Dataset Information

Magnet Patterned Superparamagnetic Fe3 O4 /Au Core-Shell Nanoplasmonic Sensing Array for Label-Free High Throughput Cytokine Immunoassay.

ABSTRACT: Rapid and accurate immune monitoring plays a decisive role in effectively treating immune-related diseases especially at point-of-care, where an immediate decision on treatment is needed upon precise determination of the patient immune status. Derived from the emerging clinical demands, there is an urgent need for a cytokine immunoassay that offers unprecedented sensor performance with high sensitivity, throughput, and multiplexing capability, as well as short turnaround time at low system complexity, manufacturability, and scalability. In this paper, a label-free, high throughput cytokine immunoassay based on a magnet patterned Fe3 O4 /Au core-shell nanoparticle (FACSNP) sensing array is developed. By exploiting the unique superparamagnetic and plasmonic properties of the core-shell nanomaterials, a facile microarray patterning technique is established that allows the fabrication of a uniform, self-assembled microarray on a large surface area with remarkable tunability and scalability. The sensing performance of the FACSNP microarray is validated by real-time detection of four cytokines in complex biological samples, showing high sensitivity (?20 pg mL-1 ), selectivity and throughput with excellent statistical accuracy. The developed immunoassay is successfully applied for rapid determination of the functional immunophenotype of leukemia tumor-associated macrophages, manifesting its potential clinical applications for real-time immune monitoring, early cancer detection, and therapeutic drug stratification toward personalized medicine.

SUBMITTER: Cai Y

PROVIDER: S-EPMC6486820 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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Magnet Patterned Superparamagnetic Fe<sub>3</sub> O<sub>4</sub> /Au Core-Shell Nanoplasmonic Sensing Array for Label-Free High Throughput Cytokine Immunoassay.

Cai Yuxin Y Zhu Jingyi J He Jiacheng J Yang Wen W Ma Chao C Xiong Feng F Li Feng F Chen Weiqiang W Chen Pengyu P

Advanced healthcare materials 20190115 4

Rapid and accurate immune monitoring plays a decisive role in effectively treating immune-related diseases especially at point-of-care, where an immediate decision on treatment is needed upon precise determination of the patient immune status. Derived from the emerging clinical demands, there is an urgent need for a cytokine immunoassay that offers unprecedented sensor performance with high sensitivity, throughput, and multiplexing capability, as well as short turnaround time at low system compl ...[more]

PMID: 30645037

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Project description:Herein, we report on developing a facile synthetic route for reusable nanocatalysts based on a combination of the supermagnetic properties of magnetite with the unique optical and catalytic properties of noble metal hybrid nanomaterials. We compare two different synthetic methods, to find out which is best from synthetic and application points of view, for the synthesis of Fe3O4 and Fe3O4@M (M = Ag or Au) core-shell hybrid nanostructures. The two different single-step synthetic methods are: thermal decomposition and hydrothermal. The structural, morphological and magnetic properties of the obtained Fe3O4 and Fe3O4@M nanoparticles were characterized by various techniques. XRD of the Fe3O4 nanoparticles exhibited sharp and strong diffraction peaks, confirming the highly crystalline structure of the Fe3O4 particles synthesized by the hydrothermal method, while broad and weak peaks were observed on using the thermal decomposition method. Both Fe3O4@Ag and Fe3O4@Au core-shells obtained by the hydrothermal method showed the reflection planes of Fe3O4 and additional planes of Ag or Au. But on the formation of Fe3O4@Ag/Au by the thermal decomposition method the peak for Fe3O4 disappeared and only the diffraction peaks of Ag or Au appeared. According to TEM analysis there was a broad particle-size distribution, random near-spherical shapes and slight particle agglomeration for Fe3O4 synthesized by the thermal decomposition method. However, there was a moderate size distribution, spherical shapes and well-dispersed particles without large aggregations for the hydrothermal method. TEM images of the synthesized nanoparticles by the two methods used showed a pronounced difference in both size and morphological shape. The catalytic performance of the synthesized nanoparticles was examined for the reduction of Congo red dye in the presence of NaBH4. The Fe3O4 nanocatalyst maintained its catalytic activity for only one cycle. In the cases of Fe3O4@Au and Fe3O4@Ag, the catalytic activity was conserved for four and ten successive cycles, respectively. Based on the obtained results, it was concluded that the hydrothermal synthesis of Fe3O4, Fe3O4@Ag and Fe3O4@Au nanostructures is highly recommended due to their selectivity and merits.

Project description:Precise monitoring of the rapidly changing immune status during the course of a disease requires multiplex analysis of cytokines from frequently sampled human blood. However, the current lack of rapid, multiplex, and low volume assays makes immune monitoring for clinical decision-making (e.g., critically ill patients) impractical. Without such assays, immune monitoring is even virtually impossible for infants and neonates with infectious diseases and/or immune mediated disorders as access to their blood in large quantities is prohibited. Localized surface plasmon resonance (LSPR)-based microfluidic optical biosensing is a promising approach to fill this technical gap as it could potentially permit real-time refractometric detection of biomolecular binding on a metallic nanoparticle surface and sensor miniaturization, both leading to rapid and sample-sparing analyte analysis. Despite this promise, practical implementation of such a microfluidic assay for cytokine biomarker detection in serum samples has not been established primarily due to the limited sensitivity of LSPR biosensing. Here, we developed a high-throughput, label-free, multiarrayed LSPR optical biosensor device with 480 nanoplasmonic sensing spots in microfluidic channel arrays and demonstrated parallel multiplex immunoassays of six cytokines in a complex serum matrix on a single device chip while overcoming technical limitations. The device was fabricated using easy-to-implement, one-step microfluidic patterning and antibody conjugation of gold nanorods (AuNRs). When scanning the scattering light intensity across the microarrays of AuNR ensembles with dark-field imaging optics, our LSPR biosensing technique allowed for high-sensitivity quantitative cytokine measurements at concentrations down to 5-20 pg/mL from a 1 ?L serum sample. Using the nanoplasmonic biosensor microarray device, we demonstrated the ability to monitor the inflammatory responses of infants following cardiopulmonary bypass (CPB) surgery through tracking the time-course variations of their serum cytokines. The whole parallel on-chip assays, which involved the loading, incubation, and washing of samples and reagents, and 10-fold replicated multianalyte detection for each sample using the entire biosensor arrays, were completed within 40 min.

Dataset Information

Magnet Patterned Superparamagnetic Fe3 O4 /Au Core-Shell Nanoplasmonic Sensing Array for Label-Free High Throughput Cytokine Immunoassay.

Publications

Magnet Patterned Superparamagnetic Fe<sub>3</sub> O<sub>4</sub> /Au Core-Shell Nanoplasmonic Sensing Array for Label-Free High Throughput Cytokine Immunoassay.

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