Multiunit controlled-release diclofenac sodium capsules using complex of chitosan with sodium alginate or pectin

被引:38
作者
Mitrevej, A [1 ]
Sinchaipanid, N [1 ]
Rungvejhavuttivittaya, Y [1 ]
Kositchaiyong, V [1 ]
机构
[1] Mahidol Univ, Dept Mfg Pharm, Fac Pharm, Bangkok 10400, Thailand
关键词
chitosan; controlled release; diclofenac sodium; pectin; sodium alginate;
D O I
10.1081/PDT-100002247
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study explored the application of chitosan-alginate (CA) and chitosan-pectin (CP) complex films as drug release regulator for the preparation of multiunit controlled-release diclofenac sodium capsules. Pellets containing drug and microcrystalline cellulose, in a ratio of 3:5, were prepared in a fluidized rotary granulator The pellets were coated with CA, CP sodium alginate, pectin, and chitosan solutions. The pellets, equivalent to 75 mg drug, were filled into capsules. After 2 h of dissolution test in acidic medium, the amount of the drug released from any preparation was negligible. The pellets were further subject to PH 6.8 phosphate buffer More than 80% drug release at 12 h was observed with the uncoated pellets and those coated with sodium alginate, pectin or chitosan. Both 1% CA and 3% CP coated pellets exhibited drug release profiles similar to that of Voltaren SR75. It was found that approximately 60% and 85% of the drug were released at 12 and 24 h, respectively. Both Differential thermal analysis (DTA) and Fourier transform infrared spectroscopy (FTIR) analyses revealed complex formation between chitosan and these anionic polymers. It could be concluded that CA and CP complex film could be easily applied to diclofenac sodium pellets to control the release of the drug.
引用
收藏
页码:385 / 392
页数:8
相关论文
共 14 条
[1]  
Adeyeye C.M., 1990, Analytical Profiles of Drug Substances, P123
[2]   CONTROLLED-RELEASE MULTIPLE-UNITS AND SINGLE-UNIT DOSES - LITERATURE-REVIEW [J].
BECHGAARD, H ;
NIELSEN, GH .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1978, 4 (01) :53-67
[3]   EFFECTS OF CORE COMPONENTS ON INDOMETHACIN RELEASE FROM FILM-COATED GRANULES [J].
LAAKSO, R ;
EERIKAINEN, S .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1991, 67 (01) :79-88
[4]   Controlled release of interleukin-2 for tumour immunotherapy using alginate/chitosan porous microspheres [J].
Liu, LS ;
Liu, SQ ;
Ng, SY ;
Froix, M ;
Ohno, T ;
Heller, J .
JOURNAL OF CONTROLLED RELEASE, 1997, 43 (01) :65-74
[5]   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
[6]   DRUG-RELEASE FROM ORAL MUCOSAL ADHESIVE TABLETS OF CHITOSAN AND SODIUM ALGINATE [J].
MIYAZAKI, S ;
NAKAYAMA, A ;
ODA, M ;
TAKADA, M ;
ATTWOOD, D .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1995, 118 (02) :257-263
[7]   PREPARATION OF CHITOSAN-REINFORCED ALGINATE GEL BEADS - EFFECTS OF CHITOSAN ON GEL MATRIX EROSION [J].
MURATA, Y ;
MAEDA, T ;
MIYAMOTO, E ;
KAWASHIMA, S .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1993, 96 (1-3) :139-145
[8]   Additive effect of chondroitin sulfate and chitosan on drug release from calcium-induced alginate gel beads [J].
Murata, Y ;
Miyamoto, E ;
Kawashima, S .
JOURNAL OF CONTROLLED RELEASE, 1996, 38 (2-3) :101-108
[9]   THE INFLUENCE OF 4 SELECTED PROCESSING AND FORMULATION FACTORS ON THE PRODUCTION OF SPHERES BY EXTRUSION AND SPHERONIZATION [J].
PINTO, JF ;
BUCKTON, G ;
NEWTON, JM .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1992, 83 (1-3) :187-196
[10]  
Sandford P., 1984, CHITIN CHITOSAN RELA, P51