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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...

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Autores principales: Kim, Kyoung Mee, Lim, Hyun Kyung, Shim, Sang Hee, Jung, Joohee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
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.
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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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