Jj. Liou et al., SOLUTIONS OF POPULATION BALANCE MODELS BASED ON A SUCCESSIVE GENERATIONS APPROACH, Chemical Engineering Science, 52(9), 1997, pp. 1529-1540
Microbial and cell cultures are composed of discrete organisms, each o
f which goes through a cell cycle that terminates in production of new
cells. The internal state of an individual cell changes as the cell p
rogresses through the cell cycle, and randomness in various features o
f the cell cycle always produces a distribution of cell states in the
culture. Rigorous models of this situation lead to the so-called popul
ation balance equations, which are integro-partial differential equati
ons. These equations are notoriously difficult to solve, and the diffi
culties increase as the number of parameters needed to describe cell s
tate increases. The cells in a culture are of different generations, a
nd cells of the (k+1)th generation originate only from divisions of ce
lls of the kth generation. A population balance equation written for t
he (k+1)th generation is therefore not an integral equation, although
it contains a source term which is an integral over the distribution o
f states of the kth generation. If competition of coexisting generatio
ns for environmental resources does not affect growth and reproduction
rates, the population balance equations for the various generations i
n a culture do not have to be solved simultaneously but rather can be
solved successively, and thus, some of the major difficulties of popul
ation balance equations written for entire populations are circumvente
d. In this paper, the successive generations approach to modeling is i
llustrated by its application to two problems where cell state is desc
ribed by a single parameter, either cell age or cell mass. It is then
applied to a problem where two parameters, namely cell age and cell ma
ss, are used to describe cell state at the same time; Analytical solut
ions of the population balance equations for the successive generation
s are found for the cases discussed, and the solutions are used to cal
culate the evolutions of the distributions of cell states with time fo
r the single parameter cases. (C) 1997 Elsevier Science Ltd.