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Novel nano-vehicle for delivery and efficiency of anticancer auraptene against colon cancer cells

The aim of this study is to devise, prepare and characterize nano encapsulated auraptene (AUR) and evaluate cytotoxic and apoptotic effects on HT-29 colon cancer cells. Herein, AUR nano formulations were prepared by triblock (PCL-PEG-PCL) and pentablock (PLA-PCL-PEG-PCL-PLA) biodegradable copolymers...

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Autores principales: Jalilzadeh, Nazila, Samadi, Naser, Salehi, Roya, Dehghan, Gholamreza, Iranshahi, Mehrdad, Dadpour, Mohammad Reza, Hamishehkar, Hamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994674/
https://www.ncbi.nlm.nih.gov/pubmed/32005894
http://dx.doi.org/10.1038/s41598-020-58527-0
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author Jalilzadeh, Nazila
Samadi, Naser
Salehi, Roya
Dehghan, Gholamreza
Iranshahi, Mehrdad
Dadpour, Mohammad Reza
Hamishehkar, Hamed
author_facet Jalilzadeh, Nazila
Samadi, Naser
Salehi, Roya
Dehghan, Gholamreza
Iranshahi, Mehrdad
Dadpour, Mohammad Reza
Hamishehkar, Hamed
author_sort Jalilzadeh, Nazila
collection PubMed
description The aim of this study is to devise, prepare and characterize nano encapsulated auraptene (AUR) and evaluate cytotoxic and apoptotic effects on HT-29 colon cancer cells. Herein, AUR nano formulations were prepared by triblock (PCL-PEG-PCL) and pentablock (PLA-PCL-PEG-PCL-PLA) biodegradable copolymers in order to increase AUR bioavailability as an anticancer agent. The preparation of nano particles (NPs) was done with rotor stator homogenization (RSH) and Ultrasonic homogenization (USH) methods. The physicochemical characteristics of prepared nanoparticles (NPs) were studied using HNMR, FTIR, GPC, DLS and SEM techniques. The smaller hydrodynamic size (110 nm) and polydispersity index (PDI: 0.288) as well as higher cellular uptake (89%) were observed in PB NPs rather than TB NPs. The highest cytotoxic and apoptotic effects were observed in AUR loaded PB NPs compared to AUR loaded TB NPs and free AUR obtained by MTT assay, cell cycle arrest, Annexin V-FITC, DAPI staining and RT-PCR techniques. Real time PCR results indicated that Bax /Bcl2 expression ratio as an apoptosis predicting criterion, in free AUR, AUR loaded TB and AUR loaded PB have increased 6, 9 and 13 times, respectively (p value < 0.05). In conclusion, using biodegradable nano-vehicles for sustained delivery of natural anti-cancer compounds may open new perspectives for treatment of cancer patients.
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spelling pubmed-69946742020-02-06 Novel nano-vehicle for delivery and efficiency of anticancer auraptene against colon cancer cells Jalilzadeh, Nazila Samadi, Naser Salehi, Roya Dehghan, Gholamreza Iranshahi, Mehrdad Dadpour, Mohammad Reza Hamishehkar, Hamed Sci Rep Article The aim of this study is to devise, prepare and characterize nano encapsulated auraptene (AUR) and evaluate cytotoxic and apoptotic effects on HT-29 colon cancer cells. Herein, AUR nano formulations were prepared by triblock (PCL-PEG-PCL) and pentablock (PLA-PCL-PEG-PCL-PLA) biodegradable copolymers in order to increase AUR bioavailability as an anticancer agent. The preparation of nano particles (NPs) was done with rotor stator homogenization (RSH) and Ultrasonic homogenization (USH) methods. The physicochemical characteristics of prepared nanoparticles (NPs) were studied using HNMR, FTIR, GPC, DLS and SEM techniques. The smaller hydrodynamic size (110 nm) and polydispersity index (PDI: 0.288) as well as higher cellular uptake (89%) were observed in PB NPs rather than TB NPs. The highest cytotoxic and apoptotic effects were observed in AUR loaded PB NPs compared to AUR loaded TB NPs and free AUR obtained by MTT assay, cell cycle arrest, Annexin V-FITC, DAPI staining and RT-PCR techniques. Real time PCR results indicated that Bax /Bcl2 expression ratio as an apoptosis predicting criterion, in free AUR, AUR loaded TB and AUR loaded PB have increased 6, 9 and 13 times, respectively (p value < 0.05). In conclusion, using biodegradable nano-vehicles for sustained delivery of natural anti-cancer compounds may open new perspectives for treatment of cancer patients. Nature Publishing Group UK 2020-01-31 /pmc/articles/PMC6994674/ /pubmed/32005894 http://dx.doi.org/10.1038/s41598-020-58527-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Jalilzadeh, Nazila
Samadi, Naser
Salehi, Roya
Dehghan, Gholamreza
Iranshahi, Mehrdad
Dadpour, Mohammad Reza
Hamishehkar, Hamed
Novel nano-vehicle for delivery and efficiency of anticancer auraptene against colon cancer cells
title Novel nano-vehicle for delivery and efficiency of anticancer auraptene against colon cancer cells
title_full Novel nano-vehicle for delivery and efficiency of anticancer auraptene against colon cancer cells
title_fullStr Novel nano-vehicle for delivery and efficiency of anticancer auraptene against colon cancer cells
title_full_unstemmed Novel nano-vehicle for delivery and efficiency of anticancer auraptene against colon cancer cells
title_short Novel nano-vehicle for delivery and efficiency of anticancer auraptene against colon cancer cells
title_sort novel nano-vehicle for delivery and efficiency of anticancer auraptene against colon cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994674/
https://www.ncbi.nlm.nih.gov/pubmed/32005894
http://dx.doi.org/10.1038/s41598-020-58527-0
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