DEVELOPMENT OF ORAL LIQUID DOSAGE FORMS OF ACETAZOLAMIDE

被引:17
作者
PARASRAMPURIA, J [1 ]
DASGUPTA, V [1 ]
机构
[1] UNIV HOUSTON,DEPT PHARMACEUT,HOUSTON,TX 77030
关键词
D O I
10.1002/jps.2600790919
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Two oral liquid dosage forms of acetazolamide have been developed. Using the solubility profiles, polyethylene glycol 400 (7%, v/v) was used as the solubilizing agent and propylene glycol (53%, v/v) as the cosolvent to keep acetazolamide in solution. Because of the bitter taste of acetazolamide, sweetening agents (simple syrup, sorbitol solution, and artificial sweeteners) and flavors (raspberry, sweet, and menthol) were added to the final formulations. A buffer (either phosphate or citrate) solution was used to maintain a pH value of 4 (pH of maximum stability as reported earlier) to minimize hydrolysis. The final dosage forms were stable for at least 90 days at 37 °C (loss of potency of 5%). According to FDA guidelines, a tentative expiry date of 2 years at 25 °C is justifiable. Copyright © 1990 Wiley‐Liss, Inc., A Wiley Company
引用
收藏
页码:835 / 836
页数:2
相关论文
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GUPTA V D, 1987, Drug Development and Industrial Pharmacy, V13, P147, DOI 10.3109/03639048709040161
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[3]  
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