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Fluidic test cassette

A technology for fluids and test strips, applied in the direction of fluid controllers, microbiological determination/inspection, laboratory containers, etc., can solve the problem of increasing storage and transportation complexity, operation and manufacturing complexity, and does not allow programming or electronics. control issues

Pending Publication Date: 2018-03-16
MESA BIOTECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, typical devices do not allow programming or electronic control of this fluid movement or the mixing of two or more fluids
Additionally, some devices utilize the pressure drop created by falling inert or pre-packaged fluids to induce a slight vacuum and draw reactants into the process chamber when oriented vertically, adding storage and shipping complexity to ensure pre-packaged Packaging Fluid Stability
Existing devices that teach moving fluids in multiple discrete steps require frangible seals or valves between chambers, complicating operation and manufacturing

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1

[0199] Example 1: Multiplexing of Purified Viral RNA (Influenza A / Influenza B (inf A / B)) and Internal Positive Control Virus Multiplexing Amplification and Detection Methods

[0200] Position the Influenza A and Influenza B test cartridges in the docking unit. Add 40 µL of sample solution to the sample port. The sample solution includes a concentration equal to 5000TCID 50 / mL of purified A / Puerto Rico influenza virus RNA at a concentration equal to 500 TCID 50 / mL of purified B / Brisbane influenza virus RNA or molecular grade water (no template control sample). Upon entering the sample port, 40 μL of sample was mixed with the lyophilized beads as they flowed into the first chamber of the assay cartridge. Lyophilized beads consisted of MS2 bacteriophage virus particles (as a positive internal control) and DTT. In the first chamber of the assay cartridge, the samples were heated to 90 °C for 1 min to promote virus cell lysis, and then cooled to 50 °C before opening the e...

example 2

[0202] Example 2: Multiplexed Amplification and Detection Method of Viral Lysate and Internal Positive Control Virus in Buffer Law

[0203] Position the Influenza A and Influenza B test cartridges in the docking unit. Add 40 µL of sample solution to the sample port. The sample solution includes a concentration equal to 5000TCID 50 / mL of A / Puerto Rico influenza virus at a concentration equal to 500 TCID 50 / mL of B / Brisbane influenza virus or molecular grade water (no template control sample). Upon entering the sample port, 40 μL of sample was mixed with the lyophilized beads as they flowed into the first chamber of the assay cartridge. Lyophilized beads consisted of MS2 bacteriophage virus particles (as a positive internal control) and DTT. In the first chamber of the assay cartridge, the samples were heated to 90 °C for 1 min to promote virus cell lysis, and then cooled to 50 °C before opening the exhaust port connected to the second chamber. Opening the vent connec...

example 3

[0205] Example 3: Multiplicity of Influenza Virus (Purified) and Internal Positive Control Virus Spiked into Negative Clinical Nasal Samples Multiplexed Amplification and Detection Methods

[0206] Nasal swab samples collected from human subjects were placed in 3 mL of 0.025% TritonX-100, 10 mM Tris, pH 8.3 and tested for influenza A and B using an FDA-approved real-time RT-PCR assay exist. Samples were confirmed to be negative for influenza A and influenza B prior to use in this study. Spike concentration equal to 5000 TCID in confirmed influenza negative nasal samples 50 / mLA / Puerto Rico influenza virus, or use as a negative control without added virus. Add 40 μL of the resulting spiked or negative control sample to the sample ports of the Influenza A and B assay cartridges. Upon entering the sample port, 40 μL of sample was mixed with the lyophilized beads as they flowed into the first chamber of the assay cartridge. Lyophilized beads consisted of MS2 bacteriophage ...

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Abstract

A disposable cassette for detecting nucleic acids or performing other assays. The cassette can be inserted into a base station during use. The cassette has numerous features to ensure correct operation of the device under gravity, such as vent pockets for enabling the flow of sample fluid from one chamber to the next when the vent pocket is unsealed. The vent pockets have protrusions to help prevent accidental resealing. The cassette also can have a gasket to ensure free air movement between open vent pockets. A flexible circuit with patterned metallic electrical components disposed on a heatstable material can be in direct contact with fluid in the chambers and has resistive heating elements aligned with the vent pockets and the chambers. The detection chamber, which houses a lateral flow detection strip can have a space below the strip that has sufficient capacity to accommodate an entire volume of the sample fluid entering the detection chamber at a height that enables the fluid toflow up the detection strip by capillary action without flooding or otherwise bypassing regions of the detection strip. The space can also contain detection particles. Recesses in in the cassette channels or chambers can have structures such as ridges or grooves to direct fluid flow to enhance rehydration of lyophilized reagents disposed in the recess. Flow diverters in the chambers can reduce the flow velocity of the sample fluid and increase the effective fluid flow path length, enabling more accurate control of fluid flow in the cassette.

Description

[0001] Cross References to Related Applications [0002] This application claims U.S. Provisional Patent Application No. 62 / 152,724, filed April 24, 2015, entitled "Fluid Test Cassette" and filed April 14, 2016, entitled "Fluid Test Cassette" Priority and benefit to U.S. Provisional Patent Application No. 62 / 322,738, "Test Cassette", the specification and claims of which are incorporated herein by reference. technical field [0003] Embodiments of the invention relate to integrated devices and related methods for the detection and identification of nucleic acids. The device may be entirely disposable, or may include a single-use portion and a reusable portion. Background technique [0004] It should be noted that the following discussion may refer to a number of publications and references. The discussion of these publications in this article is intended only to more fully present the background of the scientific rationale and is not an admission that these publications ar...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01L3/00B01L7/00C12Q1/6816
CPCB01L3/502715B01L3/502723B01L3/50273B01L3/502738B01L7/52C12Q1/6816C12Q2565/629B01L2300/123B01L2300/0883B01L2400/0406B01L2300/1827B01L2400/0677B01L2400/0457B01L2400/0694B01L2200/0689B01L2200/0621B01L2200/16B01L2200/147B01L3/5023B01L2300/0825
Inventor 马克·诺瓦科夫斯基迈克尔·王罗伯特·B·凯瑞蔡红康拉德·林德伯格马丁·布利亚内唐纳德·J·托马斯
Owner MESA BIOTECH
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