Mixed polymer coating for modified release from coated spheroids

被引:7
作者
Tan, YTF [1 ]
Heng, PWS
Wan, LSC
机构
[1] Univ Sci Malaysia, Sch Pharmaceut Sci, Minden 11800, Penang, Malaysia
[2] Natl Univ Singapore, Dept Pharm, Singapore 119260, Singapore
关键词
drug release kinetics; hydroxypropylmethylcellulose; mixed polymer coating; modified release; sodium carboxymethylcellulose; spheroid;
D O I
10.1081/PDT-100101395
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Modified-release drug spheroids coated with an aqueous mixture of high-viscosity hydroxypropylmethylcellulose (HPMC) and sodium carboxymethylcellulose (NaCMC) were formulated. The preparation of core drug spheroids and the coating procedures were performed using the rotary processor and a bottom-spray fluidized bed, respectively. Dissolution studies indicated that incorporation of suitable additives, such as poly(vinylpyrrolidone) (PVP) and poly(ethylene glycol) 400 (PEG) improved the flexibility and integrity of the coat layer by retarding the drug release. An increase in coating levels applied generally retarded the release rate of the drug. However the ratio of HPMC to NaCMC in the mixed, plasticized polymeric coat played a more dominant role in determining the dissolution T-50% values. The optimal ratio of HPMC to NaCMC for prolonged drug release was found to be 3:1, whereas an increase in the amount of NaCMC in the mixed polymer coat only increased drug release. The synergistic viscosity effect of HPMC and NaCMC in retarding drug release rate was greater in distilled water than in dissolution media of pH 1 and 7.2. Cross-sectional view of the scanning electron micrograph showed that all of the coated spheroids exhibited a well-fused continuous, and distinct layer of coating film. The drug release kinetics followed a biexponential first-order kinetic model.
引用
收藏
页码:561 / 570
页数:10
相关论文
共 16 条
[1]  
ALDERMAN D A, 1984, International Journal of Pharmaceutical Technology and Product Manufacture, V5, P1
[2]  
[Anonymous], 1988, Nonlinear regression analysis and its applications
[3]   INFLUENCE OF SURFACTANTS ON DRUG RELEASE FROM HYDROXYPROPYLMETHYLCELLULOSE MATRICES [J].
FEELY, LC ;
DAVIS, SS .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1988, 41 (1-2) :83-90
[4]   ORAL DELAYED-RELEASE SYSTEM FOR COLONIC SPECIFIC DELIVERY [J].
GAZZANIGA, A ;
IAMARTINO, P ;
MAFFIONE, G ;
SANGALLI, ME .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1994, 108 (01) :77-83
[5]  
HARRIS M.R., 1989, AQUEOUS POLYM COATIN, P63
[6]   Optimization of spheroid production by centrifugal rotary processing [J].
Heng, PWS ;
Wan, LSC ;
Tan, YTF .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1996, 143 (01) :107-112
[7]   BI-EXPONENTIAL 1ST-ORDER RELEASE KINETICS OF INDOMETHACIN FROM TABLETS CONTAINING POLYSORBATE-80 [J].
LAAKSO, R ;
KRISTOFFERSSON, E ;
MARVOLA, M .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1984, 19 (01) :35-42
[8]  
LAAKSO R, 1984, ACTA PHARM FENN, V93, P119
[9]   HIGH-VISCOSITY HPMC AS A FILM-COATING AGENT [J].
MAFFIONE, G ;
IAMARTINO, P ;
GUGLIELMINI, G ;
GAZZANIGA, A .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1993, 19 (16) :2043-2053
[10]   CONTROLLED RELEASE INDOMETHACIN MICROSPHERES PREPARED BY USING AN EMULSION SOLVENT-DIFFUSION TECHNIQUE [J].
MALAMATARIS, S ;
AVGERINOS, A .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1990, 62 (2-3) :105-111