INFLUENCE OF METHOD OF PREPARATION ON INCLUSION COMPLEXES OF NAPROXEN WITH DIFFERENT CYCLODEXTRINS

被引:79
作者
BLANCO, J
VILAJATO, JL
OTERO, F
ANGUIANO, S
机构
[1] Departamento de Farmacologia, Farmacia y Tecnologia Farmacéutica Laboratorio de Farmacia Galénica, Facultad de Farmacia, Santiago de Compostela
关键词
D O I
10.3109/03639049109040831
中图分类号
R914 [药物化学];
学科分类号
100701 [药物化学];
摘要
The aim of this study is to increase the solubility of naproxen by inclusion complex formation with alpha, beta, gamma, hydroxypropylbeta and dimethylbetacyclodextrin. The apparent stability constants were calculated from the slope and intercept of the AL-solubility diagrams. The solid inclusion complexes of naproxen with cyclodextrins in 1:1 molar ratio were prepared by the kneaded-mix, spray-drying and freeze-drying method. The formation of inclusion complexes in the solid state were confirmed by X-Ray diffractometry I.R. spectroscopy and differential scanning calorimetry. The dissolution rate of naproxen from the inclusion complexes was much more rapid than naproxen alone. The best results were obtained with beta-cyclodextrin inclusion complex prepared by the spray-drying method.
引用
收藏
页码:943 / 957
页数:15
相关论文
共 18 条
[1]
BETTINETTI GP, 1989, FARMACO, V44, P195
[2]
MECHANISM OF DRUG DISSOLUTION RATE ENHANCEMENT FROM BETA-CYCLODEXTRIN-DRUG SYSTEMS [J].
CORRIGAN, OI ;
STANLEY, CT .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1982, 34 (10) :621-626
[3]
Duchene D., 1987, CYCLODEXTRINS THEIR
[4]
Higuchi T., 1965, PHASE SOLUBILITY TEC, V4, P117
[5]
JATO JLV, 1986, ACTA PHARM TECHNOL, V32, P82
[6]
Jones S. P., 1984, ACTA PHARM TECH, V30, P263
[7]
KHAN KA, 1975, J PHARM PHARMACOL, V27, P49
[8]
NAMBU N, 1978, CHEM PHARM BULL, V25, P2952
[9]
OKAMOTO H, 1986, INT J PHARM, V30, P35, DOI 10.1016/0378-5173(86)90133-X
[10]
Szejtli J, 1982, CYCLODEXTRINS THEIR, P142