Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Añadir filtros








Intervalo de año
1.
Rev. Inst. Med. Trop. Säo Paulo ; 42(3): 153-6, May-Jun. 2000. tab
Artículo en Inglés | LILACS | ID: lil-262694

RESUMEN

The RID assay is one of the in vitro methods used for in-process control in the production of rabies vaccines for veterinary use. It has been shown to be very useful for determining antigen concentration in the final bulk product. The work presented in this paper, including the production and standardization of candidate standard reagents for use in the Radial Immunodiffusion Assay (RID) was carried out at the Pan American Institute for Food Protection and Zoonoses (INPPAZ/PAHO/WHO). The study was completed with the cooperation of the Faculty of Veterinary Sciences, National University of La Plata (NULP), Argentina, where the validation of the proposed standards and the quality control of samples from 28 different batches of rabies vaccines produced with Pasteur strain rabies virus (PV) in BHK cells were performed. The activity of the vaccines was determined by in vivo (NIH) and in vitro (RID)assays. The results of the candidate reagents for the reagent standardization tests showed stability, sensitivity and reproducibility. The Relative Potency the 1.2 between the problem vaccines and the reference vaccine was estimated by variance and regression analysis. The results of our validation study show that the INPPAZ (PAHO/WHO) is capable of producing and distributing the above-mentioned standard reagents, as well as of providing support for the incorporation of the RID technique (sensitive, rapid and inexpensive) to the laboratories that manufacture rabies vaccines in Latin America and the Caribbean.


Asunto(s)
Animales , Químicos de Laboratorio , Vacunas Antirrábicas , Inmunodifusión/métodos , Control de Calidad , Reproducibilidad de los Resultados , Sensibilidad y Especificidad , Drogas Veterinarias
2.
Rev. Inst. Med. Trop. Säo Paulo ; 35(6): 543-50, nov.-dez. 1993. ilus, tab
Artículo en Español | LILACS | ID: lil-140121

RESUMEN

El metodo recomendado por la Organizacion Mundial de la Salud (OMS) para la prueba de potencia de vacunas antirrabicas como producto final es la prueba NIH. Algunas tecnicas in vitro se han propuesto para el control durante el proceso de producion y complementan el ensayo in vivo antes mencionado. Este trabajo presenta los resultados obtenidos cuando se utilizo la tecnica de contrainmunoelectroforesis (CIE) para determinar el contenido de antigenos en muestras de 84 y 40 lotes de vacunas antirrabicas producidas em tejido nervioso de cerebro de raton lactante mediante cultivo de tejidos, respectivamente....


Asunto(s)
Humanos , Animales , Contrainmunoelectroforesis , Técnicas In Vitro , Vacunas Antirrábicas/inmunología , Virus de la Rabia/inmunología , Antígenos Virales
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA