Carbon dot based nucleus targeted fluorescence imaging and detection of nuclear hydrogen peroxide in living cells.
Kabyashree PhukanRitwick Ranjan SarmaSomarani DashRajlakshmi DeviDevasish ChowdhuryPublished in: Nanoscale advances (2021)
Investigation of the intracellular generation of H 2 O 2 , one of the most important reactive oxygen species (ROS), is crucial for preventing various diseases since it is closely linked with different physiological and complex cell signaling pathways. Despite the development of various fluorescent probes, the majority of the fluorescent probes cannot move across the nuclear membrane. However, detection of the nuclear level of H 2 O 2 is very important since it can directly cause oxidative DNA damage which ultimately leads to various diseases. Therefore, in this study, p -phenylenediamine based carbon quantum dots (B-PPD CDs) have been synthesized and integrated with 4-formylbenzeneboronic acid as a doping agent for the detection of H 2 O 2 . The detection mechanism showed that, upon exposure to H 2 O 2 , the fluorescence of the B-PPD CDs was immediately quenched. Further investigation has been done in the in vitro RAW 264.7 cell line by both exogenous and endogenous exposure of H 2 O 2 to demonstrate the feasibility of the method. It is shown successfully that the exogenous presence and endogenous generation of H 2 O 2 in RAW 264.7 cells can be detected using B-PPD CDs. The limit of detection (LOD) was determined to be 0.242 μM. The development of such imaging probes using carbon quantum dots will lead to live-cell imaging as well as ROS detection.
Keyphrases
- quantum dots
- living cells
- fluorescence imaging
- label free
- reactive oxygen species
- dna damage
- loop mediated isothermal amplification
- hydrogen peroxide
- real time pcr
- single molecule
- fluorescent probe
- sensitive detection
- small molecule
- high resolution
- energy transfer
- oxidative stress
- stem cells
- photodynamic therapy
- induced apoptosis
- signaling pathway
- epithelial mesenchymal transition
- endoplasmic reticulum stress
- nucleic acid
- single cell
- cancer therapy