pH-responsive deoxyribonucleic acid capture/release by polydopamine functionalized magnetic nanoparticles

被引:54
|
作者
Wang, Yu
Ma, Xiangdong
Ding, Chun
Jia, Li [1 ]
机构
[1] S China Normal Univ, Coll Biophoton, Key Lab Laser Life Sci, Minist Educ, Guangzhou 510631, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Polydopamine; Magnetic nanoparticles; Deoxyribonucleic acid; Bacteria; Polymerase chain reaction; Capillary electrophoresis; GENETICALLY-MODIFIED SOYBEANS; GENOMIC DNA; SURFACE MODIFICATION; PARTICLES; ADSORBENTS; PCR; MICROSPHERES; PURIFICATION; EXTRACTION; PROTEIN;
D O I
10.1016/j.aca.2015.01.009
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Polydopamine functionalized magnetic nanoparticles (PDA@Fe3O4) were prepared and characterized by transmission electron microscopy, scanning electron microscopy, zeta potential and vibrating sample magnetometry. They were found to enable highly efficient capture of genomic deoxyribonucleic acid (DNA). The adsorption capacity of PDA@Fe3O4 for genomic DNA can reach 161mg g (1). The extraction protocol used aqueous solutions for DNA binding to and releasing from the surface of the magnetic particles based on the pH inducing the charge switch of amino and phenolic hydroxyl groups on PDA@Fe3O4. The extracted DNA with high quality (A(260)/A(280) = 1.80) can be directly used as templates for polymerase chain reaction (PCR) followed by capillary electrophoresis (CE) analysis. None of the toxic chemical reagents and PCR inhibitors was used throughout the whole procedure. PDA@Fe3O4 based magnetic solid phase extraction (MSPE) method was superior to those using commercial kit and traditional phenol-chloroform extraction methods in yield of DNA. The developed PDA@Fe3O4 based MSPE-PCR-CE method was applied for simultaneous and fast detection of Listeria monocytogenes and Escherichia coli O157:H7 in milk. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:33 / 40
页数:8
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