Pengli Zuo, Jun Peng, Yuyang Yao, Wei Tan, Lan Cheng, Jinyu Zhang, Xiuhua Lu
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引用次数: 0
Abstract
Due to the unique chemical and biomedical properties of carbon dots (CDs), they have increasingly obtained the attention in many research fields, for example, bioimaging, fluorescence sensing, and drug delivery, etc. Recently, it was found that, under light excitation, CDs can also be exploited as a novel photosensitizer to prepare reactive oxygen species (ROS), which expand their applications in the field of photodynamic therapy for cancer treatment. Nevertheless, the high cost and complex fabrication approach of CDs significantly limit their applications. To address this issue, bottom-up routes usually utilize sustainable and inexpensive carbon precursor as starting materials, employed N,N-dimethylformamide (DMF) or ethanol as an environmental-friendly solvent. Bottom-up approach was energy efficient, and the purification process was relatively simple by dialysis. Therefore, carbon dots (CDs) were facilely fabricated in a one-pot solvothermal process using 1-aminoanthraquinone as a precursor, and their application as photosensitizers for in vitro antitumor cells, especially photodynamic therapy (PDT) was established. Then the photophysical and nanoscale dimensions properties of the fabricated CDs were characterized via TEM, UV-visible, fluorescence, and FT-IR spectroscopy. The synthesized N-doped CDs can easily dissolve in water, possess very low biotoxicity, yellow-light emission (maximum peak at 587 nm). More importantly, PDT studies demonstrated that the obtained CDs possess a high singlet oxygen yield of 35%, and exhibit significant phototoxicity to cancer cells upon 635 nm laser irradiation. These studies highlight that N-doped CDs can be facilely synthesized from only one precursor, and are a potentially novel theranostic agent for in vivo PDT.
由于碳点(CD)具有独特的化学和生物医学特性,它们在生物成像、荧光传感和药物输送等多个研究领域日益受到关注。最近,人们发现在光激发下,碳点还可以作为一种新型光敏剂制备活性氧(ROS),从而拓展了其在癌症光动力疗法领域的应用。然而,CD 的高成本和复杂制造方法极大地限制了其应用。为解决这一问题,自下而上的方法通常利用可持续且廉价的碳前体作为起始材料,并采用 N,N-二甲基甲酰胺(DMF)或乙醇作为环保溶剂。自下而上的方法能效高,透析纯化过程相对简单。因此,以 1-aminoanthraquinone 为前驱体,通过一锅溶热法轻松制备出了碳点(CDs),并将其应用于体外抗肿瘤细胞的光敏剂,尤其是光动力疗法(PDT)。然后通过 TEM、紫外可见光、荧光和傅立叶变换红外光谱分析了所制备 CD 的光物理和纳米尺寸特性。合成的掺杂 N 的 CD 易溶于水,具有极低的生物毒性和黄光发射(最大峰值为 587 纳米)。更重要的是,PDT 研究表明,所获得的 CD 具有高达 35% 的单线态氧产率,在 635 纳米激光照射下对癌细胞具有显著的光毒性。这些研究突出表明,掺杂 N 的 CD 只需一种前体就能轻松合成,是一种潜在的新型治疗剂,可用于体内光导放疗。
期刊介绍:
Journal of Fluorescence is an international forum for the publication of peer-reviewed original articles that advance the practice of this established spectroscopic technique. Topics covered include advances in theory/and or data analysis, studies of the photophysics of aromatic molecules, solvent, and environmental effects, development of stationary or time-resolved measurements, advances in fluorescence microscopy, imaging, photobleaching/recovery measurements, and/or phosphorescence for studies of cell biology, chemical biology and the advanced uses of fluorescence in flow cytometry/analysis, immunology, high throughput screening/drug discovery, DNA sequencing/arrays, genomics and proteomics. Typical applications might include studies of macromolecular dynamics and conformation, intracellular chemistry, and gene expression. The journal also publishes papers that describe the synthesis and characterization of new fluorophores, particularly those displaying unique sensitivities and/or optical properties. In addition to original articles, the Journal also publishes reviews, rapid communications, short communications, letters to the editor, topical news articles, and technical and design notes.