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Anticancer Effect of Cisplatin-Loaded Poly (Butylcyanoacrylate) Nanoparticles on A172 Brain Cancer Cells Line

BACKGROUND: Drug delivery systems have been designed to achieve targeted delivery and control the release rate of the drugs. A serious challenge associated with drug delivery systems is the presence of the blood-brain barrier which limits drugs penetration. In the current study, the effects of cispl...

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Autores principales: Chiani, Mohsen, Milani, Attabak Toofani, Nemati, Mahdieh, Rezaeidian, Jalal, Ehsanbakhsh, Hossein, Ahmadi, Zohre, Mazloomi, Ebrahim, Sadeghi, Vahideh, Khiyavi, Azim Akbarzadeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485583/
https://www.ncbi.nlm.nih.gov/pubmed/30678454
http://dx.doi.org/10.31557/APJCP.2019.20.1.303
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author Chiani, Mohsen
Milani, Attabak Toofani
Nemati, Mahdieh
Rezaeidian, Jalal
Ehsanbakhsh, Hossein
Ahmadi, Zohre
Mazloomi, Ebrahim
Sadeghi, Vahideh
Khiyavi, Azim Akbarzadeh
author_facet Chiani, Mohsen
Milani, Attabak Toofani
Nemati, Mahdieh
Rezaeidian, Jalal
Ehsanbakhsh, Hossein
Ahmadi, Zohre
Mazloomi, Ebrahim
Sadeghi, Vahideh
Khiyavi, Azim Akbarzadeh
author_sort Chiani, Mohsen
collection PubMed
description BACKGROUND: Drug delivery systems have been designed to achieve targeted delivery and control the release rate of the drugs. A serious challenge associated with drug delivery systems is the presence of the blood-brain barrier which limits drugs penetration. In the current study, the effects of cisplatin nanoparticles on A172 brain cancer cell line were investigated. METHODS: Cisplatin nanoparticles were produced by miniemulsion polymerization technique and their properties were evaluated. Drug release assay was performed to characterize the nanoparticles’ properties. Here, we examined the effects of cisplatin nanoparticles and free form of cisplatin on A172 cancer cell line. MTT assay was performed for different concentrations of the drug. To measure the apoptosis rate in A172 cell line in the presence of cisplatin nanoparticles or its free from, Annexin V staining method was used. RESULTS: Our results indicated that loading type of cisplatin was physical loading and only 4.7% of cisplatin was released after 68 h. Furthermore, MTT assay showed that cisplatin nanoparticles in all concentrations had more cytotoxic effects on the cells comparing with the free form of cisplatin and control groups. We also showed that cisplatin nanoparticles could increase apoptosis in cancer cells more than the drug in the free form by using flow cytometry technique. CONCLUSION: Overall, these findings proved that cisplatin loaded on poly (Butylcyanoacrylate) nanoparticles, was more efficient than the free form of cisplatin in treating A172 cancer cell line.
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spelling pubmed-64855832019-05-13 Anticancer Effect of Cisplatin-Loaded Poly (Butylcyanoacrylate) Nanoparticles on A172 Brain Cancer Cells Line Chiani, Mohsen Milani, Attabak Toofani Nemati, Mahdieh Rezaeidian, Jalal Ehsanbakhsh, Hossein Ahmadi, Zohre Mazloomi, Ebrahim Sadeghi, Vahideh Khiyavi, Azim Akbarzadeh Asian Pac J Cancer Prev Research Article BACKGROUND: Drug delivery systems have been designed to achieve targeted delivery and control the release rate of the drugs. A serious challenge associated with drug delivery systems is the presence of the blood-brain barrier which limits drugs penetration. In the current study, the effects of cisplatin nanoparticles on A172 brain cancer cell line were investigated. METHODS: Cisplatin nanoparticles were produced by miniemulsion polymerization technique and their properties were evaluated. Drug release assay was performed to characterize the nanoparticles’ properties. Here, we examined the effects of cisplatin nanoparticles and free form of cisplatin on A172 cancer cell line. MTT assay was performed for different concentrations of the drug. To measure the apoptosis rate in A172 cell line in the presence of cisplatin nanoparticles or its free from, Annexin V staining method was used. RESULTS: Our results indicated that loading type of cisplatin was physical loading and only 4.7% of cisplatin was released after 68 h. Furthermore, MTT assay showed that cisplatin nanoparticles in all concentrations had more cytotoxic effects on the cells comparing with the free form of cisplatin and control groups. We also showed that cisplatin nanoparticles could increase apoptosis in cancer cells more than the drug in the free form by using flow cytometry technique. CONCLUSION: Overall, these findings proved that cisplatin loaded on poly (Butylcyanoacrylate) nanoparticles, was more efficient than the free form of cisplatin in treating A172 cancer cell line. West Asia Organization for Cancer Prevention 2019 /pmc/articles/PMC6485583/ /pubmed/30678454 http://dx.doi.org/10.31557/APJCP.2019.20.1.303 Text en Copyright: © Asian Pacific Journal of Cancer Prevention http://creativecommons.org/licenses/BY-SA/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License
spellingShingle Research Article
Chiani, Mohsen
Milani, Attabak Toofani
Nemati, Mahdieh
Rezaeidian, Jalal
Ehsanbakhsh, Hossein
Ahmadi, Zohre
Mazloomi, Ebrahim
Sadeghi, Vahideh
Khiyavi, Azim Akbarzadeh
Anticancer Effect of Cisplatin-Loaded Poly (Butylcyanoacrylate) Nanoparticles on A172 Brain Cancer Cells Line
title Anticancer Effect of Cisplatin-Loaded Poly (Butylcyanoacrylate) Nanoparticles on A172 Brain Cancer Cells Line
title_full Anticancer Effect of Cisplatin-Loaded Poly (Butylcyanoacrylate) Nanoparticles on A172 Brain Cancer Cells Line
title_fullStr Anticancer Effect of Cisplatin-Loaded Poly (Butylcyanoacrylate) Nanoparticles on A172 Brain Cancer Cells Line
title_full_unstemmed Anticancer Effect of Cisplatin-Loaded Poly (Butylcyanoacrylate) Nanoparticles on A172 Brain Cancer Cells Line
title_short Anticancer Effect of Cisplatin-Loaded Poly (Butylcyanoacrylate) Nanoparticles on A172 Brain Cancer Cells Line
title_sort anticancer effect of cisplatin-loaded poly (butylcyanoacrylate) nanoparticles on a172 brain cancer cells line
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485583/
https://www.ncbi.nlm.nih.gov/pubmed/30678454
http://dx.doi.org/10.31557/APJCP.2019.20.1.303
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