Fast response photochromic textiles from hybrid silica surface coating

In this study, a hybrid silica sol-gel embedded with a photochromic dye has been applied to wool fabric to form a photochromic coating. The treated wool fabrics showed very quick photochromic response. Five different silanes have been used as the silica precursor, and the resultant coating showed slight differences in photochromic performance, fabric washing fastness, and surface hydrophilicity. However, the silica type had a considerable influence on fabric handle property. The silica matrix from the silane containing a long alkyl chain had a very little influence on the fabric handle and better photochromic performance than those from other different silane precursors.     

Biomedical exploitation of chitin and chitosan via mechano-chemical disassembly, electrospinning, dissolution in imidazolium ionic liquids, and supercritical drying

Recently developed technology permits to optimize simultaneously surface area, porosity, density, rigidity and surface morphology of chitin-derived materials of biomedical interest. Safe and ecofriendly disassembly of chitin has superseded the dangerous acid hydrolysis and provides higher yields and scaling-up possibilities: the chitosan nanofibrils are finding applications in reinforced bone scaffolds and composite dressings for dermal wounds. Electrospun chitosan nanofibers, in the form of biocompatible thin mats and non-wovens, are being actively studied: composites of gelatin + chitosan + polyurethane have been proposed for cardiac valves and for nerve conduits; fibers are also manufactured from electrospun particles that self-assemble during subsequent freeze-drying. Ionic liquids (salts of alkylated imidazolium) are suitable as non-aqueous solvents that permit desirable reactions to occur for drug delivery purposes. Gel drying with supercritical CO(2) leads to structures most similar to the extracellular matrix, even when the chitosan is crosslinked, or in combination with metal oxides of interest in orthopedics.     

A molecular modeling approach applied to a study of the photochromic behaviour of screen printed protein and polyamide substrates

A specifically-synthesized water-soluble photochromic acid dye has been applied by screen printing on to silk, wool and nylon. The influence of processing parameters and the nature of the substrate on the photochromic response of the printed materials has been evaluated using specifically-developed colour measurement methodology. The printed substrates show photochromic colour change from weakly coloured to an intense blue colour under sunlight or UV irradiation. In most cases, the photochromic colour build up is higher on wet substrates than after drying. Computer aided molecular modelling techniques have been used to explain aspects of the photochromic behaviour.     

The effect of bentonite concentration on the drug delivery efficacy of a pH-sensitive alginate/bentonite hydrogel

We produced a protein loaded, pH-sensitive alginate-bentonite hydrogel for wound dressings. Alginate is a nontoxic polysaccharide with favorable pH-sensitive properties that make it useful for the intestinal delivery of protein drugs. However, the use of alginate for drug delivery is limited by drug leaching and rapid dissolution of alginate at the higher pH, which may result in lower entrapment efficiency and a burst in the release of entrapped protein drugs. To overcome these problems, we created a novel cross-linked alginate-bentonite hydrogel by combining mineral-rich bentonite with the alginate matrix along with an additive to ensure controlled release. We analyzed the gel in the drug loading process in an aqueous environment by looking at the release profiles of a model protein drug (BSA) from the hydrogel at pH values of 4.5, 5.2 (skin area) and 7.4, 9.2 (wound area). The swelling ratio decreased with bentonite concentration, but did not fall below 6. The rate of drug release was slowest at a pH value of 4.5 and fastest at a pH value of 9.2. The rate of drug release decreased with bentonite concentration. The presence of bentonite prevents the rapid dissolution of alginate at the higher pH, ensuring the controlled release of the entrapped drug.     

Photochromic fabrics with improved durability and photochromic performance

Previously, we have reported a method for producing photochromic wool fabric by applying a thin layer of hybrid silica-photochromic dye onto the wool surface. While the photochromic coating showed a very fast optical response and had little influence on the fabric handle, its durability was poor. In this study, the durability of the photochromic coating layer was improved by introducing epoxy groups into the silica matrix via co-hydrolysis and co-condensation of an alkyl trialkoxysilane compound (ATAS) and 3-glycidoxypropyltrimethoxysilane (GPTMS). The presence of epoxy groups in the silica enhanced both washing and abrasion durability or fastness. In addition, the optical response speed was slightly increased as well. Effects of the type of alkyl silane and the GPTMS/alkyl silane ratio on the coating durability, fabric handle and optical response were examined.     

Mechanical and thermal properties of epoxy composites containing graphene oxide and liquid crystalline epoxy

The graphene oxide (GO) sheets are chemically grafted with γ-etheroxygentrimethoxysilane (KH560) and liquid crystalline epoxy (LCE) is synthesized from 4,4′-bis(2-hydroxyhexoxy)biphenyl (BP₂) and epichlorohydrin before being incorporated into epoxy matrix. Then we present a novel approach to the fabrication of advanced polymer composites from epoxy matrix by incorporation of two modifiers, which are grafted GO (g-GO) and LCE. The mechanical properties of epoxy composites are greatly improved by incorporating LCE/g-GO hybrid fillers. For instance, the addition of 3 wt% hybrid filler (2 wt% g-GO and 1 wt% LCE) into the epoxy matrix resulted in the increases in impact strength by 132.6 %, tensile strength by 27.6 % and flexural strength by 37.5 %. Moreover, LCE/g-GO hybrid fillers are effective to increase thermal decomposition temperature, glass transition temperature, and storage modulus by strong affinity between the fillers and epoxy matrix.     

Facile In-situ Polymerization of Thermotropic Liquid Crystalline Polymers as Thermally Conductive Matrix Materials

Although thermally conductive composites that can efficiently dissipate the heat generated from electronic devices are in high demand, most neat polymers used as matrix materials are problematic because they have poor thermal conductivities. The low thermal conductivity of polymeric materials is caused by structural defects; therefore, it can be improved by increasing the orientational regularity of the polymer chains. Here, main-chain liquid crystalline polymers (LCPs) were designed and synthesized to investigate the effects of liquid crystallinity-induced structural regularity on the thermal conductivity of the polymers. In addition, an in-situ polymerization method was devised for commercial applicability, and the thermal conductivity of the obtained polymer was compared to that of a conventionally polymerized polymer having the same structure. The designed polymers exhibited thermotropic liquid crystalline characteristics, and the polymer with longer spacers between the rigid segments showed relatively higher thermal conductivity exceeding 0.5 W·m^-1· K^-1 after sample preparation by injection molding. In addition, X-ray diffraction analysis revealed that the differences in the thermal conductivity, depending on the molding temperature during specimen preparation, were caused by variations in chain orientation within the same polymer. Based on the obtained results, it was concluded that LCPs are strong candidate matrix materials for thermally conductive composites; the suggested in-situ polymerization method could be applied practically to the polymerization of polyester-type LCPs.     

Thermotropic liquid crystal polymer reinforced poly(butylene terephthalate) composites to improve heat distortion temperature and mechanical properties

Thermotropic liquid crystal polymer (TLCP)-reinforced poly(butylene terephthalate) (PBT) composites were prepared by melt processing. The improvement in the mechanical properties and the processability of the PBT/TLCP composites was attributed to the reinforcing effect by TLCP phase and its well distribution in the PBT matrix. X-ray diffraction results demonstrated that a slow cooling process leads to the thicker lamellar structures and the formation of more regular crystallites in the composites. The incorporation of TLCP improves not only the tensile strength and flexural modulus but also the heat distortion temperature (HDT) of the PBT/TLCP composites. The HDT values of the composites were dependent on TLCP content. The improvement in the HDT values of the PBT/TLCP composites may be explained in terms with the increased flexural modulus, the development of more regular crystalline structures, and the enhancement of the ability of the composites to sustain the storage modulus by TLCP phase. In addition, the simple additivity rule makes it possible to predict the HDT values of the PBT/TLCP composites.     

Studies on the ternary blends of liquid crystalline polymer and polyesters

Thermotropic liquid crystalline polymer made up of poly(p-hydroxybenzoate) (PHB)-poly(ethylene terephthalate) (PET) 8/2 copolyester, poly(ethylene 2,6-naphthalate) (PEN) and PET were mechanically blended to pursue the liquid crystalline phase of ternary blends. Complex viscosities of blends decreased with increasing temperature and PHB content. DSC thermal analysis indicated that glass transition temperature (Tg) and melting temperature (Tm) of blends increased with increasing PHB content. Both tensile strength and initial modulus increased with raising PHB content and take-up speed of monofilaments. In the WAXS diagram, only PEN crystal reflection at 2Θ=15.5^o appeared but PET crystal reflection was not shown in all compositions. The degree of transesterification and randomness of blends increased with blending time but sequential length of both PEN and PET segment decreased.     

Mucoadhesive Chitosan Electrospun Nanofibers Containing Tetracycline and Triamcinolone as a Drug Delivery System

The mucoadhesive Chitosan (CS) nanofibers as a drug delivery system were developed. Chitosan was modified via the immobilization of thiol groups from L-cysteine as a mucoadhesive reagent. The mucoadhesive properties of the chitosan nanofibers were evaluated by tensiometer set and via tensile studies. Drug and mucoadhesive agent loading lead to decrease diameters and increased porous of nanofibers. The release of Tetracycline (Tet) and Triamcinolone (Tri) were increased with increasing immersion time and it became constant at long immersion times. Mucoadhesion studies were done at pH 2–7 and in pH 6 maximum mucoadhesive properties observed. Release studies demonstrated a sustained release of both drug continued up to 48 hours. Microbial studies were performed on the nanofibers. The drug delivery system represented a novel tool for improve the therapeutic efficacy of various drugs that are poorly absorbed from the gastrointestinal tract. Also it is an efficient system for treatment of oral ulceration.     

Cooperative photoinduced two-dimensional condensation in Langmuir films observed using nanosecond pump-probe Brewster angle microscopy

Two-dimensional condensation was initiated in a self-assembled mixed monolayer of spiropyran and octadecanol by a nanosecond laser pulse. The dynamics of the process were monitored using nanosecond pump-probe Brewster angle microscopy. Domain growth followed a power law with a growth exponent of 0.47 at a velocity approaching 20?ms(-1). This represents a limit for the rate of longitudinal signaling of pressure waves through a self-assembled amphiphilic layer at an interface and adds to our understanding of signal transmission rates in biomimetic membranes where morphological change in one region can be signaled to a more remote region.     

Marine Structure Derived Calcium Phosphate–Polymer Biocomposites for Local Antibiotic Delivery

Hydrothermally converted coralline hydroxyapatite (HAp) particles loaded with medically active substances were used to develop polylactic acid (PLA) thin film composites for slow drug delivery systems. The effects of HAp particles within PLA matrix on the gentamicin (GM) release and release kinetics were studied. The gentamicin release kinetics seemed to follow Power law Korsmeyer Peppas model with mainly diffusional process with a number of different drug transport mechanisms. Statistical analysis shows very significant difference on the release of gentamicin between GM containing PLA (PLAGM) and GM containing HAp microspheres within PLA matrix (PLAHApGM) devices, which PLAHApGM displays lower release rates. The use of HAp particles improved drug stabilization and higher drug encapsulation efficiency of the carrier. HAp is also the source of Ca²⁺ for the regeneration and repair of diseased bone tissue. The release profiles, exhibited a steady state release rate with significant antimicrobial activity against Staphylococcus aureus (S. aureus) (SH1000) even at high concentration of bacteria. The devices also indicated significant ability to control the growth of bacterial even after four weeks of drug release. Clinical release profiles can be easily tuned from drug-HAp physicochemical interactions and degradation kinetics of polymer matrix. The developed systems could be applied to prevent microbial adhesion to medical implant surfaces and to treat infections mainly caused by S. aureus in surgery.     

pH sensitive and controlled release system based on cellulose nanofibers-poly vinyl alcohol hydrogels for cisplatin delivery

Delivery of chemotherapy drugs, such as cisplatin, with controlled manner is a significant area of research in cancer treatment. The main purpose of this study was to investigate the in-vitro release of cisplatin from pH sensitive and controlled release hydrogels based on cellulose nanofibers (CNFs) and poly(vinyl alcohol) (PVA). Various hydrogels with different amounts of CNFs were prepared. This novel drug delivery system was characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and scanning electron microscopy (SEM) analyses. By in-vitro experiments the influence of CNFs contents and pH of the release media on the release rate of the drug were investigated. According to the results, the hydrogel containing 1 wt% CNFs in the release media with the pH of 7.4, efficiently sustained the drug release and so can cause to the reduction of side effects of drug. By fitting the experimental data with various kinetic models it was concluded that the release mechanism is best fitted by Korsmeyer-Peppas kinetic model suggesting the diffusion controlled release mechanism. The prepared hydrogel system is suitable for delivery of cisplatin in the small intestine with a controlled manner.     

Color evaluation of one-dimensional photonic crystal on the fabric

In this paper, the theory of 1-D photonic crystal was obtained and explained through the transfer matrix and plane wave method. Here the photonic crystal composed of SiO₂/TiO₂ thin film was assumed to be coated on fabric, the corresponding reflection and outer color can be calculated and found in the chromaticity diagram. Based on the numerical calculation of 1-D photonic crystal on fabric, if the thin film layer number varied, the reflection would change as well, and the color varied accordingly. For a certain layer number, the incident angle also influenced the observed color result. It illustrated that the constitution and observing angle of photonic crystal both influenced the structural color. The theoretical deduction and numerical calculation of photonic crystal on fabric would be very significant for designing our future structural color effect on textiles.     

A Novel Method to Fabricate High Strength Nanofiber Filaments: Morphology,Crystalline Structure,and Thermal and Mechanical Properties

Wet electrospinning is a simple and efficient method to manufacture continuous nanofiber filaments. However, polyacrylonitrile nanofiber filaments collected using a static water bath are limited for application in certain areas due to their low degree of alignment and breaking stress values. To improve these properties, a novel countercurrent flowing liquid bath collector was combined with a multi-needle electrospinning device. The morphologies, crystalline structures, thermal behaviors and mechanical properties of filaments fabricated under different countercurrent bath liquid motion conditions were investigated. In addition, the forces acting on the nanofibers in the bundling triangular zone under countercurrent liquid bath motion were analyzed. The results showed that the average nanofiber diameter of the filaments decreased with an increase in bath solution motion forces. The maximum alignment degree and breaking stress of the nanofibers were 85 % and 0.63 cN/dtex, respectively, achieved using a liquid flow rate of 80 ml/min and water inlet diameter of 6 mm. The alignment degree of the assembled nanofibers in the bundling triangular zone could be increased by 57 % when using a countercurrent flowing liquid compared with a static liquid bath.     

Photoisomerization and photo-induced optical anisotropy of polymethacrylate containing aminonitroazobenzene chromophores in the side chain

Photoresponsive side chain copolymer and homopolymer containing an aminonitroazobenzene were synthesized for studying photoisomerization behavior and photo-induced anisotropy.Trans-to-cis photoisomerization was observed under the exposure of a circularly polarized visible light with UV-Vis absorption spectroscopy. Reorientation of polar azobenzene molecules induced optical anisotropy under a linearly polarized light at 532 nm. Polarized absorption spectroscopy was employed to investigate the anisotropy of the polymer film during irradiation of the excitation light. Layers of two photosensitive polymers were used for aligning liquid crystal (LC) molecules instead of one of the rubbed polyimide layers in the conventional twisted nematic cell. For producing homogeneous alignment of a nematic LC molecule, a linearly polarized light was exposed to the films of two polymers. The stability of the LC alignment upon the linearly polarized light exposure was also studied.     

Nanostructured liquid crystalline particle assisted delivery of 2,4-dichlorophenoxyacetic acid to weeds,crops and model plants

Routine agricultural practices are heavily dependent on the use of surfactants, many of which are toxic to humans and detrimental to the environment. In proof of concept work we have previously shown the potential of nanostructured liquid crystalline particles (NLCP) to safely interact with plant leaf cuticular surfaces with minimal impact on epicuticular waxes. Here we demonstrate the use of NLCP to effectively deliver the auxin herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) to plant leaves in laboratory and field studies. In the laboratory, the physiological stress responses of lupin, Lupinus angustifolius (L.) (Fabaceae) towards NLCP spray applications were shown to be much reduced in comparison with application of two common surfactants. Phytotoxicity assays of 2,4-D loaded NLCP were used to validate the herbicidal effects on Arabidopsis thaliana (L.) Heynth. (Brassicaceae) and established a similarity with that of surfactant assisted 2,4-D delivery when tested at a concentration of 0.1%. Field trials were conducted to test the efficacy of NLCP-assisted delivery of 2,4-D in comparison with commercial surfactants for the control of the invasive weed wild radish, Raphanus raphanistrum (L.) (Brassicaceae), in wheat, Triticum aestivum (L.) (Poaceae) crop fields. Compared against Estercide 800, a commercially available 2,4-D formulation, NLCP assisted delivery of 2,4-D was effective at low concentrations of 0.03% and 0.06%. The crop yield remained similar for all the tested concentrations and formulations of 2,4-D loaded NLCP and Estercide 800. This is the first report to directly show that, as an alternative to conventional methods, NLCP can be used under both laboratory and field conditions to successfully delivery an agrochemical.     

隐花色素基因CRY2延迟拟南芥营养生长时相转变

高等植物的胚后发育经历了2个重要的时相转变,即营养生长时相转变与成花转变。这2个转变都受到内源因子与外源因子的综合调控。调控这两个转变的基因网络存在共同的因子,如部分SPL家族基因。以拟南芥叶片远轴面表皮毛的出现和mi R156的表达量为形态和分子生物学标志,研究参与成花转变的光受体基因CRY2对营养时相转变的影响,结果表明CRY2影响营养生长时相转变,突变体cry2-1的营养生长时相转变推迟。     

Synthesis and characterization of poly(N-tert-butylacrylamide-<Emphasis Type="Italic">co</Emphasis>-acrylamide) hydrogel with enhanced responsive properties

To synthesize a series of novel temperature sensitive hydrogels, N-tert-butylacrylamide (NtBA) and acrylamide (AAm) were used as the comonomers and polymerized by free-radical crosslinking copolymerizarion. The poly(ethylene glycol) (PEG) with molecular weight of 400, 4000 and 6000 g·mol^-1 was used as the porogen. The equilibrium swelling capacity, swelling/deswelling kinetics and diffusion parameters of obtained hydrogels were systematically evaluated. As revealed by SEM micrographs, the macroporous structure of hydrogels can be modulated by the crosslinking level, PEG molecular weight and dosage. FTIR analysis demonstrated that the porogen PEG was completely leached out of the gel matrix. Compared with the conventional hydrogels, the PEG-modified (PGel) hydrogels exhibited enhanced temperature sensitivity and superior kinetics during the swelling, deswelling and pulsatile swelling processes. Controlled release of salicylic acid also demonstrated the good usability of PGel hydrogel, which rendered it great potential for controlled drug delivery systems.     

Preparation and characterization of thermotropic liquid crystal microcapsules and application in textile

In this paper, thermotropic liquid-crystal microcapsules of cholesteric liquid crystal (CLC) as core material and melamine-formaldehyde (M-F) as shell material were prepared via in-situ polymerization. The core material of CLC herein was mixture of cholesteryl oleyl carbonate (COC) and cholesterol pelargonate (CPE). The optimal preparation conditions were assured based on the serial trial experiments. It was found that the prepared CLC microcapsules had spherical shape and smooth surface, and the mean particle size was about 8-10 μm. The FT-IR spectra and SEM images confirmed that the M-F shell was successfully fabricated on the surface of CLC core material. Finally, the CLC microcapsules were treated on the fabric, and the treated fabric showed color change between 33.4 °C and 38.0 °C, which is appropriate for human comfortable feeling. CIE L*a*b* values were obtained, and it confirmed the treated fabric had good color change performance. In this paper, the cholesteric liquid crystal (CLC) showed its excellent ability to change color, and the experiment result also proved that CLC microcapsules for preparing thermotropic fabric is reasonable and practicable.