Basic Principles of Pharmacology
UNIT TWO: BASIC PRINCIPLES OF PHARMACOLOGY
Pharmacokinetics
Pharmacokinetics focuses on the study of how drugs are absorbed, distributed, metabolized, and excreted in the body. The primary processes involved in pharmacokinetics include:
- Absorption: Movement of the drug from the site of administration into the bloodstream.
- Distribution: Distribution of the drug throughout the body fluids and tissues.
- Metabolism: Biochemical modification of the drug, primarily occurring in the liver.
- Excretion: Elimination of the drug and its metabolites from the body, typically through urine or feces.
Study Questions
Matching: Drug Change and Movement Terms
Match the following terms with their appropriate definitions:
- Absorption
- e. Movement into the blood
- Distribution
- c. Movement from blood into tissue and cells
- Metabolism
- a. Change in drug structure
- Excretion
- f. Movement out of the body
- Pharmacokinetics
- d. Movement into and out of the body
- Elimination
- b. Change in drug structure and movement out of the body
Matching: Methods of Drug Movement and Characteristics
Match the method of movement with their characteristics:
- May require energy or pores
- c. Passage with the aid of a transport system
- Requires small size
- a. Passage through channels
- Requires lipid solubility
- b. Direct penetration of the membrane
True or False Statements
- Cell membranes are composed of fat with phosphate.
- F
- Most drugs enter cells through channels or pores.
- F
- P-glycoprotein transports many drugs out of cells.
- T
- A transport mechanism is needed for a water-soluble drug to enter a cell.
- T
- Ionization is a process that allows a drug to enter a cell.
- F
- If a quaternary ammonium compound drug is injected into a vein, it will produce effects, but it will not if taken orally.
- T
- Polar drugs can enter fetal circulation and breast milk.
- F
- Aspirin, like most drugs, is primarily absorbed in the small intestine.
- T
- Enteric drugs should not be crushed because crushing these preparations can cause stomach distress or alter the drug due to stomach acid.
- T
- A depot intramuscular (IM) injection of an antibiotic to treat syphilis will be completely effective within 24 hours after administration.
- F
- The protein-bound portion of a drug in circulation is not able to exert its action.
- T
- First-pass effect means most of the drug is activated by the liver, so it must be administered orally.
- F
- A drug with extensive first-pass effect may be given sublingually to allow absorption directly into the systemic circulation.
- T
- Adding a drug to a patient's drug regimen can cause other drugs to be metabolized more slowly or more rapidly.
- T
- Intestinal enzymes can release drugs from bile in the duodenum, causing the drug to be reabsorbed.
- T
- The nurse would expect that an intravenous (IV) antibiotic prescribed for bacterial meningitis would most likely get to the site of infection if the drug is water-soluble.
- T
- Chemotherapy is administered through a central intravenous line because chemotherapy is caustic to the vein, and a large central vein has rapid blood flow, which dilutes and moves the medication quickly.
- T
Key Points
- P-glycoprotein functions in drug transport, specifically in moving drugs out of cells, often impacting drug efficacy and resistance.
- Polar drugs face challenges in crossing cell membranes; they often require specific transport mechanisms to facilitate entry.
- First-pass metabolism can significantly affect the bioavailability of orally administered drugs, making alternative routes (like sublingual) necessary for some medications.
- Depot IM injections are designed for sustained release, but the onset of therapeutic effects may take longer than 24 hours and is influenced by the drug's formulation and characteristics.
- Enteric-coated medications provide protection against stomach acid, which is why it is emphasized they should not be crushed.
- Understanding the principles of pharmacokinetics is crucial for effective medication administration and optimization of therapeutic outcomes.