Lesson 10: Pharmacokinetics of herbal medicines Flashcards
What is Pharmacokinetics?
The study of the absorption, distribution, metabolism and elimination of pharmacological agents in the body.
What is Pharmacodynamics?
The study of the biochemical and physiological effects of pharmacological agents on the body.
What are the 3 processes that determine Pharmacokinetics?
- absorption
- distribution
- elimination
In Pharmacokinetics what does absorption relate to?
How the drug gets into the body: is it absorbed across the small intestine to enter the circulatory system, or is absorbed across the mucous membrane of the mouth (sublingual absorption)?
In Pharmacokinetics what does distribution relate to?
Where the drug goes to in the body, so what part of the body does the drug act on.
In Pharmacokinetics what does metabolism relate to?
How the body chemically modifies the drug. Most drugs are metabolised by the liver, and drugs taken orally,will pass through the liver which may completely inactivate the drug.
In Pharmacokinetics what does elimination/excretion relate to?
How the drug is eliminated from the body. Usually drugs are removed by two main pathways: the hepatobiliary system, and the kidneys.
Which of these have been used for centuries as laxatives?
Anthraquinones
What is meant by the bioavailability of a herb?
Its ability to reach the body tissues
Which organ is involved in the first pass effect?
Liver
Which of these bind to oestrogen receptor sites?
Isoflavonoids
Which is not a major factor in determining the extent and rate of absorption of a herbal medicine?
a. Whether the herb is taken with plain water or a juice
b. Its ability to ionise
c. The blood flow at the site of administration
d. Its solubility
a. Whether the herb is taken with plain water or a juice
Which organ is most often responsible for removal of drugs from the body?
Kidney
What is the study of the absorption, distribution, metabolism and elimination of pharmacological agents in the body?
Pharmacokinetics
Which of these have a large molecular size and poor lipid solubility, resulting in low bioavailability?
Tannins