Solid dispersion of ketoprofen in pellets

被引:48
作者
Jachowicz, R
Nürnberg, E
Pieszczek, B
Kluczykowska, B
Maciejewska, A
机构
[1] Jagiellonian Univ, Coll Med, Dept Pharmaceut Technol & Biopharmaceut, PL-30688 Krakow, Poland
[2] Univ Erlangen Nurnberg, Dept Pharmaceut Technol, Nurnberg, Germany
关键词
solid dispersion; pellets; ketoprofen; Macrogol; 6000; Geliderm-tensid 3000 (KLHT);
D O I
10.1016/S0378-5173(00)00437-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The formulation of ternary solid dispersions of ketoprofen with Macrogol and kollagen hydrolizate derivative as carriers was elaborated on the basis of the results of the experiments in which different methods of solid dispersion preparation (melting, solvent method, different cooling), different concentrations of drug/carriers and molecular weight of Macrogol were tested. The best solid dispersion consisted of: ketoprofen-Macrogol 6000-KLHT (1 + 8.9 + 0.1) was chosen to formulate the pellets on the basis of the pharmaceutical availability of ketoprofen from solid dispersion and the physical chemical studies: thermomicroscopic, DSC and X-ray diffraction. The pellets were prepared by the extrusion and spheronization method. The mechanical properties of the pellets as well as ketoprofen released from pellets containing solid dispersion, in comparison with physical mixtures and the drug alone, were evaluated. The increase in the amount of released ketoprofen from solid dispersion pellets was 3.8-times greater than from the pellets containing the drug alone. The stability of solid dispersion pellets was satisfactory. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:13 / 21
页数:9
相关论文
共 12 条
[1]   Enhancement of bioavailability of ketoprofen using dry elixir as a novel dosage form [J].
Ahn, HJ ;
Kim, KM ;
Kim, CK .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1998, 24 (07) :697-701
[2]   RELEASE RATES OF KETOPROFEN FROM POLOXAMER GELS IN A MEMBRANELESS DIFFUSION CELL [J].
CHI, SC ;
JUN, HW .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1991, 80 (03) :280-283
[3]   Effect of the formulation parameters on the characteristics of pellets [J].
Fekete, R ;
Zelkó, R ;
Marton, S ;
Rácz, I .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1998, 24 (11) :1073-1076
[4]   Thermal investigation of crystallization of polyethylene glycols in solid dispersions containing oxazepam [J].
Gines, JM ;
Arias, MJ ;
Moyano, JR ;
SanchezSoto, PJ .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1996, 143 (02) :247-253
[5]  
JACHOWICZ R, 1997, P S ART SYST FORM PR, P101
[6]  
MACIEJEWSKA A, 1998, P 2 WORLD M APGI APV, P193
[7]   PHYSICAL CHARACTERISTICS AND DISSOLUTION KINETICS OF SOLID DISPERSIONS OF KETOPROFEN AND POLYETHYLENE-GLYCOL-6000 [J].
MARGARIT, MV ;
RODRIGUEZ, IC ;
CEREZO, A .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1994, 108 (02) :101-107
[8]   Influence of the preparation method on the physicochemical properties of ketoprofen-cyclodextrin binary systems [J].
Mura, P ;
Faucci, MT ;
Parrini, PL ;
Furlanetto, S ;
Pinzauti, S .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 179 (01) :117-128
[9]  
NURNBERG E, 1989, PHARM IND, V51, P1037
[10]  
NURNBERG E, 1999, PHARM TECHN EUR, V11, P41