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  2. Galenic formulation - Wikipedia

    en.wikipedia.org/wiki/Galenic_formulation

    Galenic formulation deals with the principles of preparing and compounding medicines in order to optimize their absorption.Galenic formulation is named after Claudius Galen, a 2nd Century AD Greek physician, who codified the preparation of drugs using multiple ingredients.

  3. Guide to Pharmacology - Wikipedia

    en.wikipedia.org/wiki/Guide_to_Pharmacology

    The IUPHAR/BPS Guide to PHARMACOLOGY is an open-access website, acting as a portal to information on the biological targets of licensed drugs and other small molecules. The Guide to PHARMACOLOGY (with GtoPdb being the standard abbreviation) is developed as a joint venture between the International Union of Basic and Clinical Pharmacology (IUPHAR) and the British Pharmacological Society (BPS).

  4. PK/PD model - Wikipedia

    en.wikipedia.org/wiki/PK/PD_model

    Explore the concept of PK/PD models, which integrate pharmacokinetics and pharmacodynamics to optimize drug dosing and efficacy.

  5. Inverse agonist - Wikipedia

    en.wikipedia.org/wiki/Inverse_agonist

    In pharmacology, an inverse agonist is a drug that binds to the same receptor as an agonist but induces a pharmacological response opposite to that of the agonist. A neutral antagonist has no activity in the absence of an agonist or inverse agonist but can block the activity of either; [ 1 ] they are in fact sometimes called blockers (examples ...

  6. Goodman & Gilman's The Pharmacological Basis of Therapeutics

    en.wikipedia.org/wiki/Goodman_&_Gilman's_The...

    Their new text was first published in 1941 under the title The Pharmacological Basis of Therapeutics: A Textbook of Pharmacology, Toxicology and Therapeutics for Physicians and Medical Student. [1] Because the volume was twice as long as a typical textbook, Macmillan printed few copies, but demand for a readable, up-to-date pharmacological text ...

  7. Receptor theory - Wikipedia

    en.wikipedia.org/wiki/Receptor_theory

    The receptor occupancy model, which describes agonist and competitive antagonists, was built on the work of Langley, Hill, and Clark.The occupancy model was the first model put forward by Clark to explain the activity of drugs at receptors and quantified the relationship between drug concentration and observed effect.

  8. Volume of distribution - Wikipedia

    en.wikipedia.org/wiki/Volume_of_distribution

    In pharmacology, the volume of distribution (V D, also known as apparent volume of distribution, literally, volume of dilution [1]) is the theoretical volume that would be necessary to contain the total amount of an administered drug at the same concentration that it is observed in the blood plasma. [2]

  9. Mode of action - Wikipedia

    en.wikipedia.org/wiki/Mode_of_action

    In pharmacology and biochemistry, mode of action (MoA) describes a functional or anatomical change, resulting from the exposure of a living organism to a substance. [1] In comparison, a mechanism of action (MOA) describes such changes at the molecular level.

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