Division of Pharmaceutics, Department of Pharmaceutical Technology, Jadavpur University, Kolkata 700032, India.
Division of Pharmaceutics, Department of Pharmaceutical Technology, Jadavpur University, Kolkata 700032, India.
Int J Biol Macromol. 2014 Jul;68:78-85. doi: 10.1016/j.ijbiomac.2014.04.036. Epub 2014 Apr 24.
The effect of Ca(2+) ion concentration on swelling, erosion, and drug release mechanism of Ca(2+) ion cross-linked carboxymethyl xanthan gum (Ca-CMXG) matrices was investigated. By adding CaCl2 solution, carboxymethyl xanthan gum (CMXG) was converted into Ca-CMXG matrix, which was evaluated for swelling, erosion and drug release in different dissolution media. The amount of Ca(2+) ion alters the viscosity of gel layer formed around the matrices resulting in decreased water penetration into swollen layer. The changes in amount of Ca(2+) ion considerably influenced the swelling and erosion of the matrix leading to different drug release profiles. The simultaneous swelling and erosion of matrices that were controlled by the degree of cross-linking prejudiced the drug release mechanism. The release data fitted well into the Korsmeyer-Peppas equation and the combined effect of diffusion and erosion described the overall drug transport mechanism.
研究了钙离子浓度对钙离子交联羧甲基黄原胶(Ca-CMXG)基质溶胀、侵蚀和药物释放机制的影响。通过添加 CaCl2 溶液,将羧甲基黄原胶(CMXG)转化为 Ca-CMXG 基质,在不同的溶解介质中评估其溶胀、侵蚀和药物释放。钙离子的数量改变了围绕基质形成的凝胶层的粘度,从而减少了水进入溶胀层的渗透。钙离子数量的变化对基质的溶胀和侵蚀有很大影响,导致不同的药物释放曲线。由交联度控制的基质的溶胀和侵蚀的同时发生,影响了药物释放机制。释放数据很好地符合 Korsmeyer-Peppas 方程,扩散和侵蚀的综合作用描述了整体药物传输机制。