Recent Progress of Antibacterial Carbon Dots Prepared from Marketed Small Molecule Antibacterial Drugs.

IF 3.6 4区 医学 Q2 CHEMISTRY, MEDICINAL
ChemMedChem Pub Date : 2025-06-28 DOI:10.1002/cmdc.202500248
Yuequan Wu, Meng He, Zhi-Hao Li, Hongtao Kong, Ruirui Li, Ye Qu, En Zhang
{"title":"Recent Progress of Antibacterial Carbon Dots Prepared from Marketed Small Molecule Antibacterial Drugs.","authors":"Yuequan Wu, Meng He, Zhi-Hao Li, Hongtao Kong, Ruirui Li, Ye Qu, En Zhang","doi":"10.1002/cmdc.202500248","DOIUrl":null,"url":null,"abstract":"<p><p>The massive consumption of antibiotics leads to antibiotic resistance, which is a major concern in the global health crisis. Therefore, the development of non-antibiotic antibacterial drugs occurs simultaneously with the development of antibiotics. Nanomaterial applications in antibacterial research are currently expanding. Carbon dots, termed as CD, are a novel class of nanomaterials that have garnered a lot of interest. Antibacterial CD has many outstanding characteristics, such as high biocompatibility, easy surface modification, excellent optical properties, an extensive precursor source, and a small particle size (1-10 nm). Although there are many potential sources of CD, many researchers find it challenging to screen precursors for the purpose of preparing CD with remarkable antibacterial abilities. It is often recommended to generate CD directly from antibacterial agents since the process usually maintains the part qualities of its precursors during preparation. In this paper, CDs prepared by marketed small molecule antibacterial drugs were selected as our topic. Their characteristics of preparation, biocompatibility and antibacterial activity were discussed. This review summarizes the antibacterial CDs prepared from aminoglycosides, β-lactams, quinolones, antituberculosis drugs, and nitroimidazole antibacterial drugs as precursors. Then the advantages and mechanisms of CDs, the existing problems and future possibilities of antibacterial CDs were also explored.</p>","PeriodicalId":147,"journal":{"name":"ChemMedChem","volume":" ","pages":"e202500248"},"PeriodicalIF":3.6000,"publicationDate":"2025-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemMedChem","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/cmdc.202500248","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

The massive consumption of antibiotics leads to antibiotic resistance, which is a major concern in the global health crisis. Therefore, the development of non-antibiotic antibacterial drugs occurs simultaneously with the development of antibiotics. Nanomaterial applications in antibacterial research are currently expanding. Carbon dots, termed as CD, are a novel class of nanomaterials that have garnered a lot of interest. Antibacterial CD has many outstanding characteristics, such as high biocompatibility, easy surface modification, excellent optical properties, an extensive precursor source, and a small particle size (1-10 nm). Although there are many potential sources of CD, many researchers find it challenging to screen precursors for the purpose of preparing CD with remarkable antibacterial abilities. It is often recommended to generate CD directly from antibacterial agents since the process usually maintains the part qualities of its precursors during preparation. In this paper, CDs prepared by marketed small molecule antibacterial drugs were selected as our topic. Their characteristics of preparation, biocompatibility and antibacterial activity were discussed. This review summarizes the antibacterial CDs prepared from aminoglycosides, β-lactams, quinolones, antituberculosis drugs, and nitroimidazole antibacterial drugs as precursors. Then the advantages and mechanisms of CDs, the existing problems and future possibilities of antibacterial CDs were also explored.

市售小分子抗菌药物制备抗菌碳点的研究进展。
抗生素的大量消费导致抗生素耐药性,这是全球卫生危机中的一个主要问题。因此,非抗生素类抗菌药物的发展与抗生素的发展是同步发生的。纳米材料在抗菌研究中的应用正在不断扩大。碳点,被称为CD,是一种新型的纳米材料,引起了人们的极大兴趣。抗菌CD具有生物相容性高、表面易于修饰、光学性能优异、前驱体来源广泛、粒径小(1 ~ 10 nm)等特点。虽然乳糜泻有许多潜在的来源,但许多研究人员发现筛选前体以制备具有显著抗菌能力的乳糜泻是一项挑战。通常建议直接从抗菌剂中生成CD,因为该工艺通常在制备过程中保持其前体的部分质量。本文以市售小分子抗菌药物制备cd为研究对象。讨论了它们的制备特点、生物相容性和抗菌活性。综述了以氨基糖苷类、β-内酰胺类、喹诺酮类、抗结核药物和硝基咪唑类抗菌药物为前体制备的抗菌CDs的研究进展。然后探讨了cd的优势和作用机理,以及抗菌cd存在的问题和未来的可能性。
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
ChemMedChem
ChemMedChem 医学-药学
CiteScore
6.70
自引率
2.90%
发文量
280
审稿时长
1 months
期刊介绍: Quality research. Outstanding publications. With an impact factor of 3.124 (2019), ChemMedChem is a top journal for research at the interface of chemistry, biology and medicine. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies. ChemMedChem publishes primary as well as critical secondary and tertiary information from authors across and for the world. Its mission is to integrate the wide and flourishing field of medicinal and pharmaceutical sciences, ranging from drug design and discovery to drug development and delivery, from molecular modeling to combinatorial chemistry, from target validation to lead generation and ADMET studies. ChemMedChem typically covers topics on small molecules, therapeutic macromolecules, peptides, peptidomimetics, and aptamers, protein-drug conjugates, nucleic acid therapies, and beginning 2017, nanomedicine, particularly 1) targeted nanodelivery, 2) theranostic nanoparticles, and 3) nanodrugs. Contents ChemMedChem publishes an attractive mixture of: Full Papers and Communications Reviews and Minireviews Patent Reviews Highlights and Concepts Book and Multimedia Reviews.
×
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