2011
DOI: 10.1016/j.talanta.2010.11.053
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A new potentiometric sensor for the determination of α-amylase activity

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Cited by 27 publications
(12 citation statements)
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“…These assays are mainly spectrophotometric, and require tedious sample preparation and are often high in cost. Sakač et al 52 present a theoretical approach to measuring α-amylase using a potentiometric sensor. The sensor design employed a platinum redox electrode and would be able to measure triiodide released from α-amylase promoted starch degradation.…”
Section: Potentiometric Sensorsmentioning
confidence: 99%
“…These assays are mainly spectrophotometric, and require tedious sample preparation and are often high in cost. Sakač et al 52 present a theoretical approach to measuring α-amylase using a potentiometric sensor. The sensor design employed a platinum redox electrode and would be able to measure triiodide released from α-amylase promoted starch degradation.…”
Section: Potentiometric Sensorsmentioning
confidence: 99%
“…Since the majority of the reported methods are cumbersome, less reliable, and take a lot of time to perform, most of these papers are based on modifying the available methods to increase accuracy and ease of use. In the literature, several papers describing different kinds of analytical techniques to determine α ‐amylase activity can be found . For example, techniques such as spectrometry, fluorometry, amperometry, electrophoresis, isoelectric focusing, chromatography, and immunological methods have been adapted to detect α ‐amylase activity.…”
Section: Introductionmentioning
confidence: 99%
“…In the literature, several papers describing different kinds of analytical techniques to determine α ‐amylase activity can be found . For example, techniques such as spectrometry, fluorometry, amperometry, electrophoresis, isoelectric focusing, chromatography, and immunological methods have been adapted to detect α ‐amylase activity. In addition, several methods have emerged that use different substrates, including starch, amylose, amylopectin, and some chemically modified derivatives of polymers and maltooligosaccharides of varying chain length linked to a chromophore, such as 4‐nitrophenyl or 2‐chloro‐4‐nitrophenyl .…”
Section: Introductionmentioning
confidence: 99%
“…Recently, several interesting high-throughput screening approaches have been presented, like droplet-based microfluidic system for rapid encapsulation, cultivation, assaying and sorting of yeast cells expressing heterologous hydrolytic enzymes (Beneyton et al 2017), protocols for high-throughput cultivation screening with real-time data acquisition (Back et al 2016), fluorescence-activated cell sorting (FACS) of cell-surface displayed protein mutants (Olsen et al 2000; Mattanovich and Borth 2006), or miniaturized potentiometric sensors (Sakač et al 2011) or immunosensors (Della Ventura et al 2017) for the determination of enzymatic activity. These techniques exhibit superiority in terms of high-throughput character, time-efficiency, accuracy, and precision; however, they require specialized equipment or specific structure of the DNA constructs, which might be considered as a kind of limitation.…”
Section: Introductionmentioning
confidence: 99%