Boosting transfection efficiency: A systematic study using layer-by-layer based gene delivery platform; Materials Science and Engineering: C; Vol. 126

Dades bibliogràfiques
Parent link:Materials Science and Engineering: C
Vol. 126.— 2021.— [112161, 11 p.]
Autor corporatiu: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий
Altres autors: Tarakanchikova Ya. V. Yana Vladimirovna, Linnik D. S. Dmitrii Sergeevich, Mashel T. V. Tatjyana Vyacheslavovna, Muslimov A. R. Albert, Pavlov S. I. Sergey Igorevich, Lepik K. V. Kirill Viktorovich, Zyuzin M. V. Mikhail, Sukhorukov G. B. Gleb Borisovich, Timin A. S. Aleksandr Sergeevich
Sumari:Title screen
Nowadays, the nanoparticle-based delivery approach is becoming more and more attractive in gene therapy due to its low toxicity and immunogenicity, sufficient packaging capacity, targeting, and straightforward, low-cost, large-scale good manufacturing practice (GMP) production. A number of research works focusing on multilayer structures have explored different factors and parameters that can affect the delivery efficiency of pDNA. However, there are no systematic studies on the performance of these structures for enhanced gene delivery regarding the gene loading methods, the use of additional organic components and cell/particle incubation conditions. Here, we conducted a detailed analysis of different parameters such as (i) strategy for loading pDNA into carriers, (ii) incorporating both pDNA and organic additives within one carrier and (iii) variation of cell/particle incubation conditions, to evaluate their influence on the efficiency of pDNA delivery with multilayer structures consisting of inorganic cores and polymer layers. Our results reveal that an appropriate combination of all these parameters leads to the development of optimized protocols for high transfection efficiency, compared to the non-optimized process (> 70% vs. < 7%), and shows a good safety profile. In conclusion, we provide the proof-of-principle that these multilayer structures with the developed parameters are a promising non-viral platform for an efficient delivery of nucleic acids.
Режим доступа: по договору с организацией-держателем ресурса
Idioma:anglès
Publicat: 2021
Matèries:
Accés en línia:https://doi.org/10.1016/j.msec.2021.112161
Format: Electrònic Capítol de llibre
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=667957

MARC

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200 1 |a Boosting transfection efficiency: A systematic study using layer-by-layer based gene delivery platform  |f Ya. V. Tarakanchikova, D. S. Linnik, T. V. Mashel [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 47 tit.] 
330 |a Nowadays, the nanoparticle-based delivery approach is becoming more and more attractive in gene therapy due to its low toxicity and immunogenicity, sufficient packaging capacity, targeting, and straightforward, low-cost, large-scale good manufacturing practice (GMP) production. A number of research works focusing on multilayer structures have explored different factors and parameters that can affect the delivery efficiency of pDNA. However, there are no systematic studies on the performance of these structures for enhanced gene delivery regarding the gene loading methods, the use of additional organic components and cell/particle incubation conditions. Here, we conducted a detailed analysis of different parameters such as (i) strategy for loading pDNA into carriers, (ii) incorporating both pDNA and organic additives within one carrier and (iii) variation of cell/particle incubation conditions, to evaluate their influence on the efficiency of pDNA delivery with multilayer structures consisting of inorganic cores and polymer layers. Our results reveal that an appropriate combination of all these parameters leads to the development of optimized protocols for high transfection efficiency, compared to the non-optimized process (> 70% vs. < 7%), and shows a good safety profile. In conclusion, we provide the proof-of-principle that these multilayer structures with the developed parameters are a promising non-viral platform for an efficient delivery of nucleic acids. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
338 |b Российский научный фонд  |d 20-45-01012 
338 |b Российский фонд фундаментальных исследований  |d 19-29-04025 
461 |t Materials Science and Engineering: C 
463 |t Vol. 126  |v [112161, 11 p.]  |d 2021 
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701 1 |a Tarakanchikova  |b Ya. V.  |g Yana Vladimirovna 
701 1 |a Linnik  |b D. S.  |g Dmitrii Sergeevich 
701 1 |a Mashel  |b T. V.  |g Tatjyana Vyacheslavovna 
701 1 |a Muslimov  |b A. R.  |g Albert 
701 1 |a Pavlov  |b S. I.  |g Sergey Igorevich 
701 1 |a Lepik  |b K. V.  |g Kirill Viktorovich 
701 1 |a Zyuzin  |b M. V.  |g Mikhail 
701 1 |a Sukhorukov  |b G. B.  |g Gleb Borisovich 
701 1 |a Timin  |b A. S.  |c Chemist  |c Associate Scientist of Tomsk Polytechnic University  |f 1989-  |g Aleksandr Sergeevich  |3 (RuTPU)RU\TPU\pers\37036 
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