The selection of a Diphtheria Antitoxin to serve as a replacement master standard was made. The antitoxin potency is being determined. This involves the determination of the total units per vial and the appropriateness of the preparation to serve in the following areas: 1) antitoxin potency testing in animals, 2) in vitro potency (Vero cell test in microtiter plates), and 3) rabbit skin testing.

Agency
National Institute of Health (NIH)
Institute
Food and Drug Administration (FDA)
Type
Intramural Research (Z01)
Project #
1Z01BE001004-03
Application #
3804779
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
1991
Total Cost
Indirect Cost