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  2. Distribution (pharmacology) - Wikipedia

    en.wikipedia.org/wiki/Distribution_(pharmacology)

    The distribution of a drug between tissues is dependent on vascular permeability, regional blood flow, cardiac output and perfusion rate of the tissue and the ability of the drug to bind tissue and plasma proteins and its lipid solubility. pH partition plays a major role as well. The drug is easily distributed in highly perfused organs such as ...

  3. ADME - Wikipedia

    en.wikipedia.org/wiki/ADME

    Processes in pharmacokinetics. ADME is the four-letter abbreviation (acronym) for absorption, distribution, metabolism, and excretion, and is mainly used in fields such as pharmacokinetics and pharmacology. The four letter stands for descriptors quantifying how a given drug interacts within body over time.

  4. Volume of distribution - Wikipedia

    en.wikipedia.org/wiki/Volume_of_distribution

    Volume of distribution may be increased by kidney failure (due to fluid retention) and liver failure (due to altered body fluid and plasma protein binding). Conversely it may be decreased in dehydration. The initial volume of distribution describes blood concentrations prior to attaining the apparent volume of distribution and uses the same ...

  5. Pharmacokinetics - Wikipedia

    en.wikipedia.org/wiki/Pharmacokinetics

    Pharmacokinetics (from Ancient Greek pharmakon "drug" and kinetikos "moving, putting in motion"; see chemical kinetics), sometimes abbreviated as PK, is a branch of pharmacology dedicated to describing how the body affects a specific substance after administration. [1]

  6. Table of volume of distribution for drugs - Wikipedia

    en.wikipedia.org/wiki/Table_of_volume_of...

    This is a table of volume of distribution (V d) for various medication. For comparison, those with a V d L/kg body weight of less than 0.2 are mainly distributed in blood plasma , 0.2-0.7 mostly in the extracellular fluid and those with more than 0.7 are distributed throughout total body water.

  7. Physiologically based pharmacokinetic modelling - Wikipedia

    en.wikipedia.org/wiki/Physiologically_based...

    The first pharmacokinetic model described in the scientific literature [2] was in fact a PBPK model. It led, however, to computations intractable at that time. The focus shifted then to simpler models, [3] for which analytical solutions could be obtained (such solutions were sums of exponential terms, which led to further simplifications.)

  8. PK/PD model - Wikipedia

    en.wikipedia.org/wiki/PK/PD_model

    Upload file; Permanent link; ... [2] modeling) is a technique that combines the two classical pharmacologic disciplines of pharmacokinetics and pharmacodynamics. [3] ...

  9. Category:Pharmacokinetics - Wikipedia

    en.wikipedia.org/wiki/Category:Pharmacokinetics

    Upload file; Special pages; ... This category has the following 3 subcategories, out of 3 total. ... Pages in category "Pharmacokinetics" The following 78 pages are ...