4.8 Article

AgInS2/ZnS quantum dots for noninvasive cervical cancer screening with intracellular pH sensing using fluorescence life time imaging microscopy

期刊

NANO RESEARCH
卷 15, 期 6, 页码 5193-5204

出版社

TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-022-4104-1

关键词

AIS/ZnS quantum dots; fluorescence lifetime imaging microscopy; intracellular pH sensing; cervical cancer screening; noninvasive

资金

  1. National Natural Science Foundation of China (NSFC) [62074044, 61904036, 11804350]
  2. Medical Engineering Fund of Fudan University [yg2021-022]
  3. Zhongshan-Fudan Joint Innovation Center and Jihua Laboratory Projects of Guangdong Province [X190111UZ190]
  4. Fudan University-CIOMP Joint Fund [FC2018-001]
  5. Pioneering Project of Academy for Engineering and Technology of Fudan University [gyy2018-001, gyy2018-002]
  6. Shanghai Natural Science Foundation [20ZR1405100, 20ZR1403700]
  7. Science and Technology Research Program of Shanghai [19DZ2282100]
  8. Shanghai key discipline construction plan [GWV-10.1-XK01]
  9. Shanghai Hong Kong, Macao, and Taiwan Cooperation Project [19490760900]
  10. Shanghai Engineering Technology Research Center of Hair Medicine [19DZ2250500]

向作者/读者索取更多资源

Intracellular pH plays a critical role in biological functions and diseases. This study reports on the use of an intracellular pH sensor, AIS/ZnS quantum dots, for live cell imaging and distinguishing between cancer cells and normal cells. The method offers potential for noninvasive cervical cancer screening.
Intracellular pH plays a critical role in biological functions, and abnormal pH values are related to various diseases. Here, we report on an intracellular pH sensor AgInS2 (AIS)/ZnS quantum dots (QDs) that show long fluorescence lifetimes of hundreds of nanoseconds and low toxicity. Fluorescence lifetime imaging microscopy (FLIM) combined with AIS/ZnS QDs is used for the imaging of live cells in different pH buffers and different cell lines. The FLIM images of AIS/ZnS QDs in live cells demonstrate different intracellular pH values in different regions, such as in lysosomes or cytoplasm. This method can also distinguish cancer cells from normal cells, and the fluorescence lifetime difference of the AIS/ZnS QDs between the two types of cells is 100 +/- 7 ns. Most importantly, the exfoliated cervical cells from 20 patients are investigated using FLIM combined with AIS/ZnS QDs. The lifetime difference value between the normal and cervical cancer (CC) groups is 115 +/- 9 ns, and the difference between the normal and the precancerous lesion group is 64 +/- 9 ns. For the first time, the noninvasive method has been used for cervical cancer screening, and it has shown great improvement in sensitivity compared with a clinical conventional cytology examination.

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