Aug 11 2010
Tamir Biotechnology, Inc. (Pink Sheets: ACEL) (formerly Alfacell Corporation) announced today that scientists supported by the National Institute of Allergy and Infectious Diseases (NIAID) confirmed that testing of three of our company's compounds showed in vitro results rarely seen before by the U.S. government for yellow fever.
In order to determine the effectiveness of a compound, NIAID uses a Selectivity Index (SI). The SI measures EC50 (50% virus-inhibitory (effective) concentration and EC90 (90%) cell inhibitory (cytotoxic) concentration determined in stationary cells.>
It's been over 100 years since the United States sent three doctors, led by renowned American Army surgeon Dr. Walter Reed to Cuba to study the work of Carlos Finlay, Cuban physician and scientist who first proposed proof in 1881 that yellow fever was transmitted by mosquitoes rather than direct human contact. It's been seventy-three (73) years since Max Theiler, working at the Rockefeller Foundation, discovered the 17D vaccine for yellow fever. Despite the medical advances of the twentieth century, this tropical disease remains incurable.
"Due to these compelling results, the government has informed us they will be conducting studies in animal models in the near future. This study expands the potential use of our compounds stated Charles Muniz, Chief Executive Officer of Tamir.
Source:
Tamir Biotechnology, Inc.