Synthesis and characterization of dextran esters as coating or matrix systems for oral delivery of drugs targeted to the colon

M. Beesh, P. Majewska, F. Th.
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引用次数: 4

Abstract

Different dextran esters with various degrees of substitution (1, 2 and 3) were synthesized by esterification reaction, with three acid anhydrides: acetic anhydride, propionic anhydride, and butyric anhydride, separately. These modified polysaccharides were characterized by FT-IR, 1H NMR and 13C NMR spectroscopies. Enzymatic degradation of biopolymers by dextranase was also studied. The polymers showing the best degradation profiles were chosen to design blended free films in combination with a polymethacrylate (Eudragit® RS 30D) as a sustained release system for targeting to the colon. These free films were evaluated by permeability of theophylline used as tracer in different in vitro media of the gastro intestinal tract, in presence or in absence of dextranase. From these studies, it was concluded that dextran esters having the lower degree of substitution and constituted of short carbohydrate chains showed the best and significant enzymatic degradation and could be used as a promising carrier for specific colon drug delivery system. Keywords: Colon-Specific Drug Delivery; Polysaccharides; Dextran; Dextranase; Dextran esters; Enzymatic Degradation; Eudragit® RS 30D; Sid-by-side diffusion cell
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葡聚糖酯的合成和表征作为包衣或基质系统的口服给药到结肠
分别与乙酸酐、丙酸酐和丁酸酐进行酯化反应,合成了不同取代度的葡聚糖酯(1、2、3)。通过FT-IR、1H NMR和13C NMR对改性多糖进行了表征。还研究了葡聚糖酶对生物聚合物的酶降解作用。选择具有最佳降解特性的聚合物,设计与聚甲基丙烯酸酯(Eudragit®RS 30D)结合的混合自由膜,作为针对结肠的缓释系统。用茶碱作为示踪剂,在有无葡聚糖酶的情况下,在不同的胃肠道体外培养基中对这些游离膜的渗透性进行了评价。这些研究表明,取代度较低且碳水化合物链较短的葡聚糖酯具有较好的酶解效果,可以作为特定结肠给药系统的载体。关键词:结肠特异性给药;多糖;右旋糖酐;葡聚糖酶;右旋糖酐酯;酶促降解;Eudragit®RS 30D;并排扩散电池
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