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Nanodelivery and anticancer effect of a limonoid, nimbolide, in breast and pancreatic cancer cells
INTRODUCTION: Nimbolide (Nim), a limonoid obtained from the neem tree, Azadirachta indica, has several pharmacological properties, including anticancer effects in different type of cancers. No drug-delivery system has been reported for enhancing the therapeutic application of this novel hydrophobic...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789415/ https://www.ncbi.nlm.nih.gov/pubmed/31632020 http://dx.doi.org/10.2147/IJN.S208540 |
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author | Patra, Arjun Satpathy, Swaha Hussain, Muhammad Delwar |
author_facet | Patra, Arjun Satpathy, Swaha Hussain, Muhammad Delwar |
author_sort | Patra, Arjun |
collection | PubMed |
description | INTRODUCTION: Nimbolide (Nim), a limonoid obtained from the neem tree, Azadirachta indica, has several pharmacological properties, including anticancer effects in different type of cancers. No drug-delivery system has been reported for enhancing the therapeutic application of this novel hydrophobic molecule. METHODS: In the present research, poly(lactic-co-glycolic acid) (PLGA) nanoparticles of Nim (Nim-nano) were formulated by nanoprecipitation, characterized for physicochemical properties, and screened for anticancer potential in breast (MCF-7 and MDA-MB-231) and pancreatic (AsPC-1) cancer cell lines. RESULTS: The Nim-nano had a particle size of 183.73±2.22 nm and 221.20±11.03 nm before and after lyophilization, respectively. Cryoprotectants (mannitol and sucrose) significantly inhibited growth in particle size due to lyophilization. The ζ-potential of the Nim-nano was −22.40±4.40 mV. Drug loading and encapsulation efficiency of Nim-nano were 5.25%±1.12% and 55.67%±12.42%, respectively. The Nim-nano exhibited sustained release of Nim for more than 6 days in PBS (pH 7.4) and showed two- to three-fold enhanced cytotoxicity in breast and pancreatic cancer cell lines compared with free Nim. CONCLUSION: The Nim-nano formulation has great potential for treatment of cancers, such as pancreatic and breast cancer. Further, the PLGA-polymer surface can be modified by conjugation with polyethylene glycol, receptor-binding ligands (eg, folic acid), and other that which may lead to targeted delivery of Nim in the treatment of cancer. |
format | Online Article Text |
id | pubmed-6789415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-67894152019-10-18 Nanodelivery and anticancer effect of a limonoid, nimbolide, in breast and pancreatic cancer cells Patra, Arjun Satpathy, Swaha Hussain, Muhammad Delwar Int J Nanomedicine Original Research INTRODUCTION: Nimbolide (Nim), a limonoid obtained from the neem tree, Azadirachta indica, has several pharmacological properties, including anticancer effects in different type of cancers. No drug-delivery system has been reported for enhancing the therapeutic application of this novel hydrophobic molecule. METHODS: In the present research, poly(lactic-co-glycolic acid) (PLGA) nanoparticles of Nim (Nim-nano) were formulated by nanoprecipitation, characterized for physicochemical properties, and screened for anticancer potential in breast (MCF-7 and MDA-MB-231) and pancreatic (AsPC-1) cancer cell lines. RESULTS: The Nim-nano had a particle size of 183.73±2.22 nm and 221.20±11.03 nm before and after lyophilization, respectively. Cryoprotectants (mannitol and sucrose) significantly inhibited growth in particle size due to lyophilization. The ζ-potential of the Nim-nano was −22.40±4.40 mV. Drug loading and encapsulation efficiency of Nim-nano were 5.25%±1.12% and 55.67%±12.42%, respectively. The Nim-nano exhibited sustained release of Nim for more than 6 days in PBS (pH 7.4) and showed two- to three-fold enhanced cytotoxicity in breast and pancreatic cancer cell lines compared with free Nim. CONCLUSION: The Nim-nano formulation has great potential for treatment of cancers, such as pancreatic and breast cancer. Further, the PLGA-polymer surface can be modified by conjugation with polyethylene glycol, receptor-binding ligands (eg, folic acid), and other that which may lead to targeted delivery of Nim in the treatment of cancer. Dove 2019-10-07 /pmc/articles/PMC6789415/ /pubmed/31632020 http://dx.doi.org/10.2147/IJN.S208540 Text en © 2019 Patra et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Patra, Arjun Satpathy, Swaha Hussain, Muhammad Delwar Nanodelivery and anticancer effect of a limonoid, nimbolide, in breast and pancreatic cancer cells |
title | Nanodelivery and anticancer effect of a limonoid, nimbolide, in breast and pancreatic cancer cells |
title_full | Nanodelivery and anticancer effect of a limonoid, nimbolide, in breast and pancreatic cancer cells |
title_fullStr | Nanodelivery and anticancer effect of a limonoid, nimbolide, in breast and pancreatic cancer cells |
title_full_unstemmed | Nanodelivery and anticancer effect of a limonoid, nimbolide, in breast and pancreatic cancer cells |
title_short | Nanodelivery and anticancer effect of a limonoid, nimbolide, in breast and pancreatic cancer cells |
title_sort | nanodelivery and anticancer effect of a limonoid, nimbolide, in breast and pancreatic cancer cells |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789415/ https://www.ncbi.nlm.nih.gov/pubmed/31632020 http://dx.doi.org/10.2147/IJN.S208540 |
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