“…Electrochemical biosensor has been considered as the best choice for the in situ monitoring of active compounds (e.g., phenolic) by virtue of its high sensitivity, simple instrumentation, low production cost and promising response speed (Lu et al, 2010). Excellent membrane forming ability of chitosan nanoparticles and their small response time and high sensitivity and stability (due to their high surface to volume ratio), low cost and hydrophilicity making them suitable for biosensor applications that are mostly concerned with working of enzymes for detection mechanisms (Nakorn, 2008).…”
Chitosan is an attractive natural biopolymer from renewable resources with the presence of reactive amino and hydroxyl functional groups in its structure. Due to the good biocompatibility of chitosan, it can be used in magnetic-field assisted drug delivery, enzyme or cell immobilization and many other industrial applications. In the past decade, nanotechnology has been a considerable research interest in the area of preparation of immobilized enzyme carriers. This study looks at characteristics and applications of chitosan and chitosan nanoparticles and their potentials as suitable supports for enzyme immobilization. Results indicated that activity of immobilized enzymes and performance of enzyme immobilization onto chitosan nanoparticles are higher than chitosan macro and microparticles. As compared to other biopolymers nanoparticles, application of chitosan nanoparticles to immobilize enzymes strongly increases stability of immobilized enzymes and their easy separability from the reaction mixture at the end of the biochemical process.
“…Electrochemical biosensor has been considered as the best choice for the in situ monitoring of active compounds (e.g., phenolic) by virtue of its high sensitivity, simple instrumentation, low production cost and promising response speed (Lu et al, 2010). Excellent membrane forming ability of chitosan nanoparticles and their small response time and high sensitivity and stability (due to their high surface to volume ratio), low cost and hydrophilicity making them suitable for biosensor applications that are mostly concerned with working of enzymes for detection mechanisms (Nakorn, 2008).…”
Chitosan is an attractive natural biopolymer from renewable resources with the presence of reactive amino and hydroxyl functional groups in its structure. Due to the good biocompatibility of chitosan, it can be used in magnetic-field assisted drug delivery, enzyme or cell immobilization and many other industrial applications. In the past decade, nanotechnology has been a considerable research interest in the area of preparation of immobilized enzyme carriers. This study looks at characteristics and applications of chitosan and chitosan nanoparticles and their potentials as suitable supports for enzyme immobilization. Results indicated that activity of immobilized enzymes and performance of enzyme immobilization onto chitosan nanoparticles are higher than chitosan macro and microparticles. As compared to other biopolymers nanoparticles, application of chitosan nanoparticles to immobilize enzymes strongly increases stability of immobilized enzymes and their easy separability from the reaction mixture at the end of the biochemical process.
“…Many efforts have been devoted to develop a simple and effective analytical method for the determination of phenols. Electrochemical biosensor has been considered as the best choice for in situ monitoring of phenolic compounds by virtue of its high sensitivity, simple instrumentation, low production cost and promising response speed [5], However, determination of phenols through the direct electrochemical is suffered from a number of drawbacks due to the high overvoltage, a high anodic potential needs to be applied, which open up the detection system for interfering reactions [6]. And, the high applied voltage is also followed by an increase of background current and noise level.…”
Section: Introductionmentioning
confidence: 99%
“…Electrochemical biosensors based on Tyr are simple and convenient tools for phenol assays due to their high sensitivity, effectiveness and simplicity [12]. Many nanomaterials, such as carbon-coated nickel nanoparticles [13], polyaniline (PANI) [14], hydroxyapatite [15], Fe3O4 nanoparticles [4], ZnO nanorod microarrays [16] and sonogel-carbon [17] have been used to construct Tyr biosensor for the detection of catechol (CA). It shows advantages of good reliability, fast response, inexpensive instrument, low energy consumption, simple operation, time saving and high sensitivity [18].…”
A novel catechol (CA) biosensor was developed by the immobilization of tyrosinase (Tyr) onto in situ electrochemical reduction graphene (EGR) on choline functionalized gold nanoparticals . The Tyr-EGR/AuNPs-Ch showed a good electrochemical catalytic response for the reduction of CA, with the linear range from 0.2 to 270 μM and a detection limit of 0.1 μM (S/N= 3). The apparent Michaelis-Menten constant was estimated to be 109 μM.
“…Electrochemical biosensors based on tyrosinase (Tyr) or polyphenol oxidase enzymes are con-sidered as an alternative to the conventional techniques due to their simplified sample treatment, and the possibility of portable, economic, fast, and sensitive analysis [5][6][7]. Several research groups have investigated Tyr-based bio-sensors for the detection of phenols [8][9][10]. Tyrosinasecatalysed oxidation of tyrosine and other monohydric phenols involves o-hydroxylation followed by oxidation of the resulting dihydric phenol to the corresponding o-qui-none in a single step without the release of the dihydric phenol intermediate.…”
The performance of an amperometric biosensor constructed by associating tyrosinase (Tyr) enzyme with the advantages of a 3D gold nanoelectrode ensemble (GNEE) is evaluated in a flowinjection analysis (FIA) system for the analysis of Levodopa (Ldopa). GNEEs were fabricated by electroless deposition of the metal within the pores of polycarbonate track-etched membranes. A simple solvent etching procedure based on the solubility of polycarbonate membranes is adopted for the fabrication of the 3D GNEE. Afterwards, enzyme was immobilized onto preformed self-assembled monolayers of cysteamine on the 3D GNEEs (GNEE-Tyr) via cross-linking with glutaraldehyde. The experimental conditions of the FIA system, such as the detection potential (-0.200 V (vs. Ag/ AgCl)) and flow rates (1.0 mL min -1 ) were optimized. Analytical responses for L-dopa were obtained in a wide concentration range between 1 9 10 -8 mol L -1 and 1 9 10 -2 mol L -1 . The limit of quantification was found to be 1 9 10 -8 mol L -1 with a resultant % RSD of 7.23% (n = 5). The limit of detection was found to be 1 9 10 -9 mol L -1 (S/N = 3). The common interfering compounds namely, glucose (10 mmol L -1 ), ascorbic acid (10 mmol L -1 ), and urea (10 mmol L -1 ) were studied. The recovery of L-dopa (1 9 10 -7 mol L -1 ) from spiked urine samples was found to be 96%. Therefore, the developed method is adequate to be applied in the clinical analysis.
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