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A Cationic Stearamide‐based Solid Lipid Nanoparticle for Delivering Yamanaka Factors: Evaluation of the Transfection Efficiency

Induced pluripotent stem cells (IPSC) are preferred as an alternative source for regenerative medicine, disease modeling, and drug screening due to their unique properties. As seen from the previous studies in the literature, most of the vector systems to transfer reprogramming factors are viral‐bas...

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Autores principales: Alkan, Funda, Varlı, Hanife Sevgi, Demirbilek, Murat, Kaplan, Engin, Laçin, Nelisa Türkoğlu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7668193/
https://www.ncbi.nlm.nih.gov/pubmed/33235824
http://dx.doi.org/10.1002/open.202000244
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author Alkan, Funda
Varlı, Hanife Sevgi
Demirbilek, Murat
Kaplan, Engin
Laçin, Nelisa Türkoğlu
author_facet Alkan, Funda
Varlı, Hanife Sevgi
Demirbilek, Murat
Kaplan, Engin
Laçin, Nelisa Türkoğlu
author_sort Alkan, Funda
collection PubMed
description Induced pluripotent stem cells (IPSC) are preferred as an alternative source for regenerative medicine, disease modeling, and drug screening due to their unique properties. As seen from the previous studies in the literature, most of the vector systems to transfer reprogramming factors are viral‐based and have some well‐known limitations. This study aims to develop a non‐viral vector system for the transfection of reprogramming factors. Cationic stearamide lipid nanoparticles (CSLN) were prepared via the solvent diffusion method. The obtained CSLNs were used for the delivery of plasmid DNA (pDNA) encoding Oct3/4, Sox2, Klf4, and GFP to fibroblast cell lines. The optimization studies, for zeta potential and particle size of the conjugate, was performed to achieve high cell viability. CSLN63 with 36.5±0.06 mV zeta potential and 173.6±13.91 nm size was used for the transfection of Fibroblast cells. The transfection efficiency was observed by following GFP expression and was found as 70 %±0.11. The expression of the Oct4, Sox2, Klf4 was determined by RT‐qPCR; an increase was observed after the 12th cycle in Klf4 (Ct averages: 13,41), Sox2 (Ct averages; 12,4), Oct4 (Ct average; 13,77). The tendency of colonization was observed. The upregulation efficiency of Oct4 and SSEA‐1 with CSLN and another non‐viral vector designed for the transportation of Yamanaka factors developed in our lab previously were compared with flow cytometer analysis.
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spelling pubmed-76681932020-11-23 A Cationic Stearamide‐based Solid Lipid Nanoparticle for Delivering Yamanaka Factors: Evaluation of the Transfection Efficiency Alkan, Funda Varlı, Hanife Sevgi Demirbilek, Murat Kaplan, Engin Laçin, Nelisa Türkoğlu ChemistryOpen Full Papers Induced pluripotent stem cells (IPSC) are preferred as an alternative source for regenerative medicine, disease modeling, and drug screening due to their unique properties. As seen from the previous studies in the literature, most of the vector systems to transfer reprogramming factors are viral‐based and have some well‐known limitations. This study aims to develop a non‐viral vector system for the transfection of reprogramming factors. Cationic stearamide lipid nanoparticles (CSLN) were prepared via the solvent diffusion method. The obtained CSLNs were used for the delivery of plasmid DNA (pDNA) encoding Oct3/4, Sox2, Klf4, and GFP to fibroblast cell lines. The optimization studies, for zeta potential and particle size of the conjugate, was performed to achieve high cell viability. CSLN63 with 36.5±0.06 mV zeta potential and 173.6±13.91 nm size was used for the transfection of Fibroblast cells. The transfection efficiency was observed by following GFP expression and was found as 70 %±0.11. The expression of the Oct4, Sox2, Klf4 was determined by RT‐qPCR; an increase was observed after the 12th cycle in Klf4 (Ct averages: 13,41), Sox2 (Ct averages; 12,4), Oct4 (Ct average; 13,77). The tendency of colonization was observed. The upregulation efficiency of Oct4 and SSEA‐1 with CSLN and another non‐viral vector designed for the transportation of Yamanaka factors developed in our lab previously were compared with flow cytometer analysis. John Wiley and Sons Inc. 2020-11-16 /pmc/articles/PMC7668193/ /pubmed/33235824 http://dx.doi.org/10.1002/open.202000244 Text en © 2020 The Authors. Published by Wiley-VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Full Papers
Alkan, Funda
Varlı, Hanife Sevgi
Demirbilek, Murat
Kaplan, Engin
Laçin, Nelisa Türkoğlu
A Cationic Stearamide‐based Solid Lipid Nanoparticle for Delivering Yamanaka Factors: Evaluation of the Transfection Efficiency
title A Cationic Stearamide‐based Solid Lipid Nanoparticle for Delivering Yamanaka Factors: Evaluation of the Transfection Efficiency
title_full A Cationic Stearamide‐based Solid Lipid Nanoparticle for Delivering Yamanaka Factors: Evaluation of the Transfection Efficiency
title_fullStr A Cationic Stearamide‐based Solid Lipid Nanoparticle for Delivering Yamanaka Factors: Evaluation of the Transfection Efficiency
title_full_unstemmed A Cationic Stearamide‐based Solid Lipid Nanoparticle for Delivering Yamanaka Factors: Evaluation of the Transfection Efficiency
title_short A Cationic Stearamide‐based Solid Lipid Nanoparticle for Delivering Yamanaka Factors: Evaluation of the Transfection Efficiency
title_sort cationic stearamide‐based solid lipid nanoparticle for delivering yamanaka factors: evaluation of the transfection efficiency
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7668193/
https://www.ncbi.nlm.nih.gov/pubmed/33235824
http://dx.doi.org/10.1002/open.202000244
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