A simple and reliable voltammetric method is presented for the determination of amitriptyline using a boron-doped diamond electrode in 0.1 mol L-1 sulfuric acid solution as the support electrolyte. Under optimized differential pulse voltammetry conditions (modulation time 5 ms, scan rate 70 mV s-1, and pulse amplitude 120 mV), the electrode provides linear responses to amitriptyline in the concentration range 1.05 to 92.60 µmol L-1 and at a detection limit of 0.52 µmol L-1. The proposed method was successfully applied in pharmaceutical formulations, with results similar to those obtained using UV-vis spectrophotometric method as reference (at 95% confidence level), as recommended by the Brazilian Pharmacopoeia.

Chemical imprinting technology has been widely used as a valuable tool in selective recognition of a given target analyte (molecule or metal ion), yielding a notable advance in the development of new analytical protocols. Since their discovery, molecularly imprinted polymers (MIPs) have been extensively studied with excellent reviews published. However, studies involving ion imprinted polymers (IIPs), in which metal ions are recognized in the presence of closely related inorganic ions, remain scarce. Thus, this review involved a survey of different synthetic approaches for preparing ion imprinted adsorbents and their application for the development of solid phase extraction methods, metal ion sensors (electrodes and optodes) and selective membranes.

The present study proposes a method for cloud point preconcentration of copper ions at pH 2.0 based on complexes formed with [4,5-dimercapto-1,3-dithyol-2-thionate] and subsequent determination by flame atomic absorption spectrometry (FAAS). Under optimal analytical conditions, the method provided limits of detection of 0.84 and 0.45 µg L-1, by preconcentrating 12.0 and 24.0 mL of sample, respectively. The method was applied for copper determination in water samples, synthetic saliva, guarana powder, tea samples and soft drinks and the accuracy was assessed by analyzing the certified reference materials Dogfish Liver (DOLT-4) and Lobster Hepatopancreas (TORT-2).

The present paper focuses on improving chromium (III) uptake capacity of sugarcane bagasse through its chemical modification with citric acid and/or sodium hydroxide. The chemical modifications were confirmed by infrared spectroscopy, with an evident peak observed at 1730 cm-1, attributed to carbonyl groups. Equilibrium was reached after 24 h, and the kinetics followed the pseudo-second-order model. The highest chromium (III) maximum adsorption capacity (MAC) value was found when using sugarcane bagasse modified with sodium hydroxide and citric acid (58.00 mg g-1) giving a MAC value about three times greater (20.34 mg g-1) than for raw sugarcane bagasse.

This work describes the development and validation of a dissolution test for 50 mg losartan potassium capsules using HPLC and UV spectrophotometry. A 2(4) full factorial design was carried out to optimize dissolution conditions and potassium phosphate buffer, pH 6.8 as dissolution medium, basket as apparatus at the stirring speed of 50 rpm and time of 30 min were considered adequate. Both dissolution procedure and analytical methods were validated and a statistical analysis showed that there are no significant differences between HPLC and spectrophotometry. Since there is no official monograph, this dissolution test could be applied for quality control routine.

The present work purposes the preparation of a silica gel sorbent organically modified with 2-aminoethyl-3-aminobutylmethyldimethoxysilane (AAMDMS) and imprinted with Cu2+ ions by means surface imprinting technique and its use for selective on-line sorbent preconcentration of Cu2+ ions with further UV-VIS spectrophotometric determination by flow injection analysis. The Cu2+-imprinted silica gel, when compared with non imprinted silica gel and silica gel, showed from the binary mixture of Cu2+/Ni2+ relative selectivity coefficient (k') of 6.84 and 5.43 and 6.64 and 19.83 for the mixture Cu2+/Pb2+, thus demonstrating higher selectivity of Cu2+-imprinted silica gel towards Cu2+ ions. Under optimized condition, the on-line preconcentration method provided detection limit of 3.4 μg L-1 and linear range ranging from 30.0 up to 300.0 μg L-1 (r = 0.995). The accuracy of method was successfully assessed by analyzing different kind of spiked water samples with recovery values ranging from 92.2 up to 103.0%.

Este estudo envolve a preparação de um polímero orgânico-inorgânico impresso com íon (IIP) para o enriquecimento seletivo de Ni2+ em soluções aquosas com posterior determinação por GF AAS. A rede polimérica híbrida foi preparada a partir de uma mistura do monômero funcional, 2-aminoetil-3-aminobutilmetildimetoxissilano e tetraetoxissilano como agente de ligação cruzada, contendo Ni2+ e brometo de cetiltrimetilamônio como moldes. Os polímeros foram caracterizados por IV, TG e MEV. A capacidade máxima adsortiva do IIP para os íons Ni2+, determinada pelo modelo linear de Langmuir, foi de 5,44 mg g-1. Quando o coeficiente de seletividade iônica do IIP foi comparado com os coeficientes de seletividade do NIP (non imprinted polymer) e IIP2 (ion imprinted polymer na ausência do surfactante), a partir das misturas binárias de Ni2+/Cu2+, Ni2+/Co2+, Ni2+/Cd2+ e Ni2+/Zn2+, os respectivos valores do coeficiente de seletividade relativo (k') foram 36,54 e 3,55, 1,22 e 2,03, 4,43 e 1,42, 28,60 e 1,74, demonstrando maior seletividade do IIP para os íons Ni2+. O método proposto forneceu um limite de detecção de 0,16 µg L-1 e foi aplicado com sucesso na determinação de Ni2+ em amostras de águas enriquecidas e fitoterápico (Gingko Biloba) com valores satisfatórios de recuperação.

This study involves the preparation of an ion imprinted organic-inorganic polymer (IIP) for selective sorbent enrichment of Ni2+ from aqueous solutions with further determination by GF AAS. The hybrid polymeric network was prepared from a mixture of 2-aminoethyl- 3-aminobutylmethyldimethoxysilane as functional monomer, and tetraethoxysilane as crosslinking agent, containing Ni2+ and cetyltrimethylammonium bromide as templates. The polymers were characterized by IR, TG and SEM. The maximum adsorptive capacity of IIP towards Ni2+ ions, determined by linear Langmuir model, was found to be 5.44 mg g-1. When the selectivity coefficient of IIP was compared with the selectivity coefficient of NIP (non imprinted polymer) and IIP2 (ion imprinted polymer in the absence of surfactant), from the binary mixtures of Ni2+/Cu2+, Ni2+/Co2+, Ni2+/Cd2+ and Ni2+/Zn2+, values of relative selectivity coefficient (k') were 36.54 and 3.55, 1.22 and 2.03, 4.43 and 1.42, 28.60 and 1.74, respectively, demonstrating higher selectivity of IIP for Ni2+ ions. The proposed method provided a limit of detection of 0.16 µg L-1 and was successfully applied for Ni2+ determination in spiked water samples and in a phytoterapic product (Gingko Biloba) with satisfactory recovery values.

The present work purposes the development of an analytical method for amitriptyline determination in pharmaceutical formulations using FIA system. It was based on interaction of amitriplyline with sodium lauryl sulphate in acid medium (pH 2.5) resulting in the ion-pair formation turbidimetrically detected at 410 nm. The fitting regression equation for range curve from 2.0 x 10-3 up to 3.2 x 10-3 mol L-1 was found to be analytical signal = -2.7417 + 0.1538 [amitriptyline] (r = 0.99991) with a detection limit of 1.8 x 10-3 mol L-1. The precision assessed as relative standard deviation (n = 10) was found to be 2.40 and 1.94%, for the respective concentration of amitriplyline 2.0 x 10-3 and 3.2 x 10-3 mol L-1 and the sample throughout was 60 h-1. The accuracy of method was successfully assessed in pharmaceutical formulation after comparison with a reference analytical method.

MIPs are synthetic polymers that are used as biomimetic materials simulating the mechanism verified in natural entities such as antibodies and enzymes. Although MIPs have been successfully used as an outstanding tool for enhancing the selectivity or different analytical approaches, such as separation science and electrochemical and optical sensors, several parameters must be optimized during their synthesis. Therefore, the state-of-the-art of MIP production as well as the different polymerization methods are discussed. The potential selectivity of MIPs in the extraction and separation techniques focusing mainly on environmental, clinical and pharmaceutical samples as applications for analytical purposes is presented.

The aim of this paper is the description of the strategies and advances in the use of MIP in the development of chemical sensors. MIP has been considered an emerging technology, which allows the synthesis of materials that can mimic some highly specific natural receptors such as antibodies and enzymes. In recent years a great number of publications have demonstrated a growth in their use as sensing phases in the construction of sensors . Thus, the MIP technology became very attractive as a promising analytical tool for the development of sensors.