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用于亲水性药物治疗的刺激响应水凝胶中的摄取与释放动力学及寿命

Uptake and Release Kinetics Longevity in Stimuli-Responsive Hydrogels for Hydrophilic Drug Therapy.

作者信息

Toews Parker M, Bates Jeffrey S

机构信息

Department of Materials Science and Engineering, University of Utah, 122 Central Campus Drive, Room 304, Salt Lake City, Utah 84112, United States.

出版信息

ACS Omega. 2025 Jan 29;10(5):4580-4587. doi: 10.1021/acsomega.4c08540. eCollection 2025 Feb 11.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ef2/11822526/9b062e380819/ao4c08540_0001.jpg

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