Thiolated chitosans:: development and in vitro evaluation of a mucoadhesive, permeation enhancing oral drug delivery system

被引:167
作者
Bernkop-Schnürch, A
Guggi, D
Pinter, Y
机构
[1] Leopold Franzens Univ Innsbruck, Dept Pharmaceut Technol, Inst Pharm, A-6020 Innsbruck, Austria
[2] Univ Vienna, Ctr Pharm, Inst Pharmaceut Technol & Biopharmaceut, A-1090 Vienna, Austria
关键词
thiolated chitosan; thiomers; cefadroxil; mucoadhesion; oral drug delivery;
D O I
10.1016/j.jconrel.2003.10.005
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
It was the aim of this study to develop a mucoadhesive, permeation enhancing delivery system for orally administered poorly absorbed drugs. Chitosan was modified by the immobilisation of thiol groups utilising 2-iminothiolane (Traut's reagent). The permeation enhancing effect of the resulting chitosan-4-thio-butylamidine conjugate (chitosan-TBA conjugate) in combination with the permeation mediator glutathione (GSH) was evaluated in Ussing chambers on freshly excised small intestinal mucosa from guinea pigs using rhodamine 123 as marker for passive drug uptake. The mucoadhesive properties of the chitosan-TBA conjugate adjusted to pH 3, 5 and 7 were evaluated via the rotating cylinder method and via tensile studies. Release studies were performed with tablets comprising 10% cefadroxil used as model drug, 10% GSH and 80% chitosan-TBA conjugate pH 3 in 100 mM phosphate buffer pH 6.8 at 37 degreesC. Results showed a Mold higher permeation enhancing effect of the chitosan-TBA conjugate/GSH system in comparison to unmodified chitosan. Mucoadhesion studies revealed that the lower the pH of the thiolated chitosan is, the higher are its mucoadhesive properties. Release studies showed a sustained release of both cefadroxil and GSH over several hours. This delivery system might represent a promising novel tool in order to improve the therapeutic efficacy of various drugs which are poorly absorbed from the gastrointestinal tract. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:177 / 186
页数:10
相关论文
共 26 条
  • [11] VARIATION IN GASTROINTESTINAL TRANSIT OF PHARMACEUTICAL DOSAGE FORMS IN HEALTHY-SUBJECTS
    COUPE, AJ
    DAVIS, SS
    WILDING, IR
    [J]. PHARMACEUTICAL RESEARCH, 1991, 8 (03) : 360 - 364
  • [12] de P. A, 2002, J CLIN PHARMACOL, V42, P403
  • [13] ORAL CEPHALOSPORINS - CURRENT PERSPECTIVES
    GARCIARODRIGUEZ, JA
    BELLIDO, JLM
    SANCHEZ, JEG
    [J]. INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 1995, 5 (04) : 231 - 243
  • [14] GUGGI D, 2003, IN PRESS PHARM RES
  • [15] Kasai M, 1999, CHEM PHARM BULL, V47, P1081
  • [16] Development and in vivo evaluation of an oral delivery system for low molecular weight heparin based on thiolated polycarbophil
    Kast, CE
    Guggi, D
    Langoth, N
    Bernkop-Schnürch, A
    [J]. PHARMACEUTICAL RESEARCH, 2003, 20 (06) : 931 - 936
  • [17] Thiolated polymers -: thiomers:: development and in vitro evaluation of chitosan-thioglycolic acid conjugates
    Kast, CE
    Bernkop-Schnürch, A
    [J]. BIOMATERIALS, 2001, 22 (17) : 2345 - 2352
  • [18] TRANSPORT OF CEFADROXIL, AN AMINOCEPHALOSPORIN ANTIBIOTIC, ACROSS THE SMALL INTESTINAL BRUSH-BORDER MEMBRANE
    KIMURA, T
    YAMAMOTO, T
    ISHIZUKA, R
    SEZAKI, H
    [J]. BIOCHEMICAL PHARMACOLOGY, 1985, 34 (01) : 81 - 84
  • [19] CLINICAL PHARMACOKINETICS OF NEWER CEPHALOSPORINS
    KLEPSER, ME
    MARANGOS, MN
    PATEL, KB
    NICOLAU, DP
    QUINTILIANI, R
    NIGHTINGALE, CH
    [J]. CLINICAL PHARMACOKINETICS, 1995, 28 (05) : 361 - 384
  • [20] In-vitro release kinetics of cefadroxil-loaded sodium alginate interpenetrating network beads
    Kulkarni, AR
    Soppimath, KS
    Aminabhavi, TM
    Rudzinski, WE
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2001, 51 (02) : 127 - 133