Devices and methods for manipulating deformable fluid vessels

Abstract
A fluid container comprises a first vessel, a second vessel connected or connectable to the first vessel, and a sealing partition preventing fluid flow from the second vessel. The container further includes a spherical opening element initially supported within the second vessel by the sealing partition and configured to be contacted with the sealing partition to open the sealing partition and permit fluid flow from the second vessel.
Description
FIELD OF THE INVENTION

Aspects of the invention relate to systems, methods, and apparatus for selectively opening deformable fluid vessels. One aspect of the invention relates to generating compressive forces for compressing deformable fluid vessels to displace fluid therefrom in a low profile instrument. Other aspects of the invention relate to opening the deformable fluid vessel in a manner that reduces the amount of compressive force required to displace fluid from the vessel. Other aspects of the invention relate to an apparatus for protecting the deformable fluid vessel from inadvertent exposure to external forces and for interfacing with the vessel to permit intentional application of external compressive force without removing the vessel-protective features.


BACKGROUND OF INVENTION

The present invention relates to systems, methods, and apparatus for manipulating deformable fluid vessels. An exemplary device having such deformable fluid vessels is shown in FIGS. 1A and 1B. A liquid reagent module 10 includes a substrate 12 on which a plurality of deformable fluid vessels, or blisters, are attached. Devices such as the liquid reagent module 10 are often referred to as cartridges or cards. In an embodiment, the liquid reagent module 10 includes an input port 16, which may comprise a one-way valve, for dispensing a sample fluid into the module 10. A fluid channel 18 carries fluid from the input port 16. A sample vent 14 vents excess pressure from the module 10. A labeled panel 20 may be provided for an identifying label, such as a barcode or other human and/or machine-readable information.


Liquid reagent module 10 further includes a plurality of deformable (collapsible) vessels (blisters), including, in the illustrated embodiment, an elution reagent blister 22, a wash buffer blister 24, a water blister 26, a lysis reagent blister 28, an air blister 30, a binding agent blister 32, and an oil blister 34. Note that the number and types of blisters shown are merely exemplary. Each of the blisters may be interconnected with one or more other blisters and/or the fluid channel 18 by one or more fluid channels formed in or on the substrate 12.


The liquid reagent module 10 may be processed by selectively compressing one or more of the blisters to completely or partially collapse the blister to displace the fluid therefrom. Instruments adapted to process the liquid reagent module 10, or other devices with deformable fluid vessels, include mechanical actuators, e.g., typically pneumatically or electromechanically actuated, constructed and arranged to apply collapsing pressure to the blister(s). Typically, such actuator(s) is(are) disposed and are moved transversely to the plane of the module 10—for example, if module 10 were oriented horizontally within an instrument, actuators may be provided vertically above and/or below the module 10 and would be actuated to move vertically, in a direction generally normal to the plane of the module. The liquid reagent module 10 may be processed in an instrument in which the module 10 is placed into a slot or other low profile chamber for processing. In such a slot, or low profile chamber, providing actuators or other devices that are oriented vertically above and/or below the module 10 and/or move in a vertical direction may not be practical. The pneumatic and/or electromechanical devices for effecting movement of such actuators require space above and/or below the module's substrate, space that may not be available in a slotted or other low profile instrument.


Accordingly, a need exists for methods, systems, and/or apparatus for effecting movement of an actuator for collapsing a vessel within a low profile component space of an instrument.


SUMMARY OF THE INVENTION

Aspects of the invention are embodied in an apparatus for processing a fluid module including a collapsible vessel supported on a planar substrate by applying a force compressing the vessel against the substrate. The apparatus comprises a first actuator component configured to be movable in a first direction that is generally parallel to the plane of the substrate, a second actuator component configured to be movable in a second direction having a component that is generally normal to the plane of the substrate, and a motion conversion mechanism coupling the first actuator component with the second actuator component and constructed and arranged to convert movement of the first actuator component in the first direction into movement of the second actuator component in the second direction.


According to further aspects of the invention, the first actuator component comprises an actuator plate configured to be movable in the first direction and including a cam follower element, the second actuator component comprises a platen configured to be movable in the second direction, and the motion conversion mechanism comprises a cam body having a cam surface. The cam body is coupled to the platen and is configured such that the cam follower element of the actuator plate engages the cam surface of the cam body as the actuator plate moves in the first direction thereby causing movement of the cam body that results in movement of the platen in the second direction.


According to further aspects of the invention, the cam follower element of the actuator plate comprises a roller configured to rotate about an axis of rotation that is parallel to the actuator plate and normal to the first direction, the motion conversion mechanism further comprises a chassis, and the cam body is pivotally attached at one portion thereof to the chassis and at another portion thereof to the platen.


According to further aspects of the invention, the cam surface of the cam body comprises an initial flat portion and a convexly-curved portion, and movement of the roller from the initial flat portion to the convexly-curved portion causes the movement of the cam body that results in movement of the platen in the second direction.


According to further aspects of the invention, the first actuator component comprises a cam rail configured to be movable in the first direction, the second actuator component comprises a platen configured to be movable in the second direction, and the motion conversion mechanism comprises a cam surface and a cam follower coupling the cam rail to the platen and configured to convert motion of the cam rail in the first direction into movement of the platen in the second direction.


According to further aspects of the invention, the cam surface comprises a cam profile slot formed in the cam rail, and the cam follower comprises a follower element coupling the platen to the cam profile slot such that movement of the cam rail in the first direction causes movement of the cam follower within the cam profile slot that results in the movement of the platen in the second direction.


Further aspects of the invention are embodied in an apparatus for displacing fluid from a fluid container. The fluid container includes a first vessel and a second vessel connected or connectable to the first vessel and including a sealing partition preventing fluid flow from the second vessel, and the fluid container further includes an opening device configured to be contacted with the sealing partition to open the sealing partition and permit fluid flow from the second vessel. The apparatus comprises a first actuator configured to be movable with respect to the first vessel to compress the first vessel and displace fluid contents thereof and a second actuator movable with respect to the opening device and configured to contact the opening device and cause the opening device to open the sealing partition, The second actuator is releasably coupled to the first actuator such that the second actuator moves with the first actuator until the second actuator contacts the opening device and causes the opening device to open the sealing partition, after which the second actuator is released from the first actuator and the first actuator moves independently of the second actuator to displace fluid from the first vessel.


Further aspects of the invention are embodied in a fluid container comprising a first vessel, a second vessel connected or connectable to the first vessel, a sealing partition preventing fluid flow from the second vessel, and a spherical opening element initially supported within the second vessel by the sealing partition and configured to be contacted with the sealing partition to open the sealing partition and permit fluid flow from the second vessel.


Further aspects of the invention are embodied in a fluid container comprising a first vessel, a second vessel connected or connectable to the first vessel, a sealing partition preventing fluid flow from the second vessel, and a cantilevered lance having a piercing point and disposed with the piercing point adjacent to the sealing partition and configured to be deflected until the piercing point pierces the sealing partition to permit fluid flow from the second vessel through the pierced sealing partition.


Further aspects of the invention are embodied in a fluid container comprising a first vessel, a second vessel connected or connectable to the first vessel, a sealing partition preventing fluid flow from the second vessel, and a cantilevered lance having a piercing point and being fixed at an end thereof opposite the piercing point, the cantilevered lance being disposed with the piercing point adjacent to the sealing partition and configured to be deflected until the piercing point pierces the sealing partition to permit fluid flow from the second vessel through the pierced sealing partition.


According to further aspects of the invention, the fluid container further comprises a substrate on which the first and second vessels are supported and which includes a chamber formed therein adjacent the sealing partition wherein an end of the cantilevered lance is secured to the substrate and the piercing point of the lance is disposed within the chamber.


Further aspects of the invention are embodied in a fluid container comprising a first vessel, a second vessel connected or connectable to the first vessel, a sealing partition preventing fluid flow from the second vessel, and a lancing pin having a piercing point and disposed with the piercing point adjacent to the sealing partition and configured to be moved with respect to the sealing partition until the piercing point pierces the sealing partition to permit fluid flow from the second vessel through the pierced sealing partition.


According to further aspects of the invention, the lancing pin has a fluid port formed therethrough to permit fluid to flow through the lancing pin after the sealing partition is pierced by the piercing point.


According to further aspects of the invention, the fluid container further comprises a substrate on which the first and second vessels are supported and which includes a chamber formed therein adjacent the sealing partition within which the lancing pin is disposed.


According to further aspects of the invention, the chamber in which the lancing pin is disposed comprises a segmented bore defining a hard stop within the chamber and the lancing pin includes a shoulder that contacts the hard stop to prevent further movement of the lancing pin after the piercing point pierces the sealing partition.


According to further aspects of the invention, the fluid container further comprises a fluid channel extending between the first and second vessels.


According to further aspects of the invention, the fluid container of further comprises a seal within the fluid channel, the seal being configured to be breakable upon application of sufficient force to the seal to thereby connect the first and second vessels via the fluid channel.


Further aspects of the invention are embodied in a fluid container comprising a first vessel, a second vessel disposed within the first vessel, a substrate on which the first and second vessels are supported and having a cavity formed therein adjacent the second vessel, a fixed spike formed within the cavity, and a fluid exit port extending from the cavity, wherein the first and second vessels are configured such that external pressure applied to the first vessel will collapse the second vessel and cause the second vessel to contact and be pierced by the fixed spike, thereby allowing fluid to flow from the first vessel through the pierced second vessel, the cavity, and the fluid exit port.


Further aspects of the invention are embodied in a fluid container comprising a collapsible vessel configured to be collapsed upon application of sufficient external pressure to displace fluid from the vessel, a housing surrounding at least a portion of the collapsible vessel, and a floating compression plate movably disposed within the housing. The housing includes an opening configured to permit an external actuator to contact the floating compression plate within the housing and press the compression plate into the collapsible vessel to collapse the vessel and displace the fluid contents therefrom.


Other features and characteristics of the present invention, as well as the methods of operation, functions of related elements of structure and the combination of parts, and economies of manufacture, will become more apparent upon consideration of the following description and the appended claims with reference to the accompanying drawings, all of which form a part of this specification, wherein like reference numerals designate corresponding parts in the various figures.





BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings, which are incorporated herein and form part of the specification, illustrate various, non-limiting embodiments of the present invention. In the drawings, common reference numbers indicate identical or functionally similar elements.



FIG. 1A is a top plan view of a liquid reagent module.



FIG. 1B is a side view of the liquid reagent module.



FIG. 2 is a perspective view of a blister compressing actuator mechanism embodying aspects of the present invention.



FIG. 3A is a partial, cross-sectional perspective view of the articulated blister actuator platen assembly in an initial, unactuated state.



FIG. 3B is a partial, cross-sectional side view of the articulated blister actuator platen assembly in the initial unactuated state.



FIG. 4A is a partial, cross-sectional perspective view of the articulated blister actuator platen assembly as the platen is about to be actuated.



FIG. 4B is a partial, cross-sectional side view of the articulated blister actuator platen assembly as the platen is about to be actuated.



FIG. 5A is a partial, cross-sectional perspective view of the articulated blister actuator platen assembly with the platen in a fully actuated state.



FIG. 5B is a partial, cross-sectional side view of the articulated blister actuator platen assembly with the platen in a fully actuated state.



FIG. 6A is a partial, cross-sectional perspective view of the articulated blister actuator platen assembly with the platen returned to the unactuated state.



FIG. 6B is a partial, cross-sectional side view of the articulated blister actuator platen assembly with the platen returned to the unactuated state.



FIG. 7A is a perspective view of an alternative embodiment of a blister compressing actuator mechanism in an unactuated state.



FIG. 7B is a perspective view of the blister compressing actuator mechanism of FIG. 7A in the fully actuated state.



FIG. 8A is a partial, cross-sectional side view of a collapsible fluid vessel configured to facilitate opening of the vessel.



FIG. 8B is an enlarged partial, cross-sectional side view of a vessel opening feature of the collapsible fluid vessel.



FIGS. 9A-9D are side views showing an apparatus for opening a collapsible vessel configured to facilitate opening of the vessel in various states.



FIG. 10 is a side view of an alternative embodiment of an apparatus for opening a collapsible vessel configured to facilitate opening of the vessel.



FIG. 11 is a bar graph showing exemplary burst forces for fluid-containing blisters of varying volumes.



FIG. 12 is a load versus time plot of the compression load versus time during a blister compression.



FIG. 13A is a partial, cross-sectional side view of an alternative apparatus for opening a collapsible vessel configured to facilitate opening of the vessel.



FIG. 13B is a perspective view of a cantilever lance used in the embodiment of FIG. 13A.



FIG. 14 is a partial, cross-sectional side view of an alternative apparatus for opening a collapsible vessel configured to facilitate opening of the vessel.



FIG. 15A is a partial, cross-sectional side view of an alternative apparatus for opening a collapsible vessel configured to facilitate opening of the vessel.



FIG. 15B is a perspective view of a lancing pin used in the apparatus of FIG. 15A.



FIG. 16A is a partial, cross-sectional side view of an alternative apparatus for opening a collapsible vessel configured to facilitate opening of the vessel.



FIG. 16B is a perspective view of a lancing pin used in the apparatus of FIG. 16A.



FIG. 17 is an exploded, cross-sectional, perspective view of an apparatus for protecting and interfacing with a collapsible vessel.



FIG. 18 is a cross-sectional, side view of the apparatus for protecting and interfacing with a collapsible vessel in an unactuated state.



FIG. 19 is a cross-sectional, perspective view of the apparatus for protecting and interfacing with a collapsible vessel in fully actuated state.





DETAILED DESCRIPTION OF THE INVENTION

Unless defined otherwise, all terms of art, notations and other scientific terms or terminology used herein have the same meaning as is commonly understood by one of ordinary skill in the art to which this disclosure belongs. Many of the techniques and procedures described or referenced herein are well understood and commonly employed using conventional methodology by those skilled in the art. As appropriate, procedures involving the use of commercially available kits and reagents are generally carried out in accordance with manufacturer defined protocols and/or parameters unless otherwise noted. All patents, applications, published applications and other publications referred to herein are incorporated by reference in their entirety. If a definition set forth in this section is contrary to or otherwise inconsistent with a definition set forth in the patents, applications, published applications, and other publications that are herein incorporated by reference, the definition set forth in this section prevails over the definition that is incorporated herein by reference.


As used herein, “a” or “an” means “at least one” or “one or more.”


This description may use relative spatial and/or orientation terms in describing the position and/or orientation of a component, apparatus, location, feature, or a portion thereof. Unless specifically stated, or otherwise dictated by the context of the description, such terms, including, without limitation, top, bottom, above, below, under, on top of, upper, lower, left of, right of, in front of, behind, next to, adjacent, between, horizontal, vertical, diagonal, longitudinal, transverse, etc., are used for convenience in referring to such component, apparatus, location, feature, or a portion thereof in the drawings and are not intended to be limiting.


An actuator mechanism for compressing deformable fluid vessels—such as blisters on a liquid reagent module—embodying aspects of the present invention is shown at reference number 50 in FIG. 2. The actuator mechanism 50 may include an articulated blister actuator platen assembly 52 and a sliding actuator plate 66. The sliding actuator plate 66 is configured to be movable in a direction that is generally parallel to the plane of the liquid reagent module—horizontally in the illustrated embodiment—and may be driven by a linear actuator, a rack and pinion, a belt drive, or other suitable motive means. Sliding actuator plate 66, in the illustrated embodiment, has V-shaped edges 76 that are supported in four V-rollers 74 to accommodate movement of the plate 66 in opposite rectilinear directions, while holding the sliding actuator plate 66 at a fixed spacing from the actuator platen assembly 52. Other features may be provided to guide the actuator plate 66, such as rails and cooperating grooves. A component 40—which may comprise liquid reagent module 10 described above—having one or more deformable fluid vessels, such as blisters 36 and 38, is positioned within the actuator mechanism 50 beneath the articulated blister actuator platen assembly 52.


Further details of the configuration of the articulated blister actuator platen assembly 52 and the operation thereof are shown in FIGS. 3A-6B.


As shown in FIGS. 3A and 3B, the actuator platen assembly 52 includes a chassis 54. A cam body 56 is disposed within a slot 57 of the chassis 54 and is attached to the chassis 54 by a first pivot 58. A platen 64 is pivotally attached to the cam body 56 by means of a second pivot 60. The cam body 56 is held in a horizontal, unactuated position within the slot 57 by means of a torsional spring 55 coupled around the first pivot 58.


Cam body 56 further includes a cam surface 65 along one edge thereof (top edge in the figure) which, in the exemplary embodiment shown in FIG. 3B, comprises an initial flat portion 61, a convexly-curved portion 62, and a second flat portion 63. The sliding actuator plate 66 includes a cam follow 68 (a roller in the illustrated embodiment) rotatably mounted within a slot 72 formed in the actuator plate 66. In an embodiment of the invention, one cam body 56 and associated platen 64 and cam follower 68 are associated with each deformable vessel (e.g. blister 36) of the liquid reagent module 40.


The actuator platen assembly 52 and the sliding actuator plate 66 are configured to be movable relative to each other. In one embodiment, the actuator platen assembly 52 is fixed, and the actuator plate 66 is configured to move laterally relative to the platen assembly 52, supported by the V-rollers 74. Lateral movement of the sliding actuator plate 66, e.g., in the direction “A”, causes the cam follower 68 to translate along the cam surface 65 of the cam body 56, thereby actuating the cam body 56 and the platen 64 attached thereto.


In FIGS. 3A and 3B, before the sliding actuator plate 66 has begun to move relative to the actuator platen assembly 52, the cam follower 68 is disposed on the initial flat portion 61 of the cam surface 65 of the cam body 56. In FIGS. 4A and 4B, the sliding actuator plate 66 has moved relative to the actuator platen assembly 52 in the direction “A” so that the cam follower 68 has moved across the initial flat portion 61 of the cam surface 65 and has just begun to engage the upwardly curved contour of the convexly-curved portion 62 of the cam surface 65 of the cam body 56.


In FIGS. 5A and 5B, the sliding actuator plate 66 has proceeded in the direction “A” to a point such that the cam follower 68 is at the topmost point of the convexly-curved portion 62 of the cam surface 65, thereby causing the cam body 56 to rotate about the first pivot 58. The platen 64 is lowered by the downwardly pivoting cam body 56 and pivots relative to the cam body 56 about the second pivot 60 and thereby compresses the blister 36.


In FIGS. 6A and 6B, sliding actuator plate 66 has moved to a position in the direction “A” relative to the actuator platen assembly 52 such that the cam follower 68 has progressed to the second flat portion 63 of the cam surface 65. Accordingly, the cam body 56, urged by the torsion spring 55, pivots about the first pivot 58 back to the unactuated position, thereby retracting the platen 64.


Thus, the articulated blister actuator platen assembly 52 is constructed and arranged to convert the horizontal movement of actuator plate 66 into vertical movement of the platen 64 to compress a blister, and movement of the platen does not require pneumatic, electromechanical, or other components at larger distances above and/or below the liquid module.


An alternative embodiment of a blister compression actuator mechanism is indicated by reference number 80 in FIGS. 7A and 7B. Actuator 80 includes a linear actuator 82 that is coupled to a cam rail 84. Cam rail 84 is supported for longitudinal movement by a first support rod 96 extending transversely through slot 86 and a second support rod 98 extending transversely through a second slot 88 formed in the cam rail 84. The first support rod 96 and/or the second support rod 98 may include an annular groove within which portions of the cam rail 84 surrounding slot 86 or slot 88 may be supported, or cylindrical spacers may be placed over the first support rod 96 and/or the second support rod 98 on opposite sides of the cam rail 84 to prevent the cam rail 84 from twisting or sliding axially along the first support rail 96 and/or the second support rail 98.


Cam rail 84 includes one or more cam profile slots. In the illustrated embodiment, cam rail 84 includes three cam profile slots 90, 92, and 94. Referring to cam profile slot 90, in the illustrated embodiment, slot 90 includes, progressing from left to right in the figure, an initial horizontal portion, a downwardly sloped portion, and a second horizontal portion. The shapes of the cam profile slots are exemplary, and other shapes may be effectively implemented. The actuator mechanism 80 also includes a platen associated with each cam profile slot. In the illustrated embodiment, actuator 80 includes three platens 100, 102, 104 associated with cam profile slots 90, 92, 94, respectively. First platen 100 is coupled to the cam profile slot 90 by a cam follower pin 106 extending transversely from the platen 100 into the cam profile slot 90. Similarly, second platen 102 is coupled to the second cam profile slot 92 by a cam follower pin 108, and the third platen 104 is coupled to the third cam profile slot 94 by a cam follower pin 110. Platens 100, 102, 104 are supported and guided by a guide 112, which may comprise a panel having openings formed therein conforming to the shape of each of the platens.


In FIG. 7A, cam rail 84 is in its furthest right-most position, and the platens 100, 102, 104 are in their unactuated positions. Each of the cam follower pins 106, 108, 110 is in the initial upper horizontal portion of the respective cam profile slot 90, 92, 94. As the cam rail 84 is moved longitudinally to the left, in the direction “A” shown in FIG. 7B, by the linear actuator 82, each cam follower pin 106, 108, 110 moves within its respective cam profile slot 90, 92, 94 until the cam follower pin is in the lower, second horizontal portion of the respective cam profile slot. Movement of each of the pins 106, 108, 110 downwardly within its respective cam profile slot 90, 92, 94 causes a corresponding downward movement of the associated platen 100, 102, 104. This movement of the platens thereby compresses a fluid vessel (or blister) located under each platen. Each platen may compress a vessel directly in contact with the platen or it may contact the vessel through one or more intermediate components located between the vessel and the corresponding platen.


Thus, the blister compression actuator mechanism 80 is constructed and arranged to convert the horizontal movement cam rail 84, driven by the linear actuator 82, into vertical movement of the platens 100, 102, 104 to compress blisters, and movement of the platens does not require pneumatic, electromechanical, or other components at larger distances above and/or below the liquid module.


When compressing a fluid vessel, or blister, to displace the fluid contents thereof, sufficient compressive force must be applied to the blister to break, or otherwise open, a breakable seal that is holding the fluid within the vessel. The amount of force required to break the seal and displace the fluid contents of a vessel typically increases as the volume of the vessel increases. This is illustrated in the bar graph shown in FIG. 11, which shows the minimum, maximum, and average blister burst forces required for blisters having volumes of 100, 200, 400, and 3000 microliters. The average force required to burst a blister of 400 or less microliters is relatively small, ranging from an average of 10.7 lbf to 11.5 lbf. On the other hand, the force required to burst a blister of 3000 microliters is substantially larger, with an average burst force of 43.4 lbf and a maximum required burst force of greater than 65 lbf. Generating such large forces can be difficult, especially in low profile actuator mechanisms, such as those described above, in which horizontal displacement of an actuator is converted into vertical, blister-compressing movement of a platen.


Accordingly, aspects of the present invention are embodied in methods and apparatus for opening a fluid vessel, or blister, in a manner that reduces the amount of force required to burst the vessel and displace the fluid contents of the vessel.


Such aspects of the invention are illustrated in FIGS. 8A and 8B. As shown in FIG. 8A, a fluid vessel (or blister) 122 is mounted on a substrate 124 and is connected by means of a channel 130 to a sphere blister 128. In certain embodiments, channel 130 may be initially blocked by a breakable seal. A film layer 129 may be disposed on the bottom of the substrate 124 to cover one or more channels formed in the bottom of the substrate 124 to form fluid conduits. An opening device, comprising a sphere 126 (e.g., a steel ball bearing) is enclosed within the sphere blister 128 and is supported, as shown in FIG. 8A, within the sphere blister 128 by a foil partition or septum 125. The foil partition 125 prevents fluid from flowing from the vessel 122 through a recess 127 and fluid exit port 123. Upon applying downward force to the sphere 126, however, a large local compressive stress is generated due to the relatively small surface size of the sphere 126, and the foil partition 125 can be broken with relatively little force to push the sphere 126 through the partition 125 and into the recess 127, as shown in FIG. 8B. With the foil partition 125 broken, a relatively small additional force is required to break a seal within channel 130 and force the fluid to flow from the vessel 122 through the fluid exit port 123.


In FIG. 8B, the sphere blister 128 is shown intact. In some embodiments, a force applied to the sphere 126 to push it through the foil partition 125 would also collapse the sphere blister 128.


An apparatus for opening a vessel by pushing a sphere 126 through foil partition 125 is indicated by reference number 120 in FIGS. 9A, 9B, 9C, 9D. In the illustrated embodiment, the apparatus 120 includes a ball actuator 140 extending through an opening formed through a blister plate, or platen, 132. With the blister plate 132 and an actuator 138 configured for moving the blister plate 132 disposed above the vessel 122, the ball actuator 140 is secured in a first position, shown in FIG. 9A, by a detent 136 that engages a detent collar 144 formed in the ball actuator 140.


As shown in FIG. 9B, the blister plate 132 is moved by the actuator 138 down to a position in which a contact end 142 of the ball actuator 140 contacts the top of the of the sphere blister 128. Actuator 138 may comprise a low profile actuator, such as actuator mechanisms 50 or 80 described above.


As shown in FIG. 9C, continued downward movement of the blister plate 132 by the actuator 138 causes the ball actuator 140 to collapse the sphere blister 128, thereby pushing the opening device, e.g., sphere 126, through a partition blocking fluid flow from the vessel 122. In this regard, it will be appreciated that the detent must provide a holding force sufficient to prevent the ball actuator 140 from sliding relative to the blister plate 132 until after the sphere 126 has pierced the partition. Thus, the detent must provide a holding force sufficient to collapse the sphere blister 128 and push the sphere 126 through a partition.


As shown in FIG. 9D, continued downward movement of the blister plate 132 by the actuator 138 eventually overcomes the holding force provided by the detent 136, and the ball actuator 140 is then released to move relative to the blister plate 132, so that the blister plate can continue to move down and collapse the vessel 122.


After the vessel 122 is collapsed, the blister plate 132 can be raised by the actuator 138 to the position shown in FIG. 9A. As the blister plate 132 is being raised from the position shown in FIG. 9D to the position shown in 9A, a hard stop 146 contacts a top end of the ball actuator 140 to prevent its continued upward movement, thereby sliding the ball actuator 140 relative to the blister plate 132 until the detent 136 contacts the detent collar 144 to reset the ball actuator 140.


An alternative embodiment of an apparatus for opening a vessel embodying aspects of the present invention is indicated by reference number 150 in FIG. 10. Apparatus 150 includes a pivoting ball actuator 152 configured to pivot about a pivot pin 154. A top surface 156 of the pivoting ball actuator 152 comprises a cam surface, and a cam follower 158, comprising a roller, moving in the direction “A” along the cam surface 156 pivots the actuator 152 down in the direction “B” to collapse the sphere blister 128 and force the sphere 126 through the foil partition 125. Pivoting actuator 152 may further include a torsional spring (not shown) or other means for restoring the actuator to an up position disengaged with the sphere blister 128 when the cam follower 158 is withdrawn.



FIG. 12 is a plot of compressive load versus time showing an exemplary load versus time curve for an apparatus for opening a vessel embodying aspects of the present invention. As the apparatus contacts and begins to compress the sphere blister 128, the load experiences an initial increase as shown at portion (a) of the graph. A plateau shown at portion (b) of the graph occurs after the sphere 126 penetrates the foil partition 125. A second increase in the force load occurs when the blister plate 132 makes contact with and begins compressing the vessel 122. A peak, as shown at part (c) of the plot, is reached as a breakable seal within channel 130 between the vessel 122 and the sphere blister 128 is broken. After the seal has been broken, the pressure drops dramatically, as shown at part (d) of the plot, as the vessel 122 is collapsed and the fluid contained therein is forced through the exit port 123 (See FIGS. 8A, 8B) supporting the sphere 126.


An alternative apparatus for opening a vessel is indicated by reference number 160 in FIG. 13A. As shown in FIG. 13A, a fluid vessel (or blister) 162 is mounted on a substrate 172 and is connected by means of a channel—which may or may not be initially blocked by a breakable seal—to a dimple 161. A film layer 164 may be disposed on the bottom of the substrate 172 to cover one or more channels formed in the bottom of the substrate 172 to form fluid conduits. An opening device comprising a cantilevered lance 166 is positioned within a lance chamber 170 formed in the substrate 172 where it is anchored at an end thereof by a screw attachment 168.


A foil partition or septum 165 seals the interior of the dimple 161 from the lance chamber 170. An actuator pushes the lance 170 up in the direction “A” into the dimple 161, thereby piercing the foil partition 165 and permitting fluid to flow from the blister 162 out of the lance chamber 170 and a fluid exit port. The spring force resilience of the lance 166 returns it to its initial position after the upward force is removed. In one embodiment, the lance 166 is made of metal. Alternatively, a plastic lance could be part of a molded plastic substrate on which the blister 162 is formed. Alternatively, a metallic lance could be heat staked onto a male plastic post. A further option is to employ a formed metal wire as a lance.


A further alternative embodiment of an apparatus for opening a vessel is indicated by reference number 180 in FIG. 14. A component having one or more deformable vessels includes at least one blister 182 formed on a substrate 194. In the arrangement shown in FIG. 14, an internal dimple 184 is formed inside the blister 182. Internal dimple 184 encloses an opening device comprising a fixed spike 186 projecting upwardly from a spike cavity 188 formed in the substrate 194. A film layer 192 is disposed on an opposite side of the substrate 194. As an actuator presses down on the blister 182, internal pressure within the blister 182 causes the internal dimple 184 to collapse and invert. The inverted dimple is punctured by the fixed spike 186, thereby permitting fluid within the blister 182 to flow through an exit port 190.


An alternative apparatus for opening a vessel is indicated by reference number 200 in FIG. 15A. As shown in FIG. 15A, a fluid vessel (or blister) 202 is mounted on a substrate 216 and is connected by means of a channel—which may or may not be initially blocked by a breakable seal—to a dimple 204. An opening device comprising a lancing pin 206 having a fluid port 208 formed through the center thereof (see FIG. 15B) is disposed within a segmented bore 220 formed in the substrate 216 beneath the dimple 204. A partition or septum 205 separates the dimple 204 from the bore 220, thereby preventing fluid from exiting the blister 202 and dimple 204. An actuator (not shown) presses on a film layer 212 disposed on a bottom portion of the substrate 216 in the direction “A” forcing the lancing pin 206 up within the segmented bore 220 until a shoulder 210 formed on the lancing pin 206 encounters a hard stop 222 formed in the segmented bore 220. A lancing point of the pin 206 pierces the partition 205 thereby permitting fluid to flow through the fluid port 208 in the lancing pin 206 and out of a fluid exit channel 214.


An alternative embodiment of an apparatus for opening a vessel is indicated by reference number 230 in FIGS. 16A and 16B. As shown in FIG. 16A, a fluid vessel (or blister) 232 is mounted on a substrate 244 and is connected by means of a channel—which may or may not be initially blocked by a breakable seal—to a dimple 234. An opening device comprising a lancing pin 236 is disposed within a segmented board 246 formed in the substrate 244 beneath the dimple 234. A partition or septum 235 separates the dimple 234 from the segmented bore 246. The upper surface of the substrate 244 is sealed with a film 240 before the blister 232 and dimple 234 are adhered. An actuator (not shown) pushes up on the lancing pin 236 in the direction “A” until a shoulder 238 formed on the lancing pin 236 encounters hard stop 248 within the bore 246. The pin 236 thereby pierces the partition 235 and remains in the upper position as fluid flows out along an exit channel 242 formed on an upper surface of the substrate 244. A fluid tight seal is maintained between the pin 238 and the bore 246 by a slight interference fit.


As the collapsible fluid vessels of a liquid reagent module are configured to be compressed and collapsed to displace the fluid contents from the vessel(s), such vessels are susceptible to damage or fluid leakage due to inadvertent exposures to contacts that impart a compressing force to the vessel. Accordingly, when storing, handling, or transporting a component having one or more collapsible fluid vessels, it is desirable to protect the fluid vessel and avoid such inadvertent contact. The liquid reagent module could be stored within a rigid casing to protect the collapsible vessel(s) from unintended external forces, but such a casing would inhibit or prevent collapsing of the vessel by application of an external force. Thus, the liquid reagent module would have to be removed from the casing prior to use, thereby leaving the collapsible vessel(s) of the module vulnerable to unintended external forces.


An apparatus for protecting and interfacing with a collapsible vessel is indicated by reference number 260 in FIGS. 17, 18, and 19. A component with one or more collapsible vessels includes a collapsible blister 262 formed on a substrate 264. A dispensing channel 266 extends from the blister 262 to a frangible seal 268. It is understood that, in some alternative embodiments, the dispensing channel 266 may be substituted with a breakable seal, providing an additional safeguard against an accidental reagent release.


Frangible seal 268 may comprise one of the apparatuses for opening a vessel described above and shown in any of FIGS. 8-16.


A rigid or semi-rigid housing is provided over the blister 262 and, optionally, the dispensing channel 266 as well, and comprises a blister housing cover 270 covering the blister 262 and a blister housing extension 280 covering and protecting the dispensing channel 266 and the area of the frangible seal 268.


A floating actuator plate 276 is disposed within the blister housing cover 270. In the illustrated embodiments, both the blister housing cover 270 and the floating actuator plate 276 are circular, but the housing 270 and the actuator plate 276 could be of any shape, preferably generally conforming to the shape of the blister 262.


The apparatus 260 further includes a plunger 274 having a plunger point 275 at one end thereof. Plunger 274 is disposed above the blister housing cover 270 generally at a center portion thereof and disposed above an aperture 272 formed in the housing 270.


The floating actuator plate 276 includes a plunger receiver recess 278, which, in an embodiment, generally conforms to the shape of the plunger point 275.


The blister 262 is collapsed by actuating the plunger 274 downwardly into the aperture 272. Plunger 274 may be actuated by any suitable mechanism, including one of the actuator mechanisms 50, 80 described above. Plunger 274 passes into the aperture 272 where the plunger point 275 nests within the plunger receiver recess 278 of the floating actuator plate 276. Continued downward movement by the plunger 274 presses the actuator plate 276 against the blister 262, thereby collapsing the blister 262 and displacing fluid from the blister 262 through the dispensing channel 266 to a fluid egress. Continued pressure will cause the frangible seal at 268 to break, or an apparatus for opening the vessel as described above may be employed to open the frangible seal. The plunger point 275 nested within the plunger point recess 278 helps to keep the plunger 274 centered with respect to the actuator plate 276 and prevents the actuator plate 276 from sliding laterally relative to the plunger 274. When the blister is fully collapsed, as shown in FIG. 19, a convex side of the plunger receiver recess 278 of the floating actuator plate 276 nests within a plunger recess 282 formed in the substrate 264.


Accordingly, the blister housing cover 270 protects the blister 262 from inadvertent damage or collapse, while the floating actuator plate inside the blister housing cover 270 permits and facilitates the collapsing of the blister 262 without having to remove or otherwise alter the blister housing cover 270. In components having more than one collapsible vessel and dispensing channel, a blister housing cover may be provided for all of the vessels and dispensing channels or for some, but less than all vessels and dispensing channels.


While the present invention has been described and shown in considerable detail with reference to certain illustrative embodiments, including various combinations and sub-combinations of features, those skilled in the art will readily appreciate other embodiments and variations and modifications thereof as encompassed within the scope of the present invention. Moreover, the descriptions of such embodiments, combinations, and sub-combinations is not intended to convey that the inventions requires features or combinations of features other than those expressly recited in the claims. Accordingly, the present invention is deemed to include all modifications and variations encompassed within the spirit and scope of the following appended claims.

Claims
  • 1. A fluid container comprising: a first vessel;a second vessel connected or connectable to the first vessel;a sealing partition preventing fluid flow from the second vessel; anda solid spherical opening element initially supported within the second vessel by the sealing partition and configured to be contacted with the sealing partition to open the sealing partition and permit fluid flow from the second vessel,wherein the first vessel comprises a first collapsible blister supported on a planar substrate, and the second vessel comprises a second collapsible blister supported on the substrate.
  • 2. The fluid container of claim 1, further comprising a fluid channel extending between the first and second vessels.
  • 3. The fluid container of claim 2, further comprising a seal within the fluid channel, the seal being configured to be breakable upon application of sufficient force to the seal to thereby connect the first and second vessels via the fluid channel.
  • 4. The fluid container of claim 1, further comprising a fluid channel formed in the substrate and extending between the first and second vessels.
  • 5. The fluid container of claim 1, further comprising an opening formed in the substrate below the second vessel, wherein the sealing partition is disposed over the opening and the solid spherical opening element is disposed within the second vessel and supported above the opening on the sealing partition.
  • 6. The fluid container of claim 5, wherein the solid spherical opening element is configured to be contacted with the sealing partition by collapsing the second vessel and pushing the solid spherical opening element through the sealing partition and into the opening.
  • 7. The fluid container of claim 1, wherein the solid spherical opening element comprises a steel ball.
  • 8. The fluid container of claim 1, wherein the sealing partition comprises a foil.
  • 9. The fluid container of claim 6, further comprising a channel formed in the substrate and extending from the opening to permit fluid flowing from the second vessel and into the opening to flow through the channel.
  • 10. A method for displacing fluid from a fluid container including a first vessel and a second vessel connected or connectable to the first vessel and including a sealing partition preventing fluid flow from the second vessel, wherein the fluid container further includes a solid spherical opening element disposed within the second vessel, said method comprising: (a) applying a compressive force to the second vessel sufficient to collapse the second vessel and push the solid spherical opening element disposed within the second vessel into the sealing partition with sufficient force to rupture the sealing partition to thereby permit fluid flow form the second vessel; and(b) applying a compressive force to the first vessel sufficient to collapse the first vessel and force fluid from the first vessel to the second vessel, whereby fluid forced into the second vessel flows out of the second vessel through the ruptured sealing partition.
  • 11. The method of claim 10, wherein the second vessel is supported on a substrate which comprises an opening formed in the substrate below the second vessel and wherein the sealing partition is disposed over the opening and the solid spherical opening element is supported above the opening on the sealing partition, and step (a) comprises pushing the solid spherical opening element through the sealing partition and into the opening formed in the substrate below the second vessel.
  • 12. The method of claim 10, wherein step (a) is performed with a first external actuator configured to apply a compressive force to the second vessel, and step (b) is performed with a second external actuator configured to apply a compressive force to the first vessel.
  • 13. The method of claim 10, wherein step (b) is performed after step (a) is performed.
  • 14. The method of claim 10, wherein the fluid container includes a fluid channel extending between the first vessel and the second vessel with a fluid-blocking seal within the fluid channel, and wherein step (b) comprises applying sufficient force to alter the seal and thereby connect the first and second vessels via the fluid channel.
CROSS REFERENCE OF RELATED APPLICATION

This application claims the benefit under 35 U.S.C. §119(e) of the filing date of provisional patent application Ser. No. 61/798,091 filed Mar. 15, 2013, the disclosure of which is incorporated herein by reference.

US Referenced Citations (507)
Number Name Date Kind
3641909 Baker Feb 1972 A
3687051 Baker et al. Aug 1972 A
3776425 Baker et al. Dec 1973 A
3820149 Baker et al. Jun 1974 A
4007010 Woodbridge, III Feb 1977 A
4182447 Kay Jan 1980 A
4469863 Ts'o et al. Sep 1984 A
4769333 Dole et al. Sep 1988 A
4859603 Dole et al. Aug 1989 A
4887455 Payne et al. Dec 1989 A
4978502 Dole et al. Dec 1990 A
5034506 Summerton et al. Jul 1991 A
5089233 Devaney, Jr. et al. Feb 1992 A
5098660 Devaney, Jr. Mar 1992 A
5154888 Zander et al. Oct 1992 A
5216141 Benner Jun 1993 A
5229297 Schnipelsky et al. Jul 1993 A
5234809 Boom et al. Aug 1993 A
5235033 Summerton et al. Aug 1993 A
5254479 Chemelli Oct 1993 A
5288463 Chemelli Feb 1994 A
5290518 Johnson Mar 1994 A
5374395 Robinson et al. Dec 1994 A
5386023 Sanghvi et al. Jan 1995 A
5422271 Chen et al. Jun 1995 A
5460780 Devaney, Jr. et al. Oct 1995 A
5468366 Wegner et al. Nov 1995 A
5512439 Hornes et al. Apr 1996 A
5591578 Meade et al. Jan 1997 A
5593804 Chemelli et al. Jan 1997 A
5602240 De Mesmaeker et al. Feb 1997 A
5637684 Cook et al. Jun 1997 A
5644048 Yau Jul 1997 A
5652149 Mileaf et al. Jul 1997 A
5674653 Chemelli et al. Oct 1997 A
5681702 Collins et al. Oct 1997 A
5692644 Gueret Dec 1997 A
5705348 Meade et al. Jan 1998 A
5705628 Hawkins Jan 1998 A
5714380 Neri et al. Feb 1998 A
5716852 Yager et al. Feb 1998 A
5726404 Brody Mar 1998 A
5726751 Altendorf et al. Mar 1998 A
5747349 Van Den Engh et al. May 1998 A
5748827 Holl et al. May 1998 A
5770365 Lane et al. Jun 1998 A
5807701 Payne et al. Sep 1998 A
5824473 Meade et al. Oct 1998 A
5851536 Yager et al. Dec 1998 A
5873990 Wojciechowski et al. Feb 1999 A
5876187 Afromowitz et al. Mar 1999 A
5882497 Persaud et al. Mar 1999 A
5898071 Hawkins Apr 1999 A
5932100 Yager et al. Aug 1999 A
5948684 Weigl et al. Sep 1999 A
5955028 Chow Sep 1999 A
5971158 Yager et al. Oct 1999 A
5972710 Weigl et al. Oct 1999 A
5973138 Collis Oct 1999 A
5974867 Forster et al. Nov 1999 A
6007775 Yager Dec 1999 A
6013170 Meade Jan 2000 A
6013459 Meade Jan 2000 A
6033601 Persaud et al. Mar 2000 A
6039897 Lochhead et al. Mar 2000 A
6063573 Kayyem May 2000 A
6067157 Altendorf May 2000 A
6071478 Chow Jun 2000 A
6090933 Kayyem et al. Jul 2000 A
6091502 Weigl et al. Jul 2000 A
6096273 Kayyem et al. Aug 2000 A
6110354 Saban et al. Aug 2000 A
6134950 Forster et al. Oct 2000 A
6136272 Weigl et al. Oct 2000 A
6159739 Weigl et al. Dec 2000 A
6167910 Chow Jan 2001 B1
6171865 Weigl et al. Jan 2001 B1
6180064 Persaud et al. Jan 2001 B1
6180114 Yager et al. Jan 2001 B1
6190858 Persaud et al. Feb 2001 B1
6192351 Persaud Feb 2001 B1
6221583 Kayyem et al. Apr 2001 B1
6221677 Wu et al. Apr 2001 B1
6227809 Forster et al. May 2001 B1
6232062 Kayyem et al. May 2001 B1
6235501 Gautsch et al. May 2001 B1
6236951 Payne et al. May 2001 B1
6248229 Meade Jun 2001 B1
6255477 Kleiber et al. Jul 2001 B1
6264825 Blackburn et al. Jul 2001 B1
6265155 Meade et al. Jul 2001 B1
6268136 Shuber et al. Jul 2001 B1
6277641 Yager Aug 2001 B1
6290839 Kayyem et al. Sep 2001 B1
6297061 Wu et al. Oct 2001 B1
6300138 Gleason et al. Oct 2001 B1
6321791 Chow Nov 2001 B1
6361958 Shieh et al. Mar 2002 B1
6366924 Parce Apr 2002 B1
6376232 Payne et al. Apr 2002 B1
6387290 Brody et al. May 2002 B1
6391558 Henkens et al. May 2002 B1
6399023 Chow Jun 2002 B1
6399025 Chow Jun 2002 B1
6403338 Knapp et al. Jun 2002 B1
6404493 Altendorf Jun 2002 B1
6406857 Shuber et al. Jun 2002 B1
6408884 Kamholz et al. Jun 2002 B1
6409832 Weigl et al. Jun 2002 B2
6415821 Kamholz et al. Jul 2002 B2
6426230 Feistel Jul 2002 B1
6431016 Payne Aug 2002 B1
6431212 Hayenga et al. Aug 2002 B1
6431476 Taylor et al. Aug 2002 B1
6432720 Chow Aug 2002 B2
6432723 Plaxco et al. Aug 2002 B1
6433160 Collis Aug 2002 B1
6440725 Pourahmadi et al. Aug 2002 B1
6443307 Burridge Sep 2002 B1
6451606 König et al. Sep 2002 B1
6454945 Weigl et al. Sep 2002 B1
6479240 Kayyem et al. Nov 2002 B1
6482306 Yager et al. Nov 2002 B1
6488896 Weigl et al. Dec 2002 B2
6494230 Chow Dec 2002 B2
6495104 Unno et al. Dec 2002 B1
6495323 Kayyem et al. Dec 2002 B1
6503757 Chow Jan 2003 B1
6518024 Choong et al. Feb 2003 B2
6524456 Ramsey et al. Feb 2003 B1
6537501 Holl et al. Mar 2003 B1
6541213 Weigl et al. Apr 2003 B1
6541617 Bamdad et al. Apr 2003 B1
6557427 Weigl et al. May 2003 B2
6562568 Kleiber et al. May 2003 B1
6565727 Shenderov May 2003 B1
6575188 Parunak Jun 2003 B2
6576194 Holl et al. Jun 2003 B1
6581899 Williams Jun 2003 B2
6582963 Weigl et al. Jun 2003 B1
6596483 Choong et al. Jul 2003 B1
6600026 Yu Jul 2003 B1
6602400 Choong et al. Aug 2003 B1
6627412 Manning et al. Sep 2003 B1
6642046 McGarry et al. Nov 2003 B1
6645758 Schnipelsky et al. Nov 2003 B1
6647397 Parce Nov 2003 B2
6648015 Chow Nov 2003 B1
6655010 Hatfield et al. Dec 2003 B1
6656431 Holl et al. Dec 2003 B2
6660480 Ramsey et al. Dec 2003 B2
6664104 Pourahmadi et al. Dec 2003 B2
6674525 Bardell et al. Jan 2004 B2
6686150 Blackburn et al. Feb 2004 B1
6695147 Yager et al. Feb 2004 B1
6706498 Gautsch et al. Mar 2004 B2
6712925 Holl et al. Mar 2004 B1
6739531 Taylor May 2004 B2
6740518 Duong et al. May 2004 B1
6742661 Schulte et al. Jun 2004 B1
6743399 Weigl et al. Jun 2004 B1
6753143 Tao et al. Jun 2004 B2
6761816 Blackburn et al. Jul 2004 B1
6773566 Shenderov Aug 2004 B2
6783647 Culbertson et al. Aug 2004 B2
6790341 Saban et al. Sep 2004 B1
6824669 Li et al. Nov 2004 B1
6830729 Holl et al. Dec 2004 B1
6833267 Kayyem Dec 2004 B1
6852284 Holl et al. Feb 2005 B1
6857449 Chow Feb 2005 B1
6875619 Blackburn Apr 2005 B2
6878540 Pourahmadi et al. Apr 2005 B2
6881541 Petersen et al. Apr 2005 B2
6887693 McMillan et al. May 2005 B2
6893879 Petersen et al. May 2005 B2
6914137 Baker Jul 2005 B2
6919444 Harttig et al. Jul 2005 B2
6942771 Kayyem Sep 2005 B1
6951759 Travers et al. Oct 2005 B2
6960437 Enzelberger et al. Nov 2005 B2
6960467 Shieh et al. Nov 2005 B2
6977151 Kayyem et al. Dec 2005 B2
6979424 Northrup et al. Dec 2005 B2
7010391 Handique et al. Mar 2006 B2
7011791 Weigl et al. Mar 2006 B2
7014992 Kayyem et al. Mar 2006 B1
7018523 Meade Mar 2006 B2
7030989 Yager et al. Apr 2006 B2
7045285 Kayyem et al. May 2006 B1
7056475 Lum et al. Jun 2006 B2
7056669 Kayyem et al. Jun 2006 B2
7087148 Blackburn et al. Aug 2006 B1
7090804 Kayyem et al. Aug 2006 B2
7119194 Uematsu et al. Oct 2006 B2
7125668 Kayyem et al. Oct 2006 B2
7141429 Munson et al. Nov 2006 B2
7155344 Parce et al. Dec 2006 B1
7160678 Kayyem et al. Jan 2007 B1
7163612 Sterling et al. Jan 2007 B2
7169358 Henkens et al. Jan 2007 B2
7172897 Blackburn et al. Feb 2007 B2
7192557 Wu et al. Mar 2007 B2
7201881 Cox et al. Apr 2007 B2
7208271 Bost et al. Apr 2007 B2
7223371 Hayenga et al. May 2007 B2
7226562 Holl et al. Jun 2007 B2
7238268 Ramsey et al. Jul 2007 B2
7255780 Shenderov Aug 2007 B2
7258837 Yager et al. Aug 2007 B2
7267939 Meade Sep 2007 B2
7270786 Parunak et al. Sep 2007 B2
7271007 Weigl et al. Sep 2007 B2
7312087 Duong et al. Dec 2007 B2
7323140 Handique et al. Jan 2008 B2
7343248 Parce et al. Mar 2008 B2
7364886 Hasenbank et al. Apr 2008 B2
7371830 Kleiber et al. May 2008 B2
7381525 Kayyem et al. Jun 2008 B1
7381533 Kayyem et al. Jun 2008 B2
7384749 Kayyem et al. Jun 2008 B2
7393645 Kayyem et al. Jul 2008 B2
7405054 Hasenbank et al. Jul 2008 B1
7416791 Carlson et al. Aug 2008 B1
7416892 Battrell et al. Aug 2008 B2
7419575 Culbertson et al. Sep 2008 B2
7419638 Saltsman et al. Sep 2008 B2
7439014 Pamula et al. Oct 2008 B2
7473397 Griffin et al. Jan 2009 B2
7491495 Zielenski et al. Feb 2009 B2
7514228 Meade Apr 2009 B2
7534331 Kayyem May 2009 B2
7544506 Breidford et al. Jun 2009 B2
7550267 Hawkins et al. Jun 2009 B2
7560237 O'Connor et al. Jul 2009 B2
7566534 Meade Jul 2009 B2
7569346 Petersen et al. Aug 2009 B2
7579145 Meade Aug 2009 B2
D599832 Chapin et al. Sep 2009 S
7582419 Meade Sep 2009 B2
7595153 Meade Sep 2009 B2
7601507 O'Connor et al. Oct 2009 B2
7648835 Breidford et al. Jan 2010 B2
7655129 Blackburn et al. Feb 2010 B2
7655190 Satou et al. Feb 2010 B2
7659089 Hasenbank et al. Feb 2010 B2
7713711 O'Connor et al. May 2010 B2
7727723 Pollack et al. Jun 2010 B2
7731906 Handique et al. Jun 2010 B2
7736891 Nelson et al. Jun 2010 B2
7759073 O'Connor et al. Jul 2010 B2
7763453 Clemmens et al. Jul 2010 B2
7763471 Pamula et al. Jul 2010 B2
7789270 Tanaami et al. Sep 2010 B2
7794669 Gyonouchi et al. Sep 2010 B2
7815871 Pamula et al. Oct 2010 B2
7816121 Pollack et al. Oct 2010 B2
7820030 Althaus et al. Oct 2010 B2
7820391 Chunlin Oct 2010 B2
7822510 Paik et al. Oct 2010 B2
7833708 Enzelberger et al. Nov 2010 B2
7851184 Pollack et al. Dec 2010 B2
7854897 Tanaami et al. Dec 2010 B2
7858045 Tanaami et al. Dec 2010 B2
7863035 Clemens et al. Jan 2011 B2
7867757 Karlsen et al. Jan 2011 B2
7901947 Pollack et al. Mar 2011 B2
7910294 Karlsen Mar 2011 B2
7914994 Petersen et al. Mar 2011 B2
7919330 De Guzman et al. Apr 2011 B2
7935316 Gyonouchi et al. May 2011 B2
7935481 Umek et al. May 2011 B1
7935537 Haley May 2011 B2
7939021 Smith et al. May 2011 B2
7943030 Shenderov May 2011 B2
7955836 Clemmens et al. Jun 2011 B2
7987022 Handique et al. Jul 2011 B2
7998436 Pollack et al. Aug 2011 B2
7998708 Handique et al. Aug 2011 B2
8007739 Pollack et al. Aug 2011 B2
8012743 Bamdad et al. Sep 2011 B2
8017340 Collier et al. Sep 2011 B2
8041463 Pollack et al. Oct 2011 B2
8048628 Pollack et al. Nov 2011 B2
8053239 Wheeler et al. Nov 2011 B2
8088578 Hua et al. Jan 2012 B2
8093062 Winger Jan 2012 B2
8101403 Yager et al. Jan 2012 B2
8101431 McDevitt et al. Jan 2012 B2
8105477 Althaus et al. Jan 2012 B2
8105783 Handique Jan 2012 B2
8105849 McDevitt et al. Jan 2012 B2
8110392 Battrell et al. Feb 2012 B2
8114661 O'Connor et al. Feb 2012 B2
8129118 Weindel et al. Mar 2012 B2
8133671 Williams et al. Mar 2012 B2
8133703 Ching et al. Mar 2012 B2
8137917 Pollack et al. Mar 2012 B2
8168442 Petersen et al. May 2012 B2
8187864 Wheeler et al. May 2012 B2
8201765 Rajagopal et al. Jun 2012 B2
8202686 Pamula et al. Jun 2012 B2
8202736 Mousa et al. Jun 2012 B2
8208146 Srinivasan et al. Jun 2012 B2
8216529 Ade et al. Jul 2012 B2
8216832 Battrell et al. Jul 2012 B2
8222023 Battrell et al. Jul 2012 B2
8247176 Petersen et al. Aug 2012 B2
8247191 Ritzen et al. Aug 2012 B2
8268246 Srinivasan et al. Sep 2012 B2
8273308 Handique et al. Sep 2012 B2
8304253 Yi et al. Nov 2012 B2
8313698 Pollack et al. Nov 2012 B2
8313895 Pollack et al. Nov 2012 B2
8317990 Pamula et al. Nov 2012 B2
8318109 Saltsman et al. Nov 2012 B2
8318439 Battrell et al. Nov 2012 B2
8323900 Handique et al. Dec 2012 B2
8329453 Battrell et al. Dec 2012 B2
8338166 Beer et al. Dec 2012 B2
8343636 Jen et al. Jan 2013 B2
8349276 Pamula et al. Jan 2013 B2
8356763 Rajagopal et al. Jan 2013 B2
8364315 Sturmer et al. Jan 2013 B2
8367370 Wheeler et al. Feb 2013 B2
8372340 Bird et al. Feb 2013 B2
8388909 Pollack et al. Mar 2013 B2
8389297 Pamula et al. Mar 2013 B2
8394608 Ririe et al. Mar 2013 B2
8394641 Winger Mar 2013 B2
8404440 Solli et al. Mar 2013 B2
8426213 Eckhardt et al. Apr 2013 B2
8426214 Stayton et al. Apr 2013 B2
8431389 Battrell et al. Apr 2013 B2
8440392 Pamula et al. May 2013 B2
8454905 Pope et al. Jun 2013 B2
8460528 Pollack et al. Jun 2013 B2
8470606 Srinivasan et al. Jun 2013 B2
8481125 Yi et al. Jul 2013 B2
8492168 Srinivasan et al. Jul 2013 B2
8506908 Benn et al. Aug 2013 B2
8518662 Ritzen et al. Aug 2013 B2
8541176 Pamula et al. Sep 2013 B2
8551424 Abraham-Fuchs et al. Oct 2013 B2
8557198 Saltsman et al. Oct 2013 B2
8562807 Srinivasan et al. Oct 2013 B2
8580209 Kurowski et al. Nov 2013 B2
8591830 Sudarsan et al. Nov 2013 B2
8592217 Eckhardt Nov 2013 B2
8613889 Pollack et al. Dec 2013 B2
8637317 Pamula et al. Jan 2014 B2
8637324 Pollack et al. Jan 2014 B2
8658111 Srinivasan et al. Feb 2014 B2
8685344 Sudarsan et al. Apr 2014 B2
8685754 Pollack et al. Apr 2014 B2
20020006643 Kayyem et al. Jan 2002 A1
20030025129 Hahn et al. Feb 2003 A1
20030034271 Burridge Feb 2003 A1
20030038040 Bertl et al. Feb 2003 A1
20030048631 Ladyjensky Mar 2003 A1
20030197139 Williams Oct 2003 A1
20040037739 McNeely et al. Feb 2004 A1
20040053290 Terbrueggen et al. Mar 2004 A1
20040137607 Tanaami et al. Jul 2004 A1
20040229378 Schulte et al. Nov 2004 A1
20040254559 Tanaami et al. Dec 2004 A1
20050164373 Oldham et al. Jul 2005 A1
20050201903 Weigl et al. Sep 2005 A1
20050205816 Hayenga et al. Sep 2005 A1
20050244308 Tanaami et al. Nov 2005 A1
20060057581 Karlsen et al. Mar 2006 A1
20060079834 Tennican et al. Apr 2006 A1
20060166233 Wu et al. Jul 2006 A1
20060183216 Handique et al. Aug 2006 A1
20060246575 Lancaster et al. Nov 2006 A1
20060275813 Tanaami et al. Dec 2006 A1
20060275852 Montagu et al. Dec 2006 A1
20070013733 Katsurai et al. Jan 2007 A1
20070042427 Gerdes et al. Feb 2007 A1
20070178529 Breidford et al. Aug 2007 A1
20070184547 Handique et al. Aug 2007 A1
20070241068 Pamula et al. Oct 2007 A1
20070242105 Srinivasan et al. Oct 2007 A1
20070275415 Srinivasan et al. Nov 2007 A1
20070292941 Handique et al. Dec 2007 A1
20080038810 Pollack et al. Feb 2008 A1
20080050287 Araragi et al. Feb 2008 A1
20080182301 Handique et al. Jul 2008 A1
20080227185 Schonfeld et al. Sep 2008 A1
20080230386 Srinivasan et al. Sep 2008 A1
20080248590 Gulliksen et al. Oct 2008 A1
20080274513 Shenderov et al. Nov 2008 A1
20080283439 Sullivan et al. Nov 2008 A1
20090022624 Saltsman et al. Jan 2009 A1
20090061450 Hunter Mar 2009 A1
20090148847 Kokoris et al. Jun 2009 A1
20090155902 Pollack et al. Jun 2009 A1
20090221059 Williams et al. Sep 2009 A1
20090221091 Mogi et al. Sep 2009 A1
20090263834 Sista et al. Oct 2009 A1
20090304944 Sudarsan et al. Dec 2009 A1
20090325276 Battrell et al. Dec 2009 A1
20100025250 Pamula et al. Feb 2010 A1
20100032293 Pollack et al. Feb 2010 A1
20100048410 Shenderov et al. Feb 2010 A1
20100068764 Sista et al. Mar 2010 A1
20100087012 Shenderov Apr 2010 A1
20100116640 Pamula et al. May 2010 A1
20100120130 Srinivasan et al. May 2010 A1
20100130369 Shenderov et al. May 2010 A1
20100150783 Araragi et al. Jun 2010 A1
20100151475 Tanaami et al. Jun 2010 A1
20100178697 Doebler et al. Jul 2010 A1
20100190263 Srinivasan et al. Jul 2010 A1
20100194408 Sturmer et al. Aug 2010 A1
20100206094 Shenderov Aug 2010 A1
20100224511 Boatner Sep 2010 A1
20100226199 Mogi et al. Sep 2010 A1
20100236928 Srinivasan et al. Sep 2010 A1
20100236929 Pollack et al. Sep 2010 A1
20100270156 Srinivasan et al. Oct 2010 A1
20100279374 Sista et al. Nov 2010 A1
20100282608 Srinivasan et al. Nov 2010 A1
20100288789 Tanaami et al. Nov 2010 A1
20100291578 Pollack et al. Nov 2010 A1
20100297754 Solli et al. Nov 2010 A1
20100307917 Srinivasan et al. Dec 2010 A1
20100307922 Wu Dec 2010 A1
20100308051 Weber Dec 2010 A1
20100311599 Wheeler et al. Dec 2010 A1
20100317093 Turewicz et al. Dec 2010 A1
20100323405 Pollack et al. Dec 2010 A1
20100331522 Irvine et al. Dec 2010 A1
20110048951 Wu Mar 2011 A1
20110076692 Sista et al. Mar 2011 A1
20110086377 Thwar et al. Apr 2011 A1
20110091989 Sista et al. Apr 2011 A1
20110097763 Pollack et al. Apr 2011 A1
20110104725 Pamula et al. May 2011 A1
20110104747 Pollack et al. May 2011 A1
20110104816 Pollack et al. May 2011 A1
20110114490 Pamula et al. May 2011 A1
20110180571 Srinivasan et al. Jul 2011 A1
20110186433 Pollack et al. Aug 2011 A1
20110186466 Kurowski et al. Aug 2011 A1
20110203930 Pamula et al. Aug 2011 A1
20110207621 Montagu et al. Aug 2011 A1
20110209998 Shenderov Sep 2011 A1
20110240471 Wheeler et al. Oct 2011 A1
20110303542 Srinivasan et al. Dec 2011 A1
20110311980 Pollack et al. Dec 2011 A1
20110318824 Tanaami et al. Dec 2011 A1
20110319279 Montagu et al. Dec 2011 A1
20120018306 Srinivasan et al. Jan 2012 A1
20120022695 Handique et al. Jan 2012 A1
20120044299 Winger Feb 2012 A1
20120064597 Clemmens et al. Mar 2012 A1
20120071342 Lochhead et al. Mar 2012 A1
20120083046 Watson et al. Apr 2012 A1
20120085645 Mousa et al. Apr 2012 A1
20120107811 Kelso et al. May 2012 A1
20120122108 Handique May 2012 A1
20120132528 Shenderov et al. May 2012 A1
20120142070 Battrell et al. Jun 2012 A1
20120156112 Sprague et al. Jun 2012 A1
20120156750 Battrell et al. Jun 2012 A1
20120160826 Handique Jun 2012 A1
20120164627 Battrell et al. Jun 2012 A1
20120165238 Pamula et al. Jun 2012 A1
20120171759 Williams et al. Jul 2012 A1
20120177543 Battrell et al. Jul 2012 A1
20120187117 Weber Jul 2012 A1
20120196280 Karlsen et al. Aug 2012 A1
20120252008 Brown et al. Oct 2012 A1
20120261264 Srinivasan et al. Oct 2012 A1
20120271127 Battrell et al. Oct 2012 A1
20120329142 Battrell et al. Dec 2012 A1
20130011912 Battrell et al. Jan 2013 A1
20130017544 Eckhardt et al. Jan 2013 A1
20130018611 Sturmer Jan 2013 A1
20130059366 Pollack et al. Mar 2013 A1
20130118901 Pollack et al. May 2013 A1
20130130262 Battrell et al. May 2013 A1
20130130936 Eckhardt May 2013 A1
20130142708 Battrell et al. Jun 2013 A1
20130146461 Pamula et al. Jun 2013 A1
20130164742 Pollack et al. Jun 2013 A1
20130178374 Eckhardt et al. Jul 2013 A1
20130178968 Sturmer et al. Jul 2013 A1
20130203606 Pollack et al. Aug 2013 A1
20130217103 Bauer Aug 2013 A1
20130217113 Srinivasan et al. Aug 2013 A1
20130225450 Pollack et al. Aug 2013 A1
20130225452 Pollack et al. Aug 2013 A1
20130230875 Pamula et al. Sep 2013 A1
20130233425 Srinivasan et al. Sep 2013 A1
20130233712 Pamula et al. Sep 2013 A1
20130252262 Srinivasan et al. Sep 2013 A1
20130302787 Agarwal et al. Nov 2013 A1
20130327672 Kurowski et al. Dec 2013 A1
20130331298 Rea Dec 2013 A1
20130341231 Lange et al. Dec 2013 A1
20140000223 Osterloh et al. Jan 2014 A1
20140000735 Weber et al. Jan 2014 A1
20140255275 Barry et al. Sep 2014 A1
20140263439 Wright et al. Sep 2014 A1
20140322706 Kayyem et al. Oct 2014 A1
Foreign Referenced Citations (12)
Number Date Country
0173547 Jun 1990 EP
0583833 Feb 1994 EP
0694483 Jan 1996 EP
2009161187 Jul 2009 JP
WO 9937819 Jul 1999 WO
WO 0062931 Oct 2000 WO
WO 0110729 Feb 2001 WO
WO 2004011148 Feb 2004 WO
WO 2009089466 Jul 2009 WO
WO 2009140373 Nov 2009 WO
WO 2010151705 Dec 2010 WO
WO 2012080190 Jun 2012 WO
Non-Patent Literature Citations (41)
Entry
International Search Report and Written Opinion issued in Application No. PCT/US2013/0066717, 35 pages (Feb. 3, 2014).
“Mechanisms Information/Worksheets,” World Association of Technology Teachers, 2 pages (Mar. 2, 2011). (animated display viewable at https://web.archive.org/web/20110302093447/http:www.technologystudent.com/cams/flat1.htm ).
Dobson et al., “Emerging Technologies for Point-of-Care Genetic Testing,” Future Drugs Ltd (www.future-drugs.com), 10.1586/14737159.7.4.359, Expert Rev. Mol. Diagn., pp. 359-370 (2007).
Doebler et al., “Continuous-Flow, Rapid Lysis Devices for Biodefense Nucleic Acid Diagnostic Systems,” The Association for Laboratory Automation (JALA), pp. 119-125 (Jun. 2009).
Erickson et al., “Integrated Microfluidic Devices,” Elsevier B.V., 16 pages (2003).
Findlay et al., “Automated Closed-Vessel System for in Vitro Diagnostics Based on Polymerase Chain Reaction,” Clinical Chemistry, 39:9, pp. 1927-1933, 1993).
Focke et al., “Lab-on-a-Foil: Microfluidics on Thin and Flexible Films,” The Royal Society of Chemistry, pp. 1365-1386 (2010).
Malic et al., “Current State of Intellectual Property in Microfluidic Nucleic Acid Analysis,” McGill University, Bentham Science Publishers, 18 pages (2007).
Vandeventer et al., “Mechanical Disruption of Lysis-Resistant Bacterial Cells by Use of a Miniature, Low-Power, Disposable Device,” American Society for Microbiology, Journal of Clinical Microbiology, 49:7, pp. 2533-2539 (Jul. 2011).
International Search Report and Written Opinion issued in International Patent Application No. PCT/US2014/024499, 14 pages (Dec. 11, 2014).
Beaucage et al., “Tetrahedron Report No. 329: The Functionalization of Oligonucleotides Via Phosphoramidite Derivatives,” Tetrahedron vol. 49, No. 10, pp. 1925-2963 (1993).
Bolli et al., “α-Bicyclo-DNA: Synthesis, Characterization, and Pairing Properties of α-DNA-Analogues with Restricted Conformational Flexibility in the Sugar-Phosphate Backbone,” American Chemical Society, pp. 100-117 (1994).
Brill et. al., “Synthesis of Oligodeoxynucleoside Phosphorodithioates via Thioamidites,” J. Am. Chem. Soc., pp. 2321-2322 (1989).
Carlsson et al., “Screening for Genetic Mutations” Letters to Nature, vol. 380, p. 207 (Mar. 1996).
Dempcy et al., “Synthesis of a Thymidyl Pentamer of Deoxyribonucleic Guanidine and Binding Studies with DNA Homopolynucleotides,” Proc. Natl. Acad. Sci. USA, vol. 92, pp. 6097-6101 (Jun. 1995).
Egholm et al., “Peptide Nucleic Acids (PNA). Oligonucleotide Analogues with an Achiral Peptide Backbone,” J.Am.Chem.Soc., pp. 1895-1897 (1992).
Egholm et al., “PNA hybridizes to complementary oligonucleotides obeying the Watson-Crick hydrogen-bonding rules,” Letters to Nature, pp. 566-568 (1993).
Herdewijn et al., “Hexopyranosyl-Like Oligonucleotides,” American Chemical Society, pp. 80-99 (1994).
Horn et al., “Oligonucleotides with Alternating Anionic and Cationic Phosphoramidate Linkages: Synthesis and Hybridization of Stereo-Uniform Isomers,” Tetrahedron Letters, vol. 37, No. 6, pp. 743-746 (1996).
Jeffs et al., “Unusual Confirmation of a 3-Thioformacetal Linkage in a DNA Duples,” Journal of Biomedecular NMR, pp. 17-34 (1994).
Jenkins et al., “The Biosynthesis of Carbocyclic Nucleosides,” Chemical Society Reviews, pp. 169-176 (Jan. 1995).
Kiedrowski et al., “Parabolic Growth of a Self-Replicating Hexadeoxynucleotide Bearing a 3'-5' Phosphoamidate Linkage,” Angew Chem. Intl. Ed. English 30, pp. 423-426 (1991).
Koshkin et al., “LNA (Locked Nucleic Acid): An RNA Mimic Forming Exceedingly Stable LNA: LNA Duplexes,” J. Am. Chem. Soc. vol. 120, pp. 13252-13253 (1998).
Letsinger et al., “Phosphoramidate Analogues of Oligonucleotides,” J. Org. Chem, vol. 35, No. 1, pp. 3800-3803 (1970).
Letsinger et al., “Effects of Pendant Groups at Phosphorus on Binding Properties of d-APA Analogues,” Nucleic Acids Research vol. 14, No. 8, pp. 3487-3499 (1986).
Letsinger et al., “Caionic Oligonucleotides,” J. Am. Chem. Soc., pp. 4470-4471 (1988).
Letsinger et al., “Hybridization of Alternating Cationic/ Anionic Oligonucleotides to RNA Segments,” Nucleosides & Nucleotides vol. 13, No. 6&7, pp. 1597-1605 (1994).
Maddry et al., “Synthesis of Nonionic Oligonucleotide Analogues,” American Chemical Society, pp. 40-51 (1994).
Mag et al., “Synthesis and Selective Clevage of a Oligodeoxynucleotide Containing a Bridged Internucleotide 5 Phosphorothioate Linkage,” Nucleic Acids Research, vol. 19 No. 7, pp. 1437-1441 (1991).
Meier et al., “Peptide Nucleic Acids (PNA's)-Unusual Properties of Nonionic Oligonucleotide Analogues,” Angew Intl. Ed. English 31, No. 8, pp. 1008-1010 (1992).
Mesmaeker et al., “Comparison of Rigid and Flexible Backbones in Antisense Oligonucleotides,” Bioorganic & Medicinal Chem. Letters, vol. 4, No. 3, pp. 395-398 (1994).
Mesmaeker et al., “Novel Backbone Replacements for Oligonucleotides,” American Chemical Society, pp. 24-39 (1994).
Pauwels et al., “Biological Activity of New 2-5A Analogues,” Chemica Scripta, vol. 26, pp. 141-145 (1986).
Rawls “Optomistic About Antisense,” C&EN, pp. 35-39 (Jun. 1997).
Sawai, “Synthesis and Properties of Oligoadenylic Acids Containing 2'-5' Phosphoramide Linkage,” Chemistry Letters, pp. 805-808 (1984).
Sprinzl et al., “Enzymatic Incorporation of ATP and CTP Analogues into the 3' end of RNA,” Eur. J Biochem 81, pp. 579-589 (1977).
International Search Report and Written Opinion issued in International Application No. PCT/US2013/06617, 35 pages (Feb. 3, 2014).
International Preliminary Report on Patentability and Written Opinion issued in International Application No. PCT/US2013/06617, 15 pages (Apr. 28, 2015).
Non-final Office Action issued in U.S. Appl. No. 14/062,860, 67 pages (Jul. 23, 2015).
Non-final Office Action issued in U.S. Appl. No. 14/206,817, 44 pages (Oct. 8, 2015).
International Preliminary Report on Patentability issued in International Application No. PCT/US2014/024499, 9 pages (Sep. 24, 2015).
Related Publications (1)
Number Date Country
20140261708 A1 Sep 2014 US
Provisional Applications (1)
Number Date Country
61798091 Mar 2013 US