Prado H J, Matulewicz M C, Bonelli P, Cukierman A L
Departamento de Química Orgánica, Universidad de Buenos Aires, Buenos Aires, Argentina.
Eur J Pharm Biopharm. 2008 Sep;70(1):171-8. doi: 10.1016/j.ejpb.2008.04.017. Epub 2008 Apr 29.
The formation of a novel interpolyelectrolyte complex (IPEC) between basic butylated methacrylate copolymer and kappa-carrageenan was investigated and the product formed was characterized. Turbidity measurements and elemental analyses pointed to a 1:1 interaction of the repeating units. These results and FT-IR confirmed IPEC formation. Electronic microscopy images, particle size determination by image analysis and N(2) (77K) adsorption measurements were consistent with a porous material. This IPEC formed presented very good flowability and compactibility. Two maxima were observed in the swelling behaviour as a function of pH. The performance of the IPEC as a matrix for controlled release of drugs was evaluated, using ibuprofen as a model drug. Release profiles were properly represented by a mathematical model, which indicates that the system releases ibuprofen in a zero-order manner. These profiles could be controlled by conveniently modifying the proportion of the IPEC in the tablets.
研究了碱性丁基丙烯酸酯共聚物与κ-卡拉胶之间新型聚电解质络合物(IPEC)的形成,并对形成的产物进行了表征。浊度测量和元素分析表明重复单元之间存在1:1的相互作用。这些结果和傅里叶变换红外光谱(FT-IR)证实了IPEC的形成。电子显微镜图像、通过图像分析测定的粒径以及N₂(77K)吸附测量结果与多孔材料一致。形成的这种IPEC具有非常好的流动性和可压性。观察到溶胀行为随pH值变化出现两个最大值。以布洛芬为模型药物,评估了IPEC作为药物控释基质的性能。释放曲线可以用一个数学模型很好地表示,这表明该系统以零级方式释放布洛芬。通过方便地改变片剂中IPEC的比例可以控制这些曲线。