Saliva Direct
- August 17, 2020
- Posted by: OptimizeIAS Team
- Category: DPN Topics
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Subject: Science and tech
Context :
A new, rapid diagnostic test for the novel coronavirus that uses saliva samples was granted an emergency use authorisation by the U.S. Food and Drug Administration (FDA).
Concept :
- The inexpensive test called SalivaDirecthas high sensitivity and can detect the virus even when the number of virus copies in the saliva sample is as low as 6-12 copies per microlitre.
- Collecting and testing saliva samples involves three steps — collecting saliva without preservative buffers, proteinase K treatment and heat inactivation, and dualplex RT-qPCR virus detection.
Significance:
- The new saliva test would increase efficiency and avoid shortage of crucial test components such as reagents.
- The new test makes sample collection non-invasive and reduces the need for trained healthcare workers to collect the samples, reducing the risk of infection during collection.
- In contrast, tests using nasopharyngeal swabs lead to false negative results due to errors at the time of sample collection.