冠状纳米结构:量子点与胸膜液蛋白/多肽结合,用于治疗

IF 5.4 2区 医学 Q1 BIOPHYSICS
Kerem Tok , Faezeh Ghorbanizamani , Hichem Moulahoum , Firat Baris Barlas , Emine Guler Celik , Dilara Gürsoy , Rza Memmedov , Tevfik Ilker Akcam , Kutsal Turhan , Figen Zihnioglu , Suna Timur
{"title":"冠状纳米结构:量子点与胸膜液蛋白/多肽结合,用于治疗","authors":"Kerem Tok ,&nbsp;Faezeh Ghorbanizamani ,&nbsp;Hichem Moulahoum ,&nbsp;Firat Baris Barlas ,&nbsp;Emine Guler Celik ,&nbsp;Dilara Gürsoy ,&nbsp;Rza Memmedov ,&nbsp;Tevfik Ilker Akcam ,&nbsp;Kutsal Turhan ,&nbsp;Figen Zihnioglu ,&nbsp;Suna Timur","doi":"10.1016/j.colsurfb.2025.114792","DOIUrl":null,"url":null,"abstract":"<div><div>The incorporation of protein and peptide components into nanoparticles is a revolutionary advancement in nanotheranostics, particularly in the domain of personalised medicine. This study delves into the creation of multifunctional theranostic nanoparticles by conjugating quantum dots (QDs) with proteins and peptides sourced from the pleural fluid of lung cancer patients. Our objective is to enhance the targeting and therapeutic potential of QDs through the formation of corona-like nanostructures. Pleural fluids from lung cancer patients were pooled and precipitated to enrich protein and peptide fractions. These enriched fractions, alongside untreated pooled pleural fluid, were utilized to coat QDs, forming corona-like nanostructures. Comprehensive characterization revealed robust interactions between QDs and pleural fluid proteins/peptides, resulting in heightened fluorescence and stability. Targeted in vitro assays on lung cancer cells (A549) and normal epithelial lung cells (BEAS-2B) demonstrated selective cancer cell targeting and improved therapeutic efficacy. Furthermore, combining these nanostructures with radiotherapy markedly increased cancer cell death compared to radiotherapy alone. This pioneering approach underscores the significant potential of pleural fluid-derived protein/peptide-coated QDs in developing targeted, effective multifunctional nanostructures. By leveraging the unique properties of pleural fluid proteins/peptides and QDs, this study opens new avenues for personalized medicine, poised to revolutionize cancer therapy applications.</div></div>","PeriodicalId":279,"journal":{"name":"Colloids and Surfaces B: Biointerfaces","volume":"254 ","pages":"Article 114792"},"PeriodicalIF":5.4000,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Corona-like nanostructures: Quantum dots meet pleural fluid proteins/peptides for theranostic applications\",\"authors\":\"Kerem Tok ,&nbsp;Faezeh Ghorbanizamani ,&nbsp;Hichem Moulahoum ,&nbsp;Firat Baris Barlas ,&nbsp;Emine Guler Celik ,&nbsp;Dilara Gürsoy ,&nbsp;Rza Memmedov ,&nbsp;Tevfik Ilker Akcam ,&nbsp;Kutsal Turhan ,&nbsp;Figen Zihnioglu ,&nbsp;Suna Timur\",\"doi\":\"10.1016/j.colsurfb.2025.114792\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The incorporation of protein and peptide components into nanoparticles is a revolutionary advancement in nanotheranostics, particularly in the domain of personalised medicine. This study delves into the creation of multifunctional theranostic nanoparticles by conjugating quantum dots (QDs) with proteins and peptides sourced from the pleural fluid of lung cancer patients. Our objective is to enhance the targeting and therapeutic potential of QDs through the formation of corona-like nanostructures. Pleural fluids from lung cancer patients were pooled and precipitated to enrich protein and peptide fractions. These enriched fractions, alongside untreated pooled pleural fluid, were utilized to coat QDs, forming corona-like nanostructures. Comprehensive characterization revealed robust interactions between QDs and pleural fluid proteins/peptides, resulting in heightened fluorescence and stability. Targeted in vitro assays on lung cancer cells (A549) and normal epithelial lung cells (BEAS-2B) demonstrated selective cancer cell targeting and improved therapeutic efficacy. Furthermore, combining these nanostructures with radiotherapy markedly increased cancer cell death compared to radiotherapy alone. This pioneering approach underscores the significant potential of pleural fluid-derived protein/peptide-coated QDs in developing targeted, effective multifunctional nanostructures. By leveraging the unique properties of pleural fluid proteins/peptides and QDs, this study opens new avenues for personalized medicine, poised to revolutionize cancer therapy applications.</div></div>\",\"PeriodicalId\":279,\"journal\":{\"name\":\"Colloids and Surfaces B: Biointerfaces\",\"volume\":\"254 \",\"pages\":\"Article 114792\"},\"PeriodicalIF\":5.4000,\"publicationDate\":\"2025-05-15\",\"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/S0927776525002991\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOPHYSICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Colloids and Surfaces B: Biointerfaces","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0927776525002991","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

摘要

将蛋白质和肽成分结合到纳米颗粒中是纳米治疗学的革命性进步,特别是在个性化医疗领域。本研究通过将量子点(QDs)与肺癌患者胸膜液中的蛋白质和多肽结合,深入研究了多功能治疗纳米颗粒的产生。我们的目标是通过形成冠状纳米结构来增强量子点的靶向性和治疗潜力。收集肺癌患者的胸膜液并进行沉淀,以丰富蛋白质和肽组分。这些富集的组分与未经处理的胸腔积液一起用于包裹量子点,形成冠状纳米结构。综合表征表明量子点与胸膜液蛋白/肽之间存在强大的相互作用,从而提高了荧光和稳定性。对肺癌细胞(A549)和正常肺上皮细胞(BEAS-2B)进行体外靶向实验,显示出选择性靶向癌细胞,提高了治疗效果。此外,与单独放疗相比,将这些纳米结构与放疗结合明显增加了癌细胞死亡。这种开创性的方法强调了胸膜液衍生的蛋白质/肽包被量子点在开发靶向、有效的多功能纳米结构方面的巨大潜力。通过利用胸膜液蛋白/肽和量子点的独特特性,本研究为个性化医疗开辟了新的途径,有望彻底改变癌症治疗的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Corona-like nanostructures: Quantum dots meet pleural fluid proteins/peptides for theranostic applications
The incorporation of protein and peptide components into nanoparticles is a revolutionary advancement in nanotheranostics, particularly in the domain of personalised medicine. This study delves into the creation of multifunctional theranostic nanoparticles by conjugating quantum dots (QDs) with proteins and peptides sourced from the pleural fluid of lung cancer patients. Our objective is to enhance the targeting and therapeutic potential of QDs through the formation of corona-like nanostructures. Pleural fluids from lung cancer patients were pooled and precipitated to enrich protein and peptide fractions. These enriched fractions, alongside untreated pooled pleural fluid, were utilized to coat QDs, forming corona-like nanostructures. Comprehensive characterization revealed robust interactions between QDs and pleural fluid proteins/peptides, resulting in heightened fluorescence and stability. Targeted in vitro assays on lung cancer cells (A549) and normal epithelial lung cells (BEAS-2B) demonstrated selective cancer cell targeting and improved therapeutic efficacy. Furthermore, combining these nanostructures with radiotherapy markedly increased cancer cell death compared to radiotherapy alone. This pioneering approach underscores the significant potential of pleural fluid-derived protein/peptide-coated QDs in developing targeted, effective multifunctional nanostructures. By leveraging the unique properties of pleural fluid proteins/peptides and QDs, this study opens new avenues for personalized medicine, poised to revolutionize cancer therapy applications.
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
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