Divergent Responses of Hydrophilic CdSe and CdSe@CdS Core-Shell Nanocrystals in Apoptosis and In Vitro Cancer Cell Imaging: A Comparative Analysis.
Kishan DasNeelima BhattAjith Manayil ParambilKajal KumariRaj KumarKamla RawatPaulraj RajamaniHimadri B BohidarAhmed NadeemMuthupandian SaravananRamovatar MeenaPublished in: Journal of functional biomaterials (2023)
With their distinctive core-shell design, core-shell nanocrystals have drawn interest in catalysis, medicinal research, and nanotechnology. These nanocrystals have a variety of characteristics and possible uses. The application of core-shell nanocrystals offers significant potential in increasing diagnostic and therapeutic approaches for cancer research in apoptosis and in vitro cancer cell imaging. In the present study, we investigated the fluorescence behavior of hydrophilic CdSe (core-only) and CdSe@CdS (core-shell) nanocrystals (NCs) and their potential in cancer cell imaging. The addition of a CdS coating to CdSe NCs increased the fluorescence intensity tenfold. The successful fabrication of core-shell CdSe@CdS nanocrystals was proven by a larger particle size (evaluated via DLS and TEM) and their XRD pattern and surface morphology compared to CdSe (core-only) NCs. When these NCs were used for bioimaging in MCF-7 and HEK-293 cell lines, they demonstrated excellent cellular uptake due to higher fluorescence intensity within cancerous cells than normal cells. Comparative cytotoxicity studies revealed that CdSe NCs were more toxic to all three cell lines (HEK-293, MCF-7, and HeLa) than CdSe@CdS core-shell structures. Furthermore, a decrease in mitochondrial membrane potential and intracellular ROS production supported NCs inducing oxidative stress, which led to apoptosis via the mitochondria-mediated pathway. Increased cytochrome c levels, regulation of pro-apoptotic gene expression (e.g., p53, Bax), and down-regulation of Bcl-2 all suggested cellular apoptosis occurred via the intrinsic pathway. Significantly, at an equivalent dose of core-shell NCs, core-only NCs induced more oxidative stress, resulting in increased apoptosis. These findings shed light on the role of a CdS surface coating in reducing free radical release, decreasing cytotoxicity, and improving fluorescence, advancing the field of cell imaging.
Keyphrases
- quantum dots
- energy transfer
- cell cycle arrest
- oxidative stress
- cell death
- induced apoptosis
- endoplasmic reticulum stress
- high resolution
- diabetic rats
- pi k akt
- gene expression
- dna damage
- ischemia reperfusion injury
- signaling pathway
- reactive oxygen species
- risk assessment
- fluorescence imaging
- squamous cell carcinoma
- stem cells
- single molecule
- photodynamic therapy
- anti inflammatory
- heat stress
- cell proliferation
- cell therapy
- papillary thyroid
- climate change
- drug discovery
- endothelial cells
- heat shock protein
- young adults
- atomic force microscopy
- simultaneous determination
- fluorescent probe