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ctcs captured with 25 times more than traditional cell search systems  (CellSearch inc)

 
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    Structured Review

    CellSearch inc ctcs captured with 25 times more than traditional cell search systems
    Label-dependent <t> microfluidic </t> methods for <t> CTCs </t> isolation.
    Ctcs Captured With 25 Times More Than Traditional Cell Search Systems, supplied by CellSearch inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ctcs captured with 25 times more than traditional cell search systems/product/CellSearch inc
    Average 90 stars, based on 1 article reviews
    ctcs captured with 25 times more than traditional cell search systems - by Bioz Stars, 2026-05
    90/100 stars

    Images

    1) Product Images from "Novel Isolating Approaches to Circulating Tumor Cell Enrichment Based on Microfluidics: A Review"

    Article Title: Novel Isolating Approaches to Circulating Tumor Cell Enrichment Based on Microfluidics: A Review

    Journal: Micromachines

    doi: 10.3390/mi15060706

    Label-dependent  microfluidic  methods for  CTCs  isolation.
    Figure Legend Snippet: Label-dependent microfluidic methods for CTCs isolation.

    Techniques Used: Isolation, Generated, Adsorption, High Throughput Screening Assay, Activity Assay, Filtration, Magnetic Beads, Immunofluorescence, Immunostaining

    Typical immunocapture microfluidic device. ( A ) Using aptamer cocktail to enrich CTCs in patients with lung cancer; reproduced from Reference , with a permission from Small . ( B ) Herringbone microfluidic probe. (a) The schematic shows the working process of HB-MFP, in which blood is injected through the central aperture and exits through the peripheral aperture. (b) The tip surface of 3D-printed HB-MFP. (c,d) Specifically showing the surface structure in (b); reproduced from Reference , with permission from Advanced Materials Technologies . ( C ) Scheme shows the structural composition and working principle of the Ap Octopus Chip. The chip captures CTCs, using the synergistic manner of multivalent aptamers formed by AuNP-SYL3C and a triangular DLD array design. In the sequencing curves, green, red, blue and black represent adenine (A), thymine (T), cytosine (C) and guanine (G); respectively; reproduced from Reference , with permission from Angewandte Chemie International Edition . ( D ) The process of capturing CTCs using aptamer modified AuNP surfaces; reproduced from Reference , with permission from ACS Nano .
    Figure Legend Snippet: Typical immunocapture microfluidic device. ( A ) Using aptamer cocktail to enrich CTCs in patients with lung cancer; reproduced from Reference , with a permission from Small . ( B ) Herringbone microfluidic probe. (a) The schematic shows the working process of HB-MFP, in which blood is injected through the central aperture and exits through the peripheral aperture. (b) The tip surface of 3D-printed HB-MFP. (c,d) Specifically showing the surface structure in (b); reproduced from Reference , with permission from Advanced Materials Technologies . ( C ) Scheme shows the structural composition and working principle of the Ap Octopus Chip. The chip captures CTCs, using the synergistic manner of multivalent aptamers formed by AuNP-SYL3C and a triangular DLD array design. In the sequencing curves, green, red, blue and black represent adenine (A), thymine (T), cytosine (C) and guanine (G); respectively; reproduced from Reference , with permission from Angewandte Chemie International Edition . ( D ) The process of capturing CTCs using aptamer modified AuNP surfaces; reproduced from Reference , with permission from ACS Nano .

    Techniques Used: Injection, Sequencing, Modification

    Label-independent  microfluidic  methods for  CTCs  isolation.
    Figure Legend Snippet: Label-independent microfluidic methods for CTCs isolation.

    Techniques Used: Isolation, High Throughput Screening Assay, Shear, Sample Prep

    ( A ) Schematic illustration of the double spiral microchannel to achieve cell focusing. The diagram is labeled with the inlets, outlets, and the direction of flow. The numbers 1, 2, 3 represent the flow state of cells in three different positions of the microchannel; reproduced from Reference , with permission from Frontiers in Bioengineering and Biotechnology . ( B ) Schematic illustration of the working principle of the CEA microchannel; reproduced from Reference , with permission from Analytical Chemistry . ( C ) Isolation of CTCs by a serpentine microchannel; reproduced from Reference , with permission from Micro and Nano Engineering . ( D ) Schematic illustration of the microfluidic device and working principle of inertial migration in microfluidic channel; reproduced from Reference , with permission from Microsystems & Nanoengineering . ( E ) Schematic illustration of p-MOFF device. (a) Working principle diagram. (b) Microfiltration microscopy images; reproduced from Reference , with permission from Biosensors and Bioelectronics .
    Figure Legend Snippet: ( A ) Schematic illustration of the double spiral microchannel to achieve cell focusing. The diagram is labeled with the inlets, outlets, and the direction of flow. The numbers 1, 2, 3 represent the flow state of cells in three different positions of the microchannel; reproduced from Reference , with permission from Frontiers in Bioengineering and Biotechnology . ( B ) Schematic illustration of the working principle of the CEA microchannel; reproduced from Reference , with permission from Analytical Chemistry . ( C ) Isolation of CTCs by a serpentine microchannel; reproduced from Reference , with permission from Micro and Nano Engineering . ( D ) Schematic illustration of the microfluidic device and working principle of inertial migration in microfluidic channel; reproduced from Reference , with permission from Microsystems & Nanoengineering . ( E ) Schematic illustration of p-MOFF device. (a) Working principle diagram. (b) Microfiltration microscopy images; reproduced from Reference , with permission from Biosensors and Bioelectronics .

    Techniques Used: Labeling, Isolation, Migration, Microscopy

    ( A ) Schematic illustration of the working principle of integrated microfluidic device. The device consists of two parts. The Vortex HT Chip can achieve high-throughput enrichment of CTCs, and the impedance chip can count the collected CTCs; reproduced from Reference , with permission from Cytometry Part A . ( B ) Schematic illustration of the working principle of the orthogonal vortex chip. Schematic diagram of the working principle of the vortex chip with orthogonal reversal. Enrichment of CTCs by using the generated orthogonal vortex and Dean drag force; reproduced from Reference , with permission from Analytica Chimica Acta . ( C ) TO DLD Chip Device Isolation CTCs. (a) The schematic illustration of the wide TO DLD chip. (b) The PDMS microchannel in TO DLD chip; reproduced from Reference , with permission from the Journal of Chromatography A . ( D ) Integrated Microfluidic Chip for isolation of CTCs. (a) Schematic illustration of the microfluidic chip. (b) Working schematic diagram for separating CTCs according to size inside a microchannel. (c,d) Triangular DLD arrays within the microfluidic channel for separating cells of different sizes. Cancer cells (yellow), red blood cells (red), and white blood cells (white); reproduced from Reference , with permission from Advanced Biosystems .
    Figure Legend Snippet: ( A ) Schematic illustration of the working principle of integrated microfluidic device. The device consists of two parts. The Vortex HT Chip can achieve high-throughput enrichment of CTCs, and the impedance chip can count the collected CTCs; reproduced from Reference , with permission from Cytometry Part A . ( B ) Schematic illustration of the working principle of the orthogonal vortex chip. Schematic diagram of the working principle of the vortex chip with orthogonal reversal. Enrichment of CTCs by using the generated orthogonal vortex and Dean drag force; reproduced from Reference , with permission from Analytica Chimica Acta . ( C ) TO DLD Chip Device Isolation CTCs. (a) The schematic illustration of the wide TO DLD chip. (b) The PDMS microchannel in TO DLD chip; reproduced from Reference , with permission from the Journal of Chromatography A . ( D ) Integrated Microfluidic Chip for isolation of CTCs. (a) Schematic illustration of the microfluidic chip. (b) Working schematic diagram for separating CTCs according to size inside a microchannel. (c,d) Triangular DLD arrays within the microfluidic channel for separating cells of different sizes. Cancer cells (yellow), red blood cells (red), and white blood cells (white); reproduced from Reference , with permission from Advanced Biosystems .

    Techniques Used: High Throughput Screening Assay, Cytometry, Generated, Isolation, Chromatography

    ( A ) The high-throughput taSSAW device for CTCs isolation. (a) Illustration of cell isolation in the taSSAW device. (b) Schematic illustration of the principle of taSSAW-based cell isolation. (c) Actual size image of the tasSAW cell isolation device; reproduced from Reference , with permission from the Proceedings of the National Academy of Sciences . ( B ) Schematic illustration of an ultra-compact acoustofluidic device based on np-TSAW for enrichment of CTCs; reproduced from Reference , with permission from Analytica Chimica Acta . ( C ) Schematic illustration of CTCs isolation based on multi-stage surface acoustic waves; reproduced from Reference , with permission from Sensors and Actuators B: Chemical . ( D ) Microfluidic system based on optically induced dielectrophoretic (ODEP); reproduced from Reference , with permission from Scientific Reports . ( E ) Schematic illustration of a microdevice based on LFFF-DEP; reproduced from Reference , with permission from the Journal of Chromatography B . ( F ) Microfluidic device for impedance detection and dielectrophoresis integration. (a) Structural diagram of the device. (b) Cell Flow and DEP trapping. (c) Identification of target cells by impedance; reproduced from Reference , with permission from Biosensors and Bioelectronics .
    Figure Legend Snippet: ( A ) The high-throughput taSSAW device for CTCs isolation. (a) Illustration of cell isolation in the taSSAW device. (b) Schematic illustration of the principle of taSSAW-based cell isolation. (c) Actual size image of the tasSAW cell isolation device; reproduced from Reference , with permission from the Proceedings of the National Academy of Sciences . ( B ) Schematic illustration of an ultra-compact acoustofluidic device based on np-TSAW for enrichment of CTCs; reproduced from Reference , with permission from Analytica Chimica Acta . ( C ) Schematic illustration of CTCs isolation based on multi-stage surface acoustic waves; reproduced from Reference , with permission from Sensors and Actuators B: Chemical . ( D ) Microfluidic system based on optically induced dielectrophoretic (ODEP); reproduced from Reference , with permission from Scientific Reports . ( E ) Schematic illustration of a microdevice based on LFFF-DEP; reproduced from Reference , with permission from the Journal of Chromatography B . ( F ) Microfluidic device for impedance detection and dielectrophoresis integration. (a) Structural diagram of the device. (b) Cell Flow and DEP trapping. (c) Identification of target cells by impedance; reproduced from Reference , with permission from Biosensors and Bioelectronics .

    Techniques Used: High Throughput Screening Assay, Isolation, Cell Isolation, Chromatography

    ( A ) Negative enrichment of CTCs based on GASI-ship; reproduced from Reference , with permission from Analytical Chemistry . ( B ) Monolithic chip for isolation of CTCs; reproduced from Reference , with permission from Scientific Reports . ( C ) Immunomagnetic negative enrichment coupled with flow cytometry to isolate CTCs; reproduced from Reference , with permission from Cancer . ( D ) Microfluidic Cell Concentrator for Negative Enrichment of CTCs. (a) 3D schematic diagram of the device. (b) CTCs collection process; reproduced from Reference , with permission from Methods . ( E ) μ-MixMACS chip. (a) Schematic illustration of the structure of the chip. (b) Illustration of the working principle of this chip to capture CTCs; reproduced from Reference , with permission from Sensors and Actuators B: Chemical . ( F ) Two-stage microfluidic chip. (a) Leukocyte-depleted μ-MACS chips. (b) Illustration of GASI chip; reproduced from Reference , with permission from Biosensors and Bioelectronics .
    Figure Legend Snippet: ( A ) Negative enrichment of CTCs based on GASI-ship; reproduced from Reference , with permission from Analytical Chemistry . ( B ) Monolithic chip for isolation of CTCs; reproduced from Reference , with permission from Scientific Reports . ( C ) Immunomagnetic negative enrichment coupled with flow cytometry to isolate CTCs; reproduced from Reference , with permission from Cancer . ( D ) Microfluidic Cell Concentrator for Negative Enrichment of CTCs. (a) 3D schematic diagram of the device. (b) CTCs collection process; reproduced from Reference , with permission from Methods . ( E ) μ-MixMACS chip. (a) Schematic illustration of the structure of the chip. (b) Illustration of the working principle of this chip to capture CTCs; reproduced from Reference , with permission from Sensors and Actuators B: Chemical . ( F ) Two-stage microfluidic chip. (a) Leukocyte-depleted μ-MACS chips. (b) Illustration of GASI chip; reproduced from Reference , with permission from Biosensors and Bioelectronics .

    Techniques Used: Isolation, Flow Cytometry

    ( A ) Schematic illustration of microfluidic single-cell capture principle; reproduced from Reference , with permission from Scientific Reports . ( B ) Single-cell RNA sequencing of CTCs using Hydro-Seq.; reproduced from Reference , with permission from Nature Communications . ( C ) Schematic illustration of the working principle of capturing and releasing single CTCs based on the photoelectrochemical platform; reproduced from Reference , with permission from Nature Communications . ( D ) Schematic of an integrated microvalve chip capable of capturing at the single-cell level; reproduced from Reference , with permission from Talanta . ( E ) Schematic illustration of pipette working principle based on microfluidic cell isolation technology; reproduced from Reference , with permission from Scientific Reports . ( F ) Working principle of hand-held and integrated single-cell pipettes; reproduced from Reference , with permission from the Journal of the American Chemical Society . ( G ) Single-cell isolation device based on lateral magnetophoretic isolation and microfluidic dispensing; reproduced from Reference , with permission from Analytical Chemistry .
    Figure Legend Snippet: ( A ) Schematic illustration of microfluidic single-cell capture principle; reproduced from Reference , with permission from Scientific Reports . ( B ) Single-cell RNA sequencing of CTCs using Hydro-Seq.; reproduced from Reference , with permission from Nature Communications . ( C ) Schematic illustration of the working principle of capturing and releasing single CTCs based on the photoelectrochemical platform; reproduced from Reference , with permission from Nature Communications . ( D ) Schematic of an integrated microvalve chip capable of capturing at the single-cell level; reproduced from Reference , with permission from Talanta . ( E ) Schematic illustration of pipette working principle based on microfluidic cell isolation technology; reproduced from Reference , with permission from Scientific Reports . ( F ) Working principle of hand-held and integrated single-cell pipettes; reproduced from Reference , with permission from the Journal of the American Chemical Society . ( G ) Single-cell isolation device based on lateral magnetophoretic isolation and microfluidic dispensing; reproduced from Reference , with permission from Analytical Chemistry .

    Techniques Used: RNA Sequencing, Transferring, Cell Isolation, Single-cell Isolation, Isolation

    Clinical applications of  CTCs  in cancer.
    Figure Legend Snippet: Clinical applications of CTCs in cancer.

    Techniques Used: Immunostaining, Clinical Proteomics, Immunofluorescence, Staining, Expressing, Flow Cytometry



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    CellSearch inc ctcs captured with 25 times more than traditional cell search systems
    Label-dependent <t> microfluidic </t> methods for <t> CTCs </t> isolation.
    Ctcs Captured With 25 Times More Than Traditional Cell Search Systems, supplied by CellSearch inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ctcs captured with 25 times more than traditional cell search systems/product/CellSearch inc
    Average 90 stars, based on 1 article reviews
    ctcs captured with 25 times more than traditional cell search systems - by Bioz Stars, 2026-05
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    Label-dependent  microfluidic  methods for  CTCs  isolation.

    Journal: Micromachines

    Article Title: Novel Isolating Approaches to Circulating Tumor Cell Enrichment Based on Microfluidics: A Review

    doi: 10.3390/mi15060706

    Figure Lengend Snippet: Label-dependent microfluidic methods for CTCs isolation.

    Article Snippet: , , Microfluidic ratchet mechanism , CTCs captured with 25 times more than traditional Cell Search systems. , Relatively low throughput. , UM-UC-13 , 1 , >90% , [ ] .

    Techniques: Isolation, Generated, Adsorption, High Throughput Screening Assay, Activity Assay, Filtration, Magnetic Beads, Immunofluorescence, Immunostaining

    Typical immunocapture microfluidic device. ( A ) Using aptamer cocktail to enrich CTCs in patients with lung cancer; reproduced from Reference , with a permission from Small . ( B ) Herringbone microfluidic probe. (a) The schematic shows the working process of HB-MFP, in which blood is injected through the central aperture and exits through the peripheral aperture. (b) The tip surface of 3D-printed HB-MFP. (c,d) Specifically showing the surface structure in (b); reproduced from Reference , with permission from Advanced Materials Technologies . ( C ) Scheme shows the structural composition and working principle of the Ap Octopus Chip. The chip captures CTCs, using the synergistic manner of multivalent aptamers formed by AuNP-SYL3C and a triangular DLD array design. In the sequencing curves, green, red, blue and black represent adenine (A), thymine (T), cytosine (C) and guanine (G); respectively; reproduced from Reference , with permission from Angewandte Chemie International Edition . ( D ) The process of capturing CTCs using aptamer modified AuNP surfaces; reproduced from Reference , with permission from ACS Nano .

    Journal: Micromachines

    Article Title: Novel Isolating Approaches to Circulating Tumor Cell Enrichment Based on Microfluidics: A Review

    doi: 10.3390/mi15060706

    Figure Lengend Snippet: Typical immunocapture microfluidic device. ( A ) Using aptamer cocktail to enrich CTCs in patients with lung cancer; reproduced from Reference , with a permission from Small . ( B ) Herringbone microfluidic probe. (a) The schematic shows the working process of HB-MFP, in which blood is injected through the central aperture and exits through the peripheral aperture. (b) The tip surface of 3D-printed HB-MFP. (c,d) Specifically showing the surface structure in (b); reproduced from Reference , with permission from Advanced Materials Technologies . ( C ) Scheme shows the structural composition and working principle of the Ap Octopus Chip. The chip captures CTCs, using the synergistic manner of multivalent aptamers formed by AuNP-SYL3C and a triangular DLD array design. In the sequencing curves, green, red, blue and black represent adenine (A), thymine (T), cytosine (C) and guanine (G); respectively; reproduced from Reference , with permission from Angewandte Chemie International Edition . ( D ) The process of capturing CTCs using aptamer modified AuNP surfaces; reproduced from Reference , with permission from ACS Nano .

    Article Snippet: , , Microfluidic ratchet mechanism , CTCs captured with 25 times more than traditional Cell Search systems. , Relatively low throughput. , UM-UC-13 , 1 , >90% , [ ] .

    Techniques: Injection, Sequencing, Modification

    Label-independent  microfluidic  methods for  CTCs  isolation.

    Journal: Micromachines

    Article Title: Novel Isolating Approaches to Circulating Tumor Cell Enrichment Based on Microfluidics: A Review

    doi: 10.3390/mi15060706

    Figure Lengend Snippet: Label-independent microfluidic methods for CTCs isolation.

    Article Snippet: , , Microfluidic ratchet mechanism , CTCs captured with 25 times more than traditional Cell Search systems. , Relatively low throughput. , UM-UC-13 , 1 , >90% , [ ] .

    Techniques: Isolation, High Throughput Screening Assay, Shear, Sample Prep

    ( A ) Schematic illustration of the double spiral microchannel to achieve cell focusing. The diagram is labeled with the inlets, outlets, and the direction of flow. The numbers 1, 2, 3 represent the flow state of cells in three different positions of the microchannel; reproduced from Reference , with permission from Frontiers in Bioengineering and Biotechnology . ( B ) Schematic illustration of the working principle of the CEA microchannel; reproduced from Reference , with permission from Analytical Chemistry . ( C ) Isolation of CTCs by a serpentine microchannel; reproduced from Reference , with permission from Micro and Nano Engineering . ( D ) Schematic illustration of the microfluidic device and working principle of inertial migration in microfluidic channel; reproduced from Reference , with permission from Microsystems & Nanoengineering . ( E ) Schematic illustration of p-MOFF device. (a) Working principle diagram. (b) Microfiltration microscopy images; reproduced from Reference , with permission from Biosensors and Bioelectronics .

    Journal: Micromachines

    Article Title: Novel Isolating Approaches to Circulating Tumor Cell Enrichment Based on Microfluidics: A Review

    doi: 10.3390/mi15060706

    Figure Lengend Snippet: ( A ) Schematic illustration of the double spiral microchannel to achieve cell focusing. The diagram is labeled with the inlets, outlets, and the direction of flow. The numbers 1, 2, 3 represent the flow state of cells in three different positions of the microchannel; reproduced from Reference , with permission from Frontiers in Bioengineering and Biotechnology . ( B ) Schematic illustration of the working principle of the CEA microchannel; reproduced from Reference , with permission from Analytical Chemistry . ( C ) Isolation of CTCs by a serpentine microchannel; reproduced from Reference , with permission from Micro and Nano Engineering . ( D ) Schematic illustration of the microfluidic device and working principle of inertial migration in microfluidic channel; reproduced from Reference , with permission from Microsystems & Nanoengineering . ( E ) Schematic illustration of p-MOFF device. (a) Working principle diagram. (b) Microfiltration microscopy images; reproduced from Reference , with permission from Biosensors and Bioelectronics .

    Article Snippet: , , Microfluidic ratchet mechanism , CTCs captured with 25 times more than traditional Cell Search systems. , Relatively low throughput. , UM-UC-13 , 1 , >90% , [ ] .

    Techniques: Labeling, Isolation, Migration, Microscopy

    ( A ) Schematic illustration of the working principle of integrated microfluidic device. The device consists of two parts. The Vortex HT Chip can achieve high-throughput enrichment of CTCs, and the impedance chip can count the collected CTCs; reproduced from Reference , with permission from Cytometry Part A . ( B ) Schematic illustration of the working principle of the orthogonal vortex chip. Schematic diagram of the working principle of the vortex chip with orthogonal reversal. Enrichment of CTCs by using the generated orthogonal vortex and Dean drag force; reproduced from Reference , with permission from Analytica Chimica Acta . ( C ) TO DLD Chip Device Isolation CTCs. (a) The schematic illustration of the wide TO DLD chip. (b) The PDMS microchannel in TO DLD chip; reproduced from Reference , with permission from the Journal of Chromatography A . ( D ) Integrated Microfluidic Chip for isolation of CTCs. (a) Schematic illustration of the microfluidic chip. (b) Working schematic diagram for separating CTCs according to size inside a microchannel. (c,d) Triangular DLD arrays within the microfluidic channel for separating cells of different sizes. Cancer cells (yellow), red blood cells (red), and white blood cells (white); reproduced from Reference , with permission from Advanced Biosystems .

    Journal: Micromachines

    Article Title: Novel Isolating Approaches to Circulating Tumor Cell Enrichment Based on Microfluidics: A Review

    doi: 10.3390/mi15060706

    Figure Lengend Snippet: ( A ) Schematic illustration of the working principle of integrated microfluidic device. The device consists of two parts. The Vortex HT Chip can achieve high-throughput enrichment of CTCs, and the impedance chip can count the collected CTCs; reproduced from Reference , with permission from Cytometry Part A . ( B ) Schematic illustration of the working principle of the orthogonal vortex chip. Schematic diagram of the working principle of the vortex chip with orthogonal reversal. Enrichment of CTCs by using the generated orthogonal vortex and Dean drag force; reproduced from Reference , with permission from Analytica Chimica Acta . ( C ) TO DLD Chip Device Isolation CTCs. (a) The schematic illustration of the wide TO DLD chip. (b) The PDMS microchannel in TO DLD chip; reproduced from Reference , with permission from the Journal of Chromatography A . ( D ) Integrated Microfluidic Chip for isolation of CTCs. (a) Schematic illustration of the microfluidic chip. (b) Working schematic diagram for separating CTCs according to size inside a microchannel. (c,d) Triangular DLD arrays within the microfluidic channel for separating cells of different sizes. Cancer cells (yellow), red blood cells (red), and white blood cells (white); reproduced from Reference , with permission from Advanced Biosystems .

    Article Snippet: , , Microfluidic ratchet mechanism , CTCs captured with 25 times more than traditional Cell Search systems. , Relatively low throughput. , UM-UC-13 , 1 , >90% , [ ] .

    Techniques: High Throughput Screening Assay, Cytometry, Generated, Isolation, Chromatography

    ( A ) The high-throughput taSSAW device for CTCs isolation. (a) Illustration of cell isolation in the taSSAW device. (b) Schematic illustration of the principle of taSSAW-based cell isolation. (c) Actual size image of the tasSAW cell isolation device; reproduced from Reference , with permission from the Proceedings of the National Academy of Sciences . ( B ) Schematic illustration of an ultra-compact acoustofluidic device based on np-TSAW for enrichment of CTCs; reproduced from Reference , with permission from Analytica Chimica Acta . ( C ) Schematic illustration of CTCs isolation based on multi-stage surface acoustic waves; reproduced from Reference , with permission from Sensors and Actuators B: Chemical . ( D ) Microfluidic system based on optically induced dielectrophoretic (ODEP); reproduced from Reference , with permission from Scientific Reports . ( E ) Schematic illustration of a microdevice based on LFFF-DEP; reproduced from Reference , with permission from the Journal of Chromatography B . ( F ) Microfluidic device for impedance detection and dielectrophoresis integration. (a) Structural diagram of the device. (b) Cell Flow and DEP trapping. (c) Identification of target cells by impedance; reproduced from Reference , with permission from Biosensors and Bioelectronics .

    Journal: Micromachines

    Article Title: Novel Isolating Approaches to Circulating Tumor Cell Enrichment Based on Microfluidics: A Review

    doi: 10.3390/mi15060706

    Figure Lengend Snippet: ( A ) The high-throughput taSSAW device for CTCs isolation. (a) Illustration of cell isolation in the taSSAW device. (b) Schematic illustration of the principle of taSSAW-based cell isolation. (c) Actual size image of the tasSAW cell isolation device; reproduced from Reference , with permission from the Proceedings of the National Academy of Sciences . ( B ) Schematic illustration of an ultra-compact acoustofluidic device based on np-TSAW for enrichment of CTCs; reproduced from Reference , with permission from Analytica Chimica Acta . ( C ) Schematic illustration of CTCs isolation based on multi-stage surface acoustic waves; reproduced from Reference , with permission from Sensors and Actuators B: Chemical . ( D ) Microfluidic system based on optically induced dielectrophoretic (ODEP); reproduced from Reference , with permission from Scientific Reports . ( E ) Schematic illustration of a microdevice based on LFFF-DEP; reproduced from Reference , with permission from the Journal of Chromatography B . ( F ) Microfluidic device for impedance detection and dielectrophoresis integration. (a) Structural diagram of the device. (b) Cell Flow and DEP trapping. (c) Identification of target cells by impedance; reproduced from Reference , with permission from Biosensors and Bioelectronics .

    Article Snippet: , , Microfluidic ratchet mechanism , CTCs captured with 25 times more than traditional Cell Search systems. , Relatively low throughput. , UM-UC-13 , 1 , >90% , [ ] .

    Techniques: High Throughput Screening Assay, Isolation, Cell Isolation, Chromatography

    ( A ) Negative enrichment of CTCs based on GASI-ship; reproduced from Reference , with permission from Analytical Chemistry . ( B ) Monolithic chip for isolation of CTCs; reproduced from Reference , with permission from Scientific Reports . ( C ) Immunomagnetic negative enrichment coupled with flow cytometry to isolate CTCs; reproduced from Reference , with permission from Cancer . ( D ) Microfluidic Cell Concentrator for Negative Enrichment of CTCs. (a) 3D schematic diagram of the device. (b) CTCs collection process; reproduced from Reference , with permission from Methods . ( E ) μ-MixMACS chip. (a) Schematic illustration of the structure of the chip. (b) Illustration of the working principle of this chip to capture CTCs; reproduced from Reference , with permission from Sensors and Actuators B: Chemical . ( F ) Two-stage microfluidic chip. (a) Leukocyte-depleted μ-MACS chips. (b) Illustration of GASI chip; reproduced from Reference , with permission from Biosensors and Bioelectronics .

    Journal: Micromachines

    Article Title: Novel Isolating Approaches to Circulating Tumor Cell Enrichment Based on Microfluidics: A Review

    doi: 10.3390/mi15060706

    Figure Lengend Snippet: ( A ) Negative enrichment of CTCs based on GASI-ship; reproduced from Reference , with permission from Analytical Chemistry . ( B ) Monolithic chip for isolation of CTCs; reproduced from Reference , with permission from Scientific Reports . ( C ) Immunomagnetic negative enrichment coupled with flow cytometry to isolate CTCs; reproduced from Reference , with permission from Cancer . ( D ) Microfluidic Cell Concentrator for Negative Enrichment of CTCs. (a) 3D schematic diagram of the device. (b) CTCs collection process; reproduced from Reference , with permission from Methods . ( E ) μ-MixMACS chip. (a) Schematic illustration of the structure of the chip. (b) Illustration of the working principle of this chip to capture CTCs; reproduced from Reference , with permission from Sensors and Actuators B: Chemical . ( F ) Two-stage microfluidic chip. (a) Leukocyte-depleted μ-MACS chips. (b) Illustration of GASI chip; reproduced from Reference , with permission from Biosensors and Bioelectronics .

    Article Snippet: , , Microfluidic ratchet mechanism , CTCs captured with 25 times more than traditional Cell Search systems. , Relatively low throughput. , UM-UC-13 , 1 , >90% , [ ] .

    Techniques: Isolation, Flow Cytometry

    ( A ) Schematic illustration of microfluidic single-cell capture principle; reproduced from Reference , with permission from Scientific Reports . ( B ) Single-cell RNA sequencing of CTCs using Hydro-Seq.; reproduced from Reference , with permission from Nature Communications . ( C ) Schematic illustration of the working principle of capturing and releasing single CTCs based on the photoelectrochemical platform; reproduced from Reference , with permission from Nature Communications . ( D ) Schematic of an integrated microvalve chip capable of capturing at the single-cell level; reproduced from Reference , with permission from Talanta . ( E ) Schematic illustration of pipette working principle based on microfluidic cell isolation technology; reproduced from Reference , with permission from Scientific Reports . ( F ) Working principle of hand-held and integrated single-cell pipettes; reproduced from Reference , with permission from the Journal of the American Chemical Society . ( G ) Single-cell isolation device based on lateral magnetophoretic isolation and microfluidic dispensing; reproduced from Reference , with permission from Analytical Chemistry .

    Journal: Micromachines

    Article Title: Novel Isolating Approaches to Circulating Tumor Cell Enrichment Based on Microfluidics: A Review

    doi: 10.3390/mi15060706

    Figure Lengend Snippet: ( A ) Schematic illustration of microfluidic single-cell capture principle; reproduced from Reference , with permission from Scientific Reports . ( B ) Single-cell RNA sequencing of CTCs using Hydro-Seq.; reproduced from Reference , with permission from Nature Communications . ( C ) Schematic illustration of the working principle of capturing and releasing single CTCs based on the photoelectrochemical platform; reproduced from Reference , with permission from Nature Communications . ( D ) Schematic of an integrated microvalve chip capable of capturing at the single-cell level; reproduced from Reference , with permission from Talanta . ( E ) Schematic illustration of pipette working principle based on microfluidic cell isolation technology; reproduced from Reference , with permission from Scientific Reports . ( F ) Working principle of hand-held and integrated single-cell pipettes; reproduced from Reference , with permission from the Journal of the American Chemical Society . ( G ) Single-cell isolation device based on lateral magnetophoretic isolation and microfluidic dispensing; reproduced from Reference , with permission from Analytical Chemistry .

    Article Snippet: , , Microfluidic ratchet mechanism , CTCs captured with 25 times more than traditional Cell Search systems. , Relatively low throughput. , UM-UC-13 , 1 , >90% , [ ] .

    Techniques: RNA Sequencing, Transferring, Cell Isolation, Single-cell Isolation, Isolation

    Clinical applications of  CTCs  in cancer.

    Journal: Micromachines

    Article Title: Novel Isolating Approaches to Circulating Tumor Cell Enrichment Based on Microfluidics: A Review

    doi: 10.3390/mi15060706

    Figure Lengend Snippet: Clinical applications of CTCs in cancer.

    Article Snippet: , , Microfluidic ratchet mechanism , CTCs captured with 25 times more than traditional Cell Search systems. , Relatively low throughput. , UM-UC-13 , 1 , >90% , [ ] .

    Techniques: Immunostaining, Clinical Proteomics, Immunofluorescence, Staining, Expressing, Flow Cytometry