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Single substrate-functionalized molybdenum oxide nanozyme for specific colorimetric monitoring of xanthine oxidase activity.
Li, Limin; Zhang, Cai; Zhang, Yifan; Chen, Shengnan; Shan, Shuo; Wu, Tianming; Niu, Yusheng; Xu, Yuanhong.
Affiliation
  • Li L; Institute of Biomedical Engineering, College of Life Sciences, School of Tourism and Geography Sciences, Qingdao University, Qingdao, 266071, China.
  • Zhang C; Institute of Biomedical Engineering, College of Life Sciences, School of Tourism and Geography Sciences, Qingdao University, Qingdao, 266071, China.
  • Zhang Y; The Affiliated Hospital of Qingdao University, Qingdao, 266003, China.
  • Chen S; Children's Hospital Capital Institute of Pediatrics, Beijing, 100020, China.
  • Shan S; The Second Affiliated Hospital of Hainan Medical University, Haikou, 570311, China.
  • Wu T; Institute of Biomedical Engineering, College of Life Sciences, School of Tourism and Geography Sciences, Qingdao University, Qingdao, 266071, China.
  • Niu Y; Institute of Biomedical Engineering, College of Life Sciences, School of Tourism and Geography Sciences, Qingdao University, Qingdao, 266071, China. nys@qdu.edu.cn.
  • Xu Y; Institute of Biomedical Engineering, College of Life Sciences, School of Tourism and Geography Sciences, Qingdao University, Qingdao, 266071, China. yhxu@qdu.edu.cn.
Mikrochim Acta ; 191(2): 99, 2024 01 16.
Article in En | MEDLINE | ID: mdl-38228947
ABSTRACT
Xanthine-functionalized molybdenum oxide nanodots (X-MoO3-x NDs) with peroxidase (POD)-like activity were developed for selective, sensitive, and facile colorimetric quantification of xanthine oxidase (XO). Xanthine functionalization can not only be favorable for the successful nanozyme preparation, but also for the specific recognition of XO as well as the simultaneous generation of hydrogen peroxide, which was subsequently transformed into hydroxyl radical to oxidize the chromogenic reagent based on the POD-like catalysis. Under the optimized conditions, the colorimetric biosensing platform was established for XO assay without addition of further substrates, showing good linearity relationship between absorbance difference (ΔA) and XO concentrations in the range 0.05-0.5 U/mL (R2 = 0.998) with a limit of detection (LOD) of 0.019 U/mL. The quantification of XO occurs in 25 min, which is superior to the previously reported and commercial XO assays. The proposed method has been successfully used in the assay of human serum samples, showing its high potential in the field of clinical monitoring.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Xanthine Oxidase / Colorimetry Limits: Humans Language: En Journal: Mikrochim Acta Year: 2024 Type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Xanthine Oxidase / Colorimetry Limits: Humans Language: En Journal: Mikrochim Acta Year: 2024 Type: Article Affiliation country: China