超声可切换纳米酶增强对多重耐药细菌感染的声动力治疗

IF 16 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ACS Nano Pub Date : 2020-02-05 DOI:10.1021/acsnano.9b08667
Duo Sun, Xin Pang, Yi Cheng, Jiang Ming, Sijin Xiang, Chang Zhang, Peng Lv, Chengchao Chu, Xiaolan Chen*, Gang Liu*, Nanfeng Zheng*
{"title":"超声可切换纳米酶增强对多重耐药细菌感染的声动力治疗","authors":"Duo Sun,&nbsp;Xin Pang,&nbsp;Yi Cheng,&nbsp;Jiang Ming,&nbsp;Sijin Xiang,&nbsp;Chang Zhang,&nbsp;Peng Lv,&nbsp;Chengchao Chu,&nbsp;Xiaolan Chen*,&nbsp;Gang Liu*,&nbsp;Nanfeng Zheng*","doi":"10.1021/acsnano.9b08667","DOIUrl":null,"url":null,"abstract":"<p >Ultrasound (US)-driven sonodynamic therapy (SDT) has demonstrated wide application prospects in the eradication of deep-seated bacterial infections due to its noninvasiveness, site-confined irradiation, and high-tissue-penetrating capability. However, the ineffective accumulation of sonosensitizers at the infection site, the hypoxic microenvironment, as well as rapid depletion of oxygen during SDT greatly hamper the therapeutic efficacy of SDT. Herein, an US-switchable nanozyme system was proposed for the controllable generation of catalytic oxygen and sonosensitizer-mediated reactive oxygen species during ultrasound activation, thereby alleviating the hypoxia-associated barrier and augmenting SDT efficacy. This nanoplatform ([email?protected]) was easily prepared by bridging enzyme-catalytic [email?protected] nanoplates with the organic sonosensitizer <i>meso</i>-tetra(4-carboxyphenyl)porphine (T790). It was really interesting to find that the modification of T790 onto [email?protected] could significantly block the catalase-like activity of [email?protected], whereas upon US irradiation, the nanozyme activity was effectively recovered to catalyze the decomposition of endogenous H<sub>2</sub>O<sub>2</sub> into O<sub>2</sub>. Such “blocking and activating” enzyme activity was particularly important for decreasing the potential toxicity and side effects of nanozymes on normal tissues and has potential to realize active, controllable, and disease-loci-specific nanozyme catalytic behavior. Taking advantage of this US-switchable enzyme activity, outstanding accumulation in infection sites, as well as excellent biocompatibility, the [email?protected] SDT nanosystem was successfully applied to eradicate methicillin-resistant <i>Staphylococcus aureus</i> (MRSA)-induced myositis, and the sonodynamic therapeutic progression was noninvasively monitored by photoacoustic imaging and magnetic resonance imaging. The developed US-switchable nanoenzyme system provides a promising strategy for augmenting sonodynamic eradication of deep-seated bacterial infection actively, controllably, and precisely.</p>","PeriodicalId":21,"journal":{"name":"ACS Nano","volume":"14 2","pages":"2063–2076"},"PeriodicalIF":16.0000,"publicationDate":"2020-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1021/acsnano.9b08667","citationCount":"200","resultStr":"{\"title\":\"Ultrasound-Switchable Nanozyme Augments Sonodynamic Therapy against Multidrug-Resistant Bacterial Infection\",\"authors\":\"Duo Sun,&nbsp;Xin Pang,&nbsp;Yi Cheng,&nbsp;Jiang Ming,&nbsp;Sijin Xiang,&nbsp;Chang Zhang,&nbsp;Peng Lv,&nbsp;Chengchao Chu,&nbsp;Xiaolan Chen*,&nbsp;Gang Liu*,&nbsp;Nanfeng Zheng*\",\"doi\":\"10.1021/acsnano.9b08667\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Ultrasound (US)-driven sonodynamic therapy (SDT) has demonstrated wide application prospects in the eradication of deep-seated bacterial infections due to its noninvasiveness, site-confined irradiation, and high-tissue-penetrating capability. However, the ineffective accumulation of sonosensitizers at the infection site, the hypoxic microenvironment, as well as rapid depletion of oxygen during SDT greatly hamper the therapeutic efficacy of SDT. Herein, an US-switchable nanozyme system was proposed for the controllable generation of catalytic oxygen and sonosensitizer-mediated reactive oxygen species during ultrasound activation, thereby alleviating the hypoxia-associated barrier and augmenting SDT efficacy. This nanoplatform ([email?protected]) was easily prepared by bridging enzyme-catalytic [email?protected] nanoplates with the organic sonosensitizer <i>meso</i>-tetra(4-carboxyphenyl)porphine (T790). It was really interesting to find that the modification of T790 onto [email?protected] could significantly block the catalase-like activity of [email?protected], whereas upon US irradiation, the nanozyme activity was effectively recovered to catalyze the decomposition of endogenous H<sub>2</sub>O<sub>2</sub> into O<sub>2</sub>. Such “blocking and activating” enzyme activity was particularly important for decreasing the potential toxicity and side effects of nanozymes on normal tissues and has potential to realize active, controllable, and disease-loci-specific nanozyme catalytic behavior. Taking advantage of this US-switchable enzyme activity, outstanding accumulation in infection sites, as well as excellent biocompatibility, the [email?protected] SDT nanosystem was successfully applied to eradicate methicillin-resistant <i>Staphylococcus aureus</i> (MRSA)-induced myositis, and the sonodynamic therapeutic progression was noninvasively monitored by photoacoustic imaging and magnetic resonance imaging. The developed US-switchable nanoenzyme system provides a promising strategy for augmenting sonodynamic eradication of deep-seated bacterial infection actively, controllably, and precisely.</p>\",\"PeriodicalId\":21,\"journal\":{\"name\":\"ACS Nano\",\"volume\":\"14 2\",\"pages\":\"2063–2076\"},\"PeriodicalIF\":16.0000,\"publicationDate\":\"2020-02-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1021/acsnano.9b08667\",\"citationCount\":\"200\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Nano\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsnano.9b08667\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Nano","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsnano.9b08667","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 200

摘要

超声驱动声动力治疗(SDT)因其无创、局部受限照射、高组织穿透能力等优点,在根治深部细菌感染方面具有广阔的应用前景。然而,超声增敏剂在感染部位的无效积累、低氧微环境以及SDT过程中氧的快速耗竭极大地阻碍了SDT的治疗效果。本文提出了一种us -可切换的纳米酶系统,用于在超声激活过程中可控地产生催化氧和超声敏化剂介导的活性氧,从而减轻缺氧相关屏障,增强SDT疗效。这种纳米平台([email?protected])很容易通过桥接酶催化[email?protected]来制备。用有机声敏剂中四(4-羧基苯基)卟啉(T790)保护纳米片。发现T790在[email?][Protected]可以显著阻断[email?]而在美国辐照下,纳米酶活性有效恢复,催化内源H2O2分解为O2。这种“阻断和激活”酶活性对于降低纳米酶对正常组织的潜在毒性和副作用尤为重要,并且有可能实现活性、可控和疾病位点特异性的纳米酶催化行为。利用这种us -可切换酶活性,在感染位点的显著积累以及出色的生物相容性,[电子邮件?成功应用SDT纳米系统根除耐甲氧西林金黄色葡萄球菌(MRSA)诱导的肌炎,并通过光声成像和磁共振成像无创监测声动力治疗进展。开发的us -可切换纳米酶系统提供了一种有前途的策略,可以主动、可控和精确地增强声动力根除深层细菌感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ultrasound-Switchable Nanozyme Augments Sonodynamic Therapy against Multidrug-Resistant Bacterial Infection

Ultrasound-Switchable Nanozyme Augments Sonodynamic Therapy against Multidrug-Resistant Bacterial Infection

Ultrasound (US)-driven sonodynamic therapy (SDT) has demonstrated wide application prospects in the eradication of deep-seated bacterial infections due to its noninvasiveness, site-confined irradiation, and high-tissue-penetrating capability. However, the ineffective accumulation of sonosensitizers at the infection site, the hypoxic microenvironment, as well as rapid depletion of oxygen during SDT greatly hamper the therapeutic efficacy of SDT. Herein, an US-switchable nanozyme system was proposed for the controllable generation of catalytic oxygen and sonosensitizer-mediated reactive oxygen species during ultrasound activation, thereby alleviating the hypoxia-associated barrier and augmenting SDT efficacy. This nanoplatform ([email?protected]) was easily prepared by bridging enzyme-catalytic [email?protected] nanoplates with the organic sonosensitizer meso-tetra(4-carboxyphenyl)porphine (T790). It was really interesting to find that the modification of T790 onto [email?protected] could significantly block the catalase-like activity of [email?protected], whereas upon US irradiation, the nanozyme activity was effectively recovered to catalyze the decomposition of endogenous H2O2 into O2. Such “blocking and activating” enzyme activity was particularly important for decreasing the potential toxicity and side effects of nanozymes on normal tissues and has potential to realize active, controllable, and disease-loci-specific nanozyme catalytic behavior. Taking advantage of this US-switchable enzyme activity, outstanding accumulation in infection sites, as well as excellent biocompatibility, the [email?protected] SDT nanosystem was successfully applied to eradicate methicillin-resistant Staphylococcus aureus (MRSA)-induced myositis, and the sonodynamic therapeutic progression was noninvasively monitored by photoacoustic imaging and magnetic resonance imaging. The developed US-switchable nanoenzyme system provides a promising strategy for augmenting sonodynamic eradication of deep-seated bacterial infection actively, controllably, and precisely.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信