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Altres ajuts: acords transformatius de la UAB Some inborn errors of metabolism and other diseases can result in increasing blood ammonium (hyperammonemia episodes), which can cause serious neurological complications in patients or even death. Early diagnosis, follow up and treatment are essential to minimize irreversible damages in brain. Currently, adequate analytical instrumentation for the necessary ammonium bedside determination is not available in all health centers but only in clinical laboratories of reference hospitals. We therefore have developed a low cost and portable potentiometric Point-of-Care microanalyzer (POC) to address this problem. It consists of a cyclic olefin copolymer-based microanalyzer, the size of a credit card and working in continuous flow, which integrates microfluidics, a gas-diffusion module and a potentiometric detection system. The analytical features achieved are a linear range from 30 to 1000 μmol L NH , a detection limit of 18 μmol L NH and a required sample volume of 100 μL, which comply with the medical requirements. Plasma and blood samples are analyzed with no significant differences observed between ammonium concentrations obtained with both the proposed microanalyzer and the reference method. This demonstrates the value of the developed POC for bedside clinical applications.

The design, construction and evaluation of a low cost, cyclic olefin copolymer (COC)-based continuous flow microanalyzer, with optical detection, to monitor carbon dioxide in bottled wines and beers as well as in fermentation processes, is presented. The microsystem, constructed by computer numerically controlled (CNC) micromilling and using a multilayer approach, integrates microfluidics, gas-diffusion module and an optical flow-cell in a single polymeric substrate. Its size is slightly bigger than a credit card, exactly 45 × 60 × 4 mm in the microfluidic and diffusion module zone and 22.5 × 40 × 3 mm in the flow-cell zone. The gas-diffusion module is based on a hydrophobic polyvinylidene fluoride (PVDF) membrane, which allows the transfer of the carbon dioxide present in the sample to a bromothymol blue (BTB) pH-sensitive acceptor solution, where the color change is measured optically. The detection system consisted of a LED with an emission peak at 607 nm and a photodiode integrated in a printed circuit board (PCB). The obtained analytical features after the optimization of the microfluidic platform and hydrodynamic variables are a linear range from 255 to 10000 mg L−1 of CO2 and a detection limit of 83 mg L−1 with a sampling rate of 30 samples h−1.

The construction and evaluation of a Cyclic Olefin Copolymer (COC)-based continuous flow potentiometric microanalyzer to simultaneously monitor potassium, chloride and nitrate ions in samples from an on-board water recycling process expected to be installed in future manned space missions is presented. The main goals accomplished in this work address the specific required characteristics for a miniaturized on-line monitoring system to control water quality in such missions. To begin with, the integration of three ion-selective electrodes (ISEs) and a reference electrode in a compact microfluidic platform that incorporates a simple automatic autocalibration process allows obtaining information about the concentration of the three ions with optimal analytical response characteristics, but moreover with low reagents consumption and therefore with few waste generation, which is critical for this specific application. By a simple signal processing (signal removal) the chloride ion interference on the nitrate electrode response can be eliminated. Furthermore, all fluidics management is performed by computer-controlled microvalves and micropumps, so no manual intervention of the crew is necessary. The analytical features provided by the microsystem after the optimization process were a linear range from 6.3 to 630 mg L−1 and a detection limit of 0.51 mg L−1 for the potassium electrode, a linear range from 10 to 1000 mg L−1 and a detection limit of 1.58 mg L−1 for the chloride electrode and a linear range from 10 to 1000 mg L−1 and a detection limit of 3.37 mg L−1 for the nitrate electrode with a reproducibility (RSD) of 4%, 2% and 3% respectively. Sample throughput was 12 h−1 with a reagent consumptions lower than 2 mL per analysis.

The construction and evaluation of a Low Temperature Co-fired Ceramics (LTCC)-based continuous flow potentiometric microanalyzer prototype to simultaneously monitor the presence of two ions (potassium and nitrate) in samples from the water recycling process for future manned space missions is presented. The microsystem integrates microfluidics and the detection system in a single substrate and it is smaller than a credit card. The detection system is based on two ion-selective electrodes (ISEs), which are built using all-solid state nitrate and potassium polymeric membranes, and a screen-printed Ag/AgCl reference electrode. The obtained analytical features after the optimization of the microfluidic design and hydrodynamics are a linear range from 10 to 1000 mg L−1 and from 1.9 to 155 mg L−1 and a detection limit of 9.56 mg L−1 and 0.81 mg L−1 for nitrate and potassium ions respectively.

In this paper, the universal determination of non-ionic surfactants (NIS) of the polyethoxylate type is attempted using flow-injection potentiometry. Two systems are proposed which use specifically developed tubular flow-through ion selective electrodes (ISEs). These are sensitive to NIS with an hydrophilic chain between 6 and 18 ethoxylate units, which are predominant species in the environment. An on-line pre-concentration system is designed with the aim of a possible application for the unattended monitoring of NIS in surface waters. This on-line pre-concentration is achieved by employing a column packed with a commercial solid phase extraction (SPE) sorbent for the enrichment and purification of the target analytes. The procedure outlined improves the detection limit of a direct system, decreasing it from 1×10 −4 to 3×10 −6 M by use of a pre-concentration volume of 40.0 ml and 200 μl of 75% acetonitrile in water as the eluent. Precision was estimated as 4% relative standard deviation (R.S.D.) ( n =25) for a 1×10 −6 M (0.7 ppm) nonylphenol polyethoxylate with 12 ethoxylate units when 10.0 ml of sample are pre-concentrated. Finally, the on-line pre-concentration system is applied for the total NIS determination in environmental samples from Llobregat river basin of Barcelona area (NE Spain).

The design, construction and evaluation of a versatile cyclic olefin copolymer (COC)-based continuous flow potentiometric microanalyzer to monitor the presence of ammonium ion in recycling water processes for future manned space missions is presented. The microsystem integrates microfluidics, a gas-diffusion module and a detection system in a single substrate. The gas-diffusion module was integrated by a hydrophobic polyvinylidene fluoride (PVDF) membrane. The potentiometric detection system is based on an all-solid state ammonium selective electrode and a screen-printed Ag/AgCl reference electrode. The analytical features provided by the analytical microsystem after the optimization process were a linear range from 0.15 to 500 mg L−1 and a detection limit of 0.07 ± 0.01 mg L−1. Nevertheless, the operational features can be easily adapted to other applications through the modification of the hydrodynamic variables of the microfluidic platform.

A method is described for the conductimetric determination of CO 2 . The proposed system was constructed with a pervaporator chamber coupled to a flow system comprised of a six-way solenoid valve, a conductivity cell, a conductivimeter and a PC microcomputer for data acquisition and external controls. An amount of 2 g of dry soil samples were directly weighted in the donor compartment of the pervaporation chamber. The CO 2 was determined from an analytical curve within 5.0 x 10 -3 -5.0 x 10 -2 mol kg -1 CaCO 3 . This curve was constructed with the matrix matching approach and presented a linear regression of y = 13.58 + 584.77r (r = 0.9962). Soils with different lime amounts were analyzed by the proposed methodology and with the official method, that uses the calcium difference between the total, extracted with HCl 1 mol l -1 and exchangeable, extracted with the KCl 1 mol l -1 After paired t-test application, no significant difference between the methods was found at the 95% probability level. The proposed method presented sampling rate of 17 h -1 , detection limit of 8.0 x 10 -4 mol kg -1 CaCO 3 , and R.S.D. < 3%. The use of the pervaporator allowed the in situ soil pretreatment for the residual lime determination.

A flow injection system for the determination of polyethoxylated nonionic surfactants is described. Potentiometric detection based on tubular flow-through ion-selective electrodes (ISEs) sensitive to this type of surfactants was used. As ion-exchanger, the plasticised PVC membrane incorporates the ion pair between the adduct of a nonionic surfactant with barium and tetraphenylborate. Two different membrane compositions were studied. They differed in the nonionic surfactant used in the ion-exchanger preparation: either nonylphenoxypolyethoxylate with 5 (Ig5) or 12 (Ig12) ethylene oxide units were used. Experimental results showed that the use of Ig5 membrane with a barium salt adjusting solution allowed lower detection limits, while Ig12 ISE with potassium salt solution presented enhanced sensitivity. Both FI systems were evaluated employing three different polyethoxylate standards, which could be determined down to ca. 10 −5 M. Precision was 3% R.S.D. for n = 50 using repetitive injections of a 3 × 10 −4 M Ig12 standard. Preliminary tests of an on-line preconcentration flow system employing the developed sensing devices are also shown. © 2001 Elsevier Science B.V. All rights reserved.

The fabrication of ion-sensitive electrochemical sensors for calcium is described in the present work. The membrane uses a photocurable polymer based on aliphatic diacrylated polyurethane. The use of photocurable polymers as the support matrix instead of PVC simplifies the preparation and the casting of the developed ion-sensitive membranes. Additionally, these polymers are compatible with the photolithographic fabrication techniques used in the microelectronics industry. This aspect permits the patterning of membranes on wafer level for semiconductor based sensors thus the automatization of the whole sensor fabrication. These polymer matrices show also better adhesion to silanised semiconductor surfaces, such as the gate surfaces of ion selective field effect transistors (ISFETs). Membranes sensitive to calcium ions were optimised according the type of plasticizer and the polymer/plasticizer ratio. Ion selective electrodes (ISEs) with a solid internal reference and ISFETs were used to evaluate the membrane. The resulting sensors were functional for periods of more than 8 months and the resulting sensitivities were quasi-Nernstian (26–27 mV/dec) in a range of 5×10 −6 –8×10 −2 M. These sensors were used to measure calcium activity in water samples extracted from agricultural soils. The results were compared with those yielded by standard methods, finding a good correlation between the two analytical procedures.

The development of a new electrochemical microsensor based on silicon technology with a photocurable enzyme membrane based on polyurethane acrylate is described. The use of photocurable polymers as the entrapping matrix for enzymes fulfils all the requirements expected for these materials without damaging the biological material. Additionally, the preparation of biosensor devices following this methodology is fast and simple, and this entails the main improvement shown by the new immobilisation method proposed here. The polymer used for enzyme immobilisation enhances the adhesion of the membrane to the previously silanised ion-sensitive field effect transistor (ISFET) gate and assures a long-term stability of more than one month. Additionally, this material provides a membrane deposition methodology compatible with photolithographic techniques allowing mass-production of low cost biosensors. The membrane has been optimised taking into account a good entrapment of the biological material and the effective transport of the substrate and the products through the membrane. After mixing the components of the prepolymer solution, a short exposure (30 s) to 365 nm UV-radiation produced a polymeric membrane without damaging the enzyme. The calibration parameters for the sensors prepared compared well with other methods yielding a slope of 58 mV/dec and a linear range of 0.04–36.0 mM urea in a NH4Cl pH 5.6 solution. The response time (t 95%) was approximately 2 min.

The application of optimised poly(vinyl chloride) matrix, anionic surfactant-sensitive membranes to ion-selective field-effect transistors (ISFETs) is described. The developed devices showed a lifetime longer than four months, improving reported values of PVC membrane-ISFETs. Other characteristics are Nernstian slopes from 59 to 62 mV/dec, detection limits of about 10 ˇ6 M and good linearity. They also showed response to several anionic surfactant species and to the reagent used for the potentiometric titration. This allowed the measurement of the overall anionic surfactant content in different samples. Apart from the basic characteristics of the membranes, this report also shows the results of potentiometric titrations using the developed ISFETs with known samples. The devices were useful in a range from 0.02 to 10 mM for dodecylbenzenesulphonate solutions. End-point potential jumps up to 250 mV were obtained in the titrations. The reproducibility, expressed as relative standard deviation, was estimated, using a standard 4 mM sodium dodecylsulphate solution, as 1.45% (na14). Finally, in a comparative study, there were no significant differences between the results produced with the standard, two-phase titration method and the proposed potentiometric titration method using surfactant ISFETs as end-point indicators. # 1999 Elsevier Science B.V. All rights reserved.

A flow-injection system based on potentiometric detection and designed for the monitoring of anionic surfactant content of printing plates washing solutions is described. Two new PVC membrane ion-selective electrodes, constructed with an all-solid-state tubular flow-through design, are used. The sample, with high ionic strength and extremely alkaline pH, is conditioned in a two-channel flow-injection system, allowing for surfactant determination in the 1 × 10 −4 to 1 × 10 −3 M range, with NaOH contents up to 0.3 M.

Results obtained in the evaluation of a mathematical model for flow-injection sandwich systems, in which the sample is inserted between two different carrier solutions with the aid of an eight-way injection valve, are presented. The model considers the system as a tubular reactor with axially dispersed plug flow, where chemical kinetics have been included. Only a minimum of parameters are needed for the model: the dispersion coefficients, which are obtained from experimental correlations for the different hydrodynamic conditions, and the rate constants, which are determined by univariate optimization. The behaviour of the model, when applied to the case of one analyte and one reagent, was evaluated for the enzymatic determinations of glucose or glycerol. The case of two analytes determined with two reagents was also studied in the combined determination of glucose and glycerol. Experimental profiles were compared with the simulated peaks and showed good agreement.

A simple flow-injection metod for the determination of ammonium ions in water, based on a flow-through pH-ISFET, is described. Ammonium is converted to ammonia, which diffuses through a microporous hydrophic membrane into an ammonium chloride recipient stream, forming a pH buffer which is monitored by the semiconductor detector. The linear working range extends from 0.1 to 10 mmol l−1 with a relative standard deviation of ca. 1% at the 0.7 mmol l−1 level.

Flow injection methodology based on sample insertion between two different standard solutions used as carrier streams is described. This approach provides a simple system for continuous recalibration in process control; spectrophotometric and ion-selective electrode procedures are outlined.

A simply constructed flow-through pH-ISFET detector suitable for flow-injection analysis is described. Its response characteristics are presented and discussed. The calibration plot is linear in the pH range 2–12; the slope is 53 mV per decade.

Samples (1500 μl) are inserted between zones of water and ascorbic acid solution with subsequent addition of 1,10-phenanthroline at pH 5.0. The signal provides a plateau region corresponding to Fe(Il) followed by a peak corresponding to total iron. The proposed system allows up to 90 injections per hour. Linear working ranges are 0.1–9 and 0.3–12 mg l−1 Fe(II) and total iron, with relative standard deviations of < 0.6 and 1.2%, respectively. Results obtained for various ground waters agree well with those obtained by a standard method.

A tubular PVC membrane electrode for calcium without inner reference solution and a device for location of the reference electrode are described. In the flow-injection system, calcium is determined potentiometrically and then magnesium is determined by atomic absorption spectrometry. The electrode provides linear response to calcium in the range 5 × 10 −5 /2-10 −1 M. On-line dilution of the sample allows magnesium determination in the range 0/2-10 mg l − . Flow rates between 3 and 6 ml min −1 are possible. The sampling frequency is 60/2-90 h −1 .