50935
Author
Honduvilla, N.G.;Hernando, A.;Bellón, J.M.;Buján, J.;Navlet, J.
Editor
Palacios, Fernando;Martinez, Carmen;Thomas, Barbara
Author Affiliation
Universidad de Alcalá de Henares. Dpto. Ciencias Morfológicas y Cirugia;Universidad de Alcalá de Henares. Dpto. Ciencias Morfológicas y Cirugia;Universidad de Alcalá de Henares. Dpto. Ciencias Morfológicas y Cirugia;Universidad de Alcalá de Henares. Dpto.
Title Of Article Chaper
Criopreservacion de celulas endoteliales humanas de vena de cordon umbilical
Title Of Journal Book
Sesiones del Primer Congreso Mundial y Comunicaciones Sobre Funcion y Gestion de las Colecciones de Historia Natural = First World Congress Sessions and Contributions on the Function and Management of Natural History Collections
Volume
1
Pages
107-112
Collation
6 p. : ill.
Reference Bibliography
Includes bibliographical references
Publisher
Dirección General de Bellas Artes y Archivos. Ministerio de Cultura
Publisher City
Madrid
ISBN
8474838991 (obra complete);8474839009 (Vol. 1)
Language Of Text
Spanish
Language Of Summary
English;Spanish
Literature Type
Monograph
Literature Level
Analytic
Meeting
Simposio Internacional y Primer Congreso Mundial Sobre Preservacion y Conservacion de Colecciones de Historia Natural = International Symposium and First World Congress on the Preservation and Conservation of Natural History Collections
Meeting City
Madrid
Abstract
Research into vascular prostheses lined with endothelial cells is being carried out for the purpose os using these prostheses in occlusive arterial diseases. As it is very difficult to use endothelial cells (EC) from the patient, we suggest that EC from the umbilical veins of newborns be conserved for use in the future. This paper details our present research on some experiments with EC from umbilical veins. Cells are cryopreserved following three ways: in situ in the umbilical cord; isolated and meintained in suspension; and, preservated in their own culture flask after in vitro culture. The usual culture media for cell cryopreservation techniques were used. After a preservation period in liquid nirtogen, cells were thawed, and a study of cell viability in culture was made.
pub_id
50935
Meeting Date
19920510-19920515