Related Experiment Video
Updated: Sep 13, 2025

Steady-state, Pre-steady-state, and Single-turnover Kinetic Measurement for DNA Glycosylase Activity
Published on: August 19, 2013
Rapid state-recrossing kinetics and slow escape kinetics in non-Markovian systems
Qingyuan Zhou1, Artur Bakaev1, Laura Lavacchi1
1Freie Universität Berlin, Fachbereich Physik, 14195 Berlin, Germany.
Abstract:
Barrier-crossing processes are often described using Markovian models, where reaction rates are quantified by mean first-passage times (MFPTs), barrier-escape times, or state-correlation functions. However, for systems exhibiting non-Markovian dynamics, where memory effects play a significant role, these metrics can differ substantially, complicating the interpretation of reaction kinetics from experimental or simulated time-series data. Here, we investigate the numerical evaluation of MFPTs and escape times in non-Markovian systems. For the MFPTs, we focus on two distinct computational approaches: one that considers only first arrivals between states, equivalent to the waiting or dwell time, and another that includes all first passages for a barrier-crossing event. Using extensive simulations of a one-dimensional generalized Langevin equation, we show that these methods yield equivalent results in the Markovian limit but diverge significantly under strong non-Markovian conditions. We derive a relationship between their respective passage-time distributions, which we validate against simulation data. Analysis of these distributions reveals that mean reaction times can be dominated either by rapid state recrossing or by slow escape dynamics. As such, our results highlight the importance of examining full kinetic distributions, rather than just mean values, to accurately characterize barrier-crossing dynamics in systems with memory.
Related Concept Videos
Nonlinear Pharmacokinetics: Michaelis-Menten Equation
Vmax represents the maximum achievable process rate, while KM, known as the Michaelis constant, signifies the drug concentration at which the process rate reaches half its maximum. This relationship between Vmax, KM, and Cp gives rise to three distinct...
Parameters Affecting Nonlinear Elimination: Zero-Order Input, First-Order Absorption and Two-Compartment Model
When a drug is administered through a constant intravenous infusion and eliminated via nonlinear pharmacokinetics, it follows zero-order input. For example, oral drugs undergo first-order absorption upon administration and are eliminated through nonlinear pharmacokinetics.
In the case of subcutaneously administered drugs,...
Drug Distribution as One-Compartment Model and Elimination by Nonlinear Pharmacokinetics: Overview
For instance, consider the metabolism of sodium salicylate. This compound is metabolized into two distinct substances: a glucuronide and a glycine conjugate. The rate of conjugation depends...
Fundamental Mathematical Principles in Pharmacokinetics: Rate and Order of Reaction
Pharmacokinetic reactions...
Elimination Kinetics: First-Order and Zero-Order
Drug clearance depends on the rate of drug elimination and its plasma concentration. Another important parameter is a drug's half-life, which is the time required for its concentration to decrease by half. In most cases, drug clearance follows first-order...
Nonlinear Pharmacokinetics: Dependence of Elimination Half-Life and Dose Clearance
A study on guinea pigs examined the...

