Chitosan-based mucoadhesive tablets for oral delivery of ibuprofen

被引:92
作者
Sogias, Ioannis A. [1 ]
Williams, Adrian C. [1 ]
Khutoryanskiy, Vitaliy V. [1 ]
机构
[1] Univ Reading, Sch Pharm, Reading RG6 6AD, Berks, England
基金
英国生物技术与生命科学研究理事会;
关键词
Chitosan; Mucoadhesion; Tablets; Spray-drying; Ibuprofen; Crystallinity; WATER-SOLUBILITY; DRUG-DELIVERY; N-ACETYLATION; CHITIN; PERMEABILITY; ENHANCEMENT; RELEASE;
D O I
10.1016/j.ijpharm.2012.07.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chitosan and its half-acetylated derivative have been compared as excipients in mucoadhesive tablets containing ibuprofen. Initially the powder formulations containing the polymers and the drug were prepared by either co-spray drying or physical co-grinding. Polymer-drug interactions and the degree of drug crystallinity in these formulations were assessed by infrared spectroscopy and differential scanning calorimetry. Tablets were prepared and their swelling and dissolution properties were studied in media of various pHs. Mucoadhesive properties of ibuprofen-loaded and drug-free tablets were evaluated by analysing their detachment from pig gastric mucosa over a range of pHs. Greater polymer-drug interactions were seen for spray-dried particles compared to co-ground samples and drug loading into chitosan-based microparticles (41%) was greater than the corresponding half-acetylated samples (32%). Swelling and drug release was greater with the half-acetylated chitosan tablets than tablets containing the parent polymer and both tablets were mucoadhesive, the extent of which was dependent on substrate pH. The results illustrate the potential sustained drug delivery benefits of both chitosan and its half-acetylated derivative as mucoadhesive tablet excipients. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:602 / 610
页数:9
相关论文
共 32 条
[1]   Recent advances on chitosan-based micro- and nanoparticles in drug delivery [J].
Agnihotri, SA ;
Mallikarjuna, NN ;
Aminabhavi, TM .
JOURNAL OF CONTROLLED RELEASE, 2004, 100 (01) :5-28
[2]  
Alderborn G., 2007, AULTONS PHARM DESIGN, P441
[3]   EFFECT OF CHITOSAN ON THE PERMEABILITY OF MONOLAYERS OF INTESTINAL EPITHELIAL-CELLS (CACO-2) [J].
ARTURSSON, P ;
LINDMARK, T ;
DAVIS, SS ;
ILLUM, L .
PHARMACEUTICAL RESEARCH, 1994, 11 (09) :1358-1361
[4]   IMPROVED METHOD FOR IR DETERMINATION OF THE DEGREE OF N-ACETYLATION OF CHITOSAN [J].
BAXTER, A ;
DILLON, M ;
TAYLOR, KDA ;
ROBERTS, GAF .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 1992, 14 (03) :166-169
[5]   Chitosan drug binding by ionic interaction [J].
Boonsongrit, Y ;
Mitrevej, A ;
Mueller, BW .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2006, 62 (03) :267-274
[6]  
British Pharmacopoeia, 2008, BRIT PHARMACOPOEIA
[7]   Preparation and release of salbutamol from chitosan and chitosan co-spray dried compacts and multiparticulates [J].
Corrigan, DO ;
Healy, AM ;
Corrigan, OI .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2006, 62 (03) :295-305
[8]   Effect of chitosan on epithelial permeability and structure [J].
Dodane, V ;
Khan, MA ;
Merwin, JR .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 182 (01) :21-32
[9]   An optimised method to determine the degree of acetylation of chitin and chitosan by FTIR spectroscopy [J].
Duarte, ML ;
Ferreira, MC ;
Marvao, MR ;
Rocha, J .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2002, 31 (1-3) :1-8
[10]   Solubility parameters as predictors of miscibility in solid dispersions [J].
Greenhalgh, DJ ;
Williams, AC ;
Timmins, P ;
York, P .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1999, 88 (11) :1182-1190