Mingjie Wang , Feng Xiao , Le Mi , Han Qian , Yijing Zhang , Sandra Kalil Bussadori , Vanderlei S. Bagnato , Muthumuni Managa , Mohamed Elagawany , Tebello Nyokong , Yingyuan Peng , Yijia Yan , Zhi Long Chen
{"title":"双季铵BODIPY衍生物:光物理、抗菌和抗肿瘤的光动力应用","authors":"Mingjie Wang , Feng Xiao , Le Mi , Han Qian , Yijing Zhang , Sandra Kalil Bussadori , Vanderlei S. Bagnato , Muthumuni Managa , Mohamed Elagawany , Tebello Nyokong , Yingyuan Peng , Yijia Yan , Zhi Long Chen","doi":"10.1016/j.bioorg.2025.108982","DOIUrl":null,"url":null,"abstract":"<div><div>Although Boron-dipyrromethene (BODIPY) derivatives have been explored for photodynamic antibacterial or antitumor applications, respectively, dual-activity cationic BODIPY photosensitizers have received much less attention. In addition, traditional quaternary ammonium compounds (QACs) are primarily studied as antibacterial agents, with systematic reports on their direct antitumor activity remaining scarce. We developed bis-quaternary ammonium cationic BODIPY derivatives as photosensitizers to investigate dual photodynamic antibacterial/antitumor action. All synthesized new compounds demonstrated notable UV-vis absorption in the range of 646-659 nm, intense fluorescence emission (665, 670, and 675 nm), and capabilities for reactive oxygen species (ROS) generation. Among these, brominated BODIPYs <strong>II</strong><sub><strong>3</strong></sub> and <strong>II</strong><sub><strong>5</strong></sub> exhibited high ROS generation efficiency and significant photodynamic antitumor activity against Eca-109 cells <em>in vitro</em> (IC<sub>50</sub> = 0.22 μM and 0.36 μM) and <em>in vivo</em>, comparable to the control drug <em>m</em>-THPC. Compounds <strong>I</strong><sub><strong>5</strong></sub> and <strong>II</strong><sub><strong>5</strong></sub> demonstrated substantial photodynamic antibacterial activities against pathogenic <em>Staphylococcus aureus</em> (<em>S. aureus</em>), with minimum inhibitory concentrations (MIC) of 0.5 μg/mL for both compounds. Furthermore, they achieved effective biofilm inhibition efficiencies of 86.74% and 85.23%, respectively, through the disruption of membrane integrity. These findings hold significant promise for pioneering new multifunctional photosensitizers that enable combined or sequential antimicrobial and antitumor photodynamic therapies.</div></div>","PeriodicalId":257,"journal":{"name":"Bioorganic Chemistry","volume":"165 ","pages":"Article 108982"},"PeriodicalIF":4.7000,"publicationDate":"2025-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bis-quaternary ammonium BODIPY derivatives: Photophysical, antimicrobial, and antitumor photodynamic applications\",\"authors\":\"Mingjie Wang , Feng Xiao , Le Mi , Han Qian , Yijing Zhang , Sandra Kalil Bussadori , Vanderlei S. Bagnato , Muthumuni Managa , Mohamed Elagawany , Tebello Nyokong , Yingyuan Peng , Yijia Yan , Zhi Long Chen\",\"doi\":\"10.1016/j.bioorg.2025.108982\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Although Boron-dipyrromethene (BODIPY) derivatives have been explored for photodynamic antibacterial or antitumor applications, respectively, dual-activity cationic BODIPY photosensitizers have received much less attention. In addition, traditional quaternary ammonium compounds (QACs) are primarily studied as antibacterial agents, with systematic reports on their direct antitumor activity remaining scarce. We developed bis-quaternary ammonium cationic BODIPY derivatives as photosensitizers to investigate dual photodynamic antibacterial/antitumor action. All synthesized new compounds demonstrated notable UV-vis absorption in the range of 646-659 nm, intense fluorescence emission (665, 670, and 675 nm), and capabilities for reactive oxygen species (ROS) generation. Among these, brominated BODIPYs <strong>II</strong><sub><strong>3</strong></sub> and <strong>II</strong><sub><strong>5</strong></sub> exhibited high ROS generation efficiency and significant photodynamic antitumor activity against Eca-109 cells <em>in vitro</em> (IC<sub>50</sub> = 0.22 μM and 0.36 μM) and <em>in vivo</em>, comparable to the control drug <em>m</em>-THPC. Compounds <strong>I</strong><sub><strong>5</strong></sub> and <strong>II</strong><sub><strong>5</strong></sub> demonstrated substantial photodynamic antibacterial activities against pathogenic <em>Staphylococcus aureus</em> (<em>S. aureus</em>), with minimum inhibitory concentrations (MIC) of 0.5 μg/mL for both compounds. Furthermore, they achieved effective biofilm inhibition efficiencies of 86.74% and 85.23%, respectively, through the disruption of membrane integrity. These findings hold significant promise for pioneering new multifunctional photosensitizers that enable combined or sequential antimicrobial and antitumor photodynamic therapies.</div></div>\",\"PeriodicalId\":257,\"journal\":{\"name\":\"Bioorganic Chemistry\",\"volume\":\"165 \",\"pages\":\"Article 108982\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2025-09-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bioorganic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0045206825008624\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioorganic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0045206825008624","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Bis-quaternary ammonium BODIPY derivatives: Photophysical, antimicrobial, and antitumor photodynamic applications
Although Boron-dipyrromethene (BODIPY) derivatives have been explored for photodynamic antibacterial or antitumor applications, respectively, dual-activity cationic BODIPY photosensitizers have received much less attention. In addition, traditional quaternary ammonium compounds (QACs) are primarily studied as antibacterial agents, with systematic reports on their direct antitumor activity remaining scarce. We developed bis-quaternary ammonium cationic BODIPY derivatives as photosensitizers to investigate dual photodynamic antibacterial/antitumor action. All synthesized new compounds demonstrated notable UV-vis absorption in the range of 646-659 nm, intense fluorescence emission (665, 670, and 675 nm), and capabilities for reactive oxygen species (ROS) generation. Among these, brominated BODIPYs II3 and II5 exhibited high ROS generation efficiency and significant photodynamic antitumor activity against Eca-109 cells in vitro (IC50 = 0.22 μM and 0.36 μM) and in vivo, comparable to the control drug m-THPC. Compounds I5 and II5 demonstrated substantial photodynamic antibacterial activities against pathogenic Staphylococcus aureus (S. aureus), with minimum inhibitory concentrations (MIC) of 0.5 μg/mL for both compounds. Furthermore, they achieved effective biofilm inhibition efficiencies of 86.74% and 85.23%, respectively, through the disruption of membrane integrity. These findings hold significant promise for pioneering new multifunctional photosensitizers that enable combined or sequential antimicrobial and antitumor photodynamic therapies.
期刊介绍:
Bioorganic Chemistry publishes research that addresses biological questions at the molecular level, using organic chemistry and principles of physical organic chemistry. The scope of the journal covers a range of topics at the organic chemistry-biology interface, including: enzyme catalysis, biotransformation and enzyme inhibition; nucleic acids chemistry; medicinal chemistry; natural product chemistry, natural product synthesis and natural product biosynthesis; antimicrobial agents; lipid and peptide chemistry; biophysical chemistry; biological probes; bio-orthogonal chemistry and biomimetic chemistry.
For manuscripts dealing with synthetic bioactive compounds, the Journal requires that the molecular target of the compounds described must be known, and must be demonstrated experimentally in the manuscript. For studies involving natural products, if the molecular target is unknown, some data beyond simple cell-based toxicity studies to provide insight into the mechanism of action is required. Studies supported by molecular docking are welcome, but must be supported by experimental data. The Journal does not consider manuscripts that are purely theoretical or computational in nature.
The Journal publishes regular articles, short communications and reviews. Reviews are normally invited by Editors or Editorial Board members. Authors of unsolicited reviews should first contact an Editor or Editorial Board member to determine whether the proposed article is within the scope of the Journal.