Absolute and relative bioavailability of fentanyl buccal tablet and oral transmucosal fentanyl citrate

被引:74
作者
Darwish, Mona [1 ]
Kirby, Mary [1 ]
Robertson, Philmore, Jr. [1 ]
Tracewell, William [1 ]
Jiang, John G. [1 ]
机构
[1] Cephalon Inc, Frazer, PA 19355 USA
关键词
fentanyl buccal tablet; oral transmucosal fentanyl citrate; bioavailability;
D O I
10.1177/0091270006297749
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study assessed the absolute and relative bioavailabilities and transmucosal and gastrointestinal absorbency of fentanyl buccal tablet (FBT) and oral transmucosal fentanyl citrate (OTFC). In a randomized crossover design, 26 healthy subjects received FBT 400 mu g (transmucosal), FBT 800 mu g (oral), OTFC 800 mu g (transmucosul), and fentanyl 400 mu g (intravenous). The transmucosal FBT had the highest absolute bioavailability (0.65) compared with the oral FBT (0.31) or transmucosal OTFC (0.47). More fentanyl was absorbed transmucosally from FBT than OTFC (48% vs 22%). Median t(max) values were shorter following the transmucosal FBT (47 minutes) than the oral FBT (90 minutes) or the transmucosul OTFC (91 minutes). Transmucosal administration of FBT compared with dose-normalized OTFC resulted in higher total systemic fentanyl exposure, higher early systemic exposure, and higher C-max. The rate and extent of fentanyl absorption were greater following administration of FBT compared to OTFC. An approximately 30% smaller dose of FBT achieved systemic exposures comparable to OTFC.
引用
收藏
页码:343 / 350
页数:8
相关论文
共 21 条
[1]  
[Anonymous], 2006, AM J DRUG DELIV, DOI DOI 10.2165/00137696-200604010-00001
[2]   Pharmacokinetic properties of fentanyl effervescent buccal tablets:: A phase I, open-label, crossover study of single-dose 100, 200, 400, and 800 μg in healthy adult volunteers [J].
Darwish, M ;
Kirby, M ;
Robertson, P ;
Tracewell, W ;
Jiang, JG .
CLINICAL THERAPEUTICS, 2006, 28 (05) :707-714
[3]   Relative bioavailability of the fentanyl effervescent buccal tablet (FEBT) 1080 μg versus oral transmucosal fentanyl citrate 1600 μg and dose proportionality of FEBT 270 to 1300 μg:: A single-dose, randomized, open-label, three-period study in healthy adult volunteers [J].
Darwish, M ;
Tempero, K ;
Kirby, M ;
Thompson, J .
CLINICAL THERAPEUTICS, 2006, 28 (05) :715-724
[4]   Pharmacokinetics and dose proportionality of fentanyl effervescent buccal tablets in healthy volunteers [J].
Darwish, M ;
Tempero, K ;
Kirby, M ;
Thompson, J .
CLINICAL PHARMACOKINETICS, 2005, 44 (12) :1279-1286
[5]   Mechanistic studies on effervescent-induced permeability enhancement [J].
Eichman, JD ;
Robinson, JR .
PHARMACEUTICAL RESEARCH, 1998, 15 (06) :925-930
[6]   The influence of in-vivo carbonation on GI physiological processes and drug permeability [J].
Eichman, JD ;
Yassin, AEB ;
Robinson, JR .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 1997, 44 (01) :33-38
[7]  
Food and Nutrition Board Institute of Medicine, 2005, DIETARY REFERENCE IN, P1, DOI DOI 10.17226/10925
[8]  
FRAZER P, 2006, FENTORA PRESCRIBING
[9]  
Gibaldi M., 1982, PHARMACOKINETICS, P409
[10]   PHARMACOKINETICS OF FENTANYL IN PATIENTS UNDERGOING ABDOMINAL AORTIC-SURGERY [J].
HUDSON, RJ ;
THOMSON, IR ;
CANNON, JE ;
FRIESEN, RM ;
MEATHERALL, RC .
ANESTHESIOLOGY, 1986, 64 (03) :334-338