Bartil Tahar, Bounekhel Mahmoud, Cedric Calberg, Jeerome Robert
Département de génie des procédés Faculté des sciences de l'ingénieur, Université ferhat Abbas, SETIF (19000), Algérie.
Acta Pharm. 2007 Sep;57(3):301-14. doi: 10.2478/v10007-007-0024-6.
The purpose of this study is to develop novel intestinal-specific drug delivery systems with pH sensitive swelling and drug release properties. Methacrylic-type polymeric prodrugs were synthesized by free radical copolymerization of methacrylic acid, poly(ethyleneglycol monomethyl ether methacrylate) and a methacrylic derivative of N-(4-hydroxyphenyl)-2-(4-methoxyphenyl) acetamide in the presence of ethylene glycol dimethacrylate as crosslinking agent. The effect of copolymer composition on the swelling behavior and hydrolytic degradation were studied in simulated gastric (SGF, pH 1.2) and intestinal fluids (SIF, pH 7.0). The dynamic swelling behavior of these hydrogels was investigated to determine the mechanism of water transport through these hydrogels. The mechanism of water transport through the gels was significantly affected by the pH of the swelling medium and became more relaxation-controlled in a swelling medium of pH 7.0. The swelling and hydrolytic behaviors of hydrogels were dependent on the content of methacrylic acid (MAA) groups and caused a decrease and increase in gel swelling in SGF and SIF, respectively. Drug release studies showed that the increasing content of MAA in the copolymer enhances hydrolysis in SIF. These results suggest that pH-sensitive systems could be useful for preparation of a muccoadhesive system and controlled release of N-(4-hydroxyphenyl)-2-(4-methoxyphenyl) acetamide.
本研究的目的是开发具有pH敏感溶胀和药物释放特性的新型肠道特异性药物递送系统。在乙二醇二甲基丙烯酸酯作为交联剂存在的情况下,通过甲基丙烯酸、聚(乙二醇单甲醚甲基丙烯酸酯)和N-(4-羟基苯基)-2-(4-甲氧基苯基)乙酰胺的甲基丙烯酸衍生物的自由基共聚反应合成甲基丙烯酸型聚合物前药。在模拟胃液(SGF,pH 1.2)和肠液(SIF,pH 7.0)中研究了共聚物组成对溶胀行为和水解降解的影响。研究了这些水凝胶的动态溶胀行为,以确定水通过这些水凝胶的传输机制。水通过凝胶的传输机制受溶胀介质pH值的显著影响,在pH 7.0的溶胀介质中变得更受松弛控制。水凝胶的溶胀和水解行为取决于甲基丙烯酸(MAA)基团的含量,分别导致在SGF和SIF中凝胶溶胀的降低和增加。药物释放研究表明,共聚物中MAA含量的增加会增强在SIF中的水解。这些结果表明,pH敏感系统可用于制备粘膜粘附系统和控制N-(4-羟基苯基)-2-(4-甲氧基苯基)乙酰胺的释放。