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Transdermal Drug Delivery Systems (TDDSs) Overview
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Transdermal Drug Delivery Systems (TDDSs) Overview

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Questions and Answers

What is the primary function of TDDSs?

  • To support the passage of drug substances through the skin and into the systemic circulation (correct)
  • To deliver drugs directly into the bloodstream
  • To control the rate of drug absorption in the gut
  • To enhance drug metabolism in the liver
  • What is the purpose of the polymer matrix in monolithic systems?

  • To enhance drug solubility in the skin
  • To prevent drug degradation in the skin
  • To control the rate of drug release for percutaneous absorption (correct)
  • To increase the surface area of the skin for absorption
  • What determines the rate of drug decline in monolithic systems with no excess drug?

  • The solubility limit of the stratum corneum (correct)
  • The concentration of drug in the device
  • The thickness of the skin
  • The surface area of the skin
  • What is the advantage of monolithic systems with excess drug?

    <p>They ensure continued saturation at the stratum corneum</p> Signup and view all the answers

    How are individual dosage units prepared in monolithic systems?

    <p>By cutting and assembling the gelled matrix</p> Signup and view all the answers

    What is the purpose of the backing layer in TDDSs?

    <p>To provide structural support to the device</p> Signup and view all the answers

    What is the difference between monolithic and membrane-controlled systems?

    <p>The presence or absence of a drug matrix layer</p> Signup and view all the answers

    What is the significance of Figures 11.8 to 11.10?

    <p>They depict the manufacture of TDDSs</p> Signup and view all the answers

    What is the primary purpose of having an excess of drug in most TDDSs?

    <p>To ensure continuous drug availability and absorption</p> Signup and view all the answers

    What is the role of the rate-controlling membrane in membrane-controlled transdermal systems?

    <p>To control the release rate of the drug</p> Signup and view all the answers

    What is the advantage of membrane-controlled systems over monolithic systems?

    <p>The release rate of drug remains constant as long as the drug solution in the reservoir remains saturated</p> Signup and view all the answers

    What is the purpose of placing a small quantity of drug in the adhesive layer in membrane-controlled systems?

    <p>To initiate prompt drug absorption and pharmacotherapeutic effects on skin placement</p> Signup and view all the answers

    What are the two possible rate-controlling mechanisms in TDDSs?

    <p>The artificial and natural membranes</p> Signup and view all the answers

    What is the function of the occlusive backing membrane in TDDSs?

    <p>To protect the system from environmental entry and from loss of drug from the system or moisture from the skin</p> Signup and view all the answers

    What is the difference between preconstructing the delivery unit and lamination in membrane-controlled systems?

    <p>Preconstructing is a single-step process, while lamination is a continuous process</p> Signup and view all the answers

    What determines the rate of drug transport in TDDSs?

    <p>The artificial or natural (skin) membranes</p> Signup and view all the answers

    Study Notes

    Transdermal Drug Delivery Systems (TDDSs)

    • Designed to support the passage of drug substances from the surface of the skin through its various layers and into the systemic circulation.

    Configuration and Composition of TDDSs

    • May be categorized into two types: monolithic and membrane-controlled systems.
    • Monolithic systems:
      • Incorporate a drug matrix layer between the backing and frontal layers.
      • The drug matrix layer is composed of a polymeric material in which the drug is dispersed.
      • The polymer matrix controls the rate at which the drug is released for percutaneous absorption.
      • May be of two types: with or without an excess of drug with regard to its equilibrium solubility and steady-state concentration gradient at the stratum corneum.
    • Membrane-controlled systems:
      • Designed to contain a drug reservoir, or pouch, usually in liquid or gel form; a rate-controlling membrane; and backing, adhesive, and protecting layers.
      • Examples: Transderm-Nitro (Summit) and Transderm Scop (Baxter).

    Characteristics of Monolithic Systems

    • The rate of drug release is controlled by the polymer matrix.
    • The matrix may be produced in sheet or cylindrical form, with individual dosage units cut and assembled between the backing and frontal layers.
    • Most TDDSs are designed to contain an excess of drug and thus have drug-releasing capacity beyond the time frame recommended for replacement.

    Characteristics of Membrane-Controlled Systems

    • The release rate of drug through the controlling membrane remains constant as long as the drug solution in the reservoir remains saturated.
    • A small quantity of drug is frequently placed in the adhesive layer to initiate prompt drug absorption and pharmacotherapeutic effects on skin placement.
    • May be prepared by preconstructing the delivery unit, filling the drug reservoir, and sealing or by lamination, a continuous process of construction, dosing, and sealing.

    Rate-Controlling Mechanism

    • Either the drug delivery device or the skin may serve as the rate-controlling mechanism.
    • If the drug is delivered to the stratum corneum at a rate less than the absorption capacity, the device is the controlling factor.
    • If the drug is delivered to the skin area to saturation, the skin is the controlling factor.

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    Description

    This quiz covers the basics of Transdermal Drug Delivery Systems, including their composition, configuration, and types. It also touches on their manufacture and functionality.

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