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Hydroxyl radicals (•OH) are well known as crucial chemicals for maintaining the normal activities of human cells; however, the excessive concentration of •OH disrupts their normal function, causing various diseases, including liver and heart diseases, cancers, and neurological disorders. The detection of •OH as a biomarker is thus essential for the early diagnosis of these serious conditions. Herein, a novel electrochemical sensor comprising a composite of cerium oxide nanoclusters, gold nanoparticles, and a highly conductive carbon was developed for detecting •OH. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were employed to characterize the signals generated by the interaction of the composite with •OH radicals. The CV results revealed that the developed sensor could accurately and selectively detect •OH in the Fenton reaction. The sensor demonstrated a linear relationship between the current peak and •OH concentration in the range 0.05 - 0.5 mM and 0.5 - 5 mM with a limit of detection (LOD) of 58 µM. In addition, EIS studies indicated that this electrochemical sensor could distinguish between •OH and similar reactive oxygen species (ROS), like hydrogen peroxide (H2O2). It is also worth mentioning that additional merits, such as reproducibility, repeatability, and stability of the sensor were confirmed.

 

Reactive oxygen species (ROS) have been found in plants, mammals, and natural environmental processes. The presence of ROS in mammals has been linked to the development of severe diseases, such as diabetes, cancer, tumors, and several neurodegenerative conditions. The most common ROS involved in human health are superoxide (O2•−), hydrogen peroxide (H2O2), and hydroxyl radicals (•OH). Organic and inorganic molecules have been integrated with various methods to detect and monitor ROS for understanding the effect of their presence and concentration on diseases caused by oxidative stress. Among several techniques, fluorescence and electrochemical methods have been recently developed and employed for the detection of ROS. This literature review intends to critically discuss the development of these techniques to date, as well as their application for in vitro and in vivo ROS detection regarding free-radical-related diseases. Moreover, important insights into and further steps for using fluorescence and electrochemical methods in the detection of ROS are presented. 

It is well known that an excess of hydroxyl radicals (˙OH) in the human body is responsible for oxidative stress-related diseases. An understanding of the relationship between the concentration of ˙OH and those diseases could contribute to better diagnosis and prevention. Here we present a supersensitive nanosensor integrated with an electrochemical method to measure the concentration of ˙OH in vitro. The electrochemical sensor consists of a composite comprised of ultrasmall cerium oxide nanoclusters (<2 nm) grafted to a highly conductive carbon deposited on a screen-printed carbon electrode (SPCE). Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were used to analyze the interaction between cerium oxide nanoclusters and ˙OH. The CV results demonstrated that this electrochemical sensor had the capacity of detecting ˙OH with a high degree of accuracy and selectivity, achieving a consistent performance. Additionally, EIS results confirmed that our electrochemical sensor was able to differentiate ˙OH from hydrogen peroxide (H 2 O 2 ), which is another common reactive oxygen species (ROS) found in the human body. The limit of detection (LOD) observed with this electrochemical sensor was of 0.6 μM. Furthermore, this nanosized cerium oxide-based electrochemical sensor successfully detected in vitro the presence of ˙OH in preosteoblast cells from newborn mouse bone tissue. The supersensitive electrochemical sensor is expected to be beneficially used in multiple applications, including medical diagnosis, fuel–cell technology, and food and cosmetic industries. 

One of the most significant challenges in the use of heterogeneous catalysts is the loss of activity and/or selectivity with time on stream, and researchers have explored different methods to overcome this problem. Recently, the coating of catalysts to control their deactivation has generated much research traction. This Review is aimed at studying different encapsulation techniques employed for controlling catalyst deactivation. Focus is given to the prevention of irreversible modes of deactivation, such as sintering and leaching. In this Review, we elaborate on different entrapment methods used to protect catalysts from deactivation in both liquid and gas reaction media. Relevant probe reactions are discussed with emphasis on the catalyst activity and stability. Challenges associated with those processes are also described with emphasis on the mass transfer limitations as a result of the coverage of the active sites. Finally, some future perspectives and areas for possible improvement are highlighted.