Cargando…
Efficacy of Nanofiber Sheets Incorporating Lenvatinib in a Hepatocellular Carcinoma Xenograft Model
Lenvatinib has a high response rate in unresectable advanced hepatocellular carcinoma (HCC). In this study, we investigated whether lenvatinib-incorporating poly(ε-caprolactone) sheets (lenvatinib sheets) as a drug delivery system (DDS) exerted antitumor effects in a murine HCC model. The lenvatinib...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9025678/ https://www.ncbi.nlm.nih.gov/pubmed/35458072 http://dx.doi.org/10.3390/nano12081364 |
_version_ | 1784690932420968448 |
---|---|
author | Yoshida, Terufumi Kaibori, Masaki Fujisawa, Nanami Ishizuka, Mariko Sumiyama, Fusao Hatta, Masahiko Kosaka, Hisashi Matsui, Kosuke Suzuki, Kensuke Akama, Tomoya O. Katano, Tayo Yoshii, Kengo Ebara, Mitsuhiro Sekimoto, Mitsugu |
author_facet | Yoshida, Terufumi Kaibori, Masaki Fujisawa, Nanami Ishizuka, Mariko Sumiyama, Fusao Hatta, Masahiko Kosaka, Hisashi Matsui, Kosuke Suzuki, Kensuke Akama, Tomoya O. Katano, Tayo Yoshii, Kengo Ebara, Mitsuhiro Sekimoto, Mitsugu |
author_sort | Yoshida, Terufumi |
collection | PubMed |
description | Lenvatinib has a high response rate in unresectable advanced hepatocellular carcinoma (HCC). In this study, we investigated whether lenvatinib-incorporating poly(ε-caprolactone) sheets (lenvatinib sheets) as a drug delivery system (DDS) exerted antitumor effects in a murine HCC model. The lenvatinib sheets were designed for sustained release of approximately 1 mg lenvatinib for 14 days. For 14 days, 1 mg lenvatinib was orally administered to mice. Then, we compared the antitumor effects of lenvatinib sheets with those of oral lenvatinib. The tumor volume, body weight, and serum lenvatinib level were measured for 14 days. A peritoneal dissemination model was established to examine the survival prolongation effect of the lenvatinib sheets. Tumor growth was significantly inhibited in the lenvatinib sheet group compared with that in the no treatment and oral groups. The antitumor effect was significantly higher in the lenvatinib sheet group. Regardless of the insertion site, the serum lenvatinib levels were maintained and showed similar antitumor effects. The mitotic index was significantly inhibited in the lenvatinib sheet group compared with that in the control group. Furthermore, lenvatinib sheets improved the 30-day survival. Lenvatinib sheets showed sufficient antitumor effects and may serve as an effective novel DDS for advanced HCC. |
format | Online Article Text |
id | pubmed-9025678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90256782022-04-23 Efficacy of Nanofiber Sheets Incorporating Lenvatinib in a Hepatocellular Carcinoma Xenograft Model Yoshida, Terufumi Kaibori, Masaki Fujisawa, Nanami Ishizuka, Mariko Sumiyama, Fusao Hatta, Masahiko Kosaka, Hisashi Matsui, Kosuke Suzuki, Kensuke Akama, Tomoya O. Katano, Tayo Yoshii, Kengo Ebara, Mitsuhiro Sekimoto, Mitsugu Nanomaterials (Basel) Article Lenvatinib has a high response rate in unresectable advanced hepatocellular carcinoma (HCC). In this study, we investigated whether lenvatinib-incorporating poly(ε-caprolactone) sheets (lenvatinib sheets) as a drug delivery system (DDS) exerted antitumor effects in a murine HCC model. The lenvatinib sheets were designed for sustained release of approximately 1 mg lenvatinib for 14 days. For 14 days, 1 mg lenvatinib was orally administered to mice. Then, we compared the antitumor effects of lenvatinib sheets with those of oral lenvatinib. The tumor volume, body weight, and serum lenvatinib level were measured for 14 days. A peritoneal dissemination model was established to examine the survival prolongation effect of the lenvatinib sheets. Tumor growth was significantly inhibited in the lenvatinib sheet group compared with that in the no treatment and oral groups. The antitumor effect was significantly higher in the lenvatinib sheet group. Regardless of the insertion site, the serum lenvatinib levels were maintained and showed similar antitumor effects. The mitotic index was significantly inhibited in the lenvatinib sheet group compared with that in the control group. Furthermore, lenvatinib sheets improved the 30-day survival. Lenvatinib sheets showed sufficient antitumor effects and may serve as an effective novel DDS for advanced HCC. MDPI 2022-04-15 /pmc/articles/PMC9025678/ /pubmed/35458072 http://dx.doi.org/10.3390/nano12081364 Text en © 2022 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 Yoshida, Terufumi Kaibori, Masaki Fujisawa, Nanami Ishizuka, Mariko Sumiyama, Fusao Hatta, Masahiko Kosaka, Hisashi Matsui, Kosuke Suzuki, Kensuke Akama, Tomoya O. Katano, Tayo Yoshii, Kengo Ebara, Mitsuhiro Sekimoto, Mitsugu Efficacy of Nanofiber Sheets Incorporating Lenvatinib in a Hepatocellular Carcinoma Xenograft Model |
title | Efficacy of Nanofiber Sheets Incorporating Lenvatinib in a Hepatocellular Carcinoma Xenograft Model |
title_full | Efficacy of Nanofiber Sheets Incorporating Lenvatinib in a Hepatocellular Carcinoma Xenograft Model |
title_fullStr | Efficacy of Nanofiber Sheets Incorporating Lenvatinib in a Hepatocellular Carcinoma Xenograft Model |
title_full_unstemmed | Efficacy of Nanofiber Sheets Incorporating Lenvatinib in a Hepatocellular Carcinoma Xenograft Model |
title_short | Efficacy of Nanofiber Sheets Incorporating Lenvatinib in a Hepatocellular Carcinoma Xenograft Model |
title_sort | efficacy of nanofiber sheets incorporating lenvatinib in a hepatocellular carcinoma xenograft model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9025678/ https://www.ncbi.nlm.nih.gov/pubmed/35458072 http://dx.doi.org/10.3390/nano12081364 |
work_keys_str_mv | AT yoshidaterufumi efficacyofnanofibersheetsincorporatinglenvatinibinahepatocellularcarcinomaxenograftmodel AT kaiborimasaki efficacyofnanofibersheetsincorporatinglenvatinibinahepatocellularcarcinomaxenograftmodel AT fujisawananami efficacyofnanofibersheetsincorporatinglenvatinibinahepatocellularcarcinomaxenograftmodel AT ishizukamariko efficacyofnanofibersheetsincorporatinglenvatinibinahepatocellularcarcinomaxenograftmodel AT sumiyamafusao efficacyofnanofibersheetsincorporatinglenvatinibinahepatocellularcarcinomaxenograftmodel AT hattamasahiko efficacyofnanofibersheetsincorporatinglenvatinibinahepatocellularcarcinomaxenograftmodel AT kosakahisashi efficacyofnanofibersheetsincorporatinglenvatinibinahepatocellularcarcinomaxenograftmodel AT matsuikosuke efficacyofnanofibersheetsincorporatinglenvatinibinahepatocellularcarcinomaxenograftmodel AT suzukikensuke efficacyofnanofibersheetsincorporatinglenvatinibinahepatocellularcarcinomaxenograftmodel AT akamatomoyao efficacyofnanofibersheetsincorporatinglenvatinibinahepatocellularcarcinomaxenograftmodel AT katanotayo efficacyofnanofibersheetsincorporatinglenvatinibinahepatocellularcarcinomaxenograftmodel AT yoshiikengo efficacyofnanofibersheetsincorporatinglenvatinibinahepatocellularcarcinomaxenograftmodel AT ebaramitsuhiro efficacyofnanofibersheetsincorporatinglenvatinibinahepatocellularcarcinomaxenograftmodel AT sekimotomitsugu efficacyofnanofibersheetsincorporatinglenvatinibinahepatocellularcarcinomaxenograftmodel |