Using of hydrogen ion-selective poly(vinyl chloride) membrane electrode based on calix[4]arene as thiocyanate ion-selective electrode

A hydrogen ion-selective electrode (ISE) is prepared by using 5,11,17,23-tetra-tert-butyl-25,26,27,28-tetracyanometoxy-calix[4]arene and an investigation about whether it could be used as a thiocyanate ion-selective electrode is made by using its characteristic of becoming thiocyanate sensitive in acidic regions. The electrode of the optimum characteristic has a composition of 1% ionophore, 66% 2-NPOE and 33% poly(vinyl chloride) (PVC). This electrode exhibits a linear response over the range 1.0 × 10⁻¹ to 3.0 × 10⁻⁵ M of thiocyanate with a slope of 52.0 ± 0.2 mV/pSCN. The effects of the pH and the membrane composition are also investigated. The lifetime of the electrode is at least 4 months and its response time is found to be 10–15 s. The selectivity coefficients of some anions are calculated by using mixed solution interference method. Application of the electrode to the potentiometric titration of thiocyanate ion with silver nitrate is reported. There is a good agreement between the results obtained by the proposed electrode and the Mohr method at 95% confidence level.     

Chromium(III)-selective sensor based on tri-o-thymotide in PVC matrix

Tri-o-thymotide (I) has been used as an electroactive material in PVC (poly(vinyl chloride)) matrix for fabrication of chromium(III)-selective sensor. The membrane containing tri-o-thymotide, sodium tetraphenyl borate (NaTPB), dibutyl phthalate (DBP) and PVC in the optimum ratio 5:1:75:100 (w/w) exhibits a working concentration range of 4.0 × 10⁻⁶ to 1.0 × 10⁻¹ M with a Nernstian slope of 20.0 ± 0.1 mV/decade of activity in the pH range of 2.8–5.1. The detection limit of this sensor is 2.0 × 10⁻⁷ M. The electrode exhibits a fast response time of 15 s, shows good selectivity towards Cr³⁺ over a number of mono-, bi- and trivalent cations and can also be used in partially non-aqueous medium (up to 15%, v/v) also. The assembly has been successfully used as an indicator electrode in the potentiometric titration of chromium(III) against EDTA and also to determine Cr(III) quantitatively in electroplating industry waste samples.     

Development of a wide-tuning range and high Q variable capacitor using metal-based surface micromachining process

This study aims to improve the tuning range and quality-factor (Q) of micro variable capacitors for wireless communication applications. A suspending 0.5 μm-thick gold thin-plate with two-gap structure in one-to-three ratio of spacing is designed for the maximization of tuning range. To enhance effectively the flexural rigidity of top metal-plate and improve further the tuning range of the varactor, a double-cross-type microstructure with two vertical fixed-fixed beam springs and four horizontal fixed-guided cantilever beams is introduced. Besides, a glass substrate (Corning 7740) was used to reduce substantially the power dissipation and improve the Q-factor of variable capacitor. The new glass-based double-cross-type micro variable capacitor has demonstrated many superior performances, including the wide-tuning range (2100%, at 1.0 MHz with 6.0 V), the moderate capacitance (0.56 pF, at 2.4 GHz and without DC bias), 6.5 V pull-in voltage, and the high Q-factor (40.6, at 2.4 GHz). These characteristics approximately match with the theoretical derivation or simulated results from Agilent-ADS, Ansoft-HFSS, and IntelliSuite software.     

Discovery of novel anti-leishmanial agents targeting LdLip3 lipase

Leishmaniasis is a neglected tropical disease, caused by several species of Leishmania. Being an opportunistic lipid-scavenging pathogen, Leishmania relies extensively on lipid metabolism especially for host–pathogen interaction, utilizing host lipids for energy and virulence. The rational approach is to target lipid metabolism of the pathogen focusing lipid-catabolizing lipases. The LdLip3 lipase is considered as drug target as it is constitutively expressed in both promastigote and amastigote forms. Since the LdLip3 structure is not known, we modeled its three-dimensional structure to implement structure-based drug discovery approach. Similarity-based virtual screening was carried out to identify potential inhibitors utilizing NCI diversity set on ZINC database including natural products. Implementing computational and experimental approaches, four anti-leishmanial agents were discovered. The screened molecules ZINC01821375, ZINC04008765, ZINC06117316 and ZINC12653571 had anti-leishmanial activity with IC₅₀ (% viable promastigotes vs. concentration) of 5.2 ± 1.8 μM, 13.1 ± 2.6 μM, 9.4 ± 2.6 μM and 17.3 ± 3.1 μM, respectively. The molecules showed negligible toxicity toward mouse macrophages. Based on the contact footprinting analysis, new molecules were designed with better predicted free energy of binding than discovered anti-leishmanial agents. Further validation for the therapeutic utility of discovered molecules can be carried out by the research community to combat leishmaniasis.     

Flow-injection determination of iron(III) in soil by biamperometry using two independent redox couples

A flow-injection biamperometric method for the determination of iron(III) has been described. The detector consists of two chambers separated by a salt bridge, and one platinum wire working electrode is embedded in each chamber, respectively. When iron(III) solution and hydrogen peroxide solution simultaneously flow through two chambers, the reduction of iron(III) at one platinum electrode is associated with the oxidation of hydrogen peroxide at the other platinum electrode, forming such a system as similar to a reversible couple one. The biamperometric system can perform the determination of iron(III) without any external potential difference. The linear relationship is obtained from 1.0 × 10⁻⁶ to 1.0 × 10⁻⁴ mol l⁻¹ with a detection limit of 6.0 × 10⁻⁷ mol l⁻¹. The proposed method exhibits the satisfactory reproducibility with a relative standard derivation (R.S.D.) of 1.4% for 17 successive determinations of 2.0 × 10⁻⁵ mol l⁻¹ iron(III) and is applied to the determination of iron(III) in soil.     

Designing of potential inhibitors against Staphylococcus aureus sortase A: Combined analogue and structure based approach with in vitro validation

Staphylococcus aureus sortase A is an attractive target of Gram-positive bacteria that plays a crucial role in anchoring of surface proteins to peptidoglycan present in bacterial cell wall. Inhibiting sortase A is an elementary and essential effort in preventing the pathogenesis. In this context, in silico virtual screening of in-house database was performed using ligand based pharmacophore model as a filter. The developed pharmacophore model AAHR 11 consists of two acceptors, one hydrophobic and one ring aromatic feature. Top ranked molecule KKR1 was docked into the active site of the target. After profound analysis, it was analyzed and optimized based on the observations from its binding pose orientation. Upgraded version of KKR1 was KKR2 and has improved docking score, binding interactions and best fit in the binding pocket. KKR1 along with KKR2 were further validated using 100 ns molecular dynamic studies. Both KKR1 and KKR2 contain Indole-thiazolidine moiety and were synthesized. The disk diffusion assay has good initial results (ZI of KKR1, KKR2 were 24, 38 mm at 10 μg/mL and ZI of Ampicillin was 22 at 10 μg/mL) and calculated MICs of the molecules (KKR1 5.56 ± 0.28 μg/mL, KKR2 1.32 ± 0.12 μg/mL, Ampicillin 8 ± 1.1 μg/mL) were in good agreement with standard drug Ampicillin. KKR1 has shown IC₅₀ of 1.23 ± 0.14 μM whereas the optimized lead molecule KKR2 show IC₅₀ of 0.008 ± 0.07 μM. Results from in silico were validated by in vitro studies and proved that indole-thiazolidine molecules would be useful for future development as lead molecules against S. aureus sortase A.     

Electrochemical determination of ascorbic acid in fruits on a vanadium oxide polypropylene carbonate modified electrode

A novel vanadium oxide polypropylene carbonate modified glassy carbon electrode was developed and used for the measurement of ascorbic acid (AA). The electrode was prepared by casting a mixture of vanadium tri(isopropoxide) oxide (VO(OC₃H₇)₃) and poly(propylene carbonate) (PPC) onto the surface of a glassy carbon electrode. The electrochemical behavior of the VO(OC₃H₇)₃–PPC film modified glassy carbon electrode was investigated by cyclic voltammetry and amperometry. This modified electrode exhibited electrocatalytic response to the oxidation of ascorbic acid. Compared with a bare glassy carbon electrode, the modified electrode exhibits a 220 mV shift of the oxidation potential of ascorbic acid in the cathodic direction and a marked enhancement of the current response. The response current revealed a good linear relationship with the concentration of ascorbic acid in the range of 4 × 10⁻⁸ and 1 × 10⁻⁴ mol L⁻¹ and the detection limit of 1.5 × 10⁻⁸ mol L⁻¹ (S/N = 3) in the pH 8.06 Britton–Robinson solution. Quantitative recovery of the ascorbic acid in synthetic samples has been obtained and the interferences from different species have been studied. The method has been successfully applied to the determination of ascorbic acid in fruits. The concentrations of ascorbic acid measured by this method are in good agreement with the literature value. It is much promising for the modified films to be used as an electrochemical sensor for the detection of ascorbic acid.     

Design and fabrication of a new MEMS capacitive microphone using a perforated aluminum diaphragm

In this paper, a novel single-chip MEMS capacitive microphone is presented. The novelties of the method relies on the moveable aluminum (Al) diaphragm positioned over the backplate electrode, where the diaphragm includes a plurality of holes to allow the air in the gap between the electrode and the diaphragm to escape and thus reducing acoustical damping in the microphone. Spin-on-glass (SOG) was used as a sacrificial and isolating layer. Backplate is monocrystalline silicon wafer, that it is more stiff. This work will focus on design, simulation, fabrication and characterization of the microphone. The structure has a diaphragm thickness of 3 μm, a diaphragm size of 0.5 mm × 0.5 mm, and an air gap of 1.0 μm. The results show that the pull-in voltage is 105 V, the initial stress of evaporated aluminum diaphragm is around 1500 MPa and the zero bias capacitance of microphone is 2.12 pF. Comparing with the previous works, this microphone has several advantages: the holes have been made on diaphragm, therefore no need of KOH etching to make back chamber, in this way the chip size of each microphone is reduced. The fabrication process uses minimal number of layers and masks to reduce the fabrication cost.     

Photonic crystal slabs with hexagonal air holes fabricated by selective area metal organic vapor phase epitaxy

It is shown that the photonic crystal slab (PCS) with hexagonal air holes has band gaps in the guided mode spectrum, which can be compared to that of the PCS with circular air holes, thus it is also a good candidate to be used for the PC devices. The PC with hexagonal air holes and a = 0.5 μm and r = 0.15 μm was fabricated successfully by selective area metal organic vapor phase epitaxy (SA-MOVPE). The vertical and smooth sidewalls are formed and the uniformity is very good. The same process was also used to fabricate a hexagonal air hole array with the width of 0.1 μm successfully. The air-bridge PCS with hexagonal air holes and a = 0.3 μm and r = 0.09 μm was also fabricated successfully by SA-MOVPE. Further optimization of the growth conditions for the sacrificial layer and the selective etching of the GaAs cap layer is also needed. Our experimental results indicate that SA-MOVPE is a promising method for fabricating PC devices and photonic nanostructures.     

Spin-valve planar Hall sensor for single bead detection

The planar Hall effect (PHE) sensor with a junction size of 3 μm × 3 μm for a single micro-bead detection has been fabricated successfully using a typical spin-valve thin film Ta(5)/NiFe(16)/Cu(1.2)/NiFe(2)/IrMn(15)/Ta(5) nm. The PHE sensor exhibits a sensitivity of about 7.2 μV Oe^?1 in the magnetic field range of ±7 Oe approximately. We have performed an experiment to illustrated the possibility of single micro-bead detection by using a PHE sensor. A single micro-bead of 2.8 μm diameter size is secluded from 0.1% dilute solution of the Dynabeads^® M-280 dropped on the sensor surface and is located on the sensor junction by using a micro magnetic needle. The comparison of the PHE voltage profiles in the field range from 0 to 20 Oe in the absence and presence of a single micro-bead identifies a single Dynabeads^® M-280, the maximal signal change as large as ΔV ～ 1.1 μV can be obtained at the field ～6.6 Oe. The results are well described in terms of the reversal of a basic single domain structure.     

Fabrication and characterization of a thermal switch

The development of a thermal switch based on arrays of liquid–metal micro-droplets is presented. Prototype thermal switches are assembled from a silicon substrate on which is deposited an array of 1600 30-μm liquid–metal micro-droplets. The liquid–metal micro-droplet array makes and breaks contact with a second bare silicon substrate. A gap between the two silicon substrates is filled with either air at 760 Torr, air at of 0.5 Torr or xenon at 760 Torr. Heat transfer and thermal resistance across the thermal switches are measured for “on” (make contact) and “off” (break contact) conditions using guard-heated calorimetry. The figure of merit for a thermal switch, the ratio of “off” state thermal resistance over “on” state thermal resistance, R_off/R_on, is 129 ± 43 for a xenon-filled thermal switch that opens 100 μm and 60 ± 17 for an 0.5 Torr air-filled thermal switch that opens 25 μm. These thermal resistance ratios are shown to be markedly higher than values of R_off/R_on for a thermal switch based on contact between polished silicon surfaces. Transient temperature measurements for the liquid–metal micro-droplet switches indicate thermal switching times of less than 100 ms. Switch lifetimes are found to exceed one-million cycles.     

Development of a mercury optical sensor based on immobilization of 4-(2-pyridylazo)-resorcinol on a triacetylcellulose membrane

A new optical sensor for mercury(II) ions is developed based on immobilization of 4-(2-pyridylazo)-resorcinol (PAR) on a triacetylcellulose membrane. Chemical binding of Hg²⁺ ions in solution with a PAR immobilized on the triacetylcellulose surface could be monitored spectrophotometrically at 525 nm. The optode shows excellent response over a wide concentration range of 5–3360 μM Hg(II) with a limit of detection of 1.5 μM Hg(II). The influence of factors responsible for the improved sensitivity of the sensor were studied and identified. The response time of the optode was 20 min for a stable solution, and was 15 min for a stirrer solution. The influence of potential interfering ions on the determination of 5 × 10⁻⁵ M Hg(II) was studied. The sensor was applied for determination of Hg(II) in water samples.     

Efficient organic light-emitting diodes with C60 buffer layer

Organic light-emitting diodes (OLEDs) with C₆₀ buffer layer were fabricated. The effect of C₆₀ buffer layer on the performance of the devices was investigated by inserting C₆₀ buffer layer at the interface between the electrode and organic layers. The device structures were (1) ITO/C₆₀ (0.0, 0.4, 0.7 and 1.0 nm)/NPB/Alq₃/LiF/Al and (2) ITO/NPB/Alq₃/C₆₀ (0.0, 0.4, 0.7 and 1.0 nm)/LiF/Al. The highest brightness and efficiency of the device (1) with 0.7 nm-thick C₆₀ layer reached 6439 cd/m² at 16 V and 1.80 cd/A at 6.4 V, respectively. The enhancements in brightness and efficiency are attributed to an improved balance of hole and electron injections due to C₆₀ layer blocking parts of the injected holes. On the contrary, the brightness and efficiency of the devices with the structure (2) had been hardly enhanced.     

Perchlorate-selective polymeric membrane electrode based on a cobaloxime as a suitable carrier

A cobaloxime ([chlorobis(dimethylglyoximeato)(triphenylphosphine)] cobalt (III), [Co(dmgH)₂pph₃Cl]) incorporated in a plasticized poly(vinyl chloride) membrane was used to develop a perchlorate-selective electrode. The influence of membrane composition on the electrode response was studied. The electrode exhibits a Nernstian response over the perchlorate concentration range 1.0 × 10⁻⁶ to 1 × 10⁻¹ mol l⁻¹ with a slope of −56.8 ± 0.7 mV per decade of concentration, a detection limit of 8.3 × 10⁻⁷, a wide working pH range (3–10) and a fast response time (<15 s). The electrode shows excellent selectivity towards perchlorate with respect to many common anions. The electrode was used to determine perchlorate in water and human urine.     

Simultaneous determination of epinephrine and ascorbic acid at the electrochemical sensor of triazole SAM modified gold electrode

The electrochemical sensor of triazole (TA) self-assembled monolayer (SAM) modified gold electrode (TA SAM/Au) was fabricated. The electrochemical behaviors of epinephrine (EP) at TA SAM/Au have been studied. The TA SAM/Au shows an excellent electrocatalytic activity for the oxidation of EP and accelerates electron transfer rate. The diffusion coefficient is 1.135 × 10⁻⁶ cm² s⁻¹. Under the optimum experiment conditions (i.e. 0.1 mol L⁻¹, pH 4.4, sodium borate buffer, accumulation time: 180 s, accumulation potential: 0.6 V, scan rate: 0.1 Vs⁻¹), the cathodic peak current of EP versus its concentration has a good linear relation in the ranges of 1.0 × 10⁻⁷ to 1.0 × 10⁻⁵ mol L⁻¹ and 1.0 × 10⁻⁵ to 6.0 × 10⁻⁴ mol L⁻¹ by square wave adsorptive stripping voltammetry (SWASV), with the correlation coefficient of 0.9985 and 0.9996, respectively. Detection limit is down to 1.0 × 10⁻⁸ mol L⁻¹. The TA SAM/Au can be used for the determination of EP in practical injection. Meantime, the oxidative peak potentials of EP and ascorbic acid (AA) are well separated about 200 ± 10 mV at TA SAM/Au, the oxidation peak current increases approximately linearly with increasing concentration of both EP and AA in the concentration range of 2.0 × 10⁻⁵ to 1.6 × 10⁻⁴ mol L⁻¹. It can be used for simultaneous determination of EP and AA.     

Design and synthesis of a novel class of carbonic anhydrase-IX inhibitor 1-(3-(phenyl/4-fluorophenyl)-7-imino-3H-[1,2,3]triazolo[4,5d]pyrimidin 6(7H)yl)urea

Carbonic anhydrase IX (CAIX) is a promising target in cancer therapy especially in the case of hypoxia-induced tumors. The selective inhibition of CA isozymes is a challenging task in drug design and discovery process. Here, we performed fluorescence-binding studies and inhibition assay combined with molecular docking and molecular dynamics (MD) simulation analyses to determine the binding affinity of two synthesized triazolo-pyrimidine urea derived (TPUI and TPUII) compounds with CAIX and CAII. Fluorescence binding results are showing that molecule TPUI has an excellent binding-affinity for CAIX (k_D = 0.048 μM). The TPUII also exhibits an appreciable binding affinity (k_D = 7.52 μM) for CAIX. TPUI selectively inhibits CAIX as compared to TPUII in the 4-NPA assay. Docking studies show that TPUI is spatially well-fitted in the active site cavity of CAIX, and is involve in H-bond interactions with His94, His96, His119, Thr199 and Thr200. MD simulation studies revealed that TPUI efficiently binds to CAIX and essential active site residual interaction is consistent during the entire simulation of 40 ns. These studies suggest that TPUI appeared as novel class of CAIX inhibitor, and may be used as a lead molecule for the development of potent and selective CAIX inhibitor for the hypoxia-induced cancer therapy.     

Preparation and properties of an uricase biosensor based on copolymer of o-aminophenol-aniline

An uricase biosensor of poly-o-aminophenol-aniline is firstly reported in this paper. The preparing process of the biosensor is as follows: An uricase electrode is prepared with one-step process using the copolymer of aniline and o-aminophenol, then the electrode is hydrolyzed in 6.0 mol dm⁻³ hydrochloric acid solution to remove the uricase that may be affected by monomer during copolymerization and a template with moderate apertures for immobilization uricase was obtained. Finally, active uricase is immobilized into the template based on doping and undoping of the copolymer, and a copolymer-uricase biosensor is obtained. Some factors that affect response current are studied, such as temperature, pH, potential and substrate concentration. The result of experiment indicates that the response current of the copolymer-uricase biosensor prepared with template process only decreases by about 19% for 50 days, but that of polyaniline-uricase biosensor prepared with two-step process decreases by approximately 43% for 40 h. FTIR, UV–vis and SEM are used to characterize the copolymer-uricase biosensor.     

Electrostatically actuated dip pen nanolithography probe arrays

Dip pen nanolithography (DPN) is a method of creating nanoscale chemical patterns on surfaces using an atomic force microscope (AFM) probe. Until now, efforts to increase the process throughput have focused on passive multi-probe arrays and active arrays based on thermal bimetallic actuation. This paper describes the first use of electrostatic actuation to create an active DPN probe array. Electrostatic actuation offers the benefit of actuation without the probe heating required for thermal bimetallic actuation. Actuator cross talk between neighboring probes is also reduced, permitting more densely spaced probe arrays. The array presented here consists of 10 cantilever probes, where each is 120 μm long and 20 μm wide. Each cantilever probe is actuated by the electrostatic force between the probe and a built-in counter electrode with a 20–25 μm gap. The tip-to-tip probe spacing, also called the array pitch, is 30 μm. Patterns of 1-octadecanethiol were created on gold surfaces to demonstrate single-probe actuation, simultaneous multi-probe actuation, and overlap of patterns from adjacent probes. The minimum line width was 25 nm with an average line width of 30–40 nm.     

Evaluation of response characteristics of resistive oxygen sensors based on porous cerium oxide thick film using pressure modulation method

In order to reduce the response time of resistive oxygen sensors using porous cerium oxide thick film, it is important to ascertain the factors controlling response. Pressure modulation method (PMM) was used to find the rate-limiting step of sensor response. This useful method measures the amplitude of sensor output (H(f)) for the sine wave modulation of oxygen partial pressure at constant frequency (f). In PMM, “break” response time, which is minimum period in which the sensor responds precisely, can be measured. Three points were examined: (1) simulated calculations of PMM were carried out using a model of porous thick film in which spherical particles are connected in a three-dimensional network; (2) sensor response speed was experimentally measured using PMM; and (3) the diffusion coefficient and surface reaction coefficient were estimated by comparison between experiment and calculation. The plot of log f versus log H(f) in the high f region was found to have a slope of approximately −0.5 for both porous thick film and non-porous thin film, when the rate-limiting step was diffusion. Calculations showed the response time of porous thick film was 1/20 that of non-porous thin film when the grain diameter of the porous thick film was the same as the thickness of non-porous thin film. At 973 K, “break” response time (t_b) of the resistive oxygen sensor was found by experiment to be 109 ms. It was concluded that the response of the resistive oxygen sensor prepared in this study was strongly controlled by diffusion at 923–1023 K, since the experiment revealed that the slope of plot of log f versus log H(f) in the high f region was approximately −0.5. At 923–1023 K, the diffusion coefficient of oxygen vacancy in porous ceria (D_V) was expressed as follows: D_V (m²s⁻¹) = 5.78 × 10⁻⁴ exp(−1.94 eV/kT). At 1023 K, the surface reaction coefficient (K) was found to exceed 10⁻⁴ m/s.     

Ultra high performance planar InGaAs PIN photodiodes for high speed optical fiber communication

This paper reports a front-illuminated planar InGaAs PIN photodiode with very low dark current, very low capacitance and very high responsivity on S-doped InP substrate. The presented device which has a thick absorption layer of 2.92 μm and a photosensitive area 73 μm in diameter exhibited the high performance of a very low capacitance of 0.47 pF, a very low dark current of 0.041 nA, a very high responsivity of 0.99 A/W (79% quantum efficiency) at λ = 1.55 μm, the 3 dB bandwidths of 6.89 GHz (−5 V), 7.48 GHz (−12 V) for bare chips and 4.48 GHz (−5 V), 5.02 GHz (−12 V) for the devices packaged in TO can, respectively. Furthermore, the developed PIN photodiodes possess high breakdown voltage of less than −25 V.