de Oliveira H C L, Fonseca J L C, Pereira M R
Chemistry Department, Universidade Federal do Rio Grande do Norte, Campus Universitário, Lagoa Nova, Natal RN, CEP 59078-970, Brazil.
J Biomater Sci Polym Ed. 2008;19(2):143-60. doi: 10.1163/156856208783432471.
Polyelectrolyte complex (PEC) membranes were obtained by mixing solutions of two polymers of opposite charges, chitosan (Chi) and poly(acrylic acid) PAA. Three membranes were obtained: one made of pure chitosan and two membranes with chitosan mixed with PAA at a ratio of 95:5 (one prepared using PAA solution in 3.5% formic acid, named ChiPAA3.5, and another one using a PAA solution in 10% formic acid, named ChiPAA10). The membranes were characterized by swelling experiments, FT-IR spectroscopy, scanning electron microscopy (SEM), atomic force microscopy (AFM), mechanical properties and permeability studies in relation to a drug model (sodium sulphamerazine). The calculation of degree of ionization showed that the lower the formic acid concentration was, the higher the PAA dissociation degree. Polyelectrolyte complex formation was characterized by FT-IR. Water uptake results showed that PEC membranes were more hydrophilic than pure chitosan, ChiPAA3.5 being the most. Morphological analysis by SEM and AFM showed that PAA addition changed the membranes morphology, especially for ChiPAA3.5. Mechanical properties indicated that PEC membranes were more rigid than pure chitosan membranes and that the morphology has an influence on tensile strength values. Permeability values decreased with complex formation and were lower for ChiPAA10 than ChiPAA3.5. However, as drug concentration was increased, the difference between the two complex membranes disappeared. The results were discussed considering the drug-membrane interactions. Diffusion coefficient values indicated that ChiPAA3.5 had a higher drug retention capacity than ChiPAA10.
通过混合两种带相反电荷的聚合物壳聚糖(Chi)和聚丙烯酸(PAA)的溶液,制备了聚电解质复合物(PEC)膜。制备了三种膜:一种由纯壳聚糖制成,另外两种膜是壳聚糖与PAA按95:5的比例混合而成(一种使用3.5%甲酸中的PAA溶液制备,命名为ChiPAA3.5,另一种使用10%甲酸中的PAA溶液制备,命名为ChiPAA10)。通过溶胀实验、傅里叶变换红外光谱(FT-IR)、扫描电子显微镜(SEM)、原子力显微镜(AFM)、力学性能以及与药物模型(磺胺间二甲氧嘧啶钠)相关的渗透性研究对这些膜进行了表征。电离度的计算表明,甲酸浓度越低,PAA的解离度越高。通过FT-IR对聚电解质复合物的形成进行了表征。吸水结果表明,PEC膜比纯壳聚糖更亲水,其中ChiPAA3.5的亲水性最强。通过SEM和AFM进行的形态分析表明,添加PAA改变了膜的形态,尤其是ChiPAA3.5。力学性能表明,PEC膜比纯壳聚糖膜更硬,且形态对拉伸强度值有影响。随着复合物的形成,渗透率值降低,ChiPAA10的渗透率低于ChiPAA3.5。然而,随着药物浓度的增加,两种复合膜之间的差异消失。结合药物-膜相互作用对结果进行了讨论。扩散系数值表明,ChiPAA3.5比ChiPAA10具有更高的药物保留能力。