Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
Biosensors (Basel) ; 13(6)2023 May 29.
Article in English | MEDLINE | ID: mdl-37366954

ABSTRACT

In 2019, over 21% of an estimated 10 million new tuberculosis (TB) patients were either not diagnosed at all or diagnosed without being reported to public health authorities. It is therefore critical to develop newer and more rapid and effective point-of-care diagnostic tools to combat the global TB epidemic. PCR-based diagnostic methods such as Xpert MTB/RIF are quicker than conventional techniques, but their applicability is restricted by the need for specialized laboratory equipment and the substantial cost of scaling-up in low- and middle-income countries where the burden of TB is high. Meanwhile, loop-mediated isothermal amplification (LAMP) amplifies nucleic acids under isothermal conditions with a high efficiency, helps in the early detection and identification of infectious diseases, and can be performed without the need for sophisticated thermocycling equipment. In the present study, the LAMP assay was integrated with screen-printed carbon electrodes and a commercial potentiostat for real time cyclic voltammetry analysis (named as the LAMP-Electrochemical (EC) assay). The LAMP-EC assay was found to be highly specific to TB-causing bacteria and capable of detecting even a single copy of the Mycobacterium tuberculosis (Mtb) IS6110 DNA sequence. Overall, the LAMP-EC test developed and evaluated in the present study shows promise to become a cost-effective tool for rapid and effective diagnosis of TB.


Subject(s)
Biosensing Techniques , Microelectrodes , Tuberculosis , Mycobacterium tuberculosis/genetics , Mycobacterium tuberculosis/isolation & purification , Tuberculosis/diagnosis , Tuberculosis/microbiology , Biosensing Techniques/economics , Biosensing Techniques/instrumentation , Biosensing Techniques/methods , Biosensing Techniques/standards , Carbon/chemistry , Microelectrodes/standards , Sensitivity and Specificity , Microscopy, Electron, Scanning , Reproducibility of Results , DNA, Bacterial/analysis
2.
Sensors (Basel) ; 23(9)2023 Apr 26.
Article in English | MEDLINE | ID: mdl-37177497

ABSTRACT

Underground mining operations present critical safety hazards due to limited visibility and blind areas, which can lead to collisions between mobile machines and vehicles or persons, causing accidents and fatalities. This paper aims to survey the existing literature on anti-collision systems based on computer vision for pedestrian detection in underground mines, categorize them based on the types of sensors used, and evaluate their effectiveness in deep underground environments. A systematic review of the literature was conducted following the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines to identify relevant research work on anti-collision systems for underground mining. The selected studies were analyzed and categorized based on the types of sensors used and their advantages and limitations in deep underground environments. This study provides an overview of the anti-collision systems used in underground mining, including cameras and lidar sensors, and their effectiveness in detecting pedestrians in deep underground environments. Anti-collision systems based on computer vision are effective in reducing accidents and fatalities in underground mining operations. However, their performance is influenced by factors, such as lighting conditions, sensor placement, and sensor range. The findings of this study have significant implications for the mining industry and could help improve safety in underground mining operations. This review and analysis of existing anti-collision systems can guide mining companies in selecting the most suitable system for their specific needs, ultimately reducing the risk of accidents and fatalities.

3.
BMC Infect Dis ; 16(1): 517, 2016 Sep 27.
Article in English | MEDLINE | ID: mdl-27677540

ABSTRACT

BACKGROUND: Tuberculosis (TB) is a major global health problem and remains the leading cause of morbidity and mortality in developing countries. Routinely used TB diagnostic methods, in most endemic areas, are time-consuming, often less-sensitive, expensive and inaccessible to most patients. Therefore, there is an urgent need for the development of early, easy to use and effective diagnosis tools of TB, which can be effectively integrated into resource limited settings, to anticipate the early treatment and limit further spread of the disease. Over the last decade, Loop-mediated isothermal amplification (LAMP) assays have become a powerful tool for rapid diagnosis of infectious diseases because of the simplicity of device requirements. Indeed, LAMP is a simple, quick and cost effective Isothermal Nucleic Acid Amplification diagnostic test (INAAT) that has the potential to be used in TB endemic settings of resource-poor countries. METHODS: In the present study, we have developed a simple and rapid TB molecular diagnostic test using a Single-Step Loop-mediated isothermal DNA amplification (SS-LAMP) method for the detection of Mycobacterium tuberculosis complex (MTBC) strains, with a simplified sample preparation procedure, eliminating DNA extraction prior to LAMP amplification, DNA initial denaturation and enzymatic inactivation steps during the amplification process. To perform our in-house SS-LAMP assay, a set of six specific primers was specifically designed to recognize eight distinct regions on the MTBC species-specific repetitive insertion sequence 6110 (IS6110). The amplification of the targeted DNA was carried out under isothermal conditions at 65 °C within 1 h. Our protocol was firstly optimized using 60 of confirmed MTBC isolates and a recombinant pGEMeasy-IS6110 vector for sensitivity testing. Thereafter, the assay was evaluated on liquefied sputum specimens collected from 157 Moroccan patients suspected of having TB. RESULTS: Our SS-LAMP developed assay was able to detect MTBC DNA directly from liquefied sputum samples without any prior DNA extraction, denaturation nor the final enzymatic inactivation step. When compared to routinely used Löwenstein Jensen (LJ) Culture method, our SS-LAMP assay is rapid and showed specificity and sensitivity of 99.14 % and 82.93 % respectively which are within the international standards. In addition, the limit of detection of our assay was found to be as little as 10 copies of bacterial DNA. CONCLUSION: To our knowledge, this is the first study using a single step LAMP (SS-LAMP) procedure as a rapid, easy to perform and cost effective testing for TB early detection. This innovative assay could be suitable for low-income countries with restricted health equipment facilities.

SELECTION OF CITATIONS
SEARCH DETAIL
...