Photo-activatable prodrug nanoparticles for reactive oxygen species amplification and cooperative cancer therapy

IF 5.4 2区 医学 Q1 BIOPHYSICS
Xue Li , Xu Zhang , Haizhen Guo , Zhetao Li , Lei Han , Sheng Wang
{"title":"Photo-activatable prodrug nanoparticles for reactive oxygen species amplification and cooperative cancer therapy","authors":"Xue Li ,&nbsp;Xu Zhang ,&nbsp;Haizhen Guo ,&nbsp;Zhetao Li ,&nbsp;Lei Han ,&nbsp;Sheng Wang","doi":"10.1016/j.colsurfb.2025.114775","DOIUrl":null,"url":null,"abstract":"<div><div>Photodynamic therapy (PDT), as a minimally invasive cancer therapy, demonstrates certain advantages in treating superficial tumors. However, it often faces challenges such as low reactive oxygen species (ROS) generation efficiency and non-targeted distribution of photosensitizers. The combination of chemotherapy and PDT can address the limitations of single modal therapies and improve therapeutic outcomes. In this work, we design a prodrug-based nanomedicine that can achieve photo-activated cascade drug release. Under 660 nm laser irradiation, the generated singlet oxygen can trigger the release of chemotherapeutic agent chlorambucil, cinnamaldehyde and quinone methyl. Chlorambucil can exert anti-tumor effects and cinnamaldehyde can increase intracellular hydrogen peroxide levels, while quinone methyl can consume intracellular glutathione. This process ultimately results in the amplification of ROS signals and further activation of prodrugs. This nanomedicine exhibits the ability to amplify oxidative stress and potent anticancer activity. <em>In vivo</em> experiments show that the nanomedicine can effectively inhibit tumor growth. This work provides a promising mutually beneficial strategy for achieving cooperative cancer therapy.</div></div>","PeriodicalId":279,"journal":{"name":"Colloids and Surfaces B: Biointerfaces","volume":"253 ","pages":"Article 114775"},"PeriodicalIF":5.4000,"publicationDate":"2025-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Colloids and Surfaces B: Biointerfaces","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0927776525002826","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0

Abstract

Photodynamic therapy (PDT), as a minimally invasive cancer therapy, demonstrates certain advantages in treating superficial tumors. However, it often faces challenges such as low reactive oxygen species (ROS) generation efficiency and non-targeted distribution of photosensitizers. The combination of chemotherapy and PDT can address the limitations of single modal therapies and improve therapeutic outcomes. In this work, we design a prodrug-based nanomedicine that can achieve photo-activated cascade drug release. Under 660 nm laser irradiation, the generated singlet oxygen can trigger the release of chemotherapeutic agent chlorambucil, cinnamaldehyde and quinone methyl. Chlorambucil can exert anti-tumor effects and cinnamaldehyde can increase intracellular hydrogen peroxide levels, while quinone methyl can consume intracellular glutathione. This process ultimately results in the amplification of ROS signals and further activation of prodrugs. This nanomedicine exhibits the ability to amplify oxidative stress and potent anticancer activity. In vivo experiments show that the nanomedicine can effectively inhibit tumor growth. This work provides a promising mutually beneficial strategy for achieving cooperative cancer therapy.
光活化的前药纳米粒子用于活性氧扩增和协同癌症治疗
光动力疗法(PDT)作为一种微创肿瘤治疗方法,在治疗浅表性肿瘤方面具有一定的优势。然而,它经常面临诸如活性氧(ROS)生成效率低和光敏剂的非靶向分布等挑战。化疗和PDT联合治疗可以解决单模态治疗的局限性,改善治疗效果。在这项工作中,我们设计了一种基于前体药物的纳米药物,可以实现光激活级联药物释放。在660 nm激光照射下,产生的单线态氧可触发化疗药物氯苯、肉桂醛和甲基醌的释放。氯霉素具有抗肿瘤作用,肉桂醛可增加细胞内过氧化氢水平,醌甲基可消耗细胞内谷胱甘肽。这一过程最终导致ROS信号的扩增和前药的进一步激活。这种纳米药物显示出放大氧化应激和有效抗癌活性的能力。体内实验表明,纳米药物能有效抑制肿瘤生长。这项工作为实现合作癌症治疗提供了一个有希望的互利策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Colloids and Surfaces B: Biointerfaces
Colloids and Surfaces B: Biointerfaces 生物-材料科学:生物材料
CiteScore
11.10
自引率
3.40%
发文量
730
审稿时长
42 days
期刊介绍: Colloids and Surfaces B: Biointerfaces is an international journal devoted to fundamental and applied research on colloid and interfacial phenomena in relation to systems of biological origin, having particular relevance to the medical, pharmaceutical, biotechnological, food and cosmetic fields. Submissions that: (1) deal solely with biological phenomena and do not describe the physico-chemical or colloid-chemical background and/or mechanism of the phenomena, and (2) deal solely with colloid/interfacial phenomena and do not have appropriate biological content or relevance, are outside the scope of the journal and will not be considered for publication. The journal publishes regular research papers, reviews, short communications and invited perspective articles, called BioInterface Perspectives. The BioInterface Perspective provide researchers the opportunity to review their own work, as well as provide insight into the work of others that inspired and influenced the author. Regular articles should have a maximum total length of 6,000 words. In addition, a (combined) maximum of 8 normal-sized figures and/or tables is allowed (so for instance 3 tables and 5 figures). For multiple-panel figures each set of two panels equates to one figure. Short communications should not exceed half of the above. It is required to give on the article cover page a short statistical summary of the article listing the total number of words and tables/figures.
×
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:481959085
Book学术官方微信