纳米棒
药物输送
光热治疗
聚合物
共轭体系
纳米技术
材料科学
光热效应
吸附
化学工程
微型多孔材料
肺表面活性物质
纳米囊
化学
有机化学
纳米颗粒
工程类
复合材料
作者
Berthold Reis,Robert Frenzel,Niklas Gerlach,Martin Müller,Johannes Schultz,Sarrah Putwa,Joseph A. Weatherby,Mita Dasog,Simona Schwarz
出处
期刊:Langmuir
[American Chemical Society]
日期:2025-01-23
卷期号:41 (4): 2471-2479
被引量:4
标识
DOI:10.1021/acs.langmuir.4c04164
摘要
Near-infrared (NIR) controlled drug delivery systems have drawn a lot of attention throughout the past few decades due to the deep penetration depth and comparatively minor side effects of the stimulus. In this study, we introduce an innovative approach for gastric cancer treatment by combining photothermal infrared-sensitive gold nanorods (AuNRs) with a conjugated microporous polymer (CMP) to create a drug delivery system tailored for transporting the cytostatic drug 5-fluorouracil (5-FU). CMPs are fully conjugated networks with high internal surface areas that can be precisely tailored to the adsorption and transport of active compounds through the right choice of chemical functionalities. By incorporation of surfactant-stabilized AuNRs into the CMP synthesis in dimethylformamide (DMF) the surfactant shell is destabilized and subsequently replaced by the CMP. Particularly, low initial surfactant concentrations led to uniform distribution of the AuNRs in the polymer matrix. Importantly, the integrated AuNRs maintain their plasmonic properties, as was confirmed via electron energy loss spectroscopy. Therefore, the significant photothermal properties are translated to the hybrid material as shown in a proof-of-principle experiment. Further, in an approximated gastric environment, 5-FU release studies were conducted with and without NIR stimulus. Thereby it was observed that increased Brownian motion due to the NIR irradiation not only accelerates the release but also increases the total released amount by influencing the adsorption-desorption equilibrium. This remarkable level of control of the release process underlines the immense potential of this hybrid material for precise and targeted drug delivery.
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