Targeted endothelial gene delivery by ultrasonic destruction of magnetic microbubbles carrying lentiviral vectors
- PMID: 22274557
- DOI: 10.1007/s11095-012-0678-8
Targeted endothelial gene delivery by ultrasonic destruction of magnetic microbubbles carrying lentiviral vectors
Abstract
Purpose: Site specific vascular gene delivery is a promising tool for treatment of cardiovascular diseases. By combining ultrasound mediated microbubble destruction with site specific magnetic targeting of lentiviruses, we aimed to develop a technique suitable for systemic application.
Methods: The magnetic nanoparticle coupling to lipid microbubbles was confirmed by absorbance measurements. Association of fluorescent lentivirus to magnetic microbubbles (MMB) was determined by microscopy and flow cytometry. Functionality and efficiency of GFP-encoding lentiviral MMB transduction was evaluated by endothelial (HMEC) GFP expression and cytotoxicity was measured by MTT reduction.
Results: Microbubbles with a mean diameter of 4.3 ± 0.04 μm were stable for 2 days, readily magnetizable and magnetically steerable in vitro and efficiently associated with lentivirus. Exposure of eGFP-encoding lentiviral MMB to human endothelial cells followed by application of an external static magnetic field (30 min) and ultrasonic destruction of the microbubbles did not markedly affect cellular viability. Finally, this combination led to a 30-fold increase in transduction efficiency compared to application of naked virus alone.
Conclusions: By associating microbubbles with magnetic iron nanoparticles, these function as carriers for lentiviruses achieving tissue specific deposition at the site of interest.
Similar articles
-
Targeting of Magnetic Nanoparticle-coated Microbubbles to the Vascular Wall Empowers Site-specific Lentiviral Gene Delivery in vivo.Theranostics. 2017 Jan 1;7(2):295-307. doi: 10.7150/thno.16192. eCollection 2017. Theranostics. 2017. PMID: 28042335 Free PMC article.
-
Site directed vascular gene delivery in vivo by ultrasonic destruction of magnetic nanoparticle coated microbubbles.Nanomedicine. 2012 Nov;8(8):1309-18. doi: 10.1016/j.nano.2012.03.007. Epub 2012 Apr 2. Nanomedicine. 2012. PMID: 22480917
-
Optimization of magnetic nanoparticle-assisted lentiviral gene transfer.Pharm Res. 2012 May;29(5):1255-69. doi: 10.1007/s11095-011-0660-x. Epub 2012 Jan 25. Pharm Res. 2012. PMID: 22274554
-
Ultrasonic gene and drug delivery to the cardiovascular system.Adv Drug Deliv Rev. 2008 Jun 30;60(10):1177-92. doi: 10.1016/j.addr.2008.03.004. Epub 2008 Apr 3. Adv Drug Deliv Rev. 2008. PMID: 18474407 Review.
-
Ultrasound and Magnetic Responsive Drug Delivery Systems for Cardiovascular Application.J Cardiovasc Pharmacol. 2020 Oct;76(4):414-426. doi: 10.1097/FJC.0000000000000885. J Cardiovasc Pharmacol. 2020. PMID: 32732493 Review.
Cited by
-
Vascular-targeted nanocarriers: design considerations and strategies for successful treatment of atherosclerosis and other vascular diseases.Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2016 Nov;8(6):909-926. doi: 10.1002/wnan.1414. Epub 2016 May 19. Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2016. PMID: 27194461 Free PMC article. Review.
-
Nano-mediated delivery of double-stranded RNA for gene therapy of glioblastoma multiforme.PLoS One. 2019 Mar 19;14(3):e0213852. doi: 10.1371/journal.pone.0213852. eCollection 2019. PLoS One. 2019. PMID: 30889203 Free PMC article.
-
Characterization of magnetic viral complexes for targeted delivery in oncology.Theranostics. 2015 Mar 18;5(7):667-85. doi: 10.7150/thno.10438. eCollection 2015. Theranostics. 2015. PMID: 25897333 Free PMC article.
-
Gene therapy for cardiovascular disease mediated by ultrasound and microbubbles.Cardiovasc Ultrasound. 2013 Apr 17;11:11. doi: 10.1186/1476-7120-11-11. Cardiovasc Ultrasound. 2013. PMID: 23594865 Free PMC article. Review.
-
HIF-1α Dependent Wound Healing Angiogenesis In Vivo Can Be Controlled by Site-Specific Lentiviral Magnetic Targeting of SHP-2.Mol Ther. 2017 Jul 5;25(7):1616-1627. doi: 10.1016/j.ymthe.2017.04.007. Epub 2017 Apr 20. Mol Ther. 2017. PMID: 28434868 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources