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  2. Half-life - Wikipedia

    en.wikipedia.org/wiki/Half-life

    [] = [] In order to find the half-life, we have to replace the concentration value for the initial concentration divided by 2: [] / = [] / and isolate the time: / = [] This t ½ formula indicates that the half-life for a zero order reaction depends on the initial concentration and the rate constant.

  3. Biological half-life - Wikipedia

    en.wikipedia.org/wiki/Biological_half-life

    Absorption half-life 1 h, elimination half-life 12 h. Biological half-life (elimination half-life, pharmacological half-life) is the time taken for concentration of a biological substance (such as a medication) to decrease from its maximum concentration (C max) to half of C max in the blood plasma.

  4. Plateau principle - Wikipedia

    en.wikipedia.org/wiki/Plateau_Principle

    C 0 is the initial concentration (t = 0) k e is the elimination rate constant; The relationship between the elimination rate constant and half-life is given by the following equation: = ⁡ / Because ln 2 equals 0.693, the half-life is readily calculated from the elimination rate constant.

  5. Exponential decay - Wikipedia

    en.wikipedia.org/wiki/Exponential_decay

    A more intuitive characteristic of exponential decay for many people is the time required for the decaying quantity to fall to one half of its initial value. (If N(t) is discrete, then this is the median life-time rather than the mean life-time.) This time is called the half-life, and often denoted by the symbol t 1/2. The half-life can be ...

  6. Elimination rate constant - Wikipedia

    en.wikipedia.org/wiki/Elimination_rate_constant

    C 0 is the initial concentration (at t=0) 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; Therefore, the amount of drug present in the body at time t is;

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  8. Pharmacokinetics - Wikipedia

    en.wikipedia.org/wiki/Pharmacokinetics

    Alpha phase: An initial phase of rapid decrease in plasma concentration. The decrease is primarily attributed to drug distribution from the central compartment (circulation) into the peripheral compartments (body tissues). This phase ends when a pseudo-equilibrium of drug concentration is established between the central and peripheral compartments.

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