Pharmacology · MU Sofia

6. Drug Distribution

Explains how a drug moves from the bloodstream into tissues and organs, and why this affects onset, intensity and duration of action. It works through factors such as blood flow, plasma protein binding, tissue binding, lipid solubility, molecular size and ionisation with pH, then covers central and peripheral compartments and specialised barriers like the blood-brain and placental barriers. It closes with the volume of distribution and its formula, and a set of recap questions.

Inside: 5 sections · 4 labelled pictures · 10 flashcards · 5 min

Topic 6 of 93 in the MU Sofia syllabus for Pharmacology (Medicine, Year 3). The free AceMed note covers it in 5 sections, about 739 words (5 min of reading), with 10 flashcards.

In this note

  1. Drug Distribution
  2. Factors Affecting Drug Distribution
  3. Compartments of Distribution
  4. Volume of Distribution (Vd)
  5. Recap Questions

Drug Distribution

Drug distribution refers to the process by which a drug is transported from the bloodstream to various tissues and organs of the body. Understanding drug distribution is crucial for predicting the onset, intensity, and duration of drug action, as well as its potential side effects.

Factors Affecting Drug Distribution

  1. 1. Blood Flow to Tissues
  • Highly perfused organs (e.g., heart, liver, kidneys, brain) receive drugs more rapidly than less perfused tissues (e.g., muscle, fat).
  • The rate of distribution is initially higher in organs with rich blood supply, leading to faster onset of action in these areas.
  • Poorly perfused tissues (e.g., adipose tissue, bone) act as reservoirs, releasing the drug slowly over time.
  1. 2. Plasma Protein Binding
  • Drugs can bind to plasma proteins such as albumin (for acidic drugs) and alpha-1-acid glycoprotein (for basic drugs).
  • Only the unbound (free) drug is pharmacologically active and can cross cell membranes to exert an effect.
  • High protein binding can limit the amount of free drug available for distribution, reducing drug efficacy but also prolonging its duration.
  • Conditions like hypoalbuminemia (e.g., in liver disease or nephrotic syndrome) can increase free drug levels, potentially leading to toxicity.
  1. 3. Tissue Binding
  • Drugs can bind to tissues, which act as reservoirs, prolonging the drug’s effect or leading to toxicity.
  • Lipophilic drugs tend to accumulate in fatty tissues, which can serve as a depot and slowly release the drug over time.
  • Hydrophilic drugs are more likely to distribute in the extracellular fluid, limiting their penetration into cells.
  1. 4. Lipid Solubility
  • Lipophilic (fat-soluble) drugs can easily cross cell membranes and are widely distributed in tissues, including the central nervous system (CNS).
  • Hydrophilic (water-soluble) drugs are primarily confined to the extracellular fluid and may have limited distribution in tissues.
  • Lipophilic drugs can cross protective barriers like the blood-brain barrier (BBB) and the placental barrier more easily than hydrophilic drugs.
  1. 5. Molecular Size
  • Smaller molecules diffuse more readily across cell membranes, enhancing distribution.
  • Large molecules may be restricted to plasma or extracellular fluid compartments, limiting tissue penetration.
  1. 6. Ionization and pH
  • The degree of ionization of a drug is influenced by the pH of the environment and the drug’s pKa.
  • Non-ionized forms are more lipid-soluble and can cross membranes more easily.
  • Acidic drugs are better absorbed in acidic environments (e.g., stomach), while basic drugs are better absorbed in alkaline environments (e.g., intestines).

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