Li Hongtao, Gu Xiaochen
Faculty of Pharmacy, University of Manitoba, 50 Sifton Road, Winnipeg, Manitoba, Canada R3T 2N2.
Int J Pharm. 2007 Sep 5;342(1-2):18-25. doi: 10.1016/j.ijpharm.2007.04.024. Epub 2007 May 5.
Texture analysis is a new approach in pharmaceutical research and development; this study evaluated the correlation between drug dissolution and polymer hydration from a modified release matrix tablet of pseudoephedrine hydrochloride using a texture analyzer. A series of matrix tablets of pseudoephedrine was designed and prepared. Modified drug release was achieved by combined use of matrix excipients Polyox WSR301 (PEO) and Compritol 888ATO (GB). Dissolution profiles of the tablets were assessed using USP Method II. Polymer swelling behaviors during dissolution were measured using a texture analyzer. Increase in proportion of PEO and GB in the formulation reduced drug dissolution within the first 90 min. However, drug release was complete in 6h due to high aqueous solubility of pseudoephedrine. Linear correlations were observed among drug dissolution, polymer content and parameters of texture analysis including hydrogel thickness and AUC(TA) for formulations that contained hydrophilic PEO. The study demonstrated a unique application of a texture analyzer in characterization of modified release matrix tablets.
质地分析是药物研发中的一种新方法;本研究使用质地分析仪评估了盐酸伪麻黄碱缓释基质片的药物溶出与聚合物水合之间的相关性。设计并制备了一系列伪麻黄碱基质片。通过联合使用基质辅料聚氧乙烯WSR301(PEO)和Compritol 888ATO(GB)实现了药物的缓释。使用美国药典方法II评估片剂的溶出曲线。使用质地分析仪测量溶出过程中聚合物的溶胀行为。制剂中PEO和GB比例的增加会降低前90分钟内的药物溶出。然而,由于伪麻黄碱的高水溶性,药物在6小时内释放完全。对于含有亲水性PEO的制剂,在药物溶出、聚合物含量与质地分析参数(包括水凝胶厚度和AUC(TA))之间观察到线性相关性。该研究证明了质地分析仪在表征缓释基质片方面的独特应用。