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Simple electrochemical detection of Listeria monocytogenes based on a surface-imprinted polymer-modified electrode.
Li, Qingcao; Guo, Zhen; Qiu, Xuedan; Lu, Wenjun; Yang, Wei; Wang, Qilai; Wu, Qiaoping.
Affiliation
  • Li Q; Clinical Laboratory of Ningbo Medical Centre Lihuili Hospital, Ningbo University, 1111 Jiangnan Street, Ningbo, Zhejiang 315040, PR China. lhlyywqp@163.com.
  • Guo Z; Department of Clinical Laboratory, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang 310009, PRChina.
  • Qiu X; Clinical Laboratory of Ningbo Medical Centre Lihuili Hospital, Ningbo University, 1111 Jiangnan Street, Ningbo, Zhejiang 315040, PR China. lhlyywqp@163.com.
  • Lu W; Clinical Laboratory of Ningbo Medical Centre Lihuili Hospital, Ningbo University, 1111 Jiangnan Street, Ningbo, Zhejiang 315040, PR China. lhlyywqp@163.com.
  • Yang W; Department of Clinical Laboratory, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, Zhejiang 310014, PRChina.
  • Wang Q; Department of Pulmonary Medicine, Hua Mei Hospital, University of Chinese Academy of Science, 41 Xibei Street, Ningbo, Zhejiang, 315010, PRChina. blyywql1@163.com.
  • Wu Q; Clinical Laboratory of Ningbo Medical Centre Lihuili Hospital, Ningbo University, 1111 Jiangnan Street, Ningbo, Zhejiang 315040, PR China. lhlyywqp@163.com.
Anal Methods ; 13(41): 4864-4870, 2021 10 28.
Article in En | MEDLINE | ID: mdl-34586109
ABSTRACT
Listeria monocytogenes (LM) is a foodborne pathogen, and it can pose a risk of serious diseases to the human health. Hence, the development of an effective method for the detection of LM is very important. In this study, by selecting LM as the template and 3-thiopheneacetic acid as the functional monomer, an LM-imprinted polymer (LIP)-based sensor was proposed for the first time to detect LM by electropolymerizing TPA on the glassy carbon electrode (GCE) surface in the presence of LM. After the removal of the LM template from the electrode surface, the obtained sensor was denoted as LIP/GCE, which could effectively recognize and capture LM cells. By using [Fe(CN)6]4-/3- as the probe, its peak current at LIP/GCE could be restricted when the LM cells were captured into the imprinted cavity of LIP/GCE, and the current value decreased with an increase in the LM concentration. Serious conditions were optimized for achieving highly sensitive detection, and a low detection limit (6 CFU mL-1) coupled with a wide linear range (10 to 106 CFU mL-1) was obtained for LM. Finally, the inter-electrode reproducibility, stability, selectivity, and applicability of LIP/GCE were also investigated, and the obtained results were acceptable.
Subject(s)

Full text: 1 Collection: 01-internacional Health context: 3_ND Database: MEDLINE Main subject: Molecular Imprinting / Listeria monocytogenes Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Anal Methods Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Health context: 3_ND Database: MEDLINE Main subject: Molecular Imprinting / Listeria monocytogenes Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Anal Methods Year: 2021 Document type: Article