Samantara Aneeya K, Maji Santanu, Ghosh Arnab, Bag Bamaprasad, Dash Rupesh, Jena Bikash Kumar
CSIR-Institute of Minerals and Materials Technology, Bhubaneswar 751013, Odisha, India.
J Mater Chem B. 2016 Apr 14;4(14):2412-2420. doi: 10.1039/c6tb00081a. Epub 2016 Mar 15.
Here, a facile one-step approach has been developed for the synthesis of carbon quantum dots (CQDs) from Good's buffer. The as-synthesized CQDs emit a bright greenish blue coloured fluorescence after exposure to a 365 nm UV-lamp illumination. The bright fluorescence nature of the CQDs has proven them to be excellent probes for cellular imaging. The CQDs are highly biocompatible in nature, which has been validated by an MTT assay test. The in vitro MTT assay demonstrates a more than 95% survival rate when HEK293 (human embryonic kidney) and H357 (human oral squamous carcinoma) cells were treated with CQDs. The low cytotoxicity of Good's buffer derived CQDs opens the door to biomedical applications. The anticancer drug doxorubicin (DOX) was successfully loaded on the CQDs and their delivery efficiency to the target cells via in vitro treatment of cancerous cells was explored. The CQDs supported DOX showed a higher killing rate of the cancer cells compared to bare DOX due to its ease of internalization and efficient pH-triggered release inside the cells.
在此,已开发出一种简便的一步法,用于从Good's缓冲液合成碳量子点(CQD)。合成后的CQD在365nm紫外灯照射下发出亮蓝绿色荧光。CQD的明亮荧光特性已证明它们是用于细胞成像的优秀探针。CQD本质上具有高度生物相容性,这已通过MTT测定试验得到验证。体外MTT测定表明,当用CQD处理HEK293(人胚肾)和H357(人口腔鳞状癌)细胞时,存活率超过95%。Good's缓冲液衍生的CQD的低细胞毒性为生物医学应用打开了大门。抗癌药物阿霉素(DOX)成功负载在CQD上,并通过体外处理癌细胞探索了它们对靶细胞的递送效率。与裸DOX相比,CQD负载的DOX对癌细胞的杀伤率更高,这是因为它易于内化并在细胞内实现有效的pH触发释放。