The in vitro cultivation of keratinocytes and their application in the
form of confluent sheets to cover various kinds of skin defects invol
ves a number of problematical steps which could be improved by using s
ingle cell suspensions instead. Therefore we developed a method to app
ly keratinocytes suspended as single cells in a fibrin gel. By testing
the feasibility of this method in different experimental animal model
s we found that it facilitates cultivation as well as application of t
he cells, moreover, this method allows a much more flexible use of the
cells, i.e. it is easier to consider the clinical condition of the pa
tient than by the conventional method