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The treatment efficacy of three-layered functional polymer materials as drug carrier for orthotopic colon cancer
Colorectal cancer (CRC) is a worldwide disease posing serious threats to people’s life. Surgery and postsurgical chemotherapy are still the first choices to control the rapid progression of cancer. However, tumor recurrence and even distant metastasis are prone to occur. As a result, it is in urgent...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9487963/ https://www.ncbi.nlm.nih.gov/pubmed/36101475 http://dx.doi.org/10.1080/10717544.2022.2122633 |
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author | Liu, Zhuo Wang, Dongxin Cao, Qian Li, Jiannan |
author_facet | Liu, Zhuo Wang, Dongxin Cao, Qian Li, Jiannan |
author_sort | Liu, Zhuo |
collection | PubMed |
description | Colorectal cancer (CRC) is a worldwide disease posing serious threats to people’s life. Surgery and postsurgical chemotherapy are still the first choices to control the rapid progression of cancer. However, tumor recurrence and even distant metastasis are prone to occur. As a result, it is in urgent demand to find a new method to control CRC progression while inhibiting distant metastasis. On this basis, this study developed the three-layered functionalized hydrogel-fibrous membrane-hydrogel composite materials. The Chinese traditional drugs 20 (S)-ginsenoside Rg3 (Rg3) and chemotherapeutic agent 5-fluorouracil (5-Fu) were loaded in the inner hydrogel and middle fibrous membrane and could be constantly released at the same time and space. The outer hydrogel was decorated with phenylboronic acid (PA) to interact with sialic acid expressed on the CRC cell surface. The composite materials possessed biocompatibility and showed no toxicity to normal human intestinal mucosa endothelial cells HIEC. According to the results, the cell viability of CT26 could be significantly decreased in vitro. The three-layered functionalized materials inhibited the original tumor progression and distant tumor metastasis to the liver in an orthotopic colon cancer mouse model by increasing the caspase3 expression and inhibiting the expressions of Bcl-2, Ki-67, and VEGF. In addition, the functions of major organs were not significantly damaged. Our study provides a safe and efficacious method of this three-layered functionalized hydrogel-fibrous membrane-hydrogel composite materials for CRC treatment. |
format | Online Article Text |
id | pubmed-9487963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-94879632022-09-21 The treatment efficacy of three-layered functional polymer materials as drug carrier for orthotopic colon cancer Liu, Zhuo Wang, Dongxin Cao, Qian Li, Jiannan Drug Deliv Research Article Colorectal cancer (CRC) is a worldwide disease posing serious threats to people’s life. Surgery and postsurgical chemotherapy are still the first choices to control the rapid progression of cancer. However, tumor recurrence and even distant metastasis are prone to occur. As a result, it is in urgent demand to find a new method to control CRC progression while inhibiting distant metastasis. On this basis, this study developed the three-layered functionalized hydrogel-fibrous membrane-hydrogel composite materials. The Chinese traditional drugs 20 (S)-ginsenoside Rg3 (Rg3) and chemotherapeutic agent 5-fluorouracil (5-Fu) were loaded in the inner hydrogel and middle fibrous membrane and could be constantly released at the same time and space. The outer hydrogel was decorated with phenylboronic acid (PA) to interact with sialic acid expressed on the CRC cell surface. The composite materials possessed biocompatibility and showed no toxicity to normal human intestinal mucosa endothelial cells HIEC. According to the results, the cell viability of CT26 could be significantly decreased in vitro. The three-layered functionalized materials inhibited the original tumor progression and distant tumor metastasis to the liver in an orthotopic colon cancer mouse model by increasing the caspase3 expression and inhibiting the expressions of Bcl-2, Ki-67, and VEGF. In addition, the functions of major organs were not significantly damaged. Our study provides a safe and efficacious method of this three-layered functionalized hydrogel-fibrous membrane-hydrogel composite materials for CRC treatment. Taylor & Francis 2022-09-13 /pmc/articles/PMC9487963/ /pubmed/36101475 http://dx.doi.org/10.1080/10717544.2022.2122633 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Liu, Zhuo Wang, Dongxin Cao, Qian Li, Jiannan The treatment efficacy of three-layered functional polymer materials as drug carrier for orthotopic colon cancer |
title | The treatment efficacy of three-layered functional polymer materials as drug carrier for orthotopic colon cancer |
title_full | The treatment efficacy of three-layered functional polymer materials as drug carrier for orthotopic colon cancer |
title_fullStr | The treatment efficacy of three-layered functional polymer materials as drug carrier for orthotopic colon cancer |
title_full_unstemmed | The treatment efficacy of three-layered functional polymer materials as drug carrier for orthotopic colon cancer |
title_short | The treatment efficacy of three-layered functional polymer materials as drug carrier for orthotopic colon cancer |
title_sort | treatment efficacy of three-layered functional polymer materials as drug carrier for orthotopic colon cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9487963/ https://www.ncbi.nlm.nih.gov/pubmed/36101475 http://dx.doi.org/10.1080/10717544.2022.2122633 |
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