Monitoring the in vivo siRNA release from lipid nanoparticles based on the fluorescence resonance energy transfer principle

The siRNA-loaded lipid nanoparticles have attracted much attention due to its significant gene silencing effect and successful marketization. However, the in vivo distribution and release of siRNA still cannot be effectively monitored. In this study, based on the fluorescence resonance energy transf...

Full description

Saved in:
Bibliographic Details
Main Authors: Lei Sun (Author), Jinfang Zhang (Author), Jing-e Zhou (Author), Jing Wang (Author), Zhehao Wang (Author), Shenggen Luo (Author), Yeying Wang (Author), Shulei Zhu (Author), Fan Yang (Author), Jie Tang (Author), Wei Lu (Author), Yiting Wang (Author), Lei Yu (Author), Zhiqiang Yan (Author)
Format: Book
Published: Elsevier, 2023-01-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_0b23e63d2eda42a7b5f14c0e2d1162f5
042 |a dc 
100 1 0 |a Lei Sun  |e author 
700 1 0 |a Jinfang Zhang  |e author 
700 1 0 |a Jing-e Zhou  |e author 
700 1 0 |a Jing Wang  |e author 
700 1 0 |a Zhehao Wang  |e author 
700 1 0 |a Shenggen Luo  |e author 
700 1 0 |a Yeying Wang  |e author 
700 1 0 |a Shulei Zhu  |e author 
700 1 0 |a Fan Yang  |e author 
700 1 0 |a Jie Tang  |e author 
700 1 0 |a Wei Lu  |e author 
700 1 0 |a Yiting Wang  |e author 
700 1 0 |a Lei Yu  |e author 
700 1 0 |a Zhiqiang Yan  |e author 
245 0 0 |a Monitoring the in vivo siRNA release from lipid nanoparticles based on the fluorescence resonance energy transfer principle 
260 |b Elsevier,   |c 2023-01-01T00:00:00Z. 
500 |a 1818-0876 
500 |a 10.1016/j.ajps.2022.11.003 
520 |a The siRNA-loaded lipid nanoparticles have attracted much attention due to its significant gene silencing effect and successful marketization. However, the in vivo distribution and release of siRNA still cannot be effectively monitored. In this study, based on the fluorescence resonance energy transfer (FRET) principle, a fluorescence dye Cy5-modified survivin siRNA was conjugated to nanogolds (Au-DR-siRNA), which were then wrapped with lipid nanoparticles (LNPs) for monitoring the release behaviour of siRNA in vivo. The results showed that once Au-DR-siRNA was released from the LNPs and cleaved by the Dicer enzyme to produce free siRNA in cells, the fluorescence of Cy5 would change from quenched state to activated state, showing the location and time of siRNA release. Besides, the LNPs showed a significant antitumor effect by silencing the survivin gene and a CT imaging function superior to iohexol by nanogolds. Therefore, this work provided not only an effective method for monitoring the pharmacokinetic behaviour of LNP-based siRNA, but also a siRNA delivery system for treating and diagnosing tumors. 
546 |a EN 
690 |a Survivin siRNA 
690 |a Lipid nanoparticles 
690 |a In vivo release 
690 |a Nanogolds 
690 |a Fluorescence resonance energy transfer 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Asian Journal of Pharmaceutical Sciences, Vol 18, Iss 1, Pp 100769- (2023) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S1818087622001180 
787 0 |n https://doaj.org/toc/1818-0876 
856 4 1 |u https://doaj.org/article/0b23e63d2eda42a7b5f14c0e2d1162f5  |z Connect to this object online.