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 , Faezeh Ghorbanizamani , Hichem Moulahoum , Firat Baris Barlas , Emine Guler Celik , Dilara Gürsoy , Rza Memmedov , Tevfik Ilker Akcam , Kutsal Turhan , Figen Zihnioglu , 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 , Faezeh Ghorbanizamani , Hichem Moulahoum , Firat Baris Barlas , Emine Guler Celik , Dilara Gürsoy , Rza Memmedov , Tevfik Ilker Akcam , Kutsal Turhan , Figen Zihnioglu , 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}
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.
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.