Buccal delivery of thiocolchicoside: in vitro and in vivo permeation studies

被引:55
作者
Artusi, M
Santi, P
Colombo, P
Junginger, HE
机构
[1] Univ Parma, Dept Pharm, I-43100 Parma, Italy
[2] Leiden Univ, Div Pharmaceut Technol, Leiden Amsterdam Ctr Drug Res, LACDR, NL-2300 RA Leiden, Netherlands
关键词
thiocolchicoside; buccal; formulation; permeability; enhancers; in vitro/in vivo;
D O I
10.1016/S0378-5173(02)00545-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Thiocolchicoside, a muscle-relaxant agent, is administered by the oral, intra-muscular and topical route. After oral administration the extent of bioavailability compared with intra-muscular administration is low, due to a first pass effect. In this paper, the delivery of thiocolchicoside through oral mucosa is studied to improve the bioavailability. Thiocolchicoside in vitro permeation through porcine oral mucosa and in vivo buccal transport in humans were investigated. Two dosage forms, a bioadhesive disc and a fast dissolving disc for buccal and sublingual administration of thiocolchicoside, respectively, were designed. The in vitro permeation of thiocolchicoside through porcine buccal mucosa from these dosage forms was evaluated and compared with in vivo absorption. Results from in vitro studies demonstrated that thiocolchicoside is quite permeable across porcine buccal mucosa and that permeation enhancers, such as sodium taurocholate and sodium taurodeoxycholate, were not able to increase its flux. The in vivo thiocolchicoside absorption experiments, in which the drug loss from oral cavity was measured, indicated that both formulations could be useful for therapeutic application. The fast dissolving (sublingual) form resulted in a quick uptake of 0.5 mg of thiocolchicoside within 15 min whereas with the adhesive buccal form the same dose can be absorbed over an extended period of time. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:203 / 213
页数:11
相关论文
共 25 条
[1]  
[Anonymous], 1996, DRUGS PHARM SCI
[2]  
BECKETT AH, 1967, J PHARM PHARMACOL, VS 19, pS31
[3]   LOCALIZATION OF THE PERMEABILITY BARRIER INSIDE PORCINE BUCCAL MUCOSA - A COMBINED INVITRO STUDY OF DRUG PERMEABILITY, ELECTRICAL-RESISTANCE AND TISSUE MORPHOLOGY [J].
DEVRIES, ME ;
BODDE, HE ;
VERHOEF, JC ;
PONEC, M ;
CRAANE, WIHM ;
JUNGINGER, HE .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1991, 76 (1-2) :25-35
[4]   CHANGES IN KERATIN GENE-EXPRESSION DURING TERMINAL DIFFERENTIATION OF THE KERATINOCYTE [J].
FUCHS, E ;
GREEN, H .
CELL, 1980, 19 (04) :1033-1042
[5]  
HOOGSTRAATE AJ, 1993, ADV DRUG DELIVER REV, V12, P99
[6]   In-vivo buccal delivery of fluorescein isothiocyanate dextran 4400 with glycodeoxycholate as an absorption enhancer in pigs [J].
Hoogstraate, AJ ;
Verhoef, JC ;
Tuk, B ;
Pijpers, A ;
vanLeengoed, LAMG ;
Verheijden, JHM ;
Junginger, HE ;
Bodde, HE .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1996, 85 (05) :457-460
[7]   In vivo buccal delivery of the peptide drug buserelin with glycodeoxycholate as an absorption enhancer in pigs [J].
Hoogstraate, AJ ;
Verhoef, JC ;
Pijpers, A ;
vanLeengoed, LAMG ;
Verheijden, JHM ;
Junginger, HE ;
Bodde, HE .
PHARMACEUTICAL RESEARCH, 1996, 13 (08) :1233-1237
[8]   A novel in-situ model for continuous observation of transient drug concentration gradients across buccal epithelium at the microscopical level [J].
Hoogstraate, AJ ;
Cullander, C ;
Nagelkerke, JF ;
Spies, F ;
Verhoef, J ;
Schrijvers, AHGJ ;
Junginger, HE ;
Bodde, HE .
JOURNAL OF CONTROLLED RELEASE, 1996, 39 (01) :71-78
[9]  
JANBROERS JM, 1987, ACTA THERAP, V13, P221
[10]   Recent advances in buccal drug delivery and absorption - in vitro and in vivo studies [J].
Junginger, HE ;
Hoogstraate, JA ;
Verhoef, JC .
JOURNAL OF CONTROLLED RELEASE, 1999, 62 (1-2) :149-159