Uğurlu Timucin, Karaçiçek Uğur, Rayaman Erkan
Acta Pol Pharm. 2014 Mar-Apr;71(2):311-21.
The purpose of the study was to prepare and evaluate clarithromycin (CLA) floating tablets using experimental mixture design for treatment of Helicobacter pylori provided by prolonged gastric residence time and controlled plasma level. Ten different formulations were generated based on different molecular weight of hypromellose (HPMC K100, K4M, K15M) by using simplex lattice design (a sub-class of mixture design) with Minitab 16 software. Sodium bicarbonate and anhydrous citric acid were used as gas generating agents. Tablets were prepared by wet granulation technique. All of the process variables were fixed. Results of cumulative drug release at 8th h (CDR 8th) were statistically analyzed to get optimized formulation (OF). Optimized formulation, which gave floating lag time lower than 15 s and total floating time more than 10 h, was analyzed and compared with target for CDR 8th (80%). A good agreement was shown between predicted and actual values of CDR 8th with a variation lower than 1%. The activity of clarithromycin contained optimizedformula against H. pylori were quantified using well diffusion agar assay. Diameters of inhibition zones vs. log10 clarithromycin concentrations were plotted in order to obtain a standard curve and clarithromycin activity.
本研究的目的是采用实验混合设计制备并评估克拉霉素(CLA)漂浮片,通过延长胃滞留时间和控制血浆水平来治疗幽门螺杆菌。使用Minitab 16软件,基于不同分子量的羟丙甲纤维素(HPMC K100、K4M、K15M),采用单纯形格子设计(混合设计的一个子类)生成了十种不同的制剂。碳酸氢钠和无水柠檬酸用作产气剂。片剂采用湿法制粒技术制备。所有工艺变量均固定。对第8小时的累积药物释放结果(CDR 8th)进行统计分析以获得优化制剂(OF)。对漂浮滞后时间低于15秒且总漂浮时间超过10小时的优化制剂进行分析,并与第8小时CDR的目标值(80%)进行比较。第8小时CDR的预测值与实际值之间显示出良好的一致性,变化低于1%。使用琼脂扩散法对含优化配方的克拉霉素对幽门螺杆菌的活性进行定量。绘制抑菌圈直径与log10克拉霉素浓度的关系图,以获得标准曲线和克拉霉素活性。