The effect of polymer coating systems on the preparation, tableting, and dissolution properties of sustained-release drug pellets

被引:12
作者
Li, SP
Feld, KM
Kowarski, CR
机构
[1] DERMIK LABS INC,COLLEGEVILLE,PA 19426
[2] TEMPLE UNIV,SCH PHARM,PHILADELPHIA,PA 19140
关键词
D O I
10.3109/03639049709150762
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The preparation of sustained-release (SR) drug pellets and their tablets was evaluated. Pellets containing indomethacin, pseudoephedrine hydrochloride (P-HCl), or pseudoephedrine (P) base were prepared by spraying a mixture of drug, Eudragit(R) S-100 resins, dibutyl sebacate, and alcohol onto nonpareil seeds via the Wurster-column process. The oven-dried drug/Eudragit S-100 (DS) pellets were coated with different levels of Eudragit RS and Eudragit S-100 acrylic resins. Tablets containing P-HCl or P-base SR pellets, microcrystalline cellulose, and Methocel(R) K4M were compressed. The solubility of the drug entity in the polymer solution was found to be the most critical factor affecting the yield and the physical properties of the resultant DS pellets. Dissolution studies of Eudragit RS coated drug pellets demonstrated that the release profiles depended not only on the physicochemical properties of the drug, particularly aqueous solubility, but also on the coating levels. The release rate profiles of the matrix tablets can be modified by varying the types of P-HCl or P-base SR pellets in the formulation. The release of drug from the matrix tablets is primarily matrix controlled.
引用
收藏
页码:623 / 631
页数:9
相关论文
共 14 条
[1]   COATED PELLETIZED DOSAGE FORM - EFFECT OF COMPACTION ON DRUG RELEASE [J].
BECHARD, SR ;
LEROUX, JC .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1992, 18 (18) :1927-1944
[2]   THE EFFECT OF CURING ON DRUG-RELEASE AND MORPHOLOGICAL PROPERTIES OF ETHYLCELLULOSE PSEUDOLATEX-COATED BEADS [J].
BODMEIER, R ;
PAERATAKUL, O .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1994, 20 (09) :1517-1533
[3]  
CHANG RK, 1991, INT J PHARM, V70, P261
[4]  
FORD JL, 1987, INT J PHARM, V40, P233
[5]  
GHEBRESELLASSIS RH, 1987, INT J PHARM, V37, P221
[6]   HYDROXYPROPYLMETHYLCELLULOSE SUSTAINED-RELEASE TECHNOLOGY [J].
HOGAN, JE .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1989, 15 (6-7) :975-999
[7]  
LAAKSO R, 1985, ACTA PHARM FENN, V94, P9
[8]   PREPARATION OF A CONTROLLED-RELEASE DRUG-DELIVERY SYSTEM OF INDOMETHACIN [J].
LI, SP ;
FELD, KM ;
KOWARSKI, CR .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1994, 20 (07) :1121-1145
[9]  
LI SP, 1991, DRUG DEV IND PHARM, V17, P1655
[10]  
LI SP, 1989, DRUG DEV IND PHARM, V15, P1131