首页> 外文期刊>Carbohydrate Polymers: Scientific and Technological Aspects of Industrially Important Polysaccharides >pH-sensitive cationic guar gum/poly(acrylic acid)polyelectrolyte hydrogels:Swelling and in vitro drug release
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pH-sensitive cationic guar gum/poly(acrylic acid)polyelectrolyte hydrogels:Swelling and in vitro drug release

机译:pH敏感型阳离子瓜尔胶/聚丙烯酸聚电解质水凝胶:溶胀和体外药物释放

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Novel polyelectrolyte hydrogels(coded as GA)based on cationic guar gum(CGG)and acrylic acid monomer by photoinitiated free-radical polymerization were synthesized with various feed compositions.Fourier transform infrared spectra(FTIR),scanning electron microscopy(SEM),and differential scanning calorimetry(DSC)confirmed that the formation of the polyelectrolyte hydrogels was attributed to the strong electrostatic interaction between cationic groups in CGG and anionic groups in poly(acrylic acid)(PAA).Swelling experiments provided important information on drug diffusion properties,which indicated the GA hydrogels were highly sensitive to pH environments.Potential applications of the hydrogels matrices in controlled drug delivery were also examined.The ketoprofen-loaded CGG/PAA matrices were prepared by hydrogels and directly compressed tablets,respectively.Release behavior of ketoprofen relied on the preparative methods of matrices,ratios of CGG/AA and pH environments.The release mechanism was studied by fitting experimental data to a model equation and calculating the corresponding parameters.The result showed that the kinetics of drug release from the hydrogels in pH 7.4 buffer solution was mainly non-Fickian diffusion.However,for tablets,the drug release in pH 7.4 buffer solution was mainly affected by polymer erosion.The pH of the dissolution medium appeared to have a strong effect on the drug transport mechanism.At more basic pH values,Case II transport was observed,indicating a drug release mechanism highly influenced by macromolec-ular chain relaxation.The ketoprofen release is also tested in the conditions chosen to simulate gastrointestinal tract conditions.The results implied that the GA hydrogels can be exploited as potential carriers for colon-specific drug delivery.
机译:以各种原料为原料,通过光引发的自由基聚合反应合成了基于阳离子瓜尔胶(CGG)和丙烯酸单体的新型聚电解质水凝胶(傅里叶变换红外光谱(FTIR),扫描电子显微镜(SEM)和差示法)扫描量热法(DSC)证实聚电解质水凝胶的形成是由于CGG中的阳离子基团与聚丙烯酸(PAA)中的阴离子基团之间强的静电相互作用。溶胀实验提供了有关药物扩散性质的重要信息,这表明GA水凝胶对pH值环境高度敏感。还研究了水凝胶基质在受控药物输送中的潜在应用。分别由水凝胶和直接压片制备负载酮洛芬的CGG / PAA基质。酮洛芬的释放行为依赖于基质的制备方法,CGG / AA的比值和pH环境。释放机理通过将实验数据拟合到模型方程并计算相应的参数来研究sm。结果表明,在pH 7.4缓冲溶液中从水凝胶释放药物的动力学主要是非菲克扩散。 pH 7.4缓冲溶液主要受聚合物腐蚀的影响。溶出介质的pH值似乎对药物的转运机理有很强的影响。在更碱性的pH值下,观察到了Case II的转运,表明大分子对药物释放机理的影响很大。链松弛:酮洛芬的释放也要在模拟胃肠道的条件下进行测试。结果表明,GA水凝胶可以用作结肠特异性药物递送的潜在载体。

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