Automated diagnostic analyzers having rear accessible track systems and related methods

Information

  • Patent Grant
  • 9335338
  • Patent Number
    9,335,338
  • Date Filed
    Friday, March 14, 2014
    10 years ago
  • Date Issued
    Tuesday, May 10, 2016
    8 years ago
Abstract
Example apparatus and methods related to automated diagnostic analyzers having rear accessible track systems. An example apparatus disclosed herein includes an analyzer to perform a diagnostic test, the analyzer having a first side and a second side opposite the first side. The example apparatus includes a loading bay disposed on the first side of the analyzer to receive a first carrier and a pipetting mechanism coupled to the analyzer adjacent the second side. The example apparatus also includes a first carrier shuttle to transport the first carrier from a first location adjacent the loading bay to a second location adjacent the pipetting mechanism and a track disposed adjacent the second side of the analyzer to transfer a second carrier to a third location adjacent the pipetting mechanism.
Description
FIELD OF THE DISCLOSURE

The present disclosure relates generally to automated diagnostic analyzers and, more particularly, to automated diagnostic analyzers having rear accessible track systems and related methods.


BACKGROUND

Healthcare diagnostics laboratories use diagnostic instruments for testing and analyzing specimens or samples. Known automated diagnostic analyzers employ multiple carousels and multiple pipetting mechanisms to automatically aspirate liquid from and dispense liquid to different areas in the analyzer to perform diagnostic analysis procedures. The carousels may include a carousel for reaction vessels and a carousel for reagents. By arranging multiple containers on the respective carousels, these known analyzers are capable of conducting multiple assays on multiple test samples as the carousels rotate. These analyzers typically include a pipetting mechanism that aspirates a sample from a sample container and dispenses the sample into one or more reaction vessels on one of the carousels. A robotic device is utilized to individually transport a single sample container at a time to a region near the sample pipetting mechanism for aspiration.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1A is a top view of an example analyzer having an example sample positioner in a first position in accordance with the teachings of this disclosure.



FIG. 1B shows the example analyzer of FIG. 1A with the example positioner in a second position.



FIG. 2 illustrates an example laboratory system in accordance with the teachings of this disclosure.



FIG. 3 is a block diagram of an example processing system for the example analyzers and laboratory systems shown in FIGS. 1 and 2.



FIG. 4 is a flowchart illustrating an example diagnostic testing process.



FIG. 5 is a diagram of a processor platform for use with the examples disclosed herein.





DETAILED DESCRIPTION

Certain examples are shown in the above-identified figures and described in detail below. In describing these examples, like or identical reference numbers are used to identify the same or similar elements. The figures are not necessarily to scale and certain features and certain views of the figures may be shown exaggerated in scale or in schematic for clarity and/or conciseness. Additionally, several examples have been described throughout this specification. Any features from any example may be included with, a replacement for, or otherwise combined with other features from other examples.


Diagnostics laboratories employ diagnostic instruments such as those for testing and analyzing specimens or samples including, for example, clinical chemistry analyzers, immunoassay analyzers and hematology analyzers. Specimens and biological samples are analyzed to, for example, check for the presence or absence of an item of interest including, for example, a specific region of DNA, mitochondrial DNA, a specific region of RNA, messenger RNA, transfer RNA, mitochondrial RNA, a fragment, a complement, a peptide, a polypeptide, an enzyme, a prion, a protein, an antibody, an antigen, an allergen, a part of a biological entity such as a cell or a viron, a surface protein, and/or functional equivalent(s) of the above. Specimens such as a patient's body fluids (e.g., serum, whole blood, urine, swabs, plasma, cerebra-spinal fluid, lymph fluids, tissue solids) can be analyzed using a number of different tests to provide information about the patient's health.


Generally, analysis of a test sample involves the reaction of test samples with one or more reagents with respect to one or more analytes. The reaction mixtures are analyzed by an apparatus for one or more characteristics such as, for example, the presence and/or concentration of a certain analyte in the test sample. Use of automated diagnostic analyzers improves the efficiency of the laboratory procedures as the technician (e.g., an operator) has fewer tasks to perform and, thus, the potential for operator or technician error is reduced. In addition, automated diagnostic analyzers also provide results much more rapidly and with increased accuracy and repeatability.


Automated diagnostic analyzers use multiple pipettes to move liquids between storage containers (e.g., receptacles such as open topped tubes) and containers in which the specimens are to be processed (e.g., reaction vessels). For example, a specimen may be contained in a tube that is loaded in a rack on an analyzer, and a head carrying a pipette moves the pipette into the tube where a vacuum is applied to extract a selected amount of the specimen from the tube into the pipette. The head retracts the pipette from the tube and moves the pipette to another tube or reaction vessel located at a processing station, depositing the extracted amount of the specimen from the pipette into the reaction vessel. A reagent is similarly acquired from a reagent supply.


In other examples, a track or positioner (e.g., a robotic device) is disposed at the front of an analyzer to move a sample tube or a sample carrier to a position near a pipette such that the pipette can aspirate from the sample tube. In such examples, a loading bay or rack is disposed on the front side of the analyzer to receive and hold multiple carriers, which may contain, for example, samples and/or reagents to be used in the diagnostic testing. To position samples for testing, the positioner retrieves the carrier from the loading bay and transfers the carrier to a location near an operating range of the sample pipette, which is also adjacent the front of the analyzer. After aspiration, the positioner transports the sample carrier back to the loading bay and reloads the sample carrier in a respective slot. The positioner may then retrieve a second carrier and likewise transfers the second carrier to the location near the sample pipette.


However, the pipetting mechanisms of these known analyzers are only able to aspirate samples from sample tubes that are positioned in a specific location by the positioner. In addition, because only one positioner is utilized, the positioner can only retrieve and hold one carrier at a time and, thus, there are increased time delays between aspirations from different carriers.


Additionally, for some diagnostic testing, some samples may have a higher priority for testing, some samples and/or reagents may need to be refrigerated and/or other samples and/or reagents may involve additional processing steps (e.g., centrifugation, incubation) prior to analysis. Some known laboratories use a laboratory automated system having a track to transport priority samples and other liquids (e.g., reagents, calibration fluids, control fluids, wash fluids, etc.) to the analyzers. In some known configurations, the track is located along a side of the analyzer and transports the priority samples to a location within the operating range of the sample pipetting mechanism. This arrangement increases the footprint of the analyzer particularly in configurations in which multiple analyzers (e.g., modules) are arranged next to each other. Also, the track system being disposed on the sides of the analyzers prevents the alignment (e.g., a side-by-side layout) of multiple modules, and in some examples, it may be desired to add multiple modules (e.g., analyzers) to increase throughput of a laboratory or facility utilizing the analyzers. In other known configurations, the track system is disposed along the front of the analyzers outside of the front loading bay. However, with this arrangement, additional robotic mechanisms and/or spurs are needed to move the carriers from the track system to the loading bay, and then from the loading bay into the analyzer. Additionally, with this arrangement, the track system blocks access to the front loading bay and, thus, an operator or technician is not able to manually load samples and/or reagents for diagnostic testing.


The example analyzers disclosed herein have a sample pipette (e.g., a pipetting mechanism) disposed near a rear side of the analyzer and one or more shuttle carriers to transport sample carriers from a front side of the analyzer to the rear side of the analyzer near the sample pipette. The sample pipette is positioned to aspirate sample liquid from sample tubes in the carriers and to dispense the sample liquid into one or more reaction vessels in the analyzer.


In some examples, the analyzer includes two carrier shuttles that operate independently of each other, which decreases time between aspirations and, thus, increases throughput of the analyzer. Additionally, by locating the sample pipette adjacent the rear side of the analyzer, a laboratory automated system (LAS) track can be disposed (e.g., mounted) at or along the rear side of analyzer without interfering with the layout of the laboratory. For example, multiple modules or analyzers may be aligned side-by-side, and the LAS track may traverse along the rear side of the modules for delivering additional samples (e.g., priority samples) and sample carriers to the individual analyzers. Therefore, the example analyzers may perform diagnostic testing according to traditional protocols or schedules that utilize the front loading bay and may also receive priority samples and other liquids (e.g., calibration/control liquids) from the LAS without interrupting normal operations of the analyzer. Additionally, the modularity of the example analyzers allows more or less analyzers (e.g., one, two, three, four or more) to be utilized depending on the demand (e.g., increased demand for immunoassay testing and/or clinical chemistry testing) of the laboratory or facility. In examples with multiple analyzers, the analyzers may be any combination of immunoassay or clinical chemistry analyzers. For example, there may be a laboratory system with three immunoassay analyzers coupled as modules with a clinical chemistry analyzer. In other examples, there may be two of each and/or other combinations are possible.


An example apparatus disclosed herein includes an analyzer to perform a diagnostic test, the analyzer having a first side and a second side opposite the first side. The example apparatus includes a loading bay disposed on the first side of the analyzer to receive a first carrier and a pipetting mechanism coupled to the analyzer adjacent the second side. The example apparatus also includes a first carrier shuttle to transport the first carrier from a first location adjacent the loading bay to a second location adjacent the pipetting mechanism. In addition, the example apparatus includes a track disposed adjacent the second side of the analyzer to transfer a second carrier to a third location adjacent the pipetting mechanism.


In some examples, the apparatus also includes a second carrier shuttle, wherein the loading bay is to receive a third carrier and the second carrier shuttle is to transport the third carrier from the first location adjacent the loading bay to the second location adjacent the pipetting mechanism. In some such examples, the first carrier shuttle and the second carrier shuttle are independently movable. In some examples, the apparatus also includes a positioner to transport the first carrier from a slot in the loading bay to the first carrier shuttle. In some such examples, the positioner is to transport the third carrier from a slot in the loading bay to the second carrier shuttle.


In some examples, the first carrier shuttle comprises a lead screw. In some examples, the first carrier shuttle comprises a conveyor belt.


In some examples, the first carrier shuttle is to move in a direction substantially perpendicular to the track. In some examples, the track comprises a spur to transport the first carrier to or from the third location.


In some examples, the apparatus also includes a motor to operate the first carrier shuttle, the motor being disposed at one of the first location or the second location. In some such examples, the apparatus also includes a sensor to detect movement in the first carrier shuttle, the sensor disposed at the other of the first location or the second location, opposite the motor.


In some examples, the analyzer comprises a rotatable plate having a plurality of reaction vessels, and the pipetting mechanism is to dispense liquid into one or more of the reaction vessels. In some such examples, the pipetting mechanism is to follow a first protocol of liquid transfer between at least one of the second location or the third location and the reaction vessels. In some examples, the first protocol to be suspended, the first carrier shuttle or a second carrier shuttle is to transport a third carrier from the loading bay to the second location, and the pipetting mechanism is to transfer liquid between the third carrier and at least one of the reaction vessels.


In some examples, the track is coupled to a refrigerated storage area. In some examples, the pipetting mechanism is to at least one of dispense or aspirate a sample from the second location and the third location.


Another example apparatus disclosed herein includes a first carousel, a second carousel, a first track on a first side of the first carousel, a second track on a second side of the first carousel parallel to the first track, a third track on a third side of the first carousel and a pipette to access the first carousel, the first track and the third track.


In some examples, the pipette is to pivot about a single axis to access each of the first carousel, the first track and the third track. In some examples, the third track is perpendicular to the first track. In some examples, the third track comprises a first shuttle to transport a carrier from a first position near the second track to a second position near the pipette. In some examples, the third track comprises a first shuttle and a second shuttle. In some examples, the first shuttle and second shuttle are independently movable. In some examples, the first carousel is to carry a reaction vessel and the second carousel is to carry a reagent container.


An example method is disclosed here that includes transporting a first carrier from a first side of an analyzer having a loading bay to a second side of the analyzer opposite the first side, aspirating a first liquid from the first carrier using a pipetting mechanism disposed adjacent the second side of the analyzer, and dispensing the first liquid, via the pipetting mechanism, into a first reaction vessel on the analyzer. The example method includes transporting a second carrier along a track to a position adjacent the pipetting mechanism, the track disposed along the second side of the analyzer, aspirating a second liquid from the second carrier using the pipetting mechanism, and dispensing the second liquid, via the pipetting mechanism, into a second reaction vessel on the analyzer.


In some examples, the first carrier is transported to the second side of the analyzer via a first carrier shuttle. In some such examples, the method includes transporting a third carrier from the first side of the analyzer to the second side of the analyzer. In some examples, the method includes aspirating a third liquid from the third carrier using the pipetting mechanism and dispensing the third liquid, via the pipetting mechanism, into a third reaction vessel on the analyzer. In some examples, the third carrier is transported to the second side of the analyzer via a second carrier shuttle. In some examples, the first carrier shuttle and the second carrier shuttle operate independently of each other. In some examples, one or more of the first carrier shuttle or the second carrier shuttle is a track comprising a lead screw. In some examples, one or more of the first carrier shuttle or the second carrier shuttle is a track comprising a conveyor belt. In some examples, one or more of the first carrier, the second carrier or the third carrier comprises at least one test sample tube.


Also disclosed herein is an example system that includes multiple analyzers. For example, the example system includes a first analyzer to perform a first diagnostic test and a second analyzer to perform a second diagnostic test. The example first analyzer includes a first proximal side, a first distal side opposite the first proximal side, a first pipetting mechanism adjacent the first distal side and a first loading bay disposed on the first proximal side to receive a first carrier. The example analyzer also includes a first carrier shuttle to transport the first carrier from a first location adjacent the first proximal side to a second location adjacent the first pipetting mechanism. The example second analyzer includes a second proximal side, a second distal side opposite the second proximal side, a second pipetting mechanism adjacent the second distal side and a second loading bay disposed on the second proximal side to receive a second carrier. In addition, the example second analyzer includes a second carrier shuttle to transport the second carrier from a third location adjacent the second proximal side of the second analyzer to a fourth location adjacent the second pipetting mechanism. Also, the example system includes a track disposed along the first distal side and the second distal side. The example track includes a first sidetrack to transfer a third carrier to a fifth location adjacent the first pipetting mechanism.


In some example, the example track includes a second sidetrack to transfer the third carrier to a sixth location adjacent the second pipetting mechanism.


In some examples, the first carrier shuttle and the second carrier shuttle are substantially parallel. In some examples, the first carrier shuttle is substantially perpendicular to the track.


In some examples, the first diagnostic test is an immunoassay and the second diagnostic test is a clinical chemistry assay. Also, in some examples, the first diagnostic test is an immunoassay and the second diagnostic test is an immunoassay. In addition, in some examples, the first diagnostic test is a clinical chemistry assay and the second diagnostic test is a clinical chemistry assay.


In some examples, the example system also includes a positioner disposed along the first proximal side and the second proximal side of the second analyzer. In some examples, the positioner is to transfer the second carrier from the second loading bay to the first carrier shuttle on the first analyzer.


In example system also may include a third analyzer disposed next to one of the first analyzer or the second analyzer. The example third analyzer includes a third proximal side, a third distal side opposite the third proximal side, a third pipetting mechanism adjacent the third distal side and a third loading bay disposed on the third proximal side to receive a fourth carrier. In addition, the example third analyzer includes a third carrier shuttle to transport the fourth carrier from a sixth location adjacent the third proximal side of the third analyzer to a seventh location adjacent the third pipetting mechanism. In some examples, the example track of the example system also is disposed along the third distal side of the third analyzer.


Turning now to the figures, an example automated diagnostic analyzer 100 is shown in FIGS. 1A and 1B as having a first carousel 102 and a second carousel 104. The analyzer 100 may be used, for example, to perform immunoassays, clinical chemistry tests, or any other diagnostics tests. The first carousel 102 and the second carousel 104 are rotatably coupled to a base station 106 independent of each other. The base station 106 houses different subassemblies and other components used for testing (e.g., performing diagnostic analyses) such as, for example, wash liquid, bulk reagents, a vacuum source, a pressure source, a refrigeration system, temperature sensors, a processor, motors, etc.


In the example shown, the second carousel 104 is vertically distanced (e.g., spaced) above the first carousel 102 and at least a portion of the second carousel 104 is disposed above and over the first carousel 102. In other examples, the first carousel 102 and the second carousel 104 are disposed next to each other (e.g., coplanar) or may be arranged to be concentric with each other.


In the illustrated example of FIGS. 1A and 1B, the first carousel 102 is a reagent carousel and the second carousel 104 is a reaction vessel carousel. However, in other examples, the first and second carousels 102, 104 may hold reagents, samples, reaction vessels or any combination thereof. In the illustrated examples, the first carousel 102 includes a plurality of reagent containers (including, for example, liquids having microparticles) arranged annularly around the carousel. In some examples, the first carousel 102 has an inner annular array of reagent containers and outer annular array of reagent containers, concentric with the inner annular array of containers. In the example shown, the second carousel 104 is a plate having a plurality of reaction vessels 108a-n disposed around an outer circumference of the plate. In some examples, the reaction vessels 108a-n are reusable cuvettes (e.g., washable glass cuvettes). After a test has been completed in a reaction vessel, the vessel is cleaned (e.g., sterilized) and the vessel may be used for another test. However, in other examples, the reaction vessels 108a-n are disposable cuvettes (e.g., plastic cuvettes) that are discarded after one or more tests. In operation, the second carousel 104 rotates as one or more assay tests are carried out in the reaction vessels 108a-n. A plurality of different modules or instruments may be disposed around the second carousel 104 to, for example, dispense reagents, mix the contents of the reaction vessels, incubate the contents of the reaction vessels, analyze the contents, wash the reaction vessels, etc.


The example automated diagnostic analyzers disclosed herein also include one or more pipetting mechanisms (e.g., probe arms, automated pipettes, pipettes, etc.) to aspirate and dispense liquids within the reaction vessels 108a-n on the second carousel 104. In the illustrated example shown in FIGS. 1A and 1B, the analyzer 100 includes a pipetting mechanism 110 (e.g., a sample pipette) that is coupled (e.g., mounted) to the base station 106. The pipetting mechanism 110 has multiple degrees of freedom. In the example shown, the pipetting mechanism 110 has a path of travel 112 (e.g., an arc path, a horizontal arc path, a radius of travel, an operating range), such that the pipetting mechanism 110 can aspirate (e.g., draw liquid) from or dispense liquid to containers located along the path of travel 112. As shown, the pipetting mechanism 110 is positioned to have access to one of the reaction vessels 108a-n on the second carousel 104 at point A. In some examples, the pipetting mechanism 110 has an axis of rotation and rotates a probe arm with a pipette disposed at the distal end of the probe arm. The pipetting mechanism 110 is also movable in the Z direction (e.g., the vertical direction).


In the example shown, the pipetting mechanism 110 is disposed outside of the first carousel 102 and outside of the second carousel 104, for example, coupled to the base 106 in a position at a distance from the center of the first carousel 102 and the center of the second carousel 104 that is greater than either a first diameter of the first carousel 102 or a second diameter of the second carousel 104. However, in other examples, the pipetting mechanism 110 is disposed above and over the first carousel 102 and/or adjacent the second carousel 104. In such examples, the pipetting mechanism 110 may be mounted to a platform that is disposed between the first carousel 102 and the second carousel 104. In still other examples, the pipetting mechanism 110 may be disposed over the first carousel 102 and over the second carousel 104.


In the example shown in FIGS. 1A and 1B, the example analyzer 100 has a first side 114 (e.g., a front side) and a second side 116 (e.g., a back side, a rear side) opposite the first side 114. The pipetting mechanism 110 is disposed near (e.g., adjacent, along, next to, closer to, bordering) the second side 116 of the analyzer 100. The analyzer 100 also includes a random sample handler (RSH) 118 (e.g., a loading bay) on the first side 114 of the analyzer 100 for accepting and retaining carriers having samples and/or reagents that are to be used for diagnostic testing. In the example shown, the RSH 118 includes a loading rack 120 having a plurality of slots 122a-n for receiving containers, carriers and/or trays of carriers. In the example shown, a plurality of carriers 124a-n have been inserted into the slots 122a-n in the loading rack 120. The carriers 124a-n may hold one or more containers (e.g., a tube, a vessel, an open top container, a vial, a cup, etc.). The containers may include samples, reagents, calibrations, control liquids, etc., used by the analyzer 100 for assay diagnostic testing. In some examples, an operator (e.g., a laboratory technician) loads the carriers 124a-n individually or in trays into the loading rack 120 of the RSH 118. In other examples, an automated track system transports the carriers 124a-n to the RSH 118 and loads the carriers 124a-n into respective ones of the slots 122a-n, for example, via a robotic mechanism.


In FIGS. 1A and 1B, a number of carriers 124a-n have been shown as inserted into different slots 122a-n. In the example shown, each of the carriers 124a-n is holding six containers. However, in other examples, the carriers 124a-n can be configured to hold more or fewer containers depending on the analyzer, the RSH design parameters and/or the carrier layout. The carriers 124a-n are held in the slots 122a-n until selected for testing or retesting.


In the example shown, the RSH 118 includes a positioner 126, which may be a robotic device, to transport the carriers 124a-n and containers coupled thereto to and from the loading rack 120. The positioner 126 is movable along a positioner track 128 disposed along the length of the loading rack 120 and the first side 114 of the analyzer 100. The positioner 126 has an arm 130 to engage the carriers 124a-n loaded in the RSH 118. The positioner 126 and the arm 130 operate to remove the carriers 124a-n from their respective slots 122a-n and transport the carriers 124a-n to different locations along the positioner track 128.


In the example shown in FIGS. 1A and 1B, the example analyzer 100 also includes a first carrier shuttle 134 (e.g., a transporter) and a second carrier shuttle 136 that are disposed near (e.g., along, adjacent, next to, bordering) a third side 138 (e.g., the left side of FIGS. 1A and 1B) of the analyzer 100, opposite a fourth side 140 (e.g., the right side of FIGS. 1A and 1B) of the analyzer 100. In the example shown, the first side 114, the second side 116, the third side 138 and the fourth side 140 define the outer boundaries of the analyzer 100. In the example shown, the analyzer 100 has a rectangular cross-section or footprint. However, in other examples, the analyzer 100 has a square cross-section, a circular cross-section, or any other shaped cross-section or footprint.


In the example shown, the positioner 126 transports the carriers 124a-n to and from the first carrier shuttle 134 and/or the second carrier shuttle 136. For example, in FIG. 1A, the positioner 126 engages the first carrier 124a in the loading rack 120 of RSH 118. The positioner 126 transports the first carrier 124a to, in this example, the first shuttle 134, as shown in FIG. 1B, where the positioner 126 releases or otherwise transfers the first carrier 124a onto the first carrier shuttle 134. The positioner 126 is controlled by a programmable computer for moving the carriers 124a-n as needed and/or desired (e.g., according to scheduling protocols or timetables) for testing. The RSH 118 provides random access to the carriers 124a-n on the loading rack 120. The analyzer 100 includes software that allows users to flexibly configure rules or criteria for testing samples. The software may be programmed into and/or operated from an example processor 316 (FIG. 3), which is disclosed in more detail below.


In some examples, the positioner 126 includes a label reader such as, for example, a barcode reader, a radio frequency identification (RFID) reader and/or other type of reader, to read carrier and container information. The label reader reads the labels attached to the carriers, the sample tubes and/or reagent tubes as the positioner 126 passes the carriers by the reader. An example RSH and an example positioner are disclosed in U.S. patent application Ser. No. 12/106,755, titled “ASSAY TESTING DIAGNOSTIC ANALYZER,” filed on Apr. 21, 2008, which is incorporated herein by reference in its entirety.


In the illustrated example, the first and second carrier shuttles 134, 136 operate to move carriers (e.g., the carriers 124a-n) and/or containers between a first position near the first side 114 of the analyzer 100 (e.g., adjacent the rack 120 or the RSH 118) and a second position near the second side 116 of the analyzer 100 (e.g., near the pipetting mechanism 110). Specifically, the first and second carrier shuttles 134, 136 operate to transport carriers 124a-n to a position within the path of travel 112 of the pipetting mechanism 110, such that liquid (e.g., a sample, a specimen) within the containers on the carriers 124a-n can be aspirated from the containers via the pipetting mechanism 110. The pipetting mechanism 110 may then dispense the liquid at point A into one or more of the reaction vessels 108a-n on the second carousel 104 for testing.


In the example shown, the first carrier shuttle 134 includes a first track 142 and the second carrier shuttle 136 includes a second track 144. In some examples, the first track 142 and the second track 144 are conveyor belts that move to transport carriers placed on the respective tracks 142, 144 from one position to another position along the first and second tracks 142, 144. In other examples, the first and second tracks 142, 144 include other track devices such as, for example, a belt, a chain, a carriage, a lead screw, an air cylinder, and/or a linear motor or combinations thereof. In some examples, the first carrier shuttle 134 and the second carrier shuttle 136 comprise different types of tracks. In the example shown, the first carrier shuttle 134 includes a first motor 146 (e.g., an electric motor, a servo motor, a stepper motor, etc.) to drive the first track 142 and the second carrier shuttle 136 includes a second motor 148 to drive the second track 144. In this example, the first and second tracks 142, 144 are operated independently of each other. In other examples, the operations of the first and second tracks 142, 144 are coordinated. The first and second motors 146, 148 may be used to rotate one or more pulleys or gears, which, in turn, move the tracks 142, 144. In the example shown, the first and second motors 146, 148 are rotatable in either direction to move the first and second tracks 142, 144, respectively, in either direction.


In the example shown, the first and second motors 146, 148 are located closer to the second side 116 of the analyzer 100. In the example shown, the first and second carrier shuttles 134, 136 also include respective sensors 150, 152 such as, for example, a linear encoder and/or a transducer. The first and second sensors 150, 152 are located adjacent the first and second tracks 142, 144 to sense a position/movement of the respective tracks 142, 144. Thus, the first and second sensors 150, 152 provide feedback to the first and second motors 146, 148 to indicate whether the first and second tracks 142, 144 are actually moving when the first and second motors 146, 148 are operating. In the example shown, the first and second sensors 150, 152 are positioned on the first and second carrier shuttles 134, 136 opposite the first and second motors 146, 148 as a safety feature to ensure that the tracks 142, 144 are moving when the motors 146, 148 are operating. In some instances, the first and/or second tracks 142, 144 may become dislodged, misaligned or otherwise inoperative and, thus, will not properly transport the carriers. In such an instances, the first and second motors 146, 148 may continue to operate (e.g., spin, rotate, etc.) according to a programmed testing protocol. If the sensors 150, 152 were located adjacent the first and second motors 146, 148, the continued operation of the motors 146, 148 could interfere with the readings of the sensors 146, 148, and cause the sensors 150, 152 to erroneously indicate that the tracks 142, 144 were operating normally. By locating the sensors 150, 152 at the opposite end of the carrier shuttles 134, 136 than the motors 146, 148, the sensors 150, 152 can ensure the tracks 134, 136 are actually moving in accordance with the programming of the first and second motors 146, 148. In some examples, the motors 146, 148 are disposed at, near or closer to the second side 116 of the analyzer 100, and the sensors 150, 152 are at, near or closer to the first side 114 of the analyzer 100. In other examples, this configuration may be switched, such that the motors 146, 148 are disposed at, near or closer to the first side 114 of the analyzer 100, and the sensors 150, 152 are disposed at, near or closer to the second side 116 of the analyzer 100.


The use of multiple shuttle carriers 134, 136 enables the example analyzer 100 to perform sampling (e.g., aspirating and/or dispensing) from one carrier on one track while another carrier is being loaded onto the other track. For example, a first carrier 124a can be retrieved from the RSH 118 by the positioner 126 (FIG. 1A) and deposited on the first track 142 of the first carrier shuttle 134 (FIG. 1B). In some examples, the arm 130 of the positioner 126 includes a hook to engage a tab on the end of the carrier. In other examples, the arm 130 has a gripping mechanism to grip the sides of the carrier. In either example, the arm 130 is used to grab the first carrier 124a from its respective slot 122a-n in the loading rack 120 (FIG. 1A) and then lifts to extract the first carrier 124a from of its respective slot 122a-n. After the positioner 126 retrieves the first carrier 124a, the positioner 126 moves (e.g., slides, translates) along the positioner track 128 towards the third side 138 of the analyzer 100 and, thus, towards the first and second carrier shuttles 134, 136. The arm 130 of the positioner 126 then rotates to align the first carrier on the first track 142 of the first carrier shuttle 134, as shown in the position in FIG. 1B. In the example shown, the arm 130 is capable of rotating at least about 180°.


After the first carrier 124a is placed on the first track 142 of the first carrier shuttle 134, the first motor 146 operates to move the first carrier 124a, via the first track 142, from a first position near the first side 114 of the analyzer 100 to a second position near the second side 116 of the analyzer 100 and, thus, within the path of travel 112 of the pipetting mechanism 110. The pipetting mechanism 110 may aspirate from a container on the first track 142 along the first path of travel 112 at point B. The first motor 146 operates to position the first carrier 124a so that the first path of travel 112 intersects the appropriate container on the first carrier. After aspirating from a container, the pipetting mechanism 110 moves along its first path of travel 112 to dispense the liquid into one or more of the reaction vessels 108a-n on the second carousel 104 at point A.


While the pipetting mechanism 110 is aspirating from a container on the first carrier 124a, the positioner 126 can retrieve a second carrier 124b-n from the RSH 118 and load the second carrier 124b-n onto the second track 144 of the second carrier shuttle 136. The second motor 148 operates to move the second carrier 124b-n on the second track 144 from the first position near the first side 114 of the analyzer 100 to the second side 116 of the analyzer 100 near the pipetting mechanism 110. The second motor 148 operates to position the second carrier 124b-n along the first path of travel 112 of the pipetting mechanism 110 (e.g., the position shown in FIGS. 1A and 1B). The pipetting mechanism 100 may aspirate from a container on the carrier 124b-n on the second track 144 at point C. As the second carrier shuttle 136 transports the second carrier 124b-n to/from the second position near the second side 116, and/or as the pipetting mechanism 110 aspirates from the second carrier 124b-n, the first carrier shuttle 134 may simultaneously and independently transport the first carrier 124a to/from the first position adjacent the first side 114 of the analyzer 100 and/or the second position adjacent the second side 116.


When a carrier, e.g., the first carrier 124a, returns to the first position adjacent the first side 114 of the analyzer 100, the positioner 126 unloads the first carrier 124a and places the first carrier 124a within one of the slots 122a-n in the loading rack 120. The positioner 126 is then able to retrieve the first carrier 124a or another carrier 124b-n from the loading rack 120 and deposit that carrier 124a-n on the first track 144 of the first carrier shuttle 134. By employing two carrier shuttles 134, 136, one of the carrier shuttles 134, 136 can operate to hold a carrier near the second position for aspiration while another carrier can be loaded onto the other carrier shuttle 134, 136 for subsequent transportation to the second side 116 of the analyzer 100. Thus, the time between aspirations is reduced, which increases throughput of the example analyzer 100.


In the example shown, the first and second carrier shuttles 134, 136 are aligned substantially parallel to one another and are disposed along the third side 138 of the analyzer 100. However, in other examples, the first and second carrier shuttles 136, 136 may be positioned other locations and/or not parallel to one another. In the example shown, the first and second carrier shuttles 134, 136 are disposed over a portion of the first carousel 102. In other examples, the first and/or second carrier shuttles 134, 136 are disposed outside of the first carousel 102 (i.e., next to the first carousel 102).


In some examples, test orders are programmed by an operator or downloaded via a lab information system or any network. A test order may require a plurality of assays. Once a sample is loaded, a programmable computer determines the order (e.g., scheduling, protocols) of the different sample tests based on factors including, for example, number of tests to be conducted, types of reagents to be used, number of reagents to be used, an incubation period, scheduled priority and other factors. In the example shown, the positioner 126, the first track 142, the second track 144, the first motor 146, the second motor 148 and other components are controlled in response to commands from the programmable computer.


In the illustrated example shown in FIGS. 1A and 1B, a laboratory automated system (LAS) 154 has a main track 156 and a first subtrack or spur 158, which is disposed along the second side 116 of the analyzer 100. The LAS 154 may include multiple instruments and equipment for processing and preprocessing certain samples, reagents, calibrations, controls, etc. In some examples, the LAS 154 includes and/or is coupled to a refrigerated storage area, a centrifuge, an aliquoter and/or any other processing station(s). In some examples, the LAS includes a system of tracks and robotic positioners to move carriers from one instrument to another.


In the example shown, the LAS 154 transports carriers (e.g., sample carriers) or containers to a position near the analyzer 100 and, more specifically, to a position within the first path of travel 112 of the pipetting mechanism 110. For illustrative purposes, a carrier 124c is depicted on the first subtrack or spur 158. In operation, the carrier 124c is transported along the main track 156 of the LAS 154 and when the carrier 124c arrives at the first spur 158, the carrier 124c may continue down the main track 156 or may be diverted to the first spur 158 to be sent to the position adjacent the pipetting mechanism 110. As shown, the path of travel 112 of the pipetting mechanism 110 extends beyond the second side 116 of the analyzer 110. In the example shown, the pipetting mechanism 110 may aspirate a liquid (e.g., a sample) from a container on the carrier at the first spur 158 at point D. In the example shown, the main track 156 and the spur 158 of the LAS 154 are substantially parallel to the second side 116 of the analyzer 100 and are substantially perpendicular to the first and second carrier shuttles 134, 136.


In the example shown, the pipetting mechanism 110 is located near the second side 116 of the analyzer 100 and has access (e.g., can aspirate from and/or can dispense to) to the reaction vessels 108a-n on the second carousel 104 at point A, a carrier on the first track 142 of the first carrier shuttle 134 at point B, a carrier the second track 144 of the second carrier shuttle 136 at point C and/or a carrier on the spur 158 of the LAS 154 at point D. Therefore, the pipetting mechanism 110 has access to carriers loaded in the RSH 118 at the first side 114 (e.g., the front side) of the analyzer 110 (via one or more of the carrier shuttles 134, 136) and carriers transported along the track 156 of the LAS 154 on the second side 116 (e.g., the back side) of the analyzer 100. Continuous access to carriers at different locations around the pipetting mechanism 110 points allows the pipetting mechanism 110 to aspirate from multiple sample containers more efficiently and with less idle or down time and, as a result, increases the throughput of the example analyzer 100.



FIG. 2 illustrates an example laboratory system 200 having a first diagnostic analyzer 202 (e.g., a first module), a second diagnostic analyzer 204 (e.g., a second module) and a laboratory automation system (LAS) 206. In the example shown, the first analyzer 202 includes a first carousel 208 and a second carousel 210. In the example shown, the second carousel 210 is reaction carousel having a plurality of reaction vessels for conducting diagnostic tests on one or more samples in the plurality of reaction vessels. The first analyzer 202 also includes a first random sample handler (RSH) 212 (e.g., a first loading bay) disposed along a first side 214 (e.g., a front side) of the first analyzer 202, opposite a second side 216 (e.g., a rear side) of the first analyzer 202. A first pipetting mechanism 218 is disposed on the first analyzer 202 adjacent the second side 216 of the first analyzer 202 and has a first path of travel 220 (e.g., horizontal arc path, range of access).


In the example shown, the first analyzer 202 further includes a first carrier shuttle 222 and a second carrier shuttle 224 located along a third side 226 (e.g., the left side) of the first analyzer 202, opposite a fourth side 228 (e.g., the right side) of the first analyzer 202. In the example shown, each of the first and second carrier shuttles 222, 224 has a respective track 230, 232 (e.g., lead screw) and a respective carriage 234, 236 (e.g., shuttles). The first and second tracks 230, 232 operate to move the respective carriages 234, 236 from a first position near the first side 214 of the first analyzer 202 to a second position near the second side 216 of the first analyzer 202 and within the first path of travel 220 of the first pipetting mechanism 218. In the example shown, the first and second carriages 234, 236 are platforms for holding a carrier. As the first and second tracks 230, 232 operate (e.g., rotate), the first and second carriages 234, 236 move along the longitudinal axes of the respective track 230, 232.


In the example shown, the second analyzer 204 includes similar components as the first analyzer 202 such as, for example, a third carousel 238 (e.g., a reagent carousel), a fourth carousel 240 (e.g., a reaction carousel), a second RSH 242, a first side 244 (e.g., a front side) opposite a second side 246 (e.g., a rear side), a third side 248 (e.g., a left side) opposite a fourth side 250 (e.g., a right side), a second pipetting mechanism 252 with a second path of travel 254, a third carrier shuttle 256, a fourth carrier shuttle 258, a third track 260 (e.g., a third lead screw), a fourth track 262 (e.g., a fourth lead screw), a third carriage 264 and a fourth carriage 266. The third and fourth carrier shuttles 256, 258 of the second analyzer 204 operate to transport carriers from a first position adjacent the first side 244 of the second analyzer 204 to a second position adjacent the second side 246 of the second analyzer 204 and within the second path of travel 254 of the second analyzer 204.


In the example shown, a positioner 268 is movable along a positioner path 270 between the first and second RSH 212, 242 and along the first sides 214, 244 of the first and second analyzers 202, 204. In this example, only one positioner 268 is utilized to transport carriers among the first RSH 212, the second RSH 242, the first track 230, the second track 232, the third track 260 and/or the fourth track 262. In some examples, the positioner 268 is substantially similar to the positioner 126 disclosed above in connection with FIGS. 1A and 1B. The positioner 268 may retrieve carriers loaded within the first and second RSH 212, 242 and may transport the carriers via the first, second, third or fourth carrier shuttles 222, 224, 256, 258.


In the example shown, a first plurality of carriers 272a-n are loaded in the first RSH 212, and a second plurality of carriers 274a-n are loaded in the second RSH 242. In operation, the positioner 268 is to retrieve one of the first or second plurality of carriers 272a-n, 274a-n and is to place (e.g., position, deposit, transport) the carrier on one of the first, second, third or fourth carrier shuttles 222, 224, 256, 258. The carriers 272a-n, 274a-n may then be transported via one of the carriages 234, 236, 264, 266 and tracks 230, 232, 260, 262 to a position near the second side 216, 246 of one of the analyzers 202, 204.


In the example shown, the first pipetting mechanism 218 of the first analyzer 202 may aspirate from a container in a first carrier on the first carriage 234 at point A and may aspirate from another container in a second carrier on the second carriage 236 at point B, which are both along the first path of travel 220. Similarly, the second pipetting mechanism 252 may aspirate from a container in a third carrier on the third carriage 264 at point C and may aspirate from another container in a fourth carrier on the fourth carriage 266 at point D, both of which are along the second path of travel 254 of the second pipetting mechanism 252. The first pipetting mechanism 218 may access one or more reaction vessels on the second carousel 210 at point E, and the second pipetting mechanism 252 may access one or more reaction vessels on the fourth carousel 240 at point F.


In the example system shown in FIG. 2, the LAS 206 includes a main track 276 that is disposed along the second sides 216, 246 of the first and second analyzers 202, 204. The main track 276 has a first subtrack or spur 278 and a second subtrack or spur 280. The first spur 278 displaces a carrier on the main track 276 to a position near the second side 216 of the first analyzer 202 and within the first path of travel 220 of the first pipetting mechanism 218. The second spur 280 displaces a carrier on the main track 276 to a position near the second side 246 of the second analyzer 204 and within the second path of travel 254 of the second pipetting mechanism 252. In the example shown, the first pipetting mechanism may aspirate from a container on a carrier on the first spur 278 at point G, and the second pipetting mechanism 252 may aspirate from another container on another carrier on the second spur 280 at point H.


Although only two analyzers 202, 204 are shown in this example, more (e.g, three or four) or fewer analyzers may be added to the laboratory system 200, and the track 276 of the LAS 206 may be configured to traverse along or near the analyzers to supply the analyzers with access to additional carriers. The LAS 206 transports carriers having additional liquids such as, for example, priority samples for testing, calibration and control liquids, additional reagents (including, for example, liquids with microparticles), etc. In some examples, the LAS 206 is tied to additional equipment such as, for example, a refrigerated storage area 282, a centrifuge 284 and/or an aliquoter 286.


In some example tests, such as clinical chemistry tests, a body liquid may be analyzed, such as, for example, serum or plasma. Serum is the yellow, watery part of blood that is left after blood has been allowed to clot and all blood cells have been removed such as, for example, via centrifugation, which packs the denser blood cells and platelets to the bottom of a centrifuge tube and leaves the liquid serum fraction resting above the packed cells. Plasma is similar to serum but is obtained by centrifuging blood without clotting. The LAS 206 of example system 200 enables sample liquids such as, for example, serum or plasma to be processed in the centrifuge 284 and then transported to one or more of the first and second analyzers 202, 204 for diagnostic testing. In other examples, the LAS 206 allows priority samples to be loaded onto carriers and sent along the track 276 to a position within the first and/or second paths of travel 220, 254 of the respective pipetting mechanisms 218, 252. By disposing the pipetting mechanisms 218, 252 near the second sides 216, 246 of the analyzers 202, 204, and by providing the carrier shuttles 222, 224, 256, 258 to transport carrier to and from the first and second sides 214, 244, 216, 246 of the analyzers 202, 204, the analyzers 202, 204 may receive samples in a traditional operating manner through the first sides 214, 244 and/or may receive samples from the LAS 206 at the second sides 216, 246. Additionally, by disposing the pipetting mechanisms 218, 252 near the second sides 216, 246 of the analyzers, the analyzers 202, 204 can be arranged in a side-by-side configuration without interfering with operations of the respective analyzers 202, 204 and, thus, laboratory floor space is decreased.



FIG. 3 is a block diagram of an example processing system 300 for use with any of the analyzers 100, 202, 204 and/or the LAS 154, 206 disclosed herein. Example analyzers disclosed herein are used to, for example, perform diagnostic testing on multiple test samples using one or more reagents and/or other diagnostic test procedures. The example processing system 300 includes a carousel controller 302 to control the operations (e.g., rotational sequences, locksteps, indexing, etc.) of one or more carousels on an analyzer. In some examples, an analyzer includes one or more carousels having a plurality of containers or vessels. In some examples, the analyzer includes a first carousel having a plurality of reagent containers that contain reagents for diagnostic testing and a second carousel having a plurality of vessels (e.g., reaction vessels) that are used for testing the samples. For example, the analyzer 100 disclosed above includes the first carousel 102 (e.g., a reagent carousel), and the second carousel 104 (e.g., a reaction carousel). The second carousel 104 includes a plurality of reaction vessels 108a-n and rotates the reaction vessels 108a-n in a continuous or discrete manner while a plurality of diagnostic functions are performed on the reaction vessels 108-n. The carousel controller 302 may be used, for example, to control the rotational sequence (e.g., lockstep timing) of the first and second carousels 102, 104.


The example processing system 300 includes a pipette controller 304. In some examples, an analyzer utilizes one or more pipettes (e.g., automated pipetting mechanisms, probe arms, etc.) to aspirate a fluid from one location and dispense the fluid into another location. In some examples, an analyzer has multiple pipettes such as, for example, a first pipette for dispensing a sample into a reaction vessel, a second pipette for dispensing a first reagent into a reaction vessel, a third pipette for dispensing a second reagent into a reaction vessel, etc. The pipette controller 306 operates to control the pipettes such as, for example, the movement of the pipettes, the vacuum applied to the pipettes for aspirating, the pressure applied to the pipettes for dispensing, etc. In the example analyzer 100 disclosed above, the analyzer 100 includes the pipetting mechanism 110, which moves a pipette along the path of travel 112 to aspirate and dispense fluid such as, for example, sample. In some examples, the example pipetting mechanism 110 dispenses sample into the reaction vessels 108a-n on the second carousel 104 at point A. The pipette controller 304 is used to control the pipetting mechanism 110.


The example processing system 300 includes a reader controller 306. In some examples, a reader (e.g., an analyzer) is disposed along the inside or the outside of the reaction carousel, such that as the reaction carousel rotates, the reader may analyze the contents of the respective reaction vessels. In some examples, a reaction vessel is held stationary in front of the reader for a predetermined time and a reading is taken. In other examples, one or more reaction vessels may be passed continuously in front of the reader, and the reader takes a plurality of individual readings corresponding to each reaction vessel. The reader controller 306 operates to control when the readings are taken.


The reader controller 306 may also be used to control other readers. For example, a reader positioned near the RSH 118 may be operated to read an RFID tag, a bar code, a QR code or other machine readable code to gather information about the identity of or other data related to the contents of a carrier 124a-n and/or a container coupled to the carrier 124a-n.


The example processing system 300 also includes a positioner controller 308 and a shuttle controller 310. In some examples, an analyzer includes a loading bay for receiving containers, carriers having containers and/or trays of carriers. The containers may include reagents, samples, controls, calibrations, etc. In some examples, the loading bay is disposed on a first side or front side of the analyzer. In some examples, a positioner (e.g., a robotic mechanism) retrieves the carriers from the loading bay and transports the carriers to different areas of the analyzer for testing and retesting. The positioner controller 308 controls the movement of the positioner to engage and move carriers in the analyzer. In the example analyzer 100 disclosed above, the positioner 126 translates along the track 128 on the first side 114 of the analyzer 100. The positioner 126 also has the arm 130 that rotates to engage carriers in the RSH 118. The positioner controller 308 may be used, for example, to control the movement of the positioner 126 and the arm 130 along the track 128.


In some examples, an analyzer includes one or more shuttle carriers to transport carriers from one side of the analyzer to the other side of the analyzer. In some examples, the pipette is disposed along a second side or rear side of the analyzer and the carrier shuttle(s) transports the carriers from the front of the analyzer adjacent the loading bay to a position near the back side of the analyzer and within the range of the pipette. In some examples, the carrier shuttles are operated by motors (e.g., electric motors, servo motors, stepper motors, etc.). In some examples, the shuttle carriers utilize a track system such as, for example, a conveyor belt or a lead screw, to transport the carriers. The carrier shuttle controller 310 operates to control the movement of the one or more carrier shuttles to transport carriers along the carrier shuttle(s). The carrier shuttle controller 310 may be used, for example, to control the motors 146, 148 of the respective carrier shuttles 134, 136.


The example processing system 300 includes sensors 312 communicatively coupled to the shuttle carrier controller 310. In some examples, one or more sensors (e.g., transducers, encoders, etc.) are used to sense movement of the carrier shuttles to determine whether the carrier shuttles are operating in accordance with their instructions from the carrier shuttle controller 310. In some examples, the sensors 312 are disposed at an opposite end of the carrier shuttles than the motors. In the example analyzer 100 disclosed above, the sensors 150, 152 are disposed along the tracks 142, 146 of the respective carrier shuttles 134, 136 to determine whether the tracks 142, 146 of the respective shuttle carriers 134, 136 are operating effectively and that the tracks 142, 146 are not dislodged, misaligned or otherwise inoperable.


The example processing system 300 includes a laboratory automation system (LAS) controller 314. In some examples, a laboratory automation system includes a system of tracks and instruments to transport carriers around a laboratory. Some samples, reagents, and other liquids used in diagnostic testing, require additional processing steps and/or refrigeration. The LAS may connect to various instruments and, when time for processing, the LAS may transport the liquid (e.g., a priority sample), via a carrier, to the back side of the analyzer for aspirating by the pipette. In some examples, the main track of the LAS includes a subtrack or spur to transport a carrier to the rear side of the analyzer, such that the carrier is not held stationary on the main track. The LAS controller 314 controls operation of the LAS including, for example, the main track, the spurs, and/or any equipment or instruments attached thereto. For example, the example LAS 154 disclosed above includes the main track 156 and the spur 158 to transport a carrier (e.g., 124c) to a location adjacent the rear side of the analyzer 100, such that the pipetting mechanism 110 may aspirate from the contents of the carrier.


The example processing system 300 also includes a processor 316 and a database 318. The processor interfaces with the controllers and sensors 302-314 of the processing system 300 to control the various operations of each of the components. The processor 316 is programmable to operate in accordance with desired testing protocol(s). The database 318 may be used to store, for example, information regarding tests that have occurred, are to occur, and/or are occurring, testing protocol(s), information regarding the individual samples and/or reagents data gathered from the reader(s), position(s) of the carrier(s), postioner(s), carrier shuttle(s), pipetting mechanism(s), LAS, and/or carousel(s), and/or other information.


In the example shown, the processing system components 302-318 are communicatively coupled to other components of the example system 300 via communication links 320. The communication links 320 may be any type of wired connection (e.g., a databus, a USB connection, etc.) or a wireless communication mechanism (e.g., radio frequency, infrared, etc.) using any past, present or future communication protocol (e.g., Bluetooth, USB 2.0, USB 3.0, etc.). Also, the components of the example system 300 may be integrated in one device or distributed over two or more devices.


While an example manner of implementing the analyzers 100, 202, 204 and/or the LAS 154, 206 of FIGS. 1A-2 is illustrated in FIG. 3, one or more of the elements, processes and/or devices illustrated in FIG. 3 may be combined, divided, re-arranged, omitted, eliminated and/or implemented in any other way. Further, the example carousel controller 302, the example pipette controller 304, the example reader controller 306, the example positioner controller 308, the example carrier shuttle controller 310, the example sensor(s) 312, the example LAS controller 314, the example processor 316, the example database 318 and/or, more generally, the example processing system 300 of FIG. 3 may be implemented by hardware, software, firmware and/or any combination of hardware, software and/or firmware. Thus, for example, any of the example carousel controller 302, the example pipette controller 304, the example reader controller 306, the example positioner controller 308, the example carrier shuttle controller 310, the example sensor(s) 312, the example LAS controller 314, the example processor 316, the example database 318 and/or, more generally, the example processing system 300 could be implemented by one or more analog or digital circuit(s), logic circuits, programmable processor(s), application specific integrated circuit(s) (ASIC(s)), programmable logic device(s) (PLD(s)) and/or field programmable logic device(s) (FPLD(s)). When reading any of the apparatus or system claims of this patent to cover a purely software and/or firmware implementation, at least one of the example carousel controller 302, the example pipette controller 304, the example reader controller 306, the example positioner controller 308, the example carrier shuttle controller 310, the example sensor(s) 312, the example LAS controller 314, the example processor 316 and/or the example database 318 is/are hereby expressly defined to include a tangible computer readable storage device or storage disk such as a memory, a digital versatile disk (DVD), a compact disk (CD), a Blu-ray disk, etc. storing the software and/or firmware. Further still, the example processing system 300 of FIG. 3 may include one or more elements, processes and/or devices in addition to, or instead of, those illustrated in FIG. 3, and/or may include more than one of any or all of the illustrated elements, processes and devices.


A flowchart representative of an example method 400, at least some of which are machine readable, for implementing the example analyzers 100, 202, 204, the example LAS 154, 206 and/or the example processing system 300 is shown in FIG. 4. In this example, the method 400 may be implemented using machine readable instructions that comprise a program for execution by a processor such as the processor 512 shown in the example processor platform 500 discussed below in connection with FIG. 5. The program may be embodied in software stored on a tangible computer readable storage medium such as a CD-ROM, a floppy disk, a hard drive, a digital versatile disk (DVD), a Blu-ray disk, or a memory associated with the processor 512, but the entire program and/or parts thereof could alternatively be executed by a device other than the processor 512 and/or embodied in firmware or dedicated hardware. Further, although the example program is described with reference to the flowchart illustrated in FIG. 4, many other methods of implementing the example analyzers 100, 202, 204, the example LAS 154, 206 and/or the example processing system 300 may alternatively be used. For example, the order of execution of the blocks may be changed, and/or some of the blocks described may be changed, eliminated, or combined.


As mentioned above, at least some of the elements of the process of FIG. 4 may be implemented using coded instructions (e.g., computer and/or machine readable instructions) stored on a tangible computer readable storage medium such as a hard disk drive, a flash memory, a read-only memory (ROM), a compact disk (CD), a digital versatile disk (DVD), a cache, a random-access memory (RAM) and/or any other storage device or storage disk in which information is stored for any duration (e.g., for extended time periods, permanently, for brief instances, for temporarily buffering, and/or for caching of the information). As used herein, the term tangible computer readable storage medium is expressly defined to include any type of computer readable storage device and/or storage disk and to exclude propagating signals. As used herein, “tangible computer readable storage medium” and “tangible machine readable storage medium” are used interchangeably. Additionally or alternatively, the example processes of FIG. 4 may be implemented using coded instructions (e.g., computer and/or machine readable instructions) stored on a non-transitory computer and/or machine readable medium such as a hard disk drive, a flash memory, a read-only memory, a compact disk, a digital versatile disk, a cache, a random-access memory and/or any other storage device or storage disk in which information is stored for any duration (e.g., for extended time periods, permanently, for brief instances, for temporarily buffering, and/or for caching of the information). As used herein, the term non-transitory computer readable medium is expressly defined to include any type of computer readable device or disk and to exclude propagating signals. As used herein, when the phrase “at least” is used as the transition term in a preamble of a claim, it is open-ended in the same manner as the term “comprising” is open ended.



FIG. 4 is a flowchart representing the example diagnostic testing method 400 that may be implemented, for example, by the analyzers 100, 202, 204, the LAS 154, 206 and/or the processing system 300 detailed above. The example analyzers include a first carousel and a second carousel, the second carousel being a reaction carousel having a plurality of reaction vessels for conducting diagnostic tests. As the reaction carousel rotates, a plurality of automated modules each perform assay steps on the individual reaction vessels. The example analyzers have a first side (e.g., a front side) and a second side (e.g., a back side), opposite the first side. In the example analyzers 100, 202, 204 detailed above, a pipetting mechanism is disposed near the second side of the analyzer to dispense sample into the reaction vessels on the reaction carousel as the reaction carousel rotates. In some examples, a loading bay is disposed on the first side of the example analyzer to receive carriers or trays of carriers. The example method or process 400 includes loading carriers in the first side of the analyzer (block 402). In some examples, each carrier includes multiple containers such as, for example, test tubes having test samples.


The example process 400 also includes transporting a first carrier to a first carrier shuttle (block 404). For example, the example analyzer 100 disclosed above includes a first carrier shuttle 134 and a second carrier shuttle 136 to transport carriers from the first side 114 of the analyzer 100 to the second side 116 of the analyzer 100. In some examples, a positioner is located along the loading bay to retrieve carriers from respective slots and transfer the carriers to other locations in the analyzer including, for example, to a carrier shuttle.


The example process 400 includes transporting the first carrier from the first side of the analyzer to the second side of the analyzer (block 406). In some examples, the first carrier shuttle includes a conveyor belt and a motor to transport the first carrier. In other examples, the first carrier shuttle comprises a lead screw and a carriage, such that the first carrier may be placed in the carriage and the first lead screw operates (e.g., rotates) to move the carriage (and the first carrier) from the first side of the analyzer to the second side of the analyzer. In some examples, the first carrier shuttle has a sensor (e.g., an encoder, a transducer) to sense movement of the conveyor belt, as a safety feature.


The example process 400 also includes aspirating a liquid from the first carrier (block 408). For example, the example analyzer 100 disclosed above locates the pipetting mechanism 110 adjacent the second side 116 of the analyzer 100. The first carrier shuttle 134 is to transport the first carrier from a first location near the first side 114 of the analyzer 100 to a second location near the second side 116 of the analyzer and, more specifically, within an access range (e.g., the path of travel 112, a horizontal arc path, etc.) of the pipetting mechanism 110, to enable the pipetting mechanism 110 to aspirate from the first carrier. After aspiration, the liquid is dispensed into a first reaction vessel (block 410). In some examples, the pipetting mechanism 110 has an axis of rotation and a probe arm with a pipette disposed on the distal end of the probe arm. The probe arm rotates to access liquids along a path of travel (e.g., a horizontal arc path) and dispenses the aspirated liquid into the first reaction vessel on the reaction carousel 104.


The example process includes determining whether there is a second carrier shuttle (412). In some examples, the analyzer employs only one carrier shuttle. In the example analyzers 100, 202, 204 disclosed above, a second carrier shuttle is utilized to reduce turnaround time and increase throughput. The second carrier shuttle is independently operated. Therefore, one or more of the operations of the second carrier shuttle and/or components related thereto (e.g., blocks 314, 316, 318, 320) may occur independently and/or simultaneously relative to the one or more of the operation of the first carrier shuttle and/or components related thereto (e.g., blocks 304, 306, 308, 310).


The example process 400 includes transporting a second carrier to the second carrier shuttle (block 414). For example, as mentioned above, the positioner 126 of the analyzer 100 retrieves the second carrier 124b-n from a slot 122b-n in the loading bay 120 and transports the second carrier 124b-n to the second carrier shuttle 136.


The example process 400 also includes transporting the second carrier from the first side of the analyzer to the second side of the analyzer (block 416). In some examples, the second carrier shuttle includes a conveyor belt or a lead screw. The second carrier shuttle operates to transport the second carrier from the first location near the first side of the analyzer to the second location adjacent the second side of the analyzer and, more specifically, to a location within the path of travel of the pipetting mechanism.


The example process 400 includes aspirating a liquid from the second carrier (block 418) and dispensing the liquid into a second reaction vessel on the reaction carousel (420).


In addition, the example process 400 includes transporting a third carrier to the second side of the analyzer (block 422). For example, the example analyzer 100 may include the laboratory automation system (LAS) 154. The LAS 154 has a track system 156 to transport carriers and/or containers of diagnostic testing liquid around a laboratory, and a portion of the track (e.g., 158) is disposed adjacent the second side of the analyzer. The transport of the third carrier is independent of the transport of the first and/or second carriers. Therefore, one or more of the operations of the first and second carrier shuttle and/or components related thereto (e.g., blocks 304, 308, 310, 312, 314, 316, 318, 320) may occur independently and/or simultaneously relative to the one or more of the operation of the LAS 154 and/or components related thereto (e.g., blocks 322, 324, 326).


The example process 400 also includes aspirating a liquid from the third carrier (block 424). For example, the LAS 154 includes the spur 158 that directs the third carrier 124c from the main track 156 to a position within the path of travel 112 of the pipetting mechanism 110 to enable access for aspirating the liquid from the third carrier 124c. The example process 300 also includes dispensing the liquid into a third reaction vessel on the reaction carousel (block 426). For example, the pipetting mechanism 110 may move in the path of travel 112 and dispense aspirated liquid into a reaction vessel on the second carousel 104.


The example process includes determining whether additional tests are to be performed (block 428). If further testing is desired, then the example process includes transporting the first carrier, via the first shuttle carrier, from the second location to the first location adjacent the first side of the analyzer (block 430). In some examples, the positioner removes the first carrier from the first carrier shuttle and places the first carrier in an empty slot in the loading bay. The example process may then continue with loading or transporting another carrier (block 404) onto the first carrier shuttle (i.e., as the “first” carrier in the illustrated example process 400), and the example process 400 proceeds as disclosed above. If further testing is not desired and/or needed (bock 428), then the example process 400 ends (block 432).



FIG. 5 is a block diagram of an example processor platform 500 capable of executing the instructions to be performed of FIG. 4 to implement one or more portions of the apparatus and/or systems of FIGS. 1A-3. The processor platform 500 can be, for example, a server, a personal computer, a mobile device, a personal digital assistant (PDA), an Internet appliance, and/or or any other type of computing device.


The processor platform 500 of the illustrated example includes a processor 512. The processor 512 of the illustrated example is hardware. For example, the processor 512 can be implemented by one or more integrated circuits, logic circuits, microprocessors or controllers from any desired family or manufacturer.


The processor 512 of the illustrated example includes a local memory 513 (e.g., a cache). The processor 512 of the illustrated example is in communication with a main memory including a volatile memory 514 and a non-volatile memory 516 via a bus 518. The volatile memory 514 may be implemented by Synchronous Dynamic Random Access Memory (SDRAM), Dynamic Random Access Memory (DRAM), RAMBUS Dynamic Random Access Memory (RDRAM) and/or any other type of random access memory device. The non-volatile memory 516 may be implemented by flash memory and/or any other desired type of memory device. Access to the main memory 514, 516 is controlled by a memory controller.


The processor platform 500 of the illustrated example also includes an interface circuit 520. The interface circuit 520 may be implemented by any type of interface standard, such as an Ethernet interface, a universal serial bus (USB), and/or a PCI express interface.


In the illustrated example, one or more input devices 522 are connected to the interface circuit 520. The input device(s) 522 permit(s) a user to enter data and commands into the processor 512. The input device(s) can be implemented by, for example, an audio sensor, a microphone, a camera (still or video), a keyboard, a button, a mouse, a touchscreen, a track-pad, a trackball, isopoint and/or a voice recognition system.


One or more output devices 524 are also connected to the interface circuit 520 of the illustrated example. The output devices 524 can be implemented, for example, by display devices (e.g., a light emitting diode (LED), an organic light emitting diode (OLED), a liquid crystal display, a cathode ray tube display (CRT), a touchscreen, a tactile output device and/or a light emitting diode (LED). The interface circuit 520 of the illustrated example, thus, typically includes a graphics driver card, a graphics driver chip or a graphics driver processor.


The interface circuit 520 of the illustrated example also includes a communication device such as a transmitter, a receiver, a transceiver, a modem and/or network interface card to facilitate exchange of data with external machines (e.g., computing devices of any kind) via a network 526 (e.g., an Ethernet connection, a digital subscriber line (DSL), a telephone line, coaxial cable, a cellular telephone system, etc.).


The processor platform 500 of the illustrated example also includes one or more mass storage devices 528 for storing software and/or data. Examples of such mass storage devices 528 include floppy disk drives, hard drive disks, compact disk drives, Blu-ray disk drives, RAID systems, and digital versatile disk (DVD) drives.


Coded instructions 532 to implement the method of FIG. 4 may be stored in the mass storage device 528, in the volatile memory 514, in the non-volatile memory 516, and/or on a removable tangible computer readable storage medium such as a CD or DVD. Although certain example methods, apparatus and articles of manufacture have been described herein, the scope of coverage of this patent is not limited thereto. On the contrary, this patent covers all methods, apparatus and articles of manufacture fairly falling within the scope of the claims of this patent.

Claims
  • 1. An apparatus comprising: an analyzer to perform a diagnostic test, the analyzer having a first side and a second side opposite the first side;a loading bay disposed on the first side of the analyzer to receive a first carrier;a pipetting mechanism coupled to the analyzer adjacent the second side;a first carrier shuttle to transport the first carrier from a first location adjacent the loading bay to a second location adjacent the pipetting mechanism; anda track disposed adjacent the second side of the analyzer to transfer a second carrier to a third location adjacent the pipetting mechanism.
  • 2. The apparatus of claim 1 further comprising a second carrier shuttle, wherein the loading bay is to receive a third carrier and the second carrier shuttle is to transport the third carrier from the first location adjacent the loading bay to the second location adjacent the pipetting mechanism.
  • 3. The apparatus of claim 2, wherein the first carrier shuttle and the second carrier shuttle are independently movable.
  • 4. The apparatus of claim 2 further comprising a positioner to transport the first carrier from a slot in the loading bay to the first carrier shuttle.
  • 5. The apparatus of claim 4, wherein the positioner is to transport the third carrier from a slot in the loading bay to the second carrier shuttle.
  • 6. The apparatus of claim 1, wherein the first carrier shuttle comprises a lead screw.
  • 7. The apparatus of claim 1, wherein the first carrier shuttle comprises a conveyor belt.
  • 8. The apparatus of claim 1, wherein the first carrier shuttle is to move in a direction substantially perpendicular to the track.
  • 9. The apparatus of claim 1, wherein the track comprises a spur to transport the second carrier to or from the third location.
  • 10. The apparatus of claim 1 further comprising a motor to operate the first carrier shuttle, wherein the motor is disposed at one of the first location or the second location.
  • 11. The apparatus of claim 10 further comprising a sensor to detect movement in the first carrier shuttle, wherein the sensor is disposed at the other of the first location or the second location, opposite the motor.
  • 12. The apparatus of claim 1, wherein the analyzer comprises a rotatable plate having a plurality of reaction vessels, and wherein the pipetting mechanism is to dispense liquid into one or more of the reaction vessels.
  • 13. The apparatus of claim 12, wherein the pipetting mechanism is to follow a first protocol of liquid transfer between at least one of the second location or the third location and the reaction vessels.
  • 14. The apparatus of claim 13, wherein the first protocol is to be suspended, the first carrier shuttle or a second carrier is shuttle to transport a third carrier from the loading bay to the second location, and the pipetting mechanism is to transfer liquid between the third carrier and at least one of the reaction vessels.
  • 15. The apparatus of claim 1, wherein the pipetting mechanism is to at least one of dispense or aspirate a sample from the second location and the third location.
  • 16. A method comprising: transporting a first carrier from a first side of an analyzer having a loading bay to a second side of the analyzer opposite the first side;aspirating a first liquid from the first carrier using a pipetting mechanism disposed adjacent the second side of the analyzer;dispensing the first liquid, via the pipetting mechanism, into a first vessel on the analyzer;transporting a second carrier along a track to a position adjacent the pipetting mechanism, the track disposed along the second side of the analyzer;aspirating a second liquid from the second carrier using the pipetting mechanism; anddispensing the second liquid, via the pipetting mechanism, into a second vessel on the analyzer.
  • 17. The method of claim 16, wherein the first carrier is transported to the second side of the analyzer via a first carrier shuttle.
  • 18. The method of claim 17 further comprising transporting a third carrier from the first side of the analyzer to the second side of the analyzer.
  • 19. The method of claim 18 further comprising: aspirating a third liquid from the third carrier using the pipetting mechanism; anddispensing the third liquid, via the pipetting mechanism, into a third vessel on the analyzer.
  • 20. The method of claim 18, wherein the third carrier is transported to the second side of the analyzer via a second carrier shuttle.
  • 21. The method of the claim 20, wherein the first carrier shuttle and the second carrier shuttle operate independently of each other.
  • 22. The method of claim 20, wherein one or more of the first carrier shuttle or the second carrier shuttle is a track comprising a lead screw.
  • 23. The method of claim 20, wherein one or more of the first carrier shuttle or the second carrier shuttle is a track comprising a conveyor belt.
  • 24. The method of claim 18, wherein one or more of the first carrier, the second carrier or the third carrier comprises at least one test sample tube.
  • 25. The method of claim 17 further comprising transporting the first carrier from the loading bay on the first side of the analyzer to the first carrier shuttle.
  • 26. The method of claim 25, wherein the first carrier is transported from the loading bay to the first carrier shuttle via a positioner.
  • 27. A system comprising: a first analyzer to perform a first diagnostic test, the first analyzer comprising: a first proximal side and a first distal side opposite the first proximal side;a first pipetting mechanism adjacent the first distal side;a first loading bay disposed on the first proximal side to receive a first carrier; anda first carrier shuttle to transport the first carrier from a first location adjacent the first proximal side to a second location adjacent the first pipetting mechanism;a second analyzer disposed adjacent the first analyzer, the second analyzer to perform a second diagnostic test, the second analyzer comprising: a second proximal side and a second distal side opposite the second proximal side;a second pipetting mechanism adjacent the second distal side;a second loading bay disposed on the second proximal side to receive a second carrier; anda second carrier shuttle to transport the second carrier from a third location adjacent the second proximal side of the second analyzer to a fourth location adjacent the second pipetting mechanism; anda track disposed along the first distal side and the second distal side, the track comprising a first sidetrack to transfer a third carrier to a fifth location adjacent the first pipetting mechanism.
  • 28. The system of claim 27, wherein the track further comprises a second sidetrack to transfer the third carrier to a sixth location adjacent the second pipetting mechanism.
  • 29. The system of claim 27, wherein the first carrier shuttle and the second carrier shuttle are substantially parallel.
  • 30. The system of claim 29, wherein the first carrier shuttle is substantially perpendicular to the track.
  • 31. The system of claim 27, wherein the first diagnostic test is an immunoassay and the second diagnostic test is a clinical chemistry assay.
  • 32. The system of claim 27, wherein the first diagnostic test is an immunoassay and the second diagnostic test is an immunoassay.
  • 33. The system of claim 27, wherein the first diagnostic test is a clinical chemistry assay and the second diagnostic test is a clinical chemistry assay.
  • 34. The system of claim 27 further comprising a positioner disposed along the first proximal side of the first analyzer and the second proximal side of the second analyzer.
  • 35. The system of claim 34, wherein the positioner is to transfer the second carrier from the second loading bay to the first carrier shuttle on the first analyzer.
  • 36. The system of claim 27 further comprising a third analyzer disposed next to one of the first analyzer or the second analyzer, the third analyzer comprising: a third proximal side and a third distal side opposite the third proximal side;a third pipetting mechanism adjacent the third distal side;a third loading bay disposed on the third proximal side to receive a fourth carrier; anda third carrier shuttle to transport the fourth carrier from a sixth location adjacent the third proximal side of the third analyzer to a seventh location adjacent the third pipetting mechanism.
  • 37. The system of claim 36, wherein the track is disposed along the third distal side of the third analyzer.
RELATED APPLICATION

This application claims the benefit under 35 U.S.C. §119(e) to U.S. Provisional Application 61/794,311 titled “AUTOMATED DIAGNOSTIC ANALYZERS HAVING REAR ACCESSIBLE TRACK SYSTEMS AND RELATED METHODS,” filed Mar. 15, 2013, which is incorporated herein by this reference in its entirety.

US Referenced Citations (420)
Number Name Date Kind
3449959 Grimshaw Jun 1969 A
3451433 Cunningham et al. Jun 1969 A
3484206 Loebl Dec 1969 A
4738825 Kelln et al. Apr 1988 A
4774055 Wakatake et al. Sep 1988 A
4808380 Minekane Feb 1989 A
4848917 Benin et al. Jul 1989 A
4849177 Jordan Jul 1989 A
4906433 Minekane Mar 1990 A
5037612 Takahashi et al. Aug 1991 A
5051238 Umetsu et al. Sep 1991 A
5071625 Kelln et al. Dec 1991 A
5077013 Guigan Dec 1991 A
5154896 Mochida et al. Oct 1992 A
5244633 Jakubowicz et al. Sep 1993 A
5250440 Kelln et al. Oct 1993 A
5266268 Antocci et al. Nov 1993 A
5270212 Horiuchi et al. Dec 1993 A
5311426 Donohue et al. May 1994 A
5314825 Weyrauch et al. May 1994 A
5352612 Huber et al. Oct 1994 A
5358691 Clark et al. Oct 1994 A
5360597 Jakubowicz et al. Nov 1994 A
5419871 Muszak et al. May 1995 A
5422271 Chen et al. Jun 1995 A
5424036 Ushikubo Jun 1995 A
5424212 Pinsl-Ober et al. Jun 1995 A
5434083 Mitsumaki et al. Jul 1995 A
5439646 Tanimizu et al. Aug 1995 A
5443791 Cathcart et al. Aug 1995 A
5445794 Wihlborg Aug 1995 A
5447687 Lewis et al. Sep 1995 A
5455175 Wittwer et al. Oct 1995 A
5460780 Devaney, Jr. et al. Oct 1995 A
5460968 Yoshida et al. Oct 1995 A
5462715 Koch et al. Oct 1995 A
5466574 Liberti et al. Nov 1995 A
5470744 Astle Nov 1995 A
5482834 Gillespie Jan 1996 A
5482839 Ashihara et al. Jan 1996 A
5482861 Clark et al. Jan 1996 A
5518693 Tomasso et al. May 1996 A
5525300 Danssaert et al. Jun 1996 A
5527673 Reinhartz et al. Jun 1996 A
5536475 Moubayed et al. Jul 1996 A
5536481 Mabire et al. Jul 1996 A
5538849 Uematsu et al. Jul 1996 A
5538976 Okada et al. Jul 1996 A
5548826 Sayers Aug 1996 A
5558839 Matte et al. Sep 1996 A
5559002 Uzan et al. Sep 1996 A
5567595 Kok Oct 1996 A
5571325 Ueyama et al. Nov 1996 A
5571481 Powell et al. Nov 1996 A
5575976 Choperena et al. Nov 1996 A
5576215 Burns et al. Nov 1996 A
5578269 Yaremko et al. Nov 1996 A
5578270 Reichler et al. Nov 1996 A
5580524 Forrest et al. Dec 1996 A
5582796 Carey et al. Dec 1996 A
5585068 Panetz et al. Dec 1996 A
5587129 Kurosaki et al. Dec 1996 A
5589137 Markin et al. Dec 1996 A
5595707 Copeland et al. Jan 1997 A
5599501 Carey et al. Feb 1997 A
5611994 Bailey et al. Mar 1997 A
5620898 Yaremko et al. Apr 1997 A
5632399 Palmieri et al. May 1997 A
5637275 Carey et al. Jun 1997 A
5639425 Komiyama et al. Jun 1997 A
5650327 Copeland et al. Jul 1997 A
5653940 Carey et al. Aug 1997 A
5654199 Copeland et al. Aug 1997 A
5654200 Copeland et al. Aug 1997 A
5656493 Mullis et al. Aug 1997 A
5658532 Kurosaki et al. Aug 1997 A
5658799 Choperena et al. Aug 1997 A
5670114 Sakazume et al. Sep 1997 A
5670120 Degenhardt et al. Sep 1997 A
5670375 Seaton et al. Sep 1997 A
5677188 Mitsumaki et al. Oct 1997 A
5679309 Bell Oct 1997 A
5681530 Kuster et al. Oct 1997 A
5682026 Auclair et al. Oct 1997 A
5686046 Malek et al. Nov 1997 A
5693292 Choperena et al. Dec 1997 A
5698450 Ringrose et al. Dec 1997 A
5702950 Tajima Dec 1997 A
5705062 Knobel Jan 1998 A
5714380 Neri et al. Feb 1998 A
5716583 Smethers et al. Feb 1998 A
5717148 Ely et al. Feb 1998 A
5720377 Lapeus et al. Feb 1998 A
5720923 Haff et al. Feb 1998 A
5721141 Babson et al. Feb 1998 A
5723092 Babson Mar 1998 A
5730938 Carbonari et al. Mar 1998 A
5730939 Kurumada et al. Mar 1998 A
5736101 Gianino Apr 1998 A
5736105 Astle Apr 1998 A
5736413 Uzan et al. Apr 1998 A
5738827 Marquiss Apr 1998 A
5741461 Takahashi et al. Apr 1998 A
5741708 Carey et al. Apr 1998 A
5746977 Imai et al. May 1998 A
5746978 Bienhaus et al. May 1998 A
5748978 Narayan et al. May 1998 A
5750338 Collins et al. May 1998 A
5762872 Buhler et al. Jun 1998 A
5762873 Fanning et al. Jun 1998 A
5773268 Korenberg et al. Jun 1998 A
5773296 Montalbano et al. Jun 1998 A
5773662 Imai et al. Jun 1998 A
5779981 Danssaert et al. Jul 1998 A
5786182 Catanzariti et al. Jul 1998 A
5789252 Fujita et al. Aug 1998 A
5795547 Moser et al. Aug 1998 A
5795784 Arnquist et al. Aug 1998 A
5807523 Watts et al. Sep 1998 A
5814277 Bell et al. Sep 1998 A
5816998 Silverstolpe et al. Oct 1998 A
5826129 Hasebe et al. Oct 1998 A
5827478 Carey et al. Oct 1998 A
5827479 Yamazaki et al. Oct 1998 A
5827653 Sammes et al. Oct 1998 A
5837195 Malek et al. Nov 1998 A
5843376 Ishihara et al. Dec 1998 A
5846491 Choperena et al. Dec 1998 A
5849247 Uzan et al. Dec 1998 A
5855847 Oonuma et al. Jan 1999 A
5856194 Arnquist et al. Jan 1999 A
5863506 Farren Jan 1999 A
5876668 Kawashima et al. Mar 1999 A
5876670 Mitsumaki et al. Mar 1999 A
5882594 Kawaguchi et al. Mar 1999 A
5882596 Breeser et al. Mar 1999 A
5882918 Goffe Mar 1999 A
5885353 Strodtbeck et al. Mar 1999 A
5885529 Babson et al. Mar 1999 A
5885530 Babson et al. Mar 1999 A
5888454 Leistner et al. Mar 1999 A
5897783 Howe et al. Apr 1999 A
5902549 Mimura et al. May 1999 A
5919622 Macho et al. Jul 1999 A
5928952 Hutchins et al. Jul 1999 A
5935522 Swerdlow et al. Aug 1999 A
5948691 Ekiriwang et al. Sep 1999 A
5955373 Hutchins et al. Sep 1999 A
5958763 Goffe Sep 1999 A
5972295 Hanawa et al. Oct 1999 A
5985215 Sakazume et al. Nov 1999 A
5985670 Markin Nov 1999 A
5985671 Leistner et al. Nov 1999 A
5985672 Kegelman et al. Nov 1999 A
5988869 Davidson et al. Nov 1999 A
6019945 Ohishi et al. Feb 2000 A
6027691 Watts et al. Feb 2000 A
6033574 Siddiqi Mar 2000 A
6033880 Haff et al. Mar 2000 A
6042786 Oonuma et al. Mar 2000 A
6043880 Andrews et al. Mar 2000 A
6051101 Ohtani et al. Apr 2000 A
6056923 Diamond et al. May 2000 A
6060022 Pang et al. May 2000 A
6063340 Lewis et al. May 2000 A
6068393 Hutchins et al. May 2000 A
6068978 Zaun et al. May 2000 A
6071395 Lange Jun 2000 A
6071477 Auclair et al. Jun 2000 A
6074615 Lewis et al. Jun 2000 A
6080364 Mimura et al. Jun 2000 A
6086827 Horner et al. Jul 2000 A
6096272 Clark et al. Aug 2000 A
6103193 Iwahashi et al. Aug 2000 A
6106781 Rosenberg Aug 2000 A
6110676 Coull et al. Aug 2000 A
6110678 Weisburg et al. Aug 2000 A
6117392 Hanawa et al. Sep 2000 A
6117398 Bienhaus et al. Sep 2000 A
6117683 Kodama et al. Sep 2000 A
6143578 Bendele et al. Nov 2000 A
6146592 Kawashima et al. Nov 2000 A
6156565 Maes et al. Dec 2000 A
6165778 Kedar Dec 2000 A
6174670 Wittwer et al. Jan 2001 B1
6232079 Wittwer et al. May 2001 B1
6245514 Wittwer Jun 2001 B1
6261521 Mimura et al. Jul 2001 B1
6267927 Pomar Longedo et al. Jul 2001 B1
6277332 Sucholeiki Aug 2001 B1
6293750 Cohen et al. Sep 2001 B1
6299567 Forrest et al. Oct 2001 B1
6300068 Burg et al. Oct 2001 B1
6300138 Gleason et al. Oct 2001 B1
6319718 Matsubara et al. Nov 2001 B1
6332636 Cohen et al. Dec 2001 B1
6335166 Ammann et al. Jan 2002 B1
6337050 Takahashi et al. Jan 2002 B1
6352861 Copeland et al. Mar 2002 B1
6374982 Cohen et al. Apr 2002 B1
6375898 Ulrich Apr 2002 B1
6377342 Coeurveille Apr 2002 B1
6386749 Watts et al. May 2002 B1
6399952 Maher et al. Jun 2002 B1
6436349 Carey et al. Aug 2002 B1
6444171 Sakazume et al. Sep 2002 B1
6455325 Tajima Sep 2002 B1
6461570 Ishihara et al. Oct 2002 B2
6472217 Richards et al. Oct 2002 B1
6498037 Carey et al. Dec 2002 B1
6503751 Hugh Jan 2003 B2
6509193 Tajima Jan 2003 B1
6517782 Horner et al. Feb 2003 B1
6517783 Horner et al. Feb 2003 B2
6521183 Burri et al. Feb 2003 B1
6522976 Shiba et al. Feb 2003 B2
6551833 Lehtinen et al. Apr 2003 B1
6562298 Arnquist et al. May 2003 B1
6569627 Wittwer et al. May 2003 B2
6579717 Matsubara et al. Jun 2003 B1
6586234 Burg et al. Jul 2003 B1
6592818 Ishihara et al. Jul 2003 B2
6597450 Andrews et al. Jul 2003 B1
6599749 Kodama et al. Jul 2003 B1
6605213 Ammann et al. Aug 2003 B1
6632654 Gebrian et al. Oct 2003 B1
6709634 Okada et al. Mar 2004 B1
6723288 Devlin, Sr. et al. Apr 2004 B2
6733728 Mimura et al. May 2004 B1
6752967 Farina et al. Jun 2004 B2
6764649 Ammann Jul 2004 B2
6764650 Takahashi et al. Jul 2004 B2
6776961 Lindsey et al. Aug 2004 B2
6780617 Chen Aug 2004 B2
6787338 Wittwer et al. Sep 2004 B2
6825921 Modlin et al. Nov 2004 B1
6827901 Copeland et al. Dec 2004 B2
6866821 Friedlander et al. Mar 2005 B2
6878343 Sklar et al. Apr 2005 B2
6890742 Ammann et al. May 2005 B2
6911327 McMillan et al. Jun 2005 B2
6919058 Andersson et al. Jul 2005 B2
6919175 Bienhaus et al. Jul 2005 B1
6924152 Matsubara et al. Aug 2005 B2
6943029 Copeland et al. Sep 2005 B2
6958130 Gicquel et al. Oct 2005 B1
7011792 Mimura et al. Mar 2006 B2
7028831 Veiner Apr 2006 B2
7029922 Miller Apr 2006 B2
7033820 Ammann et al. Apr 2006 B2
7081226 Wittwer et al. Jul 2006 B1
7105351 Matsubara et al. Sep 2006 B2
7115090 Lagarde Oct 2006 B2
7115384 Clark et al. Oct 2006 B2
7118892 Ammann et al. Oct 2006 B2
7118918 Copeland et al. Oct 2006 B2
7118982 Govyadinov et al. Oct 2006 B2
7132082 Aviles et al. Nov 2006 B2
7135145 Ammann et al. Nov 2006 B2
7138091 Lee et al. Nov 2006 B2
7141213 Pang et al. Nov 2006 B1
7160998 Wittwer et al. Jan 2007 B2
7169356 Gebrian et al. Jan 2007 B2
7171863 Tamura et al. Feb 2007 B2
7182912 Carey et al. Feb 2007 B2
7217513 Parameswaran et al. May 2007 B2
7220589 Richards et al. May 2007 B2
7250303 Jakubowicz et al. Jul 2007 B2
7264111 Veiner Sep 2007 B2
7267795 Ammann et al. Sep 2007 B2
7270783 Takase et al. Sep 2007 B2
7273749 Wittwer et al. Sep 2007 B1
7276208 Sevigny et al. Oct 2007 B2
7303139 Rudloff Dec 2007 B1
7331474 Veiner et al. Feb 2008 B2
7341691 Tamura et al. Mar 2008 B2
7360984 Sugiyama et al. Apr 2008 B1
7361305 Mimura et al. Apr 2008 B2
7381370 Chow et al. Jun 2008 B2
7384600 Burns et al. Jun 2008 B2
7390458 Burow et al. Jun 2008 B2
7396509 Burns Jul 2008 B2
7402281 Huynh-Ba et al. Jul 2008 B2
7407627 Rosenberg et al. Aug 2008 B1
7482143 Ammann et al. Jan 2009 B2
7524652 Ammann et al. Apr 2009 B2
7560255 Ammann et al. Jul 2009 B2
7560256 Ammann et al. Jul 2009 B2
7575937 Wiggli et al. Aug 2009 B2
7611675 Sevigny et al. Nov 2009 B2
7622078 Pagés Pinyol Nov 2009 B2
7638337 Ammann et al. Dec 2009 B2
7641855 Farina et al. Jan 2010 B2
7666602 Ammann et al. Feb 2010 B2
7666681 Ammann et al. Feb 2010 B2
7670553 Babson Mar 2010 B2
7670554 Chow et al. Mar 2010 B2
7670832 Wittwer et al. Mar 2010 B2
7700042 Matsumoto et al. Apr 2010 B2
7700043 Mimura et al. Apr 2010 B2
7731414 Vincent et al. Jun 2010 B2
7731898 Burkhardt et al. Jun 2010 B2
7745205 Wittwer et al. Jun 2010 B2
7749441 Hanawa et al. Jul 2010 B2
7785534 Watari Aug 2010 B2
7815858 Sevigny et al. Oct 2010 B2
7827874 Tsujimura et al. Nov 2010 B2
7837452 Ignatiev et al. Nov 2010 B2
7842237 Shibuya et al. Nov 2010 B1
7842504 Devlin, Sr. Nov 2010 B2
7850914 Veiner et al. Dec 2010 B2
7854892 Veiner et al. Dec 2010 B2
7855084 Jakubowicz et al. Dec 2010 B2
7858032 Le Comte et al. Dec 2010 B2
7867777 Aviles et al. Jan 2011 B2
7910294 Karlsen Mar 2011 B2
7939036 Burkhardt et al. May 2011 B2
7941904 Smith May 2011 B2
7943100 Rousseau May 2011 B2
7947225 Itoh May 2011 B2
7951329 Malyarov et al. May 2011 B2
7964140 Watari Jun 2011 B2
7985375 Edens et al. Jul 2011 B2
7998409 Veiner et al. Aug 2011 B2
7998432 Rousseau Aug 2011 B2
7998751 Evers et al. Aug 2011 B2
8003050 Burkhardt et al. Aug 2011 B2
8012419 Ammann et al. Sep 2011 B2
8038941 Devlin, Sr. Oct 2011 B2
8038942 Pang et al. Oct 2011 B2
8047086 Smith Nov 2011 B2
8066943 Kegelman et al. Nov 2011 B2
8071053 Matsuzaki et al. Dec 2011 B2
8097211 Hamada et al. Jan 2012 B2
8114351 Degenhardt Feb 2012 B2
8119080 Wiggli et al. Feb 2012 B2
8137620 Ammann et al. Mar 2012 B2
8142740 Self et al. Mar 2012 B2
8147777 Schacher et al. Apr 2012 B2
8153061 Walters et al. Apr 2012 B2
8154899 Degroot Apr 2012 B2
8158058 Shiba et al. Apr 2012 B2
8161831 Fukuma Apr 2012 B2
8163239 Fujita Apr 2012 B2
8178043 Burkhardt et al. May 2012 B2
8187558 Jacobs et al. May 2012 B2
8192992 Ammann et al. Jun 2012 B2
8221682 Ammann et al. Jul 2012 B2
8226387 Ignatiev Jul 2012 B2
8234941 Fukuda et al. Aug 2012 B2
8257650 Chow et al. Sep 2012 B2
8257664 Ogusu Sep 2012 B2
8262994 Hamada et al. Sep 2012 B2
8262999 Kaneblei et al. Sep 2012 B2
8266973 Maeda et al. Sep 2012 B2
8293191 Kohara et al. Oct 2012 B2
8309358 Ammann et al. Nov 2012 B2
8318500 Ammann et al. Nov 2012 B2
8329101 Fujita Dec 2012 B2
8333936 Miyashita et al. Dec 2012 B2
8337753 Ammann et al. Dec 2012 B2
8343423 Mori et al. Jan 2013 B2
8343754 Wittwer et al. Jan 2013 B2
8343770 Hamada et al. Jan 2013 B2
8354078 Shohmi et al. Jan 2013 B2
8355132 Xia et al. Jan 2013 B2
8356525 Hamada et al. Jan 2013 B2
8357538 Self et al. Jan 2013 B2
8366997 Degroot Feb 2013 B2
8383039 Zhou et al. Feb 2013 B2
8431079 Rosenberg et al. Apr 2013 B2
8501496 Zuk et al. Aug 2013 B2
8545757 Utsugi et al. Oct 2013 B2
8556564 Miller Oct 2013 B2
20020155590 Gebrian et al. Oct 2002 A1
20020164807 Itaya et al. Nov 2002 A1
20040134750 Luoma, II Jul 2004 A1
20050014285 Miller Jan 2005 A1
20050220670 Palmieri et al. Oct 2005 A1
20050249634 Devlin Nov 2005 A1
20060159587 Fechtner et al. Jul 2006 A1
20060263248 Gomm et al. Nov 2006 A1
20060286004 Jacobs et al. Dec 2006 A1
20070010019 Luoma Jan 2007 A1
20070059209 Pang et al. Mar 2007 A1
20070092390 Ignatiev et al. Apr 2007 A1
20080145939 Jakubowicz et al. Jun 2008 A1
20090017491 Lemme et al. Jan 2009 A1
20090148345 Hamazumi et al. Jun 2009 A1
20090227033 Hamada et al. Sep 2009 A1
20090258414 Wittwer et al. Oct 2009 A1
20100111765 Gomm et al. May 2010 A1
20100126286 Self et al. May 2010 A1
20100187253 Vincent et al. Jul 2010 A1
20100205139 Xia et al. Aug 2010 A1
20100276445 Jacobs et al. Nov 2010 A1
20100330609 Nagai et al. Dec 2010 A1
20100332144 Nagai et al. Dec 2010 A1
20110044834 Ignatiev Feb 2011 A1
20110097240 Yamashita et al. Apr 2011 A1
20110157580 Nogami et al. Jun 2011 A1
20110293475 Rosenberg et al. Dec 2011 A1
20110312082 Silverbrook et al. Dec 2011 A1
20120039748 Mimura et al. Feb 2012 A1
20120039771 Utsugi et al. Feb 2012 A1
20120114526 Watanabe et al. May 2012 A1
20120156764 Kondo Jun 2012 A1
20120183438 Shiba et al. Jul 2012 A1
20120218854 Behringer et al. Aug 2012 A1
20120258004 Ignatiev et al. Oct 2012 A1
20120294763 Fukuda et al. Nov 2012 A1
20120301359 Kraemer et al. Nov 2012 A1
20130017535 Frey et al. Jan 2013 A1
20130064737 Mori et al. Mar 2013 A1
20130065797 Silbert et al. Mar 2013 A1
20130078617 Ueda et al. Mar 2013 A1
20130089464 Sakashita et al. Apr 2013 A1
20130112014 Hamada et al. May 2013 A1
20130280129 Watanabe et al. Oct 2013 A1
20130280130 Sarwar et al. Oct 2013 A1
Foreign Referenced Citations (44)
Number Date Country
102520200 Jun 2012 CN
0576291 Dec 1993 EP
0779514 Jun 1997 EP
0871892 Jun 1997 EP
0831330 Mar 1998 EP
1414573 Mar 2003 EP
2068154 Jun 2009 EP
2362228 Aug 2011 EP
357019667 Feb 1982 JP
359116047 Jul 1984 JP
61095248 May 1986 JP
05026883 Feb 1993 JP
406027004 Feb 1994 JP
407181129 Jul 1995 JP
H1062432 Mar 1998 JP
03582240 Oct 2004 JP
2005128037 May 2005 JP
2005533641 Oct 2005 JP
2008224439 Sep 2008 JP
2008309661 Dec 2008 JP
2009031204 Feb 2009 JP
2009145202 Jul 2009 JP
2010217047 Sep 2010 JP
2011149832 Aug 2011 JP
2012021926 Feb 2012 JP
2012132721 Jul 2012 JP
2012173180 Sep 2012 JP
2012189611 Oct 2012 JP
2012233923 Nov 2012 JP
2012251804 Dec 2012 JP
2012251909 Dec 2012 JP
2012255664 Dec 2012 JP
05178891 Apr 2013 JP
9315408 Aug 1993 WO
9722006 Jun 1997 WO
03018195 Mar 2003 WO
2010095375 Aug 2010 WO
2010106885 Sep 2010 WO
2010026837 Nov 2010 WO
2012137019 Oct 2012 WO
2013111484 Jan 2013 WO
2013053023 Apr 2013 WO
2013064561 May 2013 WO
2013064562 May 2013 WO
Non-Patent Literature Citations (6)
Entry
International Search Report and Written Opinion, issued by the International Searching Authority in connection with corresponding International patent application No. PCT/US2014/029138, mailed on Jun. 23, 2014, 8 pages.
International Search Report and Written Opinion, issued by the International Searching Authority in connection with corresponding International patent application No. PCT/US2014/029118, mailed on Jun. 27, 2014, 9 pages.
International Search Report and Written Opinion, issued by the International Searching Authority in connection with International patent application No. PCT/US2013/078041, mailed on Sep. 19, 2014, 16 pages.
Invitation to Pay Additional Fees and, Where Applicable, Protest Fee and Communication Relating to the Results of the Partial International Search, issued by the International Searching Authority in connection with corresponding International patent application No. PCT/US2013/078041, mailed on Apr. 9, 2014, 6 pages.
International Preliminary Report on Patentability and Written Opinion, issued by the International Searching Authority in connection with International patent application No. PCT/US2014/029118, mailed on Sep. 24, 2015, 6 pages.
Communication Pursuant to Rules 161 and 162 EPC, issued by the European Patent Office in connection with European Patent Application 14717953.5 on Oct. 23, 2015, 2 pages.
Related Publications (1)
Number Date Country
20140273242 A1 Sep 2014 US
Provisional Applications (1)
Number Date Country
61794311 Mar 2013 US