Institute of Environmental Science, and School of Chemistry and Chemical Engineering, Shanxi University , Taiyuan 030006, P. R. China.
Acadia University , 15 University Avenue, Wolfville, Nova Scotia B4P 2R6, Canada.
ACS Appl Mater Interfaces. 2016 May 11;8(18):11288-97. doi: 10.1021/acsami.6b01577. Epub 2016 Apr 26.
Innovative phosphorus and nitrogen dual-doped hollow carbon dots (PNHCDs) have been fabricated for anticancer drug delivery and biological imaging. The functional groups of PNHCDs are introduced by simply mixing glucose, 1,2-ethylenediamine, and concentrated phosphoric acid. This is an automatic method without external heat treatment to rapidly produce large quantities of PNHCDs, which avoid high temperature, complicated operations, and long reaction times. The as-prepared PNHCDs possess small particle size, hollow structure, and abundant phosphate/hydroxyl/pyridinic/pyrrolic-like N groups, endowing PNHCDs with fluorescent properties, improving the accuracy of PNHCDs as an optical monitoring code both in vitro and in vivo. The investigation of PNHCDs as an anticancer drug nanocarrier for doxorubicin (DOX) indicates a better antitumor efficacy than free DOX owing to its enhanced nuclear delivery in vitro and tumor accumulation in vivo, which results in highly effective tumor growth inhibition and improved targeted therapy for cancer in clinical medicine.
创新性的磷氮双掺杂空心碳点(PNHCDs)已被制备用于抗癌药物输送和生物成像。PNHCDs 的功能基团通过简单地混合葡萄糖、1,2-乙二胺和浓磷酸引入。这是一种自动方法,无需外部热处理即可快速生产大量的 PNHCDs,避免了高温、复杂的操作和长反应时间。所制备的 PNHCDs 具有小的粒径、空心结构和丰富的磷酸盐/羟基/吡啶基/吡咯基样 N 基团,赋予 PNHCDs 荧光性质,提高了 PNHCDs 在体外和体内作为光学监测码的准确性。作为阿霉素(DOX)的抗癌药物纳米载体的 PNHCDs 的研究表明,由于其在体外增强的核内传递和体内肿瘤积累,其抗肿瘤功效优于游离 DOX,从而实现了高效的肿瘤生长抑制和改善癌症的靶向治疗。