Key Laboratory for Advanced Materials, Shanghai Key Laboratory of Functional Materials Chemistry, Joint International Laboratory for Precision Chemistry, Frontiers Science Center for Materiobiology & Dynamic Chemistry, and School of Chemistry & Molecular Engineering, East China University of Science and Technology, Shanghai, 200237, People's Republic of China.
Mikrochim Acta. 2020 Jul 9;187(8):435. doi: 10.1007/s00604-020-04412-6.
Lysosomes with a single-layered membrane structure are mainly involved in the scavenging of foreign substances and play an important role in maintaining normal physiological functions of living cells. In this work, near-neutrally charged fluorescent carbon dots (CDs) were prepared with lipophilicity through a facile one-pot hydrothermal carbonization of chloranil and triethylenetetramine at 160 °C for 3 h. The as-obtained CDs are proved to have good photostability, low cost, and excellent biocompatibility. Importantly, the as-prepared CDs with high quantum yield of 30.8% show excitation-dependent emission with great stability, and thus, they can be well used for the long-term target imaging of lysosomes in living cells without further modification. Meanwhile, the CDs can quickly enter into the lysosomes within 30 min, and the green fluorescence (FL) of CDs reaches the plateau when incubated for 60 min. By comparing the fluorescent intensity, the information about distribution and amount of lysosomes in different cells can be obtained. The proposed CD-based strategy demonstrates great promise for label-free target imaging of lysosomes in living cells. Graphical abstract The near-neutral carbon dots (CDs) with lipophilicity are used as label-free fluorescent nanoprobes for the long-term imaging of lysosomes in living cells.
具有单层膜结构的溶酶体主要参与外来物质的清除,在维持活细胞的正常生理功能方面发挥着重要作用。在这项工作中,通过邻位中性带电的荧光碳点(CDs),通过在 160°C 下用氯蒽和三乙烯四胺进行简单的一锅水热碳化 3 小时来制备疏水性。所得到的 CDs 被证明具有良好的光稳定性、低成本和优异的生物相容性。重要的是,所制备的具有 30.8%高量子产率的 CDs 具有激发依赖性发射,稳定性好,因此无需进一步修饰即可很好地用于活细胞溶酶体的长期靶向成像。同时,CDs 可以在 30 分钟内快速进入溶酶体,并且在孵育 60 分钟时 CDs 的绿色荧光(FL)达到平台期。通过比较荧光强度,可以获得不同细胞中溶酶体的分布和数量信息。所提出的基于 CD 的策略为活细胞中溶酶体的无标记靶向成像展示了巨大的应用潜力。