Preformulation - The Solid State Flashcards

1
Q

Describe the solid state

A
  • Physical state of matter
  • Rigid structure
  • Resistance to changes in shape and volume
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2
Q

What is the importance of the solid state?

A
  • Most medicines are solids
  • Solid properties dictate physical characteristics e.g. solubility, mechanical properties - determines drug release profile
  • Solid properties influence decisions and control over manufacturing processes
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3
Q

Describe the structure of crystalline solids

A
  • Atoms/molecules are arranged in a pattern that repeats periodically in 3 dimensions to an infinite extent
  • Defined geometric shape with flat faces
  • Sharp melting point
  • Thermodynamically stable
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4
Q

Describe the structure of salts and cocrystals.

A

Contain two or more components in the same lattice

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5
Q

How can we differentiate between salts and cocrystals?

A
  • Salts are composed of ions and cocrystals of neutral molecules
  • If the proton resides on the base (proton transfer has occurred) and the crystalline acid-base complex is a salt
  • If proton transfer has not occurred then it is a cocrystal
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6
Q

How are cocrystals formed?

A
  • By hydrogen bonds between drug and another molecule (conformer)
  • Components are not ionised in the crystal
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7
Q

Why use cocrystals?

A
  • Improve drug physiochemical properties
  • Are patentable
  • Can be made for non-ionisable drugs
  • Modulate drug solubility
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8
Q

Why use salts?

A
  • Improved physiochemical properties are possible
  • Salts are more soluble than the free acid or free base
  • Melting point of higher
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9
Q

What are solvates/hydrates

A

Molecular adducts that incorporate solvents molecules in their crystal lattices
solvent is water = hydrates
solvent is other solvents = solvates

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10
Q

why do organic compounds frequently form hydrates in presence of water?

A

Due to small molecular size of water
The multidirectional hydrogen bonding capability of water

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11
Q

What is polymorphism?

A

Crystalline forms with the same chemical composition but different internal structures.

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12
Q

Why are polymorphism and multiple crystal forms important?

A
  • Different solids show different physical, chemical and mechanical properties
  • Development will require identification of the most stable form; most stable=most desirable
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13
Q

How are polymorphs analysed?

A
  • x ray diffraction: crystal structure
  • thermal behaviour: melting point and heat fusion
  • thermodynamic stability: free energy, solubility (the more soluble polymorph = the less stable)
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14
Q

Describe amorphous solids

A
  • Amorphous solid does not posses the long-range order characteristic of a crystal
  • Solubility is improved by disarranging its crystalline lattice to produce a higher energy state of amorphous form
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15
Q

State the properties of amorphous solids.

A
  • No long range order (have short range order).
  • Exhibit a “halo” in X-ray powder diffraction patterns (compared to
    crystalline peaks).
  • Have a glass transition temperature (Tg).
  • Less physically and chemically
    stable than crystalline materials.
  • Faster dissolution than crystalline
    materials
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16
Q

What is glass transition?

A

Physical change from a glassy state to a rubbery state upon heating

17
Q

How can glass transition temp be determined?

A

Using differential scanning calorimetry.

18
Q

What is a key problem of amorphous drugs?

A
  • physical instability leads to crystallisation due to the high free energy of the amorphous state relative to the crystalline state.
19
Q

Describe solid form transformations?

A
  • One solid form spontaneously converts to another when thermodynamically favourable
  • Depends on environmental conditions
  • Generally solubility decreases as stability increases
20
Q

Why is Gibbs free energy used?

A
  • Used to determine whether a reaction is favoured or disfavoured.
  • If ΔG < 0, then products are favoured at equilibrium.
  • If ΔG > 0  “thermodynamically disfavoured”.
21
Q

State the Gibbs free energy equation.

A

△G = △ H - T △S