Magnetic porous carbon nanocomposites derived from metal-organic frameworks as a sensing platform for DNA fluorescent detection

被引:51
作者
Tan, Hongliang [1 ]
Tang, Gonge [1 ]
Wang, Zhixiong [1 ]
Li, Qian [1 ]
Gao, Jie [1 ]
Wu, Shimeng [1 ]
机构
[1] Jiangxi Normal Univ, Coll Chem & Chem Engn, Key Lab Funct Small Organ Mol, Key Lab Chem Biol Jiangxi Prov,Minist Educ, Nanchang 330022, Peoples R China
基金
高等学校博士学科点专项科研基金;
关键词
Metal-organic frameworks; Magnetic porous carbon; DNA sensing; Fluorescence; BACKGROUND SIGNAL PLATFORM; MOLECULAR APTAMER BEACON; PEROXIDASE-LIKE ACTIVITY; NUCLEIC-ACID; COLORIMETRIC DETECTION; NANOPARTICLES; NANOWIRES; NANOTUBES; EFFICIENT; SYSTEM;
D O I
10.1016/j.aca.2016.08.024
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Metal-organic frameworks (MOFs) have emerged as very fascinating functional materials due to their tunable nature and diverse applications. In this work, we prepared a magnetic porous carbon (MPC) nanocomposite by employing iron-containing MOFs (MIL-88A) as precursors through a one-pot thermolysis method. It was found that the MPC can absorb selectively single-stranded DNA (ssDNA) probe to form MPC/ssDNA complex and subsequently quench the labelled fluorescent dye of the ssDNA probe, which is resulted from the synergetic effect of magnetic nanoparticles and carbon matrix. Upon the addition of complementary target DNA, however, the absorbed ssDNA probe could be released from MPC surface by forming double-stranded DNA with target DNA, and accompanied by the recovery of the fluorescence of ssDNA probe. Based on these findings, a sensing platform with low background signal for DNA fluorescent detection was developed. The proposed sensing platform exhibits high sensitivity with detection limit of 1 nM and excellent selectivity to specific target DNA, even single-base mismatched nucleotide can be distinguished. We envision that the presented study would provide a new perspective on the potential applications of MOF-derived nanocomposites in biomedical fields. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:136 / 142
页数:7
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