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Nori Yamaguchi

Publications and source records attributed to Nori Yamaguchi.

6 recordsLinked to original sources

Spontaneous formation of an exfoliated polystyrene-clay nanocomposite using a star-shaped polymer.

Mixtures of five-arm star polystyrene with an organoclay spontaneously formed exfoliated nanocomposites when annealed, validating a recent theoretical prediction by Singh and Balazs (Polym. Int. 2000, 49, 469.). An analogous linear polystyrene sample produced only an intercalated morphology under the same conditions. The nanocomposite morphologies were characterized by X-ray diffraction and transmission electron microscopy. These results suggest a general strategy for forming exfoliated nanocomposites in commodity polymers via melt compounding.

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Supramolecular pseudorotaxane polymers from complementary pairs of homoditopic molecules.

Self-assembly of supramolecular pseudorotaxane polymers from complementary homoditopic building blocks comprised of bis(dibenzo-24-crown-8) esters derived from the hydroxymethyl crown ether and aliphatic diacid chlorides (CxC, x = number of methylene units in the diacid segment) and 1,10-bis[p-(benzylammoniomethyl)phenoxy]alkane bis(hexafluorophosphate)s (AyA, y = number of methylene units in the linker) has been studied. (1)H NMR spectroscopic studies of bis[(2-dibenzo-24-crown-8)methyl] sebacate (C8C) with dibenzylammonium hexafluorophosphate (6) showed that the two binding sites of the ditopic host are equivalent and independent (no positive or negative cooperativity). Likewise the binding sites in 1,10-bis[p-(benzylammoniomethyl)phenoxy]decane bis(hexafluorophosphate) (A10A) were shown to behave independently with dibenzo-24-crown-8 (1a). Then using (1)H NMR spectroscopy on dilute equimolar solutions (<1 mM) of CxC and AyA association constants were estimated for the formation of the linear (lin-CxC*AyA) and cyclic (cyc-CxC*AyA) dimers, thus enabling effective molarities to be estimated for the various systems. Finally (1)H NMR spectroscopy was used to semiquantitatively or qualitatively demonstrate the formation of linear supramolecular polymers lin-[CxC*AyA](n) in more concentrated solutions (up to 2.0 M) of the complementary pairs of CxC and AyA. The sizes of the assemblies (n values) are not as great as the dilute solution studies predict; this is attributed to the deleterious effect of ionic strength and exo complexation at high concentrations. However, as expected from the dilute solution results, linear extension is indeed favored with the longer building blocks, meaning that "monomer" end-to-end distance is a key factor in reducing the amount of cyclic species that form. Viscosity experiments clearly demonstrate the formation of large noncovalent polymers lin-[CxC*AyA](n) in concentrated solutions. Cohesive film and fiber formation also indicate that supramolecular polymers of sufficient size to enable entanglement self-assemble in these solutions.

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Cooperative self-assembly of dendrimers via pseudorotaxane formation from a homotritopic guest molecule and complementary monotopic host dendrons.

Interaction of the homotritopic guest 1,3,5-tris[p-(benzylammoniomethyl)phenyl]benzene tris(hexafluorophosphate) (1a) with dibenzo-24-crown-8 (DB24C8) leads to the sequential self-assembly of [2]-, [3]-, and [4]-pseudorotaxanes 7a, 8a, and 9a, respectively. The self-assembly processes were studied using NMR spectroscopy. In CD(3)CN and CD(3)COCD(3) the individual association constants K(1), K(2), and K(3) for 1:1, 1:2, and 1:3 complexes were determined by several methods. Via Scatchard plots, the three NH(2)(+) sites of 1a were shown to behave independently in binding DB24C8. K values (4.4 x 10(2), 1.4 x 10(2), and 41 M(-)(1), respectively, in CD(3)CN) directly determined from signals for the individual complexes (7a, 8a, and 9a) were somewhat higher than those estimated from the Scatchard plot because of concentration dependence, but the ratios of association constants followed the expected statistical order (K(1):K(2):K(3) = 3:1:(1)/(3)). These are believed to be the first evaluations of association constants leading to a [4]-pseudorotaxane. In the less polar CDCl(3), association constants could not be determined because approximately 90% of the dissolved tritopic guest, which by itself is insoluble, was present as the fully loaded [4]pseudorotaxane 9a! Self-assembly of homotritopic guest 1a with benzyl ether dendrons of the first, second, and third generations functionalized at the "focal point" with DB24C8 moieties (3-5) produces pseudorotaxane dendrimers. The self-assembly processes were studied using (1)H NMR spectroscopy. In CD(3)COCD(3) for all three generations the individual association constants K(1), K(2), and K(3) for [2]-, [3]-, and [4]-pseudorotaxane complexes 7c-e, 8c-e, and 9c-e indicated that the self-assembly was cooperative; that is, the ratios of the individual association constants exceeded the expected statistical ratios. Scatchard plots confirmed this behavior. Self-assembly processes in the less polar CDCl(3) were kinetically slow, requiring ca. 1, 2, and 3 days, respectively, for the first, second, and third generation systems to reach equilibrium with 1a; the slow rate is attributed to the insolubility of the homotritopic guest 1a in this medium and the steric demands of the resulting dendrimers. However, only dendrimers of 1:3 stoichiometry, that is, the nanoscopic [4]pseudorotaxanes 9, were formed! Moreover, it is noteworthy that the extent of dissolution of 1a (reflective of the overall association constant which is too high to measure) increases with generation number, presumably because of the more effective screening of the ionic guest by the larger dendrons and perhaps favorable pi-pi and CH-pi interactions. Such cooperative effects suggest a number of applications that can take advantage of the pH-switchable nature of these self-assembly processes.

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Polysaccharide-poly(ethylene glycol) star copolymer as a scaffold for the production of bioactive hydrogels.

The production of polysaccharide-derivatized surfaces, polymers, and biomaterials has been shown to be a useful strategy for mediating the biological properties of materials, owing to the importance of polysaccharides for the sequestration and protection of bioactive proteins in vivo. We have therefore sought to combine the benefits of polysaccharide derivatization of polymers with unique opportunities to use these polymers for the production of bioactive, noncovalently assembled hydrogels. Accordingly, we report the synthesis of a heparin-modified poly(ethylene glycol) (PEG) star copolymer that can be used in the assembly of bioactive hydrogel networks via multiple strategies and that is also competent for the delivery of bioactive growth factors. A heparin-decorated polymer, synthesized by the reaction of thiol end-terminated four-arm star PEG (M(n) = 10 000) with maleimide functionalized low molecular weight heparin (LMWH, M(r) = 3000), has been characterized via (1)H NMR spectroscopy and size-exclusion chromatography; results indicate attachment of the LMWH with at least 73% efficiency. Both covalently and noncovalently assembled hydrogels can be produced from the PEG-LMWH conjugate. Viscoelastic noncovalently assembled hydrogels have been formed on the basis of the interaction of the PEG-LMWH with a PEG polymer bearing multiple heparin-binding peptide motifs. The binding and release of therapeutically important proteins from the assembled hydrogels have also been demonstrated via immunochemical assays, which demonstrate the slow release of basic fibroblast growth factor (bFGF) as a function of matrix erosion. The combination of these results suggests the opportunities for producing polymer-polysaccharide conjugates that can assemble into novel hydrogel networks on the basis of peptide-saccharide interactions and for employing these materials in delivery applications.

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Rheological characterization of polysaccharide-poly(ethylene glycol) star copolymer hydrogels.

Binding interactions between low molecular weight heparin (LMWH) and heparin-binding peptides (HBP) have been applied as a strategy for the assembly of hydrogels that are capable of sequestering growth factors and delivering them in a controlled manner. In this work, the assembly of four-arm star poly(ethylene glycol) (PEG)-LMWH conjugate with PEG-HBP conjugates has been investigated. The interactions between LMWH and the heparin-binding regions of antithrombin III (ATIII) or the heparin interacting protein (HIP) have been characterized via heparin affinity chromatography and surface plasmon resonance (SPR); results indicate that the two peptides have slightly different affinities for heparin and LMWH, and bind LMWH with micromolar affinity. Solutions of the PEG-LMWH and of mixtures of the PEG-LMWH and PEG-HBP were characterized via both bulk rheology and laser tweezer microrheology. Interestingly, solutions of PEG-LMWH (2.5 wt % in PBS) form hydrogels in the absence of PEG-ATIII or PEG-HIP, with storage moduli, determined via bulk rheological measurements, in excess of the loss moduli over frequencies of 0.1-100 Hz. The addition of PEG-ATIII or PEG-HIP increases the moduli in direct proportion to the number of cross-links introduced. Characterization of the hydrogels via microrheology shows the gel microstructure is composed of polymer-rich fibrillar structures surrounded by polymer-depleted buffer. Potential applications of these hydrogels are discussed.

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Functionalizing electrospun fibers with biologically relevant macromolecules.

The development of functionalized polymers that can elicit specific biological responses is of great interest in the biomedical community, as well as the development of methods to fabricate these biologically functionalized polymers. For example, the generation of fibrous matrices with biological properties and fiber diameters commensurate with those of the natural extracellular matrix (ECM) may permit the development of novel materials for use in wound healing or tissue engineering. The goal of this work is, therefore, to create a biologically active functionalized electrospun matrix to permit immobilization and long-term delivery of growth factors. In this work, poly(ethylene glycol) functionalized with low molecular weight heparin (PEG-LMWH) was fabricated into fibers for possible use in drug delivery, tissue engineering, or wound repair applications. Electrospinning was chosen to process the LMWH into fiber form due to the small fiber diameters and high degree of porosity that can be obtained relatively quickly and using small amounts of starting material. Both free LMWH and PEG-LMWH were investigated for their ability to be incorporated into electrospun fibers. Each of the samples were mixed with a carrier polymer consisting of either a 10 wt % poly(ethylene oxide) (PEO) or 45 wt % poly(lactide-co-glycolide) (PLGA). Field emission scanning electron microscopy (FESEM), energy-dispersive X-ray analysis (EDX), UV-vis spectroscopy, and multiphoton microscopy were used to characterize the electrospun matrices. The incorporation of heparin into the electrospun PEO and PLGA fibers did not affect the surface morphology or fiber diameters. The fibers produced had diameters ranging from approximately 100 to 400 nm. Toluidine blue assays of heparin suggest that it can be incorporated into an electrospun matrix at concentrations ranging from 3.5 to 85 mug per milligram of electrospun fibers. Multiphoton microscopy confirmed that incorporation of PEG-LMWH into the matrix permits retention of the heparin for at least 14 days. Improvements in the binding of basic fibroblast growth factor to the electrospun fibers were also observed for fibers functionalized with PEG-LMWH over those functionalized with LMWH alone. The combination of these results suggests the utility for producing electrospun fibers that are appropriately functionalized for use in biomaterials applications.

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