Mostafa Kamal Masud, Daigo Natsuhara, Yuchen Dai, Javeria Bashir, Asep Sugih Nugraha, Saad M. Alshehri, Yoshio Bando, Md. Shahriar Hossain, Yusuf Valentino Kaneti, Takayuki Shibata and Yusuke Yamauchi
{"title":"用于检测传染病的基于介孔金的等离子体 SERS 微流控平台†。","authors":"Mostafa Kamal Masud, Daigo Natsuhara, Yuchen Dai, Javeria Bashir, Asep Sugih Nugraha, Saad M. Alshehri, Yoshio Bando, Md. Shahriar Hossain, Yusuf Valentino Kaneti, Takayuki Shibata and Yusuke Yamauchi","doi":"10.1039/D4TC01638F","DOIUrl":null,"url":null,"abstract":"<p >Infectious diseases, particularly those caused by pathogens and parasites, present significant global health challenges. Despite advancements in medicine, these diseases continue to result in high rates of illness, loss of function, and mortality. The continuous COVID-19 pandemic, stemming from the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), highlights the critical necessity for early detection strategies to improve patient outcomes. We present a novel microfluidics platform for the simultaneous detection of proteins (antigens) crucial for SARS-CoV-2 identification: S1, RBD, and NCD. By combining microfluidics with surface-enhanced Raman scattering (SERS), the platform enables highly sensitive and multiplexed detection of viral proteins. Furthermore, it employs an engineered mesoporous gold nanoparticle (mAuNP)-based SERS nanotags to achieve a highly sensitive readout. Demonstrating excellent analytical performance, our platform simultaneously detects three antigens, achieving detection levels as low as 14 pg mL<small><sup>−1</sup></small>, with an RSD of <5.0% (<em>n</em> = 3). Compared to existing approaches, our platform offers critical improvements for SARS-CoV-2-like infectious disease analysis. It provides a multiplex detection system alongside controls, a simple experimental setup, and a single-device-based complete assay platform. The mAuNP-based SERS nanotags eliminate the need for enzymatic amplification, while the portable SERS readout facilitates an on-site detection without sophisticated instrumentation or laboratory requirements.</p>","PeriodicalId":84,"journal":{"name":"Journal of Materials Chemistry C","volume":" 44","pages":" 17977-17985"},"PeriodicalIF":5.1000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A plasmonic mesoporous gold-based SERS-microfluidic platform for the detection of infectious diseases†\",\"authors\":\"Mostafa Kamal Masud, Daigo Natsuhara, Yuchen Dai, Javeria Bashir, Asep Sugih Nugraha, Saad M. Alshehri, Yoshio Bando, Md. 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A plasmonic mesoporous gold-based SERS-microfluidic platform for the detection of infectious diseases†
Infectious diseases, particularly those caused by pathogens and parasites, present significant global health challenges. Despite advancements in medicine, these diseases continue to result in high rates of illness, loss of function, and mortality. The continuous COVID-19 pandemic, stemming from the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), highlights the critical necessity for early detection strategies to improve patient outcomes. We present a novel microfluidics platform for the simultaneous detection of proteins (antigens) crucial for SARS-CoV-2 identification: S1, RBD, and NCD. By combining microfluidics with surface-enhanced Raman scattering (SERS), the platform enables highly sensitive and multiplexed detection of viral proteins. Furthermore, it employs an engineered mesoporous gold nanoparticle (mAuNP)-based SERS nanotags to achieve a highly sensitive readout. Demonstrating excellent analytical performance, our platform simultaneously detects three antigens, achieving detection levels as low as 14 pg mL−1, with an RSD of <5.0% (n = 3). Compared to existing approaches, our platform offers critical improvements for SARS-CoV-2-like infectious disease analysis. It provides a multiplex detection system alongside controls, a simple experimental setup, and a single-device-based complete assay platform. The mAuNP-based SERS nanotags eliminate the need for enzymatic amplification, while the portable SERS readout facilitates an on-site detection without sophisticated instrumentation or laboratory requirements.
期刊介绍:
The Journal of Materials Chemistry is divided into three distinct sections, A, B, and C, each catering to specific applications of the materials under study:
Journal of Materials Chemistry A focuses primarily on materials intended for applications in energy and sustainability.
Journal of Materials Chemistry B specializes in materials designed for applications in biology and medicine.
Journal of Materials Chemistry C is dedicated to materials suitable for applications in optical, magnetic, and electronic devices.
Example topic areas within the scope of Journal of Materials Chemistry C are listed below. This list is neither exhaustive nor exclusive.
Bioelectronics
Conductors
Detectors
Dielectrics
Displays
Ferroelectrics
Lasers
LEDs
Lighting
Liquid crystals
Memory
Metamaterials
Multiferroics
Photonics
Photovoltaics
Semiconductors
Sensors
Single molecule conductors
Spintronics
Superconductors
Thermoelectrics
Topological insulators
Transistors