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Gelatin-Functionalized Carbon Nanotubes Loaded with Cisplatin for Anti-Cancer Therapy

Cisplatin (Cp), a chemotherapeutic agent, interacts with purines on tumor DNA, causing tumor cell apoptosis. However, cisplatin has the characteristics of non-specific distribution and lack of selectivity, resulting in systemic toxicity. Moreover, it cannot maintain the drug’s high concentration in...

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Autores principales: Li, Rong, Bao, Zhenfei, Wang, Pei, Deng, Yunyun, Fan, Junping, Zhu, Xin, Xia, Xinyu, Song, Yiming, Yao, Haiyan, Li, Dongfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10458187/
https://www.ncbi.nlm.nih.gov/pubmed/37631391
http://dx.doi.org/10.3390/polym15163333
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author Li, Rong
Bao, Zhenfei
Wang, Pei
Deng, Yunyun
Fan, Junping
Zhu, Xin
Xia, Xinyu
Song, Yiming
Yao, Haiyan
Li, Dongfang
author_facet Li, Rong
Bao, Zhenfei
Wang, Pei
Deng, Yunyun
Fan, Junping
Zhu, Xin
Xia, Xinyu
Song, Yiming
Yao, Haiyan
Li, Dongfang
author_sort Li, Rong
collection PubMed
description Cisplatin (Cp), a chemotherapeutic agent, interacts with purines on tumor DNA, causing tumor cell apoptosis. However, cisplatin has the characteristics of non-specific distribution and lack of selectivity, resulting in systemic toxicity. Moreover, it cannot maintain the drug’s high concentration in the tumor-weak acid environment. These flaws of cisplatin restrict its use in clinical applications. Therefore, a pH-responsive carbon nanotube-modified nano-drug delivery system (CNTs/Gel/Cp) was constructed in this study using gelatin (Gel)-modified carbon nanotubes (CNTs/Gel) loaded with cisplatin to release drugs precisely and slowly, preventing premature inactivation and maintaining an effective concentration. When M(Cp):M(CNTs/Gel) = 1:1, the drug reaches the highest loading rate and entrapment efficiency. To achieve the sustained-release effect, CNTs/Gel/Cp can release the medicine steadily for a long time in a pH environment of 6.0. Additionally, CNTs/Gel/Cp display antitumor properties comparable to cisplatin in a manner that varies with the dosage administered. These findings indicate that CNTs/Gel/Cp have an effective, sustained release of cisplatin and a good antitumor effect, providing a theoretical and experimental basis for the clinical application of modified carbon nanotubes (CNTs) as a new drug delivery system.
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spelling pubmed-104581872023-08-27 Gelatin-Functionalized Carbon Nanotubes Loaded with Cisplatin for Anti-Cancer Therapy Li, Rong Bao, Zhenfei Wang, Pei Deng, Yunyun Fan, Junping Zhu, Xin Xia, Xinyu Song, Yiming Yao, Haiyan Li, Dongfang Polymers (Basel) Article Cisplatin (Cp), a chemotherapeutic agent, interacts with purines on tumor DNA, causing tumor cell apoptosis. However, cisplatin has the characteristics of non-specific distribution and lack of selectivity, resulting in systemic toxicity. Moreover, it cannot maintain the drug’s high concentration in the tumor-weak acid environment. These flaws of cisplatin restrict its use in clinical applications. Therefore, a pH-responsive carbon nanotube-modified nano-drug delivery system (CNTs/Gel/Cp) was constructed in this study using gelatin (Gel)-modified carbon nanotubes (CNTs/Gel) loaded with cisplatin to release drugs precisely and slowly, preventing premature inactivation and maintaining an effective concentration. When M(Cp):M(CNTs/Gel) = 1:1, the drug reaches the highest loading rate and entrapment efficiency. To achieve the sustained-release effect, CNTs/Gel/Cp can release the medicine steadily for a long time in a pH environment of 6.0. Additionally, CNTs/Gel/Cp display antitumor properties comparable to cisplatin in a manner that varies with the dosage administered. These findings indicate that CNTs/Gel/Cp have an effective, sustained release of cisplatin and a good antitumor effect, providing a theoretical and experimental basis for the clinical application of modified carbon nanotubes (CNTs) as a new drug delivery system. MDPI 2023-08-08 /pmc/articles/PMC10458187/ /pubmed/37631391 http://dx.doi.org/10.3390/polym15163333 Text en © 2023 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
Li, Rong
Bao, Zhenfei
Wang, Pei
Deng, Yunyun
Fan, Junping
Zhu, Xin
Xia, Xinyu
Song, Yiming
Yao, Haiyan
Li, Dongfang
Gelatin-Functionalized Carbon Nanotubes Loaded with Cisplatin for Anti-Cancer Therapy
title Gelatin-Functionalized Carbon Nanotubes Loaded with Cisplatin for Anti-Cancer Therapy
title_full Gelatin-Functionalized Carbon Nanotubes Loaded with Cisplatin for Anti-Cancer Therapy
title_fullStr Gelatin-Functionalized Carbon Nanotubes Loaded with Cisplatin for Anti-Cancer Therapy
title_full_unstemmed Gelatin-Functionalized Carbon Nanotubes Loaded with Cisplatin for Anti-Cancer Therapy
title_short Gelatin-Functionalized Carbon Nanotubes Loaded with Cisplatin for Anti-Cancer Therapy
title_sort gelatin-functionalized carbon nanotubes loaded with cisplatin for anti-cancer therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10458187/
https://www.ncbi.nlm.nih.gov/pubmed/37631391
http://dx.doi.org/10.3390/polym15163333
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