Chengjie Zhu, Jesús Maldonado, Hao Tang, S. Venkatesh, K. Sengupta
{"title":"cmos驱动的无气动可扩展微流体和流体处理,具有无标签细胞和生物分子传感能力,用于端到端护理系统","authors":"Chengjie Zhu, Jesús Maldonado, Hao Tang, S. Venkatesh, K. Sengupta","doi":"10.1109/ISSCC42613.2021.9365843","DOIUrl":null,"url":null,"abstract":"The emergence of the pandemic has demonstrated the necessity of point-of-care (POC) molecular diagnostic platforms that encompass an end-to-end system (from sample fluid to diagnostic information) with the ability to allow rapid analysis on the spot. While POC sensing technologies have been demonstrated in miniaturize chip-scale platforms [1–5], the bottlenecks in enabling end-to-end low-cost handheld platforms have often been bio-sample handling, filtering, mixing with re-agents that are critical to the robustness of the assay chemistry and sensing sensitivity/specificity. These processes are typically carried out either manually or by employing complex pneumatic flow control with multiple bulky syringe pumps, which have been a severe limitation to enable end-to-end biosensing systems (Fig. 18.2.1). While electrically driven droplets, molecular and cell manipulation techniques, such as electro-wetting, electrophoresis and dielectrophoresis, have been demonstrated in singular systems before [1], they do not have the ability to process bulk bio-sample fluids that is required for POC devices. In this paper, we present a scalable approach that merges the functionalities of sample processing and cellular/bio-molecular sensing in a single system and eliminates any pneumatic pumping mechanisms by exploiting CMOS-based electrically driven electro-kinetic flow of bulk fluids. We demonstrate, for the first time, a CMOS-microfluidic system that is capable of 1) pumping bulk electrolyte fluid with AC electro-osmosis, 2) cell manipulation and separation with dielectrophoresis (DEP), 3) label-free biomolecular and cell sensing, classification with dedicated 16-element impedance spectroscopy receivers. While we demonstrate these kernel functionalities in a multichip module/microfluidic interface (Fig. 18.2.1), the overall architecture, fluidics and sensing components can be massively scaled up for various POC applications due to elimination of pressure-driven flows (Fig. 18.2.1).","PeriodicalId":371093,"journal":{"name":"2021 IEEE International Solid- State Circuits Conference (ISSCC)","volume":"71 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"CMOS-Driven Pneumatic-Free Scalable Microfluidics and Fluid Processing with Label-Free Cellular and Bio-Molecular Sensing Capability for an End-to-End Point-of-Care System\",\"authors\":\"Chengjie Zhu, Jesús Maldonado, Hao Tang, S. Venkatesh, K. Sengupta\",\"doi\":\"10.1109/ISSCC42613.2021.9365843\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The emergence of the pandemic has demonstrated the necessity of point-of-care (POC) molecular diagnostic platforms that encompass an end-to-end system (from sample fluid to diagnostic information) with the ability to allow rapid analysis on the spot. While POC sensing technologies have been demonstrated in miniaturize chip-scale platforms [1–5], the bottlenecks in enabling end-to-end low-cost handheld platforms have often been bio-sample handling, filtering, mixing with re-agents that are critical to the robustness of the assay chemistry and sensing sensitivity/specificity. These processes are typically carried out either manually or by employing complex pneumatic flow control with multiple bulky syringe pumps, which have been a severe limitation to enable end-to-end biosensing systems (Fig. 18.2.1). While electrically driven droplets, molecular and cell manipulation techniques, such as electro-wetting, electrophoresis and dielectrophoresis, have been demonstrated in singular systems before [1], they do not have the ability to process bulk bio-sample fluids that is required for POC devices. In this paper, we present a scalable approach that merges the functionalities of sample processing and cellular/bio-molecular sensing in a single system and eliminates any pneumatic pumping mechanisms by exploiting CMOS-based electrically driven electro-kinetic flow of bulk fluids. We demonstrate, for the first time, a CMOS-microfluidic system that is capable of 1) pumping bulk electrolyte fluid with AC electro-osmosis, 2) cell manipulation and separation with dielectrophoresis (DEP), 3) label-free biomolecular and cell sensing, classification with dedicated 16-element impedance spectroscopy receivers. While we demonstrate these kernel functionalities in a multichip module/microfluidic interface (Fig. 18.2.1), the overall architecture, fluidics and sensing components can be massively scaled up for various POC applications due to elimination of pressure-driven flows (Fig. 18.2.1).\",\"PeriodicalId\":371093,\"journal\":{\"name\":\"2021 IEEE International Solid- State Circuits Conference (ISSCC)\",\"volume\":\"71 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-02-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2021 IEEE International Solid- State Circuits Conference (ISSCC)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/ISSCC42613.2021.9365843\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2021 IEEE International Solid- State Circuits Conference (ISSCC)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/ISSCC42613.2021.9365843","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
CMOS-Driven Pneumatic-Free Scalable Microfluidics and Fluid Processing with Label-Free Cellular and Bio-Molecular Sensing Capability for an End-to-End Point-of-Care System
The emergence of the pandemic has demonstrated the necessity of point-of-care (POC) molecular diagnostic platforms that encompass an end-to-end system (from sample fluid to diagnostic information) with the ability to allow rapid analysis on the spot. While POC sensing technologies have been demonstrated in miniaturize chip-scale platforms [1–5], the bottlenecks in enabling end-to-end low-cost handheld platforms have often been bio-sample handling, filtering, mixing with re-agents that are critical to the robustness of the assay chemistry and sensing sensitivity/specificity. These processes are typically carried out either manually or by employing complex pneumatic flow control with multiple bulky syringe pumps, which have been a severe limitation to enable end-to-end biosensing systems (Fig. 18.2.1). While electrically driven droplets, molecular and cell manipulation techniques, such as electro-wetting, electrophoresis and dielectrophoresis, have been demonstrated in singular systems before [1], they do not have the ability to process bulk bio-sample fluids that is required for POC devices. In this paper, we present a scalable approach that merges the functionalities of sample processing and cellular/bio-molecular sensing in a single system and eliminates any pneumatic pumping mechanisms by exploiting CMOS-based electrically driven electro-kinetic flow of bulk fluids. We demonstrate, for the first time, a CMOS-microfluidic system that is capable of 1) pumping bulk electrolyte fluid with AC electro-osmosis, 2) cell manipulation and separation with dielectrophoresis (DEP), 3) label-free biomolecular and cell sensing, classification with dedicated 16-element impedance spectroscopy receivers. While we demonstrate these kernel functionalities in a multichip module/microfluidic interface (Fig. 18.2.1), the overall architecture, fluidics and sensing components can be massively scaled up for various POC applications due to elimination of pressure-driven flows (Fig. 18.2.1).