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Folate-conjugated polyspermine for lung cancer–targeted gene therapy
Biodegradable polyamines have long been studied as potential recombinant viral gene vectors. Spermine (SPE) is an endogenous tetra-amine with excellent biocompatibility yet poor gene condensation capacity. We have previously synthesized a polyspermine based on SPE and poly(ethylene glycol) (PEG) dia...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951589/ https://www.ncbi.nlm.nih.gov/pubmed/27471674 http://dx.doi.org/10.1016/j.apsb.2016.03.010 |
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author | Zhang, Mei Kim, You-Kyoung Cui, Pengfei Zhang, Jialiang Qiao, Jianbin He, Yujing Lyu, Jinyuan Luo, Chengqiong Xing, Lei Jiang, Hulin |
author_facet | Zhang, Mei Kim, You-Kyoung Cui, Pengfei Zhang, Jialiang Qiao, Jianbin He, Yujing Lyu, Jinyuan Luo, Chengqiong Xing, Lei Jiang, Hulin |
author_sort | Zhang, Mei |
collection | PubMed |
description | Biodegradable polyamines have long been studied as potential recombinant viral gene vectors. Spermine (SPE) is an endogenous tetra-amine with excellent biocompatibility yet poor gene condensation capacity. We have previously synthesized a polyspermine based on SPE and poly(ethylene glycol) (PEG) diacrylate (SPE-alt-PEG) for enhanced transfection performance, but the synthesized SPE-alt-PEG still lacked specificity towards cancer cells. In this study, folic acid (FA) was incorporated into SPE-alt-PEG to fabricate a targeted gene delivery vector (FA-SPE-PEG) via an acylation reaction. FA-SPE-PEG exhibited mild cytotoxicity in both cancer cells and normal cells. FA-SPE-PEG possessed higher transfection efficiency than PEI 25 K and Lipofectamine(®) 2000 in two tested cancer cell lines at functional weight ratios, and its superiority over untargeted SPE-alt-PEG was prominent in cells with overexpressed folate receptors (FRs). Moreover, in vivo delivery of green fluorescent protein (GFP) with FA-SPE-PEG resulted in highest fluorescent signal intensity of all investigated groups. FA-SPE-PEG showed remarkably enhanced specificity towards cancer cells both in vivo and in vitro due to the interaction between FA and FRs. Taken together, FA-SPE-PEG was demonstrated to be a prospective targeted gene delivery vector with high transfection capacity and excellent biocompatibility. |
format | Online Article Text |
id | pubmed-4951589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-49515892016-07-28 Folate-conjugated polyspermine for lung cancer–targeted gene therapy Zhang, Mei Kim, You-Kyoung Cui, Pengfei Zhang, Jialiang Qiao, Jianbin He, Yujing Lyu, Jinyuan Luo, Chengqiong Xing, Lei Jiang, Hulin Acta Pharm Sin B Original Article Biodegradable polyamines have long been studied as potential recombinant viral gene vectors. Spermine (SPE) is an endogenous tetra-amine with excellent biocompatibility yet poor gene condensation capacity. We have previously synthesized a polyspermine based on SPE and poly(ethylene glycol) (PEG) diacrylate (SPE-alt-PEG) for enhanced transfection performance, but the synthesized SPE-alt-PEG still lacked specificity towards cancer cells. In this study, folic acid (FA) was incorporated into SPE-alt-PEG to fabricate a targeted gene delivery vector (FA-SPE-PEG) via an acylation reaction. FA-SPE-PEG exhibited mild cytotoxicity in both cancer cells and normal cells. FA-SPE-PEG possessed higher transfection efficiency than PEI 25 K and Lipofectamine(®) 2000 in two tested cancer cell lines at functional weight ratios, and its superiority over untargeted SPE-alt-PEG was prominent in cells with overexpressed folate receptors (FRs). Moreover, in vivo delivery of green fluorescent protein (GFP) with FA-SPE-PEG resulted in highest fluorescent signal intensity of all investigated groups. FA-SPE-PEG showed remarkably enhanced specificity towards cancer cells both in vivo and in vitro due to the interaction between FA and FRs. Taken together, FA-SPE-PEG was demonstrated to be a prospective targeted gene delivery vector with high transfection capacity and excellent biocompatibility. Elsevier 2016-07 2016-04-12 /pmc/articles/PMC4951589/ /pubmed/27471674 http://dx.doi.org/10.1016/j.apsb.2016.03.010 Text en © 2016 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Zhang, Mei Kim, You-Kyoung Cui, Pengfei Zhang, Jialiang Qiao, Jianbin He, Yujing Lyu, Jinyuan Luo, Chengqiong Xing, Lei Jiang, Hulin Folate-conjugated polyspermine for lung cancer–targeted gene therapy |
title | Folate-conjugated polyspermine for lung cancer–targeted gene therapy |
title_full | Folate-conjugated polyspermine for lung cancer–targeted gene therapy |
title_fullStr | Folate-conjugated polyspermine for lung cancer–targeted gene therapy |
title_full_unstemmed | Folate-conjugated polyspermine for lung cancer–targeted gene therapy |
title_short | Folate-conjugated polyspermine for lung cancer–targeted gene therapy |
title_sort | folate-conjugated polyspermine for lung cancer–targeted gene therapy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951589/ https://www.ncbi.nlm.nih.gov/pubmed/27471674 http://dx.doi.org/10.1016/j.apsb.2016.03.010 |
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