Transdermal fentanyl: clinical pharmacology.
摘要:
The transdermal therapeutic system (TTS) fentanyl has been designed for rate-controlled drug delivery. It provides a convenient regimen for the use of a drug previously limited by a short duration of action and a noninvasive parenteral route for a drug that is unsuitable for oral administration. TTS fentanyl has been developed to provide continuous controlled systemic delivery of fentanyl base for 72 hr. It is a rectangular, transparent unit composed of a protective peel strip and four functional layers. The amount of fentanyl released from, each system (25 μg/hr per 10 cm 2 ) is proportional to the surface area. So far, four patch sizes are available (10–40 cm 2 ). When the system is applied, a fentanyl depot concentrates in the upper skin layers. Fentanyl plasma concentration are not measurable until 2 hr after application, and it takes 8–16 hr latency until full dinical fentanyl effects are observed. Steady-state serum concentrations are obtained after several sequential 72-hr applications, and these are maintained for as long as a system is applied. Following removal, serum fentanyl concentrations decline gradually and fall about 50% in approximately 16 hr. This prolonged apparent elimination half-life occurs because fentanyl continues to be absorbed from the skin. Transdermal fentanyl transport is essentially the same between the chest, abdomen, and thigh. The skin-permeability constant is about 0.0125 mL/hr/cm 2 , much lower than the regional blood supply to a chest-skin area. Because of potential permeability variations among individuals, a special rate-controlling membrane in the system provides additional control of drug release. The rate-controlled delivery reduces the variations in skin transport by 50%. Small amounts of alcohol are used as an absorption enhancer. TTS fentanyl appears to be a valuable tool for chronic pain patients requiring continuous opiate treatment but is, due to its long delay and decay times, probably unsuitable for the routine management of short-lasting acute pain states.
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DOI:
10.1016/0885-3924(92)90048-M
被引量:
年份:
1992
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