RESUMEN
Polymers prepared by chemical vapor deposition (CVD) polymerization have found broad acceptance in research and industrial applications. However, their intrinsic lack of degradability has limited wider applicability in many areas, such as biomedical devices or regenerative medicine. Herein, we demonstrate, for the first time, a backbone-degradable polymer directly synthesized via CVD. The CVD co-polymerization of [2.2]para-cyclophanes with cyclic ketene acetals, specifically 5,6-benzo-2-methylene-1,3-dioxepane (BMDO), results in well-defined, hydrolytically degradable polymers, as confirmed by FTIR spectroscopy and ellipsometry. The degradation kinetics are dependent on the ratio of ketene acetals to [2.2]para-cyclophanes as well as the hydrophobicity of the films. These coatings address an unmet need in the biomedical polymer field, as they provide access to a wide range of reactive polymer coatings that combine interfacial multifunctionality with degradability.
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Acetales/química , Técnicas de Química Sintética/métodos , Éteres Cíclicos/química , Etilenos/química , Cetonas/química , Piperidinas/química , Polimerizacion , Polímeros/química , Acetales/síntesis química , Materiales Biocompatibles/síntesis química , Materiales Biocompatibles/química , Ciclización , Éteres Cíclicos/síntesis química , Etilenos/síntesis química , Cetonas/síntesis química , Oxepinas/síntesis química , Oxepinas/química , Piperidinas/síntesis química , Polímeros/síntesis química , VolatilizaciónRESUMEN
We use chemical vapor deposition polymerization to prepare a novel dibromomaleimide-functionalized polymer for selective and reversible binding of thiol-containing biomolecules on a broad range of substrates. We report the synthesis and CVD polymerization of 4-(3,4-dibromomaleimide)[2.2]paracyclophane to yield nanometer thick polymer coatings. Fourier transformed infrared spectroscopy and X-ray photoelectron spectroscopy confirmed the chemical composition of the polymer coating. The reactivity of the polymer coating toward thiol-functionalized molecules was confirmed using fluorescent ligands. As a proof of concept, the binding and subsequent release of cysteine-modified peptides from the polymer coating were also demonstrated via sum frequency generation spectroscopy. This reactive polymer coating provides a flexible surface modification approach to selectively and reversibly bind biomolecules on a broad range of materials, which could open up new opportunities in many biomedical sensing and diagnostic applications where specific binding and release of target analytes are desired.
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Polímeros/química , Fosfinas , Espectroscopía de Fotoelectrones , Polimerizacion , Espectroscopía Infrarroja por Transformada de FourierRESUMEN
Implantable neural microelectrodes that can record extracellular biopotentials from small, targeted groups of neurons are critical for neuroscience research and emerging clinical applications including brain-controlled prosthetic devices. The crucial material-dependent problem is developing microelectrodes that record neural activity from the same neurons for years with high fidelity and reliability. Here, we report the development of an integrated composite electrode consisting of a carbon-fibre core, a poly(p-xylylene)-based thin-film coating that acts as a dielectric barrier and that is functionalized to control intrinsic biological processes, and a poly(thiophene)-based recording pad. The resulting implants are an order of magnitude smaller than traditional recording electrodes, and more mechanically compliant with brain tissue. They were found to elicit much reduced chronic reactive tissue responses and enabled single-neuron recording in acute and early chronic experiments in rats. This technology, taking advantage of new composites, makes possible highly selective and stealthy neural interface devices towards realizing long-lasting implants.
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Electrodos Implantados , Microelectrodos , Potenciales Sinápticos , Animales , Carbono/química , Fibra de Carbono , RatasRESUMEN
A multifunctional copolymer with both aldehyde and alkyne groups is synthesized by chemical vapor deposition (CVD) for orthogonal co-immobilization of biomolecules. Surface analytical methods including FTIR and XPS are used to confirm the surface modification. Heparin-binding growth factors [basic fibroblast growth factor (bFGF) in this study] can be immobilized through interaction with heparin, which was covalently attached to the CVD surface through an aldehyde-hydrazide reaction. In parallel, an alkyne-azide reaction is used to orthogonally co-immobilize an adhesion peptide as the second biomolecule.
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Factor 2 de Crecimiento de Fibroblastos/química , Heparina/química , Polímeros/química , Aldehídos/química , Alquinos/química , Azidas/química , Factor 2 de Crecimiento de Fibroblastos/metabolismo , Gases/química , Heparina/metabolismo , Proteínas Inmovilizadas/química , Proteínas Inmovilizadas/metabolismo , Microscopía Fluorescente , Polimerizacion , Propiedades de SuperficieRESUMEN
Controlled presentation of biomolecules on synthetic substrates is an important aspect for biomaterials development. If the immobilization of multiple biomolecules is required, highly efficient orthogonal surface chemistries are needed to ensure the precision of the immobilization. In this communication, chemical vapor deposition (CVD) copolymerization is used to fabricate polymer coatings with controlled ratio of alkyne and pentafluorophenyl ester (Pfp-ester) groups. Cyclic argine-glycine-aspartic acid (cRGD) adhesion peptide and epidermal growth factor (EGF) are immobilized through alkyne-azide cycloaddtion ("click" chemistry) and active ester-amine reaction, respectively. Cell studies with human umbilical vein endothelial cells (HUVEC) and A431 cell lines demonstrate the biological activity of the coimmobilized biomolecules.
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Factor de Crecimiento Epidérmico/metabolismo , Oligopéptidos/metabolismo , Polímeros/química , Alquinos/química , Aminas/química , Azidas/química , Línea Celular Tumoral , Química Clic , Factor de Crecimiento Epidérmico/química , Ésteres , Gases/química , Células Endoteliales de la Vena Umbilical Humana , Humanos , Proteínas Inmovilizadas/química , Proteínas Inmovilizadas/metabolismo , Oligopéptidos/químicaRESUMEN
Biomolecular interactions between proteins and synthetic surfaces impact diverse biomedical fields. Simple, quantitative, label-free technologies for the analysis of protein adsorption and binding of biomolecules are thus needed. Here, we report the use of a novel type of substrate, poly-p-xylylene coatings prepared by chemical vapor deposition (CVD) polymerization, for surface plasmon resonance enhanced ellipsometry (SPREE) studies and assess the reactive coatings as spatially resolved biomolecular sensing arrays. Prior to use in binding studies, reactive coatings were fully characterized by Fourier transform infrared spectroscopy, electrochemical impedance spectroscopy, and ellipsometry. As a result, the chemical structure, thickness, and homogeneous coverage of the substrate surface were confirmed for a series of CVD-coated samples. Subsequent SPREE imaging and fluorescence microscopy indicated that the synthetic substrates supported detectable binding of a cascade of biomolecules. Moreover, analysis revealed a useful thickness range for CVD films in the assessment of protein and/or antigen-antibody binding via SPREE imaging. With a variety of functionalized end groups available for biomolecule immobilization and ease of patterning, CVD thin films are useful substrates for spatially resolved, quantitative binding arrays.
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Técnicas de Química Analítica/métodos , Fibrinógeno/análisis , Polímeros/química , Técnicas de Química Analítica/instrumentación , Técnicas Electroquímicas/métodos , Fibrinógeno/metabolismo , Microscopía de Fuerza Atómica , Estructura Molecular , Unión Proteica , VolatilizaciónRESUMEN
Along with traditional attributes such as the size, shape, and chemical structure of polymeric micro-objects, control over material distribution, or selective compartmentalization, appears to be increasingly important for maximizing the functionality and efficacy of biomaterials. The fabrication of tri- and tetracompartmental colloids made from biodegradable poly(lactide-co-glycolide) polymers via electrohydrodynamic co-jetting is demonstrated. The presence of three compartments is confirmed via flow cytometry. Additional chemical functionality is introduced via the incorporation of acetylene-functionalized polymers into individual compartments of the particles. Direct visualization of the spatioselective distribution of acetylene groups is demonstrated by confocal Raman microscopy as well as by reaction of the acetylene groups with azide-biotin via 'click chemistry'. Biotin-streptavidin binding is then utilized for the controlled assembly and orientation of bicompartmental particles onto functionalized, micropatterned substrates prepared via chemical vapor deposition polymerization.
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Coloides/química , Nanotecnología/métodos , Anisotropía , Materiales Biocompatibles/química , Polímeros/químicaRESUMEN
We report that nanostructuring via dip-pen nanolithography can be used for modification of a broad range of different substrates (polystyrene, Teflon, stainless steel, glass, silicon, rubber, etc.) without the need for reconfiguring the underlying printing technology. This is made possible through the use of vapor-based coatings that can be deposited on these substrates with excellent conformity, while providing functional groups for subsequent spatially directed click chemistry via dip-pen nanolithography. Pattern quality has been compared on six different substrates demonstrating that this approach indeed results in a surface modification protocol with potential use for a wide range of biotechnological applications.
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Nanotecnología/métodos , Impresión/métodos , Xilenos/química , Química Clic , Propiedades de Superficie , VolatilizaciónRESUMEN
We report a two-step chemical vapor deposition (CVD) method for fabrication of hierarchical polymer-coated carbon nanotube (CNT) microstructures having tunable mechanical properties and accessible chemical functionality. Diverse geometries of vertically aligned CNTs were grown from lithographically patterned catalyst films, and the CNT microstructures were chemically functionalized via poly[4-trifluoroacetyl-p-xylylene-co-p-xylylene] made by chemical vapor deposition polymerization. The polymer coating conformally coated the individual CNTs and CNT bundles within the CNT "forest". The chemical structure of the polymer films was verified by X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR). Simple control of the mechanical properties of the nanocomposite structures can be achieved by adjusting the deposition times during CVD polymerization. Increasing the polymer film thickness from 10 nm to 27 nm resulted in a change of the Young's modulus from 65 to 80 MPa. These values are substantially higher than the 36 MPa measured for the as-grown CNTs without polymer coating. The effect of the polymer coating in reinforcing the connectivity among CNTs within the structures has been understood using an analytical model. Finally, chemical functionality of the CNT composite structures after CVD polymerization was verified by a 4-fold fluorescence enhancement after binding of a dye to the coated CNT microstructures. This technique can be adapted to a wide variety of reactive coatings and facilitates attachment of chemical groups and functional nanostructures on the surfaces of the CNTs; therefore, this material could serve as a tunable platform for coupling mechanical and chemical responses in materials for environmental and biological sensing.
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Biocompatible anisotropic polymer particles with bipolar affinity towards human endothelial cells are a novel type of building blocks for microstructured biohybrid materials, report Joerg Lahann and co-workers on p. 4920. Functional polarity due to two biologically distinct hemispheres has been achieved by synthesis of anisotropic particles via electro-hydrodynamic co-jetting of two different polymer solutions and subsequent selective surface modification.
RESUMEN
Biocompatible anisotropic polymer particles with bipolar affinity towards human endothelial cells are a novel type of building blocks for microstructured bio-hybrid materials. Functional polarity due to two biologically distinct hemispheres has been achieved by synthesis of anisotropic particles via electro-hydrodynamic co-jetting of two different polymer solutions and subsequent selective surface modification.
RESUMEN
Polyethersulfone (PES)-organophilic montmorillonite (OMMT) hybrid particles, with various proportions of OMMT, were prepared by using a liquid-liquid phase separation technique, and then were used for the removal of bisphenol A (BPA) from aqueous solution. The adsorbed BPA amounts increased significantly when the OMMT were embedded into the particles. The structure of the particle was characterized by using scanning electron microscopy (SEM); and these particles hardly release small molecules below 250 degrees C which was testified by using thermogravimetric analysis (TGA). The experimental data of BPA adsorption were adequately fitted with Langmuir equations. Three simplified kinetics model including the pseudo-first-order (Lagergren equation), the pseudo-second-order, and the intraparticle diffusion model were used to describe the adsorption process. Kinetic studies showed that the adsorbed BPA amount reached an equilibrium value after 300 min, and the experimental data could be expressed by the intraparticular mass transfer diffusion model. Furthermore, the adsorbed BPA could be effectively removed by ethanol, which indicated that the hybrid particles could be reused. These results showed that the PES-OMMT hybrid particles have the potential to be used in the environmental application.
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Bentonita/química , Fenoles/aislamiento & purificación , Polímeros/química , Sulfonas/química , Adsorción , Compuestos de Bencidrilo , Cinética , Microscopía Electrónica de RastreoRESUMEN
Polyethersulfone (PES) dead-end tubes were fabricated by means of a phase inversion technique, and then were used as scaffolds for artificial lacrimal glands. The wall of the dead-end tubes could allow nutrients such as ascorbic acid, L-tryptophan, and glucose to pass through, but prevents rat IgG from passing through. Lacrimal acinar epithelial cells of Sprague-Dawley rats were cultured in vitro, and cell-associated secretory component was detected with an immunofluorescence technique to identify the acinar cells. The second passage of the cells showed high degree of cellular differentiation, and was used to seed on the PES tubes. The results showed that the PES tube could support the attachment, the growth, and the proliferation of the rat lacrimal acinar cells. Thus, PES is a substrate for the growth of lacrimal acinar cells and may be a useful scaffolding biomaterial for tissue engineering, such as a scaffold for artificial lacrimal glands.
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Órganos Bioartificiales , Células Epiteliales , Aparato Lagrimal , Polímeros , Sulfonas , Ingeniería de Tejidos , Animales , Células Cultivadas , Células Epiteliales/ultraestructura , Aparato Lagrimal/ultraestructura , Masculino , Permeabilidad , Ratas , Ratas Sprague-DawleyRESUMEN
GOAL: We extend a classic signal processing algorithm, the lock-in amplifier, to two dimensions to extract the signal in patterned images. METHODS: The algorithm was evaluated using simulated image data and experimental microscopy images to determine the fluorescence signal of fluorescently labeled proteins adsorbed on surfaces patterned with chemical vapor deposition. RESULTS: The algorithm was capable of retrieving the signal with a signal-to-noise ratio as low as -20 dB. Optimal parameters were determined for the pattern design. CONCLUSION: The lock-in algorithm is a powerful technique for 1/f noise removal. SIGNIFICANCE: The methodology holds promise not only for the measurement of adsorption events on patterned surfaces but in all situations where a signal has to be extracted from a noisy background in two or more dimensions.
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Algoritmos , Procesamiento de Imagen Asistido por Computador/métodos , Procesamiento de Señales Asistido por Computador , Simulación por Computador , MicroscopíaRESUMEN
The precise modulation of fluorescence interference contrast is achieved by introducing a nanoscopically engineered spacer layer prepared by chemical vapor deposition (CVD) of functional polymers. These novel imaging substrates are chemically identical throughout their entire detection area, yet present patterns of nanoscale thickness. A protein binding cascade is studied in real time and in the presence of high background noise.
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Nanoestructuras/química , Polímeros/química , Adsorción , Animales , Bovinos , Fluoresceína/química , Oro/química , Microscopía Fluorescente , Espectroscopía de Fotoelectrones , Albúmina Sérica Bovina/química , Propiedades de SuperficieRESUMEN
Immobilization of biomolecules, such as proteins or sugars, is a key issue in biotechnology because it enables the understanding of cellular behavior in more biological relevant environment. Here, poly(4-ethynyl-p-xylylene-co-p-xylylene) coatings have been fabricated by chemical vapor deposition (CVD) polymerization in order to bind bioactive molecules onto the surface of the material. The control of the thickness of the CVD films has been achieved by tuning the amount of precursor used for deposition. Copper-catalyzed Huisgen cycloaddition has then been performed via microcontact printing to immobilize various biomolecules on the reactive coatings. The selectivity of this click chemistry reaction has been confirmed by spatially controlled conjugation of fluorescent sugar recognizing molecules (lectins) as well as cell adhesion onto the peptide pattern. In addition, a microstructured coating that may undergo multiple click chemistry reactions has been developed by two sequential CVD steps. Poly(4-ethynyl-p-xylylene-co-p-xylylene) and poly(4-formyl-p-xylylene-co-p-xylylene) have been patterned via vapor-assisted micropatterning in replica structures (VAMPIR). A combination of Huisgen cycloaddition and carbonyl-hydrazide coupling was used to spatially direct the immobilization of sugars on a patterned substrate. This work opens new perspectives in tailoring microstructured, multireactive interfaces that can be decorated via bio-orthogonal chemistry for use as mimicking the biological environment of cells.
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Química Clic/métodos , Polímeros/química , Xilenos/química , Carbohidratos/química , Cobre/química , Gases/química , Humanos , Polimerizacion , Propiedades de SuperficieRESUMEN
In vivo regenerative gene therapy is a promising approach for bone regeneration and can help to address cell-source limitations through surgical implantation of osteoinductive materials and subsequent recruitment of host-derived cells. Localized viral delivery may reduce the risk of virus dispersion, enhance transduction efficiency, and reduce administration/injection dosing, which subsequently increases patient safety. In this manuscript, we present a custom-tailored strategy to immobilize adenovirus expressing runt-related transcription factor 2 (AdRunx2) by using reactive polymer coatings to enhance in vitro osteoblast differentiation of bone marrow stromal cells (BMSCs). A thin polymer film of poly[p-xylylene carboxylic acid pentafluorophenol ester-co-p-xylylene] equipped with amine-reactive active ester groups was deposited on the surface of poly (epsilon-caprolactone) (PCL) using the chemical vapor deposition (CVD) polymerization technique and then anti-adenovirus antibody was conjugated on the material with an amide chemical bond. Following antibody conjugation, AdRunx2 was conjugated to the PCL surface through antibody-antigen interaction. Osteoblast differentiation of BMSCs was induced by incubation in osteogenic medium. Alkaline phosphatase (ALP) activity, calcium deposition, and matrix mineralization were confirmed as markers of osteoblast formation. Incubation of the BMSCs in the presence of AdRunx2 modified PCL resulted in a 6.5-fold increase in ALP activity and significant increases in matrix mineralization when compared to controls. These results demonstrate that adenovirus vectors driving the expression of transcription factors can be delivered directly from biomaterials to direct cell differentiation.
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Células de la Médula Ósea/citología , Diferenciación Celular , Subunidad alfa 1 del Factor de Unión al Sitio Principal/fisiología , Osteoblastos/citología , Poliésteres , Células del Estroma/citología , Fosfatasa Alcalina/metabolismo , Animales , Western Blotting , Ratones , Ratones Endogámicos C57BLRESUMEN
A polyethersulfone (PES) membrane was modified by blending with a co-polymer of acrylic acid (AA) and N-vinyl pyrrolidone (VP), followed by immobilization of bovine serum albumin (BSA) onto the surface. The scanning electron microscopy results showed that PES had good miscibility with the co-polymer. X-ray photoelectron spectroscopy confirmed the existence of P(VP-AA) co-polymer on the surface of the blended membrane and the existence of BSA after the immobilization process. The amount of BSA immobilized on the surface of the membranes was determined. It was found that the protein adsorption amounts from BSA, human plasma fibrinogen and diluted human plasma solutions decreased significantly after modification. According to the circular dichroism results, the proteins kept more alpha-helix conformation in the modified membranes than in the pure PES membrane. The number of the adhered platelets was reduced, and the morphology change for the adherent platelets was also suppressed by the modification with BSA. The SEM morphological observation of the cells and the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay demonstrated that the BSA-modified PES membrane surface promoted endothelial cell adhesion and proliferation.