2008
DOI: 10.2165/00002512-200825040-00001
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Use of Transdermal Drug Formulations in the Elderly

Abstract: Transdermal drug delivery systems are pharmaceutical forms designed to administer a drug through the skin to obtain a systemic effect. They ensure a constant rate of drug administration and a prolonged action. Several different types of transdermal delivery devices are available on the market. They are either matrix or reservoir systems and their main current uses are to treat neurological disorders, pain and coronary artery disease, and as hormone replacement therapy. Transdermal drug administration has a num… Show more

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Cited by 94 publications
(53 citation statements)
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“…Reservoir TDDS should not be cut, as altering the integrity of the system could create a dose-dumping effect that can lead to drug toxicity (including death) or inadvertent drug exposure to others [8,9] . Matrix (monolithic) systems contain a similar distribution of drug throughout the patch and exist in several forms including simple matrix systems, drug-in-adhesive system, and multilayer matrix systems [1] . All matrix TDDS incorporate active drug in a polymer matrix that regulates drug release via diffusion (i.e., drug concentrations moving from high concentrations to low concentrations) compared to reservoir systems which contain a rate-controlling membrane that is responsible for controlled release of transdermal formulations [1,5,10,11] .…”
Section: Types Of Tddsmentioning
confidence: 99%
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“…Reservoir TDDS should not be cut, as altering the integrity of the system could create a dose-dumping effect that can lead to drug toxicity (including death) or inadvertent drug exposure to others [8,9] . Matrix (monolithic) systems contain a similar distribution of drug throughout the patch and exist in several forms including simple matrix systems, drug-in-adhesive system, and multilayer matrix systems [1] . All matrix TDDS incorporate active drug in a polymer matrix that regulates drug release via diffusion (i.e., drug concentrations moving from high concentrations to low concentrations) compared to reservoir systems which contain a rate-controlling membrane that is responsible for controlled release of transdermal formulations [1,5,10,11] .…”
Section: Types Of Tddsmentioning
confidence: 99%
“…In addition, transdermal formulations typically have a favorable drug concentration profile as the factors that limit gastrointestinal absorption (e.g., changes in pH, rate and extent of gastric emptying, transit times, presence/interaction with food, intestinal motilities) are avoided [1] . Delayed absorption prevents peaks and valleys associated with variations in drug concentrations.…”
Section: Safety Of Transdermal Drug Delivery Systemsmentioning
confidence: 99%
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