Salvati Anna, Söderman Olle, Lynch Iseult
Physical Chemistry 1, Center for Chemistry and Chemical Engineering, Lund University, Lund, Sweden.
J Phys Chem B. 2007 Jun 28;111(25):7367-76. doi: 10.1021/jp069051u. Epub 2007 Jun 5.
The internal structure of composite gels made of responsive microgel particles inserted into a bulk hydrogel (N-isopropylacrylamide microgel particles in a cross-linked dimethylacrylamide matrix) has been investigated from the diffusion behavior of poly(ethylene glycol) (PEG) probes through the network, in the absence of specific interactions between the diffusing molecules and the system. The effect of the different components has been examined, for example, the size of the probe, the bulk structure, and the microgel nature. Particles were characterized prior to their insertion into the hydrogel in order to describe their properties as a function of size and cross-linker content, thus revealing different swelling behaviors. The biggest effects on the diffusion of the PEG probes were related to the bulk structure, and no major effects were registered by the addition of different microgels into the hydrogel network. We attempt to rationalize this behavior in terms of the composite gel structure and discuss the results in terms of their meaning for controlled drug delivery strategies.
通过聚乙二醇(PEG)探针在网络中的扩散行为,在扩散分子与系统之间不存在特定相互作用的情况下,研究了由插入本体水凝胶(交联二甲基丙烯酰胺基质中的N-异丙基丙烯酰胺微凝胶颗粒)制成的复合凝胶的内部结构。已研究了不同组分的影响,例如探针的大小、本体结构和微凝胶性质。在将颗粒插入水凝胶之前对其进行了表征,以便描述其作为尺寸和交联剂含量函数的性质,从而揭示不同的溶胀行为。对PEG探针扩散影响最大的因素与本体结构有关,向水凝胶网络中添加不同的微凝胶未产生重大影响。我们试图根据复合凝胶结构来解释这种行为,并讨论这些结果对可控药物递送策略的意义。