Sterility test systems for product recovery.
J Pharm Sci
; 74(1): 29-32, 1985 Jan.
Article
en En
| MEDLINE
| ID: mdl-3981412
When presterilized, closed canister, membrane filter units for sterility testing are validated for process, large volumes of therapeutic products for injection can be tested for sterility, recovered, and added to a subsequent bulk prior to sterile filtration. Intermittent positive pressure, applied to the canisters through the vent filters, makes possible the relatively rapid filtration, with minimal foaming, of viscous solutions such as 25% (w/v) normal serum albumin (human). Canister systems appear to be at least as effective as the standard membrane filter method, and the canisters are particularly suited to the sterility testing of bulks.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Esterilización
/
Contaminación de Medicamentos
Idioma:
En
Revista:
J Pharm Sci
Año:
1985
Tipo del documento:
Article
Pais de publicación:
Estados Unidos