Categorieën: Alle - excretion - absorption - pharmacokinetics - transport

door Jared Hall 5 jaren geleden

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Mod 3 - Pharmacokinetics: the study of the movement of drug molecules

Pharmacokinetics is the scientific study focused on how drug molecules move through the body. Various factors influence this movement, including the drug's tendency to ionize and its affinity for protein molecules such as serum proteins like albumin.

Mod 3 - Pharmacokinetics: the study of the movement of drug molecules

Mod 3 - Pharmacokinetics: the study of the movement of drug molecules

Excretion

Feces
Exact reversal of duodenal absorption

Intact molecules cross the membrane and are immediately ionized

Urine
Active Transport

penicillins and cephalosporins.

slow penicillin’s rate of excretion by giving the patient probenecid

Affected by lipophilicity, protein binding and ionization.
KIDNEY
kidney excretes and retrieves

Re-collects water, glucose, back sodium, potassium, etc

20% free flowing through glomerulus

Transport across lipid membrane

Types of cell transport/passage

Factors that affect transport and passage
Affinity for protein molecules

serum proteins (albumin)

When a molecule that is bound to a protein molecule is going to be temporarily tied up and not available for transport.

Lipophilicity

(hydrophilic) will never get into the lipid membrane.

Tendency to ionize

Urine has highest variability

heavily defined by the pH

Ionized molecules cannot cross lipid membranes.

Oral antifungals are too big to get through. they remain in stomach. this is used to our advantage
Slip through holes
Actively transported across the membrane by enzyme systems.
Passive diffusion

Absorbed through gut wall

complications:
may be lost to bile circulation
may require reabsorption to reach heart and become systemic
much gets excreted w/o being absorbed
capillaries and venules --> Liver --> heart --> lungs -->back to the heart --> systemic circulation