[MIDTERMS] PMQA LEC - Suspensions Flashcards

1
Q

A disperse system in which solid, vehicle-insoluble particles (internal phase) are uniformly suspended by mechanical agitation and formulation design throughout the liquid vehicle (external phase).

A

Suspensions

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2
Q

Two (2) Phases of Suspensions

A
  1. Continuous Phase
  2. Discontinuous Phase
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3
Q

It is also called the External Phase or Dispersion System

A

Continuous Phase

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4
Q

It is also called the Internal Phase or Dispersed Phase

A

Discontinuous Phase

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5
Q

Purposes of Suspensions

A
  • Sustaining Effect
  • Stability
  • Taste
  • Basic Solubility
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6
Q

For sustained release preparation, the suspension necessitates drug dissolution prior to absorption.

A

Sustaining Effect

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7
Q

Drug degradation in suspension or solid dosage forms occurs much more slowly than degradation in solution form.

A

Stability

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8
Q

A drug with unpleasant taste can be converted into an insoluble form and then prepared as suspension.

A

Taste

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9
Q

When suitable solvents are not available. For example, ophthalmic suspensions provide an alternative to ophthalmic solutions.

A

Basic Solubility

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10
Q

(T/F): After gentle shaking, the medicament stays in suspension long enough for the dose to be accurately measured.

A

T

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11
Q

(T/F): Particles are small and relatively uniform in size.

A

T

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12
Q

Three (3) Steps in Ensuring Formulation of Suspension

A
  1. Control Particle Size
  2. Use of Thickeners
  3. Use of Wetting Agent
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13
Q

Diffusible Solids (Dispersible Solids)

A

Insoluble Medicament

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14
Q

Example/s of Diffusible Solids

A

• Light Kaolin
• Magnesium Trisilicate
• Light Magnesium Carbonate
• Bismuth Carbonate

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15
Q

Not Easily Wetted

A

Indiffusible Solids

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16
Q

Example/s of Indiffusible Solids

A

(Internal Use)
• Aspirin
• Chalk
• Phenobarbitone
• Sulphadimine

(External Use)
• Calamine
• Hydrocortisone
• Sulphur
• Zinc Oxide

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17
Q

Four (4) Problems Encountered when Formulating Insoluble Solid to Suspension

A
  1. Sedimentation
  2. Flocculation
  3. Wetting Agent
  4. Preservatives Used
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18
Q

(T/F): The greater the density, the greater the descent.

A

T

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19
Q

Aggregation will determine the type of suspension.

A

Flocculation

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20
Q

To prevent air trapping.

A

Wetting Agent

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21
Q

Preservatives Used

A

• Chloroform Water
• Benzoic Acid
• Hydroxybenzoates

22
Q

Two (2) Types of Suspension System

A
  1. Flocculated System
  2. Deflocculated System
23
Q

It is also known as Coagulated or Colloidally Unstable System

A

Flocculated System

24
Q

It is also known as Peptized or Colloidally Stable System

A

Deflocculated System

25
Particles appear as floccules like tufts of wool with loose fibrous structure. When the system settles two distinct layers forms clear particle free supernatant liquid and sediment. Appears to be coarse, because of the floccules formed. Exhibits minimum serious separation, depending on the solid content and the degree of flocculation that took place.
Flocculated System
26
Particles settles as the dense sediment, which becomes more compact after given time interval.
Deflocculated System
27
Two (2) Methods of Preparation of Suspensions
1. Discipitation Method 2. Precipitation Method
28
This process is done by dispersing the finely divided powders in an appropriate liquid vehicle. The use of surfactants is desirable to ensure uniform wetting of the hydrophobic surfaces.
Discipitation Method
29
This is performed by effecting precipitation in the liquid vehicle.
Precipitation Method
30
Three (3) Methods of Precipitation Methods
1. Organic Solvent Precipitation 2. Precipitation Effected by Changing the pH 3. By Double Decomposition Method
31
Water insoluble drugs are precipitated by dissolving them in the water miscible organic solvent. Then adding the organic phase to purified water under standard conditions.
Organic Solvent Precipitation
32
This is applicable to those drugs in which its solubility is dependent on pH value.
Precipitation Effected by Changing the pH
33
Where simple chemistry is involved. Example is the preparation of White Lotion USP (made by interacting zinc sulfate with sulfurated potash solution to form zinc polysulfide).
By Double Decomposition Method
34
Polyoxyethylene Esters of Mixed Fatty Acid Esters of Sorbitol Anhydride
Tweens
35
Mixed Fatty Acid Esters of Sorbitol Anhydride
Spans
36
Higher Molecular Weight Polyethylene Glycols
Carbowax
37
It forms mechanical sheath or barrier around particles.
Protective Colloids
38
Example/s of Protective Colloids
• Silica Gel • Aluminum Hydroxide
39
Suspending Agents
1. Hydrophilic Colloids (Hydrocolloids) 2. Clay Group 3. Other Agents
40
Increase the viscosity of water by binding water molecules, limiting their mobility or fluidity. It is mostly anionic, except methylcellulose (neutral) and chitosan (cationic).
Hydrophilic Colloids (Hydrocolloids)
41
These are incompatible with quarternary antibacterial agents and other positively charged ions.
Anionic Hydrocolloids
42
It is incompatible with negatively charged drugs and excipients.
Chitosan
43
It is usually 35% dispersion in water (mucilage). Its viscosity is greatest between pH 5 and 9.
Acacia
44
It is usually used as 6% dispersion in water (mucilage). The viscosity is greatest at pH 5.
Tragacanth
45
A polymer that is nonionic and stable to heat and light.
Methylcellulose
46
Example/s of Clay Group
• Bentonite • Veegum
47
They are strongly hydrated and exhibit thixotrophy.
Clay Group
48
Certain Kinds of Pharmaceutical Suspensions
1. Gels 2. Magmas and Milks 3. Lotions 4. Mixtures
49
Suspending Agent - 0.5% to 1.0% Gelling Agent - 0.5% to 2.0%
Carbomer
50
It requires high speed equipment and which is suitable for internal and external use.
Carbomer