ID | 116603 |
Author |
Ando, Hidenori
Tokushima University
Tokushima University Educator and Researcher Directory
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Mochizuki, Takashi
Tokushima University
Lila, Amr S. Abu
Zagazig University|Hail University
Akagi, Shunsuke
Tokushima University
Tajima, Kenji
Hokkaido University
Fujita, Kenji
Tokushima University
Matsushima, Tokuo
Kusano Sakko
Kusano, Takatomo
Kusano Sakko
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Keywords | nanofibrillated bacterial cellulose
bacterial cellulose
peritoneally disseminated gastric cancer
doxorubicin
intraperitoneal chemotherapy
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Content Type |
Journal Article
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Description | Natural materials such as bacterial cellulose are gaining interest for their use as drug-delivery vehicles. Herein, the utility of nanofibrillated bacterial cellulose (NFBC), which is produced by culturing a cellulose-producing bacterium (Gluconacetobacter intermedius NEDO-01) in a medium supplemented with carboxymethylcellulose (CMC) that is referred to as CM-NFBC, is described. Recently, we demonstrated that intraperitoneal administration of paclitaxel (PTX)-containing CM-NFBC efficiently suppressed tumor growth in a peritoneally disseminated cancer xenograft model. In this study, to confirm the applicability of NFBC in cancer therapy, a chemotherapeutic agent, doxorubicin (DXR), embedded into CM-NFBC, was examined for its efficiency to treat a peritoneally disseminated gastric cancer via intraperitoneal administration. DXR was efficiently embedded into CM-NFBC (DXR/CM-NFBC). In an in vitro release experiment, 79.5% of DXR was released linearly into the peritoneal wash fluid over a period of 24 h. In the peritoneally disseminated gastric cancer xenograft model, intraperitoneal administration of DXR/CM-NFBC induced superior tumor growth inhibition (TGI = 85.5%) by day 35 post-tumor inoculation, compared to free DXR (TGI = 62.4%). In addition, compared with free DXR, the severe side effects that cause body weight loss were lessened via treatment with DXR/CM-NFBC. These results support the feasibility of CM-NFBC as a drug-delivery vehicle for various anticancer agents. This approach may lead to improved therapeutic outcomes for the treatment of intraperitoneally disseminated cancers.
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Journal Title |
Nanomaterials
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ISSN | 20794991
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Publisher | MDPI
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Volume | 11
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Issue | 7
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Start Page | 1697
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Published Date | 2021-06-28
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Rights | 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/).
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DOI (Published Version) | |
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language |
eng
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TextVersion |
Publisher
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departments |
Pharmaceutical Sciences
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