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Direct visualization of the drug loading of single DNA origami nanostructures by AFM-IR nanospectroscopyf

机译:通过AFM-IR纳米光谱直接可视化单个DNA折纸纳米结构的载药量

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摘要

The efficient loading of DNA nanostructures with intercalating or groove-binding drugs is an important prerequisite for various applications in drug delivery.However,unambiguous verification and quantification of successful drug loading is often rather challenging.In this work,AFM-IR nanospectroscopy is thus employed to directly visualize the loading of DNA origami nanostructures with the photosensitizer methylene blue(MB).Single MB-loaded DNA origami nanostructures can be clearly resolved in high-resolution infrared(IR)maps and the occurrence of MB-specific IR absorption correlates well with the topographic signals of the DNA origami nanostructures.The intensity of the recorded MB absorption bands furthermore scales with the MB concentration used for MB loading.By comparing single-and multilayer DNA origami nanostructures,it is also shown that the IR signal intensity of the loaded MB increases with the thickness of the DNA origami nanostructures.This indicates that also DNA double helices located in the core of bulky 3D DNA origami nanostructures are accessible for MB loading.AFM-IR nanospectroscopy thus has the potential to become an invaluable tool for quantifying drug loading of DNA origami nanostructures and optimizing drug loading protocols.
机译:DNA纳米结构与嵌入或沟结合药物的高效负载是药物递送中各种应用的重要前提。然而,对成功的载药量进行明确的验证和量化通常相当具有挑战性。因此,利用AFM-IR纳米光谱技术直接观察了光敏剂亚甲基蓝(MB)对DNA折纸纳米结构的加载。在高分辨率红外(IR)图谱中可以清楚地解析单个MB负载的DNA折纸纳米结构,并且MB特异性IR吸收的发生与DNA折纸纳米结构的形貌信号密切相关。此外,记录的MB吸收带的强度与用于MB加载的MB浓度成正比。通过对单层和多层DNA折纸纳米结构的比较,还表明负载MB的红外信号强度随着DNA折纸纳米结构厚度的增加而增加。这表明位于大块 3D DNA 折纸纳米结构核心的 DNA 双螺旋也可用于 MB 加载。因此,AFM-IR纳米光谱有可能成为量化DNA折纸纳米结构的载药量和优化载药方案的宝贵工具。

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