Publication:
Headgroup modification of cholesterol-based cationic lipids: Synthesis, transfection efficiency evaluation, and serum compatibility

dc.contributor.authorThongbamrer C.
dc.contributor.authorNiyomtham N.
dc.contributor.authorChaiwut C.
dc.contributor.authorPosa C.
dc.contributor.authorApiratikul N.
dc.contributor.authorSangvichien E.
dc.contributor.authorOpanasopit P.
dc.contributor.authorSakee U.
dc.contributor.authorYingyongnarongkul B.-E.
dc.contributor.authorRadchatawedchakoon W.
dc.date.accessioned2021-04-05T03:02:03Z
dc.date.available2021-04-05T03:02:03Z
dc.date.issued2020
dc.date.issuedBE2563
dc.description.abstractThere were two objectives for this study. First, it focused on eight lipids having cholesterol as hydrophobic tails, carbamate linkers, and different polar headgroups. Second, it aimed to study the physicochemical properties of those eight lipids, including DNA binding, size, zeta potential, and the transfection efficiency. Cholesterol-1,2-diaminoethane and tetramethylguanidinium conjugated lipid showed the highest transfection efficacy into human embryonic kidney cells cells. The optimal formulation of this lipid was found to be 1:1 (weight/weight) for cationic lipid/DOPE, and 1:20 for DNA/liposome. GFP expression experiments further revealed that the liposome exhibited higher transfection efficiency under a 10−40% serum condition than Lipofectamine™ 2000. © 2020, Prince of Songkla University. All rights reserved.
dc.format.mimetypeapplication/pdf
dc.identifier.citationSongklanakarin Journal of Science and Technology. Vol 42, No.1 (2020), p.213-221
dc.identifier.doi10.14456/sjst-psu.2020.28
dc.identifier.issn1253395
dc.identifier.other2-s2.0-85084370377
dc.identifier.urihttps://hdl.handle.net/20.500.14740/4929
dc.rights.holderScopus
dc.titleHeadgroup modification of cholesterol-based cationic lipids: Synthesis, transfection efficiency evaluation, and serum compatibility
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85084370377&doi=10.14456%2fsjst-psu.2020.28&partnerID=40&md5=c205daaf7f831c2babd0ce2df14d0dd8

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