Buccal absorption of ergotamine tartrate using the bioadhesive tablet system in guinea-pigs

被引:25
作者
Tsutsumi, K
Obata, Y
Nagai, T
Loftsson, T
Takayama, K
机构
[1] Hoshi Univ, Dept Pharmaceut, Shinagawa Ku, Tokyo 1428501, Japan
[2] Univ Iceland, Dept Pharm, IS-127 Reykjavik, Iceland
关键词
buccal absorption; ergotamine tartrate; bioadhesive tablet system (BTS); keratinized epithelial-free membrane (KEF-membrane); in vitro-in vivo correlation;
D O I
10.1016/S0378-5173(02)00070-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The buccal administration of ergotamine tartrate (ET) combined with polyvinyl alcohol (PVA) gel brought about higher plasma concentration of ET compared with that of oral administration of capsules in guinea-pigs. T-max of ET in plasma of buccal administration was significantly smaller than that of oral administration. For the buccal dosage form of ET, the bioadhesive tablet system (BTS) was newly developed. It consisted of a reservoir of drug and an adhesive region. BTS showed better absorption of ET compared with PVA gel in guinea pigs. Among several pharmaceutical bases in the reservoir of BTS, Witepsol W-35 was most effective. It is likely that the high lipophilic property of Witepsol W-35 in which ET was dissolved facilitated the drug release by its relatively low melting point (around 35 degreesC), consequently a rapid absorption. In addition, the enhancing activity of the cod-liver oil extract (CLOE) in hydrophilic ointment on the in vivo buccal ET absorption was clarified to be comparable to that in the in vitro study utilizing the keratinized epithelial-free membrane (KEF-membrane) of the hamster cheek pouch. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:161 / 170
页数:10
相关论文
共 36 条
  • [1] LOW ORAL BIOAVAILABILITY OF DIHYDROERGOTAMINE AND 1ST-PASS EXTRACTION IN PATIENTS WITH ORTHOSTATIC HYPOTENSION
    BOBIK, A
    JENNINGS, G
    SKEWS, H
    ESLER, M
    MCLEAN, A
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 1981, 30 (05) : 673 - 679
  • [2] A mechanistic analysis to characterize oramucosal permeation properties
    Chen, LLH
    Chetty, DJ
    Chien, YW
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 184 (01) : 63 - 72
  • [3] CIERI UR, 1987, J ASSOC OFF ANA CHEM, V3, P538
  • [4] INCREASED SKIN PERMEABILITY FOR LIPOPHILIC MOLECULES
    COOPER, ER
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 1984, 73 (08) : 1153 - 1156
  • [5] ER ooper, 1982, SOLUTION BEHAV SURFA
  • [6] PERMEATION OF HAIRLESS MOUSE SKIN .2. MEMBRANE SECTIONING TECHNIQUES AND INFLUENCE ON ALKANOL PERMEABILITIES
    FLYNN, GL
    DURRHEIM, H
    HIGUCHI, WI
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 1981, 70 (01) : 52 - 56
  • [7] Physiological mechanism for enhancement of paracellular drug transport
    Hayashi, M
    Sakai, T
    Hasegawa, Y
    Nishikawahara, T
    Tomioka, H
    Iida, A
    Shimizu, N
    Tomita, M
    Awazu, S
    [J]. JOURNAL OF CONTROLLED RELEASE, 1999, 62 (1-2) : 141 - 148
  • [8] In-vivo buccal delivery of fluorescein isothiocyanate dextran 4400 with glycodeoxycholate as an absorption enhancer in pigs
    Hoogstraate, AJ
    Verhoef, JC
    Tuk, B
    Pijpers, A
    vanLeengoed, LAMG
    Verheijden, JHM
    Junginger, HE
    Bodde, HE
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 1996, 85 (05) : 457 - 460
  • [9] Human pharmacokinetics of dihydroergotamine administered by nasal spray
    Humbert, H
    Cabiac, MD
    Dubray, C
    Lavene, D
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 1996, 60 (03) : 265 - 275
  • [10] FREQUENCY AND DISTRIBUTION OF BINUCLEATE CELLS IN ORAL EPITHELIUM OF SEVERAL SPECIES OF LABORATORY RODENTS
    IBRAHIM, J
    GERSON, SJ
    MEYER, J
    [J]. ARCHIVES OF ORAL BIOLOGY, 1985, 30 (08) : 627 - 633