Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

During the first peak of the coronavirus pandemic, it became apparent that the processing of the standard COVID-19 test using nasal swab samples, while considered a gold standard, was slow, taking over 24 hours to give results in most cases.

As demand for quicker test results increased with supplies running low, scientists and engineers rushed to fill the gap at scale for rapid diagnostic testing that would replace the standard real-time reverse transcription polymerase chain reaction (rt-PCR) test.

Such technologies included rapid antigen tests, antibody tests, as well as tests using the loop-mediated isothermal amplification method (LAMP) and mass spectrometry. The UK is currently deploying “lateral flow” antigen tests, which deliver results on the spot, are cheap and easily mass produced. However they have important limitations.

With so many different types of test now on the market, how do we sort the wheat from the chaff and work out what form of testing is best for which healthcare or community setting? Our research group is testing the tests to find out.

Read the full article on The Conversation website, co-written by Gail Hayward, Nuffield Department of Primary Care Health Sciences website.

Oxford is a subscribing member of The ConversationFind out how you can write for The Conversation.