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Novel Non-Viral Vectors Based on Pluronic(®) F68PEI with Application in Oncology Field
Copolymers composed of low-molecular-weight polyethylenimine (PEI) and amphiphilic Pluronics(®) are safe and efficient non-viral vectors for pDNA transfection. A variety of Pluronic(®) properties provides a base for tailoring transfection efficacy in combination with the unique biological activity o...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9739301/ https://www.ncbi.nlm.nih.gov/pubmed/36501709 http://dx.doi.org/10.3390/polym14235315 |
Sumario: | Copolymers composed of low-molecular-weight polyethylenimine (PEI) and amphiphilic Pluronics(®) are safe and efficient non-viral vectors for pDNA transfection. A variety of Pluronic(®) properties provides a base for tailoring transfection efficacy in combination with the unique biological activity of this polymer group. In this study, we describe the preparation of new copolymers based on hydrophilic Pluronic(®) F68 and PEI (F68PEI). F68PEI polyplexes obtained by doping with free F68 (1:2 and 1:5 w/w) allowed for fine-tuning of physicochemical properties and transfection activity, demonstrating improved in vitro transfection of the human bone osteosarcoma epithelial (U2OS) and oral squamous cell carcinoma (SCC-9) cells when compared to the parent formulation, F68PEI. Although all tested systems condensed pDNA at varying polymer/DNA charge ratios (N/P, 5/1–100/1), the addition of free F68 (1:5 w/w) resulted in the formation of smaller polyplexes (<200 nm). Analysis of polyplex properties by transmission electron microscopy and dynamic light scattering revealed varied polyplex morphology. Transfection potential was also found to be cell-dependent and significantly higher in SCC-9 cells compared to the control bPEI25k cells, as especially evident at higher N/P ratios (>25). The observed selectivity towards transfection of SSC-9 cells might represent a base for further optimization of a cell-specific transfection vehicle. |
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