L38, 39 Colloids Flashcards

(95 cards)

1
Q

38

What are colloidal dispersions?

A

Colloidal dispersions are biphasic systems where one phase (dispersed phase) is distributed in another (continuous/dispersing phase), with particle sizes between 1–1000 nm.

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2
Q

38

What are the three types of dispersions in terms of particle size?

A

Molecular dispersions: <1 nm

Colloidal dispersions: 1–1000 nm

Coarse dispersions: 10–50 µm

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3
Q

38

What are the two classification types of colloids based on physical state and affinity?

A

Physical state: Sols (low viscosity), Gels (high viscosity)

Affinity: Lyophilic (high affinity for the dispersion medium), Lyophobic (low affinity)

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4
Q

38

What do hydrosols and hydrogels refer to?

A

Dispersions where the continuous phase is water.

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5
Q

38

What characterises a lyophobic colloid?

A

Low affinity for the dispersion medium

Poor solvation

Thermodynamically unstable

Requires energy to form

Decrease in entropy and increase in free energy

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6
Q

38

How are lyophobic colloids typically prepared?

A

Mechanical dispersion: Physically breaking down larger particles into fine colloids.

Controlled aggregation: Controlling particle aggregation by altering conditions.

Chemical reactions: Changing the chemical structure of materials (oxidation, reduction) to form colloids.

Solvent change: Switching from a good solvent to a bad solvent to induce colloidal formation.Mechanical dispersion

Controlled aggregation

Chemical reactions (oxidation, reduction, hydrolysis)

Solvent change (good to bad solvent)

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7
Q

38

Give an example of a lyophobic colloid used pharmaceutically.

A

Hydrophobic colloidal anhydrous silica BP, used in emulsions, gels, and semi-solid preparations.

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8
Q

38

What defines a lyophilic colloid?

A

High affinity for the dispersion medium

Forms spontaneously

Thermodynamically stable

Increase in entropy and decrease in free energy

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9
Q

38

Give an example of a lyophilic colloid.

A

Bentonite, used in Calamine Lotion BP and clay masks.

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10
Q

38

What are association colloids?

A

Colloids formed by self-association of amphiphilic molecules (e.g., surfactants, phospholipids) into structures like micelles or liposomes.

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11
Q

38

What is a micelle?

A

A spherical structure formed by surfactants in solution, where hydrophobic tails face inwards and hydrophilic heads face the solvent.

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12
Q

38

What is the Critical Micelle Concentration (CMC)?

A

The minimum concentration of surfactant above which micelles form in solution.

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13
Q

38

What drives micelle formation?

A

Entropy – release of ordered water molecules around hydrophobic tails upon micelle formation increases system entropy.

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14
Q

38

Do all amphiphilic molecules form micelles?

A

No, only some amphiphiles have the necessary structure and conditions to form micelles.

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15
Q

38

What is the Krafft point?

A

The temperature above which the solubility of a surfactant increases sharply, allowing micelle formation.

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16
Q

38

What is the cloud point?

A

The temperature above which a surfactant’s solubility decreases, leading to precipitation due to dehydration of polar heads. This is a reversible process.

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17
Q

38

What are the pharmaceutical applications of colloidal dispersions?

A

Drug Delivery:

  • Sustained release: Gradual drug release over time, reducing dosing frequency.
  • Targeted delivery: Delivers drugs specifically to desired tissues, reducing side effects.

Improved Solubility:

  • Colloids like micelles and nanosuspensions enhance the solubility of poorly water-soluble drugs, improving absorption.

Controlled Release Formulations:

  • Long-term, controlled drug release for stable therapeutic effects and reduced side effects.

Topical and Transdermal Products:

  • Liposomes and nanoemulsions improve drug penetration through the skin, allowing controlled release for local or systemic effects.

Parenteral Formulations:

  • Nanosuspensions for injectable formulations improve bioavailability and stability of poorly soluble drugs. Can provide long-acting injections.
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18
Q

38

What is the difference between thermodynamic and kinetic stability in colloids?

A

Thermodynamic stability: Whether a system forms spontaneously and remains dispersed (true for lyophilic)

Kinetic stability: Resistance to aggregation or sedimentation over time, even if not thermodynamically stable (seen in lyophobic colloids)

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19
Q

38

What types of molecular interactions stabilise lyophilic colloids?

A

Hydrogen bonding: Between colloid and solvent, enhancing dispersion.

van der Waals forces: Gentle attractive interactions supporting solubility.

Solvation layers: Solvent molecules form a stabilising barrier around particles, preventing aggregation.

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20
Q

38

What are the methods used to identify colloidal systems?

A

Light scattering (Tyndall effect)

Ultracentrifugation

Viscosity measurements

Electron microscopy

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21
Q

38

Why is entropy important in colloidal stability and micelle formation?

A

Increased entropy favours spontaneous formation of micelles and stability in lyophilic colloids due to disordering of structured water molecules.

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22
Q

38

What is the Tyndall effect?

A

The scattering of light by colloidal particles, making the path of light visible in colloidal systems.

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23
Q

38

What happens to a surfactant solution below the Krafft point?

A

The surfactant is poorly soluble and cannot form micelles; the solution may remain cloudy or precipitate.

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24
Q

38

How does temperature influence micelle formation?

A

Below Krafft point: No micelles form

Above Krafft point: Micelles form if concentration exceeds CMC

Above cloud point (for non-ionic surfactants): Micelles precipitate out due to dehydration

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25
# 38 What are some examples of lyophilic colloidal excipients?
Gelatin Acacia Tragacanth Methylcellulose Used to stabilise emulsions or suspensions, or increase viscosity.
26
# 38 What makes amphiphilic molecules suitable for micelle formation?
A balance between hydrophilic head and hydrophobic tail Chain length, ionic nature, and temperature all influence this ability
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# 38 What is the difference between a sol and a gel?
Sol: A colloidal dispersion with fluid-like consistency Gel: A semi-solid colloidal system where the dispersed phase forms a 3D network throughout the dispersion medium
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# 38 Why are lyophobic colloids more difficult to prepare than lyophilic colloids?
They require special preparation methods due to low affinity for the medium and are thermodynamically unstable.
29
# 38 What are common methods for preparing lyophobic colloids via chemical reactions?
Oxidation (e.g. forming sulphur sols) Reduction (e.g. gold sols from chloroauric acid) Hydrolysis (e.g. ferric hydroxide sols)
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# 38 What is the role of surfactants in pharmaceutical colloids?
Stabilise emulsions Enhance solubility Assist in drug delivery Reduce interfacial tension between phases
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# 38 How are association colloids classified?
Micelles (spherical, above CMC) Reverse micelles (in non-polar solvents) Vesicles (bilayer structure, e.g. liposomes)
32
# 38 What are vesicles and how do they differ from micelles?
Vesicles are bilayered structures that enclose an aqueous core Micelles have a monolayer structure with no inner core
33
# 38 What factors affect the CMC of a surfactant?
Temperature Presence of electrolytes Nature of hydrophilic and hydrophobic groups Molecular structure
34
# 38 How does the presence of electrolytes influence colloidal stability?
Electrolytes can reduce repulsion between particles, leading to aggregation or flocculation, especially in lyophobic colloids.
35
# 38 What happens when a surfactant is heated above its cloud point?
The solution becomes turbid or separates due to loss of hydration of the hydrophilic heads—reversible upon cooling.
36
# 38 Which of the following best explains why lyophobic colloids require stabilisers for long-term use in pharmaceutical formulations? A. They have a strong affinity for the dispersion medium B. They exhibit high thermodynamic stability C. They lack an electrical double layer, which prevents micelle formation D. They tend to aggregate due to poor solvation and weak intermolecular repulsion
✅ Correct Answer: D Explanation: Lyophobic colloids are not well solvated, making them prone to aggregation unless stabilised.
37
# 38 Which condition is most likely to increase the CMC of a surfactant? A. Adding a small amount of NaCl B. Replacing a methyl group in the tail with an ethyl group C. Increasing temperature beyond the Krafft point for an ionic surfactant D. Shortening the hydrophobic tail
✅ Correct Answer: D Explanation: A shorter hydrophobic tail decreases hydrophobic interactions, increasing the CMC.
38
# 38 Which of the following best differentiates association colloids from lyophilic colloids? A. Association colloids are always thermodynamically stable B. Lyophilic colloids only form above the cloud point C. Association colloids consist of amphiphilic molecules that form micelles above CMC D. Lyophilic colloids consist of particles larger than 1 μm
✅ Correct Answer: C Explanation: Association colloids form micelles from amphiphilic molecules, unlike lyophilic colloids that are often polymer-based and stable in solvents.
39
# 38 Which of the following scenarios would most likely prevent micelle formation in an aqueous surfactant solution? A. Temperature below the Krafft point B. Concentration slightly above the CMC C. pH within optimal range for head group ionisation D. Addition of a co-surfactant
✅ Correct Answer: A Explanation: Below the Krafft point, surfactant solubility is too low for micelle formation.
40
# 38 A student observes a bluish beam of light passing through a sample. What conclusion can be drawn about the nature of the sample? A. It is a true solution B. It contains molecules smaller than 1 nm C. It is a colloidal dispersion exhibiting the Tyndall effect D. It has sedimented particles
✅ Correct Answer: C Explanation: The Tyndall effect is characteristic of colloidal particles which scatter visible light.
41
# 38 What is the most likely result of increasing electrolyte concentration in a lyophobic colloidal system? A. Decreased particle size due to flocculation B. Increased repulsion between particles C. Neutralisation of surface charge leading to aggregation D. Enhanced solvation and increased viscosity
✅ Correct Answer: C Explanation: Electrolytes compress the electrical double layer, reducing repulsion and increasing aggregation.
42
# 38 Which property of a surfactant is most crucial for forming a stable micelle in aqueous solution? A. Short alkyl chains B. Balanced hydrophilic-lipophilic ratio C. Low melting point D. High cloud point
✅ Correct Answer: B Explanation: A surfactant must have the correct balance between hydrophilic and lipophilic portions to form micelles.
43
# 38 Which of the following best describes the relationship between the Krafft point and micelle formation? A. Micelles form below the Krafft point but only in presence of electrolytes B. The Krafft point represents the concentration at which micelles form C. Micelles can only form above the Krafft point if CMC is also exceeded D. The Krafft point is the temperature at which micelles begin to precipitate
✅ Correct Answer: C Explanation: Both adequate temperature (above Krafft point) and concentration (above CMC) are needed for micellisation.
44
# 38 A parenteral formulation contains a lyophobic colloid stabilised with sodium citrate. Which event is most likely if a calcium salt is added to this formulation? A. Enhanced drug solubility due to ion pairing B. Improved electrostatic repulsion between particles C. Precipitation due to charge neutralisation D. No change, as calcium has low ionic strength
✅ Correct Answer: C Explanation: Calcium ions may neutralise negative charges (e.g. citrate-stabilised particles), leading to flocculation or precipitation.
45
# 38 A patient is administered an intravenous lipid emulsion. What feature of this colloidal system prevents embolism formation? A. Low density B. High surface tension C. Steric stabilisation by phospholipids D. Complete water miscibility
✅ Correct Answer: C Explanation: Phospholipids provide steric stabilisation to keep lipid droplets dispersed and prevent coalescence.
46
# 38 A surfactant has a CMC of 2.5 mM and the solution volume is 100 mL. How many micelles are likely to form when the total surfactant added is 10 mM? (Assume each micelle contains 100 molecules) A. 7.5 × 10²⁰ B. 7.5 × 10¹⁹ C. 2.5 × 10¹⁹ D. 5.0 × 10²⁰
✅ Correct Answer: B Explanation: Surfactant available for micelles = 10 mM – 2.5 mM = 7.5 mM = 7.5 × 10⁻³ mol/L In 0.1 L: 7.5 × 10⁻³ × 0.1 = 7.5 × 10⁻⁴ mol Molecules = 7.5 × 10⁻⁴ mol × 6.022 × 10²³ ≈ 4.52 × 10²⁰ molecules Micelles = 4.52 × 10²⁰ ÷ 100 ≈ 4.5 × 10¹⁸ → Closest: B
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# 38 A 1% w/v solution of surfactant X forms micelles at 25°C. Given molar mass = 300 g/mol and CMC = 5 mM, what percentage of surfactant is in micelles? A. 20% B. 40% C. 60% D. 80%
✅ Correct Answer: D Explanation: 1% w/v = 1 g/100 mL = 10 g/L Moles = 10 ÷ 300 = 0.0333 mol = 33.3 mM Surfactant above CMC = 33.3 – 5 = 28.3 mM % in micelles = 28.3 ÷ 33.3 × 100 ≈ 85% → Closest: D
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# 38 A suspension shows rapid sedimentation despite small particle size. Which parameter most likely explains this? A. High zeta potential B. Flocculated structure C. High viscosity D. Presence of surfactant at CMC
✅ Correct Answer: B Explanation: Flocculation causes larger effective particle masses to settle rapidly, even if primary particles are small.
49
# 38 Which of the following distinguishes cloud point from Krafft point in non-ionic surfactant systems? A. Cloud point refers to turbidity from micelle breakdown B. Krafft point only applies to non-ionic surfactants C. Cloud point marks phase separation; Krafft point marks solubility threshold D. Krafft point is always lower than cloud point
✅ Correct Answer: C Explanation: Cloud point is where micelle solution turns turbid (non-ionic), Krafft is minimum temp needed for ionic surfactants to form micelles.
50
# 38 What is the most likely mechanism of drug loading in micelle-based drug delivery systems? A. Drug binds to polar heads of surfactant B. Drug is trapped within aqueous core of vesicle C. Drug is solubilised within hydrophobic core of micelles D. Drug precipitates inside the shell of micelles
✅ Correct Answer: C Explanation: Micelles can encapsulate hydrophobic drugs in their core, improving solubility.
51
# 39 What size range defines colloidal particles?
Less than 1 μm in diameter.
52
# 39 What does size distribution in colloids refer to?
The range of different particle sizes within a sample; it is not always uniform.
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# 39 How do lyophilic colloids behave in a good solvent?
They maximise interaction with the dispersing phase, adopt an extended shape, surface tension contributes almost nil to free energy, and dispersion is spontaneous.
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# 39 How do lyophobic colloids behave in a bad solvent?
They minimise interactions with the dispersing phase, adopt a compact or spherical shape, surface tension contribution is high, and dispersion requires energy input.
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# 39 What is dialysis used for in colloids?
To separate colloidal particles from small molecules or ions using a semi-permeable membrane.
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# 39 What is Brownian motion?
The random movement of colloidal particles due to thermal agitation, observable up to 5 μm.
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# 39 What is sedimentation in colloids and how is it studied?
Downward motion under gravity; studied using ultracentrifugation (~10⁶ g).
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# 39 How does diffusion work in colloids?
Particles move from areas of high concentration to low concentration along a concentration gradient.
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# 39 How does viscosity vary in colloids?
Increases with solvation, particle shape (elongated > spherical), concentration, and molecular weight.
60
# 39 How are colloidal particles visualised?
Using an ultramicroscope (as bright spots on a dark background) or electron microscope (gives size and shape).
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# 39 What does light scattering in colloids help determine?
Particle size and shape via dynamic or static light scattering.
62
# 39 What is the Faraday-Tyndall effect?
Scattering of light by colloidal particles.
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# 39 How can colloidal particles acquire charge?
Ion adsorption, ion dissolution, ionisation of surface groups; charges may be permanent or pH-dependent.
64
# 39 What is zeta potential?
The effective surface charge of a particle in a colloid; influences stability, especially in hydrophobic colloids.
65
# 39 What is the Donnan membrane effect?
The influence of charged colloids on the diffusion of small ions across a membrane.
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# 39 What forces influence colloidal stability?
Electrostatic repulsion and steric attraction (linked to solvation).
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# 39 What is the DLVO theory?
It explains colloidal stability using total potential energy: VT = VR + VA Where Vr is repulsion (electrostatic) and Va is attraction (Van der Waals).
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# 39 What causes coagulation and flocculation in lyophobic colloids?
Coagulation at the primary minimum (strong forces), flocculation at the secondary minimum (weak forces); both influenced by electrolytes.
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# 39 How can lyophilic colloids be destabilised?
With organic solvents, low electrolyte concentrations, or high salting-out conditions.
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# 39 Name pharmaceutical uses of hydrophilic colloids.
Thickening agents, stabilisers (suspensions/emulsions), tablet binders, solubilising agents (micelles), drug carriers, and detoxifying agents (e.g. activated charcoal).
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# 39 What is Brownian motion in colloidal systems?
The random, erratic movement of colloidal particles caused by collisions with dispersion medium molecules.
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# 39 Why is Brownian motion important in colloidal dispersions?
It helps prevent sedimentation, maintaining particle dispersion and stability.
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# 39 What factors affect Brownian motion?
Particle size (smaller = more movement), viscosity (lower = more movement), and temperature (higher = more movement).
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# 39 What is the significance of sedimentation in colloidal dispersions?
Sedimentation determines how fast particles settle under gravity, affecting the stability of suspensions.
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# 39 What is Stokes’ Law in relation to colloids?
It calculates the sedimentation velocity of particles based on their radius, density difference, and the medium's viscosity.
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# 39 According to Stokes’ Law, which particles sediment faster?
Larger and denser particles in low-viscosity media.
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# 39 What is the Tyndall effect?
Light scattering by colloidal particles, making the dispersion appear turbid or cloudy.
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# 39 How is the Tyndall effect used in practice?
It helps distinguish colloidal dispersions from true solutions.
79
# 39 Give a clinical example where light scattering is important.
Turbidity monitoring in IV infusions to detect contamination or aggregation.
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# 39 How does osmotic pressure of colloids compare to that of true solutions?
It is significantly lower due to fewer dispersed particles.
81
# 39 Why is osmotic pressure important in formulating IV colloids?
It influences fluid movement and volume expansion in blood vessels.
82
# 39 Name three colloidal systems used as plasma expanders.
Gelatin, dextran, and hydroxyethyl starch.
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# 39 What role do colloids play in nanomedicine?
They serve as carriers for targeted drug delivery, e.g., liposomes or nanoparticles.
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# 39 How can colloidal drug carriers be targeted to specific tissues?
By modifying their surface with ligands that bind to specific receptors.
85
# 39 A colloidal system is showing high viscosity even at low concentration. What is the most likely explanation? A. The particles are spherical and non-solvated B. The particles are elongated and highly solvated C. The system has high zeta potential D. The system is undergoing Brownian motion
Elongated, solvated particles increase viscosity even at low concentrations.
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# 39 Which of the following would most likely destabilise a lyophobic colloid? A. Increase in zeta potential B. Addition of a polymeric stabiliser C. Addition of an electrolyte above the critical coagulation concentration D. Decrease in temperature
C – Electrolytes screen the repulsive forces, reducing zeta potential and promoting coagulation.
87
# 39 A colloid has a very low zeta potential (~ -5 mV). What does this suggest about its stability? A. Highly stable due to steric repulsion B. Highly unstable due to insufficient repulsive force C. Neutral due to equilibrium of forces D. Stable only under acidic conditions
B – Low zeta potential means particles can easily aggregate.
88
# 39 What distinguishes flocculation from coagulation in colloidal dispersions? A. Flocculation is reversible, coagulation is not B. Flocculation occurs at the primary minimum C. Coagulation involves electrostatic stabilisation D. Coagulation is reversible under shear
A – Flocculation involves weak interactions (secondary minimum), while coagulation is usually irreversible.
89
# 39 A colloidal particle has a radius of 50 nm and a density of 1.2 g/cm³. If the dispersion medium is water (density = 1.0 g/cm³), what force causes sedimentation under gravity? A. Zero, due to Brownian motion B. Buoyant force exceeds gravitational force C. A net downward force due to density difference D. Cannot sediment under gravity
C – The particle is denser than the medium, so net force acts downward.
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# 39 If light scattering analysis shows an intensity distribution peak at 100 nm but number distribution peaks at 70 nm, what can be inferred? A. All particles are 100 nm B. Large particles are dominating light scattering C. Small particles have higher intensity D. Sample is monodisperse
B – Light scattering intensity is proportional to the 6th power of radius; larger particles dominate.
91
# 39 In a formulation, doubling the concentration of a lyophilic colloid increases viscosity from 0.5 to 2.0 Pa·s. What does this imply about the polymer structure? A. Likely spherical micelles B. Likely rod-like or highly solvated C. Low molecular weight polymer D. Poor solvent interaction
B – A sharp increase in viscosity with concentration indicates extended, rod-like, or highly solvated polymers.
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# 39 A patient is administered an injectable formulation with colloidal particles. Which property is most important for avoiding capillary blockage? A. High viscosity B. Small and uniform particle size C. Strong Brownian motion D. High zeta potential
B – Ensures safety in IV administration and avoids embolism risk.
93
# 39 Why is dialysis important in preparing colloidal drug carriers? A. To sterilise the colloid B. To remove residual surfactant C. To separate free drug or ions from the carrier D. To increase particle solubility
C – Dialysis separates small solutes (e.g., unencapsulated drug or ions) from the colloid.
94
# 39 A pharmacist observes phase separation in a colloidal suspension. Which adjustment is most appropriate to restore stability? A. Increase temperature B. Add salt C. Add a charged stabiliser or increase zeta potential D. Reduce solute concentration
C – Increasing electrostatic repulsion helps maintain dispersion stability.
95