The physical and chemical stability of suspensions of sustained-release diclofenac microspheres

被引:10
作者
Lewis, L
Boni, RL [1 ]
Adeyeye, CM
机构
[1] Duquesne Univ, Grad Sch Pharmaceut Sci, Pittsburgh, PA 15282 USA
[2] Univ Wisconsin, Sch Pharm, Madison, WI 53706 USA
关键词
diclofenac; microspheres; sustained-release; suspension; stability;
D O I
10.3109/02652049809008240
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The major challenge in liquid sustained-release oral suspensions is to minimize drug diffusion into the suspending medium and to retain the original properties of the microparticles during storage. Diclofenac wax microspheres prepared by the hydrophobic congealable disperse phase method were formulated as a sustained release suspension and stored at three different temperatures (25, 37 and 45 degrees C) for 3 months, to evaluate the physical and chemical stability of the suspended microspheres. Suspensions of microspheres stored at ambient temperatures were both physically and chemically stable, but at higher temperatures, up to 45 degrees C, there was a decrease in drug release due to scaling and melting on the microsphere surface as observed by scanning electron microscopy. However, on prolonged storage, up to 90 days, especially at 45 degrees C, temperature became a dominant factor causing an increase in drug release. The suspension of diclofenac microspheres was chemically stable for 3 months, while the plain drug suspension exhibited slight degradation.
引用
收藏
页码:555 / 567
页数:13
相关论文
共 10 条
[1]   Chemical, dissolution stability and microscopic evaluation of suspensions of ibuprofen and sustained release ibuprofen-wax microspheres [J].
Adeyeye, CM ;
Price, JC .
JOURNAL OF MICROENCAPSULATION, 1997, 14 (03) :357-377
[2]   DEVELOPMENT AND EVALUATION OF SUSTAINED-RELEASE IBUPROFEN-WAX MICROSPHERES .1. EFFECT OF FORMULATION VARIABLES ON PHYSICAL CHARACTERISTICS [J].
ADEYEYE, CM ;
PRICE, JC .
PHARMACEUTICAL RESEARCH, 1991, 8 (11) :1377-1383
[3]  
Chang R K., 1992, PHARM TECHNOL, V16, P134
[5]   A SPECIFIC STABILITY INDICATING HPLC METHOD TO DETERMINE DICLOFENAC SODIUM IN RAW-MATERIALS AND PHARMACEUTICAL SOLID DOSAGE FORMS [J].
KUBALA, T ;
GAMBHIR, B ;
BORST, SI .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1993, 19 (07) :749-757
[6]  
LARSEN C, 1980, Archiv for Pharmaci og Chemi, V8, P100
[7]   Effect of emulsifier blend on the characteristics of sustained release diclofenac microspheres [J].
Lewis, L ;
Boni, R ;
Adeyeye, CM .
JOURNAL OF MICROENCAPSULATION, 1998, 15 (03) :283-298
[9]  
RANI KNS, 1993, INDIAN J PHARM SCI, V56, P45
[10]   HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC DETERMINATION OF DICLOFENAC SODIUM FROM PHARMACEUTICAL PREPARATION [J].
SANE, RT ;
SAMANT, RS ;
NAYAK, VG .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1987, 13 (07) :1307-1314