RESUMO
A novel biosensor for lactate has been developed, using screen-printed carbon electrodes (SPCE) and lactate oxidase (LOx). The active surface of the electrodes was modified using a dispersion of platinum nanoparticle decorated carbon nanofibers (PtNp-CNF) in poly(diallyldimethylammonium) chloride (PDDA) solution. In this way, sensitive, disposable, low cost and reliable hydrogen peroxide sensors were obtained. The immobilisation of LOx on top of these PtNp-CNF-PDDA/SPCEs resulted in amperometric biosensors with high operational stability. The sensitivity of the optimised lactate biosensor was 36.8 (mA/Mcm(2)) with a linear range of 25-1500 µM. The limit of detection was 11 µM (S/N=3). Reproducibility, selectivity and storage stability were also evaluated. Additionally, the stability of the biosensor was also predicted by a model based on thermal degradation. Finally, lactate in sweat and blood samples was determined in a sport test using LOx/PtNp-CNF-PDDA/SPCEs and commercial biosensors respectively. Based on these data, the validity of the sweat lactate for the determination of the lactate threshold is discussed.
Assuntos
Enzimas Imobilizadas/metabolismo , Ácido Láctico/análise , Ácido Láctico/sangue , Oxigenases de Função Mista/metabolismo , Nanofibras/química , Polietilenos/química , Compostos de Amônio Quaternário/química , Técnicas Biossensoriais/métodos , Carbono/química , Enzimas Imobilizadas/química , Humanos , Ácido Láctico/metabolismo , Limite de Detecção , Oxigenases de Função Mista/química , Nanofibras/ultraestrutura , Pediococcus/enzimologia , Platina/química , Reprodutibilidade dos Testes , Suor/químicaRESUMO
The development of sensors to detect specific weak biological interactions is still today a challenging topic. Characteristics of carbohydrate-protein (lectin) interactions include high specificity and low affinity. This work describes the development of nanostructured impedimetric sensors for the detection of concanavalin A (Con A) binding to immobilized thiolated carbohydrate derivatives (D-mannose or D-glucose) onto screen-printed carbon electrodes (SPCEs) modified with gold nanoparticles. Thiolated D-galactose derivative was employed as negative control to evaluate the selectivity of the proposed methodology. After binding the thiolated carbohydrate to the nanostructured SPCEs, different functionalized thiols were employed to form mixed self-assembled monolayers (SAM). Electrochemical impedance spectroscopy (EIS) was employed as a technique to evaluate the binding of Con A to selected carbohydrates through the increase of electron transfer resistance of the ferri/ferrocyanide redox probe at the differently SAM modified electrodes. Different variables of the assay protocol were studied in order to optimize the sensor performance. Selective Con A determinations were only achieved by the formation of mixed SAMs with adequate functionalized thiols. Important differences were obtained depending on the chain lengths and functional groups of these thiols. For the 3-mercapto-1-propanesulfonate mixed SAMs, the electron transfer resistance varied linearly with the Con A concentration in the 2.2-40.0 µg mL(-1) range for D-mannose and D-glucose modified sensors. Low detection limits (0.099 and 0.078 pmol) and good reproducibility (6.9 and 6.1%, n=10) were obtained for the D-glucose and D-mannose modified sensors, respectively, without any amplification strategy.
Assuntos
Técnicas Biossensoriais , Concanavalina A/análise , Glucose/química , Ouro/química , Manose/química , Nanopartículas Metálicas/química , Carbono/química , Impedância Elétrica , Eletroquímica , EletrodosRESUMO
In this article, a disposable magnetic DNA sensor using an enzymatic amplification strategy for the detection of specific hybridization processes, based on the coupling of streptavidin-peroxidase to biotinylated target sequences, has been developed. A thiolated 19-mer capture probe was attached to gold coated ferric oxide nanoparticles and hybridization with the biotinylated target was allowed to proceed. Then, a streptavidin-peroxide was attached to the biotinylated target and the resulting modified gold coated ferric oxide nanoparticles were captured by a magnetic field on the surface of a home-made carbon screen printed electrode (SPE). Using hydroquinone as a mediator, a square wave voltammetric procedure was chosen to detect the hybridization process after the addition of hydrogen peroxide. Different aspects concerning the assay protocol and nanoparticles fabrication were optimized in order to improve the sensitivity of the developed methodology. A low detection limit (31 pM) with good stability (RSD=7.04%, n=10) was obtained without the need of polymerase chain reaction (PCR) amplification.
Assuntos
Técnicas Biossensoriais/instrumentação , Mapeamento Cromossômico/instrumentação , Materiais Revestidos Biocompatíveis/química , Compostos Férricos/química , Hibridização In Situ/instrumentação , Magnetismo/instrumentação , Nanopartículas/química , Equipamentos Descartáveis , Desenho de Equipamento , Análise de Falha de Equipamento , Ouro/química , Nanopartículas/ultraestrutura , Nanotecnologia/instrumentaçãoRESUMO
This work describes the use of a PEDOT:PSS-based conductive polymer for designing AChE-based biosensors. The transducers were obtained directly by screen-printing a PEDOT:PSS suspension on the surface of thick film carbon electrodes. The obtained working electrodes showed a high conductivity when compared with electrodes modified with conventional mediators like cobalt phthalocyanine or tetracyanoquinodimethane. The PEDOT:PSS polymer was shown to be suitable for thiocholine oxidation, allowing the measurement of AChE activity at 100 mV vs Ag/AgCl. The high conductivity of PEDOT:PSS allowed the accurate detection of the organophosphate insecticide chlorpyrifos-oxon at concentrations as low as 4x10(-9)M, corresponding to an inhibition ratio of 5%.
Assuntos
Acetilcolinesterase , Técnicas Biossensoriais/métodos , Compostos Bicíclicos Heterocíclicos com Pontes , Organofosfatos/análise , Polímeros , Clorpirifos/análise , Condutividade Elétrica , Eletrodos , Inseticidas/análise , Tiocolina/metabolismoRESUMO
The enzymatically catalyzed polymerization of 3,4-ethylenedioxythiophene in the presence of polystyrenesulfonate is introduced. This is the first time that an enzymatically catalyzed poly(3,4-ethylenedioxythiophene) (PEDOT) is reported. Horseradish peroxidase enzyme was used as a catalyst for the polymerization process leading to a water-soluble PEDOT that was characterized by UV-vis spectra, Fourier transform infrared, and electrical conductivity measurements. Water-soluble PEDOT showed excellent film formation ability as confirmed by atomic force microscopy images.