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A Logic-Gated Modular Nanovesicle Enables Programmable Drug Release for On-Demand Chemotherapy
It remains a major challenge to achieve precise on-demand drug release. Here, we developed a modular nanomedicine integrated with logic-gated system enabling programmable drug release for on-demand chemotherapy. Methods: We employed two different logical AND gates consisting of four interrelated moi...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6401502/ https://www.ncbi.nlm.nih.gov/pubmed/30867836 http://dx.doi.org/10.7150/thno.32106 |
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author | Tang, Longguang Yang, Zhen Zhou, Zijian Ma, Ying Kiesewetter, Dale O. Wang, Zhantong Fan, Wenpei Zhu, Shoujun Zhang, Mingru Tian, Rui Lang, Lixin Niu, Gang Zhang, Xianzhong Chen, Xiaoyuan |
author_facet | Tang, Longguang Yang, Zhen Zhou, Zijian Ma, Ying Kiesewetter, Dale O. Wang, Zhantong Fan, Wenpei Zhu, Shoujun Zhang, Mingru Tian, Rui Lang, Lixin Niu, Gang Zhang, Xianzhong Chen, Xiaoyuan |
author_sort | Tang, Longguang |
collection | PubMed |
description | It remains a major challenge to achieve precise on-demand drug release. Here, we developed a modular nanomedicine integrated with logic-gated system enabling programmable drug release for on-demand chemotherapy. Methods: We employed two different logical AND gates consisting of four interrelated moieties to construct the nanovesicles, denoted as v-A-CED(2), containing oxidation-responsive nanovesicles (v), radical generators (A), and Edman linker conjugated prodrugs (CED(2)). The first AND logic gate is connected in parallel by mild hyperthermia (I) and acidic pH (II), which executes NIR laser triggered prodrug-to-drug transformation through Edman degradation. Meanwhile, the mild hyperthermia effect triggers alkyl radical generation (III) which contributes to internal oxidation and degradation of nanovesicles (IV). The second AND logic gate is therefore formed by the combination of I-IV to achieve programmable drug release by a single stimulus input NIR laser. The biodistribution of the nanovesicles was monitored by positron emission tomography (PET), photoacoustic, and fluorescence imaging. Results: The developed modular nanovesicles exhibited high tumor accumulation and effective anticancer effects both in vitro and in vivo. Conclusions: This study provides a novel paradigm of logic-gated programmable drug release system by a modular nanovesicle, which may shed light on innovation of anticancer agents and strategies. |
format | Online Article Text |
id | pubmed-6401502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-64015022019-03-13 A Logic-Gated Modular Nanovesicle Enables Programmable Drug Release for On-Demand Chemotherapy Tang, Longguang Yang, Zhen Zhou, Zijian Ma, Ying Kiesewetter, Dale O. Wang, Zhantong Fan, Wenpei Zhu, Shoujun Zhang, Mingru Tian, Rui Lang, Lixin Niu, Gang Zhang, Xianzhong Chen, Xiaoyuan Theranostics Research Paper It remains a major challenge to achieve precise on-demand drug release. Here, we developed a modular nanomedicine integrated with logic-gated system enabling programmable drug release for on-demand chemotherapy. Methods: We employed two different logical AND gates consisting of four interrelated moieties to construct the nanovesicles, denoted as v-A-CED(2), containing oxidation-responsive nanovesicles (v), radical generators (A), and Edman linker conjugated prodrugs (CED(2)). The first AND logic gate is connected in parallel by mild hyperthermia (I) and acidic pH (II), which executes NIR laser triggered prodrug-to-drug transformation through Edman degradation. Meanwhile, the mild hyperthermia effect triggers alkyl radical generation (III) which contributes to internal oxidation and degradation of nanovesicles (IV). The second AND logic gate is therefore formed by the combination of I-IV to achieve programmable drug release by a single stimulus input NIR laser. The biodistribution of the nanovesicles was monitored by positron emission tomography (PET), photoacoustic, and fluorescence imaging. Results: The developed modular nanovesicles exhibited high tumor accumulation and effective anticancer effects both in vitro and in vivo. Conclusions: This study provides a novel paradigm of logic-gated programmable drug release system by a modular nanovesicle, which may shed light on innovation of anticancer agents and strategies. Ivyspring International Publisher 2019-02-14 /pmc/articles/PMC6401502/ /pubmed/30867836 http://dx.doi.org/10.7150/thno.32106 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Tang, Longguang Yang, Zhen Zhou, Zijian Ma, Ying Kiesewetter, Dale O. Wang, Zhantong Fan, Wenpei Zhu, Shoujun Zhang, Mingru Tian, Rui Lang, Lixin Niu, Gang Zhang, Xianzhong Chen, Xiaoyuan A Logic-Gated Modular Nanovesicle Enables Programmable Drug Release for On-Demand Chemotherapy |
title | A Logic-Gated Modular Nanovesicle Enables Programmable Drug Release for On-Demand Chemotherapy |
title_full | A Logic-Gated Modular Nanovesicle Enables Programmable Drug Release for On-Demand Chemotherapy |
title_fullStr | A Logic-Gated Modular Nanovesicle Enables Programmable Drug Release for On-Demand Chemotherapy |
title_full_unstemmed | A Logic-Gated Modular Nanovesicle Enables Programmable Drug Release for On-Demand Chemotherapy |
title_short | A Logic-Gated Modular Nanovesicle Enables Programmable Drug Release for On-Demand Chemotherapy |
title_sort | logic-gated modular nanovesicle enables programmable drug release for on-demand chemotherapy |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6401502/ https://www.ncbi.nlm.nih.gov/pubmed/30867836 http://dx.doi.org/10.7150/thno.32106 |
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