Effect of electrochemically dealloying Ti6Al4V abutments on human gingival fibroblasts / 口腔疾病防治

Objective@#To investigate the effects of electrochemically dealloying of Ti6Al4V abutments on human gingival fibroblasts (HGFs) and to provide experimental evidence for surface modification of implant abutments.@*Methods@#The samples were divided into an NC group (negative control, no other treatment on a smooth surface), an NM-1 group (nanomesh-1, electrochemical dealloying treatment in 1 mol/L NaOH 1 h on 2 V voltage), and an NM-2 group (nanomesh-2, electrochemical dealloying treatment in 5 mol/L NaOH 1 h on 2 V voltage). The surface morphologies of the samples and the adhesion of HGFs on the sample surfaces were observed with scanning electron microscopy (SEM). The surface hydrophilicities of the samples were measured with a contact angle measuring instrument. The proliferation of HGFs on the different samples were evaluated with CCK-8, and the expression of adhesion-related genes, including collagen Ⅰ (COL1A1), collagen Ⅲ (COL3A1), fibronectin 1 (FN1), focal adhesion kinase (FAK), vinculin (VCL), integrin α2 (ITGA2), and integrin β1 (ITGB1), on the different samples was measured with qRT-PCR. The expression of vinculin on the surfaces of HGFs was observed via confocal laser scanning microscopy (CLSM) after immunofluorescent staining. Collagen fiber secretion and syntheses of HGFs from different samples were evaluated via Sirius red staining.@*Results@#SEM revealed the formation of ordered and uniform three-dimensional mesh structures on the surfaces of the NM-1 and NM-2 groups, with grid diameters of approximately 30 nm for the NM-1 group and approximately 150 nm for the NM-2 group. Compared with that of the NC group, the water contact angles of the NM-1 group and NM-2 groups were significantly lower (P<0.000 1). Cell proliferation in the NM-1 group was significantly greater than that in the NC group (P<0.01). Moreover, there was no significant difference in the water contact angles or cell proliferation between the NM-1 group and the NM-2 group. SEM revealed that HGFs were adhered well to the surfaces of all samples, while the HGFs in the NM-1 and NM-2 groups showed more extended areas, longer morphologies, and more developed pseudopodia than did those in the NC group after 24 h. qRT-PCR revealed that the expression levels of the adhesion-related genes COL1A1, COL3A1, FN1, FAK and VCL in the NM-1 group were significantly greater than those in the NC and NM-2 groups (P<0.01). The expression of vinculin protein in the NM-1 group was the highest, and the number of focal adhesions was greatest in the NM-1 group (P<0.01). The results of Sirius red staining showed that the NM-1 group had the highest secretion and syntheses of collagen fibers (P<0.000 1).@*Conclusion@#The three-dimensional nanomechanical structure of Ti6Al4V modified by electrochemical dealloying promoted the adhesion, proliferation, collagen fiber secretion and syntheses of HGFs, and electrochemical dealloying of Ti6Al4V with a grid diameter of approximately 30 nm obviously promoted HGF formation.

Electrochemical Studies of Magnesium Coated with Modified Chitosan and Electrosprayed as an Anticorrosive Protection Method in Bone Repair / Estudios Electroquímicos del Magnesio Recubierto con Quitosano Modificado y Electrorociado como Proceso de Protección Anticorrosiva en la Reparación de Hueso

ABSTRACT Magnesium (Mg) is essential for the metabolic reactions of the human body and is known for its biocompatibility, its mechanical and physical properties are similar to human bone, which is why it is considered to have high potential in biomedical applications such as temporary and resorbable implants. Through surface modifications, the high tendency to corrosion of Mg could be controlled, such as biodegradable membranes that prevent the passage of chloride ions present in the human organism. To prepare the membrane, solutions of chitosan modified with gelatin and/or glutaraldehyde are used and by means of the electrospray method applied to protect the Mg. To simulate body fluid conditions a Kokubo saline solution (BFK) was prepared. The study focuses on evaluating the corrosion rate of Mg with a coating made of a chitosan electrosprayed membrane, applying electrochemical measurements of electrochemical impedance spectroscopy and linear polarization resistance. The key additive to improve the behavior of the membranes was observed with the use of gelatin, where the membrane with the best results lowing corrosion rates is the Mg CH+GE+GL system, which it was observed with very good physical integrity in the images of morphological analyzes of the surface after 30 days of exposure.

RESUMEN El magnesio (Mg) es esencial para las reacciones metabólicas del cuerpo humano y es conocido por su biocompatibilidad, sus propiedades mecánicas y físicas son similares a las del hueso humano, por lo que se considera que tiene un alto potencial en aplicaciones biomédicas como implantes temporales y reabsorbibles. Mediante modificaciones superficiales se podría controlar la alta tendencia a la corrosión del Mg, como por ejemplo membranas biodegradables que impidan el paso de iones cloruro presentes en el organismo humano. Para preparar la membrana se utilizan soluciones de quitosano modificado con grenetina y/o glutaraldehído y mediante el método de electrorociado se aplican para proteger el Mg. Para simular las condiciones de los fluidos corporales se preparó una solución salina de Kokubo. El estudio se enfoca en evaluar la velocidad de corrosión del Mg con un recubrimiento hecho de una membrana electrorociada con quitosano, aplicando técnicas electroquímicas de espectroscopia de impedancia electroquímica y resistencia de polarización lineal. El aditivo clave para mejorar el comportamiento de las membranas se observó con el uso de gelatina, donde la membrana con mejores resultados bajando los índices de corrosión es el sistema Mg CH+GR+GL, el cual se observó con muy buena integridad física en las imágenes de análisis morfológicos de la superficie después de 30 días de exposición.

Tumor cell membrane-coated continuous electrochemical sensor for GLUT1 inhibitor screening / 药物分析学报

Glucose transporter 1(GLUT1)overexpression in tumor cells is a potential target for drug therapy,but few studies have reported screening GLUT1 inhibitors from natural or synthetic compounds.With cur-rent analysis techniques,it is difficult to accurately monitor the GLUT1 inhibitory effect of drug molecules in real-time.We developed a cell membrane-based glucose sensor(CMGS)that integrated a hydrogel electrode with tumor cell membranes to monitor GLUT1 transmembrane transport and screen for GLUT1 inhibitors in traditional Chinese medicines(TCMs).CMGS is compatible with cell membranes of various origins,including different types of tumors and cell lines with GLUT1 expression knocked down by small interfering RNA or small molecules.Based on CMGS continuous monitoring technique,we inves-tigated the glucose transport kinetics of cell membranes with varying levels of GLUT1 expression.We used CMGS to determine the GLUT1-inhibitory effects of drug monomers with similar structures from Scutellaria baicalensis and catechins families.Results were consistent with those of the cellular glucose uptake test and molecular-docking simulation.CMGS could accurately screen drug molecules in TCMs that inhibit GLUT1,providing a new strategy for studying transmembrane protein-receptor interactions.

Research progress on surface modification of titanium implants by strontium ions / 口腔疾病防治

@#Traditional titanium implants do not completely meet the clinical requirements because they are bioinert. The surface of titanium implants, modified by strontium ions, can enhance osseointegration and reduce peri-implantitis. In this paper, the biological properties of titanium implant surfaces modified by strontium ions were reviewed. Strontium ions can be coated on the implant surface by hydrothermal treatment, electrochemical deposition, phosphate chemical conversion, flame-spraying, supramolecular self-assembly, magnetron sputtering, laser deposition and alkali etching. Implant surfaces modified by strontium ions can not only promote osteogenesis and early osseointegration but also inhibit bacterial growth and reduce postoperative infections. Even better osseointegration and antibacterial effects can be achieved when strontium ions are incorporated with other elements, such as silver, zinc, gallium, and calcium. However, most of the studies on the use of strontium ion-modified titanium implants are animal experiments and in vitro experiments, and the observation time is short compared with the actual service life of the implants. Thus, the conclusions obtained may be different from the actual clinical application, and the long-term effects need to be studied. In addition, the osteogenic effects of various modification methods also need to be compared. Future research can focus on the following points: ① to find efficient modification methods that can be widely used in the clinic; ②to study how to control the concentration of strontium ions near the implant to exert their biological function and reduce their toxic side effects; and ③ to conduct long-term follow-up clinical trials to observe their osteogenic and antibacterial effects.

Bionic optic nerve based on perovskite (CsPbBr 3) quantum-dots / 生物医学工程学杂志

The bionic optic nerve can mimic human visual physiology and is a future treatment for visual disorders. Photosynaptic devices could respond to light stimuli and mimic normal optic nerve function. By modifying (Poly(3,4-ethylenedioxythio-phene):poly (styrenesulfonate)) active layers with all-inorganic perovskite quantum dots, with an aqueous solution as the dielectric layer in this paper, we developed a photosynaptic device based on an organic electrochemical transistor (OECT). The optical switching response time of OECT was 3.7 s. To improve the optical response of the device, a 365 nm, 300 mW·cm -2 UV light source was used. Basic synaptic behaviors such as postsynaptic currents (0.225 mA) at a light pulse duration of 4 s and double pulse facilitation at a light pulse duration of 1 s and pulse interval of 1 s were simulated. By changing the way light stimulates, for example, by adjusting the intensity of the light pulses from 180 to 540 mW·cm -2, the duration from 1 to 20 s, and the number of light pulses from 1 to 20, the postsynaptic currents were increased by 0.350 mA, 0.420 mA, and 0.466 mA, respectively. As such, we realized the effective shift from short-term synaptic plasticity (100 s recovery of initial value) to long-term synaptic plasticity (84.3% of 250 s decay maximum). This optical synapse has a high potential for simulating the human optic nerve.

A descrição teórica da determinação eletroquímica do fármaco perilartina, assistida pelo oxihidróxido de cobalto, emparelhado com o seu dióxido

Introdução: perilartina é um adoçante natural potente, considerado 2000 vezes mais doce que o açúcar comum. Ela pode ser alérgica para algumas pessoas. Além disso, ela se usa apenas no Japão, o que pressupõe a possibilidade de adulterar produtos japoneses sem o seu uso. Assim, o desenvolvimento de um método eficiente da sua determinação qualificativa e quantificação é realmente atual. Metodologia: um modelo matemático de um processo anódico foi desenvolvido e analisado mediante a teoria de estabilidade linear e análise de bifurcações. O modelo inclui os cenários mais prováveis do andamento do processo eletroanalítico. Resultados: a perilartina é oxidada no meio básico, formando o poliol e o sal do "pseudoácido" correspondente, o que contribui fortemente para a força iônica da dupla camada elétrica. Isto pode ser responsável pela aparição das instabilidades oscilatória e monotônica no processo eletroanalítico. Conclusão: malgrado o supracitado, o compósito é um modificador eficiente para a determinação eletroquímica da perilartina no meio básico.

Introducción: perilartina es un edulcorante natural potente, considerado 2000 veces más dulce que el azúcar común. Esta puede causar alergia a algunas personas. Además, ella solo se usa en Japón, lo que presupone la posibilidad de falsificar productos japoneses sin su uso. Así, el desarrollo de un método eficiente de su determinación cuantitativa y cualitativa es realmente actual. Metodología: un modelo matemático de un proceso anódico fue desarrollado y analizado mediante la teoría de estabilidad lineal e análisis de bifurcaciones. El modelo incluye los escenarios más probables del curso del proceso electroanalítico. Resultados: la perilartinase oxida en el medio básico, formando el poliol y la sal del "pseudoácido" correspondiente, lo que contribuye fuertemente para la fuerza iónica de la doble capa eléctrica. Esto puede ser responsable por la aparición de las inestabilidades oscilatoria y monotónica en el proceso electroanalítico. Conclusión: a pesar de lo mencionado, el compuesto es un modificador eficaz para la determinación electroquímica de la perilartina en el medio básico.

SUMMARY Introduction: Perillartine is a strong natural sweetener, considered 2000 as sweet as a common sugar. It may be allergic to some people. Also, it is used only in Japan, which may presuppose the possibility of falsify Japanese products without its use. Thus the development of an eficiente method of its quantitative and qualitative determination is really actual. Methodology: A mathematical model of an anodic process has been developed and analyzed by means of linear stability theory and bifurcation analysis. The model includes the most probable scenarios of the course of the electroanalytical process. Results: Perillartine is oxidized in basic media, yielding the polyol and the correspondent pseudoacid salt, which strongly contributes to the double electric layer ionic force. This may be responsible for the oscillatory and monotonic instabilities appearance in the electroanalytical process. Conclusion: Despite of the above mentioned statements, the composite is na efficient modifier for the electrochemical determination of perillartine in basic media.

Descripción teórica del desempeño electroanalítico del material compuesto de oxihidróxido de vanadio con el colorante escuárico en la detección de la carfedona

Introducción: en este trabajo se evalúa desde el punto de vista mecanístico teórico el comportamiento electroanalítico del compuesto oxihidróxido de vanadio-colorante escuárico en la detección de la carfedona. El proceso electroanalítico incluye la formación de dos formas de vanadio tetravalente, incluyendo el dióxido de vanadio e ion vanadilo. Método: un mecanismo, capaz de describir el comportamiento del sensor, ha sido sugerido y un modelo matemático fue desarrollado y analizado mediante la teoría de estabilidad lineal y análisis de bifurcaciones. Resultados: el análisis del modelo ha probado que la dependencia lineal entre la concentración del fármaco y el parámetro electroquímico se mantiene firme en la ancha región topo-lógica de parámetros. Las inestabilidades oscilatoria y monotónica suelen realizarse cuando son causadas por influencias fuertes de las etapas química y electroquímica en la capacitancia de la doble capa eléctrica. Conclusiones: el compuesto de nano-partículas de oxihidróxido de vanadio (estabilizadas con el colorante escuárico) puede servir como un modificador eficiente de electrodo para la detección de la carfedona. El oxihidróxido de vanadio desempeña funciones de sustancia activa y el colorante, de la mediadora.

SUMMARY Introduction: In this work, the electroanalytical behavor of the vanadium oxyhydroxide-squaraine dye composite for the carfedon detection is evaluated. The electroanalytical process includes the formation of two tetravalent vanadium forms, including vanadium dioxide and vanadylion. Methods: A mechanism, capable to describe the sensor behavior, has been suggested, and the correspondent mathematical model has been developed and analyzed by means of the linear stability theory and bifurcation analysis. Results: The model analysis has proved that the linear dependence between the drug concentration and the concentration is firmly maintained in a wide topological parameter region. As for the oscillatory and monotonic instabilities, they may be realized, being caused by strong influences of the chemical and electrochemical stages on double electric layer capacitance. Conclusions: The vanadium oxyhydroxide composite with the squaraine dye may serve as an efficient electrode modifier for carfedone determination. The vanadium oxyhydroxide works as an active substance and the dye as a mediator.

Introdução: neste trabalho, avalia-se, do ponto de vista mecanístico teórico, o comportamento eletroanalítico do compósito oxihidróxido do vanádio-corante esquárico na detecção da carfedona. O processo eletroanalítico inclui a formação de duas formas do vanádio tetravalente, incluindo o dióxido de vanádio e íon vanadila. Método: um mecanismo, capaz de descrever o comportamento do sensor, tem sido sugerido e um modelo matemático correspondente, desenvolvido e analisado por meio da teoria de estabilidade linear e análise de bifurcações. Resultados: a análise do modelo tem provado que a dependência linear entre a concentração do fármaco e o parâmetro eletroquímico se mantém firme numa ampla região topológica de parâmetros. Já as instabilidades oscilatória e monotônica soem realizar-se, sendo causadas pelas influências fortes das etapas química e electroquímica na capacitância da dupla camada elétrica. Conclusões: o compósito de nanopartículas do oxihidróxido de vanádio, estabilizadas pelo corante esquárico, pode servir de um modificador eficaz para a detecção da carfedona. O oxihidróxido de vanádio desempenha as funções de substância ativa, e o corante, de mediador.

Green electrochemical sensors based on ionic liquid nanocomposites for detection of environmental pollutants

Industrialization and globalization have caused a huge burden on the limited natural resources, which releases various environmental pollutants such as toxic metal ions and pesticides. World Health Organisation (WHO) has set a maximum permissible limit for these toxic pollutants in water, above which, it is unsuitable for drinking purpose. There are various techniques available for the determination of such pollutants like ICP-MS, HPLC, FAAS etc. that are costly, cumbersome, and time consuming. Whereas, electrochemical sensors are portable, fast and can perform multi-analyte sensing. Electrochemical sensor can be made selective by fabricating with nanocomposites having different functional groups. Nowadays, trend of utilizing greener materials in research field is being highly appreciated in accordance with the principles of green chemistry for the application and development of electrochemical sensors. Ionic liquids having non-volatility, low toxicity, wide potential window, high electrochemical stability and conductivity have shown sustainable electrochemical sensing applications. Nanocomposite of these ionic liquids as a sensing platform have been extensively used in electrochemical detection of various pollutants. This work provides a literature survey of different ionic liquid nanocomposite based sensing platform for electrochemical detection of toxic pesticides and heavy metals. They have demonstrated good sensitivity with detection limit below WHO guidelines.

Highly sensitive electrochemical determination of rutin based on the synergistic effect of 3D porous carbon and cobalt tungstate nanosheets / 药物分析学报

Rutin,a flavonoid found in fruits and vegetables,is a potential anticancer compound with strong anti-cancer activity.Therefore,electrochemical sensor was developed for the detection of rutin.In this study,CoWO4 nanosheets were synthesized via a hydrothermal method,and porous carbon(PC)was prepared via high-temperature pyrolysis.Successful preparation of the materials was confirmed,and character-ization was performed by transmission electron microscopy,scanning electron microscopy,and X-ray photoelectron spectroscopy.A mixture of PC and CoWO4 nanosheets was used as an electrode modifier to fabricate the electrochemical sensor for the electrochemical determination of rutin.The 3D CoWO4 nanosheets exhibited high electrocatalytic activity and good stability.PC has a high surface-to-volume ratio and superior conductivity.Moreover,the hydrophobicity of PC allows large amounts of rutin to be adsorbed,thereby increasing the concentration of rutin at the electrode surface.Owing to the syn-ergistic effect of the 3D CoWO4 nanosheets and PC,the developed electrochemical sensor was employed to quantitively determine rutin with high stability and sensitivity.The sensor showed a good linear range(5-5000 ng/mL)with a detection limit of O.45 ng/mL.The developed sensor was successfully applied to the determination of rutin in crushed tablets and human serum samples.

Nitrogen-doped carbon@TiO2 double-shelled hollow spheres as an electrochemical sensor for simultaneous determination of dopamine and paracetamol in human serum and saliva / 药物分析学报

As the most commonly used antipyretic and analgesic drug,paracetamol(PA)coexists with neuro-transmitter dopamine(DA)in real biological samples.Their simultaneous determination is extremely important for human health,but they also interfere with each other.In order to improve the conductivity,adsorption affinity,sensitivity,and selectivity of TiO2-based electrochemical sensor,N-doped carbon@-TiO2 double-shelled hollow sphere(H-C/N@TiO2)is designed and synthesized by simple alcoholic and hydrothermal method,using polystyrene sphere(PS)as a template.Meanwhile,TiO2 hollow spheres(H-TiO2)or N-doped carbon hollow spheres(H-C/N)are also prepared by the same method.H-C/N@TiO2 has good conductivity,charge separation,and the highly enhanced and stable current responses for the detection of PA and DA.The detection limit and linear range are 50.0 nmol/L and 0.3-50 μmol/L for PA,40.0 nmol/L and 0.3-50 μmol/L for DA,respectively,which are better than those of carbon-based sen-sors.Moreover,this electrochemical sensor,with high selectivity,strong anti-interference,high reli-ability,and long time durability,can be used for the simultaneous detection of PA and DA in human blood serum and saliva.The high electrochemical performance of H-C/N@TiO2 is attributed to the multi-functional combination of different layers,because of good conductivity,absorption and electrons transfer ability from in-situ N-doped carbon and electrocatalytic activity from TiO2.

Construction and performance analysis of a microbial electrochemical sensor for monitoring heavy metals in water environment / 生物工程学报

A microbial fuel cell (MFC)-based microbial electrochemical sensor was developed for real-time on-line monitoring of heavy metals in water environment. The microbial electrochemical sensor was constructed with staggered flow distribution method to optimize the parameters such as external resistance value and external circulation rate. The inhibition of concentration of simulated heavy metal wastewater on voltage under optimal parameters was analyzed. The results showed that the best performance of MFC electrochemical sensor was achieved when the external resistance value was 130 Ω and the external circulation rate was 1.0 mL/min. In this case, the microbial electrochemical sensors were responsive to 1-10 mg/L Cu2+, 0.25-1.25 mg/L Cd2+, 0.25-1.25 mg/L Cr6+ and 0.25-1.00 mg/L Hg2+ within 60 minutes. The maximum rejection rates of the output voltage were 92.95%, 73.11%, 82.76% and 75.80%, respectively, and the linear correlation coefficients were all greater than 0.95. In addition, the microbial electrochemical sensor showed a good biological reproducibility. The good performance for detecting heavy metals by the newly developed microbial electrochemical sensor may facilitate the real-time on-line monitoring of heavy metals in water environment.

Direct Synthesis of Bienzyme-like Carbide-derived Carbons via Mild Electrochemical Oxidation of Ti 3AlC 2 MAX / 生物医学与环境科学（英文）

Objective@#To develop effective alternatives to natural enzymes, it is crucial to develop nanozymes that are economical, resource efficient, and environmentally conscious. Carbon nanomaterials that have enzyme-like activities have been extensively developed as substitutes for traditional enzymes.@*Methods@#Carbide-derived carbons (CDCs) were directly synthesized via a one-step electrochemical method from a MAX precursor using an ammonium bifluoride electrolyte at ambient conditions. The CDCs were characterized by systematic techniques.@*Results@#CDCs showed bienzyme-like activities similar to that of peroxidase and superoxide dismutase. We systematically studied the dependence of CDC enzyme-like activity on different electrolytes and electrolysis times to confirm activity dependence on CDC content. Additionally, the synthesis mechanism and CDC applicability were elaborated and demonstrated, respectively.@*Conclusion@#The demonstrated synthesis strategy eliminates tedious intercalation and delamination centrifugation steps and avoids using high concentrations of HF, high temperatures, and halogen gases. This study paves the way for designing two-dimensional material-based nanocatalysts for nanoenzyme and other applications.

Electrochemical immunosensor for detection of Plasmodium vivax lactate dehydrogenase

BACKGROUND Malaria is a disease that affects many tropical and subtropical countries, including Brazil. The use of tests for malaria detection is one of the fundamental strategies recommended by the World Health Organization for the control and eradication of the disease. The lack of diagnostic tests leads to an increase in transmission and non-reporting cases. OBJECTIVES This work described an electrochemical immunosensor for detecting Plasmodium vivax lactate dehydrogenase antigen (Ag-PvLDH). METHODS The device has developed by immobilising egg yolk IgY antibodies (Ab-PvLDH) on a gold electrode surface using cysteamine as linker. The immunosensor fabrication was followed by differential pulse voltammetry, and contact angle measurements were performed to characterise the modified gold electrode surface. FINDINGS The results for Ag-PvLDH determination exhibit a linear response at 10-50 µg mL-1 concentration range, with a limit of detection of 455 ng mL-1. The excellent selectivity of the device was confirmed. MAIN CONCLUSIONS The developed immunosensor showed a good performance, therefore, it can be considered an alternative test to detect malaria caused by P. vivax.

Ionic concentration in periradicular medium after dissolution of endodontic file fragments: an in vitro study

Abstract The aim of this study was to obtain ionic quantification in periradicular medium after diffusion tests of the solution used inside root canals during the electrochemical dissolution of endodontic file fragments and the NiTi-containing dissolution product via an apical foramen. Thirty single-rooted extracted human teeth had root canals prepared and were attached to Eppendorf tubes filled with sterile saline. The samples were divided into 3 groups (n = 10) according to the solution used inside the root canal during the diffusion tests: Group 1: [NaF 12 g/L + NaCl 1 g/L]; Group 2: [NaF 12 g/L + NaCl 1 g/L + NiTi 0.50 g/L]; Group 3: [NaF 6 g/L + NaCl 0.5 g/L + NiTi 0.25 g/L]. The sample in each Eppendorf tube was then analyzed to assay the ionic quantification in periradicular medium. The groups were compared in relation to ionic quantifications (Kruskal-Wallis and Dunn's tests, p ≤ 0.05). Group 2 showed significantly higher F-, Ni and Ti quantities than groups 1 and 3 (p < 0.05). Group 3 showed significantly higher Ti and Ni quantities than group 1, where no measurable quantities of Ti and Ni were observed (p < 0.05). The conclusions were that a 50% dilution of the NiTi-containing dissolution product resulted in significantly lower F-, Ni and Ti quantities compared to the undiluted product. The quantifications observed here suggest that irrigation is recommendable during the electrochemical dissolution process to reduce the resultant ion concentrations in both the root canal and the periradicular medium.

A descrição teórica da detecção eletroquímica do fármaco olanzapina, assistida pelo compósito do oxihidróxido de cobalto (III) com um corante esquaraínico

Introdução: a olanzapina é um dos fármacos antipsicóticos benzodiazepínicos mais usados no mundo. Apesar da sua eficiência, em concentrações excessivas, ela sói ser tóxica, como quaisquer outros fármacos desta classe. Assim, neste trabalho, se avaliou, pela primeira vez, a possibilidade da detecção eletroquímica do fármaco olanzapina, assistida pelo compósito do oxihidróxido de cobalto (III), emparelhado com o dióxido, com um corante esquaraínico. Método: o modelo matemático trivariante correspondente inclui dois cenários de oxidação do fármaco, possíveis para o caso, incluindo a eletropolimerização indireta da molécula da benzodiazepina condensada, bem como a oxidação do fármaco pelo átomo do enxofre. Este modelo tem sido desenvolvido e analisado mediante a teoria de estabilidade linear e análise de bifurcações. Resultados e discussão: a análise do modelo há mostrado que a hibridez do mecanismo do processo eletroanalítico, aliada à composição e descomposição dos compostos iônicos aquando da sua realização, aumenta a probabilidade da ocorrência do comportamento oscilatório, em relação ao caso mais simples e mais comum. No entretanto, a instabilidade oscilatória se realiza nos valores dos parâmetros, que estão além do limite de detecção. Por sua vez, o estado estacionário se obtém e se mantém facilmente, indicando um processo eletroanalítico eficiente, controlado pela difusão do analito. Conclusões: trata-se de um processo eletroanalítico eficiente, em que o composto de cobalto funciona como substância ativa, e o corante desempenha o papel de mediador

SUMMARY Introduction: olanzapine is one of the most used antipsychotic drugs in the world. Although it is efficient, it may be toxic in excess. Therefore, in this work the possibility of olanzapine electrochemical determination over an electrode, modified by the cobalt (III) oxyhydroxide in pair with its dioxide in a composite with squaraine dye. Methods: the trivariant correspondent mathematical model includes two scenarios of the drug oxidation, possible for the case, including the indirect electropolymerization of the condensed benzodiazepine molecule, like also its oxidation by sulfur atom. This model has been developed and analyzed by means of stability theory and bifurcation analysis. Results and discussion: the analysis of the model has shown that the mechanism hybridity of the electroanalytical process, alongside with the formation and decomposition of ionic compounds during its realization, augments the possibility for the oscillatory behavior realization, relatively to the simplest and commonest case. Nevertheless, the oscillatory instability is realized in parameter values far beyond the detection limit. On the other hand, the stable steady-state is easy to obtain and maintain, indicating an efficient electroanalytical process, controlled by the analyte diffusion. Conclusions: the electroanalytical process is efficient. The cobalt compound is acting as an active substance, and the dye is the mediator.

Introducción: la olanzapina es uno de los fármacos antipsicóticos más utilizados en el mundo. Aunque es eficaz, puede resultar tóxico en exceso. Por tanto, en este trabajo se plantea la posibilidad de la determinación electroquímica de olanzapina sobre un electrodo, modificado por el oxihidróxido de cobalto (III) en pareja con su dióxido en un composito con colorante de escuaraína. Métodos: el modelo matemático correspondiente incluye dos escenarios de oxidación del fármaco, posibles para el caso, que incluyen la electropolimerización indirecta de la molécula de benzodiazepina condensada, así como su oxidación por átomo de azufre. Este modelo ha sido desarrollado y analizado mediante teoría de estabilidad y análisis de bifurcación. Resultados y discusión: el análisis del modelo ha demostrado que el mecanismo de hibridación del proceso electroanalítico, junto con la formación y descomposición de compuestos iónicos durante su realización, aumenta la posibilidad de realización del comportamiento oscilatorio, relativamente al caso más simple y común. Sin embargo, la inestabilidad oscilatoria se realiza en valores de parámetros mucho más allá del límite de detección. Por otro lado, el estado estacionario estable es fácil de obtener y mantener, lo que indica un proceso electroanalítico eficiente, controlado por la difusión del analito. Conclusiones: el proceso electroanalítico es eficiente. El compuesto de cobalto actúa como sustancia activa y el colorante es el mediador.

A descrição matemática da detecção eletroquímica da ergina, assistida pelos novos derivados triazólicos, dopados pelo íon amavadina / The mathematical description for the ergin electrochemical detection, assisted by amavadin ion doped triazolic derivatives / Descripción matemática de la detección electroquímica de ergina, asistida por los nuevos derivados de triazol, dopados por el ión amavadina

RESUMO Introdução: Pela primeira vez, o processo eletroanalítico da detecção da ergina (LSA) sobre um elétrodo, modificado por um derivado triazólico, dopado pelo íon amavadina, tem sido descrito teoricamente. Métodos: O modelo matemático, correspondente ao desempenho do sensor, tem sido desenvolvido e analisado do ponto de vista da teoria de estabilidade linear. Foi mostrado que a amavadina pode servir de modificador eficiente para a detecção eletroanalítica da ergina. Outrossim, a presença de um material orgânico no modificador reforça a capacidade da ergina de polimerizar-se, formando um compósito polimérico. Resultados: Os comportamentos oscilatório e monotô-nico são mais prováveis que no caso mais comum, haja vista a formação-deformação de compostos iônicos aquando da detecção eletroanalítica.

SUMMARY Introduction: For the first time, the electroanalytical process of ergin (LSA) determination over an electrode, modified by triazolic derivative, doped by an amavadin-ion, has been theoretically described. Methods: The mathematical model, correspondent to the sensor function, has been developed and analyzed by means of linear stability theory. It has been shown that the amavadin may serve as an efficient electrode modifier for the electroanalytical detection of ergin. Moreover, the presence of an organic material as electrode modifier reinforces the possibility of ergin polymerization, yielding a polymer composite. Results: The oscillatory and monotonic behavior is more probable than in the common case, considering the formation and destruction of the ionic compounds during the electroanalytical detection.

RESUMEN Introducción: Por primera vez se ha descrito teóricamente el proceso eletroanalítico de detección de ergina (LSA) en un electrodo, modificado por un derivado triazólico, dopado por el ión amavadina. Métodos: El modelo matemático, correspondiente al rendimiento del sensor, ha sido desarrollado y analizado desde el punto de vista de la teoría de la estabilidad lineal. Se ha demostrado que la amavadina puede servir como un modificador eficaz para la detección eletroanalítica de ergina. Además, la presencia de un material orgánico en el modificador refuerza la capacidad de la ergina para polimerizar, formando un compuesto polimérico. Resultados: Los comportamientos oscilatorios y monótonos son más probables que en el caso más común, dada la formación-deformación de compuestos iónicos durante la detección eletroanalítica.

Descripción matemática de la determinación electroanalítica del fármaco salvarsano y su ciclooligómeros, asistida por un compuesto del colorante escuárico y oxihidróxido de cobalto / The mathematical description of the electroanalytical determination of salvarsan drug and its cyclooligomers, assisted by the composite of squaraine dye with cobalt oxyhydroxide / A descrição matemática da determinação eletroanalítica do fármaco salvarsan e seus ciclo-oligômeros, auxiliada pela composição do corante esquaraína com oxihidróxido de cobalto

RESUMEN Objetivo: En este trabajo se realiza, por primera vez, la evaluación teórica de la posibilidad de la detección electroanalítica de salvarsano, fármaco antisifilítico. El oxihidróxido de cobalto, en su compuesto con el colorante escuárico, se usa como modificador de electrodo. Metodología: Mediante el análisis de estabilidad, se ha confirmado su eficiencia en los procesos de detección de salvarsano. La linearidad de dependencia entre el parámetro electroquímico y la concentración del fármaco se obtiene y se mantiene fácilmente. Conclusión: Las inestabilidades oscilatoria y monotónica se realizan en el sistema, causadas por las influencias de las etapas electroquímicas a las capacitancias de la doble capa eléctrica (DCE).

SUMMARY Aim: In this work, the theoretical evaluation of the electroanalytical detection of antisyphilitic drug salvarsan is given for the first time. Cobalt oxyhydroxide in a composite with the squaraine dye is used as electrode modifier. Methodology: By means of the stability analysis the efficiency of the salvarsan determination is confirmed. The linearity of the dependence between the electrochemical parameter and drug concentration is easily obtained and maintained. Conclusion: The oscillatory and monotonic instabilities are realized in this system, being caused by the electrochemical stages' influences to the double electric layer (DEL).

RESUMO Objetivo: neste trabalho, a avaliação teórica da detecção eletroanalítica do antissifilítico salvarsan é feita pela primeira vez. O oxihidróxido de cobalto em um composto com o corante esquaraína é usado como modificador de eletrodo. Metodologia: por meio da análise de estabilidade é confirmada a eficiência da determinação de salvarsan. A linearidade da dependência entre o parâmetro eletroquímico e a concentração do fármaco é facilmente obtida e mantida. Conclusão: as instabilidades osci-latórias e monotônicas são percebidas neste sistema, sendo causadas pelas influências dos estágios eletroquímicos sobre a dupla camada elétrica (DEL).

Chemically modified carbon-based electrodes for the determination of paracetamol in drugs and biological samples / 药物分析学报

Paracetamol is a non-steroidal,anti-inflammatory drug widely used in pharmaceutical applications for its sturdy,antipyretic and analgesic action.However,an overdose of paracetamol can cause fulminant hepatic necrosis and other toxic effects.Thus,the development of advantageous analytical tools to detect and determine paracetamol is required.Due to simplicity,higher sensitivity and selectivity as well as costefficiency,electrochemical sensors were fully investigated in last decades.This review describes the advancements made in the development of electrochemical sensors for the paracetamol detection and quantification in pharmaceutical and biological samples.The progress made in electrochemical sensors for the selective detection of paracetamol in the last 10 years was examined,with a special focus on highly innovative features introduced by nanotechnology.As the literature is rather extensive,we tried to simplify this work by summarizing and grouping electrochemical sensors according to the by which manner their substrates were chemically modified and the analytical performances obtained.

Synthesis and electrochemical properties of environmental free L-glutathione grafted graphene oxide/ZnO nanocomposite for highly selective piroxicam sensing / 药物分析学报

A simple and reliable strategy was proposed to engineer the glutathione grafted graphene oxide/ZnO nanocomposite(glutathione-GO/ZnO)as electrode material for the high-performance piroxicam sensor.The prepared glutathione-GO/ZnO nanocomposite was well characterized by X-ray diffraction(XRD),Fourier transform infrared spectrum(FTIR),X-ray photoelectron spectroscopy(XPS),field emission scanning electron microscopy(FE-SEM),cyclic voltammetry(CV),electrochemical impedance spectros-copy(EIS)and differential pulse voltammetry(DPV).The novel nanocomposite modified electrode showed the highest electrocatalytic activity towards piroxicam(oxidation potential is 0.52 V).Under controlled experimental parameters,the proposed sensor exhibited good linear responses to piroxicam concentrations ranging from 0.1 to 500 μM.The detection limit and sensitivity were calculated as 1.8 nM and 0.2 μA/μM·cm2,respectively.Moreover,it offered excellent selectivity,reproducibility,and long-term stability and can effectively ignore the interfering candidates commonly existing in the pharmaceutical tablets and human fluids even at a higher concentration.Finally,the reported sensor was successfully employed to the direct determination of piroxicam in practical samples.

Towards wearable and implantable continuous drug monitoring:A review / 药物分析学报

Continuous drug monitoring is a promising alternative to current therapeutic drug monitoring strategies and has a strong potential to reshape our understanding of pharmacokinetic variability and to improve individualised therapy.This review highlights recent advances in biosensing technologies that support continuous drug monitoring in real time.We focus primarily on aptamer-based biosensors,wearable and implantable devices.Emphasis is given to the approaches employed in constructing biosensors.We pay attention to sensors'biocompatibility,calibration performance,long-term characteristics stability and measurement quality.Last,we discuss the current challenges and issues to be addressed in continuous drug monitoring to make it a promising,future tool for individualised therapy.The ongoing efforts are expected to result in fully integrated implantable drug biosensing technology.Thus,we may anticipate an era of advanced healthcare in which wearable and implantable biochips will automatically adjust drug dosing in response to patient health conditions,thus enabling the management of diseases and enhancing individualised therapy.