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Tunable catalytic activity of FeWO_(4) nanomaterials for sensitive assays of pyrophosphate ion and alkaline phosphatase activity
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作者 xianqing tang Jinghuang Chen +2 位作者 Mengqian Zhang Jian Sun Xiurong Yang 《Science China Chemistry》 SCIE EI CAS CSCD 2023年第6期1860-1868,共9页
Alkaline phosphatase(ALP)activity and pyrophosphate ion(PPi)levels are remarkable for the human body functions such as signal transduction pathways and metabolism.Current quantitative methods mainly focus on developin... Alkaline phosphatase(ALP)activity and pyrophosphate ion(PPi)levels are remarkable for the human body functions such as signal transduction pathways and metabolism.Current quantitative methods mainly focus on developing complicated organic substrates or employing unstable metal ions as signal-regulated medium.Herein,we have developed a facile hydrothermal method for preparing Fe WO_(4)nanomaterials with intrinsic peroxidase-like activity and further confirmed that such a catalytic activity could be significantly enhanced by adjusting the size and oxygen vacancy content.More encouragingly,PPi can easily inhibit the catalytic activity of Fe WO_(4),whereas orthophosphate ions(Pi)cannot.Therefore,we constructed an Fe WO_(4)-based colorimetric assay for sensing PPi by means of the classical 3,3′,5,5′-tetramethylbenzidine-peroxidase chromogenic reaction.A facile and reliable ALP activity assay was also designed and developed because of the logical regulation of the peroxidase-like activity of Fe WO_(4)through the ALP-catalyzed hydrolysis of PPi into Pi.Based on the clear mechanism and mimetic-enzyme Fe WO_(4)-catalyzed amplification,the sensing system exhibited excellent performance and was able to evaluate ALP activity in real serum samples and screen for potential ALP inhibitors.The proposed mimetic enzyme-involved colorimetric assay provides an alternative pathway,and Fe WO_(4)nanomaterials with excellent performance have great potential for further biosensing and biomedical applications. 展开更多
关键词 FewO4 nanomaterials mimetic enzyme oxygen vacancy COLORIMETRY pyrophosphate ion alkaline phosphatase
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