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  2. Bioequivalence - Wikipedia

    en.wikipedia.org/wiki/Bioequivalence

    In determining bioequivalence between two products such as a commercially available Branded product and a potential to-be-marketed Generic product, pharmacokinetic studies are conducted whereby each of the preparations are administered in a cross-over study (sometimes parallel study, when a cross-over study is not feasible) to volunteer subjects, generally healthy individuals but occasionally ...

  3. Binding selectivity - Wikipedia

    en.wikipedia.org/wiki/Binding_selectivity

    The concept of selectivity is used to quantify the extent to which one chemical substance, A, binds each of two other chemical substances, B and C. The simplest case is where the complexes formed have 1:1 stoichiometry. Then, the two interactions may be characterized by equilibrium constants K AB and K AC.

  4. Ligand efficiency - Wikipedia

    en.wikipedia.org/wiki/Ligand_efficiency

    Ligand efficiency is a measurement of the binding energy per atom of a ligand to its binding partner, such as a receptor or enzyme. [1]Ligand efficiency is used in drug discovery research programs to assist in narrowing focus to lead compounds with optimal combinations of physicochemical properties and pharmacological properties.

  5. Hill equation (biochemistry) - Wikipedia

    en.wikipedia.org/wiki/Hill_equation_(biochemistry)

    In contrast to this article's previous definition of the Hill equation, the IUPHAR defines the Hill equation in terms of the tissue response (), as [1] = [] + [] = + ([]) where [] is the drug concentration, is the Hill coefficient, and is the drug concentration that produces a 50% maximal response.

  6. Area under the curve (pharmacokinetics) - Wikipedia

    en.wikipedia.org/wiki/Area_under_the_curve...

    The AUC (from zero to infinity) represents the total drug exposure across time. AUC is a useful metric when trying to determine whether two formulations of the same dose (for example a capsule and a tablet) result in equal amounts of tissue or plasma exposure. Another use is in the therapeutic drug monitoring of drugs with a narrow therapeutic ...

  7. Volume of distribution - Wikipedia

    en.wikipedia.org/wiki/Volume_of_distribution

    A V D greater than the total volume of body water (approximately 42 liters in humans [5]) is possible, and would indicate that the drug is highly distributed into tissue. In other words, the volume of distribution is smaller in the drug staying in the plasma than that of a drug that is widely distributed in tissues. [6]

  8. New Mexico teen accused of killing his parents, siblings with ...

    www.aol.com/news/mexico-teen-accused-killing...

    Police in New Mexico said a 16-year-old teen killed four members of his family including his mom, dad and siblings over the weekend.

  9. PK/PD model - Wikipedia

    en.wikipedia.org/wiki/PK/PD_model

    However, if a delay is observed between the drug administration and the drug effect, a temporal dissociation needs to be taken into account and more complex models exist: [6] [7] Direct vs Indirect link PK/PD models; Direct vs Indirect response PK/PD models [8] Time variant vs time invariant; Cell lifespan models; Complex response models