Materials and Methods: GQDs nanoparticles were synthesized by pyrolysis of L-glutamic acid and its surface was coated with PEG and amine agent to create a longer half-life and more fluorescence intensity, and it was conjugated with folic acid for better binding to MCF-7 cancer cell line with folic acid receptor by thermal method. The structure of the nanocarrier was investigated using FTIR spectroscopy, fluorimetry, and TEM imaging methods. Penetration of nanoparticles into cells and their fluorescence emission were investigated by confocal microscopy.
Results: The synthesized GQDs had a uniform, relatively spherical structure and a size below 10 nm. With the addition of amine and PEG agents to GQDs nanoparticles, significant fluorescence intensities of up to 1000 a.u. were observed. According to the FTIR results, folic acid was successfully conjugated on the GQDs nanocarrier after using thermal reaction. The entry and fluorescence emission of nanoparticles into MCF-7 cells was confirmed using confocal microscopy.
Conclusion: According to the results, replacing the thermal method in the synthesis of targeted GQDs nanoparticles, instead of using chemical reagents, can provide a cost-effective and easier method. Pegylated and folated GQDs were suitable nanocarriers for targeted drug delivery to the MCF-7 breast cancer cell line.Rights and permissions | |
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