Pharmacology Definition and Scope

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Questions and Answers

What is pharmacology?

The science that deals with the study of drugs and their interaction with living systems.

What does the term 'drug' refer to?

A substance used in the diagnosis, prevention, or treatment of disease.

Which of the following is NOT a natural source of drugs?

  • Animals
  • Synthetic compounds (correct)
  • Plants
  • Minerals

What are examples of drugs derived from plants?

<p>Atropine, Morphine, Quinine, Digoxine, Pilocarpine, Physostigmine.</p> Signup and view all the answers

What is pharmacokinetics?

<p>The study of the absorption, distribution, metabolism, and excretion of drugs.</p> Signup and view all the answers

Which of the following is NOT a major transport mechanism in pharmacokinetics?

<p>Chemical Reaction (D)</p> Signup and view all the answers

What is facilitated diffusion?

<p>Carrier-mediated transport from higher to lower concentration without needing energy.</p> Signup and view all the answers

What is the most common route of drug administration?

<p>Enteral route (oral ingestion).</p> Signup and view all the answers

Match the following routes of drug administration with their characteristics:

<p>Enteral = Most common and safest route Parenteral = Administered bypassing the gastrointestinal tract Local = Applied directly to the site of action</p> Signup and view all the answers

Irritant and unpalatable drugs can be administered via the enteral route.

<p>False (B)</p> Signup and view all the answers

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Study Notes

Pharmacology Definition and Scope

  • Pharmacology studies drugs and their interactions with living systems.
  • The term originates from Greek: "pharmacon" (drug) and "logos" (study).
  • A drug is a substance used to diagnose, prevent, or treat diseases.
  • The World Health Organization (WHO) defines a drug as something used to modify or explore physiological systems or pathological states.

Drug Sources

  • Drugs originate from natural or synthetic sources.
  • Natural Sources: Plants (e.g., atropine, morphine, quinine), animals (e.g., insulin, heparin), minerals (e.g., magnesium sulfate, iron), microorganisms (e.g., penicillin, tetracycline), and humans (e.g., immunoglobulins, growth hormone).
  • Synthetic Sources: Most modern drugs are synthesized (e.g., quinolones, omeprazole). Others are obtained from cell cultures or through recombinant DNA technology (e.g., human insulin) or hybridoma technology (e.g., monoclonal antibodies).

Pharmacokinetics

  • Pharmacokinetics studies drug absorption, distribution, metabolism, and excretion (ADME) – essentially, how drugs move within the body.
  • Drug movement involves crossing biological barriers (intestinal epithelium, cell membranes, renal membranes, capillary barriers).
  • Biotransport refers to drug movement across barriers.
  • Transport Mechanisms: Passive diffusion (high to low concentration, no energy required); Carrier-mediated transport (facilitated diffusion – high to low, no energy; active transport – against concentration gradient, energy required); Pinocytosis (cell drinking); Phagocytosis (cell engulfing particles).

Passive Diffusion

  • Movement of drug molecules from high to low concentration without energy expenditure.

Carrier-Mediated Transport

  • Polar compounds and some drugs use carrier proteins to cross membranes.
  • Facilitated diffusion is carrier-mediated transport from high to low concentration without energy use. GLUT 4 is an example facilitating glucose transport.

Pinocytosis and Phagocytosis

  • Pinocytosis: Cell engulfs fluid containing drugs (e.g., insulin crossing the blood-brain barrier).
  • Phagocytosis: Cell engulfs particles (e.g., botulinum toxin poisoning).

Routes of Drug Administration

  • Drug administration routes depend on drug properties and patient needs.
  • Routes are broadly categorized as enteral, parenteral, and local.

Enteral Route (Oral Ingestion)

  • The most common, safest, and oldest route.
  • Advantages: Safest, convenient, economical, self-administrable, non-invasive
  • Disadvantages: Slower onset, unsuitable for irritants/unpalatable drugs, potential for gastric irritation/vomiting, some drugs are destroyed by gastric juices (e.g., insulin).

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