Cargando…
Ultrasound-Responsive Nrf2-Targeting siRNA-Loaded Nanobubbles for Enhancing the Treatment of Melanoma
The siRNA-mediated inhibition of nuclear factor E2-related factor 2 (Nrf2) can be an attractive approach to overcome chemoresistance in various malignant tumors, including melanoma. This work aims at designing a new type of chitosan-shelled nanobubble for the delivery of siRNA against Nrf2 in combin...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878772/ https://www.ncbi.nlm.nih.gov/pubmed/35214073 http://dx.doi.org/10.3390/pharmaceutics14020341 |
_version_ | 1784658739678150656 |
---|---|
author | Argenziano, Monica Bessone, Federica Dianzani, Chiara Cucci, Marie Angèle Grattarola, Margherita Pizzimenti, Stefania Cavalli, Roberta |
author_facet | Argenziano, Monica Bessone, Federica Dianzani, Chiara Cucci, Marie Angèle Grattarola, Margherita Pizzimenti, Stefania Cavalli, Roberta |
author_sort | Argenziano, Monica |
collection | PubMed |
description | The siRNA-mediated inhibition of nuclear factor E2-related factor 2 (Nrf2) can be an attractive approach to overcome chemoresistance in various malignant tumors, including melanoma. This work aims at designing a new type of chitosan-shelled nanobubble for the delivery of siRNA against Nrf2 in combination with an ultrasound. A new preparation method based on a water–oil–water (W/O/W) double-emulsion was purposely developed for siRNA encapsulation in aqueous droplets within a nanobubble core. Stable, very small NB formulations were obtained, with sizes of about 100 nm and a positive surface charge. siRNA was efficiently loaded in NBs, reaching an encapsulation efficiency of about 90%. siNrf2-NBs downregulated the target gene in M14 cells, sensitizing the resistant melanoma cells to the cisplatin treatment. The combination with US favored NB cell uptake and transfection efficiency. Based on the results, nanobubbles have shown to be a promising US responsive tool for siRNA delivery, able to overcome chemoresistance in melanoma cancer cells. |
format | Online Article Text |
id | pubmed-8878772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88787722022-02-26 Ultrasound-Responsive Nrf2-Targeting siRNA-Loaded Nanobubbles for Enhancing the Treatment of Melanoma Argenziano, Monica Bessone, Federica Dianzani, Chiara Cucci, Marie Angèle Grattarola, Margherita Pizzimenti, Stefania Cavalli, Roberta Pharmaceutics Article The siRNA-mediated inhibition of nuclear factor E2-related factor 2 (Nrf2) can be an attractive approach to overcome chemoresistance in various malignant tumors, including melanoma. This work aims at designing a new type of chitosan-shelled nanobubble for the delivery of siRNA against Nrf2 in combination with an ultrasound. A new preparation method based on a water–oil–water (W/O/W) double-emulsion was purposely developed for siRNA encapsulation in aqueous droplets within a nanobubble core. Stable, very small NB formulations were obtained, with sizes of about 100 nm and a positive surface charge. siRNA was efficiently loaded in NBs, reaching an encapsulation efficiency of about 90%. siNrf2-NBs downregulated the target gene in M14 cells, sensitizing the resistant melanoma cells to the cisplatin treatment. The combination with US favored NB cell uptake and transfection efficiency. Based on the results, nanobubbles have shown to be a promising US responsive tool for siRNA delivery, able to overcome chemoresistance in melanoma cancer cells. MDPI 2022-01-31 /pmc/articles/PMC8878772/ /pubmed/35214073 http://dx.doi.org/10.3390/pharmaceutics14020341 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Argenziano, Monica Bessone, Federica Dianzani, Chiara Cucci, Marie Angèle Grattarola, Margherita Pizzimenti, Stefania Cavalli, Roberta Ultrasound-Responsive Nrf2-Targeting siRNA-Loaded Nanobubbles for Enhancing the Treatment of Melanoma |
title | Ultrasound-Responsive Nrf2-Targeting siRNA-Loaded Nanobubbles for Enhancing the Treatment of Melanoma |
title_full | Ultrasound-Responsive Nrf2-Targeting siRNA-Loaded Nanobubbles for Enhancing the Treatment of Melanoma |
title_fullStr | Ultrasound-Responsive Nrf2-Targeting siRNA-Loaded Nanobubbles for Enhancing the Treatment of Melanoma |
title_full_unstemmed | Ultrasound-Responsive Nrf2-Targeting siRNA-Loaded Nanobubbles for Enhancing the Treatment of Melanoma |
title_short | Ultrasound-Responsive Nrf2-Targeting siRNA-Loaded Nanobubbles for Enhancing the Treatment of Melanoma |
title_sort | ultrasound-responsive nrf2-targeting sirna-loaded nanobubbles for enhancing the treatment of melanoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878772/ https://www.ncbi.nlm.nih.gov/pubmed/35214073 http://dx.doi.org/10.3390/pharmaceutics14020341 |
work_keys_str_mv | AT argenzianomonica ultrasoundresponsivenrf2targetingsirnaloadednanobubblesforenhancingthetreatmentofmelanoma AT bessonefederica ultrasoundresponsivenrf2targetingsirnaloadednanobubblesforenhancingthetreatmentofmelanoma AT dianzanichiara ultrasoundresponsivenrf2targetingsirnaloadednanobubblesforenhancingthetreatmentofmelanoma AT cuccimarieangele ultrasoundresponsivenrf2targetingsirnaloadednanobubblesforenhancingthetreatmentofmelanoma AT grattarolamargherita ultrasoundresponsivenrf2targetingsirnaloadednanobubblesforenhancingthetreatmentofmelanoma AT pizzimentistefania ultrasoundresponsivenrf2targetingsirnaloadednanobubblesforenhancingthetreatmentofmelanoma AT cavalliroberta ultrasoundresponsivenrf2targetingsirnaloadednanobubblesforenhancingthetreatmentofmelanoma |