Laneri Francesca, Parisi Cristina, Andrigo Vittoria, Guerra Pinto Juliana, Cortez Marcolino Luciana, Ferreira-Strixino Juliana, Natile Marta Maria, Sortino Salvatore
PhotoChemLab, Department of Drug and Health Sciences, University of Catania, Catania I-95125, Italy.
ICMATE-CNR Institute of Condensed Matter Chemistry and Technologies for Energy, National Research Council and Department of Chemical Science, University of Padova, Padova 35131, Italy.
ACS Appl Nano Mater. 2025 Jun 16;8(25):13083-13091. doi: 10.1021/acsanm.5c02198. eCollection 2025 Jun 27.
Nitric oxide (NO) and singlet oxygen (O) represent two of the most intriguing agents for unconventional phototherapeutic applications in cancer. In this contribution, N-doped carbon dots () with strong absorption in the biocompatible green region have been synthesized and covalently decorated with an otherwise blue-light-activatable NO photodonor (NOPD), leading to a nanoconjugate 3.5 nm in diameter. The core of the nanoconstruct acts as a green light antenna, permitting the release of NO from the NOPD by an intramolecular photoinduced electron transfer, with an improvement of more than 100 nm in the excitation wavelength. Simultaneously, green light excitation generates O by collisional energy transfer with molecular oxygen. Due to its emissive properties, the nanoconjugate can be visualized in 9L/LacZ brain cancer cells, where it localizes mainly in the cytoplasm. Amplified mortality of cancer cells is observed upon green light irradiation due to the mutual photodynamic action of NO and O.
一氧化氮(NO)和单线态氧(O)是癌症非传统光疗应用中最具吸引力的两种物质。在本研究中,合成了在生物相容性绿色区域具有强吸收的氮掺杂碳点(),并用一种原本可被蓝光激活的NO光供体(NOPD)进行共价修饰,得到直径为3.5 nm的纳米共轭物。该纳米结构的核心充当绿色光天线,通过分子内光诱导电子转移使NOPD释放NO,激发波长提高了100 nm以上。同时,绿色光激发通过与分子氧的碰撞能量转移产生O。由于其发光特性,该纳米共轭物可在9L/LacZ脑癌细胞中可视化,主要定位于细胞质中。由于NO和O的相互光动力作用,绿光照射后观察到癌细胞死亡率增加。