Your browser doesn't support javascript.
loading
Confined Gel-Electromembrane Extraction of Oligonucleotides.
Liu, Cong; Liu, Jie; Liu, Quan; Zhu, Qianyun; Wang, Hao; Fang, Xiangming; Zhang, Wenfang; Liu, Zilong; Huang, Chuixiu.
Afiliação
  • Liu C; Department of Forensic Medicine, Huazhong University of Science and Technology, Wuhan 430030, China.
  • Liu J; Department of Forensic Medicine, Huazhong University of Science and Technology, Wuhan 430030, China.
  • Liu Q; Hubei Key Laboratory of the Forensic Science, Hubei University of Police, Wuhan 430035, China.
  • Zhu Q; Wuhan YouFu Hospital, Wuhan 430000, China.
  • Wang H; Wuhan YouFu Hospital, Wuhan 430000, China.
  • Fang X; Wuhan YouFu Hospital, Wuhan 430000, China.
  • Zhang W; Key Laboratory of Forensic Toxicology, Ministry of Public Security, People's Republic of China (Beijing Municipal Public Security Bureau), Beijing 100000, China.
  • Liu Z; Department of Forensic Medicine, Huazhong University of Science and Technology, Wuhan 430030, China.
  • Huang C; Department of Forensic Medicine, Huazhong University of Science and Technology, Wuhan 430030, China.
Anal Chem ; 2024 Jul 30.
Article em En | MEDLINE | ID: mdl-39078883
ABSTRACT
Gel-electromembrane extraction (G-EME) is an increasingly popular green variant of electromembrane extraction (EME). However, the electroendosmosis (EEO) flow associated with G-EME greatly limits the development of this technology. To address this challenge, the current study proposed the concept of confined G-EME (CG-EME), and a three-dimensional-printed modular device was elaborately designed to realize this concept. The device blocked the EEO flow by limiting the volume of the sample compartment. Moreover, the mesh structure at the bottom of the extraction module helps to prepare thin and stable gel films, which enhance the electromigration driving force and shorten the migration path. In addition, polar oligonucleotides, a nucleic acid analyte, were extracted for the first time to prove the concept of CG-EME. After optimization, 62% of the oligonucleotides were extracted at 50 V voltage for 15 min using a 3 mm thick agarose (3%) gel film. Finally, the application capability of CG-EME was further demonstrated by recovering DNA primers and isolating disease biomarkers (miRNA-181b) from real samples. In combination with CG-EME and quantitative polymerase chain reaction (qPCR) analysis, the upregulation of miRNA-181b expression in the peripheral blood of patients with schizophrenia was observed. In conclusion, this study proposes CG-EME to diminish EEO and push EME into the clinical field to isolate nucleic acid biomarkers, which will greatly expand the application scenarios of this emerging technology.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Anal Chem Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Anal Chem Ano de publicação: 2024 Tipo de documento: Article