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Study of the Fe(3)O(4)@ZIF-8@Sor Composite Modified by Tannic Acid for the Treatment of Sorafenib-Resistant Hepatocellular Carcinoma

[Image: see text] Chemotherapeutic agents fail in clinical chemotherapy in the absence of targeting and acquired resistance. We, therefore, synthesized Fe(3)O(4)@ZIF-8@Sor@TA nanocomposite drugs based on the drug delivery properties of nanomaterials. ZIF-8 is a nanomaterial with a porous structure t...

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Autores principales: Kong, Jianqiao, Xu, Song, Dai, Yang, Wang, Yi, Zhao, Yun, Zhang, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601084/
https://www.ncbi.nlm.nih.gov/pubmed/37901534
http://dx.doi.org/10.1021/acsomega.3c04215
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author Kong, Jianqiao
Xu, Song
Dai, Yang
Wang, Yi
Zhao, Yun
Zhang, Peng
author_facet Kong, Jianqiao
Xu, Song
Dai, Yang
Wang, Yi
Zhao, Yun
Zhang, Peng
author_sort Kong, Jianqiao
collection PubMed
description [Image: see text] Chemotherapeutic agents fail in clinical chemotherapy in the absence of targeting and acquired resistance. We, therefore, synthesized Fe(3)O(4)@ZIF-8@Sor@TA nanocomposite drugs based on the drug delivery properties of nanomaterials. ZIF-8 is a nanomaterial with a porous structure that can load anticancer drugs. The nanodrug used the paramagnetic property of Fe(3)O(4) to deliver sorafenib (Sor) precisely to the tumor site, then used the pH responsiveness of ZIF-8 to slowly release Sor in the tumor microenvironment, and finally used tannic acid (TA) to inhibit P-glycoprotein to suppress the Sor resistance. The results of material characterization presented that the prepared material was structurally stable and was able to achieve a cumulative drug release of 38.2% at pH 5.0 for 72 h. The good biocompatibility of the composite was demonstrated by in vitro and in vivo experiments, which could improve antitumor activity and reduce Sor resistance through magnetic targeting TA. In conclusion, the Fe(3)O(4)@ZIF-8@Sor@TA material prepared in this study demonstrated high antitumor activity in hepatocellular carcinoma treatment, promising to reduce drug resistance and providing a novel research approach for cancer treatment.
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spelling pubmed-106010842023-10-27 Study of the Fe(3)O(4)@ZIF-8@Sor Composite Modified by Tannic Acid for the Treatment of Sorafenib-Resistant Hepatocellular Carcinoma Kong, Jianqiao Xu, Song Dai, Yang Wang, Yi Zhao, Yun Zhang, Peng ACS Omega [Image: see text] Chemotherapeutic agents fail in clinical chemotherapy in the absence of targeting and acquired resistance. We, therefore, synthesized Fe(3)O(4)@ZIF-8@Sor@TA nanocomposite drugs based on the drug delivery properties of nanomaterials. ZIF-8 is a nanomaterial with a porous structure that can load anticancer drugs. The nanodrug used the paramagnetic property of Fe(3)O(4) to deliver sorafenib (Sor) precisely to the tumor site, then used the pH responsiveness of ZIF-8 to slowly release Sor in the tumor microenvironment, and finally used tannic acid (TA) to inhibit P-glycoprotein to suppress the Sor resistance. The results of material characterization presented that the prepared material was structurally stable and was able to achieve a cumulative drug release of 38.2% at pH 5.0 for 72 h. The good biocompatibility of the composite was demonstrated by in vitro and in vivo experiments, which could improve antitumor activity and reduce Sor resistance through magnetic targeting TA. In conclusion, the Fe(3)O(4)@ZIF-8@Sor@TA material prepared in this study demonstrated high antitumor activity in hepatocellular carcinoma treatment, promising to reduce drug resistance and providing a novel research approach for cancer treatment. American Chemical Society 2023-09-12 /pmc/articles/PMC10601084/ /pubmed/37901534 http://dx.doi.org/10.1021/acsomega.3c04215 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Kong, Jianqiao
Xu, Song
Dai, Yang
Wang, Yi
Zhao, Yun
Zhang, Peng
Study of the Fe(3)O(4)@ZIF-8@Sor Composite Modified by Tannic Acid for the Treatment of Sorafenib-Resistant Hepatocellular Carcinoma
title Study of the Fe(3)O(4)@ZIF-8@Sor Composite Modified by Tannic Acid for the Treatment of Sorafenib-Resistant Hepatocellular Carcinoma
title_full Study of the Fe(3)O(4)@ZIF-8@Sor Composite Modified by Tannic Acid for the Treatment of Sorafenib-Resistant Hepatocellular Carcinoma
title_fullStr Study of the Fe(3)O(4)@ZIF-8@Sor Composite Modified by Tannic Acid for the Treatment of Sorafenib-Resistant Hepatocellular Carcinoma
title_full_unstemmed Study of the Fe(3)O(4)@ZIF-8@Sor Composite Modified by Tannic Acid for the Treatment of Sorafenib-Resistant Hepatocellular Carcinoma
title_short Study of the Fe(3)O(4)@ZIF-8@Sor Composite Modified by Tannic Acid for the Treatment of Sorafenib-Resistant Hepatocellular Carcinoma
title_sort study of the fe(3)o(4)@zif-8@sor composite modified by tannic acid for the treatment of sorafenib-resistant hepatocellular carcinoma
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601084/
https://www.ncbi.nlm.nih.gov/pubmed/37901534
http://dx.doi.org/10.1021/acsomega.3c04215
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