Ex vivo bioadhesion and in vivo testosterone bioavailability study of different bioadhesive formulations based on starch-g-poly(acrylic acid) copolymers and starch/poly(acrylic acid) mixtures

被引:47
作者
Ameye, D
Voorspoels, J
Foreman, P
Tsai, J
Richardson, P
Geresh, S
Remon, JP
机构
[1] State Univ Ghent, Fac Pharmaceut Sci, Pharmaceut Technol Lab, B-9000 Ghent, Belgium
[2] Natl Starch & Chem Corp, Bridgewater, NJ USA
[3] Ben Gurion Univ Negev, Inst Appl Res, IL-84105 Beer Sheva, Israel
关键词
starch-g-poly(acrylic acid) copolymers starch/poly(acrylic acid) mixtures; bioadhesive tablet; ex vivo bioadhesion; buccal absorption;
D O I
10.1016/S0168-3659(01)00539-9
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Starch-g-poly(acrylic acid) copolymers or grafted starches synthesized by Co-60 irradiation or chemical modification and co-freeze-dried starch/poly(acrylic acid) mixtures were evaluated on their ex vivo bioadhesion capacity. The buccal absorption of testosterone from a bioadhesive tablet formulated with the grafted starches or starch/poly(acrylic acid) mixtures was investigated. The results were compared to a reference formulation (physical mixture of 5% Carbopol(R) 974P and 95% Drum Dried Waxy Maize). Rice starch-based irradiated grafted starches showed the best bioadhesion results. Partial neutralization of the acrylic acid with Ca2+ ions resulted in significantly higher bioadhesion values compared to the reference. Ca2+ and Mg2+ partially neutralized maltodextrin-based irradiated grafted starches showed significantly higher bioadhesion values compared to the reference formulation. The chemically modified grafted starches showed significantly higher adhesion force values than for the reference tablet. None of the co-freeze-dried starch/poly(,acrylic acid) mixtures showed significantly higher bioadhesion results than the reference (Bonferroni test, P<0.05). A chemically modified grafted starch could sustain the 3 ng/ml plasma testosterone target concentration during +/-8 h (T->3 ng/ml). By lyophilization of a partially neutralized irradiated grafted starch, the in vivo adhesion time (22.0+/-7.2 h) and the T (>3 ng/ml) (13.5+/-1.3 h) could be increased. The absolute bioavailability of the lyophilized formulation approached the reference formulation. Some of the grafted starches showed to be promising buccal bioadhesive drug carriers for systemic delivery. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:173 / 182
页数:10
相关论文
共 15 条
[1]   INVITRO-INVIVO CORRELATION OF THE BIOADHESIVE PROPERTIES OF A BUCCAL BIOADHESIVE MICONAZOLE SLOW-RELEASE TABLET [J].
BOUCKAERT, S ;
LEFEBVRE, RA ;
REMON, JP .
PHARMACEUTICAL RESEARCH, 1993, 10 (06) :853-856
[2]   IN-VITRO BIOADHESION OF A BUCCAL, MICONAZOLE SLOW-RELEASE TABLET [J].
BOUCKAERT, S ;
REMON, JP .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1993, 45 (06) :504-507
[3]   Gel-forming erodible inserts for ocular controlled delivery of ofloxacin [J].
Di Colo, G ;
Burgalassi, S ;
Chetoni, P ;
Fiaschi, MP ;
Zambito, Y ;
Saettone, MF .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 215 (1-2) :101-111
[4]   Drug delivery via the buccal mucosa [J].
Hoogstraate, JAJ ;
Wertz, PW .
PHARMACEUTICAL SCIENCE & TECHNOLOGY TODAY, 1998, 1 (07) :309-316
[5]  
Lloyd NE, 1984, STARCH CHEM TECHNOLO, V2nd, P611, DOI DOI 10.1016/B978-0-12-746270-7.50027-6
[6]  
MAZER NA, 1992, J CONTROL RELEASE, V19, P347, DOI 10.1016/0168-3659(92)90089-A
[7]   MW PHARM, AN INTEGRATED SOFTWARE PACKAGE FOR DRUG-DOSAGE REGIMEN CALCULATION AND THERAPEUTIC DRUG-MONITORING [J].
PROOST, JH ;
MEIJER, DKF .
COMPUTERS IN BIOLOGY AND MEDICINE, 1992, 22 (03) :155-163
[8]   In vitro evaluation of the bioadhesive properties of hydrophobic polybasic gels containing N,N-dimethylaminoethyl methacrylate-co-methyl methacrylate [J].
Quintanar-Guerrero, D ;
Villalobos-García, R ;
Alvarez-Colín, E ;
Cornejo-Bravo, JM .
BIOMATERIALS, 2001, 22 (09) :957-961
[9]   An investigation of mucus/polymer theological synergism using synthesised and characterised poly(acrylic acid)s [J].
Riley, RG ;
Smart, JD ;
Tsibouklis, J ;
Dettmar, PW ;
Hampson, F ;
Davis, JA ;
Kelly, G ;
Wilber, WR .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 217 (1-2) :87-100
[10]   Potential applications of carbomer in oral mucoadhesive controlled drug delivery system: A review [J].
Singla, AK ;
Chawla, M ;
Singh, A .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2000, 26 (09) :913-924