexible polymer. In the approximate theory, the elastic stress is augmented by an extra stress tensor due to the spatial convection of the macroscopic material point and long range interaction, whose divergence yields the analogous extra elastic body force with respect to the nonlocal intermolecular potential. Finally, we compare the model in steady simple shear with the Doi theory for bulk monodomains of rodlike nematic polymers.

Journal Article↗

Affinity partitioning. A method for purification of proteins using specific polymer-ligands in aqueous polymer two-phase systems.

We describe a method, called affinity partitioning, for the purification of proteins containing specific ligand binding receptor sites. This method adds specificity to the procedures for protein purification with aqueous polymer two-phase systems by introduction of a polymer derivative, coupled to an appropriate ligand. The addition of a polymer-ligand that partitions predominantly into one phase shifts the protein that binds this substance to the same phase. By performing countercurrent distribution in the presence of a polymer-ligand, the protein that binds the polymer-ligand can be separated from a heterogenous mixture. One example of affinity paritioning used dextran as the polymer-ligand. Dextran was chosen since it is a constituent of the most commonly used system for partitioning proteins. In a dextran-poly(ethylene oxide) system, concanavalin A bound dextran and partitioned predominantly into the dextran-rich phase. The addition of the specific competitor, D-mannose, displaced the partition coefficient toward unity, while the application of L-fucose, a noncompetitor, had little effect. Application of affinity partitioning to the purification of another protein required the synthesis of a specific polymer-ligand. To study this we synthesized dinitrophenyl-poly-(ethylene oxide), which binds specifically to S-23 myeloma protein. Addition of dinitrophenyl-poly(ethylene oxide) to the dextran-poly(ethylene oxide) phase system shifted the S-23 myeloma protein into the poly(ethylene oxide)-rich phase. epsilon-N-dinitrophenyl-L-lysine, by competing with binding of dinitrophenyl-poly(ethylene oxide), antagonized the latter's effect on the partition coefficient of S-23 myeloma protein. By adding various amounts of dinitrophenyl-poly-(ethylene oxide), we correlated the partition coefficient with concentration of polymer-ligand. A model of the action of polymer-ligand derivatives on the partition coefficient, derived from thermodynamic considerations, was found to be consistent with the experimental data relating the concentration of polymer-ligand and partition coefficient. Affinity partitioning should prove to be a useful complement to affinity chromatography in the purification of mixtures of proteins. Since cells and subcellular particles may be purified with aqueous polymer two-phase systems, affinity partitioning might be applied to their fractionation by using polymer-ligands specific for unique surface receptors.

Animals↗

Polymers with thiol groups: a new generation of mucoadhesive polymers?

PURPOSE: To improve the mucoadhesive properties of polycarbophil by the introduction of sulfhydryl groups. METHODS: Mediated by a carbodiimide, cysteine was covalently bound to polycarbophil (PCP) forming amide bonds between the primary amino group of the amino acid and the carboxylic acid moieties of the polymer. The amount of covalently attached cysteine and the formation of disulfide bonds within the modified polymer were determined by quantifying the share of thiol groups on the polymer conjugates with Ellman's reagent. The adhesive properties of polycarbophil-cysteine conjugates were evaluated in vitro on excised porcine intestinal mucosa by determining the total work of adhesion (TWA). RESULTS: Depending on the weight-ratio of polycarbophil to cysteine at the coupling reaction, e.g., 16:1 and 2:1, 0.6+/-0.7 micromole and 5.3+/-2.4 micromole cysteine, respectively, were covalently bound per g polymer. The modified polymer displayed improved internal cohesive properties due to the formation of interchain disulfide bonds within the polymer in aqueous solutions at pH-values above 5. Adhesion studies revealed strongly improved adhesive properties. Whereas the TWA was determined to be 104+/-21 microJ for the unmodified polymer, it was 191+/-47 microJ for the polymer-cysteine conjugate 16:1 and 280+/-67 microJ for the polymer-cysteine conjugate 2:1. CONCLUSIONS: Polymers with thiol groups might represent a new generation of mucoadhesive polymers displaying comparatively stronger adhesive properties.

Acrylic Resins↗

Surface Modification of Conventional Polymers by Depositing Plasma Polymers of Trimethylsilane and of Trimethylsilane + O2.

The dynamic wetting properties of TMS (trimethylsilane) and TMS + O2 plasma-deposited films on ten low energy conventional polymers were investigated using the Wilhelmy balance method. Plasma deposition resulted in wetting properties that were independent of the underlying polymer substrate for the majority of polymers studied. TMS plasma modification resulted in virtually the same degree of hydrophobicity with an average cosine of the dynamic advancing contact angle from the first immersion, cos &theta;D,a,1 = -0.381 (&theta;D,a,1 = 112 +/- 3.6), for eight of the ten polymers. PTFE and UHMWPE were slightly more hydrophobic after TMS plasma treatment with an average cos &theta;D,a,1 = -0.785 (&theta;D,a,1 = 141 +/- 4.2). TMS + O2 plasma modification resulted in high wettability of all polymers with an average cos &theta;D,a,1 = 0.654 (&theta;D,a,1 = 49.2 +/- 11.7). Dynamic hysteresis, mainly a result of the change in meniscus shape during immersion and emersion, and intrinsic hysteresis, due to the extent of surface configuration change, were both found to vary according to the size of the polymer plate. In general, dynamic hysteresis can be quite large for more hydrophobic TMS treated polymers and considerably smaller for highly hydrophilic TMS + O2 treated polymers. The extent of intrinsic hysteresis of only TMS treated polymers was found to be independent of the underlying polymers within the time-scale of wetting. TMS + O2 plasma treatment resulted in wide variations in intrinsic hysteresis probably due to substrate specific etching of oxygen plasma species. The wettability of the untreated and TMS and TMS + O2 treated polymers, indicated by the static "advancing" contact angles from the sessile droplet method and dynamic "advancing" and "receding" contact angles from the Wilhelmy balance method, were found to conform well to the correlation, cos &theta;S = (cos &theta;D,a,1 + cos &theta;D,r,1)/2. Copyright 1999 Academic Press.

Journal Article↗

Influence of protein on polysiloxane polymer formation: evidence for induction of complementary protein-polymer interactions.

Results presented in the companion paper suggested that the protein itself might be actively involved in the polymerization process while being entrapped in polysiloxane polymers. It was speculated that the organo-functional side chains on the silanol monomers (or small oligomers) tended to associate with complementary residues on the protein surface during the polymerization process. This phenomenon might lead to complementary binding pockets for the protein on the polymer. To investigate this possibility, polysiloxane polymers were prepared from 3-aminopropyltriethoxysilane and tetraethylorthosilicate (1:3) in the presence of two proteins: urease and BSA. The entrapped proteins were removed by pronase digestion and washing and the resulting polymers evaluated for their ability to again bind the two proteins. It was found that urease preferentially bound to the polymer made in the presence of urease, and BSA preferentially bound to the polymer made in the presence of BSA. The absolute preferential binding excess was greater (30%) for urease binding relative to that observed for BSA (3%). However, in both cases the same relative binding ratio of 1.5 or 50% excess was found. A similar study using the closely related hemoglobin and myoglobin proteins failed to show comparable excess binding in the presence of the predetermined protein. In the latter case, it was demonstrated that the rebound proteins did not equilibrate with labeled solution proteins, indicating a very tight association with the polymer surface possibly masking any specificity which existed. However, it was possible to show that urea release of rebound hemoglobin from the polymer made in the presence of hemoglobin was less than for myoglobin bound to the same polymer and visa versa, again suggesting induced properties unique to the polymer prepared with the predetermined protein. To the extent that this notion of induced complementary order is correct, it may have implications in the development of protein specific adsorbants and in our understanding of polymer surface adhesion and the molding of template fine structure.

Binding Sites↗

Polymer-bridged gels of nanoparticles in solutions of adsorbing polymers.

We use a combination of polymer mean field theory and Monte Carlo simulations to study the polymer-bridged gelation, clustering behavior, and elastic moduli of polymer-nanoparticle mixtures. Polymer self-consistent field theory is first numerically implemented to quantify both the polymer induced interparticle interaction potentials and the conformational statistics of polymer chains between two spherical particles. Subsequently, the formation and structure of polymer-bridged nanoparticle gels are examined using Monte Carlo simulations. Our results indicate a universality in the fractal structure for the polymer-bridged networks over a wide range of parametric conditions. Explicitly, near the gelation transition, the fractal dimension d(f) ranges between 2.2 and 2.5, and above the gelation thresholds, the elastic moduli are found to follow a universal power law G(') proportional, variant(eta-eta(c))(nu(eta) ) with a critical exponent nu(eta) approximately 1.82. The latter suggests strong similarities between polymer-bridging induced percolation and classical elastic resistor network percolation. Our results show a very good agreement with the experimental results for polymer-particle mixtures and suggest a possible framework for experimentally distinguishing the origins of gelation phenomena observed in polymer-particle mixtures.

Journal Article↗