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  2. Lisinopril - Wikipedia

    en.wikipedia.org/wiki/Lisinopril

    Lisinopril leaves the body completely unchanged in the urine. [1] [16] The half-life of lisinopril is 12 hours, and is increased in people with kidney problems. [1] [16] While the plasma half-life of lisinopril has been estimated between 12 and 13 hours, the elimination half-life is much longer, at around 30 hours. [18]

  3. File:Lisinopril Structural Formulae V.2.svg - Wikipedia

    en.wikipedia.org/wiki/File:Lisinopril_Structural...

    The following other wikis use this file: Usage on ar.wikipedia.org ليزينوبريل; Usage on de.wikipedia.org Lisinopril; Usage on es.wikipedia.org

  4. Physiologically based pharmacokinetic modelling - Wikipedia

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

    The absorption of a chemical deposited on skin can also be modeled using first order terms. It is best in that case to separate the skin from the other tissues, to further differentiate exposed skin and non-exposed skin, and differentiate viable skin (dermis and epidermis) from the stratum corneum (the actual skin upper layer exposed).

  5. Pharmacokinetics - Wikipedia

    en.wikipedia.org/wiki/Pharmacokinetics

    That is, the closer time points are, the closer the trapezoids reflect the actual shape of the concentration-time curve. The number of time points available in order to perform a successful NCA analysis should be enough to cover the absorption, distribution and elimination phase to accurately characterize the drug.

  6. File:Lisinopril structure.svg - Wikipedia

    en.wikipedia.org/wiki/File:Lisinopril_structure.svg

    The following other wikis use this file: Usage on ca.wikipedia.org Lisinopril; Usage on cy.wikipedia.org Lisinopril; Usage on el.wikipedia.org Λισινοπρίλη

  7. 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 ...

  8. File:Lisinopril synthesis.svg - Wikipedia

    en.wikipedia.org/wiki/File:Lisinopril_synthesis.svg

    You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made.

  9. Area under the curve (pharmacokinetics) - Wikipedia

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

    In the field of pharmacokinetics, the area under the curve (AUC) is the definite integral of the concentration of a drug in blood plasma as a function of time (this can be done using liquid chromatography–mass spectrometry [1]).