Magneto-controlled aptasensor for simultaneous electrochemical detection of dual mycotoxins in maize using metal sulfide quantum dots coated silica as labels

被引:106
作者
Wang, Chengquan [1 ,3 ]
Qian, Jing [2 ]
An, Keqi [2 ]
Huang, Xingyi [1 ]
Zhao, Lufang [2 ]
Liu, Qian [2 ]
Hao, Nan [2 ]
Wang, Kun [2 ]
机构
[1] Jiangsu Univ, Sch Food & Biol Engn, Zhenjiang 212013, Peoples R China
[2] Jiangsu Univ, Sch Chem & Chem Engn, Key Lab Modern Agr Equipment & Technol, Zhenjiang 212013, Peoples R China
[3] Changzhou Coll Informat Technol, Changzhou 213164, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Electrochemical aptasensor; Magneto-controlled; Simultaneous detection; Mycotoxins; Ochratoxin A; Fumonisin B1; STEP RAPID DETECTION; IMPEDIMETRIC APTASENSOR; SIGNAL AMPLIFICATION; MULTIPLE MYCOTOXINS; NANOPARTICLE LABEL; FUMONISIN B1; OCHRATOXIN-A; IMMUNOASSAY; DNA; APTAMER;
D O I
10.1016/j.bios.2016.10.010
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Currently there is an urgent need for multi-mycotoxin detection methods due to the co-occurrence of multiple mycotoxins in food raw materials and their augmented toxicity. Herein, a magneto-controlled aptasensor has been developed for simultaneous electrochemical detection of ochratoxin A (OTA) and fumonisin B1 (FB1), two typical mycotoxins found in food crops world-wide. This aptasensor was designed using the high specificity between the target and aptamer with heavy CdTe or PbS quantum dots (QDs) coated silica as labels and the complementary DNA functionalized magnetic beads as capture probes. In presence of targets, the aptamer preferred to form the target-aptamer binding which forced the partial release of the preloaded labels from the magnetic beads. After a one-step incubation and a simple magnetic separation, the electrochemical signals of Cd2+ and Pb2+ dissolved from the reserved labels which had negative correlation with targets contents, was measured based on the difference of peak potentials. This aptasensor provided a wide detection range of 10 pg mL(-1) to 10 ng mL(-1) for OTA and 50 pg to 50 ng mL(-1) for FBI, and succeeded in real maize samples. This method provides a new avenue for high throughput screen of mycotoxins due to the advantages of simple instrument, low sample consumption, short assay times, and lower detection costs per assay. Moreover, it could be readily expanded for the simultaneous detection of a large panel of mycotoxins by using different metal sulfide QDs when their specific aptamers are available.
引用
收藏
页码:802 / 809
页数:8
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