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Omid, Hamed, paryab, amir hossien, Nakhli, Yasamin, Sajadi, Nasim, Madaah Hosseini, Hamid Reza, Ahmadbeigi, Naser, Seifalian, Alexander. (1402). The effect of SPION size and salting-out on transduction of PEGylated lentiviral vector. , 56(2), 224-232. doi: 10.22059/jufgnsm.2023.02.11
Hamed Omid; amir hossien paryab; Yasamin Nakhli; Nasim Sajadi; Hamid Reza Madaah Hosseini; Naser Ahmadbeigi; Alexander M. Seifalian. "The effect of SPION size and salting-out on transduction of PEGylated lentiviral vector". , 56, 2, 1402, 224-232. doi: 10.22059/jufgnsm.2023.02.11
Omid, Hamed, paryab, amir hossien, Nakhli, Yasamin, Sajadi, Nasim, Madaah Hosseini, Hamid Reza, Ahmadbeigi, Naser, Seifalian, Alexander. (1402). 'The effect of SPION size and salting-out on transduction of PEGylated lentiviral vector', , 56(2), pp. 224-232. doi: 10.22059/jufgnsm.2023.02.11
Omid, Hamed, paryab, amir hossien, Nakhli, Yasamin, Sajadi, Nasim, Madaah Hosseini, Hamid Reza, Ahmadbeigi, Naser, Seifalian, Alexander. The effect of SPION size and salting-out on transduction of PEGylated lentiviral vector. , 1402; 56(2): 224-232. doi: 10.22059/jufgnsm.2023.02.11

The effect of SPION size and salting-out on transduction of PEGylated lentiviral vector

Journal of Ultrafine Grained and Nanostructured Materials
مقاله 11، دوره 56، شماره 2، اسفند 2023، صفحه 224-232    اصل مقاله (1.17 M)
نوع مقاله: Research Paper
شناسه دیجیتال (DOI): 10.22059/jufgnsm.2023.02.11
نویسندگان
Hamed Omid1؛ amir hossien paryab2؛ Yasamin Nakhli2؛ Nasim Sajadi* 3؛ Hamid Reza Madaah Hosseini* 4؛ Naser Ahmadbeigi5؛ Alexander M. Seifalian6
1Gene Therapy Research Center, Digestive Disease Research Institute, Tehran University of Medical Sciences, Tehran, Iran. Department of Materials Science and Engineering, Sharif University of Technology, Azadi Avenue, Tehran, Iran; SABZ Biomedicals Science-Based Company, Tehran, Iran;
2Department of Materials Science and Engineering, Sharif University of Technology, Azadi Avenue, Tehran, Iran.
3Ali-Asghar Children Hospital, Iran University of Medical Sciences, Tehran, Iran.
4Department of Materials Science and Engineering, Sharif University of Technology, Azadi Avenue, Tehran, Iran. SABZ Biomedicals Science-Based Company, Tehran, Iran;
5Gene Therapy Research Center, Digestive Disease Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
6Nanotechnology & Regenerative Medicine Commercialisation Centre (NanoRegMed Ltd, Nanoloom Ltd, & Liberum Health Ltd), London BioScience Innovation Centre, London, UK.
چکیده
Gene editing has many promising applications for the treatment of diseases with unmet clinical needs, including cancers and autoimmune. There are two main routes for gene delivery: viral and non-viral. Recent research shows viral methods are emerging in clinical trials. Nevertheless, there are still a couple of technological obstacles that require further improvements, these include virus concentration and low efficiency of transduction. This research aimed to employ superparamagnetic iron oxide nanoparticles (SPION) to solve these problems. Three sizes of 10, 40, and 120 nm SPION were synthesized by co-precipitation and Sol-Gel methods, and characterized by XRD, FTIR, FESEM, and VSM. Conjugating SPION to viruses by polyethylene glycol (PEG) can increase the sedimentation of viruses due to magnetic and gravity forces even without ultracentrifuge. Moreover, this magnetic force can guide viruses toward cells and tremendously facilitate the transduction process. As shown, average size SPION (40 nm) revealed the best performance, especially in combination with salting-out precipitation and increased transduction efficiency of more than 20-fold. SPION size has significant effects and should be considered for this application. The combination of the salting-out method and SPION has a synergic effect and elevates transduction results tremendously.
کلیدواژه‌ها
SPION؛ Nanoparticles؛ Transduction؛ Gene editing؛ lentivirus؛ PEG
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