Abstract:Automated manipulation of discrete droplets by digital microfluidics (DMF) combined with chemiluminescence (CL) is promising to achieve automated and sensitive biosensing and bioanalysis.
“…They can be classified based on the flow control mechanisms into flow injection devices with the differential pressure flow mode, 15 microfluidic paper-based analytical devices (μPADs) driven by capillary force, 16 microchip capillary electrophoresis (MCE) devices using electrokinetic flow, 17 and digital microfluidics (DMF) employing electric fields for droplet control. 18 μPADs have been widely exploited to detect glucose, 19-21 lactate, 16,22 or H 2 O 2 23 using CL due to their advantages in fluid flow control, low cost, and disposability. The capability in fluid flow enabled by the capillary force facilitated the easy control of multiple reagents and reaction sequences on paper devices.…”
Section: Introductionmentioning
confidence: 99%
“…25 However, the chemiluminescence reaction exhibits flashtype kinetic characteristics, where emitted light sharply increases to its maximum and then rapidly decreases within less than one second. 18 The above delay method was limited in rapid sample introduction since the lateral flow requires time to reach the next reaction region. Therefore, quick contact between the oxidation products and the following reagents for chemiluminescence reading is critical.…”
Section: Introductionmentioning
confidence: 99%
“…They can be classified based on the flow control mechanisms into flow injection devices with the differential pressure flow mode, 15 microfluidic paper-based analytical devices (μPADs) driven by capillary force, 16 microchip capillary electrophoresis (MCE) devices using electrokinetic flow, 17 and digital microfluidics (DMF) employing electric fields for droplet control. 18…”
This paper reports a spin-disc paper-based device with 10 individual detection units containing electromagnetic modules controlling the sample incubation time before chemiluminescence (CL) signal detection.
“…They can be classified based on the flow control mechanisms into flow injection devices with the differential pressure flow mode, 15 microfluidic paper-based analytical devices (μPADs) driven by capillary force, 16 microchip capillary electrophoresis (MCE) devices using electrokinetic flow, 17 and digital microfluidics (DMF) employing electric fields for droplet control. 18 μPADs have been widely exploited to detect glucose, 19-21 lactate, 16,22 or H 2 O 2 23 using CL due to their advantages in fluid flow control, low cost, and disposability. The capability in fluid flow enabled by the capillary force facilitated the easy control of multiple reagents and reaction sequences on paper devices.…”
Section: Introductionmentioning
confidence: 99%
“…25 However, the chemiluminescence reaction exhibits flashtype kinetic characteristics, where emitted light sharply increases to its maximum and then rapidly decreases within less than one second. 18 The above delay method was limited in rapid sample introduction since the lateral flow requires time to reach the next reaction region. Therefore, quick contact between the oxidation products and the following reagents for chemiluminescence reading is critical.…”
Section: Introductionmentioning
confidence: 99%
“…They can be classified based on the flow control mechanisms into flow injection devices with the differential pressure flow mode, 15 microfluidic paper-based analytical devices (μPADs) driven by capillary force, 16 microchip capillary electrophoresis (MCE) devices using electrokinetic flow, 17 and digital microfluidics (DMF) employing electric fields for droplet control. 18…”
This paper reports a spin-disc paper-based device with 10 individual detection units containing electromagnetic modules controlling the sample incubation time before chemiluminescence (CL) signal detection.
“…25 Therefore, it is necessary a continuous glucose monitoring in physiological fluids to avoid complications related to anormal levels of glycemia. In this sense, spectrophotometry, [26][27][28] chromatography, [29][30][31] electrophoresis, 32,33 fluorescence, 34,35 and chemiluminescence 36,37 have been reported as traditional analytical techniques for glucose quantification; unfortunately, these ones need sample pretreatment, sophisticated instrumentation, and the use of excessive organic solvents. 38,39 Methodologies based on electrochemistry represent a viable alternative in the quantification of glucose due to their simplicity, low-cost, rapid response, and easy implementation, overcoming the drawbacks mentioned above.…”
Glucose is the principal source of energy for humans and its quantification in physiological samples can diagnose or prevent diseases. Commonly, glucose determination is based on spectrophotometric-enzymatic techniques, but since at least a decade ago, electroanalytical strategies have emerged as promising alternatives providing accuracy and precision in the determination of biomolecules. This review focuses on the development of non-enzymatic methodologies based on modified electrochemical sensors with molecularly imprinted polymers (MIPs) for glucose detection sensors in physiological samples (blood, saliva, and urine). The trends in the construction of non-enzymatic sensors base on MIP combine with materials such as carbonaceous materials, metal nanoparticles, and polymers improving their electrocatalytic properties and analytical parameters of the electro-analytical methodologies developed. Glassy carbon electrodes, carbon paste electrodes, and screen-printed electrodes are the main transductors modified with MIP for the electrochemical oxidation of glucose, and the maximum anodic peak current is taken to the analytical signal. In all reported non-enzymatic sensors, the presence of the MIP improved glucose determination compared to the bare working electrode. The reported results demonstrated that this electroanalytical approach represents a viable alternative for fast and confident analysis of the glucose molecule overcoming the drawbacks presented by enzymatic sensors.
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