Literature DB >> 11369086

Noncompartmentally-based pharmacokinetic modeling.

P Veng-Pedersen1.   

Abstract

OBJECTIVE: To present an overview of noncompartmentally-based modeling which is a modeling that makes use of systems analysis, predominantly linear systems analysis (LSA).
FINDINGS: Fundamental elements of LSA presented from a linear operational viewpoint have a sound foundation in molecular stochastic independence (MSI). Powerful LSA procedures based on MSI presented such as convolution, deconvolution and disposition decomposition analysis (DDA) enable PK predictions and evaluations of drug input and delivery using models with simple general structures and few verifiable assumptions. DDA nonparametrically differentiates the unit impulse response (UIR) into generalized elimination and distribution functions. DDA applied in a linear and nonlinear context is central to many LSA procedures such as analytically exact direct deconvolution, nonparametric evaluation of drug elimination and distribution, steady state predictions, evaluation of mean time parameters for drug delivery and disposition (mean residence time, mean transit time, mean arrival time), relative tissue affinity (residence time coefficients), nonparametric exact clearance correction of UIR, and time variant convolution and deconvolution. The general response mapping operation procedure of LSA presented provides a powerful rational alternative to problematic structured modeling of multivariate PK systems.
CONCLUSION: The wide arsenal of underutilized LSA-based kinetic analysis tools provide a rational, powerful alternative to traditional kinetic modeling.

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Year:  2001        PMID: 11369086     DOI: 10.1016/s0169-409x(01)00119-3

Source DB:  PubMed          Journal:  Adv Drug Deliv Rev        ISSN: 0169-409X            Impact factor:   15.470


  12 in total

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2.  Correlation between nasal membrane permeability and nasal absorption rate.

Authors:  Hefei Zhang; Chih-Wei Lin; Maureen D Donovan
Journal:  AAPS PharmSciTech       Date:  2012-12-07       Impact factor: 3.246

3.  C (max) and t (max) verification using Fibonacci sequence and absorption rate.

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Journal:  Eur J Drug Metab Pharmacokinet       Date:  2012-07-14       Impact factor: 2.441

4.  A 'bottom-up' approach for endo-PK/PD analysis.

Authors:  S Neelakantan; J A Widness; R L Schmidt; P Veng-Pedersen
Journal:  Biopharm Drug Dispos       Date:  2006-10       Impact factor: 1.627

5.  Prediction of the partition coefficients using QSPR modeling and simulation of paclitaxel release from the diffusion-controlled drug delivery devices.

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Journal:  Drug Deliv Transl Res       Date:  2018-10       Impact factor: 4.617

6.  Pharmacokinetic differentiation of drug candidates using system analysis and physiological-based modelling. Comparison of C.E.R.A. and erythropoietin.

Authors:  Peter Veng-Pedersen; Kevin J Freise; Robert L Schmidt; John A Widness
Journal:  J Pharm Pharmacol       Date:  2008-10       Impact factor: 3.765

7.  A system-approach method for the adjustment of time-varying continuous drug infusion in individual patients: a simulation study.

Authors:  Mária Durisová; Ladislav Dedík
Journal:  J Pharmacokinet Pharmacodyn       Date:  2002-12       Impact factor: 2.745

8.  Method of variability optimization in pharmacokinetic data analysis.

Authors:  Tomasz Grabowski; Jerzy Jan Jaroszewski; Walerian Piotrowski; Małgorzta Sasinowska-Motyl
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2013-06-19       Impact factor: 2.441

9.  Allometric analysis of tylosin tartrate pharmacokinetics in growing male turkeys.

Authors:  Błażej Poźniak; Marta Tikhomirov; Karolina Motykiewicz-Pers; Kamila Bobrek; Marcin Świtała
Journal:  J Vet Sci       Date:  2020-05       Impact factor: 1.672

10.  Physiologically based structure of mean residence time.

Authors:  Mária Durišová
Journal:  ScientificWorldJournal       Date:  2012-04-01
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