| Literature DB >> 35788853 |
Sepideh Sharif1, Chihiro Hasegawa2, Stephen B Duffull2.
Abstract
Nonlinear ordinary differential equations (ODEs) are common in pharmacokinetic-pharmacodynamic systems. Although their exact solutions cannot generally be determined via algebraic methods, their rapid and accurate solutions are desirable. Thus, numerical methods have a critical role. Inductive Linearization was proposed as a method to solve systems of nonlinear ODEs. It is an iterative approach that converts a nonlinear ODE into a linear time-varying (LTV) ODE, for which a range of standard integration techniques can then be used to solve (e.g., eigenvalue decomposition [EVD]). This study explores the properties of Inductive Linearization when coupled with EVD for integration of the LTV ODE and illustrates how the efficiency of the method can be improved. Improvements were based on three approaches, (1) incorporation of a convergence criterion for the iterative linearization process (for simulation and estimation), (2) creating more efficient step sizes for EVD (for simulation and estimation), and (3) updating the initial conditions of the Inductive Linearization (for estimation). The performance of these improvements were evaluated using single subject stochastic simulation-estimation with an application to a simple pharmacokinetic model with Michaelis-Menten elimination. The reference comparison was a standard non-stiff Runge-Kutta method with variable step size (ode45, MATLAB). Each of the approaches improved the speed of the Inductive Linearization technique without diminishing accuracy which, in this simple case, was faster than ode45 with comparable accuracy in the parameter estimates. The methods described here can easily be implemented in standard software programme such as R or MATLAB. Further work is needed to explore this technique for estimation in a population approach setting.Entities:
Keywords: (PKPD) model development; Adaptive step size algorithm; Inductive Linearization; Nonlinear ordinary differential equations; Numerical methods; Optimization
Mesh:
Year: 2022 PMID: 35788853 PMCID: PMC9338916 DOI: 10.1007/s10928-022-09813-z
Source DB: PubMed Journal: J Pharmacokinet Pharmacodyn ISSN: 1567-567X Impact factor: 2.410
Parameter values for the Michaelis–Menten example (Eq. 3)
| Parameters | Units | Values |
|---|---|---|
*Exponential error
IndLin accuracy and speed without and with the stopping rule compared with the reference solution ode45
| Methods | Final maximum absolute relative-error | Run-time (seconds) |
|---|---|---|
| – | ||
| IndLin | ||
| IndLin |
: tolerance
Comparison of the IndLin accuracy (, , and adaptive ss using ) with ode45 for simulation
| Methods | Final maximum absolute relative-error | Run-time (seconds) |
|---|---|---|
| – | 0.188 | |
| Fixed step-sizea | ||
| IndLin | 9.417 | 0.109 |
| IndLin | 7.123 | 0.993 |
| Adaptive step-sizea | ||
| IndLin (adaptive step size | 0.421 | |
| IndLin (adaptive step size | 0.055 |
aThe stopping rule for IndLin was included in these solutions with tolerance () set to 1e−6 and maximum number of iterations () to twenty ()
ss step size
Fig. 1Concentration–time profile for simulated data by typical profile from MATLAB ode45 and
Comparison of parameter estimates and speed for IndLin and ode45
| Parameters | Parameter estimates | Run time (s) | |||
|---|---|---|---|---|---|
| True parameter values | 1 | 1 | 0.2 | 0.5 | |
| IndLina | |||||
| IndLin, smart updatea | |||||
aTolerance () was set to 1e−6 and α = 0.01
Fig. 2Comparison of relative difference of estimated parameters from their nominal simulation values (%) for a ode45, b IndLin (ss = 0.1), c IndLin (ss = 0.01) and d IndLin (adaptive step size, α = 0.01)
Fig. 3Comparison of speed (seconds) among ode45, IndLin (), IndLin () and IndLin (adaptive step size, ) (a in linear scale and b in log scale)
Fig. 4Comparison of the objective function value (OFV) among ode45, IndLin (ss = 0.1), IndLin (ss = 0.01) and IndLin (adaptive step size, α = 0.01) (a in linear scale and b in log scale)