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首页> 外文期刊>International Journal of Pharmaceutical and Life Sciences >Synergistic Effects of Disintegrants on Release of poorly Water soluble drug
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Synergistic Effects of Disintegrants on Release of poorly Water soluble drug

机译:崩解剂对水溶性差的药物释放的协同作用

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We have done research work in lab to find out proper formulation of immediate release tablet by using of various types of disintegrants (crospovidone, sodium starch glycolate and sodium carboxymethylcellulose), in order to examine the effect of mode of absorption of disintegrants on release mechanism from tablets. Acetaminophen, a poor soluble drug was used as a model drug to estimate its release pattern from different formulations. The USP paddle method was selected to perform the dissolution profiles carried out by USP apparatus 2 (paddle) at 50 rpm in 900 ml phosphate buffer pH 5.8. Successive dissolution time, time required for 25%, 50% and 80% of the drug release (T 25 %, T 50 %, T 80 %) was used to evaluate the dissolution results. A One way analysis of variance (ANOVA) was used to recognize the result. Statistically significant differences were found among the drug release profile from all the formulations except mode of addition of crosspovidone. At a fixed amount of disintegrants, extragranular mode of addition seemed to be the best mode of incorporation. The best release was achieved with the sodium carboxymethylcellulose and sodium starch glycolate containing formulations. The T 50 and T 80 values were analytical of the fact that the drug release was faster from tablet formulations containing carboxymethylcellulose and sodium starch glycolate. The drug release was very much negligible difference by the mode of crospovidone addition. Two formulations found very small T 50 and T 80 values indicating very much faster release. From the all formulations corresponded extragranular mode of addition could be the best mode of incorporation. The drug release was unaffected by the mode of crospovidone addition. The mode of incorporation of disintegrants suggested enchancing the release of poor soluble drugs. DOI: http://dx.doi.org/10.3329/ijpls.v1i3.12979 International Journal of Pharmaceutical and Life Sciences Vol.1(3) 2012
机译:我们已经在实验室进行了研究工作,试图通过使用各种崩解剂(交聚维酮,淀粉羟乙酸钠和羧甲基纤维素钠)来找出速释片剂的正确制剂,从而研究崩解剂的吸收方式对从片剂中释放机理的影响。平板电脑。对乙酰氨基酚,一种难溶的药物被用作模型药物,以估计其从不同制剂中的释放模式。选择USP桨式方法以执行USP装置2(桨式)在900毫升磷酸盐缓冲液pH 5.8中以50 rpm进行的溶出曲线。连续的溶出时间,即25%,50%和80%的药物释放所需的时间(T 25%,T 50%,T 80%)用于评估溶出结果。方差的单向分析(ANOVA)用于识别结果。在所有制剂的药物释放曲线之间发现了统计学上的显着差异,除了交叉维维酮的添加方式。在固定量的崩解剂下,颗粒外添加方式似乎是最佳的掺入方式。含羧甲基纤维素钠和羟乙酸淀粉钠的配方实现了最佳释放。 T 50和T 80值分析了以下事实:从含有羧甲基纤维素和淀粉羟乙酸钠的片剂中,药物释放更快。 crospovidone添加方式的药物释放差异几乎可以忽略不计。两种配方的T 50和T 80值非常小,表明释放速度非常快。从所有配方中,相应的颗粒外添加方式可能是最佳的掺入方式。 crospovidone添加方式不会影响药物的释放。崩解剂的掺入方式建议增加难溶药物的释放。 DOI:http://dx.doi.org/10.3329/ijpls.v1i3.12979国际药学与生命科学杂志Vol.1(3)2012

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