RESUMO
We report the first use of a paper-based device coated with nanoceria as a simple, low-cost and rapid detection platform for the analysis of organophosphate (OP) pesticides using an enzyme inhibition assay with acetylcholinesterase (AChE) and choline oxidase (ChOX). In the presence of acetylcholine, AChE and ChOX catalyze the formation of H2O2, which is detected colorimetrically by a nanoceria-coated device resulting in the formation of a yellow color. After incubation with OP pesticides, the AChE activity was inhibited, producing less H2O2, and a reduction in the yellow intensity. The assay is able to analyze OP pesticides without the use of sophisticated instruments and gives detection limits of 18 ng mL(-1) and 5.3 ng mL(-1) for methyl-paraoxon and chlorpyrifos-oxon, respectively. The developed method was successfully applied to detect methyl-paraoxon in spiked vegetables (cabbage) and a dried seafood product (dried green mussel), obtaining â¼95% recovery values for both sample types. The spiked samples were also analyzed using LC-MS/MS as a comparison to the developed method and similar values were obtained, indicating that the developed method gives accurate results and is suitable for OP analysis in real samples.
Assuntos
Técnicas Biossensoriais/métodos , Cério/química , Poluentes Ambientais/análise , Nanopartículas/química , Papel , Praguicidas/análise , Oxirredutases do Álcool/antagonistas & inibidores , Animais , Técnicas Biossensoriais/instrumentação , Inibidores da Colinesterase/análise , Inibidores da Colinesterase/farmacologia , Cor , Colorimetria , Poluentes Ambientais/farmacologia , Análise de Alimentos , Peróxido de Hidrogênio/metabolismo , Limite de Detecção , Praguicidas/farmacologiaRESUMO
We report a simple, low-cost, one-step fabrication method for microfluidic paper-based analytical devices (µPAD) using only polystyrene and a patterned screen. The polystyrene solution applied through the screen penetrates through the paper, forming a three-dimensional hydrophobic barrier, defining a hydrophilic analysis zone. The optimal polystyrene concentration and paper types were first investigated. Adjusting polystyrene concentration allows for various types of paper to be used for successful device fabrication. Using an optimized polystyrene concentration with Whatman#4 filter paper, a linear relationship was found to exist between the design width and the printed width. The smallest hydrophilic channel and hydrophobic barrier that can be obtained are 670 ± 50 µm and 380 ± 40 µm, respectively. High device-to-device fabrication reproducibility was achieved yielding a relative standard deviation (%RSD) in the range of 1.12-2.54% (n = 64) of the measured diameter of the well-shaped fabricated test zones with a designed diameter of 5 and 7 mm. To demonstrate the significance of the fabricated µPAD, distance-based and well-based paper devices were constructed for the analysis of H2O2 and antioxidant activity, respectively. The analysis of H2O2 in real samples using distance-based measurement with CeO2 nanoparticles as the colorimetric agent produced the same results at 95% confidence level, as those obtained using KMnO4 titration. A proof-of-concept antioxidant activity determination based on the 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay was also demonstrated. The results verify that the polymer screen-printing method can be used as an alternative method for µPAD fabrication.
Assuntos
Técnicas Analíticas Microfluídicas/instrumentação , Poliestirenos/química , Antioxidantes/análise , Compostos de Bifenilo/química , Desenho de Equipamento , Filtração , Peróxido de Hidrogênio/análise , Microtecnologia/instrumentação , Papel , Picratos/química , ImpressãoRESUMO
Airborne particulate matter (PM) pollution significantly impacts human health, but the cellular mechanisms of PM-induced toxicity remain poorly understood. A leading hypothesis on the effects of inhaled PM involves the generation of cellular oxidative stress. To investigate PM-induced oxidative stress, analytical methods have been developed to study the chemical oxidation of dithiothreitol (DTT) in the presence of PM. Although DTT readily reacts with several forms of reactive oxygen species, this molecule is not endogenously produced in biological systems. Glutathione (GSH), on the other hand, is an endogenous antioxidant that is produced throughout the body and is directly involved in combating oxidative stress in the lungs and other tissues. We report here a new method for measuring aerosol oxidative activity that uses silver nanoparticle (AgNP) aggregation coupled to glutathione (GSH) oxidation in a paper-based analytical device. In this assay, the residual reduced GSH from the oxidation of reduced GSH to its disulfide induces the aggregation of AgNPs on a paper-based analytical device, which produces a reddish-brown product. Two methods for aerosol oxidative reactivity are presented: one based on change in color intensity using a traditional paper-based techniques and one based on the length of the color product formed using a distance-based device. These methods were validated against traditional spectroscopic assays for DTT and GSH that employ Elman's reagent. No significant difference was found between the levels measured by all three GSH methods (our two paper-based devices and the traditional method) at the 95% confidence level. PM reactivity towards GSH was less than towards DTT most likely due to the difference in the oxidation potential between the two molecules.
Assuntos
Aerossóis/química , Técnicas de Química Analítica/instrumentação , Nanopartículas/química , Papel , Prata/química , OxirreduçãoRESUMO
Human exposure to particulate matter (PM) air pollution has been linked with respiratory, cardiovascular, and neurodegenerative diseases, in addition to various cancers. Consistent among all of these associations is the hypothesis that PM induces inflammation and oxidative stress in the affected tissue. Consequently, a variety of assays have been developed to quantify the oxidative activity of PM as a means to characterize its ability to induced oxidative stress. The vast majority of these assays rely on high-volume, fixed-location sampling methods due to limitations in assay sensitivity and detection limit. As a result, our understanding of how personal exposure contributes to the intake of oxidative air pollution is limited. To further this understanding, we present a microfluidic paper-based analytical device (µPAD) for measuring PM oxidative activity on filters collected by personal sampling. The µPAD is inexpensive to fabricate and provides fast and sensitive analysis of aerosol oxidative activity. The oxidative activity measurement is based on the dithiothreitol assay (DTT assay), uses colorimetric detection, and can be completed in the field within 30 min following sample collection. The µPAD assay was validated against the traditional DTT assay using 13 extracted aerosol samples including urban aerosols, biomass burning PM, cigarette smoke, and incense smoke. The results showed no significant differences in DTT consumption rate measured by the two methods. To demonstrate the utility of the approach, personal samples were collected to estimate human exposures to PM from indoor air, outdoor air on a clean day, and outdoor air on a wildfire-impacted day in Fort Collins, CO. Filter samples collected on the wildfire day gave the highest oxidative activity on a mass normalized basis, whereas typical ambient background air showed the lowest oxidative activity.
Assuntos
Aerossóis/metabolismo , Poluentes Atmosféricos/metabolismo , Exposição Ambiental/análise , Técnicas Analíticas Microfluídicas/instrumentação , Oxidantes/metabolismo , Material Particulado/metabolismo , Ditiotreitol/análise , Ditiotreitol/metabolismo , Humanos , Limite de Detecção , Oxirredução , PapelRESUMO
Immunoassays are one of the most useful diagnostic techniques in disease assessment, drug metabolite analysis, and environmental applications due largely in part to the selectivity and sensitivity provided by antibody-antigen interactions. Here, a multiplexed immunoassay termed cleavable tag immunoassay (CTI) was performed in competitive, non-competitive, and mixed formats for the analysis of proteins and small molecule biomarkers of inflammation and tissue damage. Microchip capillary electrophoresis (MCE) with fluorescence detection was employed for the analysis of fluorescently labeled tags corresponding to the analytes of interest cleaved from the detection antibodies. For this work we have selected 3-nitrotyrosine (3-NT) a molecule indicative of reactive nitrogen species (RNS), thyroxine (T4) a molecule used to monitor thyroid gland function, and C-reactive protein (CRP) a marker of chronic inflammation as model analytes to demonstrate the assay principles. The simultaneous detection of 3-nitrotyrosine (3-NT) and thyroxine (T4) was carried out as a proof-of-principle for the competitive CTI while non-competitive CTI performance was demonstrated via the analysis of C-reactive protein (CRP). Limit of detections (LOD) and dynamic ranges were investigated. LOD for 3-NT, T4, and CRP were 0.5µg/mL, 23nM, and 5µg/mL, respectively thus demonstrating the ability of the CTI to detect proteins and small molecules within clinical reference ranges. Moreover, this is the first report of the use of mixed format CTI chemistry for the simultaneous detection of proteins (CRP) and small molecules (3-NT) in a single assay. The success of this work demonstrates the ability of CTI to analyze intact proteins and small molecule biomarkers simultaneously.
Assuntos
Anticorpos/química , Ligação Competitiva , Biomarcadores/análise , Imunoensaio/métodos , Microscopia de Fluorescência/métodos , Avidina/química , Biomarcadores/química , Proteína C-Reativa/química , Eletroforese Capilar/métodos , Fluorescência , Corantes Fluorescentes/síntese química , Corantes Fluorescentes/química , Inflamação/diagnóstico , Inflamação/imunologia , Limite de Detecção , Espécies Reativas de Nitrogênio/química , Padrões de Referência , Tiroxina/química , Tirosina/análogos & derivados , Tirosina/químicaRESUMO
Particulate matter (PM) air pollution has a significant impact on human morbidity and mortality; however, the mechanisms of PM-induced toxicity are poorly defined. A leading hypothesis states that airborne PM induces harm by generating reactive oxygen species in and around human tissues, leading to oxidative stress. We report here a system employing a microfluidic electrochemical sensor coupled directly to a particle-into-liquid sampler (PILS) system to measure aerosol oxidative activity in an on-line format. The oxidative activity measurement is based on the dithiothreitol (DTT) assay, where, after being oxidized by PM, the remaining reduced DTT is analyzed by the microfluidic sensor. The sensor consists of an array of working, reference, and auxiliary electrodes fabricated in a poly(dimethylsiloxane)-based microfluidic device. Cobalt(II) phthalocyanine-modified carbon paste was used as the working electrode material, allowing selective detection of reduced DTT. The electrochemical sensor was validated off-line against the traditional DTT assay using filter samples taken from urban environments and biomass burning events. After off-line characterization, the sensor was coupled to a PILS to enable on-line sampling/analysis of aerosol oxidative activity. Urban dust and industrial incinerator ash samples were aerosolized in an aerosol chamber and analyzed for their oxidative activity. The on-line sensor reported DTT consumption rates (oxidative activity) in good correlation with aerosol concentration (R(2) from 0.86 to 0.97) with a time resolution of approximately 3 min.
Assuntos
Aerossóis/química , Técnicas Eletroquímicas , Microfluídica , Eletrodos , Estrutura Molecular , OxirreduçãoRESUMO
Recently, the development of electrochemical biosensors as part of microfluidic devices has garnered a great deal of attention because of the small instrument size and portability afforded by the integration of electrochemistry in microfluidic systems. Electrode fabrication, however, has proven to be a major obstacle in the field. Here, an alternative method to create integrated, low cost, robust, patternable carbon paste electrodes (CPEs) for microfluidic devices is presented. The new CPEs are composed of graphite powder and a binder consisting of a mixture of poly(dimethylsiloxane) (PDMS) and mineral oil. The electrodes are made by filling channels molded in previously cross-linked PDMS using a method analogous to screen printing. The optimal binder composition was investigated to obtain electrodes that were physically robust and performed well electrochemically. After studying the basic electrochemistry, the PDMS-oil CPEs were modified with multi-walled carbon nanotubes (MWCNT) and cobalt phthalocyanine (CoPC) for the detection of catecholamines and thiols, respectively, to demonstrate the ease of electrode chemical modification. Significant improvement of analyte signal detection was observed from both types of modified CPEs. A nearly 2-fold improvement in the electrochemical signal for 100 µM dithiothreitol (DTT) was observed when using a CoPC modified electrode (4.0 ± 0.2 nA (n = 3) versus 2.5 ± 0.2 nA (n = 3)). The improvement in signal was even more pronounced when looking at catecholamines, namely dopamine, using MWCNT modified CPEs. In this case, an order of magnitude improvement in limit of detection was observed for dopamine when using the MWCNT modified CPEs (50 nM versus 500 nM). CoPC modified CPEs were successfully used to detect thiols in red blood cell lysate while MWCNT modified CPEs were used to monitor temporal changes in catecholamine release from PC12 cells following stimulation with potassium.
Assuntos
Técnicas Biossensoriais/instrumentação , Catecolaminas/análise , Dimetilpolisiloxanos/química , Técnicas Eletroquímicas/instrumentação , Grafite/química , Microfluídica/instrumentação , Compostos de Sulfidrila/análise , Animais , Dopamina/análise , Eletrodos , Desenho de Equipamento , Eritrócitos/química , Glutationa/análise , Humanos , Indóis/química , Óleo Mineral/química , Nanotubos de Carbono/química , Compostos Organometálicos/química , Células PC12 , Ratos , Sensibilidade e EspecificidadeRESUMO
A simple paper-based analytical device (PAD) has been developed to rapidly detect formaldehyde (FA) in food samples. The analysis was based on sulfite assay where FA reacted with excess sulfite to generate sodium hydroxide (NaOH) that was quantified on PAD using acid-base titration. The PAD consisted of a central sample zone connected to ten reaction and detection zones. All detection zones were pre-deposited with polyethylene glycol (PEG) with phenolphthalein (Phph) as an indicator. Reaction zones contained different amounts of the titrant, potassium hydrogen phthalate (KHP). On flowing into reaction zones, the NaOH product reacts with KHP to reach the end point. In the presence of excess NaOH, unneutralized NaOH reached the detection zone and caused Phph color change from colorless to pink. In contrast, when NaOH was less than KHP, the detection zone remained colorless. Concentration of FA can be quantified from the number of pink detection zone(s) which were correlated with a known amount of pre-deposited KHP on the PAD. Total analytical process could be completed within 5â¯min. Areas of each zone and amounts of reagents added to the corresponding zones of the PAD were optimized to obtain reproducible and accurate results. PAD gave ranges of FA detection of 100-1000â¯mgâ¯L-1 with an interval of 100â¯mgâ¯L-1 and the limit of detection (LOD) was 100â¯mgâ¯L-1. PADs were stable for up to a month under dark and cold conditions. Analysis of FA in food samples using PAD agreed well with those from the classical sulfite assay.
Assuntos
Contaminação de Alimentos/análise , Formaldeído/análise , Papel , Concentração de Íons de Hidrogênio , Hidróxido de Sódio/química , Sulfitos/químicaRESUMO
We report the first use of a paper-based device as a simple, low-cost and rapid detection platform for simultaneous determination of antioxidant activity and total phenolic content in food samples. Two antioxidant activity assays including 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulphonate) radical cation (ABTS) assay and cupric reducing antioxidant capacity (CUPRAC) assay and one total phenolic content assay, Folin Ciocaltue reagent (FC) assay were simultaneously employed as a proof-of-concept. The device composed of a central sample zone connected to four pretreatment zones and consecutive detection zones to accommodate all three assays and a sample blank measurement. The analysis was achieved by dropping the samples onto the sample zone to flow to the pretreatment and detection zones containing the stored reagents for each antioxidant assay making the color change that was measured using imageJ software. Assay optimization including key reagent concentrations, reaction time, and surface modification were carried out to obtain sensitive and wide linear rage analyses. Various antioxidant standards were then evaluated to determine the analytical features of the method. The paper-based assays were successfully applied to detect antioxidant activity and total phenolic content in 10 beverage samples with similar gallic acid equivalent (GAE) values to those obtained from traditional assays at a 95% confidence interval. Moreover, the GAE values of the samples obtained from three assay analyses were well correlated to each other with relatively high Pearson's correlation coefficients. These results indicated that the assays gave accurate results and are suitable for simultaneous analysis of antioxidant activity and total phenolic content in real samples.
Assuntos
Antioxidantes/análise , Análise de Alimentos , Contaminação de Alimentos/análise , Fenóis/análiseRESUMO
We report on a paper-based 2,2-diphenyl-1-(2,4,6-trinitrophenyl)hydrazyl (DPPH) assay for a simple, inexpensive, low reagent and sample consumption and high throughput analysis of antioxidant activity. The paper-based device was fabricated using a lamination method to create a 5-mm in diameter circular test zone that was embedded with a DPPH reagent. The analysis was carried out in one-step by dropping an antioxidant/sample onto the test zone. After reduction by the antioxidant, the DPPH radicals become stable DPPH molecules, resulting in a change in color from deep violet to pale yellow. The violet color intensity of DPPH was inversely proportional to the antioxidant activity of the samples, and was measured using imaging software. A high precision and a low limit of detection were found in the analysis of six standard antioxidants including gallic acid, trolox, ascorbic acid, caffeic acid, vanilliic acid and quercetin. The device was then validated against the traditional spectrophotometric DPPH assay by analyzing the antioxidant activity of 7 tea samples. The results showed no significant difference for gallic acid equivalent for all 7 samples obtained from the two methods at the 95% confidence level, indicating that the developed method was reliable for antioxidant activity analysis of real samples. Finally, the paper-based DPPH device was found to be stable over 10 days when stored in a refrigerator (2 - 4°C), making it an easy-to-use device for end-users.
Assuntos
Antioxidantes/análise , Compostos de Bifenilo/química , Papel , Picratos/química , RefrigeraçãoRESUMO
This work reports a portable distance-based detection paper device that has a thermometer-like shape for rapid, instrument-free determination of antioxidant activity using a nanoceria assay. The assay is based on partial reduction of cerium ion from Ce4+ to Ce3+ on nanoceria deposited along the detection channel by antioxidants present in food, giving highly reactive oxidation products. Either these products or the parent antioxidant compounds could then bind to the OH-rich ceria nanoparticles and generate charge transfer ceria-antioxidant complexes resulting in a yellow to brown color change. The distance of the brown color on the detection channel is directly proportional to antioxidant activity, and can be easily measured using an integrated ruler without the need of any external sophisticated instrument for detection. The paper sensor has been studied for the analysis of common antioxidants and its performance was validated against traditional antioxidant assays for 11 tea sample analyses. Using the Spearman rank correlation coefficient method, the antioxidant activity of tea samples obtained from the paper device correlated with the traditional assay at the 95% confidence level. The developed sensor provided a high recovery and tolerance limit and was stable for 50 days both when stored at ambient and low temperature (6 and -20°C). The results demonstrated that the developed paper device is an alternative to allow for fast, simple, instrument-free, cheap, portable and high-throughput screening of antioxidant activity analysis in real samples.
RESUMO
Human exposure to particulate matter (PM) air pollution is associated with human morbidity and mortality. The mechanisms by which PM impacts human health are unresolved, but evidence suggests that PM intake leads to cellular oxidative stress through the generation of reactive oxygen species (ROS). Therefore, reliable tools are needed for estimating the oxidant generating capacity, or oxidative load, of PM at high temporal resolution (minutes to hours). One of the most widely reported methods for assessing PM oxidative load is the dithiothreitol (DTT) assay. The traditional DTT assay utilizes filter-based PM collection in conjunction with chemical analysis to determine the oxidation rate of reduced DTT in solution with PM. However, the traditional DTT assay suffers from poor time resolution, loss of reactive species during sampling, and high limit of detection. Recently, a new DTT assay was developed that couples a Particle-Into-Liquid-Sampler with microfluidic-electrochemical detection. This 'on-line' system allows high temporal resolution monitoring of PM reactivity with improved detection limits. This study reports on a laboratory comparison of the traditional and on-line DTT approaches. An urban dust sample was aerosolized in a laboratory test chamber at three atmospherically-relevant concentrations. The on-line system gave a stronger correlation between DTT consumption rate and PM mass (R2 = 0.69) than the traditional method (R2 = 0.40) and increased precision at high temporal resolution, compared to the traditional method.