1/30
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai | Chat |
|---|
No analytics yet
Send a link to your students to track their progress
a liquid preparation of one or more chemical compounds in a suitable solvent or mixture of miscible solvents
solution
these dissociate into solvated ions in solution
electrolytes
this includes both the active pharmaceutical ingredient (API) and usually other excipients
dosage form
the chemical compound dissolved in a solvent or mixture of miscible solvents
solute
a heterogeneous mixture of finely divided solid particles in a liquid; particles can settle over time and may be removed by filtration
suspension
a feature of solutions that refers to them having uniform appearance and composition throughout
homogenous
at a constant temperature, the solubility of a gas (Cg) in a particular solvent increases as the partial pressure (Pg) of the gas above the solution increases
Henry’s law
molar volume, aqueous solubility, lipophilicity, physical form, and pKa are all examples of these
physiochemical properties
a combination of two immiscible liquids in which one is finely and uniformly subdivided throughout the second; usually translucent or opaque and cannot be separated by filtration
emulsion
these contain less than the maximum amount of dissolved solute at a given temperature
unsaturated solutions
the density of a substance relative to the density of water
specific gravity
the most common mechanism of membrane permeation for small molecule drugs
passive diffusion
BIOAVAILABILITY (F) is the fraction of administered drug that reaches circulation. Bioavailability varies across different dosage forms, routes, and formulations. Results from an IV dose are typically set as F = 100%. Which of the following likely impacts the oral bioavailability of a drug?
the drug’s solubility in intestinal fluid
both the drug’s solubility in intestinal fluid and its ability to permeate GI epithelial cells
the drug’s ability to permeate GI epithelial cells
neither the drug’s solubility in intestinal fluid nor its ability to permeate GI epithelial cells
both the drug’s solubility in intestinal fluid and its ability to permeate GI epithelial cells
Both drug A and drug B are liquid medications. Drug A is dosed orally (PO) while drug B is dosed intravenously (IV) or intramuscularly (IM). The instructions for dosing drug A say to shake well before using. Which statement is most likely to be TRUE?
Neither medication is a solution
Both medications are solutions
Only medication B is a solution
Only medication A is a solution
Only medication B is a solution
Some cancer cells overexpress the efflux transporter known as P-glycoprotein (P-gp). Some chemotherapy drugs like paclitaxel are P-gp substrates, meaning that the transporter can move the drug across cell membranes. What can you conclude about the utility of drugs like paclitaxel to treat such cells?
Drugs like paclitaxel will be less effective treatments against cancer cells that overexpress P-gp.
Drugs like paclitaxel will be more effective treatments against cancer cells that overexpress P-gp.
P-gp expression will have no effect on the effectiveness of drugs like paclitaxel.
Drugs like paclitaxel will be less effective treatments against cancer cells that overexpress P-gp.
The solubility of solids in liquids generally increases with increasing temperature.
True
False
True
Particle size reduction can enhance the absolute solubility of a pure chemical substance held at a constant temperature and pressure.
True
False
False
Unsaturated solutions contain the maximum amount of dissolved solute at a given temperature.
True
False
False
The solubility of gases in liquids decreases with increasing temperature.
True
False
True
Melting point is an example of an ____ physical property.
intensive
Density is an example of an _____ physical property.
intensive
Regardless of dosage form or route of administration, a drug must be in ________________ to be absorbed.
solution
The rate at which a solute goes into solution can vary depending on factors such as degree of agitation.
True
False
true
_______________ electrolytes dissociate partially into ions in solution.
weak
The efflux transporter known as P-glycoprotein (P-gp) is highly expressed at the blood-brain barrier. The compounds carebastine and chlorpheniramine both antagonize histamine H1 receptors. Antagonism of histamine H1 receptors in the brain is associated with drowsiness. Carebastine is a substrate of P-gp; however, chlorpheniramine is not. Given this information, and assuming doses of each compound that lead to identical concentrations in the blood, which compound will be least likely to cause drowsiness?
chlorpheniramine
carebastine
both drugs will cause drowsiness
carebastine
Categorize the following four physical properties as intensive or extensive.
Boling point =
Mass =
Specific gravity =
Volume =
intensive
extensive
intensive
extensive
What is the term for a heterogeneous mixture of finely divided solid particles dispersed in a liquid?
suspension
solution
emulsion
suspension
The absolute solubility of a pure chemical substance at a given temperature and pressure is constant, but the rate of solution varies and depends on other factors such as particle size and degree of agitation.
True
False
True
Some cancer cells overexpress the efflux transporter known as BCRP. The chemotherapy drug mitoxantrone is a substrate of BCRP, meaning that the transporter can move the drug across cell membranes. Biopsies from two cancer patients, BB and PL, determine that BB's cancer overexpresses BCRP but PL's cancer does not. Given this information, and assuming all other things are equal, which patient is more likely to respond to mitoxantrone therapy?
PL
BB
PL and BB are equally likely to respond
PL
The density of a substance relative to the density of water is known as that substance's:
specific gravity
At a constant temperature, the solubility of a gas in a particular solvent ______ as the partial pressure of the gas above the solution increases
increases