CNR-Institute of Biomolecular Chemistry, Via Paolo Gaifami 18, 95126Catania, Italy.
CIB-Interuniversity Consortium for Biotechnologies, University of Catania, Via Flavia, 23/1, 34148Trieste, Italy.
ACS Appl Mater Interfaces. 2023 Feb 1;15(4):5732-5743. doi: 10.1021/acsami.2c22500. Epub 2023 Jan 23.
Carbon-based nanostructures are attracting a lot of attention because of their very low toxicity, excellent visible light-triggered optical and photothermal properties, and intriguing applications. Currently, the development of multifunctional carbon-based nanostructures for a synergistic chemo-photothermal approach is a challenging topic for the advancement of cancer treatment. Here, we report an unprecedented example of photoresponsive carbon-based polymer dots (CPDs-PNM) obtained by a one-pot thermal process from poly(-isopropylacrylamide) (PNIPAM) without using organic solvent and additional reagents. The CPDs-PNM nanostructures were characterized by spectroscopic techniques, transmission electron microscopy, and atomic force microscopy. The CPDs-PNM exhibited high photothermal conversion efficiency, lower critical solution temperature (LCST) behavior, and good cytarabine (arabinosyl cytosine, AraC) loading capacity (62.3%). The formation of a CPDs-PNM/AraC adduct and photothermal-controlled drug release, triggered by green light excitation, were demonstrated by spectroscopic techniques, and the drug-polymer interaction and drug release mechanism were well supported by modeling simulation calculations. The cellular uptake of empty and AraC-loaded CPDs-PNM was imaged by confocal laser scanning microscopy. In vitro experiments evidenced that CPDs-PNM did not affect the viability of neuroblastoma cells, while the CPDs-PNM/AraC adduct under light irradiation exhibited significantly higher toxicity than AraC alone by a combined chemo-photothermal effect.
基于碳的纳米结构因其极低的毒性、优异的可见光触发的光学和光热性能以及有趣的应用而引起了广泛关注。目前,开发用于协同化学-光热方法的多功能碳基纳米结构是癌症治疗进展的一个具有挑战性的课题。在这里,我们报告了一个前所未有的例子,即通过一锅热过程从聚(异丙基丙烯酰胺)(PNIPAM)中获得光响应的碳基聚合物点(CPD-PNM),而无需使用有机溶剂和额外的试剂。CPD-PNM 纳米结构通过光谱技术、透射电子显微镜和原子力显微镜进行了表征。CPD-PNM 表现出高的光热转换效率、更低的临界溶液温度(LCST)行为和良好的阿糖胞苷(阿拉伯糖胞嘧啶,AraC)负载能力(62.3%)。通过光谱技术证明了 CPD-PNM/AraC 加合物的形成和光热控制的药物释放,通过绿光激发触发,药物-聚合物相互作用和药物释放机制得到了建模模拟计算的很好支持。通过共聚焦激光扫描显微镜对空的和载有 AraC 的 CPD-PNM 的细胞摄取进行了成像。体外实验表明,CPD-PNM 不影响神经母细胞瘤细胞的活力,而在光照射下,CPD-PNM/AraC 加合物通过协同化学-光热作用表现出比单独 AraC 更高的毒性。
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