Ultrasensitive DNA Detection with Hydrodynamic Separation of Plasmonic Nanoparticles and Isothermal Amplification

被引:9
|
作者
Draz, Mohamed Shehata [1 ,2 ]
Ma, Luyao [1 ]
Lu, Xiaonan [1 ]
机构
[1] Univ British Columbia, Fac Land & Food Syst, Food Nutr & Hlth Program, Vancouver, BC V6T 1Z4, Canada
[2] Tanta Univ, Fac Sci, Tanta 31527, Egypt
基金
加拿大自然科学与工程研究理事会;
关键词
LAMP; Nucleic Acid; Isothermal Amplification; Plasmonic; Gold Nanoparticle; Colorimetric; ROLLING CIRCLE AMPLIFICATION; NANOGOLD HYBRIDIZATION PROBE; GOLD NANOPARTICLES; COLORIMETRIC DETECTION; ANALYTICAL ULTRACENTRIFUGATION; SENSITIVE DETECTION; STRANDED-DNA; CENTRIFUGATION; ASSAY; IDENTIFICATION;
D O I
10.1166/jbn.2018.2507
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Nucleic acid based assays are routinely used to detect diseases and monitor medical treatment. Here, we demonstrated a novel approach for colorimetric DNA detection using plasmonic gold nanoparticles (AuNPs) as hydrodynamic separators coupled with differential centrifugation. This approach relies upon the change in the sedimentation rate of AuNPs when conjugated to DNA amplicons. Isothermal nucleic acid amplification results in the formation of unique DNA amplicons that is large enough to prevent the sedimentation of conjugated AuNPs at a specific centrifugal force. In contrast, free nanoparticles are readily centrifuged and the solution color changes to colorless, enabling accurate and quantitative detection of the targeted DNA. This approach was challenged for the detection of sdfI gene of Salmonella. The decline of the red color intensity of AuNPs was linear to the concentration of the targeted DNA from 1.2 x 10(1) copies/ml to 1.2 x 10(7) copies/ml and the detection limit was as low as 120 copies/ml (S/N = 3). This simple platform could be used to establish inexpensive and sensitive assays for clinical and in-field diagnostic applications.
引用
收藏
页码:1025 / 1038
页数:14
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