In Situ NADH-Activated BODIPY-Based Macrocyclic Supramolecular Photosensitizer for Chemo-Photodynamic Synergistic Tumor Therapy

IF 6.8 1区 医学 Q1 CHEMISTRY, MEDICINAL
Zhuo Lei, Ya-Hui Song, Yuan-Li Leng, Yi-Jun Gu, Miao Yu, Yong Chen, Qilin Yu and Yu Liu*, 
{"title":"In Situ NADH-Activated BODIPY-Based Macrocyclic Supramolecular Photosensitizer for Chemo-Photodynamic Synergistic Tumor Therapy","authors":"Zhuo Lei,&nbsp;Ya-Hui Song,&nbsp;Yuan-Li Leng,&nbsp;Yi-Jun Gu,&nbsp;Miao Yu,&nbsp;Yong Chen,&nbsp;Qilin Yu and Yu Liu*,&nbsp;","doi":"10.1021/acs.jmedchem.5c0009410.1021/acs.jmedchem.5c00094","DOIUrl":null,"url":null,"abstract":"<p >Photodynamic therapy (PDT) based on supramolecular assembly has been receiving wide attention due to its great potential application in clinical treatment. Herein, we report a supramolecular photoelectron “reservoir” (SPR) constructed by tetracationic boron dipyrromethene (BODIPY)-based macrocycle (<b>BBox·</b>4Cl), doxorubicin (Dox), and tumor-targeted β-cyclodextrin-grafted hyaluronic acid (HACD). Upon irradiation, <b>BBox·</b>4Cl can in situ catalyze nicotinamide adenine dinucleotide (NADH) to continuously generate electrons to inject into SPR, which further transfers electrons to oxygen, inducing highly efficient hydroxyl radical generation even under hypoxia. Synergistically, Dox in SPR as “pump” can be encapsulated by <b>BBox·</b>4Cl and transport photoelectrons between two BODIPY units, while HACD as “sponge” can enrich <b>BBox·</b>4Cl by the electrostatic interaction to concentrate them closer in space, which facilitates intramolecular and intermolecular photoelectron transfer, respectively, and significantly enhances the generation of hydroxyl radicals. Meanwhile, electron replenishment in SPR causes NADH depletion and redox dysfunction, thereby accelerating the apoptosis and achieving highly effective synergistic tumor therapy.</p>","PeriodicalId":46,"journal":{"name":"Journal of Medicinal Chemistry","volume":"68 5","pages":"5891–5906 5891–5906"},"PeriodicalIF":6.8000,"publicationDate":"2025-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Medicinal Chemistry","FirstCategoryId":"3","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jmedchem.5c00094","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

Photodynamic therapy (PDT) based on supramolecular assembly has been receiving wide attention due to its great potential application in clinical treatment. Herein, we report a supramolecular photoelectron “reservoir” (SPR) constructed by tetracationic boron dipyrromethene (BODIPY)-based macrocycle (BBox·4Cl), doxorubicin (Dox), and tumor-targeted β-cyclodextrin-grafted hyaluronic acid (HACD). Upon irradiation, BBox·4Cl can in situ catalyze nicotinamide adenine dinucleotide (NADH) to continuously generate electrons to inject into SPR, which further transfers electrons to oxygen, inducing highly efficient hydroxyl radical generation even under hypoxia. Synergistically, Dox in SPR as “pump” can be encapsulated by BBox·4Cl and transport photoelectrons between two BODIPY units, while HACD as “sponge” can enrich BBox·4Cl by the electrostatic interaction to concentrate them closer in space, which facilitates intramolecular and intermolecular photoelectron transfer, respectively, and significantly enhances the generation of hydroxyl radicals. Meanwhile, electron replenishment in SPR causes NADH depletion and redox dysfunction, thereby accelerating the apoptosis and achieving highly effective synergistic tumor therapy.

Abstract Image

基于原位nadh活化bodipy的大环超分子光敏剂用于化学-光动力协同肿瘤治疗
基于超分子组装的光动力疗法(PDT)因其在临床治疗中的巨大应用潜力而受到广泛关注。在此,我们报道了一个由四离子型二吡咯甲基硼(BODIPY)基大环(BBox·4Cl)、阿霉素(Dox)和靶向肿瘤的β-环糊精接片透明质酸(HACD)构建的超分子光电子“储层”(SPR)。辐照后,BBox·4Cl能原位催化烟酰胺腺嘌呤二核苷酸(nictinamide adenine dinucleotide, NADH)不断生成电子注入SPR, SPR再将电子传递给氧,即使在缺氧条件下也能高效生成羟基自由基。协同作用下,SPR中的Dox作为“泵”可被BBox·4Cl包封,并在两个BODIPY单元之间传递光电子,而HACD作为“海绵”可通过静电相互作用富集BBox·4Cl,使其在空间上更紧密地集中,分别促进分子内和分子间光电子传递,并显著增强羟基自由基的生成。同时,SPR中的电子补充引起NADH耗竭和氧化还原功能障碍,从而加速细胞凋亡,实现高效的协同肿瘤治疗。
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
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry 医学-医药化学
CiteScore
4.00
自引率
11.00%
发文量
804
审稿时长
1.9 months
期刊介绍: The Journal of Medicinal Chemistry is a prestigious biweekly peer-reviewed publication that focuses on the multifaceted field of medicinal chemistry. Since its inception in 1959 as the Journal of Medicinal and Pharmaceutical Chemistry, it has evolved to become a cornerstone in the dissemination of research findings related to the design, synthesis, and development of therapeutic agents. The Journal of Medicinal Chemistry is recognized for its significant impact in the scientific community, as evidenced by its 2022 impact factor of 7.3. This metric reflects the journal's influence and the importance of its content in shaping the future of drug discovery and development. The journal serves as a vital resource for chemists, pharmacologists, and other researchers interested in the molecular mechanisms of drug action and the optimization of therapeutic compounds.
×
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