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  5. Targeting and Enrichment of Viral Pathogen by Cell Membrane Cloaked Magnetic Nanoparticles for Enhanced Detection.
 
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Targeting and Enrichment of Viral Pathogen by Cell Membrane Cloaked Magnetic Nanoparticles for Enhanced Detection.

Journal
ACS applied materials & interfaces
Date Issued
2017
Author(s)
HUI-WEN CHEN  
Fang, Zih-Syun
Chen, You-Ting
Chen, Yuan-I
Yao, Bing-Yu
Cheng, Ju-Yun
Chien, Chen-Ying
Chang, Yuan-Chih
Hu, Che-Ming J.
DOI
10.1021/acsami.7b09931
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/404849
https://www.scopus.com/record/display.uri?eid=2-s2.0-85034958341&origin=resultslist
Abstract
Attachment to cellular surfaces is a major attribute among infectious pathogens for initiating disease pathogenesis. In viral infections, viruses exploit receptor-ligand interactions to latch onto cellular exterior prior to subsequent entry and invasion. In light of the selective binding affinity between viral pathogens and cells, nanoparticles cloaked in cellular membranes are herein employed for virus targeting. Using the influenza virus as a model, erythrocyte membrane cloaked nanoparticles are prepared and modified with magnetic functionalities (RBC-mNP) for virus targeting and isolation. To maximize targeting and isolation efficiency, density gradient centrifugation and nanoparticle tracking analysis were applied to minimize the presence of uncoated particles and membrane vesicles. The resulting nanoparticles possess a distinctive membrane corona, a sialylated surface, and form colloidally stable clusters with influenza viruses. Magnetic functionality is bestowed to the nanoparticles through encapsulation of superparamagnetic iron-oxide particles, which enable influenza virus enrichment via magnetic extraction. Viral samples enriched by the RBC-mNPs result in significantly enhanced virus detection by multiple virus quantification methods, including qRT-PCR, immunnochromatographic strip test, and cell-based titering assays. The demonstration of pathogen targeting and isolation by RBC-mNPs highlights a biologically inspired approach toward improved treatment and diagnosis against infectious disease threats. The work also sheds light on the efficient membrane cloaking mechanism that bestows nanoparticles with cell mimicking functionalities. ? 2017 American Chemical Society.
Subjects
cell membrane cloaked nanoparticles; host-pathogen interaction; influenza virus; membrane corona; superparamagnetic iron oxide nanoparticles
SDGs

[SDGs]SDG3

Other Subjects
Binding energy; Cell membranes; Cells; Computer viruses; Cytology; Diagnosis; Diseases; Iron oxides; Magnetism; Membranes; Nanoparticles; Pathogens; Superparamagnetism; Viruses; Density gradient centrifugation; Host-pathogen interactions; Influenza virus; Magnetic nano-particles; Nanoparticle tracking analysis; Receptor-ligand interactions; Superparamagnetic iron oxide nanoparticles; Superparamagnetic iron oxides; Nanomagnetics; magnetite nanoparticle; erythrocyte membrane; magnetism; Erythrocyte Membrane; Magnetics; Magnetite Nanoparticles
Type
journal article

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To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

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