Jeevanandham S, Sekar M, Dhachinamoorthi D, Muthukumaran M, Sriram N, Joysaruby J
Department of Pharmaceutics, Santhiram College of Pharmacy, Andhra Pradesh, India.
J Young Pharm. 2010 Jan;2(1):15-20. doi: 10.4103/0975-1483.62207.
This study examines the sustained release behavior of both water-soluble (acetaminophen, caffeine, theophylline and salicylic acid) and water-insoluble (indomethacin) drugs from Leucaena leucocephala seed Gum isolated from Leucaena leucocephala kernel powder. It further investigates the effect of incorporation of diluents like microcrystalline cellulose and lactose on release of caffeine and partial cross-linking of the gum (polysaccharide) on release of acetaminophen. Applying exponential equation, the mechanism of release of soluble drugs was found to be anomalous. The insoluble drug showed near case II or zero-order release mechanism. The rate of release was in the decreasing order of caffeine, acetaminophen, theophylline, salicylic acid and indomethacin. An increase in release kinetics of drug was observed on blending with diluents. However, the rate of release varied with type and amount of blend in the matrix. The mechanism of release due to effect of diluents was found to be anomalous. The rate of release of drug decreased on partial cross-linking and the mechanism of release was found to be super case II.
本研究考察了从银合欢籽仁粉中分离得到的银合欢籽胶对水溶性药物(对乙酰氨基酚、咖啡因、茶碱和水杨酸)和水不溶性药物(吲哚美辛)的缓释行为。进一步研究了加入微晶纤维素和乳糖等稀释剂对咖啡因释放的影响,以及胶(多糖)的部分交联对乙酰氨基酚释放的影响。应用指数方程,发现可溶性药物的释放机制为非正规扩散。不溶性药物表现出近似Ⅱ型或零级释放机制。释放速率由高到低依次为咖啡因、对乙酰氨基酚、茶碱、水杨酸和吲哚美辛。与稀释剂混合时,药物释放动力学增加。然而,释放速率随基质中混合物的类型和用量而变化。发现由于稀释剂作用导致的释放机制为非正规扩散。药物的释放速率在部分交联时降低,且释放机制为超Ⅱ型。