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The development of poly-L-arginine-coated liposomes for gene delivery

In this study, liposomes coated with cationic polymers, poly-L-arginine (PLA), were assessed as a promising gene transfer system in human cervical carcinoma (HeLa) cells and human hepatoma cell line (Huh7) cells. The liposomes were prepared using egg yolk phosphatidylcholine and sodium oleate in the...

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Autores principales: Opanasopit, Praneet, Tragulpakseerojn, Jintana, Apirakaramwong, Auayporn, Ngawhirunpat, Tanasait, Rojanarata, Theerasak, Ruktanonchai, Uracha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3215165/
https://www.ncbi.nlm.nih.gov/pubmed/22114488
http://dx.doi.org/10.2147/IJN.S25336
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author Opanasopit, Praneet
Tragulpakseerojn, Jintana
Apirakaramwong, Auayporn
Ngawhirunpat, Tanasait
Rojanarata, Theerasak
Ruktanonchai, Uracha
author_facet Opanasopit, Praneet
Tragulpakseerojn, Jintana
Apirakaramwong, Auayporn
Ngawhirunpat, Tanasait
Rojanarata, Theerasak
Ruktanonchai, Uracha
author_sort Opanasopit, Praneet
collection PubMed
description In this study, liposomes coated with cationic polymers, poly-L-arginine (PLA), were assessed as a promising gene transfer system in human cervical carcinoma (HeLa) cells and human hepatoma cell line (Huh7) cells. The liposomes were prepared using egg yolk phosphatidylcholine and sodium oleate in the molar ratio of 10:2 with an ultrasonic generator and then coated with PLA. The PLA-coated liposomes (PCLs) formed complexes with plasmid DNA encoding green fluorescent protein. The complexes were characterized by agarose gel electrophoresis and investigated for their transfection efficiency in HeLa and Huh7 cells. The data were compared with PLA/DNA complexes and the positive control Lipofectamine 2000(™). The results showed that complete PCL/DNA complexes were formed at weight ratios of more than 0.05. Efficient gene transfer by PCLs was dependent on the cell type. The transfection efficiency of PCLs was about two times higher than that of PLA/DNA complexes in both HeLa cells and Huh7 cells. Cytotoxicity was determined by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay and showed that 80%–100% of both of the cells were viable after treating PCL/DNA complexes. The present results demonstrate that PCLs are a promising, nonviral gene carrier with low toxicity.
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spelling pubmed-32151652011-11-23 The development of poly-L-arginine-coated liposomes for gene delivery Opanasopit, Praneet Tragulpakseerojn, Jintana Apirakaramwong, Auayporn Ngawhirunpat, Tanasait Rojanarata, Theerasak Ruktanonchai, Uracha Int J Nanomedicine Original Research In this study, liposomes coated with cationic polymers, poly-L-arginine (PLA), were assessed as a promising gene transfer system in human cervical carcinoma (HeLa) cells and human hepatoma cell line (Huh7) cells. The liposomes were prepared using egg yolk phosphatidylcholine and sodium oleate in the molar ratio of 10:2 with an ultrasonic generator and then coated with PLA. The PLA-coated liposomes (PCLs) formed complexes with plasmid DNA encoding green fluorescent protein. The complexes were characterized by agarose gel electrophoresis and investigated for their transfection efficiency in HeLa and Huh7 cells. The data were compared with PLA/DNA complexes and the positive control Lipofectamine 2000(™). The results showed that complete PCL/DNA complexes were formed at weight ratios of more than 0.05. Efficient gene transfer by PCLs was dependent on the cell type. The transfection efficiency of PCLs was about two times higher than that of PLA/DNA complexes in both HeLa cells and Huh7 cells. Cytotoxicity was determined by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay and showed that 80%–100% of both of the cells were viable after treating PCL/DNA complexes. The present results demonstrate that PCLs are a promising, nonviral gene carrier with low toxicity. Dove Medical Press 2011 2011-10-07 /pmc/articles/PMC3215165/ /pubmed/22114488 http://dx.doi.org/10.2147/IJN.S25336 Text en © 2011 Opanasopit et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Opanasopit, Praneet
Tragulpakseerojn, Jintana
Apirakaramwong, Auayporn
Ngawhirunpat, Tanasait
Rojanarata, Theerasak
Ruktanonchai, Uracha
The development of poly-L-arginine-coated liposomes for gene delivery
title The development of poly-L-arginine-coated liposomes for gene delivery
title_full The development of poly-L-arginine-coated liposomes for gene delivery
title_fullStr The development of poly-L-arginine-coated liposomes for gene delivery
title_full_unstemmed The development of poly-L-arginine-coated liposomes for gene delivery
title_short The development of poly-L-arginine-coated liposomes for gene delivery
title_sort development of poly-l-arginine-coated liposomes for gene delivery
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3215165/
https://www.ncbi.nlm.nih.gov/pubmed/22114488
http://dx.doi.org/10.2147/IJN.S25336
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