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Improved chemotherapeutic efficacy of injectable chrysin encapsulated by copolymer nanoparticles
Chrysin is a flavone that is found in several plants and in honeycomb and possesses various biological activities. However, its low solubility means it has poor bioavailability, which must be resolved to enable its pharmaceutical applications. In the present study, chrysin was incorporated into meth...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352247/ https://www.ncbi.nlm.nih.gov/pubmed/28331315 http://dx.doi.org/10.2147/IJN.S132043 |
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author | Kim, Kyoung Mee Lim, Hyun Kyung Shim, Sang Hee Jung, Joohee |
author_facet | Kim, Kyoung Mee Lim, Hyun Kyung Shim, Sang Hee Jung, Joohee |
author_sort | Kim, Kyoung Mee |
collection | PubMed |
description | Chrysin is a flavone that is found in several plants and in honeycomb and possesses various biological activities. However, its low solubility means it has poor bioavailability, which must be resolved to enable its pharmaceutical applications. In the present study, chrysin was incorporated into methoxy poly(ethylene glycol)-β-polycaprolactone nanoparticles (chrysin-NPs) using the oil-in-water technique in order to overcome problems associated with chrysin. The properties of chrysin-NPs were analyzed, and their anticancer effects were investigated in vitro and in vivo. Chrysin-NPs were 77 nm sized (as determined by dynamic laser light scattering) and showed a monodisperse distribution. The zeta potential of chrysin-NPs was −2.22 mV, and they were spherically shaped by cryo-transmission electron microscopy (cryo-TEM). The loading efficiency of chrysin-NPs was 46.96%. Chrysin-NPs retained the cytotoxicity of chrysin in A549 cells. The therapeutic efficacies of chrysin-NPs were compared with those of chrysin in an A549-derived xenograft mouse model. Chrysin-NPs were intravenously injected at a 10 times lower dosage than chrysin 3 times per week (q2d×3/week). However, free chrysin was orally administrated 5 times per week (q1d×5/week). Chrysin-NP-treated group showed significant tumor growth delay, which was similar to that of chrysin-treated group, despite the considerably lower total dosage. These results suggest that the injectable chrysin-NPs enhance therapeutic efficacy in vivo and offer a beneficial formulation for chemotherapy. |
format | Online Article Text |
id | pubmed-5352247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53522472017-03-22 Improved chemotherapeutic efficacy of injectable chrysin encapsulated by copolymer nanoparticles Kim, Kyoung Mee Lim, Hyun Kyung Shim, Sang Hee Jung, Joohee Int J Nanomedicine Original Research Chrysin is a flavone that is found in several plants and in honeycomb and possesses various biological activities. However, its low solubility means it has poor bioavailability, which must be resolved to enable its pharmaceutical applications. In the present study, chrysin was incorporated into methoxy poly(ethylene glycol)-β-polycaprolactone nanoparticles (chrysin-NPs) using the oil-in-water technique in order to overcome problems associated with chrysin. The properties of chrysin-NPs were analyzed, and their anticancer effects were investigated in vitro and in vivo. Chrysin-NPs were 77 nm sized (as determined by dynamic laser light scattering) and showed a monodisperse distribution. The zeta potential of chrysin-NPs was −2.22 mV, and they were spherically shaped by cryo-transmission electron microscopy (cryo-TEM). The loading efficiency of chrysin-NPs was 46.96%. Chrysin-NPs retained the cytotoxicity of chrysin in A549 cells. The therapeutic efficacies of chrysin-NPs were compared with those of chrysin in an A549-derived xenograft mouse model. Chrysin-NPs were intravenously injected at a 10 times lower dosage than chrysin 3 times per week (q2d×3/week). However, free chrysin was orally administrated 5 times per week (q1d×5/week). Chrysin-NP-treated group showed significant tumor growth delay, which was similar to that of chrysin-treated group, despite the considerably lower total dosage. These results suggest that the injectable chrysin-NPs enhance therapeutic efficacy in vivo and offer a beneficial formulation for chemotherapy. Dove Medical Press 2017-03-09 /pmc/articles/PMC5352247/ /pubmed/28331315 http://dx.doi.org/10.2147/IJN.S132043 Text en © 2017 Kim et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Kim, Kyoung Mee Lim, Hyun Kyung Shim, Sang Hee Jung, Joohee Improved chemotherapeutic efficacy of injectable chrysin encapsulated by copolymer nanoparticles |
title | Improved chemotherapeutic efficacy of injectable chrysin encapsulated by copolymer nanoparticles |
title_full | Improved chemotherapeutic efficacy of injectable chrysin encapsulated by copolymer nanoparticles |
title_fullStr | Improved chemotherapeutic efficacy of injectable chrysin encapsulated by copolymer nanoparticles |
title_full_unstemmed | Improved chemotherapeutic efficacy of injectable chrysin encapsulated by copolymer nanoparticles |
title_short | Improved chemotherapeutic efficacy of injectable chrysin encapsulated by copolymer nanoparticles |
title_sort | improved chemotherapeutic efficacy of injectable chrysin encapsulated by copolymer nanoparticles |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352247/ https://www.ncbi.nlm.nih.gov/pubmed/28331315 http://dx.doi.org/10.2147/IJN.S132043 |
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