whereξ_f,ξ_b are the velocities of the direct and reverse reaction
passes, respectively. Substituting expressions (7) and (6)into(5)is
obtained:
S_i¼_ξf_ξb ln
ξ_f
ξ_b
0 ð 8 Þ
Formula (8)[14] is fulfilled regardless of whether the network
of chemical reactions is close or far from equilibrium and also ends
the controversy related to the divorce between classic thermody-
namics and chemical kinetics.
Using the expression for the Gibbs equation,GHTS, the
affinityAcan be evaluated as
A¼
∂H
∂ξ
Tp
þT
∂S
∂ξ
Tp
ð 9 Þ
The term ∂∂Hξ
Tp
represents the heat of process,qTp. Some-
times, it is possible to neglect the term ∂∂Sξ
Tp
, due to
qTp
∂∂Sξ
Tp
[12]. Taking into account (Eq.4), we get that the
entropy production rate can be rewritten as
δSi
∂t
¼S_i¼
1
T
Aξ_
qTpξ_
T
¼
1
T
δq
dt
Tp
ð 10 Þ
Formula (10) is an approximation to the entropy production
rate of a living organism [12]. Equation (10) can be rewritten
according to Zotin [15] using the metabolic rate δdtq
Tp
q_ as
follows:
S_i¼q_
O 2 þq_Gl
T
ð 11 Þ
whereq_O 2 ,q_Glare the metabolic rates of oxygen consumptionq_O 2 ,
due to oxidative phosphorylation (OxPhos) and due also to glycol-
ysisq_Gl, respectively. Under aerobic conditionsq_Gl is negligible,
except in cancerous cells where the glycolysis is the main
process [16].
Sometimes, it is convenient [12] to use the so-called dissipation
function, ΨTS_i, introduced by Lord Rayleigh. According to
Eq. (11) the dissipation function can be rewritten as
ΨTS_i¼q_O 2 þq_Gl ð 12 Þ
In the tumor cells the glycolysis is the main process [16], thus
Eq. (12) can be written as
S_iq_Gl
T
ð 13 Þ
Parameters Estimation in Phase-Space Landscape Reconstruction of Cell Fate... 131