首页> 外文期刊>Der Pharma Chemica: journal for medicinal chemistry, pharmaceutical chemistry and computational chemistry >Synthesis and in vitro evaluation of acrylate-based macromolecular prodrugs containing mesalazine for colon-specific drug delivery
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Synthesis and in vitro evaluation of acrylate-based macromolecular prodrugs containing mesalazine for colon-specific drug delivery

机译:含美沙拉嗪的丙烯酸酯基大分子前药的合成及体外评价

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This work, describes synthesis and in vitro evaluation of new acrylic-type polymeric prodrugs containing mesalazine, as colon targeted drug delivery systems. First, mesalazine reacted with formic acid, and the obtained material was reacted with 2-hydroxypropyl methacrylat in the presence of 1,1-carbonyldiimidazole to produce methacryloyloxypropyl 5-amino salicylate. The resulted acrylic-derivative of mesalazine was then polymerized with various acrylic monomers by free radical solution polymerization, utlizing azobisisobutyronitrile as an initiator at 70±2°C. The obtained polymer-drug conjugates were characterized by FT-IR, 1H-NMR, elemental analysis, gel permeation chromatography, and differential scanning calorimetery techniques. The release studies were performed into dialysis bags by hydrolysis buffered solutions at 37°C. Detection of hydrolysis by UV spectrophotometer at free drug λmax (300 nm for pH 1; 339 nm for pH 7 and 8) in selected intervals showed that the mesalazine can be released by selective hydrolysis of the ester bond at the side of drug moiety. The release profiles indicated that the hydrophobicity of polymers and the pH value of the hydrolysis media have strongly effects on the hydrolytic behavior of the polymeric prodrugs.
机译:这项工作描述了合成和体外评估含美沙拉嗪的新型丙烯酸类聚合物前药,并将其作为结肠靶向药物递送系统。首先,将美沙拉嗪与甲酸反应,将得到的物质在1,1-羰基二咪唑存在下与2-羟丙基甲基丙烯酸酯反应,生成甲基丙烯酸酰氧基丙基5-氨基水杨酸酯。然后通过自由基溶液聚合将所得的美沙拉嗪的丙烯酸衍生物与各种丙烯酸单体聚合,在70±2℃下使用偶氮二异丁腈作为引发剂。通过FT-IR,1 H-NMR,元素分析,凝胶渗透色谱和差示扫描量热技术对所得的聚合物-药物缀合物进行表征。通过在37°C下使用水解缓冲液将释放研究放到透析袋中进行。通过紫外分光光度计在选定的间隔内以游离药物λmax(pH 1为300 nm; pH 7和8为339 nm)检测紫外光水解表明,美沙拉嗪可通过选择性水解药物部分一侧的酯键来释放。释放曲线表明,聚合物的疏水性和水解介质的pH值对聚合物前药的水解行为有强烈影响。

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