Surface tension reduction channel

Weigl, Bernhard H.

Patent Application Summary

U.S. patent application number 10/114864 was filed with the patent office on 2002-10-17 for surface tension reduction channel. Invention is credited to Weigl, Bernhard H..

Application Number20020150502 10/114864
Document ID /
Family ID23076003
Filed Date2002-10-17

United States Patent Application 20020150502
Kind Code A1
Weigl, Bernhard H. October 17, 2002

Surface tension reduction channel

Abstract

A structure for use with a microfluidic channel to reduce the effects of surface tension and capillary forces. A macroscale reservoir is connected to a microscale channel by a microscale section extending from the reservoir, which fills with fluid and flows smoothly into the microscale channel.


Inventors: Weigl, Bernhard H.; (Seattle, WA)
Correspondence Address:
    JERROLD J. LITZINGER
    SENTRON MEDICAL, INC.
    4445 LAKE FOREST DR.
    SUITE 600
    CINCINNATI
    OH
    45242
    US
Family ID: 23076003
Appl. No.: 10/114864
Filed: April 3, 2002

Related U.S. Patent Documents

Application Number Filing Date Patent Number
60281114 Apr 3, 2001

Current U.S. Class: 422/400 ; 422/68.1
Current CPC Class: B01L 3/50273 20130101; F16K 2099/008 20130101; F16K 99/0059 20130101; F16K 2099/0084 20130101; A61M 2206/11 20130101; B01L 3/502753 20130101; B01L 2400/0406 20130101; G01N 2015/0288 20130101; A61M 1/14 20130101; B01L 3/5027 20130101; G01N 2015/1486 20130101; B01L 3/502776 20130101; B01L 2200/0647 20130101; G01N 2001/4061 20130101; F16K 7/17 20130101; B01L 2400/0487 20130101; B01L 2200/027 20130101; F16K 99/0001 20130101; B01L 2300/0874 20130101; B01L 3/502761 20130101; G01N 2015/1413 20130101; B01L 3/502707 20130101; F16K 99/0025 20130101; B01L 2400/084 20130101; Y10T 436/2575 20150115; B01L 3/502738 20130101; B01D 21/0012 20130101; B01L 2200/028 20130101; B01L 2400/0436 20130101; G01N 15/1456 20130101; G01N 2001/4094 20130101; G01N 2035/00247 20130101; B01L 2200/0668 20130101; B01L 2300/0829 20130101; B01L 2300/0883 20130101; B01L 2400/0457 20130101; G01N 15/05 20130101; G01N 15/0255 20130101; B01L 3/502746 20130101; G01N 2001/4016 20130101; B01L 2300/0861 20130101; F16K 99/0015 20130101; B01D 21/283 20130101; Y10T 436/25375 20150115; B01L 2200/0636 20130101; G01N 2015/1411 20130101; G01N 2015/144 20130101
Class at Publication: 422/58 ; 422/55; 422/68.1
International Class: G01N 021/05

Claims



What is claimed is:

1. A microfluidic device, comprising: a first fluid vessel having only macrofluidic dimensions; a second fluid vessel having at least one microfluidic dimension; a microfluidic channel having first and second ends, said first end attached to at least one portion of at least one side of said first fluid vessel and said second end attached to at least one portion of at least one side of said second fluid vessel such that said attachment to said first vessel is larger in at least one dimension than said attachment to said vessel.
Description



CROSS REFERENCE TO RELATED APPLICATIONS

[0001] This application claims benefit from U.S. Provisional Patent Application Serial No. 60/281,114, filed Apr. 3, 2001, which application is incorporated herein by reference.

BACKGROUND OF THE INVENTION

[0002] 1. Field of the Invention

[0003] This invention relates generally to microfluidic devices for performing analytic testing, and, in particular, to a device for reducing the effect of surface tension on fluids flowing in microfluidic channels.

[0004] 2. Description of the Related Art

[0005] Microfluidic devices have recently become popular for performing analytic testing. Using tools developed by the semiconductor industry to miniaturize electronics, it has become possible to fabricate intricate fluid systems which can be inexpensively means produced. Systems have been developed to perform a variety of analytical techniques for the acquisition of information for the medical field.

[0006] Microfluidic devices may be constructed in a multi-layer laminated structure where each layer has channels and structures fabricated from a laminate material to form microscale voids or channels where fluid flow. A microscale channel is generally defined as a fluid passage which has at least one internal cross-sectional dimension that is less than 500 .mu.m and typically between about 0.1 .mu.m and about 500 .mu.m. The control and pumping of fluids through these channels is affected by either external pressurized fluid forced into the laminate, or by structures located within the laminate.

[0007] U.S. Pat. No. 5,716,852 teaches a method for analyzing the presence and concentration of small particles in a flow cell using diffusion principles. This patent, the disclosure of which is incorporated herein by reference, discloses a channel cell system for detecting the presence of analyte particles in a sample stream using a laminar flow channel having at least two inlet means which provide an indicator stream and a sample stream, where the laminar flow channel has a depth sufficiently small to allow laminar flow of the streams and length sufficient to allow diffusion of particles of the analyte into the indicator stream to form a detection area, and having an outlet out of the channel to form a single mixed stream. This device, which is known at a T-Sensor, may contain an external detecting means for detecting changes in the indicator stream. This detecting means may be provided by any means known in the art, including optical means such as optical spectroscopy, or absorption spectroscopy of fluorescence.

[0008] U.S. Pat. No. 5,932,100, which patent is also incorporated herein by reference, teaches another method for analyzing particles within microfluidic channels using diffusion principles. A mixture of particles suspended in a sample stream enters an extraction channel from one upper arm of a structure, which comprises microchannels in the shape of an "H". An extraction stream (a dilution stream) enters from the lower arm on the same side of the extraction channel and due to the size of the microfluidic extraction channel, the flow is laminar and the streams do not mix. The sample stream exits as a by-product stream at the upper arm at the end of the extraction channel, while the extraction stream exits as a product stream at the lower arm. While the streams are in parallel laminar flow is in the extraction channel, particles having a greater diffusion coefficient (smaller particles such as albumin, sugars, and small ions) have time to diffuse into the extraction stream, while the larger particles (blood cells) remain in the sample stream. Particles in the exiting extraction stream (now called the product stream) may be analyzed without interference from the larger particles. This microfluidic structure, commonly known as an "H-Filter," can be used for extracting desired particles from a sample stream containing those particles.

[0009] Surface effects describe the character of a surface on a micro scale. Materials often have unbound electrons, exposed polar molecules, or other molecular level features that generate a surface charge or reactivity characteristic. Due to scaling, these surface effects or surface forces are substantially more pronounced in microstructures than they are in traditionally sized devices. This is particularly true in microscale fluid handling systems where the dynamics of fluid movement are governed by external pressures and by attractions between liquids and the materials they are flowing through.

[0010] This invention deals with the passive control of fluids within a microfluidic circuit. The passive control is generated by using the natural forces that exist on a microscale, specifically capillarity, which is caused by the attraction or repulsion of a fluid toward certain materials.

SUMMARY OF THE INVENTION

[0011] It is therefore an object of the present invention to provide a device for reducing the effect of surface tension on fluids flowing within a microfluidic channel.

[0012] It is a further object of the present invention to provide a microfluidic structure in which fluids flow from a macrochannel into a microchannel to insure smooth flow within the microfluidic structure.

[0013] These and other objects of the present invention will be more readily apparent from the description and drawings that follow.

BRIEF DESCRIPTION OF THE DRAWINGS

[0014] FIG. 1 is a plan view of a microfluidic structure including an H-Filter using the principles of the present invention; and

[0015] FIG. 2 is a fragmentary, cross-sectional side view of the microfluidic structure shown in FIG. 1.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

[0016] FIG. 1 shows a microfluidic analysis card 10 which contains an H-Filter 12, which structure is described in detail in U.S. Pat. No. 5,932,100, incorporating the present invention. H-Filter 12 includes a first reservoir 14 and a second reservoir 16. An outlet channel 18 of reservoir 14 and an outlet channel 20 of reservoir 16 are both connected to a flow channel 24 at a first end 26. A second end 28 of flow channel 24 is coupled to an exit channel 30, which is connected to a reservoir 32 and also to an exit channel 34, which is coupled to a reservoir 36. Reservoir 36 is also coupled to a bellows 38 via a channel 40. It should be understood that H-Filter 12 will also operate using gravity as a driving force.

[0017] Reservoir 14 contains a vent hole 42 and an inlet port 44, while reservoir 16 contains an inlet port 46. Reservoir 14 also contains a narrowed lower section 50, which extends across the lower length of reservoir 14, while reservoir 16 also contains a similarly narrowed lower section 52 across the lower length of reservoir 16.

[0018] Operation of H-Filter 12 is as follows: a sample fluid is placed into inlet port 46 of reservoir 16 while an extractor solution is placed into port 44 of reservoir 14. The fluids form a stream and flow through channels 20, 18 respectively to end 26 of channel 24. The fluids form a stream and flow laminarly within channel 24 while particles from the sample fluid diffuse across the laminar junction into the extractor fluid. As the stream reaches end 28 of channel 24, the extractor fluid containing particles flow through channel 30 into reservoir 32, while the sample fluid flows through channel 34 into reservoir 36.

[0019] Narrowed section 50 of reservoir 14 fills with sample fluid when the sample is loaded into inlet port 44. Since the structure of reservoir 14 is not microscale, and outlet channel 18 is of a microscale dimension, the effect of surface tension would generally prevent the fluid from flowing smoothly from reservoir 14 to channel 18. However, as can be clearly seen in FIGS. 1 and 2, the narrow lower section 50, which runs the entire length of reservoir 14, is of essentially the same microdimensions of channel 18; thus, fluid moves smoothly and consistently from reservoir 14 into channel 18 and through the rest of the H-Filter structure. This is also true for fluids flowing from reservoir 16 into channel 20, as the narrow lower section 52 of reservoir 16 fills with fluid and flows smoothly into channel 20 with little or no surface tension effect.

[0020] While the present invention has been shown and described in terms of a preferred embodiment thereof, it will be understood that this invention is not limited to this particular embodiment and that changes and modifications may be made without departing from the true spirit and scope of the invention as defined in the appended claims.

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