双氯灭痛(DC-Na)亲水凝胶骨架片及不溶性骨架片体外均能控制DC-Na释药12h,亲水凝胶骨架片释药机理符合一级动力学,lg(1-F)=0.1865-0.1177t,相关系数r=0.9928,不溶性骨架片释药机理符合Higuchi方程,F=0.3226t?-0.1503,相关系数r=0.9916,释药递质的pH对DC-Na释药速度没有明显影响,转篮转达为50或100r/min释药速度没有明显变化。
Abstract
Diclofenac sodium can be released continuously from hydrophilic and insolublematrices for more than 12 hours in vitro. The mechanism of hydrophilic matrix is first-orderkinetics,lg(1-F)=0.1865-0.1177t,r=-0.9928 and that of insoluble matrix is the square rootkinetics,F=0. 3226t1/2-0.1503,r=0.9916.Medium pH affects significantly the release rate ofDiclofenal sodium, There is no notable effect in stirring rate between 50 and 100 r/min for therelease rate of Diclofenal sodium.
关键词
亲水凝胶骨架片 /
不溶性骨架片 /
双氯灭痛 /
释药机理
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Key words
hydrophilic matrix /
insoluble matrix /
Dlclofenac sodium /
release mechanism
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参考文献
1王尔华.双氯灭痛合成工艺评述.药学进展,1989,13(3) :20.
2Wilis JV,Kendall MJ,Jack DB. The influence of food on the absorption of DC-Na after single and multiple oral doses. Eur J Clin Pharmacol 91979,16 :405.
3Kiess W, Scand. The pharmaceutics of DC-Na in man. J Rheumato,l978,22:17.
4何铭新,杨彦新.感冒通中双氯灭痛含量測定.药物分析杂志,1987,7(1):54.
5Lieberman HA, Lachman L. Pharm Dosage Form, vol 3.edl. New York. Marcel Dekker Ine,1981:160.
6Hguchi T. The mechanism of the drug release fron granules. J Pharm Sci ,1963,52:1145.
7Hatem Fessl,Marty J PjPuist EUXF^et al. Square root of time dependence of matrix formulations with low drug content. J Pharm Sd, 1982,71 (7) * 749.
8Yoshihko Hirotani,Yukio Arakawa9Yoshimi Maeda,et al.Preparation of controlled-release grannies of DC-Na. Chem Pharm 1987,35:3049.
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脚注
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