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pH-Sensitive nanodiamond co-delivery of retinal and doxorubicin boosts breast cancer chemotherapy
Herein for the first time we take the advantage of nanodiamonds (NDs) to covalently immobilize all-trans retinal (NPA) by an imine bond, allowing pH-mediated drug release. DOX is then physically adsorbed onto NPA to form an NPA@D co-loaded double drug in the sodium citrate medium, which is also susc...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10498152/ https://www.ncbi.nlm.nih.gov/pubmed/37711368 http://dx.doi.org/10.1039/d3ra03907b |
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author | Cui, Jicheng Hu, Bo Fu, Yuejun Xu, Zhengkun Li, Yingqi |
author_facet | Cui, Jicheng Hu, Bo Fu, Yuejun Xu, Zhengkun Li, Yingqi |
author_sort | Cui, Jicheng |
collection | PubMed |
description | Herein for the first time we take the advantage of nanodiamonds (NDs) to covalently immobilize all-trans retinal (NPA) by an imine bond, allowing pH-mediated drug release. DOX is then physically adsorbed onto NPA to form an NPA@D co-loaded double drug in the sodium citrate medium, which is also susceptible to pH-triggered DOX dissociation. The cytotoxicity results showed that NPA@D could markedly inhibit the growth of DOX-sensitive MCF-7 cells in a synergetic way compared to the NP@D system of single-loaded DOX, while NPA basically showed no cytotoxicity and weak inhibition of migration. In addition, NPA@D can overcome the drug resistance of MCF-7/ADR cells, indicating that this nanodrug could evade the pumping of DOX by drug-resistant cells, but free DOX is nearly ineffective against these cells. More importantly, the fluorescence imaging of tumor-bearing mice in vivo and ex vivo demonstrated that the NPA@D was mainly accumulated in the tumor site rather than any other organ by intraperitoneal injection after 24 h, in which the fluorescence intensity of NPA@D was 19 times that of the free DOX, suggesting that a far reduced off-target effect and side effects would be expected. Therefore, this work presents a new paradigm for improving chemotherapy and reversing drug resistance using the ND platform for co-delivery of DOX and ATR. |
format | Online Article Text |
id | pubmed-10498152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-104981522023-09-14 pH-Sensitive nanodiamond co-delivery of retinal and doxorubicin boosts breast cancer chemotherapy Cui, Jicheng Hu, Bo Fu, Yuejun Xu, Zhengkun Li, Yingqi RSC Adv Chemistry Herein for the first time we take the advantage of nanodiamonds (NDs) to covalently immobilize all-trans retinal (NPA) by an imine bond, allowing pH-mediated drug release. DOX is then physically adsorbed onto NPA to form an NPA@D co-loaded double drug in the sodium citrate medium, which is also susceptible to pH-triggered DOX dissociation. The cytotoxicity results showed that NPA@D could markedly inhibit the growth of DOX-sensitive MCF-7 cells in a synergetic way compared to the NP@D system of single-loaded DOX, while NPA basically showed no cytotoxicity and weak inhibition of migration. In addition, NPA@D can overcome the drug resistance of MCF-7/ADR cells, indicating that this nanodrug could evade the pumping of DOX by drug-resistant cells, but free DOX is nearly ineffective against these cells. More importantly, the fluorescence imaging of tumor-bearing mice in vivo and ex vivo demonstrated that the NPA@D was mainly accumulated in the tumor site rather than any other organ by intraperitoneal injection after 24 h, in which the fluorescence intensity of NPA@D was 19 times that of the free DOX, suggesting that a far reduced off-target effect and side effects would be expected. Therefore, this work presents a new paradigm for improving chemotherapy and reversing drug resistance using the ND platform for co-delivery of DOX and ATR. The Royal Society of Chemistry 2023-09-13 /pmc/articles/PMC10498152/ /pubmed/37711368 http://dx.doi.org/10.1039/d3ra03907b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Cui, Jicheng Hu, Bo Fu, Yuejun Xu, Zhengkun Li, Yingqi pH-Sensitive nanodiamond co-delivery of retinal and doxorubicin boosts breast cancer chemotherapy |
title | pH-Sensitive nanodiamond co-delivery of retinal and doxorubicin boosts breast cancer chemotherapy |
title_full | pH-Sensitive nanodiamond co-delivery of retinal and doxorubicin boosts breast cancer chemotherapy |
title_fullStr | pH-Sensitive nanodiamond co-delivery of retinal and doxorubicin boosts breast cancer chemotherapy |
title_full_unstemmed | pH-Sensitive nanodiamond co-delivery of retinal and doxorubicin boosts breast cancer chemotherapy |
title_short | pH-Sensitive nanodiamond co-delivery of retinal and doxorubicin boosts breast cancer chemotherapy |
title_sort | ph-sensitive nanodiamond co-delivery of retinal and doxorubicin boosts breast cancer chemotherapy |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10498152/ https://www.ncbi.nlm.nih.gov/pubmed/37711368 http://dx.doi.org/10.1039/d3ra03907b |
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