X射线光电子能谱
离子键合
阳离子聚合
聚合物
扫描电子显微镜
材料科学
光化学
骨料(复合)
离子强度
接受者
质谱法
化学工程
化学
离子
纳米技术
高分子化学
物理化学
有机化学
色谱法
物理
凝聚态物理
工程类
复合材料
水溶液
作者
Kongqi Chen,Dong He,Qiong Liu,Yuanzhong Fan,Zhiming Wang,Weijie Zhang,Ben Zhong Tang
出处
期刊:Small
[Wiley]
日期:2023-03-21
卷期号:19 (26)
被引量:2
标识
DOI:10.1002/smll.202208052
摘要
The formation of nanoaggregates makes a great difference to the improvement of photodynamic therapy (PDT) performance to some extent, but constructing stable aggregates with a clear structure is simultaneously a big challenge for us. Herein, just by electrostatic interaction, cationic 2PAHs and anionic FBA351, regarded as acceptor (A) and donor (D), respectively, are utilized to prepare stable aggregate of ionic-bonds coupled polymer (ICP) with repeated "D-A" structure, which is fully characterized by nuclear magnetic resonance (NMR), time-of-flight mass spectrometry, X-ray photoelectron spectroscopy (XPS), and scanning electron microscopy (SEM). Remarkably, aggregate ICP with multiple "D-A" structures showed enhanced photosensitization efficiency over its precursor 2PAHs and FBA351, which is in accord with the image-guided photodynamic anticancer therapy. Such results not only offer a simple way to obtain stable aggregate but also give us a guideline to design efficient photosensitizers.
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