{"title":"可扩展和可定制的三材料微针电化学生物传感器平台与无尘室制造","authors":"Kazim Haider;Trevor Tilly;Victoria Coyle;Colin Dalton","doi":"10.1109/LSENS.2025.3596869","DOIUrl":null,"url":null,"abstract":"This work reports a rapid, cleanroom-free route for fabricating three-electrode microneedle electrochemical biosensors by repurposing the high speed wire bonding technique from the semiconductor industry. The 50 µm diameter Au, Pt, and 30 µm Ag wires were bonded to commercial printed circuit boards (PCBs) to produce freestanding microneedles (MNs) that served as working (WE), counter (CE), and reference (RE) electrodes. Ag MNs were galvanostatically chlorinated to form Ag/AgCl reference electrodes with low drift, −3 ± 0.3 mV over 24 h in phosphate-buffered saline. Au MNs were coated with PEDOT:PSS/glucose oxidase for amperometric glucose sensing from 5–25 mM (sensitivity = 0.37 µA mM-1, +0.50 V working voltage), covering the physiologic range for diabetes management. Platform versatility was demonstrated by nanomolar-range detection after the addition of an aptamer self-assembled monolayer on wire bonded Au MNs. This fully automated, additive wire bonding process provides submillimetre electrode spacing, < US$2 materials cost per trielectrode array, and seamless integration with external sensing hardware for wearable applications owing to the PCB-substrate based approach. We demonstrate a scalable pathway toward multiplexed MN patches for continuous interstitial fluid monitoring and other microneedle-based minimally invasive biosensing applications.","PeriodicalId":13014,"journal":{"name":"IEEE Sensors Letters","volume":"9 9","pages":"1-4"},"PeriodicalIF":2.2000,"publicationDate":"2025-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=11119430","citationCount":"0","resultStr":"{\"title\":\"Scalable and Customizable Trimaterial Microneedle Electrochemical Biosensor Platform With Cleanroom-Free Fabrication\",\"authors\":\"Kazim Haider;Trevor Tilly;Victoria Coyle;Colin Dalton\",\"doi\":\"10.1109/LSENS.2025.3596869\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This work reports a rapid, cleanroom-free route for fabricating three-electrode microneedle electrochemical biosensors by repurposing the high speed wire bonding technique from the semiconductor industry. The 50 µm diameter Au, Pt, and 30 µm Ag wires were bonded to commercial printed circuit boards (PCBs) to produce freestanding microneedles (MNs) that served as working (WE), counter (CE), and reference (RE) electrodes. Ag MNs were galvanostatically chlorinated to form Ag/AgCl reference electrodes with low drift, −3 ± 0.3 mV over 24 h in phosphate-buffered saline. Au MNs were coated with PEDOT:PSS/glucose oxidase for amperometric glucose sensing from 5–25 mM (sensitivity = 0.37 µA mM-1, +0.50 V working voltage), covering the physiologic range for diabetes management. Platform versatility was demonstrated by nanomolar-range detection after the addition of an aptamer self-assembled monolayer on wire bonded Au MNs. This fully automated, additive wire bonding process provides submillimetre electrode spacing, < US$2 materials cost per trielectrode array, and seamless integration with external sensing hardware for wearable applications owing to the PCB-substrate based approach. We demonstrate a scalable pathway toward multiplexed MN patches for continuous interstitial fluid monitoring and other microneedle-based minimally invasive biosensing applications.\",\"PeriodicalId\":13014,\"journal\":{\"name\":\"IEEE Sensors Letters\",\"volume\":\"9 9\",\"pages\":\"1-4\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-08-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=11119430\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IEEE Sensors Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://ieeexplore.ieee.org/document/11119430/\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ENGINEERING, ELECTRICAL & ELECTRONIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IEEE Sensors Letters","FirstCategoryId":"1085","ListUrlMain":"https://ieeexplore.ieee.org/document/11119430/","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
Scalable and Customizable Trimaterial Microneedle Electrochemical Biosensor Platform With Cleanroom-Free Fabrication
This work reports a rapid, cleanroom-free route for fabricating three-electrode microneedle electrochemical biosensors by repurposing the high speed wire bonding technique from the semiconductor industry. The 50 µm diameter Au, Pt, and 30 µm Ag wires were bonded to commercial printed circuit boards (PCBs) to produce freestanding microneedles (MNs) that served as working (WE), counter (CE), and reference (RE) electrodes. Ag MNs were galvanostatically chlorinated to form Ag/AgCl reference electrodes with low drift, −3 ± 0.3 mV over 24 h in phosphate-buffered saline. Au MNs were coated with PEDOT:PSS/glucose oxidase for amperometric glucose sensing from 5–25 mM (sensitivity = 0.37 µA mM-1, +0.50 V working voltage), covering the physiologic range for diabetes management. Platform versatility was demonstrated by nanomolar-range detection after the addition of an aptamer self-assembled monolayer on wire bonded Au MNs. This fully automated, additive wire bonding process provides submillimetre electrode spacing, < US$2 materials cost per trielectrode array, and seamless integration with external sensing hardware for wearable applications owing to the PCB-substrate based approach. We demonstrate a scalable pathway toward multiplexed MN patches for continuous interstitial fluid monitoring and other microneedle-based minimally invasive biosensing applications.