The potential use of mixed films of pectin, chitosan and HPMC for bimodal drug release

被引:95
作者
Macleod, GS [1 ]
Collett, JH [1 ]
Fell, JT [1 ]
机构
[1] Univ Manchester, Sch Pharm & Pharmaceut Sci, Manchester M13 9PL, Lancs, England
关键词
polyelectrolyte complex (PEC); pectin USP; chitosan; viscosity;
D O I
10.1016/S0168-3659(98)00168-0
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polyelectrolyte complex (PEC) formation between pectin USP and chitosan was investigated by examining the viscosities of supernatant solutions after removal of the precipitated complex. The amount of pectin, relative to chitosan, required for optimal PEC formation increased as the pH of the solution was reduced. At pH values of less than 1.3, there was no evidence for the formation of the PEG. Swelling studies conducted on pectin/chitosan films, showed minimal swelling occurring when the pectin:chitosan weight ratio was optimal for PEC formation, suggesting the formation of the PEC in situ. The permeability of the films to paracetamol as a model compound was dependent on film composition and was markedly increased after exposure to pectinolytic enzymes, used to mimic conditions in the colon. It may be implied from the results that similar formulations, applied as a film coat to tablets, could be used to achieve bimodal drug release with colonic conditions acting as a trigger for an increased rate of release. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:303 / 310
页数:8
相关论文
共 23 条
[1]   STUDY OF THE STOICHIOMETRIC POLYELECTROLYTE COMPLEX BETWEEN CHITOSAN AND CARBOXYMETHYL CELLULOSE [J].
ARGUELLESMONAL, W ;
GARCIGA, M ;
PENICHECOVAS, C .
POLYMER BULLETIN, 1990, 23 (03) :307-313
[2]   AN EVALUATION OF PECTIN AS A CARRIER FOR DRUG TARGETING TO THE COLON [J].
ASHFORD, M ;
FELL, J ;
ATTWOOD, D ;
SHARMA, H ;
WOODHEAD, P .
JOURNAL OF CONTROLLED RELEASE, 1993, 26 (03) :213-220
[3]   STUDIES ON PECTIN FORMULATIONS FOR COLONIC DRUG-DELIVERY [J].
ASHFORD, M ;
FELL, J ;
ATTWOOD, D ;
SHARMA, H ;
WOODHEAD, P .
JOURNAL OF CONTROLLED RELEASE, 1994, 30 (03) :225-232
[4]  
CHEVASIT V, 1988, POLYM B, V19, P223
[5]   MEASUREMENT OF GASTROINTESTINAL PH PROFILES IN NORMAL AMBULANT HUMAN-SUBJECTS [J].
EVANS, DF ;
PYE, G ;
BRAMLEY, R ;
CLARK, AG ;
DYSON, TJ ;
HARDCASTLE, JD .
GUT, 1988, 29 (08) :1035-1041
[6]  
MAGGI L, 1996, P 16 PAHRM TECH C, V2, P38
[7]   EFFECT OF INTERPOLYMER COMPLEX-FORMATION OF CHITOSAN WITH PECTIN OR ACACIA ON THE RELEASE BEHAVIOR OF CHLORPROMAZINE HCL [J].
MESHALI, MM ;
GABR, KE .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1993, 89 (03) :177-181
[8]   Amylose as a coating for drug delivery to the colon: Preparation and in vitro evaluation using 5-aminosalicylic acid pellets [J].
Milojevic, S ;
Newton, JM ;
Cummings, JH ;
Gibson, GR ;
Botham, RL ;
Ring, SG ;
Stockham, M ;
Allwood, C .
JOURNAL OF CONTROLLED RELEASE, 1996, 38 (01) :75-84
[9]   Amylose as a coating for drug delivery to the colon: Preparation and in vitro evaluation using glucose pellets [J].
Milojevic, S ;
Newton, JM ;
Cummings, JH ;
Gibson, GR ;
Botham, RL ;
Ring, SG ;
Stockham, M ;
Allwood, MC .
JOURNAL OF CONTROLLED RELEASE, 1996, 38 (01) :85-94
[10]   THE INFLUENCE OF SUBSTITUTION TYPE ON THE PERFORMANCE OF METHYLCELLULOSE AND HYDROXYPROPYLMETHYCELLULOSE IN GELS AND MATRICES [J].
MITCHELL, K ;
FORD, JL ;
ARMSTRONG, DJ ;
ELLIOTT, PNC ;
HOGAN, JE ;
ROSTRON, C .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1993, 100 (1-3) :143-154