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The half-life of a first-order reaction is often expressed as t 1/2 = 0.693/k (as ln(2) ... the kinetics will approximate first order (or pseudo-first order). As the ...
Most drugs are eliminated from the blood plasma with first-order kinetics. For this reason, when a drug is introduced into the body at a constant rate by intravenous therapy, it approaches a new steady concentration in the blood at a rate defined by its half-life. Similarly, when the intravenous infusion is ended, the drug concentration ...
In this situation it is generally uncommon to talk about half-life in the first place, but sometimes people will describe the decay in terms of its "first half-life", "second half-life", etc., where the first half-life is defined as the time required for decay from the initial value to 50%, the second half-life is from 50% to 25%, and so on. [7]
As useful rules of thumb, a first-order reaction with a rate constant of 10 −4 s −1 will have a half-life (t 1/2) of approximately 2 hours. For a one-step process taking place at room temperature, the corresponding Gibbs free energy of activation (Δ G ‡ ) is approximately 23 kcal/mol.
In first-order (linear) kinetics, ... t 1/2 is the half-life time of the drug, which is the time needed for the plasma drug concentration to drop to its half;
Using the Eyring equation, there is a straightforward relationship between ΔG ‡, first-order rate constants, and reaction half-life at a given temperature. At 298 K, a reaction with ΔG ‡ = 23 kcal/mol has a rate constant of k ≈ 8.4 × 10 −5 s −1 and a half life of t 1/2 ≈ 2.3 hours, figures that are often rounded to k ~ 10 −4 s ...
In this one-compartment model, the most common model of elimination is first order kinetics, where the elimination of the drug is directly proportional to the drug's concentration in the organism. This is often called linear pharmacokinetics , as the change in concentration over time can be expressed as a linear differential equation d C d t ...
Clearance is variable in zero-order kinetics because a constant amount of the drug is eliminated per unit time, but it is constant in first-order kinetics, because the amount of drug eliminated per unit time changes with the concentration of drug in the blood. [3] [4]