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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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.
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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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