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The Medicine 2 - Sem 2 > Pre-formulation considerations > Flashcards

Pre-formulation considerations Flashcards

1
Q

Capsules are cheaper to manufacture than tablets. True or false?

A

false, tablets are cheaper

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2
Q

What is preformulation?

A

it is the process before formulating a drug where a drug candidate is turned into a drug product and the physiochemical properties are determined

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3
Q

What is needed during preformulation?

A

Large amounts of sample

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4
Q

How can the molecular or intrinsic properties of the inherent drug be modified?

A

can only be changed by modifying the structure

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5
Q

What are the molecular properties that can be modified by changing the chemical structure of the drug?

A

stability to oxidation, hydrolysis, solubility, hygroscopy, pKa partition coefficient

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6
Q

Macroscopic/bulk properties can’t be changed. True or false?

A

false, can be changed and change based on other excipients present

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7
Q

For the final drug to be given orally as a solid form, what solubility is preferred?

A

10mg/ml

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8
Q

What is hygroscopicity?

A

the tendency of a substance to attract water from its immediate environment by absorption or adsorption

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9
Q

Does water selectively bind to polar or non-polar regions of a solid surface?

A

polar, so the extent of absorption is related to the degree of polarity

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10
Q

Adsorption of water onto most crystalline solids causes the solid to dissolve. True or false?

A

False

Does not cause it to dissolve

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11
Q

Why doesn’t adsorption of water onto crystalline solids cause the solid to dissolve?

A

because only a few layers of water molecules adsorb onto the surface so the volume isn’t sufficient enough to allow dissolution

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12
Q

Salts have a greater tendency to absorb water than free acid or base. True or false?

A

True

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13
Q

How is water uptake is usually determined?

A

Measuring an uptake in mass – thermogravimetric analysis (TGA). Dynamic vapour sorption (DVS)

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14
Q

What is the enthalpy of fusion?

A

The change in enthalpy resulting from heating a given quantity of a substance to change its state from solid to liquid

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15
Q

Melting point doesn’t give any information about the purity of a drug. True or false?

A

False

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16
Q

What technique is used to measure melting point and enthalpy of fusion?

A

differential scanning calorimetry

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17
Q

Particle size and surface area do not affect dissolution rates. True or false?

A

False

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18
Q

A scanning electron microscope is used to determine particle size and shape, true or false?

A

False

A light microscope

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19
Q

It’s easy to determine particle size when the particle is spherical. True or false?

A

True

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20
Q

Particles with a diameter of 50 or less have good flow properties, true or false?

A

False

Poor flow

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21
Q

Why is it important for powder to have good flow properties?

A

to ensure blend uniformity and optimal filling of tablet presses or capsule filling machines

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22
Q

In preformulation testing, which two measures are used to determine powder flow?

A

Carr index & angle of repose

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23
Q

The higher the angle of repose, the better the powder flow. True or false?

A

False

high angle of repose is bad, and a low angle of repose is good

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24
Q

Powders with an angle of repose higher than ? degrees have unsatisfactory flow properties

A

45

25
Q

Powders with an angle of repose close to ? degrees have excellent powder flow properties

A

25

26
Q

What are bulk density and tapped density used to measure?

A

compaction or compressibility (Carr index)

27
Q

How is bulk density measured?

A

adding a known mass of powder to a graduated cylinder. The density is calculated as mass/volume

28
Q

How is tapped density measured?

A

mechanically tapping the graduated cylinder to see whether further volume change is observed

29
Q

Which is better for manufacturing, a powder that is compressible or non-compressible?

A

non-compressible (ie low Carr index, higher bulk density)

30
Q

Compaction is the result of ? and ?

A

Compression and cohesion

31
Q

Compaction of drug powders is usually good, true or false?

A

false – usually poor so excipients are added which have good compaction properties

32
Q

As amorphous materials have no lattice energy, they are unstable and overtime they will convert to a crystalline form. True or false?

A

true

33
Q

Amorphous materials exhibit worse solubility and slower dissolution than crystalline equivalents. True or false?

A

False

Better absolute solubility and faster dissolution rates

34
Q

Converting a poorly soluble compound into an amorphous material will improve its bioavailability. True or false?

A

True

35
Q

What is meant by polymorphism?

A

when a compound exists in at least two different molecular arrangements in the solid state

36
Q

The most stable polymorph has the highest melting point. True or false?

A

True

37
Q
  1. The most stable polymorph exists in a thermodynamic position of equilibrium and all other forms won’t convert to it overtime. True or false?
A

False

They will convert to it

38
Q

What is the use of X-ray powder diffraction in pre-formulation?

A

provides structural data to identify polymorphisms

39
Q

Differential scanning calorimetry differentiates polymorphs based on what?

A

Melting points & enthalpy of fuision

40
Q

All polymorphs have the same physiochemical properties. True or false?

A

False

Different physiochemical properties

41
Q

The most stable polymorph always has the best bioavailability. True or false?

A

False

May have the worst processing ability or bioavailability

42
Q

Why will an anhydrous polymorph of a drug dissolve more quickly than a trihydrous form?

A

Because the anhydrous is not associated with water so dissolves more quickly but as the trihydrous is already associated with water, there is less of an energy change and so will have a slower dissolution rate

43
Q

Amorphous compounds have a higher solubility than crystalline compounds. True or false?

A

True

44
Q

Which factors determine which API is chosen for formulation and in which dosage form?

A

solubility, salt formation, rheology, wettability

45
Q

How is solubility analysed in pre-formulation?

A

Rotating OR disc methods are used

drug is packed into a non-disintegrating disc, only one face of the disc is exposed to the dissolution medium, disc is either held in place or rotated, samples of dissolution medium are taken at given ties, SA remains constant, under these conditions, the amount of drug dissolved per unit time and unit surface area can be determined – providing the intrinsic dissolution rate

46
Q

Esterification of a drug will increase its solubility. True or false?

A

False

Reduce solubility as its non-polar

47
Q

Degree of ionisation for most polar compounds is not linked to solubility. True or false?

A

False

48
Q

A large Ka (small pKa) implies a high or low solubility?

A

High

Molecule is hydrophillic

49
Q

If the pKa is low ie less than 5 the salt is unlikely to be stable at physiological pH. True or false?

A

Truw

50
Q

What is wettability?

A

It describes the ability of a liquid to maintain contact with a solid surface. It is defined by measuring the contact angle of a drop of fluid on its surface

51
Q

Strong cohesive forces within the liquid allow for good wettability. True or false?

A

False

poor wettability

52
Q

Strong adhesive forces between a liquid and solid are good for wettability. True or false?

A

True

53
Q

What does a contact angle of less than 90 degrees show in terms of wettability?

A

Wetting is very favourable

54
Q

What can be used to increase wettability?

A

Surfactants

55
Q

What is rheology?

A

The study of flow matter

56
Q

Most pharmaceutical fluids are Newtonian. True or false?

A

False

Non-newtonian

57
Q

You are asked to quantify the cohesiveness of the powdered material. Give one method to do this and which characteristics do you need to measure for this method.

A

Cohesiveness of a powder is best quantified by the Hausner Factor or Carr’s index, and for both you would need to measure the bulk density and the tapped density of the powder.

58
Q

Give the difference between plastic and pseudoplastic flow

A

Both plastic and pseudoplastic flow are shear thinning, but plastic flow is newtonian flow with a yield stress, pseudoplastic is never newtonian

The Medicine 2 - Sem 2 (14 decks)

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