1/31
30 fill-in-the-blank flashcards covering key concepts of ADMET related to drug absorption, distribution, metabolism, elimination, and pharmacokinetics.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai |
|---|
No analytics yet
Send a link to your students to track their progress
Drugs go through the process of __, Distribution, Metabolism, Elimination, and Toxicology.
ADMET
The __ phase concerns the study of parameters that control the journey of drug from point of administration to its point of action.
Pharmacokinetic (PK)
The __ of a drug determines its interactions with enzymes, receptors, or other molecules in the body.
Drug Action
The pharmacokinetic phase includes absorption, distribution, metabolism, and __.
Elimination
The major mechanism involved in oral absorption of drugs is __ diffusion.
Passive
During first-pass metabolism, a large fraction of the dose is absorbed into the __ vein blood flow.
Portal
LogP affects drug __ and absorption.
Solubility
A drug’s __ affects its ability to cross cell membranes.
Degree of ionization
The ideal pH environment for a drug's ionization will determine its __ in the body.
Solubility
An increase in drug concentration in the blood can affect drug __.
Pharmacological activity
The degree a drug penetrates the blood-brain barrier is influenced by its __.
LogP value
Fatty foods impact gastric emptying time, which can slow __.
Drug absorption
First-pass metabolism typically occurs in the __.
Liver
Pharmacodynamic phase relates to the __ nature of the relationship between drug and its target.
Chemical
Membrane permeability is significantly affected by the drug's __.
Lipid/water solubility
The __ pathway contributes minimally to drug distribution compared to circulatory blood.
Lymphatic system
Drugs that bypass first-pass metabolism can provide __ efficacy.
Enhanced
One common route of drug administration is __, which allows for quick absorption.
Intravenous
A neutral compound is more likely to be __ through membranes than a charged compound.
Absorbed
Log P is a logarithm of the partition coefficient, expressed as log of concentration of drug in __ over concentration of drug in water.
Octanol
Hydrophobic interactions often dictate a drug’s ability to __ across lipid membranes.
Permeate
Oral absorption ideally requires a balance of drug solubility and membrane __.
Permeability
A drug's ability to bind to __ can determine its pharmacokinetic profile.
Plasma proteins
The __ is the most concentrated serum protein that binds acidic and neutral drugs.
Serum Albumin
Drug metabolism primarily occurs in the __.
Liver
Renal clearance is the primary route for the elimination of drugs and __.
Metabolites
An example of a non-oral route is __ administration, which typically avoids first-pass metabolism.
Topical
The mechanism of drug elimination includes both metabolism and __.
Excretion
A major concern in drug development is the formation of __ metabolites during metabolism.
Toxic
A drug's __ can substantially influence its distribution and efficacy in target tissues.
Concentration
Hydrophilic drugs are generally better absorbed in an __ environment.
Aqueous
By the end of their course, most drugs are __ before being excreted from the body.
Metabolized