Сationic liposomes as delivery systems for nucleic acids

Objectives. Gene therapy is based on the introduction of genetic material into cells, tissues, or organs for the treatment of hereditary or acquired diseases. A key factor in the success of gene therapy is the development of delivery systems that can efficiently transfer genetic material to the plac...

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Main Authors: A. A. Mikheev, E. V. Shmendel, E. S. Zhestovskaya, G. V. Nazarov, M. A. Maslov
Format: Article
Language:Russian
Published: MIREA - Russian Technological University 2020-03-01
Series:Тонкие химические технологии
Subjects:
Online Access:https://www.finechem-mirea.ru/jour/article/view/1582
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spelling doaj-eff474613d0545fc9c9d7e475380291a2021-07-28T13:24:02ZrusMIREA - Russian Technological UniversityТонкие химические технологии2410-65932686-75752020-03-0115172710.32362/2410-6593-2020-15-1-7-271574Сationic liposomes as delivery systems for nucleic acidsA. A. Mikheev0E. V. Shmendel1E. S. Zhestovskaya2G. V. Nazarov3M. A. Maslov4Scientific Center “Signal”MIREA – Russian Technological University (M.V. Lomonosov Institute of Fine Chemical Technologies)Scientific Center “Signal”Scientific Center “Signal”MIREA – Russian Technological University (M.V. Lomonosov Institute of Fine Chemical Technologies)Objectives. Gene therapy is based on the introduction of genetic material into cells, tissues, or organs for the treatment of hereditary or acquired diseases. A key factor in the success of gene therapy is the development of delivery systems that can efficiently transfer genetic material to the place of their therapeutic action without causing any associated side effects. Over the past 10 years, significant effort has been directed toward creating more efficient and biocompatible vectors capable of transferring nucleic acids (NAs) into cells without inducing an immune response. Cationic liposomes are among the most versatile tools for delivering NAs into cells; however, the use of liposomes for gene therapy is limited by their low specificity. This is due to the presence of various biological barriers to the complex of liposomes with NA, including instability in biological fluids, interaction with serum proteins, plasma and nuclear membranes, and endosomal degradation. This review summarizes the results of research in recent years on the development of cationic liposomes that are effective in vitro and in vivo. Particular attention is paid to the individual structural elements of cationic liposomes that determine the transfection efficiency and cytotoxicity. The purpose of this review was to provide a theoretical justification of the most promising choice of cationic liposomes for the delivery of NAs into eukaryotic cells and study the effect of the composition of cationic lipids (CLs) on the transfection efficiency in vitro.Results. As a result of the analysis of the related literature, it can be argued that one of the most promising delivery systems of NAs is CL based on cholesterol and spermine with the addition of a helper lipid DOPE. In addition, it was found that varying the composition of cationic liposomes, the ratio of CL to NA, or the size and zeta potential of liposomes has a significant effect on the transfection efficiency.Conclusions. Further studies in this direction should include optimization of the conditions for obtaining cationic liposomes, taking into account the physicochemical properties and established laws. It is necessary to identify mechanisms that increase the efficiency of NA delivery in vitro by searching for optimal structures of cationic liposomes, determining the ratio of lipoplex components, and studying the delivery efficiency and properties of multicomponent liposomes.https://www.finechem-mirea.ru/jour/article/view/1582liposomesnucleic acidsgene therapylipidsdelivery
collection DOAJ
language Russian
format Article
sources DOAJ
author A. A. Mikheev
E. V. Shmendel
E. S. Zhestovskaya
G. V. Nazarov
M. A. Maslov
spellingShingle A. A. Mikheev
E. V. Shmendel
E. S. Zhestovskaya
G. V. Nazarov
M. A. Maslov
Сationic liposomes as delivery systems for nucleic acids
Тонкие химические технологии
liposomes
nucleic acids
gene therapy
lipids
delivery
author_facet A. A. Mikheev
E. V. Shmendel
E. S. Zhestovskaya
G. V. Nazarov
M. A. Maslov
author_sort A. A. Mikheev
title Сationic liposomes as delivery systems for nucleic acids
title_short Сationic liposomes as delivery systems for nucleic acids
title_full Сationic liposomes as delivery systems for nucleic acids
title_fullStr Сationic liposomes as delivery systems for nucleic acids
title_full_unstemmed Сationic liposomes as delivery systems for nucleic acids
title_sort сationic liposomes as delivery systems for nucleic acids
publisher MIREA - Russian Technological University
series Тонкие химические технологии
issn 2410-6593
2686-7575
publishDate 2020-03-01
description Objectives. Gene therapy is based on the introduction of genetic material into cells, tissues, or organs for the treatment of hereditary or acquired diseases. A key factor in the success of gene therapy is the development of delivery systems that can efficiently transfer genetic material to the place of their therapeutic action without causing any associated side effects. Over the past 10 years, significant effort has been directed toward creating more efficient and biocompatible vectors capable of transferring nucleic acids (NAs) into cells without inducing an immune response. Cationic liposomes are among the most versatile tools for delivering NAs into cells; however, the use of liposomes for gene therapy is limited by their low specificity. This is due to the presence of various biological barriers to the complex of liposomes with NA, including instability in biological fluids, interaction with serum proteins, plasma and nuclear membranes, and endosomal degradation. This review summarizes the results of research in recent years on the development of cationic liposomes that are effective in vitro and in vivo. Particular attention is paid to the individual structural elements of cationic liposomes that determine the transfection efficiency and cytotoxicity. The purpose of this review was to provide a theoretical justification of the most promising choice of cationic liposomes for the delivery of NAs into eukaryotic cells and study the effect of the composition of cationic lipids (CLs) on the transfection efficiency in vitro.Results. As a result of the analysis of the related literature, it can be argued that one of the most promising delivery systems of NAs is CL based on cholesterol and spermine with the addition of a helper lipid DOPE. In addition, it was found that varying the composition of cationic liposomes, the ratio of CL to NA, or the size and zeta potential of liposomes has a significant effect on the transfection efficiency.Conclusions. Further studies in this direction should include optimization of the conditions for obtaining cationic liposomes, taking into account the physicochemical properties and established laws. It is necessary to identify mechanisms that increase the efficiency of NA delivery in vitro by searching for optimal structures of cationic liposomes, determining the ratio of lipoplex components, and studying the delivery efficiency and properties of multicomponent liposomes.
topic liposomes
nucleic acids
gene therapy
lipids
delivery
url https://www.finechem-mirea.ru/jour/article/view/1582
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