Roy Pallab, Shahiwala Aliasgar
Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research - Ahmedabad, C/o B.V. Patel Pharmaceutical Education and Research Development (PERD) Centre, Sarkhej-Gandhinagar Highway, Thaltej, Gujarat, India.
Eur J Pharm Sci. 2009 Jun 28;37(3-4):363-9. doi: 10.1016/j.ejps.2009.03.006. Epub 2009 Mar 24.
Present work conceptualizes a specific technology, based on combining floating and pulsatile principles to develop drug delivery system, intended for chronotherapy in nocturnal acid breakthrough. This approach will be achieved by using a programmed delivery of ranitidine hydrochloride from a floating tablet with time-lagged coating. In this study, investigation of the functionality of the outer polymer coating to predict lag time and drug release was statistically analyzed using the response surface methodology (RSM). RSM was employed for designing of the experiment, generation of mathematical models and optimization study. The chosen independent variables, i.e. percentage weight ratios of ethyl cellulose to hydroxypropyl methyl cellulose in the coating formulation and coating level (% weight gain) were optimized with a 3(2) full factorial design. Lag time prior to drug release and cumulative percentage drug release in 7h were selected as responses. Results revealed that both, the coating composition and coating level, are significant factors affecting drug release profile. A second-order polynomial equation fitted to the data was used to predict the responses in the optimal region. The optimized formulation prepared according to computer-determined levels provided a release profile, which was close to the predicted values. The proposed mathematical model is found to be robust and accurate for optimization of time-lagged coating formulations for programmable pulsatile release of ranitidine hydrochloride, consistent with the demands of nocturnal acid breakthrough.
目前的工作基于将漂浮和脉动原理相结合,概念化了一种特定技术,用于开发药物递送系统,旨在用于夜间酸突破的时间疗法。这种方法将通过从具有时滞包衣的漂浮片剂中进行盐酸雷尼替丁的程序化递送来实现。在本研究中,使用响应面法(RSM)对外部聚合物包衣的功能进行了研究,以预测滞后时间和药物释放,并进行了统计分析。RSM用于实验设计、数学模型的生成和优化研究。采用3(2)全因子设计对选定的自变量,即包衣配方中乙基纤维素与羟丙基甲基纤维素的重量百分比和包衣水平(增重百分比)进行优化。选择药物释放前的滞后时间和7小时内的药物累积释放百分比作为响应指标。结果表明,包衣组成和包衣水平都是影响药物释放曲线的重要因素。将拟合数据的二阶多项式方程用于预测最佳区域内的响应。根据计算机确定的水平制备的优化制剂提供了与预测值接近的释放曲线。发现所提出的数学模型对于优化用于盐酸雷尼替丁可编程脉动释放的时滞包衣制剂是稳健且准确的,符合夜间酸突破的要求。