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1.
Denise Tofanello Gimenes Polyana Fernandes Pereira Rafael Rodrigues Cunha Rodrigo Amorim Bezerra da Silva Rodrigo Alejandro Abarza Munoz Eduardo Mathias Richter 《Electroanalysis》2012,24(9):1805-1810
In this study, we describe for the first time the application of an internal standard method to compensate for random errors associated with the injection procedure in batch injection analysis (BIA) systems with multiple pulse amperometric detection. A sequence of potential pulses was selected in such a way that the internal standard (IS) compound was detected individually at one potential pulse and both the IS and analyte, were detected at another potential pulse. The current ratio (IIS+analyte/IIS) was used in the construction of the calibration curve and then to compensate for random errors. The use of disposable syringes or manual pipettes in BIA systems increases the robustness of the method and dispenses with skilled operators. 相似文献
2.
We consider a certain type of second-order neutral delay differential systems and we establish two results concerning the oscillation of solutions after the system undergoes controlled abrupt perturbations (called impulses). As a matter of fact, some particular non-impulsive cases of the system are oscillatory already. Thus, we are interested in finding adequate impulse controls under which our system remains oscillatory. 相似文献
3.
Development of a Simple and Fast Electrochemical Method for Screening and Stoichiometric Determination of Dimenhydrinate 下载免费PDF全文
Jhonys Machado Freitas Thiago da Costa Oliveira Polyana Luiza Silva Denise Tofanello Gimenes Rodrigo Alejandro Abarza Munoz Eduardo Mathias Richter 《Electroanalysis》2014,26(9):1905-1911
Dimenhydrinate (DIM) is a salt composed by the combination of two active pharmaceutical ingredients: diphenhydramine (DIP) and 8‐chlorotheophylline (CTP). In this work, the use of batch injection analysis with multiple pulse amperometric detection (BIA‐MPA) was proposed for the first time for fast stoichiometric determination of DIM. DIP (cation) and CTP (anion) were determined simultaneously in pharmaceutical samples with a simple and fast injection procedure (70 injections h?1). Additional strategies were also proposed for rapid screening of samples containing the DIM salt. By a simple injection of a sample into the BIA system (without using of calibration curve), reliable information about stoichiometry of the DIM salt (1 : 1; DIP:CTP) and presence or absence of interfering species (electroactive) can be achieved. 相似文献
4.
Denise Tofanello Gimenes Wallans Torres Pio dos Santos Rodrigo Alejandro Abarza Munoz Eduardo Mathias Richter 《Electrochemistry communications》2010,12(2):216-218
In this work, we describe for the first time the use of the internal standard method in flow injection analysis (FIA) with amperometric detection. The method is based on the application of sequential potential pulses to the working electrode in an electrochemical flow cell. The sequence of potential pulses is selected in such a way that the analyte and internal standard compound are detected and monitored individually and independently at the same working electrode. This approach compensates for random errors associated with variations of flow rate, injection volume, ionic strength difference between standards and samples, and accidental insertion or formation of air bubbles in the carrier stream. In addition, this method can overcome the major drawback of amperometric detection using solid electrodes, which is gradual electrode passivation. To illustrate the potential of this method, the flow-injection amperometric detection of uric acid using [Fe(CN)6]3? as an internal standard (IS) is presented as an example. 相似文献
5.
Wallans Torres Pio dos Santos Edimar Gledison Nascimento de Almeida Humberto Eustáquio Alves Ferreira Denise Tofanello Gimenes Eduardo Mathias Richter 《Electroanalysis》2008,20(17):1878-1883
The present work reports a simple and quick strategy for simultaneous determination of paracetamol (PC) and ascorbic acid (AA) in pharmaceutical formulations using flow injection method with multiple pulse amperometric detection. The method allows the resolution of the mixture without chemical pretreatment of the sample or electrode modification or the use of chemometric techniques for data analysis. The compounds are detected by applying four sequential pulses (waveform) in function of time to a three‐electrode amperometric system that uses a wall‐jet cell with gold as working electrode. AA is direct detected at +0.40 V and PC is indirectly detected at 0.0 V by the reduction (desorption) of the oxidation product (N‐acetyl‐p‐benzoquinoneimine) electrochemically generated at +0.65 V. The fourth potential pulse (?0.05 V) is applied for the complete regeneration (cleaning) of the gold electrode surface. The linear response range was optimized between 5 and 24 mg L?1 for AA and 50 and 240 mg L?1 for PC. The difference between the two responses ranges (10‐fold) present correlation with the concentration of these compounds in two different pharmaceutical formulations available in the Brazilian market. The analytical frequency was calculated in 60 injections per hour. The use of the proposed methodology for PC quantification in the presence of higher AA concentrations was also carried out. Using the standard addition method, it was possible to detect PC in trace levels (LD=0.2 mg L?1) in the presence of 880‐fold more of AA (176 mg L?1). 相似文献
6.
Alexandre Minami Fioroto Gislayne Aparecida Rodrigues Kelmer Luiza Gimenes Rodrigues Albuquerque Thiago Régis Longo César Paixão 《光谱学快报》2017,50(10):550-556
A systematic approach is proposed to evaluate microwave-assisted digestion in a single reaction chamber for the simultaneous determination of elements in the mineral fertilizer and raw material by inductively coupled plasma optical emission spectrometry. A reference material was digested using 12 acid mixtures containing nitric, hydrochloric, orthophosphoric, hydrofluoric or boric acid. Principal components analysis was applied for data treatment. Three digestion procedures based on diluted acids exhibited the most accurate results, with relative errors for reference values ranging from ?15% to +?9%. Limits of quantification were in the range of 0.2?mg cadmium kg?1 up to 1000?mg aluminum kg?1. 相似文献
7.
When a time harmonic electromagnetic wave impinges on a slaba certain portion of the wave creates heat within the slab throughdipolar and ohmic heating. The electrical and thermal propertiesof the material dictate the dynamical nature of the heatingprocess, as well as the steady-state temperature profile. Thematerial considered here is a slab of fluid. We consider thecase where the fluid is bounded by thin rigid layers of transparentmaterial. The steady-state heating profile governs the typesof convective motions that can occur and also affects the stabilitycharacteristics of temperature, pressure and velocity perturbationsintroduced in the slab. The main objective here is to examinesuch stability characteristics, initially in the linear regime.Both rigid-rigid and rigid-free configurations are considered. 相似文献
8.
Faria Luis F. Figueiredo Gimenes Maria Antonieta P. Nobrega Ronaldo Pereira Nei 《Applied biochemistry and biotechnology》2002,98(1-9):449-458
Oxygen availability is the most important environmental parameter in the production of xylitol by yeasts, directly affecting
yields and volumetric productivity. This work evaluated the cell behavior in fermentations carried out with different dissolved
oxygen concentrations (0.5–30.0% of saturation), as well as a limited oxygen restriction (0% of saturation), at several oxygen
volumetric transfer coefficients (12 ≤ k
L
a ≤ 70 h−1). These experiments allowed us to establish the specific oxygen uptake rate limits to ensure high yields and volumetric productivity.
When oxygen availability was limited, the specific oxygen uptake rate values were between 12 and 26 mg of O2/of g cell·h, resulting in a yield of 0.71 g of xylitol/xylose consumed, and 0.85 g/[L·h] for the volumetric productivity.
According to the results, the effective control of the specific oxygen uptake rate makes it possible to establish complete
control over this fermentative process, for both cell growth and xylitol production. 相似文献
9.
Rafael R. Cunha Denise T. Gimenes Rodrigo A. A. Munoz Claudimir L. do Lago Eduardo M. Richter 《Electrophoresis》2013,34(9-10):1423-1428
This paper presents a method for fast and simultaneous determination of diclofenac (DCF) and its common counter‐ions (potassium, sodium, and diethylammonium) using CE with capacitively coupled contactless conductivity detection (CE‐C4D). On the basis of a single electropherogram (about 50 s), the proposed method allows the determination of the stoichiometry, absolute quantification and evaluation of the degradation degree of the active pharmaceutical ingredient (DCF). A linear working range from 100 to 500 μmol/L was obtained for all analytes in an equimolar TRIS/TAPS (10 mmol/L) solution as the background electrolyte as well as adequate LOD (7, 6, 7, and 10 μmol/L for K+, Na+, diethylammonium, and DCF, respectively). The proposed method was applied to the analysis of pharmaceutical formulations (tablets and spray form) with similar results to those achieved by HPLC (DCF) or flame photometry (K and Na) at a 95% confidence level. 相似文献
10.
Wesley C. Silva Polyana F. Pereira Mariana C. Marra Denise T. Gimenes Rafael R. Cunha Rodrigo A. B. da Silva Rodrigo A. A. Munoz Eduardo M. Richter 《Electroanalysis》2011,23(12):2764-2770
In this work, we report a simple and novel strategy for simultaneous analysis using flow injection analysis with multiple pulse amperometric (FIA‐MPA) detection. The proposed strategy was successfully used for simultaneous determination of paracetamol and caffeine (model analytes) in pharmaceutical formulations. A sequence of potential pulses (waveform) was selected in such a way that PA is selectively oxidized at E1 (+1.20 V/50 ms) and both compounds (PA+CA) are simultaneously oxidized at E2 (+1.55 V/50 ms); hence, current subtraction (using a correction factor) can be used for the selective determination of CA. The proposed FIA method is simple, cheap, fast (140 injections h?1), and present selectivity for the determination of both compounds in pharmaceutical samples, with results similar to those obtained by HPLC at a 95 % confidence level. 相似文献