Boosting transfection efficiency: A systematic study using layer-by-layer based gene delivery platform
Creators
- 1. Nanobiotechnology Laboratory, St. Petersburg Academic University, 194021 St. Petersburg (Russian Federation)
- 2. Peter the Great St. Petersburg Polytechnic University, Polytechnicheskaya, 29, 195251 St. Petersburg (Russian Federation)
- 3. Department of Applied Optics, ITMO University, Kronverkskiy pr. 49, 197101 St. Petersburg (Russian Federation)
- 4. Ioffe Institute, Politekhnicheskaya Ulitsa, 26, 194021 St. Petersburg (Russian Federation)
- 5. R.M. Gorbacheva Research Institute for Pediatric Oncology, Hematology and Transplantation, Pavlov University, Lev Tolstoy str., 6/8, 197022 St. Petersburg (Russian Federation)
- 6. Department of Physics and Engineering, ITMO University, Lomonosova 9, 191002 St. Petersburg (Russian Federation)
- 7. School of Engineering and Material Science, Queen Mary University of London, London (United Kingdom)
- 8. Skolkovo Institute of Science and Technology, 143026 Moscow (Russian Federation)
- 9. National Research Tomsk Polytechnic University, Lenin Avenue, 30, 634050 Tomsk (Russian Federation)
Description
Highlights: • LbL-based delivery systems provide variability in genetic material loading. • The influence of different parameters on the transfection efficiency was verified. • Loading of PLA/DNase II inh. in one carrier increases the transfection efficiency. 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.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.msec.2021.112161Additional details
Identifiers
- DOI
- 10.1016/j.msec.2021.112161;
- PII
- S0928493121003003;
Publishing Information
- Journal Title
- Materials Science and Engineering. C, Biomimetic Materials, Sensors and Systems
- Journal Volume
- 126
- Journal Page Range
- vp.
- ISSN
- 0928-4931
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54043256
- Subject category
- S77: NANOSCIENCE AND NANOTECHNOLOGY; S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- CALCIUM CARBONATES; GENE THERAPY; GENES; GENETICS; NANOPARTICLES; NUCLEIC ACIDS; PERFORMANCE; POLYMERS
- Descriptors DEC
- ALKALINE EARTH METAL COMPOUNDS; BIOLOGY; CALCIUM COMPOUNDS; CARBON COMPOUNDS; CARBONATES; MEDICINE; ORGANIC COMPOUNDS; OXYGEN COMPOUNDS; PARTICLES; THERAPY
Optional Information
- Copyright
- Copyright (c) 2021 Elsevier B.V. All rights reserved.