Designing siRNA-conjugated plant oil-based nanoparticles for gene silencing and cancer therapy

In this study, the anticancer activities of two siRNA carriers were compared using a human lung adenocarcinoma epithelial cell line (A549). Firstly, poly(styrene)-graft-poly(linoleic acid) (PS-g-PLina) and poly(styrene)-graft-poly(linoleic acid)-graft-poly(ethylene glycol) (PS-g-PLina-g-PEG) graft copolymers were synthesized by free-radical polymerization. PS-PLina and PS-PLina-PEG nanoparticles (NPs) were prepared by solvent evaporation method and were then characterized. The size was found as 150 ± 10 nm for PS-PLina and 184 ± 6 nm for PS-PLina-PEG NPs. The NPs were functionalized with poly(l-lysine) (PLL) for c-myc siRNA conjugation. siRNA entrapment efficiencies were found in the range of 4–63% for PS-PLina-PLL and 6–42% for PS-PLina-PEG-PLL NPs. The short-term stability test was realised for 1 month. siRNA release profiles were also investigated. In vitro anticancer activity of siRNA-NPs was determined by MTT, flow cytometry, and fluorescence microscopy analyses. Obtained findings showed that both NPs systems were promising as siRNA delivery tool for lung cancer therapy. © 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.

Eser Adı
[dc.title]
Designing siRNA-conjugated plant oil-based nanoparticles for gene silencing and cancer therapy
Yazar
[dc.contributor.author]
Anılmış, Nur Merve
Yazar
[dc.contributor.author]
Kara, Göknur
Yazar
[dc.contributor.author]
Kılıçay, Ebru
Yazar
[dc.contributor.author]
Hazer, Baki
Yazar
[dc.contributor.author]
Denkbaş, Emir Baki
Yayın Yılı
[dc.date.issued]
2019
Yayıncı
[dc.publisher]
Taylor and Francis Ltd
Yayın Türü
[dc.type]
article
Özet
[dc.description.abstract]
In this study, the anticancer activities of two siRNA carriers were compared using a human lung adenocarcinoma epithelial cell line (A549). Firstly, poly(styrene)-graft-poly(linoleic acid) (PS-g-PLina) and poly(styrene)-graft-poly(linoleic acid)-graft-poly(ethylene glycol) (PS-g-PLina-g-PEG) graft copolymers were synthesized by free-radical polymerization. PS-PLina and PS-PLina-PEG nanoparticles (NPs) were prepared by solvent evaporation method and were then characterized. The size was found as 150 ± 10 nm for PS-PLina and 184 ± 6 nm for PS-PLina-PEG NPs. The NPs were functionalized with poly(l-lysine) (PLL) for c-myc siRNA conjugation. siRNA entrapment efficiencies were found in the range of 4–63% for PS-PLina-PLL and 6–42% for PS-PLina-PEG-PLL NPs. The short-term stability test was realised for 1 month. siRNA release profiles were also investigated. In vitro anticancer activity of siRNA-NPs was determined by MTT, flow cytometry, and fluorescence microscopy analyses. Obtained findings showed that both NPs systems were promising as siRNA delivery tool for lung cancer therapy. © 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.
Kayıt Giriş Tarihi
[dc.date.accessioned]
2019-12-23
Açık Erişim Tarihi
[dc.date.available]
2019-12-23
Yayın Dili
[dc.language.iso]
eng
Konu Başlıkları
[dc.subject]
lung cancer
Konu Başlıkları
[dc.subject]
nanoparticles
Konu Başlıkları
[dc.subject]
PS-g-PLina
Konu Başlıkları
[dc.subject]
PS-g-PLina-PEG
Konu Başlıkları
[dc.subject]
siRNA
Künye
[dc.identifier.citation]
Anilmis, N. M., Kara, G., Kilicay, E., Hazer, B. ve Denkbas, E. B. (2019). Designing siRNA-conjugated plant oil-based nanoparticles for gene silencing and cancer therapy. Journal of Microencapsulation, 36(7), 635-648. doi:10.1080/02652048.2019.1665117
Haklar
[dc.rights]
info:eu-repo/semantics/closedAccess
ISSN
[dc.identifier.issn]
0265-2048
Sponsor YAYINCI
[dc.description.sponsorship]
BAGP-001, BEU-2016, 33496813-01
Sponsor YAYINCI
[dc.description.sponsorship]
This work was financially supported by Bulent Ecevit University Research Fund (Grant no. BEU-2016?33496813-01) and Kapadokya University #K?N(0).2018-BAGP-001. The authors thank Faruk Bahad?r for helping us to the preparation step of polymer.
İlk Sayfa Sayısı
[dc.identifier.startpage]
635
Son Sayfa Sayısı
[dc.identifier.endpage]
648
Dergi Adı
[dc.relation.journal]
Journal of Microencapsulation
Dergi Sayısı
[dc.identifier.issue]
7
Dergi Cilt Bilgisi
[dc.identifier.volume]
36
Tek Biçim Adres
[dc.identifier.uri]
https://dx.doi.org/10.1080/02652048.2019.1665117
Tek Biçim Adres
[dc.identifier.uri]
https://hdl.handle.net/20.500.12628/5018
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poly(styrene)-graft-poly(linoleic PS-PLina-PEG PS-PLina anticancer Limited trading Taylor profiles Francis release realised stability short-term PS-PLina-PEG-PLL 6–42% PS-PLina-PLL investigated siRNA-NPs activity Obtained cancer delivery promising systems showed findings analyses therapy microscopy fluorescence Informa cytometry determined 4–63% (PS-g-PLina-g-PEG)
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