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Use of Saponinosomes from Ziziphus spina-christi as Anticancer Drug Carriers

[Image: see text] Saponins 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 advantageou...

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Autores principales: Nazemoroaya, Zahra, Sarafbidabad, Mohsen, Mahdieh, Athar, Zeini, Darya, Nyström, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9386697/
https://www.ncbi.nlm.nih.gov/pubmed/35990496
http://dx.doi.org/10.1021/acsomega.2c03109
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author Nazemoroaya, Zahra
Sarafbidabad, Mohsen
Mahdieh, Athar
Zeini, Darya
Nyström, Bo
author_facet Nazemoroaya, Zahra
Sarafbidabad, Mohsen
Mahdieh, Athar
Zeini, Darya
Nyström, Bo
author_sort Nazemoroaya, Zahra
collection PubMed
description [Image: see text] Saponins 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.
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spelling pubmed-93866972022-08-19 Use of Saponinosomes from Ziziphus spina-christi as Anticancer Drug Carriers Nazemoroaya, Zahra Sarafbidabad, Mohsen Mahdieh, Athar Zeini, Darya Nyström, Bo ACS Omega [Image: see text] Saponins 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. American Chemical Society 2022-08-04 /pmc/articles/PMC9386697/ /pubmed/35990496 http://dx.doi.org/10.1021/acsomega.2c03109 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Nazemoroaya, Zahra
Sarafbidabad, Mohsen
Mahdieh, Athar
Zeini, Darya
Nyström, Bo
Use of Saponinosomes from Ziziphus spina-christi as Anticancer Drug Carriers
title Use of Saponinosomes from Ziziphus spina-christi as Anticancer Drug Carriers
title_full Use of Saponinosomes from Ziziphus spina-christi as Anticancer Drug Carriers
title_fullStr Use of Saponinosomes from Ziziphus spina-christi as Anticancer Drug Carriers
title_full_unstemmed Use of Saponinosomes from Ziziphus spina-christi as Anticancer Drug Carriers
title_short Use of Saponinosomes from Ziziphus spina-christi as Anticancer Drug Carriers
title_sort use of saponinosomes from ziziphus spina-christi as anticancer drug carriers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9386697/
https://www.ncbi.nlm.nih.gov/pubmed/35990496
http://dx.doi.org/10.1021/acsomega.2c03109
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