Pharmaceutics 1: Colloidal Stability Overview
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Questions and Answers

What does the Schultze-Hardy Rule state about the flocculating power of ions?

  • Proportional to the fifth power of their charge
  • Proportional to their charge squared
  • Proportional to the sixth power of their charge (correct)
  • Proportional to the square of their charge
  • DLVO theory is effective for both monovalent and multivalent ions.

    False

    What effect does high electrolyte concentration have on k in relation to particle stability?

    Increases k and promotes aggregation

    The thickness of the electrical double layer is altered by electrolyte concentrations and is described by the _______ law.

    <p>Debye-Huckel</p> Signup and view all the answers

    Match the ion type with its flocculating power:

    <p>Monovalent = 1 Divalent = 64 Trivalent = 729</p> Signup and view all the answers

    What is formed by ions being attracted to or repelled from the charged surface of a colloid particle?

    <p>Electrical double layer</p> Signup and view all the answers

    Electrostatic forces between particles with the same charge are attractive.

    <p>False</p> Signup and view all the answers

    What constant represents the Debye-Huckel length?

    <p>1/κ</p> Signup and view all the answers

    The potential difference across the double layer is known as __________ potential.

    <p>Zeta</p> Signup and view all the answers

    Match the following terms with their definitions:

    <p>Stern Layer = Layer of ions closely associated with the colloid particle's surface Gouy-Chapman Layer = Diffuse layer of ions extending into the solution Zeta Potential = Potential at the shear surface of charged particles Debye-Huckel Constant = Constant used in describing potential interactions in colloids</p> Signup and view all the answers

    Which of the following best describes the Stern layer?

    <p>It is a fixed layer of counter-ions attracted to the surface.</p> Signup and view all the answers

    The Gouy-Chapman layer is the first layer of ions adjacent to the colloid's surface.

    <p>False</p> Signup and view all the answers

    What are forces responsible for the interaction of the electrical double layer called?

    <p>Electrostatic forces</p> Signup and view all the answers

    What happens to the repulsion experienced between particles when the electrical double layers overlap?

    <p>There is no repulsion until particles are very close.</p> Signup and view all the answers

    The Debye-Huckel Constant (κ) increases as the Debye-Huckel Length (1/κ) increases.

    <p>False</p> Signup and view all the answers

    What effect does high electrolyte concentration have on Debye-Huckel Length?

    <p>It decreases the Debye-Huckel Length.</p> Signup and view all the answers

    The potential energy graph shows that __________ occurs at low electrolyte concentrations.

    <p>no secondary minimum</p> Signup and view all the answers

    Match the following electrolyte concentrations with their effect on VR:

    <p>High Electrolyte Concentration = Small 1/κ, Large κ Low Electrolyte Concentration = Large 1/κ, Small κ Intermediate Electrolyte Concentration = Balanced 1/κ and κ Very High Electrolyte Concentration = No primary maximum in VT</p> Signup and view all the answers

    What is the primary effect of the Debye-Huckel Length on the potential energy (VT)?

    <p>Creates a primary maximum and secondary minimum.</p> Signup and view all the answers

    In a low electrolyte concentration scenario, there is a strong attraction between particles at large separations.

    <p>True</p> Signup and view all the answers

    How does increasing particle separation (H) affect VR?

    <p>VR decreases.</p> Signup and view all the answers

    As __________ of the Debye-Huckel Constant (κ) increases, VR decreases.

    <p>the value</p> Signup and view all the answers

    At high electrolyte concentrations, the primary maximum in VT disappears.

    <p>True</p> Signup and view all the answers

    Study Notes

    Introduction to Pharmaceutics 1: Colloidal Stability

    • Pharmaceutics 1 lecture on colloidal stability focuses on suspensions.
    • The lecture aims to explain physical instability in disperse systems.
    • It describes the electrical double layer surrounding particles in aqueous electrolyte solutions and the forces governing physical instability.
    • The lecture covers how electrolyte concentrations affect electrical double layers, repulsive forces, and instability in disperse systems.
    • It also discusses the influence of electrolyte valency on flocculation in disperse systems.

    Disperse Systems and Colloids

    • Colloids are disperse systems where one phase consists of tiny particles or droplets.
    • Liquid-in-liquid colloids are called emulsions.
    • Solid-in-liquid colloids are called suspensions.

    Physical Instability in Suspensions

    • Physical instability in suspensions is observed as sedimentation (particles settling due to density differences) and caking (high-density sediment forming).
    • Redispersing a solid-liquid colloid often requires shaking.

    Flocculation

    • Flocculation involves particles/droplets clustering together with maintained individual identity (unlike coagulation).
    • Flocculation can be redispersed by shaking.
    • Flocculation is desirable in formulations to prevent caking.

    Coagulation

    • Coagulation involves strong attractive forces between particles and droplets.
    • Coagulated particles form small aggregates that cannot be redispersed by shaking, resulting in permanent medication failure (caking).

    Forces Acting on Particles in Disperse Systems

    • Particles less than 2 microns in diameter move due to Brownian motion, kinetic energy influenced by temperature and external forces.
    • As particles approach, they experience repulsive electrostatic interactions (VR) and attractive van der Waals forces (VA).
    • Steric forces (Vs) also arise if non-ionic surfactants are present.
    • The total potential energy (VT) is determined by the combined interactions: VT = VA + VR + Vs

    DVLO Theory

    • DVLO theory describes the balance between electrostatic repulsion and attractive forces in charged particles.
    • In the case of charged particles, steric forces (Vs) are insignificant, simplifying the equation to VT = VA + VR

    Forces and Particle Separation

    • The attractive and repulsive forces change with the distance between particles (H).
    • Potential diagrams visualize force (V) plotted against particle separation (H).
    • The attractive force (VA) inversely depends on the particle separation distance(1/H).

    Repulsive Forces

    • Colloidal particles are often charged.
    • Charge arises from ion dissolution (e.g., drug uneven dissolution).
    • Ion adsorption (e.g., surfactants) can also cause surface charge.
    • Electrostatic repulsion (VR) occurs between particles with similar charges.
    • VR is related to particle separation and charge density as defined by; VR = 2πεαψ2(exp(-кH)).
    • VR decreases rapidly with increasing particle separation distance.
    • VR also decreases with increasing Debye-Huckel Constant (к)

    Debye-Huckel Length and Electrolyte Concentration

    • The Debye-Huckel length (1/к) signifies the extent of the electrical double layer.
    • High electrolyte concentrations reduce the Debye-Huckel length, increasing the Debye-Huckel Constant, and thus decreasing VR.
    • Low electrolyte concentrations increase the Debye-Huckel length, decreasing the Debye-Huckel Constant, and thus increasing VR
    • Intermediate electrolyte concentrations result in both attractive and repulsive forces, leading to a stable suspension

    Total Potential Energy

    • The total potential energy (VT) combines attractive and repulsive forces.
    • Different electrolyte concentrations lead to diverse VT profiles and thus differing colloidal stability.
    • High electrolyte concentration creates a situation where the primary maximum is absent, resulting in an unstable colloidal suspension.
    • All kinetic energy levels will lead to coagulation.
    • Intermediate electrolyte concentration results in both attractive forces and a secondary minimum, fostering colloidal stability.

    Effect of Multivalent Ions

    • DLVO theory simplifies the interactions that determine colloidal stability.
    • The Schulze-Hardy rule highlights the significant flocculating power of multivalent ions (proportionally related to their charge to the power of 6).
    • The addition of divalent or trivalent ions can negatively impact stability.

    Summary

    • Attractive and repulsive forces influence colloidal stability and physical instability.
    • Electrolyte concentration changes the thickness of the electrical double layer and ultimately impacts colloidal stability.
    • The addition of multivalent ions must be avoided for many disperse systems in order to maintain colloidal stability.

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    Description

    This quiz covers key concepts from the Pharmaceutics 1 lecture on colloidal stability, focusing on the physical instability of disperse systems such as suspensions. It explores the role of the electrical double layer, electrolyte concentrations, and their impacts on stability. Prepare to test your understanding of colloids and the mechanisms behind their behavior in various solutions.

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