Gupta College of Technological Sciences, Ashram More, G.T. Road, Asansol 713301, West Bengal, India.
Gupta College of Technological Sciences, Ashram More, G.T. Road, Asansol 713301, West Bengal, India.
Int J Biol Macromol. 2017 Oct;103:347-354. doi: 10.1016/j.ijbiomac.2017.04.059. Epub 2017 Apr 27.
Gum Ghatti (GG) is a water soluble complex polysaccharide obtained from Anogeissus latifolia. Due to its non toxic and excellent emulsifying characteristics, it was widely used in different pharmaceutical preparations. Currently another facet was explored for its utility as release retardant polymer in oral controlled drug delivery system. As GG solely was incapable of forming microspheres therefore modification of GG to Sodium carboxymethyl (NaCMGG) derivative was done by carboxymethylation process and its gel forming capacity was explored by the use of trivalent cation (Aluminium chloride) which results into complete microbead system in a complete aqueous environment for controlled delivery of Ropinirole Hydrochloride (RHCl). Rheological property of NaCMGG showed pseudoplastic shear thinning behavior. Spherical shape of bead was observed under scanning electron microscope. Depending upon the formulation variables, Drug entrapment efficiency (DEE) varies from 47.66±3.51 % to 71.4±2.65%., and 80 to 90% drug was released in 6h in pH 6.8 phosphate buffer. Drug release was governed by both fickian diffusion and polymer relaxation simultaneously. Compatible environment for drug entrapment was established by Fourier transform infrared (FTIR) spectroscopy and differential scanning calorimetry (DSC). Thus the modified derivative NaCMGG could be a promising polymer in biomedical application.
树胶 Ghatti(GG)是一种水溶性复合多糖,从印楝属植物中提取得到。由于其无毒且具有出色的乳化特性,因此被广泛应用于各种药物制剂中。目前,人们又探索了其在口服控释药物传递系统中作为缓释聚合物的用途。由于 GG 本身不能形成微球,因此通过羧甲基化过程对 GG 进行改性,制备出羧甲基化 GG(NaCMGG)衍生物,并利用三价阳离子(氯化铝)探索其凝胶形成能力,在完全水性环境中形成完整的微球体系,以实现盐酸罗匹尼罗(RHCl)的控释。NaCMGG 的流变特性表现出假塑性剪切变稀行为。扫描电子显微镜下观察到微球呈球形。根据配方变量,药物包封效率(DEE)在 47.66±3.51%至 71.4±2.65%之间变化,在 pH6.8 磷酸盐缓冲液中 80%至 90%的药物在 6 小时内释放。药物释放同时受到菲克扩散和聚合物松弛的控制。傅里叶变换红外(FTIR)光谱和差示扫描量热法(DSC)证明了药物包封的环境具有相容性。因此,改性衍生物 NaCMGG 可能成为生物医学应用中有前途的聚合物。