Wash process for a sample being analyzed

Description

BACKGROUND OF THE INVENTION

[0001] 1. Field of the Invention

[0002] The present invention relates to a process for removing an undesired component from a bound desired component, in particular for improving the bound-free separation efficiency. In particular, the present invention relates to a process for separating or washing a bound analyte being analyzed in an automated clinical analyzer from unbound label, particularly without decreasing processing efficiency or speed.

[0003] 2. Description of the Related Art

[0004] Methods and systems for washing containers that hold samples being analyzed, such as analyzers for conducting clinical assays are known, e.g., wash stations in clinical analyzer immunochemical assay systems. For example, U.S. Pat. No. 6,096,561 and U.S. application Ser. No. 09/482,599 filed Jan. 13, 2000 entitled “Failure Detection in Automatic Clinical Analyzers” describe immunoassay analyzers that include container wash stations for washing containers containing one or more analytes bound to coated sample containers that are measured, for example, by chemiluminescence. Such systems typically contain a sample wash station that may include a wash fluid dispense nozzle and an aspirating nozzle. The sample containing analyte and reagent, e.g., label, is aspirated out of the container after it has been incubated. Wash fluid is then dispensed into and aspirated out of the container one or more times to remove any excess analyte and reagent not bound to the coating, such as streptavidin, at the side of the container. Some known surface coated containers have features, such as pockets or ledges, near the top of the container that can trap unbound material, such as unbound label, analyte, etc. These features may be the result of the process used to mold the containers and/or to keep the containers separated in a stack. See, e.g., U.S. Pat. No. 5,441,895, which describes stackable containers. The incubation, reagent metering and mixing processes involved in immunochemical assay analysis move the sample in the container in a manner that leaves a film of sample containing unbound label and/or analyte on the pockets and ledges that are in the upper regions of the container.

[0005] Typically in immunochemical assay systems, an important aspect that affects the performance is bound-free separation. The bound-free separation is controlled by two primary factors:

[0006] (1) the component or material, such as the bound label, that is intended to produce signal remains behind and intact; and

[0007] (2) the unbound (i.e., free) component or material is removed as completely as possible.

[0008] In particular, there are several assays that have clinically significant performance very close to the background of the assay. This means that small amounts of unbound material present during the measurement portion of the process, particularly signal producing material, can produce a substantial adverse impact on performance.

[0009] To remove unbound material as completely as possible, a container wash process typically includes multiple wash cycles, such as filling a surface coated container to a first height on the container with a wash fluid and aspirating the wash fluid after a predetermined amount of time. For example, in one known process, a dispensing nozzle fills the container, which has a 300 μl capacity up to a height of 270 μl and then sets the soak height to 230 μl so the well can be transported during the wash incubation step (≅37-40 seconds). These steps, including the incubation step, are repeated multiple times (e.g., four times) using the same fluid heights. Unbound material that can be present in the upper regions of the container is only removed by inadvertent exposure to the wash fluid. Considerable erroneous signal can be generated when the wash fluid makes contact with unbound material in the upper regions of the container where the material is re-hydrated but not removed. The unbound material can then drop into the signal reagent during the last processing step that is intended to detect the amount of label bound to the container surface.

[0010] Another problem with the known art that removes fluid by aspiration is that the outer surface of an aspirating nozzle can become contaminated with the wash fluid containing unbound material. This can lead to contamination of the container with unbound material in subsequent wash cycles (in that particular test or across subsequent tests). All of the problems described above lead to the unbound material remaining in the test container and possibly interfering with the subsequent analysis of the analyte, leading to tests that need to be repeated at considerable inconvenience and expense due to inaccurate results.

[0011] It is known in the art that the unbound material in the upper regions of the container can be removed more completely if the fluid were to be filled higher in the container and remain there for the soak cycle (i.e., container wash incubation). This is not practical for a random access analyzer system since the test element needs to be transported during the soak cycle so other tests elements can be processed. Batch analyzers leave the test element static during this process step, which allows the fluid level moved to the very top of the container (positive meniscus). Even analyzers that fill the test element to the very top of the container may still have issues with not completely removing unbound label at the very top, if there are features in this region that can trap or retain unbound material. This is especially true when each wash processing cycle raises the fluid to the same height. In this process, the last processing step can cause any residual unbound material to flow into a region of the test element where it can interact with the signal generating reagents, thus producing erroneous results.

SUMMARY OF THE INVENTION

[0012] One object of the invention is to overcome the disadvantages of the known art described above. Another object of the invention is to provide an improved wash process for washing a container holding a sample being analyzed; in particular, a wash process that allows separation of undesired unbound material from desired bound material. Still another object of the invention is to provide an improved wash process for an immunochemical assay system that removes unbound material without substantially reducing the amount of signal from the bound fraction. Yet another object of the invention is to provide an improved process for analyzing an analyte having a signal strength close to the background noise. Another object of the invention is to provide for improved removal of unbound material in a time frame of ˜2.5 seconds (excluding wash incubation time), which enables the test elements to be processed without any significant and preferably no degradation in the system throughput (efficiency or number or tests per hour).

[0013] The foregoing and further objects of the invention are accomplished according to one aspect of the invention that provides a method for removing an undesired component from a bound desired component in an analysis that includes the steps of: (a) providing a container having a desired component bound thereto and an undesired component; (b) dispensing a wash fluid in the container at a first level sufficient to contact at least a portion of the bound desired component; (c) oscillating the level of the wash fluid in the container; and (d) removing at least a portion of the wash fluid from the container. Another aspect of the invention provides a method for washing an analyte bound to the walls of a surface coated container of an analyzer that includes: (a) providing a surface coated container having an analyte bound thereto; (b) dispensing a wash fluid in the container at a first level sufficient to contact at least a portion of the analyte bound thereto; (c) oscillating the level of the wash fluid in the container; and (d) removing the wash fluid from the surface coated container.

[0014] Still another aspect of the invention provides a method for removing an undesired component from a bound desired component in an analysis that includes the steps of: (a) providing a container having a desired bound component bound thereto and an undesired component; (b) dispensing a wash fluid in the container at a first level sufficient to wash at least a portion of the bound desired component; (c) removing the wash fluid from the container; (d) subsequently dispensing a wash fluid in the container at a subsequent level that is lower than the first level and is sufficient to wash at least a portion of the bound desired substrate; and (e) removing the wash fluid from the container.

[0015] Yet another aspect of the invention provides a method for washing an analyte bound to the walls of a surface coated container of an analyzer that includes the steps of: (a) providing a surface coated container having an analyte bound thereto; (b) dispensing a wash fluid in the container at a first level sufficient to wash at least a portion of the analyte bound thereto; (c) removing the wash fluid from the surface coated container; (d) subsequently dispensing a wash fluid in the sample container at a second level that is lower than the first level and sufficient to wash at least a portion of the analyte bound thereto; and (e) removing the wash fluid from the sample container.

[0016] Still another aspect of the invention provides a method of determining the amount of an analyte in a sample, that includes the steps of: (a) providing a sample containing an analyte in a coated container; (b) providing a reagent in the container; (c) optionally incubating the combined sample and reagent; (d) performing a wash as described above; (e) optionally adding a signal reagent; and (f) analyzing the sample for an analyte. Preferably, the analyte being measured is Troponin I.

[0017] Another aspect of the invention provides the methods described above implemented by a computer program interfacing with a computer, and an article of manufacture that includes a computer usable medium having computer readable program code configured to conduct the methods described above.

[0018] Another aspect of the invention provides for improved removal of unbound material in a time frame of ˜2.5 seconds (excluding wash incubation time), which enables the test elements to be processed without any significant and preferably no degradation in the system throughput (efficiency or number or tests per hour).

[0019] Further objects, features and advantages of the present invention will be apparent to those skilled in the art from detailed consideration of the preferred embodiments that follow.

BRIEF DESCRIPTION OF THE DRAWINGS

[0020]
FIG. 1 shows a cup-shaped container according to one embodiment of the present invention.

[0021]
FIG. 2 shows a container wash dispenser according to one embodiment of the present invention.

[0022]
FIG. 3 shows a graph comparing assay performance using a wash process according to a preferred embodiment of the present invention and a conventional wash process.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

[0023] The present invention provides a method for washing a container containing a sample being analyzed, in order to assure that components (such as analyte and bound label) in the sample bound to the substrate remain, while unbound components, such as unbound label, are removed from the container. While much of the foregoing and following description is related to automated immunochemical assay analyzers, the present invention is not so limited. In particular, the present process can be applied to any analysis or separation, chemical, immunological or otherwise. The coated container being washed includes those components (single or multiple) of the sample that are bound and those components (single or multiple) of the sample that need to be removed, such as excess analyte (e.g., Troponin I), excess reagents, such as biotin or unbound label (e.g., HRP), the liquid phase, undesired materials/interferents (e.g., hemoglobin), etc. The coated container can also include streptavidin coated containers that have not been further modified or treated, such as biotinylation. In this instance, the bound material is the streptavidin coating and the unbound material is any impurity to be removed before further treatment in the process.

[0024] According to a first preferred embodiment, a container suitable for containing a wash fluid and sample is provided. The container can include materials such as plastic, glass, metal, etc. and can be configured as a cup, well, cuvette, test tube, etc. As noted above, the container can include features from an injection molding process and/or features from stacking the containers. Prior to the wash process, the container and the sample may have been through previous processes, such as reagent addition or incubation as will be described more fully below. As used herein, a “wash cycle” is the dispensing and aspirating of wash fluid into and out of the container and does not include the incubation time, which is generally on the order of ≅37.5 seconds.

[0025] Prior to the first dispense of wash fluid, the container may have any liquid phase and/or solids not containing the portion of the sample, e.g., the analyte, not being washed, first removed, such as by aspiration. The wash fluid is then dispensed into the container. It should be understood that in some cases, it is possible for the wash fluid to be first dispensed before the sample is present in the container. However, in a preferred aspect of the invention, the sample, including the analyte and label, are present in the container prior to the first dispense. Upon dispensing, the wash fluid contacts at least a portion of the container containing the bound desired material or component to ensure removal of the undesired and unbound material or component into the wash fluid. The dispense can be accomplished with a dispensing nozzle, or any other satisfactory fluid dispensing apparatus. If a dispense nozzle is used, it can be the same or different than the aspirate nozzle, described below. In those embodiments where a pre-wash is performed before a sample is added to the container, the wash fluid may be of a different composition than the wash fluid typically used. For example, the wash fluid for a pre-wash cycle may include a protein, such as bovine serum albumin (BSA) to act as a blocking agent.

[0026] After a selected time of contact, the wash fluid is removed from the container, such as by aspirating with a nozzle, resulting in the completion of a wash cycle. Alternatively, the fluid removal can be accomplished with any other known fluid removal devices, such as inversion of the container, etc.

[0027] According to a particularly preferred embodiment, the wash cycle can include an oscillating process. Upon dispensing the wash fluid into the container, small amounts (i.e., a less than complete emptying of the container, for example,) of wash fluid are dispensed and removed from the container. The oscillating action of the wash fluid creates a moving meniscus. The moving meniscus reduces the concentration gradient at the boundary layer of the container wall by constantly refreshing the wash fluid at the surface on the container wall in contact with the moving meniscus. The meniscus moving along the surface of the container forces the wash fluid to drain from the container surface providing convective transport along the surface. That is, the moving meniscus made possible by the oscillation, enhances the fluid velocity as close as possible to the boundary layer to maximize the concentration gradient at the boundary. While moving meniscus are known to enhance diffusion at boundary layers, the present inventors believe that this is the first time such a concept has been applied to the present invention. In a preferred embodiment, two complete oscillations may be provided, one oscillation being up and down nozzle travel, or vice versa. Applicants have found that, even with the oscillation, it is possible to provide a wash cycle that takes approximately the same time as known wash processes, even though there are several additional steps that are required by the oscillation. Preferably, the wash cycle takes approximately 3 seconds, more preferably approximately 2.5 seconds.

[0028] According to another preferred aspect, after removal in the first wash cycle, a wash incubation step of approximately 37.5 seconds follows. After the wash incubation step, a further dispense and removal wash cycle may be provided. The dispense step in the further wash cycle or cycles dispenses fluid into the container at a level which is lower than a previous wash cycle. This ensures that once the upper portion of the container has been cleaned and removed of sufficient undesired material, it will no longer contact subsequent washes and not allow for the possibility of recontamination of the upper reaches of the container in subsequent wash cycles.

[0029] As many wash cycles as required can be used according to the present invention. A preferred number of wash cycles is four. Also, other steps during the wash cycle can also be performed, if desired. Moreover, the oscillating process embodiment described above can be carried out during one or all of the wash cycles.

[0030] In systems where an aspirating nozzle is used to remove the wash fluid, the rate of the nozzle descent is generally balanced with the amount of wash liquid being removed from the container. That is, the aspirating nozzle relative to the surface of the fluid will remain substantially constant. In the present invention, the inventors have found that reducing the rate of the aspirate nozzle descent and elimination of any fluid dispense during the aspirate nozzle descent, particularly in the final wash, preferably the fourth wash, reduces the likelihood that the aspirate nozzle will be submerged in the wash fluid. Submerging the nozzle in the wash fluid on the final wash cycle makes it likely that any unbound material on the outside of the nozzle will be washed off the nozzle and leave residual undesired or unbound material in the container that can give an incorrect result, such as an elevated signal. In a preferred embodiment, the rate of descent is ⅓ slower relative to the rate of descent in previous wash cycles (where the previous wash cycle rate of descent is where the fluid aspirate rate and rate of descent are balanced as described above).

[0031] In some embodiments, particularly in systems where the wash fluid is temperature controlled, the wash fluid dispense may be on during the aspirate nozzle descent. This is done to further improve the control of the wash fluid temperature during the soak cycle where the temperature control device is in the wash nozzle head 50 (FIG. 2). The nozzle contains fluid (˜80 μl) that is retained by the nozzle after the temperature control element in the wash head so this amount of fluid quickly reaches room temperature. By dispensing and quickly aspirating during nozzle descent, the colder fluid in the nozzle not at wash temperature is quickly removed. In this embodiment, the present inventors have found it particularly advantageous to turn off the wash fluid dispense during the final wash aspirate nozzle descent in order to reduce the curvature of the fluid meniscus in the container. This further reduces the likelihood that the aspirate nozzle will be submerged and become contaminated.

[0032] In a particularly preferred embodiment, the wash process is employed in an immunodiagnostic assay analyzer, such as those described in U.S. Pat. No. 6,069,561 and copending U.S. application Ser. No. 09/482,599 filed Jan. 13, 2000 entitled “Failure Detection in Automated Clinical Analyzers,” both of which are incorporated by reference in their entireties. In preferred immunodiagnostic analyzers, the container is cup-shaped. Preferred containers are 0.35 ml, conical containers coated with a material complementary to the reagents. Container coatings can comprise materials such as streptavidin and/or other materials useful for immunochemical analysis as is well known in the art to facilitate binding by a biotinylated antigen or antibody to which an analyte binds as part of the assay chemistry. An exemplary container 10 is shown in FIG. 1. Also preferred are separate wash dispense and aspirating probes, such as the wash dispense 20 and aspiration nozzles 30 in wash unit 40 shown in FIG. 2.

[0033] In a typical immunodiagnostic analyzer, the analyzer is categorized into systems and subsystems of components that perform different processes in the sequence of measuring a sample for an analyte, such as those described in the '599 application. A typical process involves a sample being dispensed into a container that may or may not already have a reagent present in the container that is dispensed by a reagent metering system. After the reagent is added, the sample is diluted, if necessary, and then incubated. After incubation, the container is washed, in this instance according to the inventive wash. After washing, a signal reagent is added, followed by further incubation, if necessary. The signal produced by the combination bound analyte/signal reagent is read by the appropriate detector, e.g., a luminometer.

[0034] The wash process according to the present invention can be implemented by a computer program, having computer readable program code, interfacing with the computer controller of the analyzer as is known in the art.

[0035] A particularly preferred wash sequence (not including the wash incubation) is as follows (with a typical wash sequence shown for comparison).

1Process stepPro-(preferredcessembodi-stepment) ofPresent inventionWash(kno-Known washpresentpreferred wash#wn)processinventionprocess11Turn on vacuum1Starts downwardbefore startingtravel with vacuumnozzle downwardofftravel12Starts to dispense2Finds sample + reagentfluid when aspiratefluidnozzle is at the topheightof the incubatorring. Start of 80 μlpredispense13Travels to bottom3Turns on vacuumof container andand turns on startwaits until for 80 μlof 80 μl predispensedispense to becomplete14Reverses direction4Travels to bottomwith vacuum on (noof container anddelay) and starts towaits until for 80 μldispense 270 μldispense to bevolumecomplete15Waits for 270 μl of5Waits 30 ms atfluid to be dispensebottom of containerwith vacuum onand dispense off16Lowers nozzle to6Reverses directionthe 230 μl positionwith vacuum onwith the vacuum onand starts toand thendispense 270 μlimmediatelyvolume waiting atreverses directionthe 270 μl positionlifting nozzle tohome with vacuumon for 800 ms toclear fluid fromnozzle and line177With dispense onand vacuum onnozzle raises to 320 μlposition and waits60 ms (sufficient timedispense of >60 μl)188With dispense andvacuum on nozzlelowers to 250 μlposition199With dispense onand vacuum onnozzle raises to 320 μlposition and waits60 ms (sufficient timedispense of >60 μl)11010Nozzle moves downto 270 μl positionremains steady for50 ms and thendispense is turned offand waits an other 30 ms111Nozzle lowers to230 μl height withvacuum on and staysthere for 30 ms beforelifting112Nozzle lifts to homeposition andincubator starts toturn with nozzlevacuum still on for500 ms to evaluatenozzle and line offluid21Turn on vacuum1Starts downwardbefore startingtravel with vacuumnozzle downwardofftravel22Starts to dispense2Finds soak volumefluid when aspiratefrom wash #1 (shouldnozzle is at the topbe at 230 μl)of the incubatorring. Start of 80 μlpredispense23Travels to bottom3Turns on vacuumof container andand turns on start ofwaits until for 80 μl80 μl predispensedispense to becomplete24Reverses direction4Travels to bottom ofwith vacuum on (nocontainer and waitsdelay) and starts tountil for 80 μldispense 270 μldispense to bevolumecomplete25Waits for 270 μl of5Waits 30 ms atfluid to be dispensebottom of containerwith vacuum on anddispense off26Lowers nozzle to6Reverses directionthe 230 μl positionwith vacuum on andwith the vacuum onstarts to dispenseand then270 μl volume waitingimmediatelyat the 270 μl positionreverses directionlifting nozzle tohome with vacuumon for 800 ms toclear fluid fromnozzle and line277With dispense onand vacuum onnozzle raises to 320 μlposition and waits60 ms (sufficient timedispense of >60 μl)288With dispense andvacuum on nozzlelowers to 250 μlposition299With dispense onand vacuum onnozzle raises to 320 μlposition and waits60 ms (sufficient timedispense of >60 μl)21010Nozzle moves downto 270 μl positionremains steady for50 ms and thendispense is turned offand waits another 30 ms211Nozzle lowers to230 μl height withvacuum on and staysthere for 30 ms beforelifting212Nozzle lifts to homeposition andincubator starts toturn with nozzlevacuum still on for500 ms to evaluatenozzle and line offluid31Turn on vacuum1Starts downwardbefore startingtravel with vacuumnozzle downwardofftravel32Starts to dispense2Finds soak volumefluid when aspiratefrom wash #2 (shouldnozzle is at the topbe at 230 μl)of the incubatorring. Start of 80 μlpredispense33Travels to bottom3Turns on vacuumof container andand turns on start ofwaits until for 80 μl80 μl predispensedispense to becomplete34Reverses direction4Travels to bottom ofwith vacuum on (nocontainer and waitsdelay) and starts tofor 80 μl dispense todispense 270 μlbe completevolume35Waits for 270 μl of5Waits 30 ms atfluid to be dispensebottom of containerwith vacuum on anddispense off36Lowers nozzle to6Reverses directionthe 230 μl positionwith vacuum on andwith the vacuum onstarts to dispenseand then270 μl volume waitingimmediatelyat the 270 μl positionreverses directionlifting nozzle tohome with vacuumon for 800 ms toclear fluid fromnozzle and line377With dispense offand vacuum onnozzle lowers to220 μl position andwaits 30 ms388With dispense andvacuum on nozzleraises to 270 μlposition waits therefor the dispense tocomplete the 40 μldispense (40 ms)399The dispense isturned off and thenozzle lowers to220 μl position andwaits there 30 ms totop control the fluidheight31010The dispense isturned on and thenozzle raises to250 μl position waitingfor the 30 μl dispenseto be completed311The dispense isturned off and thenozzle lowers to230 μl height withvacuum on and staysthere for 30 ms beforelifting (which is thesoak height)312Nozzle lifts to homeposition andincubator starts toturn with nozzlevacuum still on for500 ms to clearnozzle and line offluid1Turn on vacuum1Starts downwardbefore startingtravel with vacuumnozzle downwardoff and finds soaktravelheight of wash #3with level sensing42Starts to dispense2Turn on vacuumfluid when aspiratebefore starting nozzlenozzle is at the topdownward travelof the incubatordropping at a speedring. Start of 80 μlthat is 1/3 slowerpredispensethan the baselinewash rate of nozzledescent (goes to thebottom of thecontainer).Note that there is no80 μl dispense43Travels to bottom3Waits at the bottomof container andof the container forwaits until for 80 μl30 ms beforedispense to bereversing directioncomplete44Reverses direction4Turns on thewith vacuum on (nodispense and lifts thedelay) and starts tonozzle to the 230 μldispense 270 μlheight waiting forvolume230 μl of fluid to bedispensed45Waits for 270 μl of5Turns off thefluid to be dispensedispense and thenozzle drops to thebottom of thecontainer with thevacuum on at theslower rate of decline(same as the firstpart of wash #4)46Lowers nozzle to6The nozzle waits inthe bottom of thethe bottom of thecontainer with thecontainer for 500 msvacuum onwith the vacuum on(the total amount oftime that thecontainer is beingevacuated is thesame since theslower rate of declinetook an additional300 ms)47Waits at the bottom7The nozzle is liftedof the container forwith the vacuum on800 ms with thevacuum on toreduce the amountof wash residual48Lifts the nozzle to8Nozzle lifts to homehome with theposition andvacuum on andincubator starts toleaves the vacuumturn with nozzleon for 800 msvacuum still on forbefore the ring500 ms to clearmovesnozzle and line offluid

[0036] The present invention has proved to be particularly useful in improving the analysis performance of Troponin I (cTnI), a protein detectable in the bloodstream 4 to 6 hours after an acute myocardial infraction. Using the above wash process (both known and the present invention), several runs were carried out to determine levels of Troponin I according to the procedure set out below.

[0037] Biotin reagent was added to streptavidin-coated containers containing samples to initiate a reaction between biotinylated anti-cTnI antibody, the streptavidin coated container and the cTnI present in the sample. HRP conjugate reagent was also added to initiate a reaction between HRP-conjugated anti-cTnI antibody and the cTnI in the sample. The sample was then incubated for 8 minutes and 37° C. After incubation, the containers containing the samples were washed according to the present invention and according to the known wash process. Following washing, signal reagent containing a luminol derivative, a peracid salt and a substituted acetanilide electron transfer agent was added to produce luminescence that was read using a luminometer. The results are shown in the graph set forth in FIG. 3. As the graph shows, the results using the wash process of the present invention are much more consistent and have fewer outliers than the results using the known wash process.

[0038] It will be apparent to those skilled in the art that various modifications and variations can be made to the compounds, compositions and processes of this invention. Thus, it is intended that the present invention cover such modifications and variations, provided they come within the scope of the appended claims and their equivalents.

[0039] The disclosure of all publications cited above are expressly incorporated herein by reference in their entireties to the same extent as if each were incorporated by reference individually.

Claims

1. A method for removing an undesired component from a bound desired component in an analysis comprising the steps of: (a) providing a container having a desired component bound thereto and an undesired component; (b) dispensing a wash fluid in the container at a first level sufficient to contact at least a portion of the bound desired component; (c) oscillating the level of the wash fluid in the container; and (d) removing at least a portion of the wash fluid from the container.
2. A method according to claim 1, wherein steps (b)-(d) take about 2.5 seconds or less.
3. A method according to claim 1, further comprising after step (d), incubating the container containing the wash fluid.
4. A method according to claim 3, wherein the incubation takes about 37.5 seconds.
5. A method according to claim 1, further comprising: a subsequent dispensing of a wash fluid in the container at a level that is lower than the first level and is sufficient to contact at least a portion of the bound desired component; and a subsequent removing of the wash fluid from the container, wherein the oscillating (c) occurs between any of the dispensing and removing steps.
6. A method according to claim 5, wherein the oscillating occurs during a dispensing and removing step subsequent to the first dispensing and removing step.
7. A method according to claim 1, wherein the removing the wash fluid includes aspirating the wash fluid out of the container with an aspirating nozzle.
8. A method according to claim 1, wherein the container is cup-shaped with features at the upper end.
9. A method according to claim 7, wherein during the removing of the wash fluid step no additional wash fluid is dispensed and the rate of descent of the aspirating nozzle is reduced relative to a previous removing of the wash fluid to reduce or avoid the contact of the outer surface of the nozzle with the wash fluid.
10. A method for washing an analyte bound to the walls of a surface coated container of an analyzer comprising: (a) providing a surface coated container having an analyte bound thereto; (b) dispensing a wash fluid in the container at a first level sufficient to contact at least a portion of the analyte bound thereto; (c) oscillating the level of the wash fluid in the container; and (d) removing the wash fluid from the surface coated container.
11. A method according to claim 10, further comprising: a subsequent dispensing of a wash fluid in the container at a level that is lower than the first level and is sufficient to contact at least a portion of the bound analyte; and a subsequent removing of the wash fluid from the container, wherein the oscillating (c) occurs between any of the dispensing and removing steps.
12. A method according to claim 11, wherein the oscillating occurs during a dispensing and removing step subsequent to the first dispensing and removing step.
13. A method according to claim 10, wherein the analyzer is an immunodiagnostic assay analyzer.
14. A method according to claim 13, wherein the container is cup-shaped and is coated with an antibody.
15. A method according to claim 13, wherein the analyte being measured is Troponin I.
16. A method according to claim 10, wherein the removing the wash fluid steps includes aspirating the wash fluid out of the container with an aspirating nozzle.
17. A method for removing an undesired component from a bound desired component in an analysis comprising the steps of: (a) providing a container having a desired bound component bound thereto and an undesired component; (b) dispensing a wash fluid in the container at a first level sufficient to wash at least a portion of the bound desired component; (c) removing the wash fluid from the container; (d) subsequently dispensing a wash fluid in the container at a subsequent level that is lower than the first level and is sufficient to wash at least a portion of the bound desired substrate; and (e) removing the wash fluid from the container.
18. A method according to claim 17, further comprising oscillating the level of the wash fluid between at least one of the dispensing and the removing steps.
19. A method according to claim 18, wherein the oscillating occurs during a dispensing and removing step subsequent to the first dispensing and removing step.
20. A method according to claim 17, wherein the removing the wash fluid step (e) includes aspirating the wash fluid out of the container with an aspirating nozzle.
21. A method according to claim 17, wherein the container is cup-shaped with features at the upper end.
22. A method according to claim 20, wherein during the removing of the wash fluid step (e) no additional wash fluid is dispensed and the rate of descent of the aspirating nozzle is reduced relative a previous removal of the wash fluid to reduce or avoid the contact of the outer surface of the nozzle with the wash fluid.
23. A method for washing an analyte bound to the walls of a surface coated container of an analyzer comprising: (a) providing a surface coated container having an analyte bound thereto; (b) dispensing a wash fluid in the container at a first level sufficient to wash at least a portion of the analyte bound thereto; (c) removing the wash fluid from the surface coated container; (d) subsequently dispensing a wash fluid in the sample container at a second level that is lower than the first level and sufficient to wash at least a portion of the analyte bound thereto; and (e) removing the wash fluid from the sample container.
24. A method according to claim 23, wherein the dispensing and removing the wash fluid steps occurs at least four times, with the subsequent wash fluid levels lower than or equal to previous levels and at least one subsequent level lower than a previous level.
25. A method according to claim 23, wherein the analyzer is an immunodiagnostic assay analyzer.
26. A method according to claim 25, wherein the container is cup-shaped and is coated with an antibody.
27. A method according to claim 23, wherein the container is cup-shaped and is coated with an antibody.
28. A method according to claim 25, wherein the analyte being measured is Troponin I.
29. A method according to claim 23, wherein the removing the wash fluid steps includes aspirating the wash fluid out of the container with an aspirating nozzle.
30. A method according to claim 24, wherein the removing the wash fluid steps includes aspirating the wash fluid out of the container with an aspirating nozzle.
31. A method according to claim 30, wherein during the fourth removal of the wash fluid, no additional wash relative to an earlier removal of the wash fluid is dispensed and the rate of descent of the aspirating nozzle is reduced relative to an earlier removal of the wash fluid to reduce or avoid the contact of the outer surface of the nozzle with the wash fluid.
32. A method of determining the amount of an analyte in a sample, comprising the steps of: (a) providing a sample containing an analyte in a coated container; (b) providing a reagent in the container; (c) optionally incubating the combined sample and reagent; (d) performing the wash according to claim 10;(e) optionally adding a signal reagent; and (f) analyzing the sample for an analyte.
33. A method of determining the amount of an analyte in a sample, comprising the steps of: (g) providing a sample containing an analyte in a coated container; (h) providing a reagent in the container; (i) optionally incubating the combined sample and reagent; (j) performing the wash according to claim 23;(k) optionally adding a signal reagent; and (l) analyzing the sample for an analyte.
34. A method according to claim 1 implemented by a computer program interfacing with a computer.
35. An article of manufacture comprising a computer usable medium having computer readable program code configured to conduct the process of claim 1.

Wash process for a sample being analyzed

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Description

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