基于miR-21对肿瘤成像和治疗反应的双功能氧化石墨烯药物传递系统。

IF 3.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Dutao Yang, Sen Li, Yanfei Cai, Jian Jin and Zhaoqi Yang*, 
{"title":"基于miR-21对肿瘤成像和治疗反应的双功能氧化石墨烯药物传递系统。","authors":"Dutao Yang,&nbsp;Sen Li,&nbsp;Yanfei Cai,&nbsp;Jian Jin and Zhaoqi Yang*,&nbsp;","doi":"10.1021/acs.langmuir.5c01921","DOIUrl":null,"url":null,"abstract":"<p >Cancer, a category of diseases that pose a serious threat to human health, has received widespread attention in recent years. Although the small-molecule anticancer drug like Doxorubicin (Dox) has obvious therapeutic effects, it lacks targeting ability and is prone to causing cytotoxicity to normal cells or tissues, thus limiting its clinical application. In this study, a novel drug-loaded nanosystem, which was composed of graphene oxide (GO) modified by molecular beacon (MB) and Dox, was developed to respond to small-molecular RNA (miR-21) and release Dox for killing tumor cells. When the nanosystem was internalized by CD44 receptor-overexpressing cancer cells, the MBs on the GO hybridized with the overexpressed miR-21, thereby opening the hairpin structure and allowing the release of Dox in tumor cells. Our research results indicate that this nanosystem has a good inhibitory effect on cancer cells while exhibiting negligible side effects on normal cells. This treatment strategy provides a new approach to the safe delivery of small-molecule drugs.</p>","PeriodicalId":50,"journal":{"name":"Langmuir","volume":"41 29","pages":"19400–19408"},"PeriodicalIF":3.9000,"publicationDate":"2025-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bifunctional Graphene Oxide Drug Delivery System Based on miR-21 Response for Tumor Imaging and Therapy\",\"authors\":\"Dutao Yang,&nbsp;Sen Li,&nbsp;Yanfei Cai,&nbsp;Jian Jin and Zhaoqi Yang*,&nbsp;\",\"doi\":\"10.1021/acs.langmuir.5c01921\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Cancer, a category of diseases that pose a serious threat to human health, has received widespread attention in recent years. Although the small-molecule anticancer drug like Doxorubicin (Dox) has obvious therapeutic effects, it lacks targeting ability and is prone to causing cytotoxicity to normal cells or tissues, thus limiting its clinical application. In this study, a novel drug-loaded nanosystem, which was composed of graphene oxide (GO) modified by molecular beacon (MB) and Dox, was developed to respond to small-molecular RNA (miR-21) and release Dox for killing tumor cells. When the nanosystem was internalized by CD44 receptor-overexpressing cancer cells, the MBs on the GO hybridized with the overexpressed miR-21, thereby opening the hairpin structure and allowing the release of Dox in tumor cells. Our research results indicate that this nanosystem has a good inhibitory effect on cancer cells while exhibiting negligible side effects on normal cells. This treatment strategy provides a new approach to the safe delivery of small-molecule drugs.</p>\",\"PeriodicalId\":50,\"journal\":{\"name\":\"Langmuir\",\"volume\":\"41 29\",\"pages\":\"19400–19408\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-07-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Langmuir\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.langmuir.5c01921\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Langmuir","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.langmuir.5c01921","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

癌症是一类严重威胁人类健康的疾病,近年来受到了广泛关注。阿霉素(Dox)等小分子抗癌药物虽然具有明显的治疗效果,但缺乏靶向性,易对正常细胞或组织产生细胞毒性,限制了其临床应用。在这项研究中,开发了一种新的载药纳米系统,该系统由分子信标(MB)修饰的氧化石墨烯(GO)和Dox组成,可响应小分子RNA (miR-21)并释放Dox杀死肿瘤细胞。当纳米系统被过表达CD44受体的癌细胞内化时,氧化石墨烯上的mb与过表达的miR-21杂交,从而打开发夹结构,允许Dox在肿瘤细胞中释放。我们的研究结果表明,该纳米系统对癌细胞具有良好的抑制作用,而对正常细胞的副作用可以忽略不计。这种治疗策略为小分子药物的安全输送提供了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Bifunctional Graphene Oxide Drug Delivery System Based on miR-21 Response for Tumor Imaging and Therapy

Bifunctional Graphene Oxide Drug Delivery System Based on miR-21 Response for Tumor Imaging and Therapy

Cancer, a category of diseases that pose a serious threat to human health, has received widespread attention in recent years. Although the small-molecule anticancer drug like Doxorubicin (Dox) has obvious therapeutic effects, it lacks targeting ability and is prone to causing cytotoxicity to normal cells or tissues, thus limiting its clinical application. In this study, a novel drug-loaded nanosystem, which was composed of graphene oxide (GO) modified by molecular beacon (MB) and Dox, was developed to respond to small-molecular RNA (miR-21) and release Dox for killing tumor cells. When the nanosystem was internalized by CD44 receptor-overexpressing cancer cells, the MBs on the GO hybridized with the overexpressed miR-21, thereby opening the hairpin structure and allowing the release of Dox in tumor cells. Our research results indicate that this nanosystem has a good inhibitory effect on cancer cells while exhibiting negligible side effects on normal cells. This treatment strategy provides a new approach to the safe delivery of small-molecule drugs.

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
Langmuir
Langmuir 化学-材料科学:综合
CiteScore
6.50
自引率
10.30%
发文量
1464
审稿时长
2.1 months
期刊介绍: Langmuir is an interdisciplinary journal publishing articles in the following subject categories: Colloids: surfactants and self-assembly, dispersions, emulsions, foams Interfaces: adsorption, reactions, films, forces Biological Interfaces: biocolloids, biomolecular and biomimetic materials Materials: nano- and mesostructured materials, polymers, gels, liquid crystals Electrochemistry: interfacial charge transfer, charge transport, electrocatalysis, electrokinetic phenomena, bioelectrochemistry Devices and Applications: sensors, fluidics, patterning, catalysis, photonic crystals However, when high-impact, original work is submitted that does not fit within the above categories, decisions to accept or decline such papers will be based on one criteria: What Would Irving Do? Langmuir ranks #2 in citations out of 136 journals in the category of Physical Chemistry with 113,157 total citations. The journal received an Impact Factor of 4.384*. This journal is also indexed in the categories of Materials Science (ranked #1) and Multidisciplinary Chemistry (ranked #5).
×
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