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Define Pharmacokinetics, give the three major mechanisms of drug absorption, and suggest the mechanism of absorption for NaCl in the GIT.

Biology

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2. a) Define Pharmacokinetics.
Pharmacokinetics is the study of how the body affects a drug. It describes the quantitative relationship between drug dose and drug concentration in the body over time, encompassing the processes of Absorption, Distribution, Metabolism, and Excretion (ADME).

Pharmacokinetics: The study of drug ADME (Absorption, Distribution, Metabolism, Excretion).\boxed{\text{Pharmacokinetics: The study of drug ADME (Absorption, Distribution, Metabolism, Excretion).}}

b) Give the three major mechanisms of drug absorption.
The three major mechanisms of drug absorption across biological membranes are:

  1. Passive Diffusion: Movement of a drug from an area of higher concentration to an area of lower concentration, directly across the lipid bilayer, without the need for a carrier or energy.
  2. Facilitated Diffusion: Movement of a drug across a membrane down its concentration gradient, aided by a specific carrier protein, but without the expenditure of metabolic energy.
  3. Active Transport: Movement of a drug across a membrane against its concentration gradient, requiring a specific carrier protein and the expenditure of metabolic energy (ATP).

c) Suggest the mechanism of absorption undergone by the following in the GIT:

  • i) Sodium chloride: Sodium ions are primarily absorbed via active transport mechanisms (e.g., Na+^+-K+^+ ATPase, Na+^+-glucose cotransport, Na+^+-H+^+ exchange), while chloride ions often follow passively or via specific chloride channels.

    Sodium chloride: Active transport\boxed{\text{Sodium chloride: Active transport}}
  • ii) Glucose: Glucose is absorbed by both facilitated diffusion (via GLUT2 transporters) and secondary active transport (via SGLT1 cotransporters, which use the sodium gradient).

    Glucose: Facilitated diffusion and secondary active transport\boxed{\text{Glucose: Facilitated diffusion and secondary active transport}}
  • iii) Ethanol: Ethanol is a small, lipid-soluble molecule that is readily absorbed across biological membranes primarily by passive diffusion.

    Ethanol: Passive diffusion\boxed{\text{Ethanol: Passive diffusion}}
  • iv) Acetyl Salicylic acid: Acetyl salicylic acid (aspirin) is a weak acid. In the acidic environment of the stomach, it exists predominantly in its unionized, lipid-soluble form, allowing it to be absorbed efficiently by passive diffusion.

    Acetyl Salicylic acid: Passive diffusion\boxed{\text{Acetyl Salicylic acid: Passive diffusion}}
  • v) Water: Water is absorbed across the gastrointestinal tract primarily by osmosis, which is a form of passive movement across semi-permeable membranes, driven by osmotic gradients.

    Water: Osmosis (passive diffusion)\boxed{\text{Water: Osmosis (passive diffusion)}}
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