Experimental composite guidance conduits for peripheral nerve repair: An evaluation of ion release

Poly (lactide-co-glycolide) (PLGA) — Pluronic F127 — glass composites have demonstrated excellent potential, from the perspective of controlled mechanical properties and cytocompatibility, for peripheral nerve regeneration. In addition to controlling the mechanical properties and cytotoxicity for such composite devices, the glass component may mediate specific responses upon implantation via degradation in the physiological environment and release of constituent elements. However, research focused on quantifying the release levels of such therapeutic ions from these experimental medical devices has been limited. To redress the balance, this paper explores the ion release profiles for Si⁴⁺, Ca²⁺, Na⁺, Zn²⁺, and Ce⁴⁺ from experimental composite nerve guidance conduits (CNGC) comprising PLGA (at 12.5, and 20 wt.%), F127 (at 0, 2.5 and 5 wt.%) and various loadings of Si–Ca–Na–Zn–Ce glass (at 20 and 40 wt.%) for incubation periods of up to 28 days. The concentration of each ion, at various time points, was determined using Inductively Coupled Plasma–Atomic Emission Spectrometry (Perkin Elmer Optima 3000). It was observed that the Si⁴⁺, Na⁺, Ca²⁺, Zn²⁺ release from CNGCs in this study ranged from 0.22 to 6.477 ppm, 2.307 to 3.277 ppm, 40 to 119 ppm, and 45 to 51 ppm, respectively. The Ce⁴⁺ concentrations were under the minimum detection limits for the ICP instrument utilized. The results indicate that the ion release levels may be appropriate to mediate therapeutic effects with respect to peripheral nerve regeneration. The data generated in this paper provides requisite evidence to optimize composition for pre-clinical evaluation of the experimental composite.     

Novel,simple and reproducible method for preparation of composite hierarchal porous structure scaffolds

Demand to develop a simple and adaptable method for preparation the hierarchical porous scaffolds for bone tissue regeneration is ever increasing. This study presents a novel and reproducible method for preparing the scaffolds with pores structure spanning from nano, micro to macro scale. A macroporous Sr-Hardystonite (Sr–Ca₂ZnSi₂O₇, Sr–HT) scaffold with the average pore size of ~ 1200 μm and porosity of ~ 95% was prepared using polymer sponge method. The struts of the scaffold were coated with a viscous paste consisted of salt (NaCl) particles and polycaprolactone (PCL) to provide a layer with thickness of ~ 300–800 μm. A hierarchical porous scaffold was obtained with macro, micro and nanopores in the range of 400–900 μm, 1–120 μm and 40–290 nm, after salt leaching process. These scales could be easily adjusted based on the starting foam physical characteristics, salt particle size, viscosity of the paste and salt/PCL weight ratio.     

Cytocompatibility,degradation, mechanical property retention and ion release profiles for phosphate glass fibre reinforced composite rods

Fibre reinforced composites have recently received much attention as potential bone fracture fixation applications. Bioresorbable composites based on poly lactic acid (PLA) and phosphate based glass fibre were investigated according to ion release, degradation, biocompatibility and mechanical retention profiles. The phosphate based glass fibres used in this study had the composition of 40P₂O₅–24MgO–16CaO–16Na₂O–4Fe₂O₃ in mol% (P40). The degradation and ion release profiles for the composites showed similar trends with the amount of sodium and orthophosphate ions released being greater than the other cations and anions investigated. This was attributed to low Dietzal's field strength for the Na⁺ in comparison with Mg^2 + and Ca^2 + and breakdown of longer chain polyphosphates into orthophosphate ions. P40 composites exhibited good biocompatibility to human mesenchymal stem cells (MSCs), which was suggested to be due to the low degradation rate of P40 fibres. After 63 days immersion in PBS at 37 °C, the P40 composite rods lost ~ 1.1% of mass. The wet flexural, shear and compressive strengths for P40 UD rods were ~ 70%, ~ 80% and ~ 50% of their initial dry values after 3 days of degradation, whereas the flexural modulus, shear and compressive strengths were ~ 70%, ~ 80%, and ~ 65% respectively. Subsequently, the mechanical properties remained stable for the duration of the study at 63 days. The initial decrease in mechanical properties was attributed to a combination of the plasticisation effect of water and degradation of the fibre–matrix interface, with the subsequent linear behaviour being attributed to the chemical durability of P40 fibres. P40 composite rods showed low degradation and ion release rates, good biocompatibility and maintained mechanical properties similar to cortical bone for the duration of the study. Therefore, P40 composite rods have huge potential as resorbable intramedullary nails or rods.     

Functionally graded hydroxyapatite-alumina-zirconia biocomposite: Synergy of toughness and biocompatibility

Functionally Gradient Materials (FGM) are considered as a novel concept to implement graded functionality that otherwise cannot be achieved by conventional homogeneous materials. For biomedical applications, an ideal combination of bioactivity on the material surface as well as good physical property (strength/toughness/hardness) of the bulk is required in a designed FGM structure. In this perspective, the present work aims at providing a smooth gradation of functionality (enhanced toughening of the bulk, and retained biocompatibility of the surface) in a spark plasma processed hydroxyapatite-alumina-zirconia (HAp-Al₂O₃-YSZ) FGM bio-composite. In the current work HAp (fracture toughness ~ 1.5 MPa.m^1/2) and YSZ (fracture toughness ~ 6.2 MPa.m^1/2) are coupled with a transition layer of Al₂O₃ allowing minimum gradient of mechanical properties (especially the fracture toughness ~ 3.5 MPa.m^1/2). The in vitro cyto-compatibilty of HAp-Al₂O₃-YSZ FGM was evaluated using L929 fibroblast cells and Saos-2 Osteoblast cells for their adhesion and growth. From analysis of the cell viability data, it is evident that FGM supports good cell proliferation after 2, 3, 4 days culture. The measured variation in hardness, fracture toughness and cellular adhesion across the cross section confirmed the smooth transition achieved for the FGM (HAp-Al₂O₃-YSZ) nanocomposite, i.e. enhanced bulk toughness combined with unrestricted surface bioactivity. Therefore, such designed biomaterials can serve as potential bone implants.     

Fabrication of novel composites of ZnO-nanoparticles and magadiite

Novel composites of ZnO-nanoparticles and magadiite were successfully prepared by a simple ion-exchange technique in an aqueous suspension of magadiite (Na₂Si₁₄O₂₉·nH₂O) and Zn(NO₃)₂. The TEM and STEM measurements showed that the composites have a structure in which ZnO-nanoparticles with relatively uniform particle sizes are well dispersed within the interlaminar spaces of the magadiite matrix. The particle sizes of the ZnO-nanoparticles were found to depend on the heat-treatment temperature; the average particle sizes are ~ 2.6, ~ 2.8, ~ 4.4 and ~ 4.6 nm, respectively, for the temperatures of 40, 180, 300 and 600 °C. It was also found that the ZnO nanoparticles crystallize and form a single-crystalline particle when the temperature exceeds ~ 300 °C.     

Mechanical properties and microstructure of spark plasma sintered nanostructured p-type SiGe thermoelectric alloys

SiGe based thermoelectric (TE) materials have been employed for the past four decades for power generation in radio-isotope thermoelectric generators (RTG). Recently “nanostructuring” has resulted in significantly increasing the figure-of-merit (ZT) of both n and p-type of SiGe and thus nanostructured Si₈₀Ge₂₀ alloys are evolving as a potential replacement for their conventional bulk counterparts in designing efficient RTGs. However, apart from ZT, their mechanical properties are equally important for the long term reliability of their TE modules. Thus, we report the mechanical properties of p-type nanostructured Si₈₀Ge₂₀ alloys, which were synthesized employing spark plasma sintering of mechanically alloyed nanopowders of its constituent elements with 1.2% boron doping. Nanostructured p-type Si₈₀Ge₂₀ alloys exhibited a hardness of ~ 9 ± 0.1 GPa, an elastic modulus of ~ 135 ± 1.9 GPa, a compressive strength of 108 ± 0.2 MPa, and fracture toughness of ~ 1.66 ± 0.04 MPa√m with a thermal shock resistance value of 391 ± 21 Wm^− 1. This combination of good mechanical properties coupled with higher reported ZT of nanostructured p-type Si₈₀Ge₂₀ alloys are rendered to be a potential material for power generation applications, compared to its bulk counterpart.     

Antibacterial effects of silver-doped hydroxyapatite thin films sputter deposited on titanium

Since many orthopedic implants fail as a result of loosening, wear, and inflammation caused by repeated loading on the joints, coatings such as hydroxyapatite (HAp) on titanium with a unique topography have been shown to improve the interface between the implant and the natural tissue. Another serious problem with long-term or ideally permanent implants is infection. It is important to prevent initial bacterial colonization as existing colonies have the potential to become encased in an extracellular matrix polymer (biofilm) that is resistant to antibacterial agents. In this study, plasma-based ion implantation was used to examine the effects of pre-etching on plain titanium. Topographical changes to the titanium samples were examined and compared via scanning electron microscopy. Hydroxyapatite and silver-doped hydroxyapatite thin films were then sputter deposited on titanium substrates etched at ? 700 eV. For silver-doped films, two concentrations of silver (~ 0.5 wt.% and ~ 1.5 wt.%) were used. Silver concentrations in the film were determined using energy dispersive X-ray spectroscopy. Hydroxyapatite film thicknesses were determined by measuring the surface profile using contact profilometry. Staphylococcus epidermidis and Pseudomonas aeruginosa adhesion studies were performed on plain titanium, titanium coated with hydroxyapatite, titanium coated with ~ 0.5 wt.% silver-doped hydroxyapatite, and titanium coated with ~ 1.5 wt.% silver-doped hydroxyapatite. Results indicate that less bacteria adhered to surfaces containing hydroxyapatite and silver; further, as the hydroxyapatite films delaminated, silver ions were released which killed bacteria in suspension.     

High conductive ethylene vinyl acetate composites filled with reduced graphene oxide and polyaniline

A conductive network composed of reduced graphene oxide (RGO) planes and polyaniline (PANI) chains was designed and fabricated by in situ polymerization of aniline monomer on the RGO planes. It was further used for fabrication of conductive composites with a polymer matrix–ethylene vinyl acetate (EVA). The composites achieve improved conductivity at a low filler loading although the host polymer–EVA–is of insulator. For instance, compared to the pure EVA polymer, the conductivity of the composite filled with 4.0 wt.% RGO and 8.0 wt.% PANI increases from 1.2 × 10^?14 S cm^?1 to 1.07 × 10^?1 S cm^?1. In addition, thermal stability of the composites is also enhanced by the filler loading.     

Flexible polymer microtubes and microchannels via electrospinning

Here we report an approach to fabricate flexible polymer self standing films embedded with continuous aligned microtubes/microchannels via electrospinning. The scheme is to wash the electrospun fibers selectively to form either microtubes/microchannels. Optical microscope (OM) and Scanning electron microscope images are evident for the well aligned microtubes and microchannels respectively with a diameter of ~ 8 μm and a length of ~ 4 cm. Meniscus of tetrahydrofuran in the microtubes can be observed explicitly in the OM images. Mutually perpendicular microtubes are also fabricated on a polymer film. Angular distribution of aligned microstructures indicates the standard deviation is not more than 1°. These tubes/channels can be potential for tissue engineering as they could provide a directional template for the growth when a biodegradable polymer such as Poly(vinylalcohol) is used.     

Novel photoluminescent mesogenic Schiff-base ligands bearing [N4O4] donors and their bimetallic Zn(II) complexes

Novel photoluminescent salicylaldimine ligands condensed from 3^/, 3^/, 4^/, 4^/-tetraminobiphenyl and 4-substituted long alkoxy salicylaldehyde possessing two sets of tetradentate [N₂O₂] donor site and their binuclear zinc(II) complexes have been synthesized. The mesogenic and photophysical properties were investigated. The compounds were characterized by FT-IR, ¹H and ¹³C NMR, UV–vis, elemental analyses, solution electrical conductivity measurements and FAB mass spectrometry. The mesomorphic behavior of these compounds was probed by differential scanning calorimetry and polarized optical microscopy. The ligand with six carbon chain length showed monotropic nematic mesomorphism at 128° C. However, the ligand with alkoxy tail of carbon length 12 showed enantiotropic SmC phase. The complexes are devoid of any mesomorphism. The low molar conductance values in CH₂Cl₂ indicate that the complexes are non-electrolytes. At 330 nm excitation, the ligand emits green light at ~ 516 nm (Φ = 30%) and ~ 549 nm (Φ = 16%) in solution and solid state, respectively. At similar excitation wavelength, the complexes exhibit blue light in solution at ~ 452 nm (Φ = 20%) and green light in solid state ~ 555 nm (Φ = 11%). The DFT calculations were performed using DMol3 program at BLYP/DNP level to ascertain the stable electronic structure of the complex.     

Li4Ti5O12/Li3SbO4/C composite anode for high rate lithium-ion batteries

Nanocrystalline Li₄Ti₅O₁₂/Li₃SbO₄/C composite-prepared by mechanical ball-milling of Li₄Ti₅O₁₂ (synthesized by aqueous combustion), Li₃SbO₄ (synthesized by solid state method) and activated carbon, has been investigated as anode in lithium-ion coin cells and compared to pristine Li₄Ti₅O₁₂. Galvanostatic charge–discharge measurements in the potential window of 0.05–2.0 V show three plateau regions corresponding to Li insertion/extraction in the composite: a large flat plateau at ~ 1.52/1.59 V, followed by a second plateau at ~ 0.75/1.1 V and a sloppy tail at ~ 0.4/0.6 V. While the plateaus at ~ 0.4/0.6 V and ~ 1.52/1.59 V correspond to Li₄Ti₅O₁₂, the other one at ~ 0.75/1.1 V corresponds to Li₃SbO₄. At a high rate of ~ 15 C, the capacity for Li₄Ti₅O₁₂/Li₃SbO₄/C composite is found to be 105 mAhg^?1 retaining ~ 78% of its initial capacity compared to only 58 mAhg^?1 (~ 27% of the initial capacity) at 14 C for pristine Li₄Ti₅O₁₂ up to 100 cycles. Thus, such composite material might find application in lithium-ion batteries requiring high rate of charge and discharge.     

Structural and optical properties of chlorinated plasma polymers

Amorphous hydrogenated chlorinated carbon (a-C:H:Cl) films were produced by the plasma polymerization of chloroform–acetylene–argon mixtures in a radiofrequency plasma enhanced chemical vapor deposition system. The main parameter of interest was the proportion of chloroform in the feed, R_C, which was varied from 0 to 80%. Deposition rates of 80 nm min^? 1 were typical for the chlorinated films. Infrared reflection–absorption spectroscopy revealed the presence of C–Cl groups in all the films produced with chloroform in the feed. X-ray photoelectron spectroscopy confirmed this finding, and revealed a saturation of the chlorine content at ~ 47 at.% for R_C ≥ 40%. The refractive index and optical gap, E₀₄, of the films were roughly in the 1.6 to 1.7, and the 2.8 to 3.7 eV range. These values were calculated from transmission ultraviolet–visible-near infrared spectra. Chlorination leads to an increase in the water surface contact angle from ~ 40° to ~ 77°.     

Modification of porous calcium phosphate surfaces with different geometries of bioactive glass nanoparticles

In this study, the effects of bioactive glass nanoparticles' (nBGs) size and shape incorporated into hydroxyapatite/β-tricalcium phosphate (BCP) scaffolds were investigated. We prepared a highly porous (> 85%) BCP scaffold and coated its surface with a nanocomposite layer consisted of polycaprolactone (PCL) and rod (~ 153 nm in height and ~ 29 nm in width) or spherical (~ 33 nm and 64 nm in diameter) nBGs. Osteogenic gene expression by primary human osteoblast-like cells (HOB) was investigated using quantitative real time polymerase chain reaction (q-RT-PCR). We demonstrated for the first time that in vitro osteogenesis is dramatically affected by the shape of the nBGs, whereby rod shaped nBGs showed the most significant osteogenic induction, compared to spherical particles (regardless of their size). Importantly, the good biological effect observed for the rod shaped nBGs was coupled by a marked increase in the modulus (~ 48 MPa), compressive strength (~ 1 MPa) and failure strain (~ 6%), compared to those for the BCP scaffolds (~ 4 MPa, ~ 1 MPa and ~ 0.5% respectively). The findings of this study demonstrated that the shape of the nBGs is of significant importance when considering bone regeneration.     

Preparation and characterization of biocompatible carbon electrodes

Electron transfer in microbial fuel cell and biosensors could be facilitated through high conductive materials with enhanced active surface area and appropriate redox potential suited to microbial metabolism. In the first strategy based on bulk doping, graphite/epoxy composite electrode (GECE) bulk was modified with six types of metal ion which were prepared through a wet impregnation procedure. In the second strategy, immobilization of redox dye on carbon cloth and graphite sheet was carried out using N,N′-dicyclohexylcarbodiimide for surface modification. Crystallinity, morphology, surface chemistry and electrochemical properties of all modified electrodes were investigated. Influence of redox behavior of electrodes suited to microbial metabolism and conducive to biofilm formation have been examined. It was observed that the Fe³⁺ doped GECE surfaces exhibited significantly high biofilm formation of 1.10(±0.18) × 10⁷ CFU/cm² as compared to other dopants. The microbial growth on the carbon cloth electrode and carbon fiber reinforced plate were found to be less (2.6(±0.97) × 10⁴, 4.8(±1.8) × 10³ CFU/cm² respectively) compared to GECEs.     

Characterisation of bacterial cellulose partly acetylated by dimethylacetamide/lithium chloride

Cellulose is a water-insoluble polysaccharide used at an industrial scale for the manufacture of paper and films or in the dust form, natural, hydrolysed or derivatised. The cellulose produced by G. hansenii (former A. xylinum) has a structure identical to that of plants, but is free of lignin and hemicellulose, with several unique physical–chemical properties. The main barrier to the use of cellulose is its insolubility in water and most organic solvents, but soluble derivatives can be obtained with the use of ionic solvents. Bacterial cellulose, produced in a static, 4% glucose medium, was dissolved in hot DMAc/LiCl (120, 150 or 170 °C). The solution was analysed by ¹³C NMR, and the effect of the dissolution on the crystalline state was shown by X-ray crystallography. The crystalline structure was lost upon dissolution, becoming amorphous; this was also observed for Avicel^® plant cellulose. The soluble cellulose was partly acetylated in acetic anhydride with acetic anhydride-cellulose ratios of 1:50, 1:6 and 1:12 (w/v). The resulting cellulose acetates were examined by infrared spectroscopy, and the best result was 43% (w/v). The degree of acetylation was determined via ¹H NMR spectroscopy by comparing the area of the glucose ring at 2.60–5.20 ppm and that of the methyl proton of the acetate group at 1.80–2.20 ppm. The ¹³C NMR spectra showed acetylation at C6 ? C2 > C3 at 60–80 ppm, with C1 signals at ~ 100–104 ppm. The derivatisation of bacterial cellulose in DMAc/LiCl/acetic anhydride (1:4:50, v/v/v) gave rise to 87% substitution. The process of dissolution of the bacterial cellulose is essential for the analysis of the insoluble polymer in water, facilitating analysis and characterisation of these composites by ¹³C NMR spectroscopy, size exclusion chromatography and light scattering techniques.     

Template-assisted electrohydrodynamic atomization of polycaprolactone for orthopedic patterning applications

This paper presents the development of the novel deposition of biodegradable polycaprolactone (PCL) polymer patterns on a metallic substrate using a jet spraying technique, template-assisted electrohydrodynamic atomization (TAEA), at ambient temperature. The structure of patterns was controlled by systematically varying the polymer concentration (2–15 wt.%) and the flow rate (1–25 μl min^? 1). Polymer deposition was carried out in the stable cone-jet mode to precisely control the surface structure and morphology. The patterns were studied by optical microscopy, scanning electron microscopy and profilometry, and a high degree of control over the pattern geometry and thickness was achieved by varying the spraying time. The hardness and the effective elastic modulus of the polymer patterns were estimated using nanoindentation. The effect of load, loading rate and the holding time on the hardness and effective elastic modulus was derived. Optimal results were obtained with 5 wt.% PCL in DMAC solution sprayed within the stable cone-jet mode operating window at a flow rate of 15 μl min^? 1 for 300 s at 11.1 kV with a working distance of 60 mm. Hexagonal patterns were well-defined and repeatable with thickness of ~ 34 μm. The hardness is 1.6 MPa at a loading rate of 0.1 μN/s and nearly halved when the load rate was increased to 1 μN/s. The effective elastic modulus of ~ 12 MPa is obtained for a load rate of 0.1 μN/s.     

Microstructure,thermooxidation and mechanical behavior of a novel highly linear,vitamin E stabilized,UHMWPE

A novel, vitamin E-stabilized, medical grade ultra-high molecular polyethylene, MG003 (DSM Biomedical; The Netherlands), has been very recently introduced for use in total joint replacements. This homopolymer resin features average molecular weight similar to that of conventional GUR 1050 resin (5.5–6*10⁶ g/mol), but a higher degree of linearity. The aim of this study was to characterize the microstructure, thermal and thermooxidation properties as well as the mechanical behavior of this novel MG003 resin before and after gamma irradiation in air to 90 kGy. For this purpose, a combination of experimental techniques were performed including differential scanning calorimetry (DSC), thermogravimetry (TG), transmission electron microscopy (TEM), X-Ray Diffraction, electron paramagnetic resonance (EPR), and uniaxial tensile tests. As-consolidated MG003 materials exhibited higher crystalline contents (~ 62%), transition temperatures (~ 140 °C), crystal thickness (~ 36 nm), yield stress (~ 25 MPa) and elastic modulus (~ 400 MPa) than GUR 1050 controls (55%, 136 °C, 27 nm, 19 MPa, and 353 MPa, respectively). Irradiation produced similar changes in both MG003 and GUR 1050 materials, specifically increased crystallinity (63% and 60%, respectively), crystal thickness (39 nm and 30 nm), yield stress (27 MPa and 21 MPa), but, above of all, loss of elongation to breakage (down to 442 and 469%, respectively). Thermogravimetric and EPR results suggest comparable susceptibilities to oxidation for both MG003 and GUR 1050 polyethylenes. Based on the present findings, MG003 appears as a promising alternative medical grade polyethylene and it may satisfactorily contribute to the performance of total joint replacements.     

Highly elastic and transparent multiwalled carbon nanotube/polydimethylsiloxane bilayer films as electric heating materials

Highly elastic and transparent bilayer films composed of MWCNT and polydimethylsiloxane (PDMS) layers were fabricated by spin-coating of MWCNT aqueous solution on glass plates and following curing of PDMS applied on the MWCNT layer. Morphological feature, optical transparency, tensile property, electrical property, and electric heating behavior of the bilayer films with different MWCNT layer thicknesses of 65–185 nm were investigated. SEM images confirmed that pristine MWCNTs were uniformly deposited on glass substrates and the PDMS layer was combined well with the MWCNT layer, resulting in high structural stability of the bilayer films to high elongational or twisting deformations. With the increase of the thickness of the MWCNT layer, the sheet resistance of the bilayer films decreased substantially from ~ 10⁵ Ω/sq to ~ 10³ Ω/sq, in addition to the change of the optical transmittance from ~ 75% to ~ 40% at a 550 nm wavelength. The electric heating behavior of MWCNT/PDMS bilayer films was strongly dependent on the thickness of the MWCNT layer as well as the applied voltage. Even under high twisting by 540° or continuous stepwise voltage changes for long periods of time, the MWCNT/PDMS bilayer films retained stable electrical heating performance in aspects of temperature responsiveness, steady-state maximum temperature, and electric power efficiency.     

Thermal stability of hierarchical and multiphase nanolaminated TiZrAlV

Microstructures, thermal stabilities and microstructures and properties evolutions of a new β TiZrAlV alloy have been investigated in this paper. Various hierarchical and multiphase nanolaminated (HMN) structures have been successfully produced in the alloy via appropriate thermomechanical processing treatments. The higher thermal stability (T_p ~ 275 °C), i.e., onset temperature of phase transformation, is achieved in a specific HMN structure consisting of nanoscale acicular isothermal α″ martensites, submicroscale α plates and large microscale primary α_p grains, compared with that (T_p ~ 105 °C) of its coarse-laminated counterpart without primary α_p grains. For this specific HMN structure, thermal exposures at 300–400 °C lead to further precipitation of isothermal α″ martensites, which enhances evidently the strength and reduces the ductility, while the reverse transformation of α″/α to β and the coarsening of previously formed α plates concur during thermal exposures at 500–600 °C, which leads to dramatically decreased strength and increased ductility.     

Third-order nonlinear optical properties of bis(tetrabutylammonium)bis(4,5-dithiolato-1,3-dithiole-2-thione)copper

Bis(tetrabutylammonium)bis(4,5-dithiolato-1,3-dithiole-2-thione)copper (BCDT) was synthesized and its third-order optical nonlinearity was characterized using picosecond Z-scan at 1064 nm. The Z-scan spectra reveal a large negative nonlinear refraction coefficient n₂ as high as 4.0 × 10⁻¹⁸ m²/W and a slight two-photon absorption β, which is determined to be 3.4 × 10⁻¹² m/W. The molecular second-order hyperpolarizability γ was calculated to be 6.5 × 10⁻³² esu. All these results suggest that this material has potential for the application of all-optical switching.