Gohel M C, Patel M M, Amin A F
Department of Pharmaceutics and Pharmaceutical Technology, L. M. College of Pharmacy, Navrangpura, Ahmedabad, India.
Drug Dev Ind Pharm. 2003 May;29(5):565-74. doi: 10.1081/ddc-120018645.
This article reports the preparation of tartaric acid treated ispaghula husk powder for the development of modified release tablets of diltiazem HCl by adopting direct compression technique and a 32 full factorial design. The modified ispaghula husk powder showed superior swelling and gelling as compared to untreated powder. Addition of compaction augmenting agent such as dicalcium phosphate was found to be essential for obtaining tablets with adequate crushing strength. In order to improve the crushing strength of diltiazem HCl tablets, to modulate drug release pattern, and to obtain similarity of dissolution profiles in distilled water and simulated gastric fluid (pH 1.2), modified guar gum was used along with modified ispaghula husk powder and tartaric acid. A novel composite index, which considers a positive or a negative deviation from an ideal value, was calculated considering percentage drug release in 60, 300, and 540 min as dependent variables for the selection of a most appropriate batch. Polynomial equation and contour plots are presented. The concept of similarity factor (f2) was used to prove similarity of dissolution in water and simulated gastric fluid (pH 1.2).
本文报道了采用直接压片技术和32全因子设计制备酒石酸处理的卵叶车前子壳粉,用于开发盐酸地尔硫卓缓释片。与未处理的粉末相比,改性卵叶车前子壳粉表现出更好的溶胀和胶凝性能。发现添加压实增强剂如磷酸二钙对于获得具有足够抗压强度的片剂至关重要。为了提高盐酸地尔硫卓片的抗压强度、调节药物释放模式并在蒸馏水和模拟胃液(pH 1.2)中获得相似的溶出曲线,将改性瓜尔胶与改性卵叶车前子壳粉和酒石酸一起使用。考虑到60、300和540分钟时的药物释放百分比作为因变量,计算了一个考虑与理想值的正偏差或负偏差的新型复合指数,以选择最合适的批次。给出了多项式方程和等高线图。使用相似因子(f2)的概念来证明在水和模拟胃液(pH 1.2)中溶出的相似性。