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Published on: November 17, 2018
Visualization and Cytotoxicity of Fluorescence-Labeled Dimeric Magnetite-Gold Nanoparticles Conjugated with
S K Pirutin1,2, M V Efremova3,4, A I Yusipovich3
1M. V. Lomonosov Moscow State University, Moscow, Russia. pirutin@yandex.ru.
Abstract:
We demonstrated the possibility of penetration of magnetite-gold nanoparticles conjugated with prostate-specific membrane antigen into mouse macrophages. It was found that after 3-h incubation with nanoparticles in a concentration of 15 mg/liter at 37oC, they were seen in only 13% macrophages. In about 90% cells, the nanoparticles were detected within the cytoplasm. Under these conditions, membrane damage was revealed in 25% cells. These results should be taken into account in further development and application of nanomaterials for diagnostic and therapeutic purposes in oncology.
Insights
Magnetite-gold nanoparticles conjugated with prostate-specific membrane antigen can enter mouse macrophages. While uptake was limited, nanoparticles were found in the cytoplasm, with some cells showing membrane damage, impacting oncology applications.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Oncology
Background:
- Nanoparticles are increasingly used in oncology for diagnostics and therapeutics.
- Targeted delivery of nanoparticles to specific cells is crucial for efficacy.
- Understanding nanoparticle-cell interactions, including uptake and potential toxicity, is essential.
Purpose of the Study:
- To investigate the cellular uptake of magnetite-gold nanoparticles conjugated with prostate-specific membrane antigen in mouse macrophages.
- To assess the intracellular localization and potential cytotoxic effects of these nanoparticles.
Main Methods:
- Incubation of mouse macrophages with magnetite-gold nanoparticles conjugated with prostate-specific membrane antigen.
- Quantification of nanoparticle uptake using microscopy.
- Assessment of macrophage membrane integrity.
Main Results:
- Magnetite-gold nanoparticles conjugated with prostate-specific membrane antigen demonstrated limited uptake (13%) in mouse macrophages after 3-hour incubation at 15 mg/L and 37°C.
- Nanoparticles were predominantly found within the cytoplasm (approx. 90% of positive cells).
- Cell membrane damage was observed in 25% of macrophages under these conditions.
Conclusions:
- The study shows that targeted nanoparticles can penetrate macrophages, but with limited efficiency.
- Intracellular localization and potential for membrane damage require consideration for safe and effective nanomedicine development.
- These findings are critical for the future design of nanomaterials in cancer diagnostics and therapy.
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