Solubility Flashcards

(55 cards)

1
Q

What is solubility?

A

Concentration of a solute when the solvent has dissolved all that solute that it can at a given temperature.

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2
Q

What is solubility in reference to equilibrium?

A

Concentration of solute in a saturated solution at equilibrium.

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3
Q

What type of property is solubility?

A

Physical property

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4
Q

Miscible meaning.

A

Refers to a solute when it is a liquid. This solute can form a solution with a solvent over any concentration range.

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5
Q

What are the factors affecting solubility?

A

Temperature = principal factor
Pressure = unimportant in pharm. applications
Polarity (and hydrogen bonding)
Particle size

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6
Q

What is NOT a factor of solubility?

A

How fast a substance dissolves

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7
Q

What is heat of solution?

A

Overall energy exchange when a solute dissolves in a solvent

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8
Q

What is lattice energy?

A

energy released when one mole of ionic solid is formed from gaseous ions

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9
Q

What is heat of hydration?

A

Enthalpy change associated with dissolution of one mole of ion in water

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10
Q

Heat of solution equation.

A

∆Hsolution= ∆Hsolute + ∆Hhydration

∆Hsolute - always endo

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11
Q

What are the steps of solution formation?

A
  1. separation of solute particles
  2. separation of solvent particles
  3. mixing of solute and solvent particles.
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12
Q

Describe the separation of solute part. steps.

A

Attractive forces between solute part. are cleaved with energy

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13
Q

Describe the separation of solvent part. steps.

A

Attractive forces between solvent part. are cleaved with energy

endothermic

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14
Q

Describe the mixing of solute and solvent part.

A

solute and solvent particles create bonds which releases energy

exothermic

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15
Q

What is Hess’s law?

A

net enthalpy change is sum of the enthalphy change in each step

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16
Q

Relationship between boiling point and solubility.

A

higher melting point = lower solubility

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17
Q

Cis E isomer vs Trans Z isomer

A

Cis e isomer is more soluble
Cis e has lower melting points

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18
Q

Describe the solubility of strong electrolytes in water.

A

soluble

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19
Q

Describe the solubility of weak electrolytes in water.

A

often not soluble

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20
Q

Describe the solubility of non electrolytes in water.

A

little to no solubility.

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21
Q

What is dissolution?

A

The process by which solid solute enters into a solution in the presence of a solvent.

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22
Q

List the basis of dissolution.

A

diffusion layer model
noyes-whitney relationship
hixson-crowell cube-root relationship

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23
Q

What is the diffusion layer model?

A

Concentration gradient between concentration of the drug in the diffusion layer (Cs) and concentration of the drug in the bulk medium (Cb)

(Cs-Cb)

24
Q

Describe the noyes-whitney relationship.

A

Amount of drug dissolved from solid particles in a function of time (Quantitative Analysis)

25
Describe the Hixson-crowell cube-root relationship.
The decrease in the size of particles changes the effective area.
26
Name of apparatus 1.
rotating basket
27
Assemblt of apparatus 1.
cylindrical, stainless steel basket shaft assembly
28
Use of apparatus 1.
capsules suppositories tablets with low density/dissolve very slowly
29
Name of apparatus 2
paddle
30
assembly of apparatus 2
paddle and shaft assembly
31
use of apparatus 2
formulations that sink but does not touch the bottom
32
List the factors affecting drug dissolution.
Physicochemical properties of the drug formulation factors physiologic factors
33
What are the factors under physicochemical properties?
ionized and unionzed forms particle size crystalline state
34
Explain how ionized and unionized forms of drugs affect dissolution?
ionized form = more water soluble = faster dissolution
35
Unionized vs ionized: absorption
Unionized drug forms results in more efficient absorption
36
Explain how crystalline state of drugs affect dissolution.
weakly bound amorphous and metastable forms are dissolve faster
37
What increases rate of dissolution in solid dosage forms?
disintegration disaggregation
38
How does viscosity affect dissolution?
increased viscosity = dissolution rate decreases
39
How does change in crystalline structure affect dissolution?
Change in the crystalline structure of the drug particles in aged suspensions = dissolution rate decreases
40
What factor affects dissolution rate of semi solid forms?
type of base used
41
What is the normal GET?
15 mins to 2 hours
42
Explain the variation in GET.
fasted state - faster fed state - slower
43
List the formulation factors affecting dissolution.
solid dosage forms suspensions and emulsions semisolid dosage forms
44
List the physiologic affecting dissolution.
gastric emptying time intestinal transit time variability of pH
45
State the partition law
A solute will distribute itself between two immiscible solvents so that the ratio of its concentration in each solvent is equal to the ratio of its solubility in each one.
46
What is the partition coefficient?
Measure of a drug concentration in a nonpolar organic phase to that in a polar aqueous phase
47
What is the partition orientation of strong electrolytes?
completely dissociated in aqueous solutions.
48
What is the partition orientation of nonelectrolytes?
dissociates in both aqueous and organic solvents
49
What is the partition orientation of weak electrolytes?
orientation depends on pH of solution
50
How does increasing unsaturation affect solubility?
Increase solubility in polar solvent
51
Dissolution profile of a drug can be used in the formulation the drug for maximum [?]
bioavailability
52
[?] of a drug can be used in the formulation the drug for maximum bioavailability
dissolution profile
53
What is dieelectric properties?
ability to store charge.
54
pH of stomach
1-3 pH
55
pH of intestine
pH 5-7