State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201600, China.
Engineering Research Center of Advanced Glasses Manufacturing Technology, College of Materials Science and Engineering, Donghua University, Shanghai 201600, China.
ACS Appl Mater Interfaces. 2020 Nov 18;12(46):51225-51235. doi: 10.1021/acsami.0c14665. Epub 2020 Nov 9.
drug release systems have recently received tremendous attention because they allow noninvasive, convenient, and prolonged administration of pharmacological agents. On-demand epidermal drug release systems can improve treatment efficiency, prevent multidrug resistance, and minimize drug toxicity to healthy cells. In addition, real-time monitoring of drug content is also essential for guiding the determination of drug dosage and replacing drug carriers in time. Therefore, it is important to integrate the above properties in one ideal epidermal patch. Herein, photonic crystals (PCs) based on FeO@C nanoparticles were introduced into drug-loaded poly(-isopropylacrylamide--acrylic acid) (P(NIPAM-AAc)) hydrogel-functionalized textiles. Drug loading and release depended on the expansion and contraction of the hydrogels. The lower critical solution temperature (LCST) of the hydrogels was adjusted to 40 °C, which is higher than the skin temperature, by varying the content of hydrophilic comonomer acrylic acid (AAc) to store the drug at room temperature, and on-demand release was achieved by mild thermal stimulation. Moreover, the lattice spacing () of PCs varied with the expansion and contraction of the hydrogels, which can cause the color of P(NIPAM-AAc) hydrogel-functionalized textiles to change. These synchronous thermoresponsive chromic drug uptake and release behaviors provided an effective method for visual and real-time monitoring of drug content. Furthermore, in view of the poor mechanical properties of hydrogel wound dressings, textile matrices were composited to prevent holistic breaking during the stretching process. Biological experiments proved that the drug-loaded P(NIPAM-AAc) hydrogel-functionalized textiles had good antibacterial properties and wound-healing effects.
药物释放系统最近受到了极大的关注,因为它们允许非侵入性、方便和延长给药的药理学试剂。按需表皮药物释放系统可以提高治疗效率、防止多药耐药性,并将药物毒性最小化到健康细胞。此外,实时监测药物含量对于指导药物剂量的确定和及时更换药物载体也至关重要。因此,将上述特性集成到一个理想的表皮贴片中非常重要。在此,引入了基于 FeO@C 纳米粒子的光子晶体 (PCs) 到载药的聚(-异丙基丙烯酰胺--丙烯酸) (P(NIPAM-AAc)) 水凝胶功能化纺织品中。药物的负载和释放取决于水凝胶的膨胀和收缩。通过改变亲水性单体丙烯酸 (AAc) 的含量来调整水凝胶的低临界溶液温度 (LCST) 至 40°C,使其高于皮肤温度,从而在室温下储存药物,并通过温和的热刺激实现按需释放。此外,PCs 的晶格间距 () 随水凝胶的膨胀和收缩而变化,这会导致 P(NIPAM-AAc) 水凝胶功能化纺织品的颜色发生变化。这些同步的热响应变色药物摄取和释放行为为药物含量的可视化和实时监测提供了一种有效的方法。此外,鉴于水凝胶伤口敷料的机械性能较差,将纺织基质复合以防止在拉伸过程中整体断裂。生物实验证明,载药的 P(NIPAM-AAc) 水凝胶功能化纺织品具有良好的抗菌性能和伤口愈合效果。