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Questions and Answers
What is the primary function of TDDSs?
What is the primary function of TDDSs?
What is the purpose of the polymer matrix in monolithic systems?
What is the purpose of the polymer matrix in monolithic systems?
What determines the rate of drug decline in monolithic systems with no excess drug?
What determines the rate of drug decline in monolithic systems with no excess drug?
What is the advantage of monolithic systems with excess drug?
What is the advantage of monolithic systems with excess drug?
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How are individual dosage units prepared in monolithic systems?
How are individual dosage units prepared in monolithic systems?
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What is the purpose of the backing layer in TDDSs?
What is the purpose of the backing layer in TDDSs?
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What is the difference between monolithic and membrane-controlled systems?
What is the difference between monolithic and membrane-controlled systems?
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What is the significance of Figures 11.8 to 11.10?
What is the significance of Figures 11.8 to 11.10?
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What is the primary purpose of having an excess of drug in most TDDSs?
What is the primary purpose of having an excess of drug in most TDDSs?
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What is the role of the rate-controlling membrane in membrane-controlled transdermal systems?
What is the role of the rate-controlling membrane in membrane-controlled transdermal systems?
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What is the advantage of membrane-controlled systems over monolithic systems?
What is the advantage of membrane-controlled systems over monolithic systems?
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What is the purpose of placing a small quantity of drug in the adhesive layer in membrane-controlled systems?
What is the purpose of placing a small quantity of drug in the adhesive layer in membrane-controlled systems?
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What are the two possible rate-controlling mechanisms in TDDSs?
What are the two possible rate-controlling mechanisms in TDDSs?
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What is the function of the occlusive backing membrane in TDDSs?
What is the function of the occlusive backing membrane in TDDSs?
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What is the difference between preconstructing the delivery unit and lamination in membrane-controlled systems?
What is the difference between preconstructing the delivery unit and lamination in membrane-controlled systems?
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What determines the rate of drug transport in TDDSs?
What determines the rate of drug transport in TDDSs?
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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.