An investigation into the characteristics of chitosan/Kollicoat SR30D free films for colonic drug delivery

被引:25
作者
He Wei [1 ,3 ]
Fan Li-Fang [2 ,4 ]
Xiang Bai
Li Chun-Lei [3 ]
Du Qing
Chang Yong-Zhen [5 ]
Cao De-Ying
机构
[1] Hebei Med Univ, Sch Pharmaceut Sci, Dept Pharmaceut, Shijiazhuang 050017, Peoples R China
[2] Hebei Med Univ, Dept Pharmaceut Anal, Shijiazhuang 050017, Peoples R China
[3] CSPC Pharmaceut Technol Co Ltd, Shijiazhuang, Peoples R China
[4] Hebei Med Univ, Inst Med, Hebei Yiling Pharmaceut Grp, Beijing, Peoples R China
[5] Hebei Med Univ, XingTai Med Coll, Dept Pharmaceut, Xingtai, Peoples R China
关键词
Chitosan; Kollicoat SR30D; Colonic drug delivery; Mixed-film; Permeability; SYSTEMS; PERMEABILITY; COATINGS; BACTERIA; POLYMER; ACETATE; PH; DISSOLUTION; PRODRUGS; RELEASE;
D O I
10.1016/j.ejpb.2008.10.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of the study was to establish the physico-mechanical, digestibility, permeability and swelling properties of chitosan/Kollicoat SR30D films as potential coatings for colonic drug delivery. Free films containing different ratios of chitosan to Kollicoat SR30D were prepared by casting/solvent evaporation method. The resultant mixed films were characterized in terms of puncture strength and elongation (%), glass transition temperature, swellability, polymer miscibility, permeability, and digestibility under different media. The mixed films possessed good mechanical properties, which could be used as film-coating materials for drug delivery. The extent of digestion was directly proportional to the amount of chitosan present within the film. No apparent miscibility was detected between the chitosan and Kollicoat SR30D, regardless of the film composition. The films were found to be susceptible to digestion by bacterial or beta-glucosidase enzymes in simulated colonic fluid (SCF). The SCF with rat cecal bacterial enzymes had a more profound hydrolytic activity than that with beta-glucosidase enzyme for the digestion of chitosan within the mixed films. Overall, the results indicated that such chitosan/Kollicoat SR30D films had potential as a coating system for drug delivery to the colon. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:266 / 274
页数:9
相关论文
共 45 条
[1]   PERMEABILITY AND BLOOD COMPATIBILITY PROPERTIES OF CHITOSAN-POLY(ETHYLENE OXIDE) BLEND MEMBRANES FOR HEMODIALYSIS [J].
AMIJI, MM .
BIOMATERIALS, 1995, 16 (08) :593-599
[2]  
AURORA J., 2006, EUR GASTRO REV, V1-6, P2006
[3]   Advances in colonic drug delivery [J].
Basit, AW .
DRUGS, 2005, 65 (14) :1991-2007
[4]   PERMEABILITY OF PROGESTERONE AND A SYNTHETIC PROGESTIN THROUGH METHACRYLIC FILMS [J].
BLANCHON, S ;
COUARRAZE, G ;
RIEGFALSON, F ;
COHEN, G ;
PUISIEUX, F .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1991, 72 (01) :1-10
[5]   MECHANICAL-PROPERTIES OF DRY AND WET CELLULOSIC AND ACRYLIC FILMS PREPARED FROM AQUEOUS COLLOIDAL POLYMER DISPERSIONS USED IN THE COATING OF SOLID DOSAGE FORMS [J].
BODMEIER, R ;
PAERATAKUL, O .
PHARMACEUTICAL RESEARCH, 1994, 11 (06) :882-888
[6]  
Chourasia MK, 2003, J PHARM PHARM SCI, V6, P33
[7]   Physicochemical and release properties of pellets coated with Kollicoat® SR 30 D, a new aqueous polyvinyl acetate dispersion for extended release [J].
Dashevsky, A ;
Wagner, K ;
Kolter, K ;
Bodmeier, R .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 290 (1-2) :15-23
[8]  
DASHEVSKY A, 2000, AAPS ANN M S, V2
[9]   Dissolution of pH responsive formulations in media resembling intestinal fluids:: bicarbonate versus phosphate buffers [J].
Fadda, HM ;
Basit, AW .
JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2005, 15 (04) :273-279
[10]   Characterization of coating systems [J].
Felton L.A. .
AAPS PharmSciTech, 8 (4)