Pharmaceutical Suspensions

🧪 Disperse Systems Overview

Disperse systems consist of two components:

  • Dispersed phase (internal phase): could be molecules, particles, or droplets.

  • Continuous phase (external phase): the medium in which the dispersed phase is distributed.

🔬 Classification of Disperse Systems

Type

Particle Size

Examples

Solutions

< 1 nm

Salt in water

Colloidal dispersions

0.001 – 0.5 µm

Surfactant micelles

Suspensions

0.1 – 10 µm

Pharmaceutical suspensions

Coarse dispersions

10 – 50 µm

Emulsions, aerosols


💊 Pharmaceutical Suspensions

Suspensions are heterogeneous mixtures where insoluble particles are dispersed in a liquid.

🔄 Differences: Solutions vs Suspensions

Feature

Solution

Suspension

Uniformity

Homogeneous

Heterogeneous

Solubility

Solute is dissolved

Particles are insoluble

Appearance

Clear

Cloudy, may settle over time

Example

Sugar in water

Chalk in water


📦 Classification of Suspensions

1. By Route of Administration

  • Oral: Paediatric formulations, antacids (e.g. amoxicillin)

  • Topical: Calamine lotion

  • Parenteral: Procaine penicillin G, vaccines (must be sterile)

  • Inhalation: Asthma treatments (fine particles)

  • Ophthalmic: Sterile, small particle size

2. By Solid Concentration

  • Dilute suspensions (2–10% w/w)
    E.g. Prednisolone acetate eye drops

  • Concentrated suspensions (up to 50% w/w)
    E.g. Zinc oxide topical formulations

3. By Particle Size

Type

Size

Colloidal

< 1 µm

Nanosuspensions

Nano range

Coarse suspensions

> 1 µm


📈 Bioavailability (Absorption Rate) Order

From slowest to fastest:

  1. Coated tablets

  2. Compressed tablets

  3. Capsules

  4. Suspensions

  5. Solutions


💡 Pharmaceutical Uses of Suspensions

  • To deliver poorly soluble drugs (e.g. Prednisolone acetate)

  • To enhance stability (e.g. Oxytetracycline)

  • To mask taste (e.g. Chloramphenicol palmitate)

  • For topical use (e.g. Calamine lotion)

  • In injections/vaccines (e.g. Cholera vaccine)

  • In X-ray contrast agents (e.g. Barium sulphate)


Pros and Cons of Suspensions

Advantages

  • Useful for insoluble/stable drugs

  • Palatable for paediatric use

  • Easy to swallow

  • Higher drug loading

  • Allow modified/sustained drug release

Disadvantages

  • Dosing accuracy may be poor

  • Requires shaking before use

  • Bulky, risk of breakage/leakage

  • Storage (may need refrigeration)


Properties of an Ideal Suspension

  • Slow sedimentation

  • Easily redispersible after settling

  • Pourable and smooth

  • Uniform particle size to avoid grittiness

  • Stable appearance


🧱 Components of Suspensions

Types of Dispersed Solids

a) Diffusible powders
  • Light and evenly suspended

  • No suspending agent required

  • Examples: Light Kaolin BP, Magnesium Trisilicate BP

b) Indiffusible powders
  • Heavy, settle quickly

  • Need a suspending agent

  • Examples: Calamine BP, Zinc Oxide BP, Aspirin BP


Suspension Challenges

1. Sedimentation

  • Particles settle due to gravity

  • Controlled by suspending agents and viscosity control

2. Caking

  • Formation of a non-redispersible layer

  • Avoided by creating flocculated systems


🧪 Suspending Agents

Purpose: Maintain particles in suspension by:

  • Preventing aggregation

  • Increasing viscosity

Examples:

  • Natural gums (acacia)

  • Cellulose derivatives (HPMC)

  • Clays (bentonite)

Note: Must balance between:

  • Sedimentation rate

  • Pourability

  • Drug release rate


Particle Size Considerations

  • < 5 µm: Avoid grittiness

  • > 25 µm: May block needles

  • Too small: Risk of hard cake formation


🍭 Other Formulation Components

  • Flavours: Improve palatability

  • Preservatives: Prevent microbial growth (e.g. Benzoic acid)

  • Colours

  • Sweeteners: e.g. Sucrose, Glycerol

  • Packaging: Amber bottles (oral), fluted (topical/eye/ear)


🏷 Labelling & Storage

  • Label: "Shake well before use", "For external use only", etc.

  • Storage: Refrigeration may be required

  • Transport: Avoid breakage/leakage


📊 Quality Control

  • Content uniformity (85–115% of label claim)

  • Preservative efficacy

  • Shelf life: ≥ 90% active after expiry

  • Appearance, pH, viscosity