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Questions and Answers
What is the outcome of particles in a deflocculated suspension?
What is the outcome of particles in a deflocculated suspension?
Why are pharmaceutical suspensions preferred over solid dosage forms?
Why are pharmaceutical suspensions preferred over solid dosage forms?
What characteristic does a fully flocculated system exhibit?
What characteristic does a fully flocculated system exhibit?
What is the main problem associated with deflocculated suspensions?
What is the main problem associated with deflocculated suspensions?
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Which of the following describes a key feature of a flocculated suspension?
Which of the following describes a key feature of a flocculated suspension?
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What is the effect of Stokes' law on particle behavior in a flocculated suspension?
What is the effect of Stokes' law on particle behavior in a flocculated suspension?
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When classifying suspensions, which factor is NOT considered?
When classifying suspensions, which factor is NOT considered?
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Which of the following statements describes the characteristics of a deflocculated suspension?
Which of the following statements describes the characteristics of a deflocculated suspension?
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What is the significance of particle surface area in the formulation of suspensions?
What is the significance of particle surface area in the formulation of suspensions?
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What is a defining characteristic of colloidal particles?
What is a defining characteristic of colloidal particles?
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Which of the following is an example of a lyophobic colloid?
Which of the following is an example of a lyophobic colloid?
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Why are lyophobic dispersions considered thermodynamically unstable?
Why are lyophobic dispersions considered thermodynamically unstable?
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What is meant by 'disperse phase' in a colloidal system?
What is meant by 'disperse phase' in a colloidal system?
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What distinguishes lyophilic colloids from lyophobic colloids?
What distinguishes lyophilic colloids from lyophobic colloids?
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Which of the following is true about the size of colloidal particles?
Which of the following is true about the size of colloidal particles?
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What does a colloidal system primarily use for drug delivery?
What does a colloidal system primarily use for drug delivery?
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Which of the following systems can be classified as colloids?
Which of the following systems can be classified as colloids?
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What defines a colloidal solution when water is the solvent?
What defines a colloidal solution when water is the solvent?
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Which of the following is an example of a liquid/liquid emulsion?
Which of the following is an example of a liquid/liquid emulsion?
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What is the primary kinetic property that prevents the destruction of colloidal systems?
What is the primary kinetic property that prevents the destruction of colloidal systems?
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According to Stokes' law, what factors affect the velocity of sedimentation for spherical particles?
According to Stokes' law, what factors affect the velocity of sedimentation for spherical particles?
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What is the formula used to calculate the velocity of sedimentation?
What is the formula used to calculate the velocity of sedimentation?
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Which option would likely increase the velocity of sedimentation for a particle?
Which option would likely increase the velocity of sedimentation for a particle?
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What happens to a colloidal system when aggregation occurs?
What happens to a colloidal system when aggregation occurs?
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How does Brownian motion influence colloidal systems?
How does Brownian motion influence colloidal systems?
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What is the primary advantage of using a narrow particle size range for suspended drugs?
What is the primary advantage of using a narrow particle size range for suspended drugs?
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Which thickening agent is NOT mentioned as a modifier for viscosity?
Which thickening agent is NOT mentioned as a modifier for viscosity?
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What characteristic of large particles, greater than 5 μm diameter, is NOT a concern during formulation?
What characteristic of large particles, greater than 5 μm diameter, is NOT a concern during formulation?
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What is the formula for calculating the sedimentation volume ratio?
What is the formula for calculating the sedimentation volume ratio?
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Which factor does NOT contribute to the issues related to flocculated systems?
Which factor does NOT contribute to the issues related to flocculated systems?
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Which of the following is an example of a potential irritation caused by large particles in formulations?
Which of the following is an example of a potential irritation caused by large particles in formulations?
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Which thickening agent is commonly used to control viscosity in suspensions?
Which thickening agent is commonly used to control viscosity in suspensions?
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What risk is associated with using particles greater than 25 μm in diameter?
What risk is associated with using particles greater than 25 μm in diameter?
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Study Notes
MPharm Programme - Colloids & Suspensions
- Colloids are large molecules or finely divided particles dispersed in a medium. They lie between true solutions and coarse suspensions.
- Colloidal particles are visible with an electron microscope but not through semi-permeable membranes.
- Their size ranges from 10⁻⁹ m to 10⁻⁶ m, with at least one dimension between 1 nm and 1 μm.
- All three dimensions are not always in the colloidal range (e.g., fibers).
- Distinguishing colloidal from non-colloidal systems can be challenging.
- Examples of colloidal systems include aerosols, cosmetics, paints, cement, rubber, and pharmaceuticals. These applications often use colloidal systems for drug delivery and nanotechnology applications.
Classification of Colloidal Particles
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Lyophobic colloids are solvent-hating (e.g., water-insoluble drugs, clays, oily phases, suspensions of microorganisms, blood, and metals).
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Lyophobic dispersions are not spontaneously formed in the medium.
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They are thermodynamically unstable and will separate (although some may remain suspended for extended periods).
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Size and high surface area contribute to the instability by affecting free energy (reducing surface area is favorable).
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Be aware that some water-insoluble drugs, like kaolin, are often classified as lyophobic but not 'water-hating'
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Lyophilic colloids are solvent-loving (e.g., surfactants, proteins, gums).
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These solutions (colloidal, not true) form spontaneously, making them thermodynamically stable.
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These are termed 'hydrophilic' when water is the solvent.
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Examples of lyophilic colloidal systems include foams, milk, and smoke (liquid in gas, liquid/liquid emulsion, solid in gas).
Properties of Colloids - Kinetic
- Kinetic properties relate to the motion of colloidal particles.
- Interactions between particles can lead to aggregation or coalescence (if liquid droplets) and destroy the colloidal system.
- Brownian motion describes random collisions between particles in a liquid (or gas) dispersion medium. This results in particles travelling in a zig-zag fashion.
- Stokes' Law describes the velocity of sedimentation (or creaming) for spherical particles falling through a liquid: V = 2r²g(σ-ρ)/9η, where:
- V = velocity of sedimentation/creaming
- r = radius of particle
- g = acceleration due to gravity
- σ = density of particle
- ρ = density of liquid
- η = dynamic viscosity of liquid
- Reducing sedimentation velocity involves reducing particle size, increasing the viscosity of the continuous phase, or decreasing the density difference between the phases
Diffusion
- Colloidal particles spontaneously diffuse from higher concentration regions to lower concentration regions.
- Fick's first law describes the rate of diffusion. dm/dt = -DA dC/dx where:
- dm/dt = mass of substance diffusing per unit time
- D = diffusion coefficient
- A = area across which diffusion occurs
- dC/dx = concentration gradient
Pharmaceutical Suspensions
- Suspensions are dispersions of insoluble drugs in a continuous liquid phase (aqueous or non-aqueous).
- Colloidal or slightly coarser particles are used, with gravity having a significant impact.
- The advantages of suspensions include overcoming difficulties in swallowing solid dosage forms and maintaining drug stability (e.g., preventing hydrolysis).
- Taste and high surface area are also inherent properties of suspensions.
- Common problems associated with suspensions include sedimentation, caking, flocculation, and particle growth (including recrystallization).
Types of Suspensions
- Classified by dispersion medium (aqueous or oily), formulation type (flocculated or deflocculated), and drug stability (ready-to-use or reconstituted powders).
- Common uses include oral, parenteral, topical, ocular, and x-ray contrast media formulations.
Formulation of Suspensions
- Practice involves avoiding aggregation/caking, adhesion of particles to vessel surfaces, and creating a flocculated system (loose assembly of particles).
- Ideal suspensions are partially, not fully, flocculated.
- Fully flocculated systems exhibit a clear supernatant, large sediment volumes, rapid sedimentation, and easy redispersal.
Electrical Properties of Colloids
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Most colloidal particles dispersed in water possess a surface charge due to ionisation or adsorption.
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This charge affects the distribution of ions in the medium. A layer of counterions, and then co-ions build up a double layer adjacent to the particles. Zeta potential reflects this charge build up.
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Zeta potential: a measure of the electrical potential at the shear plane.
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A value above ±30 mV usually indicates sufficient repulsion to prevent particle aggregation and ensure colloidal stability.
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Changes in zeta potential can be used to predict stability with the addition of surfactants and electrolytes.
Modification of zeta potential
- Zeta potential modification can impact suspension stability and is affected by various factors including the presence of ions like electrolytes and the presence of surfactants.
Quality Control of Suspensions
- Quality control aspects include physical appearance, particle size analysis, ease of redispersal, sedimentation volume ratio, zeta potential, rheology (shear thinning/thixotropy is favorable).
Other Important Concepts
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Size reduction: Coarse suspensions (>1 µm) requiring size reduction (e.g., to avoid grit, prevent issues with hypodermic needles, and improve drug release/bioavailability).
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Surfactants: Used for wetting (interfacial tension reduction), controlling flocculation through various mechanisms of charge and interactions.
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Electrolytes: Modification of zeta potential through modifying the charge on the particle.
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Thickening agents: Used (e.g., Acacia, starch, hydroxypropylcellulose, and carmellose sodium) to modify the viscosity of the suspension vehicle.
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Schultz-Hardy rule: The ability of an electrolyte to induce flocculation/aggregation depends on the valence of the ions. Trivalent > divalent > monovalent ions.
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Description
Test your knowledge on pharmaceutical suspensions, including their characteristics, advantages over solid dosage forms, and the behavior of particles in flocculated and deflocculated systems. This quiz covers key features of colloidal systems and their stability.