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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...

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Autores principales: Zhang, Mei, Kim, You-Kyoung, Cui, Pengfei, Zhang, Jialiang, Qiao, Jianbin, He, Yujing, Lyu, Jinyuan, Luo, Chengqiong, Xing, Lei, Jiang, Hulin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
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.
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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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