Sample-in-result-out closed microfluidic device for nucleic acid molecular point-of-care testing detection

Patent metadata

Field	Value
Publication number	US-12582985-B2
Application number	US-202217816769-A
Country	US
Kind code	B2
Filing date	Aug 2, 2022
Priority date	Aug 2, 2022
Publication date	Mar 24, 2026
Grant date	Mar 24, 2026

Abstract

A molecular point-of-care testing (POCT) diagnostic device for molecular detection of various diseases with “sample-in-result-out” principle is provided. The device has a sample tube in which a test sample is mixed with a sample buffer, a microfluidic-based reaction tube with a simple flow-based system for amplifying the sample buffer mixed with the test sample to form an amplified result, and a closed-system, disposable result interpretation using colorimetric- or lateral flow assay-based for assaying the amplified result. The device is portable and simple to use, which can help bring laboratory detection to the field.

First claim

What is claimed is:

1 . A molecular point-of-care testing (POCT) diagnostic device for assaying a test sample, the device comprising:
a sample tube for receiving the test sample, the sample tube including a sample buffer for mixing with the test sample; a microfluidic-based reaction tube insertable into the sample tube for receiving the sample buffer that is mixed with the test sample, the reaction tube including one or more reaction chambers installed at a first end portion of the reaction tube, an individual reaction chamber of the one or more reaction chambers being arranged to receive a portion of the received sample buffer, the individual reaction chamber including an amplification reagent for amplifying a test-sample content in the received portion to yield an amplified result used for assaying the test sample; and an inner tube configured to filter the sample buffer before the sample buffer reaches the reaction tube, the inner tube being connectable to the reaction tube such that the reaction tube receives the sample buffer from the sample tube via the inner tube; wherein:
the reaction tube is configured to lock and seal the reaction tube and the sample tube together to create a closed enclosure confining the sample buffer for avoiding contamination of the sample buffer from outside the sample tube and the reaction tube during generation of the amplified result;
the individual reaction chamber is installed with a capillary tube configured to passively transport the portion of the received sample buffer from a second end portion of the reaction tube to the individual reaction chamber via a combination of capillary action and centrifugal acceleration induced by a manual inversion of the device, the second end portion being opposite to the first end portion;
the individual reaction chamber is further installed with a channel connecting the individual reaction chamber to the second end portion of the reaction tube;
the capillary tube is positioned inside the channel;
the reaction tube further includes a first O-ring located at a lateral side of the reaction tube as a static seal between the reaction tube and the sample tube to create the closed enclosure when the reaction tube is inserted into the sample tube, thereby preventing leakage to the external environment when the reaction tube is locked;
the reaction tube further includes a second O-ring located at the lateral side of the reaction tube for locking and sealing the reaction tube and the inner tube when the reaction tube is connected to the inner tube;
the reaction tube further includes a crevice gap located between the first and second O-rings for exposing respective channels installed for the one or more reaction chambers to outside the reaction tube;
one or more holes are formed on the channel at the crevice gap for displacing air in the individual reaction chamber during transfer of the sample buffer; and
the crevice gap has an adjustable width for adjusting a volume of the portion of the received sample buffer to be transferred into the individual reaction chamber.

2 . The device in accordance with claim 1 , wherein the capillary tube is sealed with a heat-sensitive valve, the heat-sensitive valve being openable when exposed to heat.

3 . The device in accordance with claim 1 , wherein:
the one or more reaction chambers consist of four respective reaction chambers such that four respective channels are installed in the device; and the four respective channels are arranged in an X shape.

4 . The device in accordance with claim 1 , wherein the individual reaction chamber comprises a silicone seal enclosing a junction between the individual reaction chamber and the channel for sealing the junction.

5 . The device in accordance with claim 1 , wherein the inner tube is housed inside the sample tube when the reaction tube connected with the inner tube is inserted into the sample tube, and wherein the inner tube comprises:
an inner-tube opening for receiving the sample buffer from the sample tube; and a filter proximal to the inner-tube opening for filtering the sample buffer before the sample buffer reaches the reaction tube to thereby prevent possible cell debris from entering into the reaction tube.

6 . The device in accordance with claim 1 , wherein the amplification reagent is a dried amplification reagent.

7 . The device in accordance with claim 1 , wherein the one or more reaction chambers consist of four or more respective reaction chambers, the four or more respective reaction chambers being configured for simultaneous multiplex amplification of distinct targets.

8 . The device in accordance with claim 1 further comprising a heating block for heating the reaction tube.

9 . The device in accordance with claim 1 further comprising a reading cassette for assaying the amplified result, the reading cassette comprising:
a main body formed with a hollow tube used for receiving the reaction tube;
a lateral flow assay (LFA) strip housing for housing a LFA strip used to perform LFA;
a puncturing blade located at the hollow tube for rupturing the one or more reaction chambers when the reaction tube is inserted into the hollow tube, thereby releasing the amplified result from the one or more reaction chambers; and
a glass fiber connecting the puncturing blade and the LFA strip housing for transporting the released amplified result to the LFA strip such that the test sample is assayed.

10 . The device in accordance with claim 9 , wherein:
the one or more reaction chambers consist of four respective reaction chambers; and the puncturing blade is shaped as a 4-point wide barbed arrowhead such that all the four respective reaction chambers are ruptured when the reaction tube is inserted into the hollow tube.

11 . The device in accordance with claim 1 , wherein a centrally-open plug is embedded into the channel, the centrally-open plug covering the channel and allowing the capillary tube to go through the channel so as to prevent uncontrolled spill of the sample buffer into the individual reaction chamber while allowing the portion of the received sample buffer to enter into the individual reaction chamber.

Assignees

• Univ City Hong Kong

Inventors

• Yang Mengsu
• Ayele Bereket
• Gunawan Renardi

Classifications

• B01L2200/10

  Integrating sample preparation and analysis in single entity, e.g. lab-on-a-chip concept · CPC title

• B01L2300/1805

  Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks · CPC title

• B01L2300/087

  Multiple sequential chambers · CPC title

• B01L2200/16

  Reagents, handling or storing thereof · CPC title

• B01L2400/0406

  capillary forces · CPC title