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Biophysical characterization of siRNA-loaded lipid nanoparticles with different PEG content in an aqueous systemopen access

Authors
Kim, Ki HyunBhujel, RipeshMaharjan, RaviLee, Jae ChulJung, Hun SoonKim, Hye JeongKim, Nam AhJeong, Seong Hoon
Issue Date
Sep-2023
Publisher
ELSEVIER
Keywords
siRNA; PEGylated LNPs; Colloidal stability; Flow imaging microscopy; Aggregation
Citation
European Journal of Pharmaceutics and Biopharmaceutics, v.190, pp 150 - 160
Pages
11
Indexed
SCIE
SCOPUS
Journal Title
European Journal of Pharmaceutics and Biopharmaceutics
Volume
190
Start Page
150
End Page
160
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/21089
DOI
10.1016/j.ejpb.2023.07.013
ISSN
0939-6411
1873-3441
Abstract
Although lipid nanoparticles (LNP) are potential carriers of various pharmaceutical ingredients, further inves-tigation for maintaining their stability under various environmental stressors must be performed. This study evaluated the influence of PEGylation and stress conditions on the stability of siRNA-loaded LNPs with different concentrations of PEG (0.5 mol%; 0.5 % PEG-LNP and 1.0 mol%; 1.0 % PEG-LNP) anchored to their surface. We applied end-over-end agitation, elevated temperature, and repeated freeze and thaw (F/T) cycles as physico-chemical stressors of pH and ionic strength. Dynamic light scattering (DLS), flow imaging microscopy (FIM), and ionic-exchange chromatography (IEX) were to determine the degree of aggregation and change in siRNA content. The results indicate that 0.5 % PEG-LNP resisted aggregation only at low pH levels or with salt, whereas 1.0 % PEG-LNP had increased colloidal stability except at pH 4. 0.5 % PEG-LNP withstood aggregation until 71 degrees C and three cycles of F/T. In contrast, 1.0 % PEG-LNP maintained colloidal stability at 90 degrees C and seven F/T cycles. Moreover, 1.0 % PEG-LNP had higher siRNA stability under all stress conditions. Therefore, to ensure the sta-bility of LNP and encapsulated siRNA, the PEG concentration must be carefully controlled while considering LNPs' colloidal instability mechanisms under various stress conditions.
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