Accessioning and automation compatible anterior nares swab design.

J Virol Methods

Department of Systems Biology, Harvard Medical School, Boston, MA, 02115, USA; Laboratory of Systems Pharmacology, Harvard Medical School, Boston, MA, 02115, USA; Massachusetts Consortium on Pathogen Readiness, Boston, MA, 20115, USA. Electronic address:

Published: August 2021

AI Article Synopsis

  • The COVID-19 pandemic necessitated a significant increase in viral testing for effective economic reopening.
  • An innovative anterior nares swab, called the Rhinostic, has been developed to facilitate automated sample processing and has shown similar performance to existing swabs for collecting viral samples.
  • Testing with Rhinostic swabs demonstrated 100% accuracy when compared to CLIA-approved nasal swabs, and the product is designed to be cost-effective and compatible with laboratory automation to improve testing efficiency.

Article Abstract

The COVID-19 pandemic has resulted in an unparalleled need for viral testing capacity across the world and is a critical requirement for successful re-opening of economies. The logistical barriers to near-universal testing are considerable. We have designed an injection molded polypropylene anterior nares swab, the Rhinostic, with a screw cap integrated into the swab handle that is compatible with fully automated sample accessioning and processing. The ability to collect and release both human and viral material is comparable to that of several commonly used swabs on the market. SARS-CoV-2 is stable on dry Rhinostic swabs for at least 3 days, even at 42 °C, and elution can be achieved with small volumes. To test the performance of the Rhinostic in patients, 119 samples were collected with Rhinostic and the positive and negative determinations were 100 % concordant with samples collected using Clinical Laboratory Improvement Amendments (CLIA) use approved nasal swabs at a clinical lab. The Rhinostic swab and barcoded tube set can be produced, sterilized, and packaged cost effectively and is designed to be adopted by clinical laboratories using automation to increase throughput and dramatically reduce the cost of a standard SARS-CoV-2 detection pipeline.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8108477PMC
http://dx.doi.org/10.1016/j.jviromet.2021.114153DOI Listing

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