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dc.date.accessioned2023-02-17T18:05:27Z
dc.date.available2023-02-17T18:05:27Z
dc.date.created2022-10-27T15:04:52Z
dc.date.issued2022
dc.identifier.citationNazemoroaya, Zahra Sarafbidabad, Mohsen Mahdieh, Athar Zeini, Darya Nyström, Bo . Use of Saponinosomes from Ziziphus spina-christi as Anticancer Drug Carriers. ACS Omega. 2022, 7(32), 28421-28433
dc.identifier.urihttp://hdl.handle.net/10852/100095
dc.description.abstractSaponins are plant glycosides with different structures and biological activities, such as anticancer effects. Ziziphus spina-christi is a plant rich in saponin, and this compound is used to treat malignant melanoma in the present study. Nanophytosomes can be used as an advantageous nanodrug delivery system for plant extracts. The aim of this work is to use the saponin-rich fraction (SRF) from Z. spina-christi and prepare SRF-loaded nanophytosomes (saponinosomes) and observe the in vitro and in vivo effects of these carriers. First, the SRF was obtained from Z. spina-christi by a solvent–solvent fractionation method. Then, Fourier transform infrared (FTIR) analyses were performed to confirm the presence of saponins in the extracted material. Subsequently, the saponinosomes were prepared by the solvent injection method (ether injection method) using a 1:1:1 ratio of lecithin/cholesterol/SRF in the mixture. Characterization of the prepared saponinosomes was performed by FTIR, dynamic light scattering (DLS), field-emission scanning electron microscopy (FE-SEM), and atomic force microscopy (AFM) analyses. In addition, a UV–vis spectrophotometer was used to determine the entrapment efficiency (EE) and in vitro release of the SRF. Finally, cell cytotoxicity of the different formulations was evaluated using a 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide (MTT) assay on both mouse melanoma cells (B16F10) and fibroblasts (L929). Using DLS, AFM, and FE-SEM analyses, the particle size was determined to be 58 ± 6 nm with a zeta potential of −32 ± 2 mV. The calculated EE was 85 ± 3%. The results of the in vitro release profile showed that 68.2% of the SRF was released from the saponinosome after 48 h. The results of the MTT assay showed that the SRF and saponinosomes have high toxicity on B16F10 melanoma cells, but saponinosomes showed a significant decrease in cytotoxicity on L929 fibroblast cells compared with that of the SRF. Our results indicate that the SRF from Z. spina-christi has anticancer activity, and the saponinosomes prepared in this work can control tumor growth, improve therapeutic efficacy, and reduce the side effects of saponins.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleUse of Saponinosomes from Ziziphus spina-christi as Anticancer Drug Carriers
dc.title.alternativeENEngelskEnglishUse of Saponinosomes from Ziziphus spina-christi as Anticancer Drug Carriers
dc.typeJournal article
dc.creator.authorNazemoroaya, Zahra
dc.creator.authorSarafbidabad, Mohsen
dc.creator.authorMahdieh, Athar
dc.creator.authorZeini, Darya
dc.creator.authorNyström, Bo
cristin.unitcode185,15,23,10
cristin.unitnameSeksjon for galenisk farmasi og samfunns
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin2065691
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=ACS Omega&rft.volume=7&rft.spage=28421&rft.date=2022
dc.identifier.jtitleACS Omega
dc.identifier.volume7
dc.identifier.issue32
dc.identifier.startpage28421
dc.identifier.endpage28433
dc.identifier.doihttps://doi.org/10.1021/acsomega.2c03109
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2470-1343
dc.type.versionPublishedVersion


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