Nimesulide-modified gum karaya solid mixtures: Preparation, characterization, and formulation development

被引:12
作者
Babu, GVMM [1 ]
Kumar, NR [1 ]
Himasankar, K [1 ]
Seshasayana, A [1 ]
Murthy, KVR [1 ]
机构
[1] Andhra Univ, Dept Pharmaceut Sci, Div Ind Pharm, Visakhapatnam 530003, Andhra Pradesh, India
关键词
nimesulide; modified gum karaya; dissolution enhancement; solid mixtures;
D O I
10.1081/DDC-120024181
中图分类号
R914 [药物化学];
学科分类号
100701 [药物化学];
摘要
Solid Mixtures of nimesulide (NS) and modified guru karaya (MGK) were prepared to improve the dissolution rate of NS. The effect of drug-carrier ratio on dissolution rate of NS was investigated by preparing the solid Mixtures of different ratios by cogrinding method. Solid mixtures were also prepared by physical mixing, kneading, and solid dispersion techniques to Study the influence of method of preparation. Differential Scanning Calorimetry (DSC), X-ray Diffraction (XRD), and equilibrium solubility Studies were performed to explain the results of in vitro dissolution rate Studies. It was clearly evident from the results that the NS dissolution rate was dependent oil the concentration of MGK in the solid mixtures, and optimum weight ratio was found to be 1:4 (NS:MGK). Though the dissolution rate of NS from all solid mixtures prepared by different methods improved significantly, maximum improvement in dissolution rate was observed with solid dispersions. The order of methods basing on their effect on dissolution efficiency is solid dispersion > kneading > cogrinding > physical mixing > pure NS. Tablets of pure drug and solid mixtures (1:4 w/w, NS:MGK) were prepared. Though the best results from the dissolution test were obtained for the tablets containing solid dispersions, tablets containing cogrinding mixture were found to be suitable, from a practical point of view, for commercialization.
引用
收藏
页码:855 / 864
页数:10
相关论文
共 21 条
[1]
ACATURK F, 1992, INT J PHARM, V85, P1
[2]
Investigation of the triamterene-beta-cyclodextrin system prepared by co-grinding [J].
Arias, MJ ;
Moyano, JR ;
Gines, JM .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1997, 153 (02) :181-189
[3]
Babu GVMM, 2002, INT J PHARM, V234, P1
[4]
Improvement of dissolution of poorly soluble drugs by solid deposition on a super disintegrant .2. The choice of super disintegrants and effect of granulation [J].
Bolhuis, GK ;
Zuurman, K ;
teWierik, GHP .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 1997, 5 (02) :63-69
[5]
Chowdary KP, 2000, INDIAN DRUGS, V37, P299
[6]
NIMESULIDE - AN UPDATE OF ITS PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES, AND THERAPEUTIC EFFICACY [J].
DAVIS, R ;
BROGDEN, RN .
DRUGS, 1994, 48 (03) :431-454
[7]
EGAWA H, 1992, CHEM PHARM BULL, V40, P819
[8]
FORD JL, 1986, PHARM ACTA HELV, V61, P69
[9]
Giunchedi P, 1990, Boll Chim Farm, V129, P17
[10]
Gohel M. C., 2000, Pharmacy and Pharmacology Communications, V6, P433