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 dropsConcentrated 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:
Coated tablets
Compressed tablets
Capsules
Suspensions
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