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diameter drill bit  (NS Tool Co Ltd)

 
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    NS Tool Co Ltd diameter drill bit
    Establishment of a <t>microfluidic</t> system using an organ-on-chip system and feline mammary tumor (FMT) organoids. Overview of organoids-on-a-chip experiments ( A ). Representative H&E-stained image (Left panel) and expression of a mammary tumor marker HER2 (Right panel) in FMT organoids are shown ( B ). Scale bar: 50 μm. After generating organoids from a cat with mammary tumor disease, the organoids were mounted on a microfluidic device, and drug perfusion was performed. After perfusion, the organoids were collected for genetic analysis and cell survival measurements. The device was created by CAD design and acrylic cutting. The width and height of the flow channel were 0.4 and 0.5 mm, respectively, and the diameter of the chamber was set at 5 mm ( C ). Liquid flows in from the left side of the device and flows out in three separate directions ( D ). The device was connected to a syringe pump and perfused in a CO 2 incubator at 37 ℃ for 48 h ( E ).
    Diameter Drill Bit, supplied by NS Tool Co Ltd, 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/product/diameter+drill+bit/pmc11697305-83-3-12?v=NS+Tool+Co+Ltd
    Average 90 stars, based on 1 article reviews
    diameter drill bit - by Bioz Stars, 2026-07
    90/100 stars

    Images

    1) Product Images from "A microfluidics platform for simultaneous evaluation of sensitivity and side effects of anti-cancer drugs using a three-dimensional culture method"

    Article Title: A microfluidics platform for simultaneous evaluation of sensitivity and side effects of anti-cancer drugs using a three-dimensional culture method

    Journal: Scientific Reports

    doi: 10.1038/s41598-024-84297-0

    Establishment of a microfluidic system using an organ-on-chip system and feline mammary tumor (FMT) organoids. Overview of organoids-on-a-chip experiments ( A ). Representative H&E-stained image (Left panel) and expression of a mammary tumor marker HER2 (Right panel) in FMT organoids are shown ( B ). Scale bar: 50 μm. After generating organoids from a cat with mammary tumor disease, the organoids were mounted on a microfluidic device, and drug perfusion was performed. After perfusion, the organoids were collected for genetic analysis and cell survival measurements. The device was created by CAD design and acrylic cutting. The width and height of the flow channel were 0.4 and 0.5 mm, respectively, and the diameter of the chamber was set at 5 mm ( C ). Liquid flows in from the left side of the device and flows out in three separate directions ( D ). The device was connected to a syringe pump and perfused in a CO 2 incubator at 37 ℃ for 48 h ( E ).
    Figure Legend Snippet: Establishment of a microfluidic system using an organ-on-chip system and feline mammary tumor (FMT) organoids. Overview of organoids-on-a-chip experiments ( A ). Representative H&E-stained image (Left panel) and expression of a mammary tumor marker HER2 (Right panel) in FMT organoids are shown ( B ). Scale bar: 50 μm. After generating organoids from a cat with mammary tumor disease, the organoids were mounted on a microfluidic device, and drug perfusion was performed. After perfusion, the organoids were collected for genetic analysis and cell survival measurements. The device was created by CAD design and acrylic cutting. The width and height of the flow channel were 0.4 and 0.5 mm, respectively, and the diameter of the chamber was set at 5 mm ( C ). Liquid flows in from the left side of the device and flows out in three separate directions ( D ). The device was connected to a syringe pump and perfused in a CO 2 incubator at 37 ℃ for 48 h ( E ).

    Techniques Used: Staining, Expressing, Marker



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    Establishment of a <t>microfluidic</t> system using an organ-on-chip system and feline mammary tumor (FMT) organoids. Overview of organoids-on-a-chip experiments ( A ). Representative H&E-stained image (Left panel) and expression of a mammary tumor marker HER2 (Right panel) in FMT organoids are shown ( B ). Scale bar: 50 μm. After generating organoids from a cat with mammary tumor disease, the organoids were mounted on a microfluidic device, and drug perfusion was performed. After perfusion, the organoids were collected for genetic analysis and cell survival measurements. The device was created by CAD design and acrylic cutting. The width and height of the flow channel were 0.4 and 0.5 mm, respectively, and the diameter of the chamber was set at 5 mm ( C ). Liquid flows in from the left side of the device and flows out in three separate directions ( D ). The device was connected to a syringe pump and perfused in a CO 2 incubator at 37 ℃ for 48 h ( E ).
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    Image Search Results


    Drilling groups tested in vitro.

    Journal: Bioengineering

    Article Title: Comparison of One-Drill Protocol to Sequential Drilling In Vitro and In Vivo

    doi: 10.3390/bioengineering12010051

    Figure Lengend Snippet: Drilling groups tested in vitro.

    Article Snippet: Thermal video recordings taken during the implant bed preparation procedure for the 4.0 mm diameter new-generation drill bit used in a one-drill protocol and Straumann BLT drill bits used in sequential drilling were analyzed and maximum temperatures at osteotomy depths of 0, 2, 4, 6, 8, and 10 mm were recorded and organized into the bar graph seen in .

    Techniques:

    Animal study groups.

    Journal: Bioengineering

    Article Title: Comparison of One-Drill Protocol to Sequential Drilling In Vitro and In Vivo

    doi: 10.3390/bioengineering12010051

    Figure Lengend Snippet: Animal study groups.

    Article Snippet: Thermal video recordings taken during the implant bed preparation procedure for the 4.0 mm diameter new-generation drill bit used in a one-drill protocol and Straumann BLT drill bits used in sequential drilling were analyzed and maximum temperatures at osteotomy depths of 0, 2, 4, 6, 8, and 10 mm were recorded and organized into the bar graph seen in .

    Techniques: Control, Modification

    Establishment of a microfluidic system using an organ-on-chip system and feline mammary tumor (FMT) organoids. Overview of organoids-on-a-chip experiments ( A ). Representative H&E-stained image (Left panel) and expression of a mammary tumor marker HER2 (Right panel) in FMT organoids are shown ( B ). Scale bar: 50 μm. After generating organoids from a cat with mammary tumor disease, the organoids were mounted on a microfluidic device, and drug perfusion was performed. After perfusion, the organoids were collected for genetic analysis and cell survival measurements. The device was created by CAD design and acrylic cutting. The width and height of the flow channel were 0.4 and 0.5 mm, respectively, and the diameter of the chamber was set at 5 mm ( C ). Liquid flows in from the left side of the device and flows out in three separate directions ( D ). The device was connected to a syringe pump and perfused in a CO 2 incubator at 37 ℃ for 48 h ( E ).

    Journal: Scientific Reports

    Article Title: A microfluidics platform for simultaneous evaluation of sensitivity and side effects of anti-cancer drugs using a three-dimensional culture method

    doi: 10.1038/s41598-024-84297-0

    Figure Lengend Snippet: Establishment of a microfluidic system using an organ-on-chip system and feline mammary tumor (FMT) organoids. Overview of organoids-on-a-chip experiments ( A ). Representative H&E-stained image (Left panel) and expression of a mammary tumor marker HER2 (Right panel) in FMT organoids are shown ( B ). Scale bar: 50 μm. After generating organoids from a cat with mammary tumor disease, the organoids were mounted on a microfluidic device, and drug perfusion was performed. After perfusion, the organoids were collected for genetic analysis and cell survival measurements. The device was created by CAD design and acrylic cutting. The width and height of the flow channel were 0.4 and 0.5 mm, respectively, and the diameter of the chamber was set at 5 mm ( C ). Liquid flows in from the left side of the device and flows out in three separate directions ( D ). The device was connected to a syringe pump and perfused in a CO 2 incubator at 37 ℃ for 48 h ( E ).

    Article Snippet: After milling the microfluidic features, a 1 mm diameter drill bit (MHR230, NS Tool Co., Ltd., Japan) was used to segment the acrylic sheet into individual sections, each measuring 3 × 4 cm and containing a complete microfluidic channel network.

    Techniques: Staining, Expressing, Marker