Volume 9, Issue 4 (Autumn 2020)
aumj 2020, 9(4): 367-379 |
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Khamehchian S, Hosseinkhani S, Nikkhah M. Effect of Peptide Derived from Scorpion Toxin on Enhanced Permeability of Doxorubicin Conjugated Gold Nanoparticles in HeLa and MDA-MB-231 Cells. aumj 2020; 9 (4) :367-379
URL: http://aums.abzums.ac.ir/article-1-1144-en.html
URL: http://aums.abzums.ac.ir/article-1-1144-en.html
1- Department of Venomous Animals and Antivenom Production, Razi Vaccine and Serum Research Institute, Agricultural Research Education and Extension Organization (AREEO), Karaj, Iran , s.khamehchian@rvsri.ac.ir
2- Department of Nanobiotechnology, Faculty of Biological Science, Tarbiat Modares University, Tehran, Iran
2- Department of Nanobiotechnology, Faculty of Biological Science, Tarbiat Modares University, Tehran, Iran
Abstract: (2572 Views)
Background: Cell penetrating peptides (CPPs) can enter a cell through the cell membrane, and used in the fields of drug delivery, gene therapy, and cancer therapy by their property transporting various molecules into cytoplasm. Gold nanospheres (GNSs) are a useful tool for molecular imaging, because they are not cytotoxic and have high solubility, excellent light scattering property and ease of synthesis. We constructed a drug delivery system by developing gold nanospheres conjugated to MCaUF1-9-C, a CPP derived from maurocalcine (MCa) scorpion toxin. We examined the applicability of this cell-selective anti-cancer drug delivery system by evaluating its cell-penetrating and cell death activities.
Methods: Cell viability of HeLa and MDA-MB-231 cells, against 500 nanomolar concentration of doxorubicin (DOX)-conjugated gold nanoparticles (DOX-GNPs, and DOX-MCaUF1–9-C-GNP) were evaluated using MTT assay. Cell penetrability of MCaUF1-9-C peptide conjugated to gold nanoparticles investigated using of dark field imaging and atomic absorption spectroscopy (AAS).
Results: HeLa cell viability was about 87% when treated with DOX-GNP and DOX-MCaUF1-9-C-GNP, whereas DOX-MCaUF1–9-C-GNP induced high cytotoxicity in MDA-MB-231 cells (30%). Dark field imaging demonstrated higher affinity of MCaUF1–9-C-GNP for the MDA-MB-231 cell compared with HeLa cells. Moreover, atomic absorption spectrometry data analysis showed that 33% of the total amounts of the applied MCaUF1–9-C-GNP were internalized in MDA-MB-231 cells.
Conclusion: These results demonstrated that peptide conjugated GNP would be a useful tool for the development of a cell-selective drug delivery system.
Methods: Cell viability of HeLa and MDA-MB-231 cells, against 500 nanomolar concentration of doxorubicin (DOX)-conjugated gold nanoparticles (DOX-GNPs, and DOX-MCaUF1–9-C-GNP) were evaluated using MTT assay. Cell penetrability of MCaUF1-9-C peptide conjugated to gold nanoparticles investigated using of dark field imaging and atomic absorption spectroscopy (AAS).
Results: HeLa cell viability was about 87% when treated with DOX-GNP and DOX-MCaUF1-9-C-GNP, whereas DOX-MCaUF1–9-C-GNP induced high cytotoxicity in MDA-MB-231 cells (30%). Dark field imaging demonstrated higher affinity of MCaUF1–9-C-GNP for the MDA-MB-231 cell compared with HeLa cells. Moreover, atomic absorption spectrometry data analysis showed that 33% of the total amounts of the applied MCaUF1–9-C-GNP were internalized in MDA-MB-231 cells.
Conclusion: These results demonstrated that peptide conjugated GNP would be a useful tool for the development of a cell-selective drug delivery system.
Type of Study: Research |
Subject:
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Received: 2020/07/26 | Accepted: 2020/10/01 | Published: 2020/10/01
Received: 2020/07/26 | Accepted: 2020/10/01 | Published: 2020/10/01
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