Toews Parker M, Bates Jeffrey S
Department of Materials Science and Engineering, University of Utah, 122 Central Campus Drive, Room 304, Salt Lake City, Utah 84112, United States.
ACS Omega. 2025 Jan 29;10(5):4580-4587. doi: 10.1021/acsomega.4c08540. eCollection 2025 Feb 11.
The uptake and release of target molecules were studied in hydrogels as a function of time over a month to determine what, if any, deviation exists in these properties. Through the use of spectroscopic techniques such as FT-IR and UV-vis-NIR in combination with drug release kinetics and swelling kinetics studies, both the effect of imprinting and the effect of time could be substantially analyzed for hydrogels. Molecular imprinting provides a significant advantage over nonimprinted hydrogel samples through the sustainment of a first-order release profile throughout the month without significant deviations in the releasable concentration, while nonimprinted samples struggle in their capability to be consistently load-cycled. Changes between the imprinted and nonimprinted samples are not evidenced to be significant chemical deviations; rather, they are attributable to functionality differences between the release mechanisms of these hydrogels.
研究了水凝胶中目标分子的摄取和释放随时间变化的情况,为期一个月,以确定这些性质是否存在任何偏差。通过使用傅里叶变换红外光谱(FT-IR)和紫外可见近红外光谱(UV-vis-NIR)等光谱技术,并结合药物释放动力学和溶胀动力学研究,可以对水凝胶的印迹效应和时间效应进行充分分析。与未印迹的水凝胶样品相比,分子印迹具有显著优势,即在整个月内维持一级释放曲线,可释放浓度无明显偏差,而未印迹的样品在持续加载循环能力方面存在困难。印迹样品和未印迹样品之间的变化并非显著的化学偏差;相反,它们归因于这些水凝胶释放机制之间的功能差异。