Biopharmaceutics and pharmacokinetics distribution slideshare

  • 9, 2019•383 likes•127,451 views.
    Health & Medicine.
    Biopharmaceutics is defined as the study of factors influencing the rate and amount of drug that reaches the systemic circulation and the use of this information to optimise the therapeutic efficacy of the drug products.
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    S.Sep 9, 2019
  • How does drug distribution occur?

    After a drug enters the systemic circulation, it is distributed to the body's tissues.
    Distribution is generally uneven because of differences in blood perfusion, tissue binding (eg, because of lipid content), regional pH, and permeability of cell membranes..

  • What are the factors affecting distribution in pharmacokinetics?

    Factors affecting distribution of drug

    Organ or tissue perfusion.Binding of drug to Tissue component.
    Binding of drug to blood.
    Binding of drug to extra vascular component..

  • What are the factors affecting distribution in pharmacokinetics?

    Several factors impact drug distribution.
    These factors include the concentration of drug transporters in blood, pH, perfusion, body water composition, body fat composition, and most certainly disease conditions (e.g., volume depletion, burns, third spacing)..

  • What is distribution of drugs in pharmacokinetics?

    Drug distribution is the disbursement of an unmetabolized drug as it moves through the body's blood and tissues.
    The efficacy or toxicity of a drug depends on the distribution in specific tissues and in part explains the lack of correlation between plasma levels and the effects that are seen..

  • What is meant by distribution in biopharmaceutics and pharmacokinetics?

    Distribution in pharmacology is a branch of pharmacokinetics which describes the reversible transfer of a drug from one location to another within the body.
    Once a drug enters into systemic circulation by absorption or direct administration, it must be distributed into interstitial and intracellular fluids..

  • What is pharmacokinetics distribution process?

    Distribution is the process by which drug passes from the bloodstream to body tissues and organs.
    It is how a drug moves from intravascular space, e.g. blood vessels, to extravascular space, e.g. body tissues, as it is carried around the body by the circulatory system (figure 1)..

  • What is the distribution phase of pharmacokinetics?

    Distribution: Describes the journey of the drug through the bloodstream to various tissues of the body.
    Metabolism: Describes the process that breaks down the drug.
    Excretion: Describes the removal of the drug from the body..

  • What is the importance of distribution in pharmacokinetics?

    Drug distribution is the disbursement of an unmetabolized drug as it moves through the body's blood and tissues.
    The efficacy or toxicity of a drug depends on the distribution in specific tissues and in part explains the lack of correlation between plasma levels and the effects that are seen..

  • What is the pharmacokinetic distribution?

    Distribution.
    Distribution is the process by which drug passes from the bloodstream to body tissues and organs..

  • What is the pharmacokinetic process of distribution?

    Distribution is the process by which drug passes from the bloodstream to body tissues and organs.
    It is how a drug moves from intravascular space, e.g. blood vessels, to extravascular space, e.g. body tissues, as it is carried around the body by the circulatory system (figure 1)..

  • What is volume of distribution in pharmacokinetics SlideShare?

    Volume of distribution (V) relates the amount of drug in the body to the concentration of drug (C) in blood or plasma: Drugs with very high volumes of distribution have much higher concentrations in extravascular tissue than in the vascular compartment, ie, they are not homogeneously distributed..

  • Where can drugs be distributed?

    Each drug is uniquely distributed in the body.
    Some drugs distribute mostly into fat, others remain in extracellular fluid, and others are bound extensively to specific tissues.
    Many acidic drugs (eg, warfarin, aspirin) are highly protein-bound and thus have a small apparent volume of distribution..

  • Where does distribution occur in pharmacokinetics?

    Distribution in pharmacology is a branch of pharmacokinetics which describes the reversible transfer of a drug from one location to another within the body.
    Once a drug enters into systemic circulation by absorption or direct administration, it must be distributed into interstitial and intracellular fluids..

  • After a drug enters the systemic circulation, it is distributed to the body's tissues.
    Distribution is generally uneven because of differences in blood perfusion, tissue binding (eg, because of lipid content), regional pH, and permeability of cell membranes.
  • Drug distribution is impacted by several factors related to the drug and the body.
    The drug-related factors include blood and tissue binding proteins, pH, and perfusion.
    The body-related factors include body water composition, fat composition, diseases (e.g., volume depletion, burns, third spacing).
  • Volume of distribution (V) relates the amount of drug in the body to the concentration of drug (C) in blood or plasma: Drugs with very high volumes of distribution have much higher concentrations in extravascular tissue than in the vascular compartment, ie, they are not homogeneously distributed.
  • Volume of distribution (Vd), represents the apparent volume into which the drug is distributed to provide the same concentration as it currently is in blood plasma.
    It is calculated by the amount of the drug in the body divided by the plasma concentration [19].
Pharmacokinetics byLeon Shargel Clinical biopharmaceutics and pharmacokinetics byGibaldi Biopharmaceutics and Pharmacokinetics by Brahmankar. AboutSupport 
Distribution which involves reversible transfer of a drug between compartments. 2.Elimination which involves irreversible loss of drug from the body. It 

What are the three processes of drug distribution?

It involves the processes of drug absorption, bioavailability, clearance, and distribution. Although these processes are theoretically separate, from a practical standpoint in-vivo, they are all inter-connected.
After the drug is absorbed from the site of administration, it is distributed to extracellular fluids.

What is drug distribution in pharmacology?

DEFINITION Drug Distribution is defined as the Reversible transfer of drug between one compartment (blood) to another (extra vascular tissue) 5.
Significance :- Pharmacological action of drug depends upon its concentration at the site of action Thus distribution plays important role in Onset of Action Intensity of Action Duration of Action 6.


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