PubMed Health⌕ Search

Biomedical subjects

Paul F Nealey

Publications and source records attributed to Paul F Nealey.

At least 19 recordsLinked to original sources

Phase behavior of symmetric ternary block copolymer-homopolymer blends in thin films and on chemically patterned surfaces.

The phase diagram of symmetric ternary blends of diblock copolymers and homopolymers in thin films was determined as a function of increasing volume fraction of homopolymer (phi(H)) and was similar to that for these materials in the bulk. Blends with compositions in the lamellar region of the diagram (phi(H)< or =0.4) could be directed to assemble into ordered lamellar arrays on chemically striped surfaces if the characteristic blend dimension (L(B)) and the period of the stripes (L(S)) were commensurate such that L(S)=L(B)+/-0.10L(B). Blends with compositions in the microemulsion region of the diagram (phi(H) approximately 0.6) assembled into defect-free lamellar phases on patterned surfaces with L(S)> or =L(B), but formed coexisting lamellar (with period L(S)) and homopolymer-rich phases when L(S)<L(B).

Journal Article↗

Side-chain-grafted random copolymer brushes as neutral surfaces for controlling the orientation of block copolymer microdomains in thin films.

Random copolymers of P(S-r-MMA-r-HEMA)s with a distribution of surface reactive hydroxyl groups were synthesized to formulate neutral surface layers on a SiO2 substrate. The layers were designed to drive vertical orientation of lamellar microdomains in a top P(S-b-MMA) thin film. Copolymers with a styrene weight fraction (f(St)) of 0.58 and a HEMA fraction (f(HEMA)) ranging from 0.01 to 0.03, with a corresponding MMA fraction (f(MMA)) ranging from 0.41 to 0.39, in the P(S-r-MMA-r-HEMA) copolymer showed neutral surface characteristics. The morphology of block copolymer thin films was studied by scanning electron microscopy (SEM). P(S-r-MMA-r-HEMA) copolymers prepared by both living and classical free-radical polymerizations were equally effective in demonstrating the neutrality of the surface. These side-chain-grafted random copolymer brushes showed faster grafting kinetics than the end-chain-grafted P(S-r-MMA) because of multipoint attachment to the surface. The modified surfaces had a very thin layer of random copolymer brush (5-7 nm), which is desirable for effective pattern transfer. Furthermore, neutral surfaces could be obtained even when the grafting time was reduced to 3 h. These results indicate that the composition of the random copolymer brush, rather than its PDI or molecular weights, is the most important factor in controlling the neutrality of the surface. These results also demonstrate the feasibility of using a third comonomer (C) in the random copolymer brush P(A-r-B-r-C) to alter the interfacial and surface energies of a diblock copolymer (A-b-B).

Journal Article↗

A new method to characterize chemically and topographically nanopatterned surfaces.

Surface chemistry of topographically patterned grooved samples with ridges of 150 nm width, adsorbed with self-assembled monolayers (SAMs) of alkanethiols on gold, have been characterized by near edge X-ray absorption fine structure (NEXAFS) spectroscopy. Analysis reveals that NEXAFS may discriminate between different chemistries adsorbed to the tops, sidewalls and grooves of the patterns.

Coated Materials, Biocompatible↗

The effect of environmental factors on the response of human corneal epithelial cells to nanoscale substrate topography.

We have previously shown that human corneal epithelial cells sense and react to nanoscale substrate topographic stimuli [Teixeira AI, Abrams GA, Bertics PJ, Murphy CJ, Nealey PF. Epithelial contact guidance on well-defined micro- and nanostructured substrates. J Cell Sci 2003;116(10):1881-92; Karuri NW, Liliensiek S, Teixeira AI, Abrams G, Campbell S, Nealey PF, et al. Biological length scale topography enhances cell-substratum adhesion of human corneal epithelial cells. J Cell Sci 2004;117(15):3153-64]. Here we demonstrate that cellular responses to nanoscale substrate topographies are modulated by the context in which these stimuli are presented to cells. In Epilife medium, cells aligned preferentially in the direction perpendicular to nanoscale grooves and ridges. This is in contrast to a previous study where cells cultured in DMEM/F12 medium aligned in the direction parallel to nanoscale topographic features [Teixeira AI, Abrams GA, Bertics PJ, Murphy CJ, Nealey PF. Epithelial contact guidance on well-defined micro- and nanostructured substrates. J Cell Sci 2003;116(10):1881-92]. Additionally, cell alignment in Epilife medium was dependent on pattern pitch. Cells switched from perpendicular to parallel alignment when the pitch was increased from 400 to 4,000 nm. There was a transition region (between 800 and 1,600 nm pitch) where both parallel and perpendicular alignments were favored compared to all other cellular orientations. Cells formed focal adhesions parallel to the substrate topographies in this transition region. On the nano- and microscale patterns, 400 and 4,000 nm pitch, focal adhesions were almost exclusively oriented obliquely to the topographic patterns.

Biocompatible Materials↗

Fabrication of complex three-dimensional nanostructures from self-assembling block copolymer materials on two-dimensional chemically patterned templates with mismatched symmetry.

A study is presented of the self-assembly of a lamella-forming blend of a diblock copolymer and its respective homopolymers on periodically patterned substrates consisting of square arrays of spots, that preferentially attract one component, as a function of pattern dimensions and film thickness. The blend morphology follows the pattern at the substrate and forms a single quadratically perforated lamella (QPL). At intermediate film thicknesses necks connect this QPL to the film surface, resulting in a bicontinuous morphology. The necks do not register with the underlying square lattice but exhibit a substantial amount of hexagonal short-range order. For thicker films we observe bicontinuous morphologies consisting of parallel lamellae with disordered perforations. These results demonstrate a promising strategy for the fabrication of complex interfacial nanostructures from two-dimensional chemically patterned templates.

Journal Article↗

Nano- and microscale holes modulate cell-substrate adhesion, cytoskeletal organization, and -beta1 integrin localization in SV40 human corneal epithelial cells.

Human corneal epithelial cells (HCECs) interface with a basement membrane in vivo that possesses complex nanoscale topographic features. We report that synthetic substrates patterned with nano- and microscale holes differentially modulate the proliferation, shape and adhesion of SV40 human corneal epithelial cells (SV40-HCECs) as a function of feature size: 1) Cell proliferation was inhibited on nanoscale features (features size less than 800 nm in pitch) compared to microscale features or planar substrates in identical culture conditions. 2) Cells on nanoscale holes had a stellate morphology compared to those on microscale features that were more evenly spread. 3) Cells adhered more to nanoscale features than to microscale features when exposed to shear stress in a laminar flow chamber. Transmission electron microscopy showed that cells cultured on the 400 nm pitch patterns had longer and more numerous filopodia and retraction fibers than cells cultured on the 1600 nm pitch patterns. Immunogold labeling of -beta1 integrins revealed that these receptors were localized at the cell periphery and in the aforementioned cytoskeletal elements. Our findings indicate that surface discontinuities and the activation of mechanochemical cell signaling mechanisms may contribute to the observed responses exhibited by SV40-HCECs cultured on nano- and microscale topography.

Cell Adhesion↗

Local mechanical properties of polymeric nanocomposites.

The inclusion of a nanoparticle into a polymer matrix is studied by efficient Monte Carlo simulations. The resulting structural changes in the melt and glass exhibit a strong dependence on the strength of the polymer attraction to the surface of the filler. The mechanical properties of the nanocomposite are analyzed in detail through a formalism that permits calculation of local elastic constants. The average shear and Young's modulus of the nanocomposite are higher than those of the pure polymer for neutral or attractive nanoparticles. For repulsive particles, these moduli are lower. Simulation of local properties reveals that a glassy layer is formed in the vicinity of the attractive filler, contributing to the increased strength of the composite material. In contrast, a region of negative moduli emerges around repulsive fillers, which provides a mechanism for frustration relief and a lowering of the glass transition temperature.

Journal Article↗

Fidelity of micropatterned cell cultures.

Methods that enable the culture of micropatterned cells may help advance our fundamental understanding of cell-cell and cell-surface interactions, while facilitating the development and implementation of cell-based biological assays. However, the long-term stability of the cell patterns can limit the time scales over which such methods can be informative. Here we used self-assembling monolayers (SAMs) to localize the adsorption of baby hamster kidney (BHK-21) cells as well as cells from a murine astrocytoma-derived cell line (delayed brain tumor) in linear arrays. We tested the effects of surface chemistries, fibronectin pre-treatments, array dimensions, and cell types on pattern fidelity. Changes in patterns were monitored by phase-contrast microscopy up to 96 h post-plating, followed by digital imaging, and these changes were quantified by measuring an "intrusion distance" or the average distance cells extend beyond the initial adhesive/non-adhesive boundary. Loss of pattern boundaries involved different mechanisms for different cells. Treatment of patterned surfaces with fibronectin prior to plating of cells tended to promote earlier loss of pattern fidelity, and the extent of pattern loss was further augmented for SAMs formed using hydrophobic monolayers. Finally, reduction of gap spacing between adjacent cell arrays promoted pattern loss.

Adsorption↗

Directed assembly of block copolymer blends into nonregular device-oriented structures.

Self-assembly is an effective strategy for the creation of periodic structures at the nanoscale. However, because microelectronic devices use free-form design principles, the insertion point of self-assembling materials into existing nanomanufacturing processes is unclear. We directed ternary blends of diblock copolymers and homopolymers that naturally form periodic arrays to assemble into nonregular device-oriented structures on chemically nanopatterned substrates. Redistribution of homopolymer facilitates the defect-free assembly in locations where the domain dimensions deviate substantially from those formed in the bulk. The ability to pattern nonregular structures using self-assembling materials creates new opportunities for nanoscale manufacturing.

Journal Article↗

Local dynamic mechanical properties in model free-standing polymer thin films.

High-frequency sinusoidal oscillations of a coarse-grained polymer model are used to calculate the local dynamic mechanical properties (DMPs) of free-standing polymer thin films. The storage modulus G(') and loss modulus G(") are examined as a function of position normal to the free surfaces. It is found that mechanically soft layers arise near the free surfaces of glassy thin films, and that their thickness becomes comparable to the entire film thickness as the temperature approaches the glass transition T(g). As a result, the overall stiffness of glassy thin films decreases with film thickness. It is also shown that two regions coexist in thin films just at the bulk T(g); a melt-like region (G(') G(")) in the middle of the film. Our findings on the existence of a heterogeneous distribution of DMPs in free-standing polymer thin films provide insights into recent experimental measurements of the mechanical properties of glassy polymer thin films.

Journal Article↗

Cooperative modulation of neuritogenesis by PC12 cells by topography and nerve growth factor.

Understanding axonal formation and contact guidance are of critical importance for the design of materials that interface with neuronal tissue. Contact guidance of neurites by topographic features is well known, but the role that topography plays in the modulation of neuritogenesis has not been addressed. To test this, we cultured PC12 cells with a range of nerve growth factor (NGF) concentrations on surfaces with ridge widths ranging from 70 to 1900 nm. We find that neuritogenesis by PC12 cells cultured with sub-optimal concentrations of NGF (25 and 5 ng/ml) is modulated by topographic feature size. The threshold for induction of neuritogenesis was markedly reduced when cells were cultured on ridges of 70 and 250 nm. In contrast, contact guidance of neurites was independent of feature size. These results suggest that the scale of topographic features can act cooperatively with NGF signaling to regulate the formation of neurites. These findings may have general relevance to differentiation processes in neurons as well as in other cell types.

Animals↗

Directed assembly of cylinder-forming block copolymer films and thermochemically induced cylinder to sphere transition: a hierarchical route to linear arrays of nanodots.

A morphological transition from cylinders to spheres was induced in an asymmetric diblock copolymer, poly(styrene)-block-poly(tert-butyl acrylate) (PS-b-PtBA). The periodic arrays of the poly(tert-butyl acrylate) (PtBA) domains were transformed to the ordered poly(acrylic anhydride) (PAA) spheres via the thermal deprotection of tert-butyl acrylate linkages and the subsequent volume change of the minority block. Coupled with techniques to direct the assembly of cylinder-forming block copolymers, this finding provides new routes to fabricate ordered geometries of nanodot arrays.

Acrylates↗

Responses of human keratocytes to micro- and nanostructured substrates.

We have previously shown that human corneal epithelial cells respond to synthetic topographic features with dimensions similar to those found in the native human corneal basement membrane. Epithelial cells integrated inputs from substrate topography and soluble factors in the culture medium to generate alignment responses to substrate topographic anisotropies. Human keratocytes are the main cellular components of the stroma, the tissue that underlies the corneal epithelium. Here we report that keratocytes aligned more strongly than epithelial cells along topographic patterns of grooves and ridges. On patterns with pitches of 800 nm and larger approximately 70% of keratocytes were aligned along the patterns compared to 35% for epithelial cells. On 70 nm-wide ridges on a 400-nm pitch, keratocyte alignment dropped to 45%, whereas epithelial cell alignment remained constant. Similarly to epithelial cells, focal adhesions and associated stress fibers in keratocytes were aligned mainly along the substrate topographies, although oblique orientations were also observed. Furthermore, keratocytes cultured on the nanoscale patterns had fewer stress fibers and focal adhesions than cells cultured on microscale patterns or on smooth substrates.

Cell Movement↗

Mechanical heterogeneities in model polymer glasses at small length scales.

Molecular simulations of a model, deeply quenched polymeric glass show that the elastic moduli become strongly inhomogeneous at length scales comprising several tens of monomers; these calculations reveal a broad distribution of local moduli, with regions of negative moduli coexisting within a matrix of positive moduli. It is shown that local moduli have the same physical meaning as that traditionally ascribed to moduli obtained from direct measurements of local constitutive behaviors of macroscopic samples.

Journal Article↗

Biological length scale topography enhances cell-substratum adhesion of human corneal epithelial cells.

The basement membrane possesses a rich 3-dimensional nanoscale topography that provides a physical stimulus, which may modulate cell-substratum adhesion. We have investigated the strength of cell-substratum adhesion on nanoscale topographic features of a similar scale to that of the native basement membrane. SV40 human corneal epithelial cells were challenged by well-defined fluid shear, and cell detachment was monitored. We created silicon substrata with uniform grooves and ridges having pitch dimensions of 400-4000 nm using X-ray lithography. F-actin labeling of cells that had been incubated for 24 hours revealed that the percentage of aligned and elongated cells on the patterned surfaces was the same regardless of pitch dimension. In contrast, at the highest fluid shear, a biphasic trend in cell adhesion was observed with cells being most adherent to the smaller features. The 400 nm pitch had the highest percentage of adherent cells at the end of the adhesion assay. The effect of substratum topography was lost for the largest features evaluated, the 4000 nm pitch. Qualitative and quantitative analyses of the cells during and after flow indicated that the aligned and elongated cells on the 400 nm pitch were more tightly adhered compared to aligned cells on the larger patterns. Selected experiments with primary cultured human corneal epithelial cells produced similar results to the SV40 human corneal epithelial cells. These findings have relevance to interpretation of cell-biomaterial interactions in tissue engineering and prosthetic design.

Actins↗

Ultrastructural basement membrane topography of the bladder epithelium.

The basement membrane underlies epithelium and separates it from deeper tissues. Recent studies suggest that nanoscale topography of the surface of basement membrane may modulate adhesion, migration, proliferation and differentiation of overlying epithelium. This study was performed to elucidate nanoscale topographic features of basement membrane of the bladder. Bladder tissues were obtained from three adult female rhesus macaques. A process was developed to remove the epithelium while preserving the underlying basement membrane, and tissues were evaluated by immunohistochemistry and scanning electron microscopy (SEM). Detailed measurements were made of stereo SEM images to quantitatively define topographic features. Measurements made from multiple SEM images of bladder basement membrane provided the following values for topographic features: mean feature height, 178+/-57 nm; mean fiber diameters, 52+/-28 nm; mean pore diameter, 82+/-49 nm; and mean interpore distance (center to center), 127+/-54 nm. These dimensions are similar to those reported previously for basement membranes of other species and anatomical locations. This information provides a rational basis for design of nanostructured biomaterials to produce composite grafts for repair or replacement of segments of the urinary tract.

Animals↗

Epitaxial self-assembly of block copolymers on lithographically defined nanopatterned substrates.

Parallel processes for patterning densely packed nanometre-scale structures are critical for many diverse areas of nanotechnology. Thin films of diblock copolymers can self-assemble into ordered periodic structures at the molecular scale (approximately 5 to 50 nm), and have been used as templates to fabricate quantum dots, nanowires, magnetic storage media, nanopores and silicon capacitors. Unfortunately, perfect periodic domain ordering can only be achieved over micrometre-scale areas at best and defects exist at the edges of grain boundaries. These limitations preclude the use of block-copolymer lithography for many advanced applications. Graphoepitaxy, in-plane electric fields, temperature gradients, and directional solidification have also been demonstrated to induce orientation or long-range order with varying degrees of success. Here we demonstrate the integration of thin films of block copolymer with advanced lithographic techniques to induce epitaxial self-assembly of domains. The resulting patterns are defect-free, are oriented and registered with the underlying substrate and can be created over arbitrarily large areas. These structures are determined by the size and quality of the lithographically defined surface pattern rather than by the inherent limitations of the self-assembly process. Our results illustrate how hybrid strategies to nanofabrication allow for molecular level control in existing manufacturing processes.

Journal Article↗

Epithelial contact guidance on well-defined micro- and nanostructured substrates.

The human corneal basement membrane has a rich felt-like surface topography with feature dimensions between 20 nm and 200 nm. On the basis of these findings, we designed lithographically defined substrates to investigate whether nanotopography is a relevant stimulus for human corneal epithelial cells. We found that cells elongated and aligned along patterns of grooves and ridges with feature dimensions as small as 70 nm, whereas on smooth substrates, cells were mostly round. The percentage of aligned cells was constant on substrate tomographies with lateral dimensions ranging from the nano- to the micronscale, and increased with groove depth. The presence of serum in the culture medium resulted in a larger percentage of cells aligning along the topographic patterns than when no serum was added to the basal medium. When present, actin microfilaments and focal adhesions were aligned along the substrate topographies. The width of the focal adhesions was determined by the width of the ridges in the underlying substrate. This work documents that biologic length-scale topographic features that model features encountered in the native basement membrane can profoundly affect epithelial cell behavior.

Actin Cytoskeleton↗