Abstract
In the present study it is shown that poloxamer 188, added before or immediately after an electrical pulse used for electroporation, decreases the number of dead cells and at the same time does not reduce the number of reversible electropores through which small molecules (cisplatin, bleomycin, or propidium iodide) can pass/diffuse. It was suggested that hydrophobic sections of poloxamer 188 molecules are incorporated into the edges of pores and that their hydrophilic parts act as brushy pore structures. The formation of brushy pores may reduce the expansion of pores and delay the irreversible electropermeability. Tumors were implanted subcutaneously in both flanks of nude mice using HeLa cells, transfected with genes for red fluorescent protein and luciferase. The volume of tumors stopped to grow after electrochemotherapy and the use of poloxamer 188 reduced the edema near the electrode and around the subcutaneously growing tumors. © 2010 Iana Tsoneva et al.
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CITATION STYLE
Tsoneva, I., Iordanov, I., Berger, A. J., Tomov, T., Nikolova, B., Mudrov, N., & Berger, M. R. (2010). Electrodelivery of drugs into cancer cells in the presence of poloxamer 188. Journal of Biomedicine and Biotechnology, 2010. https://doi.org/10.1155/2010/314213
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