We
report a simple one-pot microwave-assisted green-synthesis route
for the fabrication of bright red-luminescent graphene quantum dots
(GQDs) using ethanolic extracts of Mangifera indica (mango) leaves, hence addressing them as mGQDs. The mGQDs were quantum-sized
ranging from 2 to 8 nm and exhibited excitation-independent fluorescence
emission in the near-infrared (NIR) region between 650 and 750 nm.
The mGQDs showed defects in their structure and were highly crystalline
in nature as confirmed by Raman spectroscopy and powdered X-ray diffraction
analysis, respectively. These mGQDs showed 100% cellular uptake and
excellent biocompatibility on L929 cells even at high concentration
(0.1 mg/mL) 24 h post-treatment. Cell cycle analysis showed increased
proliferation in L929 cells upon mGQDs treatment. Furthermore, the
mGQDs were demonstrated as NIR-responsive fluorescent bioimaging probes,
self-localizing themselves selectively in the cell cytoplasm. Also,
the temperature-dependent fluorescence intensity of these GQDs proved
them as a very competent temperature sensing probe (at 10–80
°C). The temperature sensing stability analysis showed that the
temperature signal remains stable even after multiple cycles of temperature
switching between 30–80 °C. Furthermore, we analyzed intracellular
temperature (25–45 °C) of live L929 cells based on the
fluorescence intensity of the mGQDs. It was observed that with an
increasing temperature there was a decrease in the fluorescence intensity
of the mGQDs making it a suitable probe for temperature sensing. In
sum, a biocompatible, scalable, photostable, green synthesis based
mGQDs were prepared for NIR imaging and nanothermometry applications
which can play a pivotal role in biomedical nanotechnology.
We report a simple one-pot microwave assisted “green synthesis” of Graphene Quantum Dots (GQDs) using grape seed extract as a green therapeutic carbon source. These GQDs readily self-assemble, hereafter referred to as “self-assembled” GQDs (sGQDs) in the aqueous medium. The sGQDs enter via caveolae and clathrin-mediated endocytosis and target themselves into cell nucleus within 6–8 h without additional assistance of external capping/targeting agent. The tendency to self-localize themselves into cell nucleus also remains consistent in different cell lines such as L929, HT-1080, MIA PaCa-2, HeLa, and MG-63 cells, thereby serving as a nucleus labelling agent. Furthermore, the sGQDs are highly biocompatible and act as an enhancer in cell proliferation in mouse fibroblasts as confirmed by in vitro wound scratch assay and cell cycle analysis. Also, photoluminescence property of sGQDs (lifetime circa (ca.) 10 ns) was used for optical pH sensing application. The sGQDs show linear, cyclic and reversible trend in its fluorescence intensity between pH 3 and pH 10 (response time: ~1 min, sensitivity −49.96 ± 3.5 mV/pH) thereby serving as a good pH sensing agent. A simple, cost-effective, scalable and green synthetic approach based sGQDs can be used to develop selective organelle labelling, nucleus targeting in theranostics, and optical sensing probes.
An Indian fig tree serves as a green factory by providing withered leaves as a carbon source for graphene quantum dots synthesis. The quantum dots are multi-functional and have tremendous theranostic biomedical applications.
Developing a nanotheranostic agent with better image resolution and high accumulation into solid tumor microenvironment is a challenging task. Herein, we established a light mediated phototriggered strategy for enhanced tumor accumulation of nanohybrids. A multifunctional liposome based nanotheranostics loaded with gold nanoparticles (AuNPs) and emissive graphene quantum dots (GQDs) were engineered named as NFGL. Further, doxorubicin hydrochloride was encapsulated in NFGL to exhibit phototriggered chemotherapy and functionalized with folic acid targeting ligands. Encapsulated agents showed imaging bimodality for in vivo tumor diagnosis due to their high contrast and emissive nature. Targeted NFGL nanohybrids demonstrated near infrared light (NIR, 750 nm) mediated tumor reduction because of generated heat and Reactive Oxygen Species (ROS). Moreover, NFGL nanohybrids exhibited remarkable ROS scavenging ability as compared to GQDs loaded liposomes validated by antitumor study. Hence, this approach and engineered system could open new direction for targeted imaging and cancer therapy.
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