Development of a new fluorescent sensor based on a triazolo-thiadiazin derivative immobilized in polyvinyl chloride membrane for sensitive detection of lead(II) ions

A new sensor membrane based on a novel triazolo-thiadiazin derivative immobilized in polyvinyl chloride has been developed for the determination of Pb(II) ions that displays excellent performance. The parameters involved in the preparation of the optode and determination of Pb(II) were optimized. Under the optimal conditions, the proposed sensor displays a calibration response for Pb(II) over a wide concentration range of 5.0 × 10⁻⁸ to 3.8 × 10⁻⁴ M with the detection limit of 2.2 × 10⁻⁸ M. In addition to high reproducibility and reversibility of the fluorescence signal, the sensor also exhibits good selectivity over common metal ions. The optode membrane developed is easily prepared, stable, rapid, and simple for the determination of Pb(II). The accuracy of the proposed sensor was confirmed by analyzing standard reference materials of natural water and surface water. The sensor was successfully used for the determination of Pb(II) ions in water samples with satisfactory results.     

Selective potentiometric determination of uric acid with uricase immobilized on ZnO nanowires

In this study, a potentiometric uric acid biosensor was fabricated by immobilization of uricase onto zinc oxide (ZnO) nanowires. Zinc oxide nanowires with 80-150 nm in diameter and 900 nm to 1.5 μm in lengths were grown on the surface of a gold coated flexible plastic substrate. Uricase was electrostatically immobilized on the surface of well aligned ZnO nanowires resulting in a sensitive, selective, stable and reproducible uric acid biosensor. The potentiometric response of the ZnO sensor vs Ag/AgCl reference electrode was found to be linear over a relatively wide logarithmic concentration range (1-650 μM) suitable for human blood serum. By applying a Nafion^® membrane on the sensor the linear range could be extended to 1-1000 μM at the expense of an increased response time from 6.25 s to less than 9 s. On the other hand the membrane increased the sensor durability considerably. The sensor response was unaffected by normal concentrations of common interferents such as ascorbic acid, glucose, and urea.     

Development of an optical sensor for determination of zinc by application of PC-ANN

A very sensitive and reversible optical chemical sensor based on dithizone as chromoionophore immobilized within a plasticized carboxylated PVC film for Zn²⁺ determination is described. At optimum conditions (i.e. pH 5.0), the proposed sensor displays a linear response to Zn²⁺ over 5.0 × 10⁻⁸-5.0 × 10⁻⁶ mol L⁻¹ range. This range was improved to 2.5 × 10⁻⁸-5.8 × 10⁻⁵ mol L⁻¹ range by applying principle component-feed forward artificial neural network with back-propagation training algorithm (PC-ANNB). Detection limit of 8.0 × 10⁻⁹ mol L⁻¹ was obtained. The sensor is fully reversible within the dynamic range and the response time (t_95%) is approximately 4 min under batch conditions. In addition to its high stability and reproducibility, the sensor shows good selectivity towards Zn²⁺ ion with respect to common metal cations. The sensor was successfully applied for determination of Zn²⁺ ion in hair sample.     

Finite element analysis and experiments on a silicon membrane actuated by an epitaxial PZT thin film for localized-mass sensing applications

In this paper, we investigate the performance of a piezoelectric membrane actuated by an epitaxial piezoelectric Pb(Zr_0.2Ti_0.8)O₃ (PZT) thin film for localized-mass sensing applications. The fabrication and characterization of piezoelectric circular membranes based on epitaxial thin films prepared on a silicon wafer are presented. The dynamic behavior and mass sensing performance of the proposed structure are experimentally investigated and compared to numerical analyses. A 1500 μm diameter silicon membrane actuated by a 150 nm thick epitaxial PZT film exhibits a strong harmonic oscillation response with a high quality factor of 110-144 depending on the resonant mode at atmospheric pressure. Different aspects related to the effect of the mass position and of the resonant mode on the mass sensitivity as well as the minimum detectable mass are evaluated. The operation of the epitaxial PZT membrane as a mass sensor is determined by loading polystyrene microspheres. The mass sensitivity is a function of the mass position, which is the highest at the antinodal points. The epitaxial PZT membrane exhibits a mass sensitivity in the order of 10⁻¹² g/Hz with a minimum detectable mass of 5 ng. The results reveal that the mass sensor realized with the epitaxial PZT thin film, which is capable of generating a high actuating force, is a promising candidate for the development of high performance mass sensors. Such devices can be applied for various biological and chemical sensing applications.     

Ultrasensitive immunosensing of tuberculosis CFP-10 based on SPR spectroscopy

An antigen (Ag), CFP-10, found in tissue fluids of tuberculosis (TB) patients may be an ultimate candidate for use as a sensitive TB marker with a sensing method for early simplified diagnosis of TB. In this study, chemical and optical optimizations were carried out using novel immuno-materials for establishment of a self-assembled surface plasmon resonance (SPR) optical immunosensor system for detection of CFP-10, which is valuable for pre-clinical work, prior to conduct of massive clinical observations. For creation of a simple sensing interface, a monoclonal antibody (anti-CFP-10) was immobilized directly on a gold surface, followed by blocking with cystamine. Orientation and accessibility of anti-CFP-10 were assessed by the selective binding of CFP-10. Recent results indicate that the reusability of the sensor chip adopting the cystamine method was found to be preferable to other immobilization methods. A linear relationship was well correlated between SPR angle shift and CFP concentrations in the range from 100 ng mL⁻¹ to 1 μg mL⁻¹. Modification of the SPR chip with antibody provides a simple experimental platform for investigation of isolated proteins under experimental conditions resembling those of their native environment.     

A novel porous anodic alumina based capacitive sensor towards trace detection of PCBs

To detect polychlorinated biphenyls (PCBs), a novel porous anodic alumina (PAA) based capacitive sensor working at room temperature has been developed. The parallel nanopores of PAA not only provide large surface area for PCB adsorption, but also benefit for the enhancement of capacitive response. By dropping the PCB methanol solution on the surface of PAA, it is convenient to load PCB into the nanopores by solvent evaporation. 3,3′,4,4′-tetrachlorobiphenyl (PCB77) was chosen as a typical sample of PCBs to investigate the sensing properties of the capacitive sensor. The capacitance of the PAA membrane shows remarkable enhancement after PCB77 solution was loaded while no significant change can be seen after the pure solvent was loaded. The capacitive sensor also shows good response to PCB77 even in the presence of the interferent of benzene. The sensing mechanism has been qualitatively discussed based on a parallel plate capacitor model. The detection limit is down to 8 × 10⁻⁸ M towards PCB77. The novel PAA based capacitive sensor exhibits great potential for practical application in trace detection of PCBs.     

All fiber-optic sensing of light using side-polished fiber overlaid with photoresponsive liquid crystals

This study presents a highly sensitive, all-fiber sensor for in situ detecting light. A fiber-optic light sensing platform was created by overlaying an in-line side-polished fiber (SPF) with a photoresponsive liquid crystal (P-LC) consisting of an azobenzene dye, a chiral dopant, and a nematic LC. The resulting P-LC overlaid SPF light sensor is sensitive to three different light sources, including 380 nm light emitting diode (LED), mercury lamp, and office ceiling lights. Under the light illumination, the energy of irradiation from short wavelengths of light (<450 nm) initiates the trans-to-cis photoisomerization of azobenzene. The photochemical LC-phase transition induced by the generated cis-moiety of azobenzene changes the refractive index of LC-overlaid side-polished area. Light illumination increased the attenuation of the input laser signal. After turning off the illumination, the attenuation returned to its original value, allowing the fiber-optic light sensor to be reused. The sensitivity of the resulting fiber-optic light sensor was 0.16 dB/(μW/cm²) with a detection limit of 5 μW/cm² and 0.06 dB/lx with a detection limit of 45 lx when a 380 nm LED and office ceiling lights were used as illumination sources, respectively. The detection limit increased from 45 to 12 lx when P-LC containing 20 wt% azobenzene was used as light sensing material. The proposed fiber-based light sensor has potential use in harsh environments, such as severely humid and corrosive environments, which could damage mechanical and electronic light sensors.     

DC humidity sensing properties of BaTiO3 nanofiber sensors with different electrode materials

Barium titanate (BaTiO₃) nanofibers were synthesized by electrospinning and calcination techniques. Two direct current (DC) humidity sensors with different electrodes (Al and Ag) were fabricated by loading BaTiO₃ nanofibers as the sensing material. Compared with the Al electrode sensor, the Ag electrode sensor exhibits larger sensitivity and quicker response/recovery. The current of Al electrode sensor increases from 4.08 × 10⁻⁹ to 1.68 × 10⁻⁷ A when the sensor is switched from 11% to 95% relative humidity (RH), while the values are 2.19 × 10⁻⁹ and 3.29 × 10⁻⁷ A for the Ag electrode sensor, respectively. The corresponding response and recovery times are 30 and 9 s for Al electrode sensor, and 20 and 3 s for Ag electrode sensor, respectively. These results make BaTiO₃ nanofiber-based DC humidity sensors good candidates for practical application. Simultaneously, the comparison of sensors with different electrode materials may offer an effective route for designing and optimizing humidity sensors.     

Study on design and application of fully automatic miniature surface plasmon resonance concentration analyzer

A fully automatic miniature surface plasmon resonance (SPR) concentration analyzer having high performance and low cost and developed using a Spreeta™ sensor was designed for field applications and concentration analysis. As in the case of Biacore™ instruments, the automatic sampling system of this device can introduce air segments between the sample/regeneration solution and buffer solution in the pipeline, which effectively prevents mixing of the solutions. A temperature sensor (AD 590) and temperature compensation method are used, which make the device insensitive to temperature fluctuations. A real-time data-smoothing algorithm for the SPR detection data is adopted; this can reduce the noise level to 5 × 10⁻⁷ RIU (refractive index units). The noise level of the sensorgram is 3.5% of the original level. Two types of self-prepared sensing chips—SMX-BSA (bovine serum albumin coated with sulfamethoxazole) and SMX-CM5 (carboxymethyl dextran coated with sulfamethoxazole)—are used to analyze the concentrations of sulfamethoxazole (SMX) standard solutions. Each chip's SMX calibration curve is established within the measurement range of 0-2000 ng/ml, and both limits of detection (LOD) are 2 ng/ml. One cycle of assay time is less than 15 min.     

Terbium doped strontium cerate enabled long period fiber gratings for high temperature sensing of hydrogen

This paper reports on a novel optical fiber based sensor for hydrogen detection at high temperatures (>600 °C). The optical sensor consists of a perovskite-type ceramic, SrCe_0.95Tb_0.05O_3−δ, as the sensing material, which is coated on the cladding layer of long period fiber gratings. Upon exposure to hydrogen, the reduction of Ce⁴⁺ to Ce³⁺ on the surface of SrCe_0.95Tb_0.05O_3−δ particle causes decrease in its refractive index. As a result, the resonance wavelength of long period fiber gratings shifts to a higher value. The rate of the shift is dependent on the hydrogen partial pressure and can be used as the sensing signal. The high temperature optical H₂ sensor exhibits high sensitivity for H₂ detection at a partial pressure of 0.005 atm, and a short response time. The sensor is reversible as exposing the sensor to air oxidizes Ce³⁺ to Ce⁴⁺.     

A selective and highly sensitive fluorescent probe of Hg in organic and aqueous media: The role of a polymer network in extending the sensing phenomena to water environments

This paper describes the preparation of a hydrophilic copolymer membrane with two comonomers: 1-vinyl-2-pyrrolidone (commercial) and a new water insoluble piperazinedione derivative, which is a fluorogenic mercury sensing motif. The dense membrane permitted the fluorogenic detection of Hg²⁺ in aqueous media. The sensitivity of the membrane this cation was significantly high, with a detection limit of 10 ppt. This limit of detection is much lower than that of DMSO/water solutions of the sensing monomer, which is 10 ppb, and significantly lower than the maximum contaminant level (EPA) in drinking water, 2 ppb.     

Free chlorine sensing using an interferometric sensor

A waveguide interferometer based free-chlorine sensing technique has been developed. A polymer film for a specific free chlorine binding was designed, synthesized and applied on the surface of a waveguide. The material is based on cyanuric acid moieties along each repeating unit covalently tethered to poly(norbornene)s. Chlorine sensing was accomplished by measuring the refractive index change of the polymer, as a result of the reaction between cyanuric acid and free chlorine, interferometrically by the evanescent field extended above the waveguide surface. The free chlorine binding to cyanuric acid is reversible and a linear calibration curve from 0.1 to 10 mg L⁻¹ of HOCl concentration was obtained with the level of detection (LOD) and level of quantification (LOQ) of 0.047 and 0.328 mg L⁻¹ of HOCl, respectively. A free chlorine measurement with less interference from combined chlorine than DPD based colorimetric method was developed as a result of the different sensing responses of free and combined chlorine. Free chlorine residual was measured in samples collected from tap water and poultry processing waters by both optical sensor and DPD-based colorimetric method. Good agreement between both methods was observed although the levels for free chlorine measured by the optical sensor are systematically lower than the readings obtained from the DPD method. The difference might be the result of the interference from combined chlorine during the DPD measurement.     

Direct oxidation of methionine at screen printed graphite macroelectrodes: Towards rapid sensing platforms

The direct electrochemical oxidation of methionine has been achieved at bare carbon based electrodes and for the first time at screen printed graphite electrodes in aqueous solutions. Due to scales of economy and intended use as a potential point-of-care sensor, the quantification of methionine was explored at screen printed electrodes, allowing linear ranges over the range 0.05-5.0 mM with a detection limit of 95 × 10⁻⁶ mol L⁻¹ possible in model solutions. Application of this sensor was used for the determination of methionine in a pharmaceutical product containing a complex mixture of vitamins, amino acids, chelated minerals and additional factors with the results agreeing with manufacturers’ specification suggesting that this sensing platform holds promise as a rapid, sensitive and disposable sensor for methionine determination.     

Noble metal dispersed multiwalled carbon nanotubes immobilized ss-DNA for selective detection of dopamine

A hybrid nanocomposite consisting of Pt nanoparticles decorated functionalized multiwalled carbon nanotubes (f-MWNT) immobilized with single strand-DNA (ss-DNA) has been devised for the selective detection of dopamine (DA). AFM and TEM analyses show that wrapping of ss-DNA over Pt/f-MWNT reduces the aggregation of the nanotubes arising from van der Waals interaction. In addition to serving as a noncovalent dispersion agent, ss-DNA facilitated electron transfer towards dopamine, as analyzed by cyclic voltammetric studies (CV) and amperometry. The sequence dependency of ss-DNA for DA detection has been analyzed using AC and GT ss-DNA. The hybrid nanocomposite biosensor consisting of AC/ss-DNA exhibits linearity of detection upto ∼315 μM, with a detection limit 0.8 μM towards dopamine. The best sensing performance with linearity of ∼800 μM and detection limit ∼0.45 μM has been obtained with GT/ss-DNA immobilized Pt/f-MWNT sensor. Further, the nafion coated ss-DNA wrapped Pt/f-MWNT immobilized biosensor exhibits good stability, fast response time (<3 s) and selective detection of DA in the presence of ascorbic acid and uric acid.     

Simultaneous kinetic spectrophotometric determination of sulfide and sulfite ions by using an optode and the partial least squares (PLS) regression

The characterization of an optical sensor membrane is described for simultaneous determination of sulfite and sulfide ions based on the immobilization of crystal violet on a triacetylcellulose membrane. The absorbance of the membranes decreased by increasing sulfite and sulfide concentration. The partial least squares (PLS-1) calibration model based on spectrophotometric measurement for simultaneous determination of sulfite and sulfide ions was applied. This method is based on the difference between the rate of the reaction of sulfide and sulfite with membranes in pH 7.0 buffer solution and at 25 °C. The experimental calibration matrix for partial least squares (PLS-1) calibration was designed with 18 samples. The cross-validation method was used for selecting the number of factors. The results showed that simultaneous determination could be performed in the range of 200–2000 μg mL⁻¹ (2.5–25 mmol L⁻¹) and 80–900 μg mL⁻¹ (2.5–28.125 mmol L⁻¹) for sulfite and sulfide, respectively. The sensor can readily be regenerated with water and the color is fully reversible. The sensor was successfully applied to the simultaneous determination of sulfide and sulfite in water samples.     

Enhanced room temperature response of SnO2 thin film sensor loaded with Pt catalyst clusters under UV radiation for LPG

The room temperature response characteristics of SnO₂ thin film sensor loaded with platinum catalyst clusters are investigated for LPG under the exposure of ultraviolet radiation. The SnO₂-Pt cluster sensor structures have been prepared using rf sputtering. Combined effect of UV radiation exposure (λ = 365 nm) and presence of Pt catalyst clusters (10 nm thick) on SnO₂ thin film sensor surface is seen to lead to an enhanced response (4.4 × 10³) for the detection of LPG (200 ppm) at room temperature whereas in the absence of UV illumination a comparable response (∼5 × 10³) could be obtained but only at an elevated temperature of 220 °C. The present study therefore investigates the effect of UV illumination on LPG sensing characteristics of SnO₂ sensors loaded with Pt clusters of varying thickness values. Results indicate the possibility of utilizing the sensor structure with novel dispersal of Pt catalyst clusters on SnO₂ film surface for efficient detection of LPG at room temperature under the illumination of UV radiations.     

Nanoporous polystyrene fibers functionalized by polyethyleneimine for enhanced formaldehyde sensing

Here we report a novel fabrication approach to highly sensitive formaldehyde sensors by the surface modification of the electrospun nanofibrous membranes. The three-dimensional fibrous membranes comprising nanoporous polystyrene (PS) fibers were electrospun deposition on quartz crystal microbalance (QCM), followed by the functionalization of the sensing polyethyleneimine (PEI) on the membranes. The morphology and Brunauer-Emmett-Teller (BET) surface area of the fibrous PS membranes with fiber diameter of 110-870 nm were controllable by tuning the concentrations of PS solutions. After PEI modification, PEI particles in clusters of varying sizes (50 nm to 1.2 μm) were immobilized onto the surface of the bead-on-string structured nanoporous fibers. The developed formaldehyde-selective sensors exhibited fast response and low detection limit (3 ppm) at room temperature. This high sensitivity is attributed to the high surface-area-to-volume ratio (∼47.25 m²/g) of the electrospun porous PS membranes and efficient nucleophilic addition reaction between formaldehyde molecules and primary amine groups of PEI.     

Tethered DNA scaffolds on optical sensor platforms for detection of hipO gene from Campylobacter jejuni

DNA biosensors have gained increased attention over traditional diagnostic methods due to their fast and responsive operation and cost-effective design. The specificity of DNA biosensors relies on single-stranded oligonucleotide probes immobilized to a transduction platform. Here, we report the development of biosensors to detect the hippuricase gene (hipO) from Campylobacter jejuni using direct covalent coupling of thiol- and biotin-labeled single-stranded DNA (ssDNA) on both surface plasmon resonance (SPR) and diffraction optics technology (DOT, dotLab) transduction platforms. This is the first known report of the dotLab to detect targeted DNA. Application of 6-mercapto-1-hexanol as a spacer thiol for SPR gold surface created a self-assembled monolayer that removed unbound ssDNA and minimized non-specific detection. The detection limit of SPR sensors was shown to be 2.5 nM DNA while dotLab sensors demonstrated a slightly decreased detection limit of 5.0 nM (0.005 μM). It was possible to reuse the SPR sensor due to the negligible changes in sensor sensitivity (∼9.7 × 10⁻⁷ ΔRU) and minimal damage to immobilized probes following use, whereas dotLab sensors could not be reused. Results indicated feasibility of optical biosensors for rapid and sensitive detection of the hipO gene of Campylobacter jejuni using specific ssDNA as a probe.     

High sensitive optode for selective determination of Ni based on the covalently immobilized thionine in agarose membrane

A novel Ni²⁺ optode was prepared by covalent immobilization of thionine, 3,7-diamine-5-phenothiazoniom thionineacetate, in a transparent agarose membrane. Influences of various experimental parameters on Ni²⁺ sensing, including the reaction time, the solution pH and the concentration of reagents were investigated. Under the optimized conditions, a linear response was obtained for Ni²⁺ concentrations ranging from 1.00 × 10⁻¹⁰ to 1.00 × 10⁻⁷ mol l⁻¹ with an R² value of 0.9985. The detection limit (3σ) of the method for Ni²⁺ was 9.30 × 10⁻¹¹ mol l⁻¹. The influence of several potentially interfering ions such as Ag⁺, Hg²⁺, Cd²⁺, Zn²⁺, Pb²⁺, Cu²⁺, Mn²⁺, Co³⁺, Cr³⁺, Al³⁺ and Fe³⁺ on the determination of Ni²⁺ was studied and no significant interference was observed. The membrane showed a good durability and short response time with no evidence of reagent leaching. The membrane was successfully applied for the determination of Ni²⁺ in environmental water samples.     

Flexible sensorial system based on capacitive chemical sensors integrated with readout circuits fully fabricated on ultra thin substrate

In this paper we present the design and fabrication of a fully flexible sensorial system, composed of three different sensor units implemented on an ultrathin polyimide substrate of 8 μm thick. Each unit is composed by a capacitive chemical sensor integrated with readout electronics. The sensors are parallel plate capacitors with the top electrode properly patterned to allow analytes diffusion into the dielectric that acts as chemical interactive material. Three different polymers, poly(tetrafluoroethene) (PTFE), poly(methyl 2-methylpropenoate) (PMMA) and benzocyclobutene (BCB), were used as dielectrics. A ring oscillator circuit, implemented with polysilicon thin film transistors (PS-nTFT), was used to convert the capacitance variations into frequency shifts. The electronic tests show oscillating frequencies of about 211 ± 2 kHz and negligible frequency shifts under different bending radius conditions. Furthermore, system response to some alcohols concentrations (Methanol, ethanol, 1-butanol, and 1-propanol) is reported and data analysis proves that the system is able to discriminate methanol from ethanol.