This invention relates generally to microfluidic devices, and in particular, to a device and method to facilitate the prepackaging, handling and use of small volumes of fluids.
Due to the lower cost, simpler protocols, and less reagent waste, assays are continually transforming towards the smaller scale. Unfortunately, this transformation and the general acceptance of microscale technologies has been slowed due to both technological limitations and the lack of general acceptance by users. More specifically, users are skeptical of new technologies that differ significantly from those to which they are accustomed. Hence, in order to gain acceptance by users, microscale technologies must be reliable and easy to use. Further, the technology must be transitional, so as to constitute an incremental step from current technologies.
To facilitate and to simplify assays and facilitate distribution of microscale technologies, kits have been developed which include all of the reagents and protocols necessary to complete a task. Despite this transition, methods of prepackaging small volumes (e.g., nano- to micro-liter volumes) of reagents remain limited. In addition, even if small volumes of the reagent were prepackaged in a standard tube, recovery of these small volumes of the reagent can be difficult, if not impossible, thereby requiring excess volume of the reagent to be shipped to the user. Thus, it can be appreciated that a technology which enables the prepackaging of small volumes of reagents and enables full recovery of the reagent could bring forth a paradigm shift in the use of microscale technologies.
It is noted that small volume fluid handling capabilities are ubiquitous and required by both industry and academics, spanning multiple disciplines, including: biology, pharmacology, and agriculture, to list a few. The standard tool, used by almost every lab, for measuring and manipulating small volumes of fluids is the pipette. Pipettes have a usable range from approximately 0.2 microliters (μl) to 25 milliliters (ml), with the most accurate low-volume pipettes having a usable range from 0.2 μl to 2 μl. Despite its usable range, these low-volume pipettes carry high levels of imprecision, which increases as the volume decreases. The most prominent sources for this imprecision come from: 1) fluid stuck to the walls (both inside and outside walls) of the pipette; and 2) improper pipetting techniques, both of which are amplified when pipetting high viscosity or low surface energy fluids. This imprecision represents difficulties for many assays which require measurement of small volumes, including: PCR, staining assays, etc. Thus, a technology that can more precisely measure small volumes of fluid, despite the viscosity or surface energy of the fluid, would enable new assays and provide value.
Therefore, it is a primary object and feature of the present invention to provide a device and method to facilitate the prepackaging, handling and use of small volumes of fluids.
It is a further object and feature of the present invention to provide a device and method to facilitate the prepackaging, handling and use of small volumes of fluids that are amenable to a wide variety of reagents.
It is a still further object and feature of the present invention to provide a device to facilitate the prepackaging, handling and use of small volumes of fluids that is simple to manufacture and easy to use.
In accordance with the present invention, a device is provided to facilitate the handling of a volume of fluid. The device includes an elongated tube having an open first end and a second end. The tube defines a reservoir for receiving the volume of fluid. A stanchion has a first end received within the reservoir of the tube and a second end projecting from the open end of the elongated tube.
The reservoir has a volume less than 10 microliters, and preferably in the range of 0.01 microliters to 6 microliters. The tube has a diameter in the range of 50 micrometers to 1.5 millimeters and a length of 1 millimeter and 15 millimeters. The second end of the tube may be closed, for example, by a seal provided in the second end of the tube. The first end of the stanchion may be fixed to the seal.
In accordance with a further aspect of the present invention, a method is provided for facilitating the handling of volume of fluid. The method includes the step of positioning an elongated tube in a first capsule having the fluid therein. The tube has an open end. The first capsule is centrifuged such that the volume of fluid is received in the tube through the open end.
After the first capsule is centrifuged, the tube is removed from the first capsule. Thereafter, the tube may be positioned in a second capsule free of fluid and having a closed end such that the open end of the tube is spaced from the closed end of the second capsule. The second capsule is centrifuged such that the volume of fluid is expelled from the tube into the second capsule.
It is contemplated for the open end of the tube to be spaced from the closed end of the second capsule by a stanchion. The stanchion extends from the open end of the tube. The tube also includes a second end which is closed, for example, by a seal received within the second end of the tube. The stanchion has a first end fixed within the tube, e.g., to the seal, and a second end positioned outside of the tube.
In accordance with a further aspect of the present invention, a method is provided for facilitating the handling a volume of fluid. The method includes the step of positioning an elongated tube having a reservoir and an open end communicating with the reservoir in a first capsule such that the open end of the tube is spaced from a closed end of the first capsule. The reservoir includes the volume of fluid therein. Thereafter, the first capsule is centrifuged such that the volume of fluid is expelled from the reservoir of the tube into the first capsule.
Prior to positioning the tube in the first capsule, the method may include the additional steps of positioning the tube in a second capsule having the fluid therein; and centrifuging the second capsule such that the volume of the fluid is urged into the tube through the open end. The open end of the tube is spaced from the closed end of the first capsule by a stanchion. The stanchion extends from the open end of the tube. The tube also includes a second end that is closed by, for example, a seal. The stanchion has a first end fixed within the tube, e.g., to the seal, and a second end positioned outside of the tube.
In accordance with a still further aspect of the present invention, a method is provided for facilitating the handling of a volume of fluid. The method includes the step of positioning an elongated tube in a first capsule having fluid therein. The tube has an open end. The first capsule is centrifuged such that the volume of fluid is received in a reservoir in the tube through the open end. The tube is removed from the first capsule and positioned in a second capsule such that the open end of the tube is spaced from a closed end of the second capsule. The second capsule is centrifuged such that the volume of fluid is expelled from the reservoir of the tube.
The tube includes a second end that is closed, e.g., by a seal. The open end of the tube is spaced from the closed end of the second capsule by a stanchion. The stanchion has a first end fixed within the tube, e.g., to the seal, and a second end positioned outside of the tube.
The drawings furnished herewith illustrate a preferred construction of the present invention in which the above aspects, advantages and features are clearly disclosed as well as others which will be readily understood from the following description of the illustrated embodiments.
In the drawings:
Referring to
Wall 14 includes a first upper end 22 and a second lower end 24. Upper and lower ends 22 and 24, respectively, define corresponding upper and lower orifices 26 and 28, respectively, which communicate with reservoir 18. Seal 30 is receivable in reservoir 18 of tube 12 through lower orifice 28. Seal 30 extends along a longitudinal axis and includes a generally concave upper surface 32 and a generally concave lower surface 34 interconnected by a generally cylindrical outer surface 36 and a generally cylindrical inner surface 38 radially spaced therefrom. With seal 30 received within reservoir 18 of tube 12, it is intended for outer surface 36 of seal 30 to form a fluidic seal with inner surface 16 of wall 14 so as to prevent fluid received in reservoir 18 from exiting reservoir 18 though orifice 28. In the depicted embodiment, radially outer edge 39 at the intersection of lower surface 34 and outer surface 36 of seal 30 is generally coplanar with lower end 24 of wall 14.
Inner surface 38 of seal 30 includes an upper edge intersecting upper surface 32 of seal 30 so as to define opening 46 and a lower edge intersecting lower surface 34 of seal 30 so as to define opening 48. Inner surface 38 of seal 30 defines a passageway 40 which extends between openings 46 and 48 along the longitudinal axis of seal 30 and which is adapted for receiving a lower end 42 of stanchion 44, as hereinafter described. Openings 46 and 48 are centrally located in upper and lower surfaces 32 and 34, respectively, of seal 30, for reasons hereinafter described.
As previously noted, lower end 42 of stanchion 44 is received within passageway 40 of seal 30 such that lower surface 50 of stanchion 44 is substantially coplanar with lower end 24 of wall 14. It is intended for portion 52 of outer surface 54 of stanchion 44 to engage inner surface 38 of seal 30 so as to form a fluidic seal therewith and prevent fluid received in reservoir 18 from exiting reservoir 18 though passageway 40 in seal 30. With lower end 42 received within passageway 40 of seal 30, stanchion 44 extends axially along the longitudinal axis of seal 30 and through reservoir 18 such that upper end 56 of stanchion 44 is positioned outside of tube 12. More specifically, upper surface 58 of stanchion 44 lies in a plane generally parallel to and spaced from a plane containing upper end 22 of wall 14 by a distance D.
Referring to
In operation, in order to fill reservoir 18 of tube 12 with a desired volume of a fluid, such as reagent 59, reagent 59 is provided in capsules of a conventional centrifuge machine 60. Referring to
With lid 70 of first capsule 62 in an open position, device 10 is positioned within interior 74 of first capsule 62 such that lower surface 34 of seal 30 is directed towards closed tip 76 of tapered portion 68 of first capsule 62. In addition, interior 74 of first capsule 62 is filled with a sufficient volume of a desired reagent 59 such that desired reagent 59 overlaps upper orifice 26 defined by wall 14 of tube 12. Thereafter, lid 70 is moved to the closed position and first capsule 62 is deposited in a corresponding retainer 80 in centrifuge machine 60. In a similar manner, a second device 10a, identical to device 10, is positioned within interior 74 of second capsule 64 such that lower surface 34 of seal 30 is directed towards closed tip 76 of tapered portion 68 of second capsule 64. In addition, interior 74 of second capsule 64 is filled with a sufficient volume of a desired reagent 59 such that desired reagent 59 in second capsule 64 overlaps upper orifice 26 defined by wall 14 of tube 12 of second device 10a. Thereafter, lid 70 is moved to the closed position and second capsule 64 is deposited in a corresponding retainer 80 in centrifuge machine 60.
With first and second capsules 62 and 64, respectively, received in corresponding retainers 80 in centrifuge machine 60, centrifuge machine 60 is actuated so as to centrifuge first and second capsules 62 and 64, respectively, for a desired time period (e.g. 30 seconds) at user selected revolutions per minute. As first and second capsules 62 and 64, respectively, (and hence, first and second devices 10 and 10a, respectively) are centrifuged, portions of reagents 59 in first and second capsules 62 and 64, respectively, are urged into corresponding reservoirs 18 in devices 10 and 10a such that the air, previously in reservoirs 18, is expelled therefrom,
Referring to
Referring to
Device 10 is positioned within interior 74 of third capsule 62 such that upper end 56 of stanchion 44 is directed towards, and preferably engages, closed tip 76 of tapered portion 68 of third capsule 82. Thereafter, lid 70 is moved to the closed position and third capsule 82 is deposited in a corresponding retainer 80 in centrifuge machine 60. In a similar manner, a second device 10a, identical to device 10, is positioned within interior 74 of second capsule 64 such that upper end 56 of stanchion 44 is directed towards, and preferably engages, closed tip 76 of tapered portion 68 of fourth capsule 84. Thereafter, lid 70 is moved to the closed position and fourth capsule 84 is deposited in a corresponding retainer 80 in centrifuge machine 60.
With third and fourth capsules 82 and 84, respectively, received in corresponding retainers 80 in centrifuge machine 60, centrifuge machine 60 is actuated so as to centrifuge third and fourth capsules 82 and 84, respectively, for a desired time period (e.g. 30 seconds) at user selected revolutions per minute. As third and fourth capsules 82 and 84, respectively, (and hence, first and second devices 10 and 10a, respectively) are centrifuged, reagents 59 in reservoirs 18 of devices 10 and 10a are urged from reservoirs 18 and into corresponding interiors 74 of third and fourth capsules 82 and 84, respectively,
It is noted that since devices 10 and 10a are small, a number of devices 10 and 10a can be bundled together in a single capsule, e.g., first capsule 62, so as to allow for the simultaneous filling of multiple devices 10 and 10a. Further, it is understood that a number of devices 10 and 10a containing different reagents can be bundled together in a single capsule, e.g., third capsule 82, so as to allow for the simultaneous delivery of several different reagents to the interior 74 of such capsule.
Referring to
Wall 104 includes a first upper end 112 and a second lower end 114. Upper and lower ends 112 and 114, respectively, define corresponding upper and lower orifices 116 and 118, respectively, which communicate with reservoir 108. Seal 120 is receivable in reservoir 108 of tube 102 through lower orifice 118. Seal 120 extends along a longitudinal axis and includes a generally cylindrical outer surface 122. It is intended for outer surface 122 of seal 120 to form a fluidic seal with inner surface 106 of wall 104 so as to prevent fluid received in reservoir 108 from exiting reservoir 108 though lower orifice 118. In the depicted embodiment, lower surface 124 of seal 120 is generally coplanar with lower end 114 of wall 104.
Seal 130 is receivable in reservoir 108 of tube 102 through upper orifice 116. Seal 130 extends along a longitudinal axis and includes a generally cylindrical outer surface 132. It is intended for outer surface 132 of seal 130 to form a fluidic seal with inner surface 106 of wall 104 so as to prevent fluid received in reservoir 108 from exiting reservoir 108 though upper orifice 116. In the depicted embodiment, upper surface 134 of seal 130 is generally coplanar with upper end 112 of wall 104. It is contemplated to provide opening 136 through wall 104 at a location spaced from the intersection of outer surface 132 of seal 130 and inner surface 106 of wall 104 such that opening 136 communicates with reservoir 108. Upper portion 136a of opening 136 is generally coplanar with lower surface 138 of seal 130 to facilitate the flow of fluid into and out of reservoir 108, as hereinafter described.
Stanchion 140 projects from upper surface 134 of seal 130, for example, along the longitudinal axis of seal 130. However, stanchion 140 may project from other locations of or along other angles to upper surface 134 of seal 130. It is contemplated for upper surface 142 of stanchion 140 to lie in a plane generally parallel to and spaced from a plane containing upper end 112 of wall 104.
In order to fill device 100, device 100 is positioned within interior 74 of a capsule, e.g, first capsule 62, such that upper surface 142 of stanchion 140 is directed away from closed tip 76 of tapered portion 68 of first capsule 62. In addition, interior 74 of first capsule 62 is filled with a sufficient volume of a desired reagent 59 such that desired reagent 59 overlaps opening 136 in wall 104 of tube 102. Thereafter, lid 70 is moved to the closed position and first capsule 62 is deposited in a corresponding retainer 80 in centrifuge machine 60. With first capsule 62 received in a corresponding retainer 80 in centrifuge machine 60, centrifuge machine 60 is actuated so as to centrifuge first capsule 62 for a desired time period (e.g. 30 seconds) at user selected revolutions per minute. As first capsule 62 (and hence, device 100) is centrifuged, a portion of reagent 59 in first capsule 62 is urged into corresponding reservoir 108 in device 100 such that the air, previously in reservoir 108, is expelled therefrom. The volume of fluid received in reservoir 108 of device 100 is controlled by the geometry and the volume of reservoir 108. By way of example, it is contemplated for each reservoir 108 to have a volume less than 10 microliters, and preferably, in the range of 0.01 microliters to 6 microliters, Reservoir 18 may have a diameter in the range of 50 micrometers to 1.5 millimeters and a length in the range of 1 millimeter and 15 millimeters. More specifically, it is contemplated for reservoir 108 to have a diameter of approximately 0.66 mm and a length of approximately 8 mm. However, other diameters and lengths are possible without deviating from the scope of the present invention. Once reservoir 108 is filled with reagent 59, as heretofore described, device 100 may be removed from capsule 62. This “prepackaged” device 100 may be transported to an end user. It is noted that small area of opening 136 in device 100 severely limits evaporation, and hence, mitigates the risk of evaporative loss of reagent 59 from reservoir 108.
In order to remove the reagent 59 from reservoir 108 of device 100, device 100 is positioned within a corresponding capsule, e.g. third capsule 82, such that upper surface 142 of stanchion 140 is directed towards, and preferably engages, closed tip 76 of tapered portion 68 of third capsule 82. Thereafter, lid 70 is moved to the closed position and third capsule 82 is deposited in a corresponding retainer 80 in centrifuge machine 60. With third capsule 82 received in retainer 80 in centrifuge machine 60, centrifuge machine 60 is actuated so as to centrifuge third capsule 82 for a desired time period (e.g. 30 seconds) at user selected revolutions per minute. As third capsule 82 (and hence, device 100) is centrifuged, reagent 59 in reservoir 108 of device 100 is urged from reservoir 108 through opening 136 and into corresponding interior 74 of third capsule 82. It can be appreciated that during the centrifugation process, stanchion 140 maintains opening 136 in device 100 in spaced relation to closed tip 76 of tapered portion 68 of third capsule 82 thereby assuring that all of the fluidic contents of reservoir 108 has been expelled from device 100 into corresponding interior 74 of third capsule 82, respectively. As this point, the nano- or micro-volumes of reagent 59 has been delivered to interior 74 of third capsule 82 and is accessible for downstream dilutions or applications.
Referring to
Device 150 further includes generally planar base 172 with first and second opposite sides 174 and 176, respectively,
In order to fill lid 151 of device 150, device 150 is positioned within interior 74 of a capsule, e.g, first capsule 62, such that openings 167 in cylindrical tubes 158 are directed away from closed tip 76 of tapered portion 68 of first capsule 62. In addition, interior 74 of first capsule 62 is filled with a sufficient volume of a desired reagent 59 such that desired reagent 59 overlaps openings 167. Thereafter, lid 70 is moved to the closed position and first capsule 62 is deposited in a corresponding retainer 80 in centrifuge machine 60. With first capsule 62 received in a corresponding retainer 80 in centrifuge machine 60, centrifuge machine 60 is actuated so as to centrifuge first capsule 62 for a desired time period (e.g. 30 seconds) at user selected revolutions per minute. As first capsule 62 (and hence, device 100) is centrifuged, a portion of reagent 59 in first capsule 62 is urged into corresponding reservoirs 168 in cylindrical tubes 158 through openings 167 such that the air, previously in reservoirs 168, is expelled therefrom. The volumes of fluid received in reservoirs 168 of cylindrical tubes 158 are controlled by the geometry and the volume of reservoirs 168. By way of example, it is contemplated for each reservoir 168 to have a volume less than 10 microliters, and preferably, in the range of 0.01 microliters to 6 microliters. Reservoir 168 may have a diameter in the range of 50 micrometers to 1.5 millimeters and a length in the range of 1 millimeter and 15 millimeters. More specifically, it is contemplated for reservoir 168 to have a diameter of approximately 0.66 mm and a length of approximately 8 mm. However, other diameters and lengths are possible without deviating from the scope of the present invention.
Once reservoir 168 is filled with reagent 59, as heretofore described, lid 151 of device 150 may be removed from capsule 62 and interconnected to base 172 so as to form device 150. More specifically, to form device 150, lid 151 is inserted into base 172 such that cylindrical tubes 158 of lid 151 are received in corresponding cylindrical recesses 178 in base 172. As such, the “prepackaged” device 150 may be transported to an end user. It is noted that lid 151 interconnected to base 172, openings 167 in cylindrical tubes 178 of lid 151 are spaced from corresponding inner surfaces 196 of end walls 194 partially defining reservoirs 188 of base 172.
In order to remove the reagent 59 from reservoirs 168 of lid 151, device 150, namely, the lid 151 and base 172 combination is centrifuged. By way of example, lid 151 and base 172 combination may be positioned within a corresponding capsule, e.g. third capsule 82 such that outer surfaces 198 of end walls 194 of base 172 are directed towards closed tip 76 of tapered portion 68 of third capsule 82. However, it can be appreciated that other arrangements for centrifuging lid 151 and base 172 combination are contemplated as being within the scope of the present invention. Thereafter, once lid 151 and base 172 combination is positioned within a corresponding capsule, e.g. third capsule 82, lid 70 is moved to the closed position and third capsule 82 is deposited in a corresponding retainer 80 in centrifuge machine 60. With third capsule 82 received in retainer 80 in centrifuge machine 60, centrifuge machine 60 is actuated so as to centrifuge third capsule 82 for a desired time period (e.g. 30 seconds) at user selected revolutions per minute. As third capsule 82 (and hence, device 100) is centrifuged, reagents 59 in reservoirs 168 of lid 151 are urged from reservoir 168 and into corresponding reservoirs 188 in cylindrical recesses 178 of base 172. It can be appreciated that during the centrifugation process, the spacing between openings 167 in cylindrical tubes 178 of lid 151 and the corresponding inner surfaces 196 of end walls 194 partially defining reservoirs 188 of base 172 allows for all of the fluidic contents of reservoirs 168 to be expelled therefrom into corresponding reservoirs 188 in cylindrical recesses 178 abase 172. After removal of lid 151 from base 172, the nano- or micro-volumes of reagents 59 in reservoirs 188 in cylindrical recesses 178 of base 172 are accessible for downstream dilutions or applications.
It can be appreciated that the above descriptions of devices are merely exemplary of the present invention. Various modes of carrying out the invention are contemplated as being within the scope of the following claims particularly pointing out and distinctly claiming the subject matter, which is regarded as the invention.
This application is a divisional of U.S. application Ser. No. 15/277,029, filed Sep. 27, 2016.
This invention was made with government support under CA160344 awarded by the National Institutes of Health. The government has certain rights in the invention.
Number | Name | Date | Kind |
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20120277697 | Haghgooie et al. | Nov 2012 | A1 |
20140309096 | Wilkinson et al. | Oct 2014 | A1 |
Entry |
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“Rapid DNA Isolation From Mammalian Cell Lysates Using the Gilson Extractman(TM)”, Gilson, Inc., Middleton, WI 53562, downloaded from www.gilson.com/Resources/TRANS0615_EXTRACTMAN_DNA.pdf on Dec. 30, 2016. |
Number | Date | Country | |
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20210016285 A1 | Jan 2021 | US |
Number | Date | Country | |
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Parent | 15277029 | Sep 2016 | US |
Child | 17032671 | US |