Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmacy, Petra University, Amman, Jordan.
Pharm Dev Technol. 2013 Sep-Oct;18(5):1204-12. doi: 10.3109/10837450.2011.620968. Epub 2011 Oct 6.
In the present systematic study, a sustained release of terbutaline sulfate tablet (TBS) was developed and optimized by employing the hydrophilic polymers; chitosan and xanthan gum mixed with sodium bicarbonate as a release modifying agent. This formulation was developed using direct compression technology. In vitro release studies indicated rapid swelling and drug release in the initial period of the acid stage from a matrix composed of chitosan and xanthan gum solely. Addition of sodium bicarbonate to the matrix resulted in sustained drug release. Various formulation factors such as polymer to polymer ratio, polymer viscosity and particle size were altered and their effect on dissolution pattern was illustrated. Manufacturing variables such as compression force and lubricant percentage were investigated and found not to influence the drug release profile of the resulted tablets. The release mechanism follows Korsmeyer-Peppas equation with n value indicating non-Fickian diffusion. The release profiles were analyzed using statistical method (one-way ANOVA) and f2 metric values and found to be similar to the commercial product Bricanyl(®). Reproducible data were obtained when scale-up of the formulation was performed.
在本系统研究中,通过使用亲水性聚合物壳聚糖和黄原胶与碳酸氢钠混合作为释放改性剂,开发并优化了硫酸特布他林片的缓释制剂。该制剂采用直接压片技术制备。体外释放研究表明,在酸性阶段的初始时期,由壳聚糖和黄原胶组成的基质会迅速溶胀并释放药物。向基质中添加碳酸氢钠可实现药物的持续释放。改变各种制剂因素,如聚合物与聚合物的比例、聚合物的黏度和粒径,并说明了它们对溶解模式的影响。考察了压片力和润滑剂百分比等制造变量,发现它们不影响所得片剂的药物释放曲线。释放机制符合 Korsmeyer-Peppas 方程,n 值表示非 Fickian 扩散。使用统计方法(单因素方差分析)和 f2 度量值对释放曲线进行分析,发现与商业产品 Bricanyl(®)相似。当对制剂进行放大时,可获得重现性数据。