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Sona Nanotech Inc C.SONA

Alternate Symbol(s):  SNANF

Sona Nanotech Inc. is a nanotechnology life sciences company that has developed multiple methods for the manufacturing of various types of gold nanoparticles. The Company is engaged in the research and development of its technology for use in multiplex diagnostic testing platforms and biomedical applications. Its gold nanotechnologies are adapted for use in applications, as a safe and delivery system for multiple medical treatments, for the approval of various regulatory boards, including Health Canada and the Food and Drug administration (FDA). Its gold nanorod particles are manufactured without the use of CTAB (cetyltrimethylammonium), eliminating the toxicity risks associated with the use of other gold nanorod technologies in medical applications. The Company leverages its core proprietary gold nanorod (GNR) manufacturing technology and laboratory assets to focus on the development of diagnostic tests and biologic reagents, and the advancement of its GNR intellectual property.


CSE:SONA - Post by User

Comment by JoeScotiaon Oct 02, 2020 5:10pm
326 Views
Post# 31661674

RE:RE:Awaiting Response From Manufacturer

RE:RE:Awaiting Response From ManufacturerThere is evidence to indicate that the two South Korean tests on HC’s list of antigen test applications that are awaiting response from manufacturer could be in a lot of trouble. I know the wait for validation of Sona’s test was difficult for all investors but I expect hindsight will show that 3rd party validation was a brilliant move on the part of Sona’s management. I can not find any evidence that either of the Korean tests was 3rd party validated.

The Biocredit Covid-19 Ag test from Rapigen Inc. (South Korea) is in HC’s “awaiting response” status. The Journal of Clinical Virology did a study on the test and found it only detected 11.1% to 45.7% from RT-PCR positive samples from Covid-19 patients. Furthermore it’s LOD was deemed to be a 1,000 times less sensitive than a viral culture and 1,000,000 times less sensitive than a RT-PCR test. Major red flags for any regulator. https://www.sciencedirect.com/science/article/pii/S1386653220302420

The Standard Q COVID-19 AG Test from SD Biosensor, Inc. (Korea) is also in HC’s “awaiting response” status. The WHO said they were going to buy 120M tests (SD Biosensor and Abbott’s BinaxNow) in their Sept 28 press release https://www.who.int/news-room/detail/28-09-2020-global-partnership-to-make-available-120-million-affordable-quality-covid-19-rapid-tests-for-low--and-middle-income-countries. Then this article said it failed evaluation “because it fell short of World Health Organization (WHO) standards". Furthermore, it “only posted 71% sensitivity” when the WHO has a minimum sensitivity standard of 80%. https://www.msn.com/en-ph/news/national/sd-biosensor-covid-19-antigen-test-fails-doh-evaluation/ar-BB19yzZv and https://cnnphilippines.com/news/2020/9/30/SD-Biosensor-rapid-antigen-test-kit-RITM-study-COVID-19.html
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