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Simultaneous monitoring of multiple prohibited drugs in various aquatic products.
Nian, Qixun; Meng, Erqiong; Li, Feng; Wang, Chunmin; Zhang, Qiuping; Li, Jingjing; Xu, Qian.
  • Nian Q; Key Laboratory of Environmental Medicine Engineering, Ministry of Education, School of Public Health, Southeast University, Nanjing 210009, China.
  • Meng E; Key Laboratory of Environmental Medicine Engineering, Ministry of Education, School of Public Health, Southeast University, Nanjing 210009, China.
  • Li F; Key Laboratory of Environmental Medicine Engineering, Ministry of Education, School of Public Health, Southeast University, Nanjing 210009, China.
  • Wang C; Suzhou Municipal Center for Disease Prevention and Control, Suzhou 215004, China.
  • Zhang Q; Suzhou Municipal Center for Disease Prevention and Control, Suzhou 215004, China.
  • Li J; Jiangxi Science and Technology Normal University, Nanchang 330013, China.
  • Xu Q; Key Laboratory of Environmental Medicine Engineering, Ministry of Education, School of Public Health, Southeast University, Nanjing 210009, China. Electronic address: q_xu68@163.com.
Food Chem ; 456: 139974, 2024 Oct 30.
Article en En | MEDLINE | ID: mdl-38850605
ABSTRACT
Both sedative and antipathogenic drugs are often found to be illegally used in aquaculture, but there is a lack of simultaneous monitoring methods. A method for simultaneously monitoring multiple prohibited drugs in various aquatic product samples was developed in this work, including fish, shrimp, crab, and shellfish. Sulfonic acid-functionalized magnetic graphitic carbon nitride (S-MGCN) was synthesized and validated to efficiently co-extract all targets (adsorption efficiency over 90.07%) through various adsorption mechanisms such as electrostatic interaction, hydrogen bonding, and π-π interaction while demonstrating good sample matrix purification ability (matrix effect below 13.60%). A new magnetic solid-phase extraction method based on S-MGCN was subsequently established. Coupled with UPLC-MS/MS, the detection limits were 0.030.075 µg /kg, and the recoveries ranged from 88.76% to 111.74% with the RSDs lower than 14.60%, indicating that the developed method has good sensitivity, accuracy, and precision. Further validation of its practicality was achieved through actual sample analysis.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Mariscos / Contaminación de Alimentos / Alimentos Marinos / Espectrometría de Masas en Tándem / Extracción en Fase Sólida / Peces Límite: Animals Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Mariscos / Contaminación de Alimentos / Alimentos Marinos / Espectrometría de Masas en Tándem / Extracción en Fase Sólida / Peces Límite: Animals Idioma: En Año: 2024 Tipo del documento: Article