Martinez Leticia, Agnely Florence, Leclerc Bernard, Siepmann Juergen, Cotte Marine, Geiger Sandrine, Couarraze Guy
Faculté de Pharmacie, Université Paris-Sud, Châtenay-Malabry, France.
Eur J Pharm Biopharm. 2007 Sep;67(2):339-48. doi: 10.1016/j.ejpb.2007.02.012. Epub 2007 Feb 24.
The major aim of this study was to get deeper insight into the process of polymer cross-linking and the resulting structure of beads based on chitosan (CS) or chitosan/poly(ethylene oxide) (CS/PEO) semi-interpenetrating networks (semi-IPNs) as new carrier materials for oral drug delivery. Spherical hydrogels were prepared by a dropping method. The uptake kinetics of the cross-linking agent glyoxal into the beads were monitored and quantitatively described using Fick's second law of diffusion. High-resolution synchrotron infrared microspectroscopy (SIRM) was used to characterize the inner structures of the beads. Importantly, the diffusion of glyoxal through the hydrogels was found to be much slower than the cross-linking reaction and the mesh size of the created networks to be much larger than the hydrodynamic diameter of glyoxal. The presence of PEO chains slightly decreased the diffusivity of glyoxal due to obstruction effects. However, the cross-linking reaction was not affected. Interestingly, the polymers were homogeneously cross-linked throughout the beads, except for a thin outer shell showing an elevated cross-linking density. Thus, the obtained cross-linked hydrogel-based beads exhibit well-defined polymeric structures and offer an interesting potential as novel oral drug delivery systems.
本研究的主要目的是更深入地了解聚合物交联过程以及基于壳聚糖(CS)或壳聚糖/聚环氧乙烷(CS/PEO)半互穿网络(semi-IPNs)的珠粒结构,这些珠粒作为口服给药的新型载体材料。通过滴加法制备球形水凝胶。使用菲克第二扩散定律监测并定量描述交联剂乙二醛进入珠粒的吸收动力学。采用高分辨率同步辐射红外显微光谱(SIRM)对珠粒的内部结构进行表征。重要的是,发现乙二醛在水凝胶中的扩散比交联反应慢得多,且所形成网络的网孔尺寸比乙二醛的流体动力学直径大得多。由于阻碍作用,PEO链的存在略微降低了乙二醛的扩散率。然而,交联反应并未受到影响。有趣的是,除了显示出较高交联密度的薄外壳外,聚合物在整个珠粒中均匀交联。因此,所获得的基于交联水凝胶的珠粒具有明确的聚合物结构,并作为新型口服给药系统展现出有趣的潜力。