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界面工程化吡啶假双子表面活性剂作为 DNA、siRNA 和 mRNA 的多功能高效超分子递药系统。

Interfacially Engineered Pyridinium Pseudogemini Surfactants as Versatile and Efficient Supramolecular Delivery Systems for DNA, siRNA, and mRNA.

机构信息

Department of Pharmaceutical Sciences and Moulder Center of Drug Discovery Research, Temple University School of Pharmacy , Philadelphia, Pennsylvania 19140, United States.

出版信息

ACS Appl Mater Interfaces. 2017 Sep 6;9(35):29481-29495. doi: 10.1021/acsami.7b07066. Epub 2017 Aug 25.


DOI:10.1021/acsami.7b07066
PMID:28809098
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7774514/
Abstract

This article presents the synthesis, self-assembly, and biological activity as transfection agents for pDNA, siRNA, and mRNA of novel pyridinium pseudogemini surfactants, interfacially engineered from the most efficient gemini surfactants and lipids generated in our amphiphile research program. Formulation of novel amphiphiles in water revealed supramolecular properties very similar to those of gemini surfactants, despite their lipidlike charge/mass ratio. This dual character was found also to enhance endosomal escape and significantly increase the transfection efficiency. We were also successful in identifying the parameters governing the efficient delivery of pDNA, siRNA, and mRNA, drawing valuable structure-activity and structure-property relationships for each nucleic acid type, and establishing DNA/siRNA/mRNA comparisons. Several supramolecular complexes identified in this study proved to be extremely efficient nucleic acid delivery systems, displaying excellent serum stability and tissue penetration in three-dimensional organoids.

摘要

本文介绍了新型吡啶阳离子假双子表面活性剂的合成、自组装以及作为 pDNA、siRNA 和 mRNA 的转染试剂的生物活性,这些表面活性剂是从我们的两亲分子研究计划中生成的最有效的双子表面活性剂和脂质界面工程设计而来。在水中形成新型两亲物时,尽管其荷质比类似于脂质,但仍表现出与双子表面活性剂非常相似的超分子性质。这种双重特性还被发现能够增强内涵体逃逸,并显著提高转染效率。我们还成功地确定了有效递送 pDNA、siRNA 和 mRNA 的参数,为每种核酸类型绘制了有价值的结构-活性和结构-性质关系,并建立了 DNA/siRNA/mRNA 的比较。本研究中鉴定的几种超分子复合物被证明是非常有效的核酸递送系统,在三维类器官中显示出优异的血清稳定性和组织穿透性。

相似文献

[1]
Interfacially Engineered Pyridinium Pseudogemini Surfactants as Versatile and Efficient Supramolecular Delivery Systems for DNA, siRNA, and mRNA.

ACS Appl Mater Interfaces. 2017-8-25

[2]
Modulation of pyridinium cationic lipid-DNA complex properties by pyridinium gemini surfactants and its impact on lipoplex transfection properties.

Mol Pharm. 2014-2-3

[3]
Interfacial engineering of pyridinium gemini surfactants for the generation of synthetic transfection systems.

Biomaterials. 2013-6-12

[4]
Spacer structure and hydrophobicity influences transfection activity of novel polycationic gemini amphiphiles.

Bioorg Med Chem Lett. 2017-8-1

[5]
Novel polymerizable surfactants with pH-sensitive amphiphilicity and cell membrane disruption for efficient siRNA delivery.

Bioconjug Chem. 2007

[6]
Novel pyridinium surfactants for efficient, nontoxic in vitro gene delivery.

Proc Natl Acad Sci U S A. 1997-2-18

[7]
Self-assembling complexes between binary mixtures of lipids with different linkers and nucleic acids promote universal mRNA, DNA and siRNA delivery.

J Control Release. 2017-2-1

[8]
Structural studies of the formation of lipoplexes between siRNA and selected bis-imidazolium gemini surfactants.

Colloids Surf B Biointerfaces. 2016-10-1

[9]
Ammonium Gemini Surfactants Form Complexes with Model Oligomers of siRNA and dsDNA.

Int J Mol Sci. 2019-11-7

[10]
Development of lyophilized gemini surfactant-based gene delivery systems: influence of lyophilization on the structure, activity and stability of the lipoplexes.

J Pharm Pharm Sci. 2012

引用本文的文献

[1]
Lipid-based nucleic acid therapeutics with in vivo efficacy.

Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2023-3

[2]
Lipids and Lipid Derivatives for RNA Delivery.

Chem Rev. 2021-10-27

[3]
Novel Synthesis of Substituted 2-Trifluoromethyl and 2-Perfluoroalkyl -Arylpyridinium Compounds-Mechanistic Insights.

Molecules. 2019-6-25

[4]
A Gemini Cationic Lipid with Histidine Residues as a Novel Lipid-Based Gene Nanocarrier: A Biophysical and Biochemical Study.

Nanomaterials (Basel). 2018-12-16

[5]
Transfection by cationic gemini lipids and surfactants.

Medchemcomm. 2018-7-17

[6]
Nanoscale platforms for messenger RNA delivery.

Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2018-5-4

本文引用的文献

[1]
Synthesis, Physicochemical Characterization, and Interaction with DNA of Long-Alkyl-Chain Gemini Pyridinium Surfactants.

Chempluschem. 2015-6

[2]
Enhancement of liposome mediated gene transfer by adding cholesterol and cholesterol modulating drugs.

Biochim Biophys Acta. 2016-12

[3]
A Virus-Mimicking, Endosomolytic Liposomal System for Efficient, pH-Triggered Intracellular Drug Delivery.

ACS Appl Mater Interfaces. 2016-8-22

[4]
Interactions between DNA and Gemini surfactant: impact on gene therapy: part I.

Nanomedicine (Lond). 2016-1-20

[5]
Gene therapy returns to centre stage.

Nature. 2015-10-15

[6]
Modified mRNA as an alternative to plasmid DNA (pDNA) for transcript replacement and vaccination therapy.

Expert Opin Biol Ther. 2015

[7]
Applications of the CRISPR-Cas9 system in cancer biology.

Nat Rev Cancer. 2015-7

[8]
Synthetic vectors for gene delivery: An overview of their evolution depending on routes of administration.

Biotechnol J. 2015-9

[9]
Cationic lipophosphoramidates containing a hydroxylated polar headgroup for improving gene delivery.

Mol Pharm. 2015-6-1

[10]
Influence of cholesterol on liposome stability and on in vitro drug release.

Drug Deliv Transl Res. 2015-6

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