Literature DB >> 29801966

Novel carbamate-linked quaternary ammonium lipids containing unsaturated hydrophobic chains for gene delivery.

Hengjun Zhou1, Jian Yang2, Yanyan Du2, Shuang Fu3, Chenxi Song3, Defu Zhi2, Yinan Zhao2, Huiying Chen2, Shubiao Zhang4, Shufen Zhang5.   

Abstract

In this paper, two novel carbamate-linked pan class="Chemical">quaternary ammonium lipids (MU18: a lipid with a mono-ammonium head; GU18: a lipid with a Gemini-ammonium head) containing unsaturated hydrophobic chains were designed and synthesized. The chemical structures of the synthetic lipids were characterized by infrared spectrum, ESI-MS, 1H NMR, 13C NMR, and HPLC. For investigating the effect of unsaturation on gene delivery, the previous reported saturated cationic liposomes (MS18 and GS18) were used as comparison. Cationic liposomes were prepared by using these cationic lipids and neutral lipid DOPE at the molar ratio of 1:1. Particle sizes and zeta potentials of the cationic liposomes were studied to show that they were suitable for gene transfection. The binding abilities of the cationic liposomes were investigated by gel electrophoresis at various N/P ratios from 0.5/1 to 8/1. The results indicated that the binding ability of GU18 was much better than MU18 and the saturated cationic liposomes (MS18 and GS18). DNA transfection of these liposomes comparable to commercially available reagent (DOTAP) was achieved in vitro against Hela, HepG-2 and NCI-H460 cell lines. GU18 showed higher transfection at the N/P ratio of 3/1 than other cationic liposomes and the positive control, DOTAP. All of the liposomes presented a relatively low cytotoxicity, which was measured by MTT. Therefore, the synthetic lipids bearing unsaturated hydrophobic chains and Gemini-head could be promising candidates for gene delivery.
Copyright © 2018 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Cytotoxicity; Gene delivery; Hydrophobic chains; Quaternary ammonium lipids; Transfection

Mesh:

Substances:

Year:  2018        PMID: 29801966     DOI: 10.1016/j.bmc.2018.05.029

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  2 in total

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