The present disclosure generally relates to the field of clinical analysis and medical diagnostics and, more particularly, to fluidic systems, fluid containers and processes for washing fluid lines of a fluidic system. The disclosure also relates to fluid containers for connection to reagent lines of fluidic systems.
A strong demand for the automated analysis of liquid samples can be observed which is primarily due to the fact that there is an ongoing increase in the number of clinical analyses. Sample analysis typically involves combining the samples with one or more reagents to determine absence/presence and optionally concentration of one or more analytes contained therein.
Commercially available analyzers typically use pipetting robots for combining samples and reagents. These systems normally have many fast and nearly continuously moving parts, which may require frequent maintenance and replacement operations. Otherwise, conventional analyzers have limited flexibility with regard to the type of the analytical method and can only be operated with comparably low precision due to the variability of pipetting operations. Since reagents are exposed to the ambient air, they may have a reduced shelf life.
Due to low sample consumption, fast analysis times and high sample throughput, many efforts have been made to develop integrated fluidic systems for the automated analysis of liquid samples. U.S. Application Publication No. 2011/0189052 A1 describes an integrated fluidic system for the automated analysis of liquid samples, the disclosure of which is hereby incorporated herein by reference.
It is against the above background that the embodiments of the present invention provide certain unobvious advantages and advancements over the prior art. In particular, the inventors have recognized a need for improvements in fluidic systems, fluid containers and processes for washing fluid lines.
Although the embodiments of the present invention are not limited to specific advantages or functionality, it is noted that the present disclosure provides efficient processes for washing fluid lines of integrated fluidic systems for the automated combining of liquid samples with reagents.
According to an embodiment of the invention, a process for washing fluid lines of a fluidic system for combining liquid samples with one or more reagents is provided. The fluidic system comprises at least one main line connected to one or more reagent lines for feeding reagents to the main line, at least one sample intake for intaking samples, e.g., into the main line, and at least one pressure actuator for generating a positive or negative pressure in the fluid lines. In the system, each of the reagent lines is connectable to one reagent container containing reagent by means of a fluidic connector. In some embodiments, in the fluidic system, each of the fluid lines is operatively coupled to at least one controllable fluid valve, adapted to inhibit or release fluid flow in the fluid line. In some embodiments, each of the reagent lines includes at least one controllable line valve.
According to an embodiment of the invention, the process for washing fluid lines comprises the following steps of one or more procedures, selected from the following group of procedures.
According to a first procedure (I), the process for washing fluid lines of the fluidic system comprises steps of drawing wash fluid from a wash fluid reservoir connected to the main line via a fluidic connection other than (different from) the reagent lines into the main line and discharging wash fluid into a waste compartment for receiving waste fluid of a cleaning container connected to at least one reagent line by the fluidic connector. In some embodiments, the process includes a step of releasing fluid flow between the main line and the reagent line connected to the cleaning container by means of a controllable fluid valve which is operatively coupled to the reagent line so as to allow wash fluid to be discharged into the waste compartment of the cleaning container. In some embodiments, the process comprises a step of connecting the cleaning container to at least one reagent line by means of the fluidic connector. In some embodiments, the process comprises a step of disconnecting at least one reagent container from a reagent line and connecting the cleaning container to the reagent line by means of the fluidic connector, i.e., replacing at least one reagent container by the cleaning container. In some embodiments, an empty reagent container is used as cleaning container.
According to a second procedure (II), the process for washing fluid lines of the fluidic system comprises steps of drawing wash fluid from at least one fluid compartment containing wash fluid of at least one cleaning container connected to at least one reagent line into the main line and discharging wash fluid from the main line into at least one waste compartment for receiving waste fluid of the cleaning container. In some embodiments, the process includes a step of releasing fluid flow between the main line and the reagent line to which the cleaning container is connected by means of a controllable fluid valve which is operatively coupled to the reagent line so as to allow wash fluid to be drawn from the fluid compartment into the main line and to be discharged from the main line into the waste compartment. In some embodiments, the process comprises a step of connecting the cleaning container to at least one reagent line. In some embodiments, the process comprises a step of disconnecting at least one reagent container from a reagent line and connecting the cleaning container to the reagent line, i.e., replacing at least one reagent container by the cleaning container. In some embodiments, wash fluid is drawn from the at least one fluid compartment into the main line until the wash fluid compartment is empty and used wash fluid is discharged into the at least one empty fluid compartment to be used as waste compartment for receiving waste fluid.
According to a third procedure (III), the process for washing fluid lines of the fluidic system comprises steps of drawing wash fluid from at least one fluid compartment containing wash fluid of a cleaning container connected to at least one first reagent line into the main line and discharging wash fluid from the main line into at least one waste compartment for receiving waste fluid of a cleaning container connected to at least one second reagent line being different from the at least one first reagent line. In some embodiments, the process includes a step of releasing fluid flow between the main line and the first cleaning container container-connected and second cleaning container-connected reagent lines by means of fluid valves operatively coupled thereto so as to allow that wash fluid can be drawn from the fluid compartment into the main line and that wash fluid can be discharged from the main line into the waste compartment. In some embodiments, the process comprises a step of connecting the first cleaning container to at least one first reagent line and to connect the at least one second cleaning container to at least one second reagent line. In some embodiments, the process comprises a step of disconnecting at least two reagent containers from reagent lines and connecting the first and second cleaning containers to these reagent lines, i.e., to replace the reagent containers by the first and second cleaning containers.
In some embodiments of the process according to the second and third procedures, the process comprises steps of drawing wash fluid from a wash fluid reservoir connected to the main line via a fluidic connection other than (different from) the reagent lines into the main line and discharging wash fluid into at least one waste compartment of the cleaning container.
In some embodiments of the process according to the second and third procedures, plural wash fluids different with respect to each other contained in plural fluid compartments of one or more cleaning containers are successively drawn into the main line.
In some embodiments of the process according to the first to third procedures, the process comprises a step of discharging wash fluid through the sample intake. Specifically, in some embodiments, the process includes a step of releasing fluid flow between the main line and the sample intake by means of a fluid valve operatively coupled to the sample intake so as allow that wash fluid can be discharged from the main line through the sample intake.
In some embodiments of the process according to the first to third procedures, at least one reagent container connected to one reagent line is automatically replaced by one cleaning container.
According to another embodiment of the invention, another process for washing fluid lines of a fluidic system for combining liquid samples with one or more reagents as described above is provided. Accordingly, the process comprises the following steps of connecting at least one cleaning container provided with at least one fluid compartment containing wash fluid to at least one reagent line, drawing wash fluid from the fluid compartment into the main line and discharging wash fluid from the main line through a fluid waste port of the main line.
According to yet another embodiment of the invention, a cleaning container for connection by at least one fluidic connector to at least one reagent line of a fluidic system for combining liquid samples with reagents as described above is provided. The cleaning container comprises at least one waste compartment for receiving waste fluid and/or at least one fluid compartment containing wash fluid. It further contains at least one container-sided connector part, adapted for connection to a reagent line-sided connector part of the reagent line for forming the fluidic connector.
In some embodiments, the cleaning container comprises at least one controllable or non-controllable fluid valve, adapted to release or inhibit fluid flow between the reagent line and one or more compartments in one or both flow directions. In some embodiments, the cleaning container comprises at least one fluid compartment containing wash fluid and a bi-directionally operable fluid valve adapted to selectively control fluid flow in either one of two flow directions so that the at least one empty fluid compartment can be used as waste compartment for receiving waste fluid.
In some embodiments, the cleaning container comprises a septum closing a fluid opening wherein the septum is adapted to be broken by a protruding element of the reagent line-sided connector part. Specifically, in some embodiments, the septum is arranged nearer to the fluid opening than a septum of a similar container-sided connector part of a reagent container for connection to the reagent line.
According to still yet another embodiment of the invention, a fluidic system for combining liquid samples with one or more reagents is provided.
The fluidic system can, e.g., be used for analyzing liquid samples. Specifically, in some embodiments, the fluidic system is adapted for analyzing liquid samples. Although the fluidic system is particularly suitable in (bio-)chemical applications including in-vitro diagnostics it will also be useful with a wide variety of non-(bio-)chemical applications. In some embodiments, the fluidic system can be used for diagnostic assays such as clinical-chemistry assays and immunoassays. Typical diagnostic assays comprise the qualitative and/or quantitative analysis of analytes such as albumin, ALP (alkaline phosphatase), ALT (alanine aminotransferase), ammonia, amylase, aspartat, aminotransferase, bicarbonate, bilirubin, calcium, cardiac markers, cholesterol, creatinine kinase, D-dimer, ethanol, g-glutamyltransferase, glucose, HBA1c (haemoglobin A1c), HDL-cholesterol, iron, lactate, lactate dehydrogenase, LDL-cholesterol, lipase, magnesium, phosphorus inorganic, potassium, sodium, total protein, triglycerides, UREA, and uric acid. This list is not exhaustive.
Specifically, the fluidic system of this embodiment of the present invention comprises a main line for conveying liquid fluids connected to a wash fluid reservoir and plural reagent lines connected to the main line for feeding reagents to the main line, wherein each of the reagent lines is connectable to a reagent container containing reagent by a fluidic connector. The system further comprises at least one sample intake directly or indirectly connected to the main line for feeding samples, e.g., into the main line. In some embodiments of the fluidic system, each of the fluid lines is coupled to at least one controllable fluid valve, adapted to inhibit or release fluid flow in the fluid line. Specifically, in some embodiments, each of the fluid lines includes one fluid valve. The system yet further comprises at least one pressure actuator which is adapted for generating a positive or negative pressure in the fluid lines. Furthermore, the system comprises one or more reagent containers containing reagents, wherein each of the reagent containers is connected to one reagent line by one fluidic connector. The system further comprises at least one cleaning container provided with at least one waste compartment for receiving waste fluid connected to at least one reagent line by the fluidic connector. The system yet further comprises a controller for controlling the activity of components which require control such as the pressure actuator and fluid valves, wherein the controller is set up to control activity of the pressure actuator and fluid valves in a manner to draw wash fluid from the wash fluid reservoir into the main line and to discharge wash fluid from the main line into the waste compartment.
According to yet still another embodiment of the present invention, another fluidic system for combining liquid samples with one or more reagents is proposed. Specifically, the fluidic system comprises a main line for conveying liquid fluids and plural reagent lines connected to the main line for feeding reagents to the main line, wherein each of the reagent lines is connectable to a reagent container containing reagent by a fluidic connector. The system further comprises at least one sample intake which is directly or indirectly connected to the main line for feeding samples, e.g., into the main line. In some embodiments of the fluidic system, each of the fluid lines is coupled to at least one controllable fluid valve, adapted to inhibit or release fluid flow in the fluid line. Specifically, in some embodiments, each of the fluid lines includes the fluid valve. The system yet further comprises at least one pressure actuator which is adapted for generating a positive or negative pressure in the fluid lines. Furthermore, the system comprises one or more reagent containers containing reagents, wherein each of the reagent containers is connected to one reagent line by one fluidic connector. The system further comprises at least one cleaning container provided with at least one waste compartment for receiving waste fluid and at least one wash compartment containing wash fluid connected to at least one reagent line. The system yet further comprises a controller set up to control activity of the pressure actuator and fluid valves in a manner to draw wash fluid from the wash compartment into the main line and to discharge wash fluid from the main line into the waste compartment. In some embodiments of the fluidic system the main line is connected to a wash fluid reservoir containing wash fluid and wherein the controller is set up to draw wash fluid from the wash fluid reservoir into the main line and to discharge wash fluid from the main line into at least one waste compartment.
In some embodiments of the above-described fluidic systems, the cleaning container comprises plural fluid compartments containing wash fluids different with respect to each other, wherein the controller is set up to selectively draw the wash fluids into the main line.
In some embodiments of the above-described fluidic systems, the main line is connected to a waste fluid port, wherein the controller is set up to discharge wash fluid through the waste fluid port.
In some embodiments of the above-described fluidic systems, the system comprises an automated positioning mechanism, adapted for positioning individual containers, wherein the controller is set up to replace at least one reagent container connected to one reagent line by the cleaning container.
These and other features and advantages of the embodiments of the present invention will be more fully understood from the following detailed description taken together with the accompanying claims. It is noted that the scope of the claims is defined by the recitations therein and not by the specific discussion of features and advantages set forth in the present description.
The following detailed description of the embodiments of the present invention can be best understood when read in conjunction with the following drawings, where like structure is indicated with like reference numerals and in which:
1 Fluidic system
2 Main line
3 Waste fluid port
4 Receiving chamber
5 Pressure actuator
6 Connecting line
7 Sample intake
8 Reagent line
9 Reagent container
10 Set
11 Cleaning container
12 Fluid compartment
13 Waste compartment
14 Processing unit
15 Fluidic connector
16 Controller
17 Positioning mechanism
18 Housing
19 Wash fluid reservoir
20 Fluid valve
21 Container valve
22 Container duct
23 First connector portion
24 Second connector portion
25 Connector duct
26 Junction
27 Septum
28 Fluid opening
29 Gasket
30 Protruding element
31 Protrusion
32 Slot
33 Wall
34 Ball
35 Spring
36 Recess
37 Analytical unit
38 Optical detector
39 Reagent unit
30 Sample unit
41 Sample tube loading mechanism
42 Sample tube
43 Distribution unit
44 Belt
45 Rack
46 Flow-through cell
47 Connecting channel
48 Waste container
Skilled artisans appreciate that elements in the figures are illustrated for simplicity and clarity and have not necessarily been drawn to scale. For example, the dimensions of some of the elements in the figures may be exaggerated relative to other elements to help improve understanding of the embodiments of the present invention.
As used herein, the term “sample” generally relates to biological and non-biological (chemical) fluids. Biological fluids such as body fluids like blood, serum, urine, saliva and cerebrospinal fluid can, e.g., be subject to analyses and assays in medical and pharmaceutical research and clinical diagnosis. Non-biological fluids can, e.g., be subject to chemical analyses and assays, e.g., drug interaction screening, environmental analysis and identification of organic substances. Samples can also be pre-processed fluids such as extracts of body fluids.
As used herein, the term “reagent” generally relates to any liquid fluid. In the more strict sense of the term, a reagent is a liquid solution containing a reactant such as a compound or agent capable of binding to or transforming one or more analytes present in a liquid sample. Accordingly, reagents may contain reactants for reaction with one or more analytes contained in the sample. Examples of reactants are enzymes, enzyme substrates, conjugated dyes, protein-binding molecules, nucleic acid binding molecules, antibodies, chelating agents, promoters, inhibitors, epitopes, antigens and catalysts. Reagents, however, can also be non-reacting fluids such as buffers, solvents and diluting fluids.
As used herein, the term “fluid line” or “line” generally relates to a flow channel configured for conveying liquid fluids and optionally gaseous fluids.
As used herein, the term “connected” generally relates to a fluidic connection which can be direct or indirect. Fluid lines connected with respect to each other can be equipped with flow regulating means such as fluid valves.
As used herein, the term “fluid valve” or “valve” generally relates to controllable or non-controllable means for regulating fluid flow. Controllable valves can be brought into one of two distinct states: a valve open state in which liquid fluid can pass through the valve and a valve closed state in which liquid fluid is inhibited to pass the valve.
Specifically, valves can, e.g., be configured as freeze-thaw valves which can selectively be brought into one of three distinct states with respect to liquid and gaseous fluids: a valve open state in which both liquid and gaseous fluids can pass through the valve, a first valve closed state in which gaseous fluid can pass through the valve but liquid fluid is blocked to pass the valve, and a second valve closed state in which both liquid and gaseous fluids are blocked to pass the valve. If not specified in more detail, a “valve closed state” of the freeze-thaw valve can be the first or the second valve closed state. Freeze-thaw valves are well-known to those of skill in the art and in the patent literature, e.g., are described in U.S. Pat. No. 6,557,575 and U.S. Pat. No. 6,311,713 B1.
As used herein, the term “positive pressure” relates to pressures greater than atmospheric (ambient) pressure and the term “negative pressure” relates to pressures less than atmospheric pressure.
In order that the embodiments of the invention may be more readily understood, reference is made to the following examples, which are intended to illustrate the invention, but not limit the scope thereof.
By way of illustration, specific exemplary embodiments in which the invention may be practiced are described. With particular reference to
Accordingly, in some embodiments, the fluidic system 1 configured as a flow-through system includes a processing unit 14 provided with a main line 2 for conveying liquid fluids which, in some embodiments, freely opens into a waste fluid container 48 for discharging waste fluid. The fluidic system 1 can, e.g., be part of a diagnostic instrument, e.g., for clinical chemistry, immunochemistry, coagulation, etc. As illustrated, the main line 2 includes a (flow-through) receiving chamber 4 for receiving liquid fluids. While only one receiving chamber 4 is illustrated for the purpose of illustration only, those of skill in the art will appreciate that more than one receiving chamber 4, e.g., in parallel arrangement with respect to each other, can be envisaged according to the specific demands of the user, in accordance with this disclosure.
In some embodiments, the receiving chamber 4 is operatively coupled to one or more detecting means related to one or more analytical methods. Specifically, in some embodiments, the receiving chamber 4 is operatively coupled to an ion-selective electrode (ISE), a biosensor such as an enzymatic-electrochemical detector, an electro-chemoluminescence detector (ECL), an optical detector, e.g., embodied as photometer to detect light emitted from reaction products contained in the receiving chamber 4 and the like (not shown).
In some embodiments, a pressure actuator 5 such as a pump is connected to the main line 2 via connecting line 6 for generating a positive or negative pressure therein. In some embodiments, the pressure actuator 5 is adapted for pumping gaseous fluids. In some embodiments, the pressure actuator 5 is adapted for pumping liquid and gaseous fluids. The pressure actuator 5 can be embodied as continuous or discontinuous pressure actuator such as, for example, a pump of the membrane pump type, syringe pump type, rotary displacement pump type and bellow pump type. While only one pressure actuator 5 is illustrated for the purpose of illustration only, those of skill in the art will appreciate that more than one pressure actuator 5 can be envisaged according to the specific demands of the user, in accordance with this disclosure.
In some embodiments, one sample intake 7 is connected to the main line 2 for feeding samples to the main line 2 and receiving chamber 4, respectively. In some embodiments, the sample intake 7 is a metallic needle. Accordingly, samples can be aspirated via the sample intake 7 into the main line 2, e.g., from a sample tube (not illustrated) by action of the pressure actuator 5. While only one sample intake 7 is illustrated for the purpose of illustration only, those of skill in the art will appreciate that more than one sample intake 7 can be envisaged according to the specific demands of the user, and in accordance with the present disclosure.
In some embodiments, in the fluidic system 1, a plurality of reagent lines 8 is connected to the main line 2 for feeding one or more reagents to the main line 2 and receiving chamber 4, respectively. In some embodiments, each of the reagent lines 8 is connected to one reagent container 9, e.g., configured as cassette containing reagent by means of one fluidic connector 15 (not further detailed in
As illustrated in
While not illustrated, in some embodiments of the fluidic system 1, each of the reagent lines 8 is operatively coupled to at least one controllable fluid valve, adapted for inhibiting and releasing fluid flow in the reagent line 8. In some embodiments, the fluid valves are included in the reagent lines 8, e.g., adjacent the main line 2. Furthermore, in some embodiments of the fluidic system 1, the sample intake 7 is operatively coupled to at least one controllable fluid valve, adapted for inhibiting and releasing fluid flow in the sample intake 7.
With continued reference to
As illustrated, in some embodiments, the fluidic system 1 further includes a controller 16 set up to control washing fluid lines of the fluidic system 1. In some embodiments, the controller 16 is a programmable logic controller running a computer-readable program provided with instructions to perform operations in accordance with a process plan. The controller 16 is electrically connected to the system components which require control and/or provide information. Specifically, the controller 16 is electrically connected to the pressure actuator 5, the automated positioning mechanism 17 and the various controllable fluid valves (not illustrated). Specifically, the controller 16 is set up to control intake of samples and reagents by generating a negative pressure in the main line 2. Otherwise, as illustrated in
With particular reference to
The combined cleaning container 11 has many advantages. One major advantage is that the wash fluid can be taken back into its origin so that no additional waste has to be handled in the fluidic system 1. In the case of configuring the fluidic system 1 as a disposable analytical unit this can be of certain interest since only solid waste is generated on the analytical part and no fluid waste. The fluid compartment 12 contains a wash fluid such as a cleaning solution, e.g., sodium hydroxide solution, hydrochloric acid, sodium hypochlorite, a detergent solution, an enzyme solution, or similar chemicals. The cleaning container 11 can, e.g., be configured as a re-usable cassette intended for multiple use allowing the fluid compartment 12 to be refilled with wash fluid and the waste compartment 13 to be emptied. Alternatively, the cleaning container 11 can be configured as a disposable subject intended for single-use only. The cleaning container 11 can, e.g., be made of a chemically inert, inexpensive polymeric material such as high-density polyethylene (HDPE) and polypropylene (PP).
With continued reference to
With yet continued reference to
With particular reference to
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As described above, the cleaning container 11 can contain several wash fluids, e.g., to wash by acidic and alkaline solutions using a same cleaning container 11. Otherwise, the cleaning container 11 can contain fluids such as buffer solutions containing detergent to wash out previously used aggressive wash fluids which could possibly interfere with the following reagent. Stated more particularly, some wash fluids such as strong acids and bases can interfere with assay reagents, e.g., by (de)-protonation, pH-change or chemical reactions with some ingredients of the assay. This may lead to a wrong assay composition and potentially compromise the result(s). Strong wash solutions are typically accordingly washed out by flushing the fluid lines with buffer or purified water.
With continued reference to
With particular reference to
In some alternative embodiments, not illustrated, instead of being discharged into the waste container 48, the wash fluid can also be discharged into an empty waste compartment 13 of the cleaning container 11, e.g., configured as illustrated in
With particular reference to
With particular reference to
With particular reference to
As illustrated by the various scenarios for washing fluid lines of the fluidic system 1, by connecting the cleaning container 11 to at least one reagent line 8, cleaning of the fluidic system 1, especially of the permanent connection part from the fluidic connector 15 to the main line 2, that is to say, of the reagent lines 8, can be performed. In particular, in the case of a reagent change, e.g., a change from an assay A to an assay B, the reagent lines 8 can be thoroughly washed so as to avoid carry-over of the old assay A to the new assay B. Hence, the risk of various types of wrong results like false analyte concentrations or even false negative or false positive results can advantageously be avoided. The cleaning containers 11 can specifically be adapted to wash the reagent lines 8, e.g., by means of a highly-effective cleaner which normally is not on-board of analytical instruments. Hence, the carry-over rate can be strongly reduced to an extent that is lower than a significant amount. Therefore, use of the cleaning container 11 allows exchange of reagent containers 9 containing different reagents on one reagent line 8. In other words, reagent assays become interchangeable without changing parts of instruments, like fluid lines 2, 8 or fluidic connections 15. The fluidic system 1 no longer has fixed reagent channels. Furthermore, in case reagent lines 8 are clogged, wash fluid from the cleaning container 11 can help unblocking the fluid line by use of, e.g., aggressive wash agents.
With particular reference to
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With particular reference to
The analytical unit 37 further includes one flow-through cell 46 coupled to an instrument to detect light emitted from reaction products of sample and one or more reagents transferred to the flow-through cell 46. The optical detector 38 is coupled to a first subset of processing units 14 while the flow-through cell 46 is fluidically connected to a second subset of processing units 14 by manifold connecting channel 47. The optical detector 38 and the flow-through cell 46 are related to different types of analytical methods.
In the system 1, the distribution unit 43 is a planar body which has a plate-like shape. It is provided with a plurality of fluid lines or channels (not shown) for transporting fluids. The distribution or main channels are connected to the reagent containers 9 by means of reagent lines 8 so as to connect each of the reagent containers 9 to individual distribution channels. Each of the processing units 14 is fluidically connected to an individual sample intake 7, e.g., embodied as a metallic needle. Each of the sample intakes 7 can be dipped into the sample tubes 43, e.g., by lifting the sample tubes 43 for aspirating sample contained therein.
As illustrated in
The various embodiments of the present invention thus have many advantages over the prior art. It allows cleaning of fluid lines with a non-permanent connection of the wash agent to the fluidic system. Multiple non-permanent cleaners are available on-board. The embodiments especially allow cleaning from the reagent side and not only the system side. Due to the possibility to clean the reagent lines, carry-over which could be caused by a reagent exchange can be avoided. The wash fluids can be drawn from the cleaning container into the fluidic lines and can also be discharged back to the cleaning container. Otherwise, wash fluid can be discharged via the sample intake and through the fluid waste port. Since the cleaning container has the same outer dimensions as the reagent containers, any reagent container can readily be exchanged with the cleaning container.
It is noted that terms like “typically” are not utilized herein to limit the scope of the claimed subject matter or to imply that certain features are critical, essential, or even important to the structure or function of the embodiments disclosed herein. Rather, these terms are merely intended to highlight alternative or additional features that may or may not be utilized in a particular embodiment.
It is also noted that the terms “substantially” and “about” may be utilized herein to represent the inherent degree of uncertainty that may be attributed to any quantitative comparison, value, measurement, or other representation. These terms are also utilized herein to represent the degree by which a quantitative representation may vary from a stated reference without resulting in a change in the basic function of the subject matter at issue.
It will be apparent to those skilled in the art that various modifications and variations can be made to the embodiments described herein without departing from the spirit and scope of the claimed subject matter. Thus it is intended that the specification cover the modifications and variations of the various embodiments described herein provided such modifications and variations come within the scope of the appended claims and their equivalents.
Number | Date | Country | Kind |
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10195180.4 | Dec 2010 | EP | regional |