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Synergistic Combination of Irinotecan and Rapamycin Orally Delivered by Nanoemulsion for Enhancing Therapeutic Efficacy of Pancreatic Cancer
In recent years, combining different types of therapy has emerged as an advanced strategy for cancer treatment. In these combination therapies, oral delivery of anticancer drugs is more convenient and compliant. This study developed an irinotecan/rapamycin-loaded oral lecithin-based self-nanoemulsif...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963937/ https://www.ncbi.nlm.nih.gov/pubmed/36839795 http://dx.doi.org/10.3390/pharmaceutics15020473 |
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author | Liu, Yu-Hsuan Chen, Ling-Chun Cheng, Wen-Ting Wei, Pu-Sheng Hsieh, Chien-Ming Sheu, Ming-Thau Lin, Shyr-Yi Ho, Hsiu-O Lin, Hong-Liang |
author_facet | Liu, Yu-Hsuan Chen, Ling-Chun Cheng, Wen-Ting Wei, Pu-Sheng Hsieh, Chien-Ming Sheu, Ming-Thau Lin, Shyr-Yi Ho, Hsiu-O Lin, Hong-Liang |
author_sort | Liu, Yu-Hsuan |
collection | PubMed |
description | In recent years, combining different types of therapy has emerged as an advanced strategy for cancer treatment. In these combination therapies, oral delivery of anticancer drugs is more convenient and compliant. This study developed an irinotecan/rapamycin-loaded oral lecithin-based self-nanoemulsifying nanoemulsion preconcentrate ((LB)SNENP(ir/ra)) and evaluated its synergistic combination effects on pancreatic cancer. (LB)SNENP loaded with irinotecan and rapamycin at a ratio of 1:1 ((LB)SNENP(ir10/ra10)) had a better drug release profile and smaller particle size (<200 nm) than the drug powder. Moreover, (LB)SNENP(ir10/ra10) exhibited a strong synergistic effect (combination index [CI] < 1.0) in cell viability and combination effect studies. In the tumor inhibition study, the antitumor activity of (LB)SNENP(ir10/ra10/sily20) against MIA PaCa-2 (a human pancreatic cancer cell line) was significantly increased compared with the other groups. When administered with rapamycin and silymarin, the area under the curve and the maximum concentration of irinotecan significantly improved compared with the control. We successfully developed an irinotecan/rapamycin-loaded oral self-nanoemulsifying nanoemulsion system to achieve treatment efficacy for pancreatic cancer. |
format | Online Article Text |
id | pubmed-9963937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99639372023-02-26 Synergistic Combination of Irinotecan and Rapamycin Orally Delivered by Nanoemulsion for Enhancing Therapeutic Efficacy of Pancreatic Cancer Liu, Yu-Hsuan Chen, Ling-Chun Cheng, Wen-Ting Wei, Pu-Sheng Hsieh, Chien-Ming Sheu, Ming-Thau Lin, Shyr-Yi Ho, Hsiu-O Lin, Hong-Liang Pharmaceutics Article In recent years, combining different types of therapy has emerged as an advanced strategy for cancer treatment. In these combination therapies, oral delivery of anticancer drugs is more convenient and compliant. This study developed an irinotecan/rapamycin-loaded oral lecithin-based self-nanoemulsifying nanoemulsion preconcentrate ((LB)SNENP(ir/ra)) and evaluated its synergistic combination effects on pancreatic cancer. (LB)SNENP loaded with irinotecan and rapamycin at a ratio of 1:1 ((LB)SNENP(ir10/ra10)) had a better drug release profile and smaller particle size (<200 nm) than the drug powder. Moreover, (LB)SNENP(ir10/ra10) exhibited a strong synergistic effect (combination index [CI] < 1.0) in cell viability and combination effect studies. In the tumor inhibition study, the antitumor activity of (LB)SNENP(ir10/ra10/sily20) against MIA PaCa-2 (a human pancreatic cancer cell line) was significantly increased compared with the other groups. When administered with rapamycin and silymarin, the area under the curve and the maximum concentration of irinotecan significantly improved compared with the control. We successfully developed an irinotecan/rapamycin-loaded oral self-nanoemulsifying nanoemulsion system to achieve treatment efficacy for pancreatic cancer. MDPI 2023-01-31 /pmc/articles/PMC9963937/ /pubmed/36839795 http://dx.doi.org/10.3390/pharmaceutics15020473 Text en © 2023 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 Liu, Yu-Hsuan Chen, Ling-Chun Cheng, Wen-Ting Wei, Pu-Sheng Hsieh, Chien-Ming Sheu, Ming-Thau Lin, Shyr-Yi Ho, Hsiu-O Lin, Hong-Liang Synergistic Combination of Irinotecan and Rapamycin Orally Delivered by Nanoemulsion for Enhancing Therapeutic Efficacy of Pancreatic Cancer |
title | Synergistic Combination of Irinotecan and Rapamycin Orally Delivered by Nanoemulsion for Enhancing Therapeutic Efficacy of Pancreatic Cancer |
title_full | Synergistic Combination of Irinotecan and Rapamycin Orally Delivered by Nanoemulsion for Enhancing Therapeutic Efficacy of Pancreatic Cancer |
title_fullStr | Synergistic Combination of Irinotecan and Rapamycin Orally Delivered by Nanoemulsion for Enhancing Therapeutic Efficacy of Pancreatic Cancer |
title_full_unstemmed | Synergistic Combination of Irinotecan and Rapamycin Orally Delivered by Nanoemulsion for Enhancing Therapeutic Efficacy of Pancreatic Cancer |
title_short | Synergistic Combination of Irinotecan and Rapamycin Orally Delivered by Nanoemulsion for Enhancing Therapeutic Efficacy of Pancreatic Cancer |
title_sort | synergistic combination of irinotecan and rapamycin orally delivered by nanoemulsion for enhancing therapeutic efficacy of pancreatic cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963937/ https://www.ncbi.nlm.nih.gov/pubmed/36839795 http://dx.doi.org/10.3390/pharmaceutics15020473 |
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