Search

Amino-terminated oligoglycines non-covalently self-assemble, through cooperative hydrogen bonding formation, into biocompatible rigid 2D nanostructures called tectomers, either in solution or in surfacepromoted processes. Tectomers effectively coat carboxylated multi-walled carbon nanotubes (MWCNT-COOH) and strongly interact with graphene oxide (GO). Electrostatic interactions and hydrogen bonding formation accounts for the strong interfacial interaction of tectomers with MWCNTCOOH and GO, respectively. The resulting composites were characterized by electron- and atomic force microscopies, UV-vis and X-ray photoelectron (XPS) spectroscopies and contact angle measurements. Because of this high affinity of tectomers to GO, tectomers efficiently coat wet-spun GO fibers (Fig. 1). We also show that, due to their versatile surface chemistry, tectomers act as supramolecular peptidic adhesives for the immobilization of a variety of carbon nanomaterials, nanoparticles, molecules and drugs on the GO fiber surface therefore allowing GO fiber functionalization. The resulting ultrathin coatings exhibit remarkable water-resistant properties. This tectomer-based “double-sided sticky tape” fiber functionalization strategy can be extended to other fibers, fabrics and substrates, making it very attractive for technological and smart textile applications

Amino-terminated oligoglycines non-covalently self-assemble, through cooperative hydrogen bonding formation, into biocompatible rigid 2D nanostructures called tectomers. Tectomers effectively coat carboxylated multi-walled carbon nanotubes (MWCNT-COOH) and strongly interact with graphene oxide (GO). Electrostatic interactions and hydrogen bonding formation accounts for the strong interfacial interaction of tectomers with MWCNT-COOH and GO, respectively. Because of the high affinity of tectomers to GO, tectomers have been used to coat wet-spun GO fibers. We here show that, due to their versatile surface chemistry, tectomers act as supramolecular adhesives for nanomaterial and molecule immobilization on the GO fiber surface. Tectomer-coated GO fibers can then be subsequently decorated with a variety of carbon nanomaterials (carbon nanotubes, carbon nanohorns, carbon nanocones, and highly fluorescent nanodiamonds), metal (gold, platinum, iron) nanoparticles, acrylate-based polymer nanoparticles, fluorophores and drugs. The resulting ultrathin coatings exhibit remarkable water resistant properties. We show that this tectomer-based “double-sided sticky tape” fiber functionalization strategy can be extended to other fibers and fabrics, such as polyurethane/PEDOT:PSS, poly(methyl methacrylate) and polyester, making it very attractive for a variety of technological and smart textile applications.

Amino-terminated oligoglycine two-dimensional (2D) peptide self-assemblies (known as tectomers) have a versatile surface chemistry that allows them to interact with a variety of nanomaterials and to actas supramolecular adhesives for surface functionalization. Here, we have exploited the strong hydrogen-bond based interaction between tectomers and graphene oxide (GO) to functionalize GO fiber surfaces with different carbon nanomaterials (carbon nanotubes, carbon nanohorns, carbon nanocones, and highly fluorescent nanodiamonds), metal (gold, platinum, iron) nanoparticles, acrylate-based polymernanoparticles, fluorophores and drugs. The resulting ultrathin coatings exhibit remarkable water resis-tant properties. This tectomer-mediated fiber decoration strategy allows coating functionalities to be tailored by choosing the appropriate nanomaterials or other molecules. We show that this strategy can be extended to other fibers and fabrics, such as polyurethane/PEDOT:PSS, poly(methyl methacrylate) and polyester, making it very attractive for a variety of technological and smart textile applications.

High quality opal-like photonic crystals containing graphene are fabricated using evaporation-driven self-assembly of soft polymer colloids. A miniscule amount of pristine graphene within a colloidal crystal lattice results in the formation of colloidal crystals with a strong angle-dependent structural color and a stop band that can be reversibly shifted across the visible spectrum. The crystals can be mechanically deformed or can reversibly change color as a function of their temperature, hence their sensitive mechanochromic and thermochromic response make them attractive candidates for a wide range of visual sensing applications. In particular, it is shown that the crystals are excellent candidates for visual strain sensors or integrated time-temperature indicators which act over large temperature windows. Given the versatility of these crystals, this method represents a simple, inexpensive, and scalable approach to produce multifunctional graphene infused synthetic opals and opens up exciting applications for novel solution-processable nanomaterial based photonics., Funding Agencies|EPSRCEngineering & Physical Sciences Research Council (EPSRC) [EP/L02263X/1 (EP/M008576/1), EP/M027791/1]

Melt-electrospinning is an eco-friendly method for producing ultra-fine fibers without using any solvent. We prepared webs of poly(ethylene terephthalate) (PET) through melt-electrospinning using CO2 laser irradiation for heating. The PET webs comprised ultra-fine fibers of uniform diameter (average fiber diameter = 1.66 μm, coefficient of variation = 19%). The co-existence of fibers with high and low molecular orientation was confirmed through birefringence measurements. Although the level of high orientation corresponded to that of commercial highly oriented yarn, crystalline diffraction was not observed in the wide-angle X-ray diffraction (WAXD) analysis of the webs. The crystallinity of the webs was estimated using differential scanning calorimetry (DSC). The fibers with higher birefringence did not exhibit any cold crystallization peak. After annealing the web at 116 °C for 5 min, a further increase in the birefringence of the fibers with higher orientation was observed. The WAXD results revealed that the annealed webs showed crystalline diffraction peaks with the orientation of the c-axis along the fiber axis. In summary, the formation of fibers with a unique non-crystalline structure with extremely high orientation was confirmed.

Engineering of 3D regenerative skeletal muscle tissue constructs (skMTCs) using hydrogels containing muscle precursor cells (MPCs) is of potential benefit for repairing Volumetric Muscle Loss (VML) arising from trauma (e.g., road/industrial accident, war injury) or for restoration of functional muscle mass in disease (e.g., Muscular Dystrophy, muscle atrophy). Additive Biofabrication (AdBiofab) technologies make possible fabrication of 3D regenerative skMTCs that can be tailored to specific delivery requirements of VML or functional muscle restoration. Whilst 3D printing is useful for printing constructs of many tissue types, the necessity of a balanced compromise between cell type, required construct size and material/fabrication process cyto-compatibility can make the choice of 3D printing a secondary alternative to other biofabrication methods such as wet-spinning. Alternatively, wet-spinning is more amenable to formation of fibers rather than (small) layered 3D-Printed constructs. This study describes the fabrication of biosynthetic alginate fibers containing MPCs and their use for delivery of dystrophin-expressing cells to dystrophic muscle in the mdx mouse model of Duchenne Muscular Dystrophy (DMD) compared to poly(DL-lactic-co-glycolic acid) copolymer (PLA:PLGA) topically-seeded with myoblasts. In addition, this study introduces a novel method by which to create 3D layered wet-spun alginate skMTCs for bulk mass delivery of MPCs to VML lesions. As such, this work introduces the concept of “Trojan Horse” Fiber MTCs (TH-fMTCs) and 3d Mesh-MTCs (TH-mMTCs) for delivery of regenerative MPCs to diseased and damaged muscle, respectively.

[Background/ Objectives and Goals] Amino-terminated oligoglycines non-covalently self-assemble, through cooperative hydrogen bonding formation, into biocompatible rigid 2D nanostructures called tectomers, either in solution or in surface-promoted processes [1,2]. We here explore the ability of tectomers to form hybrids with graphene oxide (GO), so the interaction at the interface of these 2D nanomaterials is maximized, providing new functionalities to GO. [Expected Results/ Conclusion/ Contribution] Tectomers strongly interact with GO leading to GO instant flocculation and to the formation of novel multilayered hybrid assemblies. Hydrogen bonding formation accounts for the strong interfacial interaction of tectomers with GO [2]. Because of this high affinity of tectomers to GO, tectomers efficiently coat wet-spun GO fibers. We also show that, due to their versatile surface chemistry, tectomers act as supramolecular peptidic adhesives for the immobilization of a variety of carbon nanomaterials, nanoparticles, molecules and drugs on the GO fiber surface therefore allowing GO fiber functionalization. This tectomer-based functionalization strategy can be extended to other fibers, fabrics and substrates, making it very attractive for technological and smart textile applications [3]., [Methods] GO/tectomer hybrids were prepared by mixing oligoglycine peptide solutions with aqueous GO solutions. The resulting composites were characterized by electron- and atomic force microscopies techniques, by UV-vis and X-ray photoelectron (XPS) spectroscopies, and contact angle measurements.