Melissa S Monteiro, Marina S Mesquita, Leidiane M Garcia, Paulo R Dos Santos, Cássia C de Marangoni de Viveiros, Ronei D da Fonseca, Mary A Xavier, Gabriel Ws de Mendonça, Suélia Srf Rosa, Saulo Lp Silva, Leonardo G Paterno, Paulo C Morais, Sônia N Báo
{"title":"基于氧化石墨烯的纳米复合材料的射频驱动抗肿瘤效应:希尔模型分析。","authors":"Melissa S Monteiro, Marina S Mesquita, Leidiane M Garcia, Paulo R Dos Santos, Cássia C de Marangoni de Viveiros, Ronei D da Fonseca, Mary A Xavier, Gabriel Ws de Mendonça, Suélia Srf Rosa, Saulo Lp Silva, Leonardo G Paterno, Paulo C Morais, Sônia N Báo","doi":"10.2217/nnm-2023-0312","DOIUrl":null,"url":null,"abstract":"<p><p><b>Aim:</b> This report proposes using the Hill model to assess the benchmark dose, the 50% lethal dose, the cooperativity and the dissociation constant while analyzing cell viability data using nanomaterials to evaluate the antitumor potential while combined with radiofrequency therapy. <b>Materials & methods:</b> A nanocomposite was synthesized (graphene oxide-polyethyleneimine-gold) and the viability was evaluated using two tumor cell lines, namely LLC-WRC-256 and B16-F10. <b>Results:</b> Our findings demonstrated that while the nanocomposite is biocompatible against the LLC-WRC-256 and B16-F10 cancer cell lines in the absence of radiofrequency, the application of radiofrequency enhances the cell toxicity by orders of magnitude. <b>Conclusion:</b> This result points to prospective studies with the tested cell lines using tumor animal models.</p>","PeriodicalId":74240,"journal":{"name":"Nanomedicine (London, England)","volume":" ","pages":"397-412"},"PeriodicalIF":0.0000,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Radiofrequency driving antitumor effect of graphene oxide-based nanocomposites: a Hill model analysis.\",\"authors\":\"Melissa S Monteiro, Marina S Mesquita, Leidiane M Garcia, Paulo R Dos Santos, Cássia C de Marangoni de Viveiros, Ronei D da Fonseca, Mary A Xavier, Gabriel Ws de Mendonça, Suélia Srf Rosa, Saulo Lp Silva, Leonardo G Paterno, Paulo C Morais, Sônia N Báo\",\"doi\":\"10.2217/nnm-2023-0312\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Aim:</b> This report proposes using the Hill model to assess the benchmark dose, the 50% lethal dose, the cooperativity and the dissociation constant while analyzing cell viability data using nanomaterials to evaluate the antitumor potential while combined with radiofrequency therapy. <b>Materials & methods:</b> A nanocomposite was synthesized (graphene oxide-polyethyleneimine-gold) and the viability was evaluated using two tumor cell lines, namely LLC-WRC-256 and B16-F10. <b>Results:</b> Our findings demonstrated that while the nanocomposite is biocompatible against the LLC-WRC-256 and B16-F10 cancer cell lines in the absence of radiofrequency, the application of radiofrequency enhances the cell toxicity by orders of magnitude. <b>Conclusion:</b> This result points to prospective studies with the tested cell lines using tumor animal models.</p>\",\"PeriodicalId\":74240,\"journal\":{\"name\":\"Nanomedicine (London, England)\",\"volume\":\" \",\"pages\":\"397-412\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nanomedicine (London, England)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2217/nnm-2023-0312\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/12/19 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanomedicine (London, England)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2217/nnm-2023-0312","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/12/19 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
Radiofrequency driving antitumor effect of graphene oxide-based nanocomposites: a Hill model analysis.
Aim: This report proposes using the Hill model to assess the benchmark dose, the 50% lethal dose, the cooperativity and the dissociation constant while analyzing cell viability data using nanomaterials to evaluate the antitumor potential while combined with radiofrequency therapy. Materials & methods: A nanocomposite was synthesized (graphene oxide-polyethyleneimine-gold) and the viability was evaluated using two tumor cell lines, namely LLC-WRC-256 and B16-F10. Results: Our findings demonstrated that while the nanocomposite is biocompatible against the LLC-WRC-256 and B16-F10 cancer cell lines in the absence of radiofrequency, the application of radiofrequency enhances the cell toxicity by orders of magnitude. Conclusion: This result points to prospective studies with the tested cell lines using tumor animal models.