Unmodified gold nanoparticles for direct and rapid detection of Mycobacterium tuberculosis complex

被引:49
|
作者
Hussain, Marwa M. [1 ,2 ,3 ]
Samir, Tamer M. [1 ,2 ,3 ]
Azzazy, Hassan M. E. [1 ,2 ]
机构
[1] Amer Univ Cairo, Dept Chem, New Cairo 11835, Egypt
[2] Amer Univ Cairo, Sch Sci & Engineer, Yousef Jameel Sci & Technol Res Ctr, New Cairo 11835, Egypt
[3] Misr Univ Sci & Technol, Fac Pharm, Dept Microbiol, 6th October City, Egypt
关键词
Mycobacterium tuberculosis complex; Unmodified gold nanoparticles; TB detection; IDENTIFICATION; DIAGNOSIS; ASSAY; DNA; PROSPECTS;
D O I
10.1016/j.clinbiochem.2012.12.020
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objectives: This work aims to develop rapid nano-gold assay prototypes for specific detection of Mycobacterium tuberculosis complex (MTBC). Design and methods: Spherical gold nanoparticles (AuNPs, 14 nm) were synthesized by citrate reduction method and characterized by spectrophotometry and SEM. MTB 16s rDNA regions were amplified by PCR and amplicons were detected using genus- and species-specific oligotargeters and AuNPs. In a second prototype, MTBC unamplified genomic DNA was directly detected using species-specific oligo-targeters and AuNPs. Results: Detection limits were 1 ng for PCR product and 40 ng for genomic DNA. The nano-gold prototype detected 45 positive genomic DNA samples which were also positive with automated liquid culture system (BACTEC (TM) MGIT (TM)) and semi-nested PCR (100% concordance). Following DNA extraction, using standard procedures, the TB nano-gold prototype turnaround time is about 1 h. Conclusions: We have developed nano-gold assay prototype for direct and inexpensive detection of MTBC. The developed prototypes are simple, sensitive, rapid and can substitute PCR-based detection. The developed assay may show potential in the clinical diagnosis of TB especially in developing countries. (C) 2013 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:633 / 637
页数:5
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