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The Annals of Thoracic Surgery, Vol 21, 230-236, Copyright © 1976 by The Society of Thoracic Surgeons
LK Watts, P Duffy, RB Field, EG Stafford and MF O'Brien
A method for determining the viability of homograft valves has been
developed based on sequential measurements of glucose and pH levels of the
culture medium in which cardiac valves have been maintained for short
periods at 37 degrees C. Viable valves, as determined by tissue culture,
showed a characteristic pattern of glucose utilization and pH reduction
that was absent in nonviable valves. Upon explantation of valve leaflet
fragments into tissue culture, only fragments from valves that metabolized
glucose produced viable fibroblast cultures. The method reported here is
rapid, requires no specialized equipment, is nondestructive, and can
directly determine the viability of the valve homograft within 24 to 48
hours.
ARTICLES
Establishment of a viable homograft cardiac valve bank: a rapid method of determining homograft viability
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