Patent Application
20210178399
The present invention relates to a bottle compartment of an analyzer instrument for consumable liquids used by the analyzer instrument.
Analyzer instruments use different kinds of liquids in their analyzing processes. The used liquids include different types of reagent liquids, such as organic solvents and mild acids, and washing liquids for example. The used liquids also set requirements for the materials used with the analyzer instruments, so that parts in contact with the liquids endure the continuous contact without dissolving anything into the liquids.
The liquids used in analyzer instruments are generally contained in bottles and inserted in the analyzer instrument into compartments reserved for the bottles. The insertion process typically requires removing the used liquid bottle, opening a new liquid bottle, and setting the new bottle in the analyzer instrument together with setting of the aspiration tubes for aspiration of the liquid from the bottle. This replacement and insertion process is often time consuming and messy with droplets of liquid splashing from the aspiration tubes removed from the used liquid bottle and/or the new bottle when it is set at its place, which may create a hazardous chemical problem. Further, replacement processes may also allow for possible contaminants to enter the analyzer system.
In one known solution for this problem the bottle compartment may be closed using a vertically slidable hatch, wherein movement of the hatch is combined with insertion and removal of the aspiration tube. In this embodiment the hatch is opened by sliding the hatch vertically upwards, which simultaneously moves the aspiration tube vertically upwards and out from the liquid bottle located in the bottle compartment. And when a new liquid bottle is inserted in the bottle compartment, the closing of the hatch, which takes place by sliding the hatch vertically downwards, also moves the aspiration tube vertically inside the new bottle. This type of solution is used in MiSeq desktop sequencer by Illumina, Inc. However, this solution creates new problems, for example in that it requires significantly more space for the vertical movement, and the raised aspiration tube can drop liquid droplets in the bottle compartment when the bottle is removed underneath.
A further source of analysis errors and incorrect results may result from improper liquids used in the analyzing process. This compromises the patient safety due to incorrect analyzing results.
Both FDA (US Food and Drug Administration) and MDD/IVD standard ISO 13485 require that patient results generated by in vitro diagnostic (IVD) instruments must be traceable back to the original patient samples and to all analytically critical components of the analyzer systems including liquid consumables and disposables used in the analyzing processes.
In the context of the present invention a microbiology laboratory has several rooms or laboratories for different kinds of sample types. These rooms are also categorized based on biosafety levels (BSL) of the biological agents handled to BSL-1, BSL-2, BSL-3, and BSL-4. Many hazardous microbes, such as mycobacteria for example, are processed in BSL-3 level laboratories and non-hazardous microbes are processed in BSL-1 level laboratories. Samples from these laboratory rooms are transferred to a separate analyzing room for analysis, which analyzing room is equipped with suitable analyzer instruments and serve several different laboratory rooms.
Generally, the samples to be analyzed are prepared in a sample preparation station located at the BSL room or rooms. The sample preparation station comprises an instrument to facilitate movement of primary samples (e.g. bacterial colony) from original sample media (e.g. agar plate, blood culture bottle) to a sample vessel in an ergonomic manner which further reduces errors.
As an example, a primary sample in an agar plate is taken to the sample preparation station and identification data of the primary sample, which is stored in a barcode, radio frequency identification (RFID) tag or other indicia, is read to the sample preparation station with a suitable reader. Once confirmation of the data input is received, for example by a visual or audio signal, a specimen sample is taken from the primary sample with a sampling device, and the primary sample is returned to its storage. Next a sample vessel is taken, and its identification data is read to the sample preparation station with a suitable reader as was done with the primary sample. Then the sample in the sampling tool is inserted in the sample vessel, and the sample is transferred to the vessel for example by detaching the end of the sampling tool containing the sample inside the sample vessel by twisting the sample tool, for example. The remaining part of the sampling tool is discarded and the lid or cap of the sample vessel is closed. The sample vessel together with the sample is placed in an empty position of a sample vessel rack located in the sample preparation station in a proper orientation. The sample preparation station detects the location of the newly inserted sample vessel in the sample vessel rack and connects identification data obtained from the primary sample and the new sample vessel to the location of the sample vessel in the sample vessel rack.
When the sample vessel rack contains the required number of sample vessels, the sample vessel rack is removed from the sample vessel preparation station. In one example, the removal action also activates a locking means in the sample vessel rack. The locking means prevent the removal of any of the sample vessels located in the rack when locking is activated. The sample vessel rack is then inserted into an analyzing instrument, which insertion action optionally deactivates the locking means in the sample vessel rack, allowing removal of the sample vessels from the sample vessel rack for analysis operations.
The obtained analysis results are connected to the identification data of the sample from the sample preparation station, so that each analysis result can be tracked to a single sample.
The present invention provides a bottle compartment for an analyzer instrument to be used in the above described process, the use of which greatly simplifies the liquid insertion process and guarantees proper setting of the liquid as well as decreases the possibility of contamination and splashes of the liquid during the insertion process. The present invention also requires the use of correct and properly prepared liquids, which enhances the accuracy and traceability of the analyzing results.
In the context of the present invention the features “bottle compartment” and related “bottle of liquid” or “liquid bottle” is to be interpreted at their widest meaning, and especially the “bottle” feature is to be interpreted to include any suitable liquid containers, such as bottles, cans, bags, jars, cartons and tins for example, made of any suitable materials, such as metal, glass or plastic materials for example.
The bottle compartment of the invention for an analyzer instrument comprises a frame with a location for a bottle of liquid used in the operation of the analyzer instrument, a tube for aspiration of liquid from a bottle at the location for a bottle by the analyzer instrument, a handle mechanism connected turnably to the frame, which handle mechanism in an open position allows access to the location for a bottle for insertion and removal of a bottle and in a closed position prevents access to the location for a bottle, and that the tube for aspiration of liquid is connected to the handle mechanism so that when the handle mechanism is turned to an open position the end of the tube is simultaneously moved from a bottle at the location for a bottle and when the handle mechanism is turned to a closed position the end of the tube is simultaneously moved into inside of a bottle at the location for a bottle. Thus the used bottle of liquid can be removed and a new bottle can be inserted simply by turning the handle mechanism to an open position, and once the handle is turned to a closed position after the change of bottle, liquid can be aspired by the analyzer instrument.
In an embodiment of the bottle compartment of the invention the tube for aspiration of liquid from a bottle passes through and is connected to a cap, which cap in a closed position of the handle mechanism is located on top of the opening of a bottle at the location for bottle. The cap prevents evaporation of the liquid in the bottle when the handle mechanism of the bottle compartment is in a closed position but preferably still allows air to enter to the bottle. The cap may be replaced with a cone member, which cone member in a closed position of the handle mechanism is located in the area of the opening of a bottle located in the location of the bottle, especially in cases where the opening of the bottle is covered with a sealing member. In this context the sealing member is a member used to cover the opening of the bottle, preferably hermetically. The sealing member may be a foil, a membrane, a sticker or a similar member made from a suitable material, for example. The sealing member is generally fixed to the bottle after the bottle is filled.
In an embodiment of the bottle compartment of the invention the handle mechanism comprises a cover, or is formed as a cover, covering the bottle at the location of the bottle substantially completely when the handle mechanism is in a closed position. This embodiment keeps the needle hidden from the user, which increases the safety of the user as well as increases the sterility of the needle.
In an embodiment of the bottle compartment of the invention the bottle located at the location for a bottle is in a slanted position. This slanted position of the bottle allows the liquid in the bottle to gather at one end of the bottom of the bottle, especially when the liquid volume in the bottle is low, so that the bottle can be emptied more thoroughly before replacement is required.
In an embodiment of the bottle compartment of the invention the bottle compartment comprises an intermediate storage container for liquid aspired from a bottle at the location for a bottle. This allows the analyzer instrument to store a quantity of liquid from the bottle to an intermediate storage so that the empty bottle may be changed without interrupting the operation of the analyzer instrument.
In an embodiment of the bottle compartment of the invention the bottle compartment comprises a RFID reader and writer for reading a RFID tag in a bottle located in the location for a bottle and for adding information to a RFID tag in a bottle located in the location for a bottle. With this embodiment the information about the liquid contained in the bottle with a RFID tag can be read directly to the analyzer system without any need for manual inputting, which enhances usability and result traceability. Further, with the RFID writing ability the analyzer system can tag used bottle as used, so that bottles refilled with non-validated liquids may not be used in order to improve quality of analyzer results and patient safety. This embodiment also prevents the use of bottles without RFID tags or bottles with incorrect RFID tags.
In an embodiment of the bottle compartment of the invention at least the end portion of the tube for aspiration of liquid from a bottle is made of metal, such as aluminum, stainless steel or acid-resistant steel, for example. This allows the end of the tube to pierce a sealing member of a bottle substantially without bending and thus the use of bottles with sealing members with the bottle compartment without the need to remove the sealing member before inserting the bottle to the bottle compartment. Other suitable materials for the end portion of the tube are for example glass, plastics (such as PTFE (Teflon®), PEEK (polyester ketone) or PP (polypropylene)) or ceramics, for example. It is to be noted, however, that in a preferred embodiment the end portion is needle-like to facilitate smooth piercing of the sealing member, and a flexible plastic tube as such, for example, is not suitable as the tube must be able to pierce the foil without substantial bending. In an embodiment the tube is made of rigid, hard material coated with softer material.
In an embodiment of the bottle compartment of the invention the bottle compartment comprises a suitable locking mechanism, such as a solenoid lock, for locking the handle mechanism at its open position and/or a closed position. The locking at an open position prevents closing of the bottle compartment while an unauthorized liquid bottle is located in the bottle compartment and thus the contamination of the tubing. The locking mechanism preferably releases its locking only after the liquid bottle placed in the bottle compartment has been identified and the liquid contained therein certified, which also prevents closing of the bottle compartment when it is empty. The locking at a closed position allows prevention of the replacement of the bottle too early, and any undesired access to the bottle compartment during the use of the analyzer instrument, for example. The locking function can also be obtained by automating the opening and closing operations of the bottle compartment with suitable actuators, such as servo motors, for example.
In an embodiment of the bottle compartment of the invention the bottle compartment is a bottle compartment of an IVD (in vitro diagnostics) analyzer instrument.
The features defining a bottle compartment of the invention are more precisely presented in claim 1. Dependent claims present advantageous features and embodiments of the invention.
An exemplifying embodiment and its advantages are explained in greater detail below in the sense of an example and with reference to the accompanying figures, where
The bottle compartment 1 comprises a frame 3 to which the handle mechanism 2 is movably connected. The frame 3 comprises a location 4 for a bottle of liquid used in the analyzing processes.
In the frame 3 of the bottle compartment 1 is located a RFID reader and writer 5 for reading information from a RFID tag located in a bottle of liquid to be inserted in the location 4, and for inputting information to the RFID tag of the bottle of liquid.
The handle mechanism 2 comprises a handle 6 for operating the handle mechanism, i.e. for turning the handle mechanism to an open or a closed position. The handle mechanism 2 also comprises a curved metal tube 7, which is connected to the opposite end of the handle mechanism with respect to the handle 6 and which tube is used to aspire liquid from a bottle of liquid located in the location 4 of the bottle compartment 1. On and around the tube 7 is located and connected a cap 8.
The bottle compartment 1 also comprises an intermediate storage container 9 connected to the frame 3.
In
In
When the liquid is aspired from the newly inserted bottle 10 of liquid in the bottle compartment 1, it is first pumped to the intermediate storage 9, from where it is then used by the analyzer instrument. Thus when the bottle 10 is empty, the analyzer instrument informs of the need to change the bottle to the user of the analyzer instrument, but can still continue the analyzing processes without interruption with the use of the intermediate storage 9.
When a new bottle 10 of liquid is placed at its location 4 in the bottle compartment 1, the RFID reader and writer 5 reads information from a RFID tag located in the bottle to the analyzer system. This information may include type of liquid and amount of liquid contained in the bottle 10, for example. Thus the information is input directly to the analyzer system, so that no additional user actions, such as barcode reading with related tools, are required. Further, when the bottle 10 in the bottle compartment 1 is empty, the RFID reader and writer 5 adds this information to the RFID tag of the bottle, so that the same bottle may not be refilled with non-validated liquid. This enhances the patient safety, since the analyzer system only allows the use of validated liquids.
The embodiment of the bottle compartment 1 of the invention shown in figures and discussed above is preferably a bottle compartment of an IVD analyzer instrument, but may be used with other analyzer instruments that require use of liquids during the analyzing processes.
This embodiment of
In the embodiment of
Further, in this embodiment the tube 24 is also covered by the cover of the handle mechanism 22, which shields the tube from the user when the bottle 23 is changed, thus increasing the sterility of the tube and removing the user's access to the tube itself.
As can be best seen from
In relation to the embodiments discussed above it is to be noted, that the opening and closing of the handle mechanism can be implemented manually, or through the automatic control system of the analyzer instrument so that the automatic control system closes and/or opens the handle mechanism.
The specific exemplifying embodiment of the invention shown in figures and discussed above should not be construed as limiting. A person skilled in the art can amend and modify the embodiment in many evident ways within the scope of the attached claims. Thus the invention is not limited merely to the embodiments described above.
| Number | Date | Country | Kind |
|---|---|---|---|
| 20155109 | Feb 2015 | FI | national |
This application is a continuation of U.S. application Ser. No. 15/551,933 filed Aug. 18, 2017, which is a 371 of International Application No. PCT/F12016/050106 filed Feb. 19, 2016, which claims the benefit of Finnish Application No. 20155109 filed Feb. 19, 2015, all disclosures are incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15551933 | Aug 2017 | US |
| Child | 17179172 | US |
