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Intracellular Delivery of siRNA by Polycationic Superparamagnetic Nanoparticles

The siRNA transfection efficiency of nanoparticles (NPs), composed of a superparamagnetic iron oxide core modified with polycationic polymers (poly(hexamethylene biguanide) or branched polyethyleneimine), were studied in CHO-K1 and HeLa cell lines. Both NPs demonstrated to be good siRNA transfection...

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Detalles Bibliográficos
Autores principales: Castillo, Betzaida, Bromberg, Lev, López, Xaira, Badillo, Valerie, González Feliciano, Jose A., González, Carlos I., Hatton, T. Alan, Barletta, Gabriel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437298/
https://www.ncbi.nlm.nih.gov/pubmed/22970377
http://dx.doi.org/10.1155/2012/218940
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author Castillo, Betzaida
Bromberg, Lev
López, Xaira
Badillo, Valerie
González Feliciano, Jose A.
González, Carlos I.
Hatton, T. Alan
Barletta, Gabriel
author_facet Castillo, Betzaida
Bromberg, Lev
López, Xaira
Badillo, Valerie
González Feliciano, Jose A.
González, Carlos I.
Hatton, T. Alan
Barletta, Gabriel
author_sort Castillo, Betzaida
collection PubMed
description The siRNA transfection efficiency of nanoparticles (NPs), composed of a superparamagnetic iron oxide core modified with polycationic polymers (poly(hexamethylene biguanide) or branched polyethyleneimine), were studied in CHO-K1 and HeLa cell lines. Both NPs demonstrated to be good siRNA transfection vehicles, but unmodified branched polyethyleneimine (25 kD) was superior on both cell lines. However, application of an external magnetic field during transfection (magnetofection) increased the efficiency of the superparamagnetic NPs. Furthermore, our results reveal that these NPs are less toxic towards CHO-K1 cell lines than the unmodified polycationic-branched polyethyleneimine (PEI). In general, the external magnetic field did not alter the cell's viability nor it disrupted the cell membranes, except for the poly(hexamethylene biguanide)-modified NP, where it was observed that in CHO-K1 cells application of the external magnetic field promoted membrane damage. This paper presents new polycationic superparamagnetic NPs as promising transfection vehicles for siRNA and demonstrates the advantages of magnetofection.
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spelling pubmed-34372982012-09-11 Intracellular Delivery of siRNA by Polycationic Superparamagnetic Nanoparticles Castillo, Betzaida Bromberg, Lev López, Xaira Badillo, Valerie González Feliciano, Jose A. González, Carlos I. Hatton, T. Alan Barletta, Gabriel J Drug Deliv Research Article The siRNA transfection efficiency of nanoparticles (NPs), composed of a superparamagnetic iron oxide core modified with polycationic polymers (poly(hexamethylene biguanide) or branched polyethyleneimine), were studied in CHO-K1 and HeLa cell lines. Both NPs demonstrated to be good siRNA transfection vehicles, but unmodified branched polyethyleneimine (25 kD) was superior on both cell lines. However, application of an external magnetic field during transfection (magnetofection) increased the efficiency of the superparamagnetic NPs. Furthermore, our results reveal that these NPs are less toxic towards CHO-K1 cell lines than the unmodified polycationic-branched polyethyleneimine (PEI). In general, the external magnetic field did not alter the cell's viability nor it disrupted the cell membranes, except for the poly(hexamethylene biguanide)-modified NP, where it was observed that in CHO-K1 cells application of the external magnetic field promoted membrane damage. This paper presents new polycationic superparamagnetic NPs as promising transfection vehicles for siRNA and demonstrates the advantages of magnetofection. Hindawi Publishing Corporation 2012 2012-08-30 /pmc/articles/PMC3437298/ /pubmed/22970377 http://dx.doi.org/10.1155/2012/218940 Text en Copyright © 2012 Betzaida Castillo et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Castillo, Betzaida
Bromberg, Lev
López, Xaira
Badillo, Valerie
González Feliciano, Jose A.
González, Carlos I.
Hatton, T. Alan
Barletta, Gabriel
Intracellular Delivery of siRNA by Polycationic Superparamagnetic Nanoparticles
title Intracellular Delivery of siRNA by Polycationic Superparamagnetic Nanoparticles
title_full Intracellular Delivery of siRNA by Polycationic Superparamagnetic Nanoparticles
title_fullStr Intracellular Delivery of siRNA by Polycationic Superparamagnetic Nanoparticles
title_full_unstemmed Intracellular Delivery of siRNA by Polycationic Superparamagnetic Nanoparticles
title_short Intracellular Delivery of siRNA by Polycationic Superparamagnetic Nanoparticles
title_sort intracellular delivery of sirna by polycationic superparamagnetic nanoparticles
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437298/
https://www.ncbi.nlm.nih.gov/pubmed/22970377
http://dx.doi.org/10.1155/2012/218940
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