Physicochemical characterization, in vitro dissolution behavior, and pharmacodynamic studies of rofecoxib-cyclodextrin inclusion compounds.: Preparation and properties of rofecoxib hydroxypropyl β-cyclodextrin inclusion complex:: A technical note -: art. no. 14

被引:50
作者
Baboota, S [1 ]
Dhaliwal, M [1 ]
Kohli, K [1 ]
机构
[1] Hamdard Univ, Fac Pharm, Dept Pharmaceut, New Delhi 110062, India
关键词
rofecoxib; HPb-CD; inclusion complexes; in vitro dissolution; anti-inflammatory; ulcerogenic activity;
D O I
10.1208/pt060114
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
[No abstract available]
引用
收藏
页码:E83 / E90
页数:8
相关论文
共 12 条
[1]  
Baboota S, 2003, PHARMAZIE, V58, P73
[2]   Physicochemical characterization and in vitro dissolution behavior of nicardipine-cyclodextrins inclusion compounds [J].
Fernandes, CM ;
Vieira, MT ;
Veiga, FJB .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 15 (01) :79-88
[3]  
Higuchi T., 1965, Interscience, New York, V4, P117
[4]   Cyclodextrin conjugate-based controlled release system: repeated- and prolonged-releases of ketoprofen after oral administration in rats [J].
Kamada, M ;
Hirayama, F ;
Udo, K ;
Yano, H ;
Arima, H ;
Uekama, K .
JOURNAL OF CONTROLLED RELEASE, 2002, 82 (2-3) :407-416
[5]  
Mukne AP, 2004, AAPS PHARMSCITECH, V5
[6]  
Nagarsenker M. S., 1997, INDIAN J PHARM SCI, V59, P174
[7]  
Nalluri Buchi N, 2003, AAPS PharmSciTech, V4, pE2
[8]  
NAMBU N, 1978, CHEM PHARM BULL, V26, P3609
[9]   Meloxicam [J].
Noble, S ;
Balfour, JA .
DRUGS, 1996, 51 (03) :424-430
[10]   Characterization of the Interaction of 2-hydroxypropyl-β-cyclodextrin with itraconazole at pH 2, 4, and 7 [J].
Peeters, J ;
Neeskens, P ;
Tollenaere, JP ;
Van Remoortere, P ;
Brewster, ME .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 91 (06) :1414-1422