Molecule-Responsive SERS Sensors for Urine Diagnosis of Kidney Diseases Enhanced by Neural Networks.

Journal: Analytical chemistry
Published Date:

Abstract

Early diagnosis of kidney disease is crucial for treatment and prognosis. Compared with kidney biopsy, a noninvasive urine-based diagnosis method of kidney disease can be more convenient and less painful for patients. Urine is closely associated with kidney disease, including nephritis, kidney failure, and kidney cancer. Since it contains various biomolecules, including small-molecule metabolites, proteins, and so on, urine is an appropriate sample for diagnosing and monitoring kidney disease progression. Herein, we developed a liquid biopsy method for diagnosing various kidney diseases based on a specific SERS sensing mode combined with neural network models, which allows an integrated response to multiple types of targets with a single probe and facilitates the detection of complex samples from multiple target groups. Compared to label-free SERS, this method relies on changes in the probe molecule, which facilitates the sensitivity of the assay. Two kinds of silver nanoparticle-casting films assist this method with the surface decoration of molecule-responsive Raman reporter molecules: -mercaptobenzoic acid (MBA) and -aminothiophenol (PATP). MBA responds to amino components in urine by SERS spectral changes caused by molecular polarizability. PATP illustrates the level of small-molecule metabolites in urine according to SERS changes resulting from the rate of the hot hole-catalyzed reactions. These interactions were evidenced by density functional theory and molecular docking simulations. Through these two SERS sensors, we acquired the SERS data sets of urine samples and established a classifier by incorporating neural network models, enabling the effective discrimination of healthy and kidney disease samples. The method is helpful for clinical validation and shows promise for use in long-term kidney disease monitoring programs.

Authors

  • Jiaqi Wang
  • Sijun Huang
    Key Laboratory for Molecular Enzymology and Engineering of Ministry of Education, National Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin University, Changchun, China.
  • Fanxiang Meng
    State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun 130012, P. R. China.
  • Qiuting Huang
    State Key Laboratory of Marine Environmental Science, Fujian Provincial Key Laboratory for Coastal Ecology and Environmental Studies, Center for Marine Environmental Chemistry & Toxicology, College of the Environment and Ecology, Xiamen University, Xiamen 361102, P. R. China.
  • Xue Xia
    Rheumatology and Immunology Department, China-Japan Union Hospital of Jilin University, Changchun 130033, P. R. China.
  • Weiqing Xu
    Key Laboratory of Pesticide and Chemical Biology of Ministry of Education, International Joint Research Center for Intelligent Biosensing Technology and Health, College of Chemistry, Central China Normal University, Wuhan, 430079, People's Republic of China.
  • Yi Guo
    Department of Respiratory and Critical Care Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
  • Guokun Liu
    State Key Laboratory of Marine Environmental Science, Fujian Provincial Key Laboratory for Coastal Ecology and Environmental Studies, Center for Marine Environmental Chemistry & Toxicology, College of the Environment and Ecology, Xiamen University, Xiamen 361102, P. R. China.
  • Weigang Wang
    Department of Statistics and Mathematics, Zhejiang Gongshang University, Hangzhou, 310018, China. wangweigang@zjgsu.edu.cn.
  • Ping Li
    Department of Gastroenterology, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
  • Shuping Xu
    State Key Laboratory of Supramolecular Structure and Materials , Jilin University , 2699 Qianjin Avenue , Changchun 130012 , P. R. China.