Zero-order release of theophylline from a core-in-cup tablet in sequenced simulated gastric and intestinal fluid

被引:5
作者
Danckwerts, MP
van der Watt, JG
Moodley, I
机构
[1] Univ Witwatersrand, Sch Med, Dept Pharm, ZA-2193 Johannesburg, South Africa
[2] Potchefstroom Univ Christian Higher Educ, Sch Pharm, ZA-2520 Potchefstroom, South Africa
关键词
D O I
10.3109/03639049809085601
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Core-in-cup tablets containing theophylline were evaluated for their dissolution characteristics in sequenced simulated gastric fluid (SGF) followed by simulated intestinal fluid (SIF). Core-in-cup tablets containing 10% w/w, 20% w/w, and 30% w/w acacia as binder were evaluated for their effects on the time course of release of theophylline. This was done to optimize a formula that could release theophylline at a zero-order rate of release for 8-16 hr in simulated gastrointestinal fluids. Theophylline was released and dissolved from the core-in-cup tablets at a rate that is more consistent with a zero-order dissolution rate than a first-order dissolution rate in both SIG and SIF. The dissolution rates of theophylline from the 10%, 20%, and 30% acacia core-in-cup tablets were 0.87 mg/min, 0.53 mg/min, and 0.27 mg/min, respectively in SGF, and 0.61 mg/min, 0.30 mg/min, and 0.20 mg/min, respectively in SIF. The results indicate that a concentration of 32% w/w acacia in the core tablet will release theophylline at a rate of 0.14 mg/min in SGF for 2 hr followed by SIF for 10 hr.
引用
收藏
页码:163 / 167
页数:5
相关论文
共 12 条
[1]   A THEORETICAL BASIS FOR A BIOPHARMACEUTIC DRUG CLASSIFICATION - THE CORRELATION OF IN-VITRO DRUG PRODUCT DISSOLUTION AND IN-VIVO BIOAVAILABILITY [J].
AMIDON, GL ;
LENNERNAS, H ;
SHAH, VP ;
CRISON, JR .
PHARMACEUTICAL RESEARCH, 1995, 12 (03) :413-420
[2]   A NOVEL-APPROACH TO THE ORAL DELIVERY OF MICRO-PARTICLES OR NANOPARTICLES [J].
BODMEIER, R ;
CHEN, HG ;
PAERATAKUL, O .
PHARMACEUTICAL RESEARCH, 1989, 6 (05) :413-417
[3]   SPHERICAL AGGLOMERATES OF WATER-INSOLUBLE DRUGS [J].
BODMEIER, R ;
PAERATAKUL, O .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1989, 78 (11) :964-967
[4]   The effect of processing variables on the release of ibuprofen and caffeine from controlled-release nonswellable core-in-cup compressed tablets [J].
Danckwerts, MP ;
vanderWatt, JG ;
Moodley, I .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1996, 22 (07) :681-687
[5]   THE EFFECT OF PROCESSING VARIABLES ON THE COMPRESSION PROPERTIES OF CONTROLLED-RELEASE CORE-IN-CUP COMPRESSED TABLETS FROM A NEW ADJUSTABLE PUNCH [J].
DANCKWERTS, MP ;
VANDERWATT, JG .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1995, 123 (01) :85-94
[6]   IMPORTANCE OF DRUG TYPE, TABLET SHAPE AND ADDED DILUENTS ON DRUG RELEASE KINETICS FROM HYDROXYPROPYLMETHYLCELLULOSE MATRIX TABLETS [J].
FORD, JL ;
RUBINSTEIN, MH ;
MCCAUL, F ;
HOGAN, JE ;
EDGAR, PJ .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1987, 40 (03) :223-234
[7]  
Korsmeyer R. W., 1983, INT J PHARMACEUT, V15, P23, DOI DOI 10.1016/0378-5173(83)90064-9
[8]   CALCIUM ALGINATE BEADS AS CORE CARRIERS OF 5-AMINOSALICYLIC ACID [J].
LIN, SY ;
AYRES, JW .
PHARMACEUTICAL RESEARCH, 1992, 9 (09) :1128-1131
[9]   TOPOGRAPHICAL DISSOLUTION CHARACTERIZATION FOR CONTROLLED RELEASE PRODUCTS - A NEW TECHNIQUE [J].
SKELLY, JP ;
YAMAMOTO, LA ;
SHAH, VP ;
YAU, MK ;
BARR, WH .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1986, 12 (8-9) :1159-1175
[10]   INVITRO TOPOGRAPHICAL CHARACTERIZATION AS A PREDICTOR OF INVIVO CONTROLLED RELEASE QUINIDINE GLUCONATE BIOAVAILABILITY [J].
SKELLY, JP ;
YAU, MK ;
ELKINS, JS ;
YAMAMOTO, LA ;
SHAH, VP ;
BARR, WH .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1986, 12 (8-9) :1177-1201