{"title":"光驱动纳米机器人群体聚集肿瘤靶向的动力学与动力学","authors":"Luyao Zhang;Yue Sun;Dong Du;Yifan Chen","doi":"10.1109/TMBMC.2025.3546207","DOIUrl":null,"url":null,"abstract":"This study proposes a novel light-driven nanorobots swarm (NS) aggregation method to enhance tumor targeting efficiency. To replicate the structured and directional flow of density blood vessels near tumors, we employed a Manhattan-geometry vasculature (MGV) model, which mimics the complex, density-connected vasculature near the tumor site. This model significantly influences NS navigation and aggregation behavior, providing more realistic movement dynamics insights. We analyzed NS dynamics under light illumination, focusing on drag and thermophoretic forces. Comparisons with magnetic field-driven and non-external force strategies across three objective functions show that light-driven targeting increases efficiency by 4% to 46% and reduces targeting time by up to 27.9%. The MGV model enables precise predictions of NS movement, optimizing aggregation toward tumor tissues. These findings demonstrate the potential of light-driven NS aggregation to enhance tumor-targeting therapies, offering advantages over magnetic control in complex biological environments, with implications for photothermal therapy and precision drug delivery.","PeriodicalId":36530,"journal":{"name":"IEEE Transactions on Molecular, Biological, and Multi-Scale Communications","volume":"11 2","pages":"269-282"},"PeriodicalIF":2.4000,"publicationDate":"2025-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dynamics and Kinetics of Light-Driven Nanorobots Swarm Aggregation for Tumor Targeting\",\"authors\":\"Luyao Zhang;Yue Sun;Dong Du;Yifan Chen\",\"doi\":\"10.1109/TMBMC.2025.3546207\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This study proposes a novel light-driven nanorobots swarm (NS) aggregation method to enhance tumor targeting efficiency. To replicate the structured and directional flow of density blood vessels near tumors, we employed a Manhattan-geometry vasculature (MGV) model, which mimics the complex, density-connected vasculature near the tumor site. This model significantly influences NS navigation and aggregation behavior, providing more realistic movement dynamics insights. We analyzed NS dynamics under light illumination, focusing on drag and thermophoretic forces. Comparisons with magnetic field-driven and non-external force strategies across three objective functions show that light-driven targeting increases efficiency by 4% to 46% and reduces targeting time by up to 27.9%. The MGV model enables precise predictions of NS movement, optimizing aggregation toward tumor tissues. These findings demonstrate the potential of light-driven NS aggregation to enhance tumor-targeting therapies, offering advantages over magnetic control in complex biological environments, with implications for photothermal therapy and precision drug delivery.\",\"PeriodicalId\":36530,\"journal\":{\"name\":\"IEEE Transactions on Molecular, Biological, and Multi-Scale Communications\",\"volume\":\"11 2\",\"pages\":\"269-282\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2025-02-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IEEE Transactions on Molecular, Biological, and Multi-Scale Communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://ieeexplore.ieee.org/document/10904191/\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENGINEERING, ELECTRICAL & ELECTRONIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IEEE Transactions on Molecular, Biological, and Multi-Scale Communications","FirstCategoryId":"1085","ListUrlMain":"https://ieeexplore.ieee.org/document/10904191/","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
Dynamics and Kinetics of Light-Driven Nanorobots Swarm Aggregation for Tumor Targeting
This study proposes a novel light-driven nanorobots swarm (NS) aggregation method to enhance tumor targeting efficiency. To replicate the structured and directional flow of density blood vessels near tumors, we employed a Manhattan-geometry vasculature (MGV) model, which mimics the complex, density-connected vasculature near the tumor site. This model significantly influences NS navigation and aggregation behavior, providing more realistic movement dynamics insights. We analyzed NS dynamics under light illumination, focusing on drag and thermophoretic forces. Comparisons with magnetic field-driven and non-external force strategies across three objective functions show that light-driven targeting increases efficiency by 4% to 46% and reduces targeting time by up to 27.9%. The MGV model enables precise predictions of NS movement, optimizing aggregation toward tumor tissues. These findings demonstrate the potential of light-driven NS aggregation to enhance tumor-targeting therapies, offering advantages over magnetic control in complex biological environments, with implications for photothermal therapy and precision drug delivery.
期刊介绍:
As a result of recent advances in MEMS/NEMS and systems biology, as well as the emergence of synthetic bacteria and lab/process-on-a-chip techniques, it is now possible to design chemical “circuits”, custom organisms, micro/nanoscale swarms of devices, and a host of other new systems. This success opens up a new frontier for interdisciplinary communications techniques using chemistry, biology, and other principles that have not been considered in the communications literature. The IEEE Transactions on Molecular, Biological, and Multi-Scale Communications (T-MBMSC) is devoted to the principles, design, and analysis of communication systems that use physics beyond classical electromagnetism. This includes molecular, quantum, and other physical, chemical and biological techniques; as well as new communication techniques at small scales or across multiple scales (e.g., nano to micro to macro; note that strictly nanoscale systems, 1-100 nm, are outside the scope of this journal). Original research articles on one or more of the following topics are within scope: mathematical modeling, information/communication and network theoretic analysis, standardization and industrial applications, and analytical or experimental studies on communication processes or networks in biology. Contributions on related topics may also be considered for publication. Contributions from researchers outside the IEEE’s typical audience are encouraged.