In a new study, researchers in Taiwan describe a simple, colour-based diagnostic approach with the potential to detect target DNA sequences found in TB-causing mycobacteria - in just a fraction of the time required for established diagnostic tests.
The standard method for TB detection in a clinical setting involves culturing the Mycobacterium tuberculosis bacillus, which requires 3-6 weeks to grow on solid culture media or 9-16 days in rapid liquid culture media.
A faster alternative is the polymerase chain reaction (PCR) technology.
In their study, Tsung-Ting Tsai and colleagues employed gold nanoparticles and microfluidic paper-based analytical devices to achieve rapid diagnosis without the need for complex and time-consuming laboratory processes.
They easily detected TB mycobacterium target sequences, and the turnaround time was approximately one hour after the human DNA was extracted from patients.
Although the authors are still optimising their technology, they already believe that it will result in "affordable, sensitive, specific, user-friendly, rapid and robust, equipment-free, and highly end-user-deliverable diagnostic applications".
According to World Health Organisation estimates, there were 8.7 million new cases in 2011 and 1.4 million deaths.
Most new cases occur in developing countries that lack the facilities and trained personnel required for early detection of TB, they said.
The study was published in the journal Science and Technology of Advanced Materials (STAM).
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