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

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dc.contributor.authorKim, Ki Hyun-
dc.contributor.authorBhujel, Ripesh-
dc.contributor.authorMaharjan, Ravi-
dc.contributor.authorLee, Jae Chul-
dc.contributor.authorJung, Hun Soon-
dc.contributor.authorKim, Hye Jeong-
dc.contributor.authorKim, Nam Ah-
dc.contributor.authorJeong, Seong Hoon-
dc.date.accessioned2024-08-08T10:00:48Z-
dc.date.available2024-08-08T10:00:48Z-
dc.date.issued2023-09-
dc.identifier.issn0939-6411-
dc.identifier.issn1873-3441-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/21089-
dc.description.abstractAlthough 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.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER-
dc.titleBiophysical characterization of siRNA-loaded lipid nanoparticles with different PEG content in an aqueous system-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.ejpb.2023.07.013-
dc.identifier.scopusid2-s2.0-85166328412-
dc.identifier.wosid001049402600001-
dc.identifier.bibliographicCitationEuropean Journal of Pharmaceutics and Biopharmaceutics, v.190, pp 150 - 160-
dc.citation.titleEuropean Journal of Pharmaceutics and Biopharmaceutics-
dc.citation.volume190-
dc.citation.startPage150-
dc.citation.endPage160-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusMESSENGER-RNA DELIVERY-
dc.subject.keywordPlusPOLYMORPHIC TRANSFORMATIONS-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusFORMULATION-
dc.subject.keywordPlusAGGREGATION-
dc.subject.keywordPlusSTABILITY-
dc.subject.keywordPlusCRYOPROTECTANTS-
dc.subject.keywordPlusDEGRADATION-
dc.subject.keywordPlusREACTIVITY-
dc.subject.keywordPlusGELATION-
dc.subject.keywordAuthorsiRNA-
dc.subject.keywordAuthorPEGylated LNPs-
dc.subject.keywordAuthorColloidal stability-
dc.subject.keywordAuthorFlow imaging microscopy-
dc.subject.keywordAuthorAggregation-
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