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Anti-tumor effects of PEGylated-nanoliposomes containing ginger extract in colorectal cancer-bearing mice

OBJECTIVE(S): This study aimed to develop a nanoliposomal formulation containing ginger ethanolic extract with a higher therapeutic effect for cancer treatment. MATERIALS AND METHODS: The present study aimed to prepare PEGylated nanoliposomal ginger through the thin film hydration method plus extrus...

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Autores principales: Yavari, Maryam, Jaafari, Mahmoud Reza, Mirzavi, Farshad, Mosayebi, Ghasem, Ghazavi, Ali, Ganji, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9392564/
https://www.ncbi.nlm.nih.gov/pubmed/36033959
http://dx.doi.org/10.22038/IJBMS.2022.63870.14075
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author Yavari, Maryam
Jaafari, Mahmoud Reza
Mirzavi, Farshad
Mosayebi, Ghasem
Ghazavi, Ali
Ganji, Ali
author_facet Yavari, Maryam
Jaafari, Mahmoud Reza
Mirzavi, Farshad
Mosayebi, Ghasem
Ghazavi, Ali
Ganji, Ali
author_sort Yavari, Maryam
collection PubMed
description OBJECTIVE(S): This study aimed to develop a nanoliposomal formulation containing ginger ethanolic extract with a higher therapeutic effect for cancer treatment. MATERIALS AND METHODS: The present study aimed to prepare PEGylated nanoliposomal ginger through the thin film hydration method plus extrusion. Physicochemical characteristics were evaluated, and the toxicity of the prepared liposomes was assessed using the MTT assay. In addition, tumor size was monitored in colorectal cancer-bearing mice. Also, the anticancer effects of liposomal ginger were evaluated by gene expression assay of Bax and Bcl-2 and cytokines including TNF-α, TGF-β, and IFN-γ by Real-time PCR. Also, cytotoxic T lymphocytes (CTLs) and regulatory T lymphocytes (Treg cells) were counted in spleen and tumor tissue by flow cytometry assay. RESULTS: The nanoliposomes’ particle size and polydispersity index (PDI) were 94.95 nm and 0.246 nm, respectively. High encapsulation capacity (80 %) confirmed the technique’s efficiency, and the release rate of the extract was 85% at pH 6.5. In addition, this study showed that liposomal ginger at 100 mg/kg/day enhanced the expression of Bax (P<0.05) and IFN-γ (P<0.01) compared with ginger extract in the mouse model. Also, the number of tumor-infiltrating lymphocytes (TILs) and CTLs cell count in tumor tissue showed a significant increase in the LipGin group compared with the Gin group (P<0.05). CONCLUSION: Results indicated that the liposomal ginger enhanced the antitumor activity; therefore, the prepared liposomal ginger can be used in future clinical trials.
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spelling pubmed-93925642022-08-26 Anti-tumor effects of PEGylated-nanoliposomes containing ginger extract in colorectal cancer-bearing mice Yavari, Maryam Jaafari, Mahmoud Reza Mirzavi, Farshad Mosayebi, Ghasem Ghazavi, Ali Ganji, Ali Iran J Basic Med Sci Original Article OBJECTIVE(S): This study aimed to develop a nanoliposomal formulation containing ginger ethanolic extract with a higher therapeutic effect for cancer treatment. MATERIALS AND METHODS: The present study aimed to prepare PEGylated nanoliposomal ginger through the thin film hydration method plus extrusion. Physicochemical characteristics were evaluated, and the toxicity of the prepared liposomes was assessed using the MTT assay. In addition, tumor size was monitored in colorectal cancer-bearing mice. Also, the anticancer effects of liposomal ginger were evaluated by gene expression assay of Bax and Bcl-2 and cytokines including TNF-α, TGF-β, and IFN-γ by Real-time PCR. Also, cytotoxic T lymphocytes (CTLs) and regulatory T lymphocytes (Treg cells) were counted in spleen and tumor tissue by flow cytometry assay. RESULTS: The nanoliposomes’ particle size and polydispersity index (PDI) were 94.95 nm and 0.246 nm, respectively. High encapsulation capacity (80 %) confirmed the technique’s efficiency, and the release rate of the extract was 85% at pH 6.5. In addition, this study showed that liposomal ginger at 100 mg/kg/day enhanced the expression of Bax (P<0.05) and IFN-γ (P<0.01) compared with ginger extract in the mouse model. Also, the number of tumor-infiltrating lymphocytes (TILs) and CTLs cell count in tumor tissue showed a significant increase in the LipGin group compared with the Gin group (P<0.05). CONCLUSION: Results indicated that the liposomal ginger enhanced the antitumor activity; therefore, the prepared liposomal ginger can be used in future clinical trials. Mashhad University of Medical Sciences 2022-07 /pmc/articles/PMC9392564/ /pubmed/36033959 http://dx.doi.org/10.22038/IJBMS.2022.63870.14075 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Yavari, Maryam
Jaafari, Mahmoud Reza
Mirzavi, Farshad
Mosayebi, Ghasem
Ghazavi, Ali
Ganji, Ali
Anti-tumor effects of PEGylated-nanoliposomes containing ginger extract in colorectal cancer-bearing mice
title Anti-tumor effects of PEGylated-nanoliposomes containing ginger extract in colorectal cancer-bearing mice
title_full Anti-tumor effects of PEGylated-nanoliposomes containing ginger extract in colorectal cancer-bearing mice
title_fullStr Anti-tumor effects of PEGylated-nanoliposomes containing ginger extract in colorectal cancer-bearing mice
title_full_unstemmed Anti-tumor effects of PEGylated-nanoliposomes containing ginger extract in colorectal cancer-bearing mice
title_short Anti-tumor effects of PEGylated-nanoliposomes containing ginger extract in colorectal cancer-bearing mice
title_sort anti-tumor effects of pegylated-nanoliposomes containing ginger extract in colorectal cancer-bearing mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9392564/
https://www.ncbi.nlm.nih.gov/pubmed/36033959
http://dx.doi.org/10.22038/IJBMS.2022.63870.14075
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