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Nanoemulsions as Delivery Systems for Poly-Chemotherapy Aiming at Melanoma Treatment
Aims: Advanced melanoma is characterized by poor outcome. Despite the number of treatments having been increased over the last decade, current pharmacological strategies are only partially effective. Therefore, the improvement of the current systemic therapy is worthy of investigation. Methods: a na...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281359/ https://www.ncbi.nlm.nih.gov/pubmed/32397484 http://dx.doi.org/10.3390/cancers12051198 |
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author | Dianzani, Chiara Monge, Chiara Miglio, Gianluca Serpe, Loredana Martina, Katia Cangemi, Luigi Ferraris, Chiara Mioletti, Silvia Osella, Sara Gigliotti, Casimiro Luca Boggio, Elena Clemente, Nausicaa Dianzani, Umberto Battaglia, Luigi |
author_facet | Dianzani, Chiara Monge, Chiara Miglio, Gianluca Serpe, Loredana Martina, Katia Cangemi, Luigi Ferraris, Chiara Mioletti, Silvia Osella, Sara Gigliotti, Casimiro Luca Boggio, Elena Clemente, Nausicaa Dianzani, Umberto Battaglia, Luigi |
author_sort | Dianzani, Chiara |
collection | PubMed |
description | Aims: Advanced melanoma is characterized by poor outcome. Despite the number of treatments having been increased over the last decade, current pharmacological strategies are only partially effective. Therefore, the improvement of the current systemic therapy is worthy of investigation. Methods: a nanotechnology-based poly-chemotherapy was tested at preclinical level. Temozolomide, rapamycin, and bevacizumab were co-loaded as injectable nanoemulsions for total parenteral nutrition (Intralipid(®)), due to suitable devices, and preliminarily tested in vitro on human and mouse cell models and in vivo on the B16-F10 melanoma mouse model. Results: Drug combination was efficiently loaded in the liquid lipid matrix of Intralipid(®), including bevacizumab monoclonal antibody, leading to a fast internalization in tumour cells. An increased cytotoxicity towards melanoma cells, as well as an improved inhibition of tumour relapse, migration, and angiogenesis were demonstrated in cell models for the Intralipid(®)-loaded drug combinations. In preliminary in vivo studies, the proposed approach was able to reduce tumour growth significantly, compared to controls. A relevant efficacy towards tumour angiogenesis and mitotic index was determined and immune response was involved. Conclusions: In these preliminary studies, Intralipid(®) proved to be a safe and versatile poly-chemotherapy delivery system for advanced melanoma treatment, by acting on multiple mechanisms. |
format | Online Article Text |
id | pubmed-7281359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72813592020-06-19 Nanoemulsions as Delivery Systems for Poly-Chemotherapy Aiming at Melanoma Treatment Dianzani, Chiara Monge, Chiara Miglio, Gianluca Serpe, Loredana Martina, Katia Cangemi, Luigi Ferraris, Chiara Mioletti, Silvia Osella, Sara Gigliotti, Casimiro Luca Boggio, Elena Clemente, Nausicaa Dianzani, Umberto Battaglia, Luigi Cancers (Basel) Article Aims: Advanced melanoma is characterized by poor outcome. Despite the number of treatments having been increased over the last decade, current pharmacological strategies are only partially effective. Therefore, the improvement of the current systemic therapy is worthy of investigation. Methods: a nanotechnology-based poly-chemotherapy was tested at preclinical level. Temozolomide, rapamycin, and bevacizumab were co-loaded as injectable nanoemulsions for total parenteral nutrition (Intralipid(®)), due to suitable devices, and preliminarily tested in vitro on human and mouse cell models and in vivo on the B16-F10 melanoma mouse model. Results: Drug combination was efficiently loaded in the liquid lipid matrix of Intralipid(®), including bevacizumab monoclonal antibody, leading to a fast internalization in tumour cells. An increased cytotoxicity towards melanoma cells, as well as an improved inhibition of tumour relapse, migration, and angiogenesis were demonstrated in cell models for the Intralipid(®)-loaded drug combinations. In preliminary in vivo studies, the proposed approach was able to reduce tumour growth significantly, compared to controls. A relevant efficacy towards tumour angiogenesis and mitotic index was determined and immune response was involved. Conclusions: In these preliminary studies, Intralipid(®) proved to be a safe and versatile poly-chemotherapy delivery system for advanced melanoma treatment, by acting on multiple mechanisms. MDPI 2020-05-09 /pmc/articles/PMC7281359/ /pubmed/32397484 http://dx.doi.org/10.3390/cancers12051198 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Dianzani, Chiara Monge, Chiara Miglio, Gianluca Serpe, Loredana Martina, Katia Cangemi, Luigi Ferraris, Chiara Mioletti, Silvia Osella, Sara Gigliotti, Casimiro Luca Boggio, Elena Clemente, Nausicaa Dianzani, Umberto Battaglia, Luigi Nanoemulsions as Delivery Systems for Poly-Chemotherapy Aiming at Melanoma Treatment |
title | Nanoemulsions as Delivery Systems for Poly-Chemotherapy Aiming at Melanoma Treatment |
title_full | Nanoemulsions as Delivery Systems for Poly-Chemotherapy Aiming at Melanoma Treatment |
title_fullStr | Nanoemulsions as Delivery Systems for Poly-Chemotherapy Aiming at Melanoma Treatment |
title_full_unstemmed | Nanoemulsions as Delivery Systems for Poly-Chemotherapy Aiming at Melanoma Treatment |
title_short | Nanoemulsions as Delivery Systems for Poly-Chemotherapy Aiming at Melanoma Treatment |
title_sort | nanoemulsions as delivery systems for poly-chemotherapy aiming at melanoma treatment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281359/ https://www.ncbi.nlm.nih.gov/pubmed/32397484 http://dx.doi.org/10.3390/cancers12051198 |
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