feooh辅助形成的杂化聚合物纳米纺锤体用于高效铁传递和铁下垂肿瘤治疗

IF 4 2区 化学 Q1 BIOCHEMICAL RESEARCH METHODS
Heng Liu, Lu Wang, Hao Jin, Kepeng Tao, Xuanqi Zhu, Mengsi Zhang, Yuchuan Hou*, Shuwei Liu* and Hao Zhang, 
{"title":"feooh辅助形成的杂化聚合物纳米纺锤体用于高效铁传递和铁下垂肿瘤治疗","authors":"Heng Liu,&nbsp;Lu Wang,&nbsp;Hao Jin,&nbsp;Kepeng Tao,&nbsp;Xuanqi Zhu,&nbsp;Mengsi Zhang,&nbsp;Yuchuan Hou*,&nbsp;Shuwei Liu* and Hao Zhang,&nbsp;","doi":"10.1021/acs.bioconjchem.4c0054610.1021/acs.bioconjchem.4c00546","DOIUrl":null,"url":null,"abstract":"<p >Exogenous iron delivery using iron-containing nanomaterials is an alternative strategy for enhancing the efficacy in ferroptosis tumor therapy but limited by the problems of low iron content, low tumor enrichment, low cellular uptake, and uncontrolled release of iron ions. To solve the problems, an FeOOH-assisted approach is demonstrated to produce iron hybrid polymer nanospindles (IHPNSs) for efficient iron delivery and ferroptosis tumor therapy. The IHPNSs are prepared through the cohydrolysis of FeCl<sub>3</sub>·6H<sub>2</sub>O with aniline, pyrrole, or amino-pyrrole. On the one hand, the hydrolysis of Fe<sup>3+</sup> generates FeOOH particles, which further act as the templates to form fusiform architectures. On the other hand, Fe<sup>3+</sup> triggers the oxidative polymerization of aniline, pyrrole, or amino-pyrrole. The as-prepared polymers are capable of coordinating with excessive Fe<sup>3+</sup> and locate on the FeOOH templates, thus producing Fe<sup>3+</sup>/polymer composite-coated FeOOH nanospindles. Systematic studies indicate that the one-dimension-like morphology facilitates tumor enrichment and cellular uptake of IHPNSs. Besides the high iron content of IHPNSs, the controlled release of Fe<sup>3+</sup> stimulated by the overexpressed glutathione (GSH) in the tumor microenvironment is achieved. The released Fe<sup>3+</sup> is further transformed to Fe<sup>2+</sup> by scavenging GSH, which leads to excessive accumulation of reactive oxygen species and lipid peroxides and finally induces ferroptosis of tumor cells. As a proof of concept, the IHPNSs show good efficacy in the treatment of a rat model of bladder tumors in situ.</p>","PeriodicalId":29,"journal":{"name":"Bioconjugate Chemistry","volume":"36 3","pages":"464–475 464–475"},"PeriodicalIF":4.0000,"publicationDate":"2025-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"FeOOH-Assisted Formation of Hybrid Polymer Nanospindles for Efficient Iron Delivery and Ferroptosis Tumor Therapy\",\"authors\":\"Heng Liu,&nbsp;Lu Wang,&nbsp;Hao Jin,&nbsp;Kepeng Tao,&nbsp;Xuanqi Zhu,&nbsp;Mengsi Zhang,&nbsp;Yuchuan Hou*,&nbsp;Shuwei Liu* and Hao Zhang,&nbsp;\",\"doi\":\"10.1021/acs.bioconjchem.4c0054610.1021/acs.bioconjchem.4c00546\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Exogenous iron delivery using iron-containing nanomaterials is an alternative strategy for enhancing the efficacy in ferroptosis tumor therapy but limited by the problems of low iron content, low tumor enrichment, low cellular uptake, and uncontrolled release of iron ions. To solve the problems, an FeOOH-assisted approach is demonstrated to produce iron hybrid polymer nanospindles (IHPNSs) for efficient iron delivery and ferroptosis tumor therapy. The IHPNSs are prepared through the cohydrolysis of FeCl<sub>3</sub>·6H<sub>2</sub>O with aniline, pyrrole, or amino-pyrrole. On the one hand, the hydrolysis of Fe<sup>3+</sup> generates FeOOH particles, which further act as the templates to form fusiform architectures. On the other hand, Fe<sup>3+</sup> triggers the oxidative polymerization of aniline, pyrrole, or amino-pyrrole. The as-prepared polymers are capable of coordinating with excessive Fe<sup>3+</sup> and locate on the FeOOH templates, thus producing Fe<sup>3+</sup>/polymer composite-coated FeOOH nanospindles. Systematic studies indicate that the one-dimension-like morphology facilitates tumor enrichment and cellular uptake of IHPNSs. Besides the high iron content of IHPNSs, the controlled release of Fe<sup>3+</sup> stimulated by the overexpressed glutathione (GSH) in the tumor microenvironment is achieved. The released Fe<sup>3+</sup> is further transformed to Fe<sup>2+</sup> by scavenging GSH, which leads to excessive accumulation of reactive oxygen species and lipid peroxides and finally induces ferroptosis of tumor cells. As a proof of concept, the IHPNSs show good efficacy in the treatment of a rat model of bladder tumors in situ.</p>\",\"PeriodicalId\":29,\"journal\":{\"name\":\"Bioconjugate Chemistry\",\"volume\":\"36 3\",\"pages\":\"464–475 464–475\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2025-03-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bioconjugate Chemistry\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.bioconjchem.4c00546\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioconjugate Chemistry","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.bioconjchem.4c00546","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

摘要

使用含铁纳米材料外源性铁递送是提高铁上吊肿瘤治疗效果的另一种策略,但受铁含量低、肿瘤富集低、细胞摄取低和铁离子释放不受控制等问题的限制。为了解决这一问题,一种feooh辅助的方法被证明可以生产铁杂化聚合物纳米纺锤体(IHPNSs),用于有效的铁递送和铁下垂肿瘤治疗。IHPNSs是通过FeCl3·6H2O与苯胺、吡咯或氨基吡咯共水解制备的。一方面,Fe3+水解生成FeOOH颗粒,FeOOH颗粒进一步作为模板形成纺锤状结构。另一方面,Fe3+引发苯胺、吡咯或氨基吡咯的氧化聚合。所制备的聚合物能够与过量的Fe3+配合并定位在FeOOH模板上,从而产生Fe3+/聚合物复合包覆的FeOOH纳米纺锤。系统研究表明,一维样形态有利于肿瘤富集和IHPNSs的细胞摄取。IHPNSs除了具有高铁含量外,还可通过过表达谷胱甘肽(GSH)刺激肿瘤微环境中Fe3+的控释。释放的Fe3+通过清除GSH进一步转化为Fe2+,导致活性氧和脂质过氧化物的过度积累,最终诱导肿瘤细胞铁下垂。作为概念的证明,IHPNSs在大鼠原位膀胱肿瘤模型中显示出良好的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

FeOOH-Assisted Formation of Hybrid Polymer Nanospindles for Efficient Iron Delivery and Ferroptosis Tumor Therapy

FeOOH-Assisted Formation of Hybrid Polymer Nanospindles for Efficient Iron Delivery and Ferroptosis Tumor Therapy

Exogenous iron delivery using iron-containing nanomaterials is an alternative strategy for enhancing the efficacy in ferroptosis tumor therapy but limited by the problems of low iron content, low tumor enrichment, low cellular uptake, and uncontrolled release of iron ions. To solve the problems, an FeOOH-assisted approach is demonstrated to produce iron hybrid polymer nanospindles (IHPNSs) for efficient iron delivery and ferroptosis tumor therapy. The IHPNSs are prepared through the cohydrolysis of FeCl3·6H2O with aniline, pyrrole, or amino-pyrrole. On the one hand, the hydrolysis of Fe3+ generates FeOOH particles, which further act as the templates to form fusiform architectures. On the other hand, Fe3+ triggers the oxidative polymerization of aniline, pyrrole, or amino-pyrrole. The as-prepared polymers are capable of coordinating with excessive Fe3+ and locate on the FeOOH templates, thus producing Fe3+/polymer composite-coated FeOOH nanospindles. Systematic studies indicate that the one-dimension-like morphology facilitates tumor enrichment and cellular uptake of IHPNSs. Besides the high iron content of IHPNSs, the controlled release of Fe3+ stimulated by the overexpressed glutathione (GSH) in the tumor microenvironment is achieved. The released Fe3+ is further transformed to Fe2+ by scavenging GSH, which leads to excessive accumulation of reactive oxygen species and lipid peroxides and finally induces ferroptosis of tumor cells. As a proof of concept, the IHPNSs show good efficacy in the treatment of a rat model of bladder tumors in situ.

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
Bioconjugate Chemistry
Bioconjugate Chemistry 生物-化学综合
CiteScore
9.00
自引率
2.10%
发文量
236
审稿时长
1.4 months
期刊介绍: Bioconjugate Chemistry invites original contributions on all research at the interface between man-made and biological materials. The mission of the journal is to communicate to advances in fields including therapeutic delivery, imaging, bionanotechnology, and synthetic biology. Bioconjugate Chemistry is intended to provide a forum for presentation of research relevant to all aspects of bioconjugates, including the preparation, properties and applications of biomolecular conjugates.
×
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