Field of the Invention

The present invention relates to a cold processing device which is developed for the portioning and storage of the tissues of the treated animal during animal experiments and for the non-mixing and transportation of the tissues, and for the transportation and protection of blood and similar liquid materials taken from the animal, for helping to ensure standardization in experiments.

The present invention relates to the prevention of a trauma that may occur on the tissue during transportation or external factors that may change the analysis to be made, with the help of the equal cold effect on every part of the tissue taken from the animal since the inventive cold processing device is for animal experiments in preclinical studies, it is a cold storage and transport system.

Prior Art

Today, it is known that preclinical studies, which must be carried out before the application of active substances and medical devices to humans, are continuing rapidly all over the world. It is crucial that all kinds of new active substances and medical devices discovered in the field of health sciences pass through the preclinical phase before they are applicable to humans. Animal experiments applied within this scope include very difficult procedures from planning and finalizing. It is very crucial that each of the tissues taken is treated equally and stored under equal conditions in these experiments, which are carried out by experienced teams and using effective/quality products. The tissues must be put in the refrigerator and kept in a cold area during and after the portioning process of each tissue which is prepared for the unit where it will be analyzed. It is crucial that these obligatory applications are carried out in certain standardization. Tissues taken from experimental animals should be portioned in a suitable cold environment without losing their freshness. Portioned animal tissues must be stored and quickly delivered to the units where they will be analyzed. Traditional methods used for this may affect the results of the analysis to be made and may cause the researcher's effort to be wasted. The cold environment requirement for all processes of these processes has become obligatory for the proper transmission of the tissue.

Today, heat conduction is the transfer of heat from a hot region to a colder region in a solid material or stagnant fluid. In case there are temperature differences in a solid body, heat passes from the high temperature zone to the low temperature zone by conduction. The heat transmission coefficient is a factor that shows how well or how fast a material conducts heat (unit value is given as heat transfer coefficient W/m.K.). Heat conduction is a distinctive feature for substances. The heat conduction law explains the relationship between the amount of heat energy transferred and the type of substance with the ratio of the heat transmission coefficient. The heat transfer coefficient is the power value required to increase the temperature of a point one meter away from a substance by 1 Kelvin. The heat transmission coefficient differs according to the product from which the material is produced. Heat conduction is a distinctive feature particularly for solid substances. For example, while the thermal conductivity coefficient of styrofoam polystyrene, that is, insulation foam material, is 0.039 W/m.K (TS EN 13163), heat transfer coefficient of poly lactic acid (PLA) is 0.13 W/m.K. These values determine the isolation value.

In the state of the art, the aluminum foil wrapped around the battery, which they use as a bench to cut the tissues taken from the animal, is torn at each scalpel stroke during the process. The foil edges also damage the tissue during this tissue cutting process on aluminum foil. However, each time a new tissue arrives, the battery must be wrapped with foil again so as to prevent any contamination and not affect the analysis results. The aluminum foil wrapped around the battery partially provides the cold environment, cannot provide the required flat surface and is constantly damaged during the operation with the scalpel tip. There is also a prolongation of the test times due to this process. Therefore, this method used in the state of the art is disadvantageous.

In the state of the art, it is necessary to have a standard system that provides the same degree of cold exposure in all directions for the refrigerated storage of the portioned tissues taken from the animal. In cases where the tissue is not exposed to the same degree of cold in all directions, the quality of the tissue is affected. However, there is no such a system used in the state of the art. A lot of ice or batteries are placed in the foam container used for the tissues that need to be transmitted to the analysis units. However, these materials are not always available. In addition to this, these materials do not last long enough for longterm transportation. Besides all these, it is insufficient as the cold cannot be provided to all parts of the tissue equally.

A slicing device for laboratory biological research is disclosed in the document numbered CN113776908A in the state of the art. It is a tissue/paraffin tissue slicing device used especially for laboratory biological research. It prevents any contamination and damage to the tissue sample. In addition to this, it is a device maintained so as to prevent the tissue sample from being affected by temperature. It is effective due to the short distance between it and the tissue sample by conveying cold air from a cold air hole. The diffusion range is small and the contact distance with the tissue sample is close, which causes the tissue sample to be constantly exposed to cold. In addition, it comprises a method developed for cutting the portioned and paraffinized samples into thin slices. The device is fixed laboratory equipment and does not include a method for transporting, storing and keeping samples. On the contrary, there must be a device which is developed for preserving the structure of the tissue slice, which prevents the curling of the slices by means of the cold air and prevents the paraffin of the cut slices from melting, while taking thin slices from the paraffinized tissue after portioning. Said device does not have elements such as exposure to cold during tissue portioning, transportation/storage of tissue and the like.

The document numbered US4615183A, known in the state of the art, relates to a cold plate for laboratory use, particularly useful for tissue micro and macro dissection procedures. Said invention provides improved dissection of frozen tissues, provides tissue micro and macro dissection such as brain tissue dissection, provides a dissection that will cool homogeneously. It is combined with a remotely operated cooling unit so as to cool said cold plate to any desired cold temperature. In addition to this, it is a cold plate with a protective holding slot. It has the property of not melting a sample placed thereon early. Besides, the structure is made of a thermally conductive material in a rectangular configuration such as iron or copper. The device is fixed laboratory equipment and does not include a method for transporting, storing and keeping samples. Said device does not have elements such as exposure to cold during tissue portioning, transportation/storage of tissue and the like.

Since there are no standard storage containers in the prior art, an eppendorf tube is a material used for tissues. Eppendorf tube has a narrow area in structure. Therefore, placing the tissue in an area where it will be compressed may also cause damage to the tissue or adversely affect the analysis results.

In the state of the art, blood, serum and similar biological materials must be transported. The surroundings of the spore equipment in which blood and serum are placed are open and open to being exposed to the external environment. Cold chain is often required for the transportation of these products. All samples are not exposed to the same cold, and problems may occur during transportation in the cold chains where these small-sized samples are transported.

There are plastic separators in the prior art used for storing or separating or transporting tissues after portioning. Although these separators do not have a cooler, portioned tissues are again wrapped in a product (aluminum foil, etc.) and taken to the refrigerator after they are placed in separator boxes, or transported by placing the same in a foam box with dry ice. Said plastic separator which is used only to separate the tissues from each other and to cut off their contact with the surfaces, has disadvantages such as not comprising any cooling system and giving damage to the tissue as the box areas are narrow for some tissue portions.

As can be seen in the methods used in the state of the art, there is no complete system apart from the absence of standard storage containers except organ transplant containers used in human-to-human organ transplantation. Disadvantages and product deficiencies in the state of the art make it necessary to make an R.&D study in this field.

The Aim of the Invention

The main aim of the present invention is to provide cold tissue cutting bench, refrigerated tissue storage container and cooled spore structures for the transport of blood and similar liquids so as to prevent disruptions that may occur during transport and external factors that change the analysis by allowing the cutting of small-sized tissues taken from animals, and also providing a standardized storage condition since it will be a tissue storage container.

One of the main aims of the present invention is to provide a continuous and even cooling effect with the help of a base and a cooling material division positioned in the base and to prevent the tissues to be used for analysis from being damaged by the temperature difference by placing a tissue cutting machine on the base, where the portioning of the tissues taken is carried out or by placing spores containing slots in which biochemistry tubes will be placed, or by placing a cover containing divisions that allow tissues to be transported.

An aim of the present invention is to provide equal exposure to cold effect to every area of the sampled animal tissue used for the experiment and thus to prevent trauma on the tissue during transportation.

Another aim of the present invention is to use the same not only for experimental animals, but also for portioning pathological preparations and similar experimental animal applications, with a structure that allows cutting, storing and transporting small-sized tissues.

Another aim of the present invention is to use the same for the transportation of small-sized tissues after portioning, while simultaneously to provide transportation even between cities with dry ice supplement.

An aim of the invention is to ensure that blood, serum and similar biological materials can be subjected to long-term transport processes within a cold environment.

Another aim of the present invention is to keep the taken tissues at a volumetric homogeneous temperature during transportation and processing, to distribute the temperature equally to all parts of the tissue and to ensure that every point of the tissue is protected at the same temperature.

Another aim of the present invention is to prevent the tissue from being exposed to excessive cold by preventing overflow and leakage by closing the structure containing the divisions where the cooling material placed in the base will travel with a sealing gasket after putting the cooling material through the hole in the center area. An aim of the present invention is to transport both tissue and biochemistry samples at the same time as well as to protect tissue or blood or serum samples taken from animals during the cutting of the tissue by being equally exposed to a constant cold from all directions without being affected by the temperature difference.

Another aim of the present invention is to ensure that the system can be easily stored by placing the same in a transport cabinet, together with the base, for the transportation of tissue sample or blood or serum samples and to allow the preservation of the required temperature in long-term storage of tissues.

Another aim of the present invention is to ensure that tissue, blood or serum samples are transported without any damage over distances of 3 hours only with the transport container with the help of the extra protection and insulation of the same with the transport container, and at distances of 5 hours and more with the support of dry ice.

Description of the Figures

Figures of the cold processing device are given below.

Figure - 1 is the Perspective View of the Interior Division

Figure - 2 is the Rear View of the Interior Division and Cooler Walls

Figure - 3 is the Joint View of the Cooler Case and Interior Division.

Figure - 4 is the Joint View of the Cooler Case and Cutting Bench.

Figure - 5 is the Joint View of the Spore Body and the Cooler Case.

Figure - 6 is the Front Side Perspective View of the Spore Body.

Figure - 7 is the Joint View of the Tissue Handling Unit and Cooler Case

Figure - 8 is the General Perspective View of the Transport Cabin

Reference Numbers:

1. Tissue Cutting Bench 1.1 Waste Division

1.2. Cutting Surface

1.3. Protrusion

1.4. Cooler Surface

2. Cooler Case

2.1. Channel

2.2. Exterior wall

2.3. Interior Wall

3. Interior Division

3.1. Lock Housing

3.2. Upper Housing

3.3. Cooler Wall

3.4. Lower Housing

4. Spore Body

4.1. Spore Housing

4.2. Spore Division

5. Transport Cabin

5.1. Handle

5.2. Slot

6 Tissue Handling Unit

6.1. Tissue Divisions

Detailed Description of the Invention

A cold processing device which is the subject of the invention comprises of a cooler case (2), detailed in Figure 3, in which the cooling material and covers are accommodated, an interior division (3) located inside the cooler case (2), which allows the processes to be carried out in a cold environment or to be protected or transported during the test. There are a total of three parts positioned on the cooler case (2). These are as follows; a tissue cutting bench (1) for the cutting process taken from experimental animals, a spore body (4) in which blood, serum and similar materials taken from experimental animals are placed, and a tissue handling unit (6) that allows the tissues taken to be separated and transported after portioning.

The cooler case (2) comprises an interior wall (2.3) and an exterior wall (2.2). There is a channel (2.1) between the interior wall (2.3) and the exterior wall (2.2). The thicknesses of the exterior wall (2.2) and the interior wall (2.3) are adjusted as 3 mm. The interior wall (2.3) and the exterior wall (2.2) provide external insulation with the help of the cooling material added to the channel

(2.1) of the cooler case (2). Thus, it is ensured that the cold is transmitted equally to all parts of the equipment such as the spore body (4), the tissue cutting bench (1) and the tissue handling unit (6), which are positioned on the cooler case (2). The cooler case (2) is made of poly lactic acid (PLA) material. The thermal conductivity coefficient of the PLA material used is 0.13 W/m.K, thus making it a suitable material for insulation. The thickness of the exterior wall

(2.2) and the interior wall (2.3) made of the PLA material used is 3 mm.

The interior division (3), the detail of which is shown in Figure - 1 comprises a lock housing (3.1) in which the sealing gasket is located, an upper housing (3.2) that allows the cooling material to be added from the top, a lower housing (3.4) that allows the cooling material to spread out from the lower surface, cooler walls (3.3) that allow the cooling material coming out of the lower housing (3.4) to spread evenly to the inner body of the cooler case (2). The interior division (3) is made of poly lactic acid (PLA) material. The thermal conductivity coefficient of the PLA material used is 0.13 W/m.K, thus making it a suitable material for insulation. The samples placed on the apparatus such as the spore body (4), the tissue cutting bench (1) and the tissue handling unit (6) placed on the cooler case (2) are equally exposed to the cold from all directions with the help of the interior division (3). Cooling material is filled into the cooler walls (3.3). Thus, the cooling material coming out of the lower housing (3.4) is spread along the cooler walls (3.3) and every area is exposed to cold equally. (Figure - 2) The interior division (3) positioned in the cooler case (2) ensures that the cooling material is distributed evenly in the middle area of the case. After the interior division (3) is positioned inside the cooler case (2), the cooling material is added from the upper housing (3.2) of the interior division (3). The added cooling material reaches the lower housing (3.4) of the interior division (3) and spreads to the cooler walls (3.3). Overflow or spillage of the cooling material is prevented by adding a sealing gasket to the lock housing (3.1) of the interior division (3) upper housing (3.2), after the cooling case (2) and the interior division (3) are positioned together and the cooling material is added. The cooler case (2) is placed in the refrigerator to further increase the desired cold effect after the cooling material is added.

A tissue cutting bench (1), detailed in Figure - 4, is used to cut and portion the tissues taken from the experimental animal after the cooler case (2) is prepared for processing. The tissue cutting bench (1) comprises a cooler surface (1.4) in contact with the interior division (3), a protrusion (1.3) on the edge such that the tissues do not mix with each other, a cutting surface (1.2) which is positioned on the cooler surface (1.4) and enables tissue cutting and portioning on a cold surface and a waste division (1.1) that separates the cut tissues such that they do not mix with each other. The tissue cutting bench (1) is made of poly lactic acid (PI_A) material. The thermal conductivity coefficient of the PLA material used is 0.13 W/m.K, thus making it a suitable material for insulation.

The tissue cutting bench (1) is positioned on the cooler case (2), which has been made ready by positioning the interior division (3), to which the cooling material has been added. Subsequently, a cutting surface (1.2) is positioned on the cooler surface (1.4) and the cutting process is performed. Therefore, the cooler surface (1.4), which is in contact with the interior division (3) during the cutting and portioning of the tissues, ensures that the tissues in the process performed on the cutting surface (1.2) are equally exposed to the cold. The cutting surface (1.2) is scratch-proof (it is made of non-scratchable material), and the heat transmission coefficient is 0.13 W/m.K. In addition, the scratch-proof cutting surface (1.2) is hygienically reusable. After the portioned tissues are placed in the waste division (1.1), the process continues. The waste division (1.1) is 13 mm deep and serves as a waiting area for tissues. The protrusion (1.3) on the cooler surface (1.4) edges prevents the tissues from mixing. A tissue cutting bench (1) with cooler is obtained with all these components.

Since all tissues portioned during the process will be exposed to cold equally, they are not exposed to any deterioration during the process and the experiment. All materials constituting the assembly are made of poly lactic acid (PLA) material. The thermal conductivity coefficient of the PI_A material used is 0.13 W/m.K, thus making it a suitable material for insulation. Distilled water or cooling material to be circulated on the cooler walls (3.3) according to the sensitivity of the tissues is added from the upper housing (3.2) of the system, it spreads to the cooler walls (3.3) passing through its lower housing (3.4). Therefore, it is ensured that the portioned tissues for analysis are kept at a homogeneous temperature value, a proper portioning is provided without being affected by external effects due to temperature difference or surface difference. Thus, it is prevented from affecting the analysis results. The cold affects every part of the tissue equally with the help of the cooler case (2). Although the cutting surface (1.2) is not scratched, it is manufactured in such a way that adhesion to the surface or adhesion of tissue parts to each other is minimized.

Likewise, blood, serum and similar materials are taken from experimental animals for analysis. A spore body (4), the detail of which can be seen in Figure 6 is positioned on the cooler case (2), which has been made ready by positioning the interior division (3), to which the cooling material has been added. There are spore divisions (4.2) located on the spore body (4). After the blood or serum or other fluid samples taken from the animal are taken into biochemistry tubes, they are placed in the spore housings (4.1) of the spore divisions (4.2). The lower surfaces of the spore housings (4.1) are in contact with the interior division (3), it is ensured that the samples positioned in the spore housings (4.1) with biochemistry tubes are exposed to a cold environment with the help of both the cooling material circulating in the cooler case (2) channel (2.1) and the cooling material circulating on the cooler walls (3.3) and the base of the interior division (3). Thus, while the skilled person is taking or preparing other samples, the other samples are not exposed to any temperature-related deterioration during the experiment. That is to say, even if the samples are not processed or stored immediately, they remain cold throughout the experiment with the help of the cooler case (2). Similar to the other covers, the spore body (4) is also made of PLA material. The thermal conductivity coefficient of the material is 0.13 W/m.K, thus making it a suitable material for insulation. (Figure - 5)

The spore body (4) used ensures that the samples taken from 6 experimental animals are divided into 4 different areas and used in different sections. The thickness of the walls is 3mm in the structure made of PLA material. The spore body (4) consists of a total of 24 equal divisions. The value of each compartment is 0 20 mm and their depth is 55 mm. The system is reusable by using distilled water and similar cooling materials around the spore housings (4.1) where blood tubes are placed. Also, the body (4) ensures that the blood tubes named during the experiment are stored systematically without loss of time and confusion.

The cooler case (2) and the interior division (3) are positioned similarly before the tissue handling unit (6) detailed in Figure 7 is positioned on the cooler case (2) and then the cooling material is added to make it ready for processing. Subsequently, a tissue handling unit (6) with tissue divisions (6.1) thereon positioned on the cooler case (2). The tissue handling unit (6) is capable of both separating the tissues for different analysis processes and allowing them to be transported or stored for a certain period of time. Portioned tissues are separated by placing them in tissue divisions (6.1) on the tissue handling unit (6). The tissues are modeled as a system where 6 different tissues of 3 different animals can be taken. The tissue divisions (6.1) have a depth of 55 mm. It is made of PLA material, the thermal conductivity coefficient of the material is 0.13 W/m.K, thus making it a suitable material for insulation. The thickness of the walls is 3mm in the structure made of PLA material.

After the tissue handling unit (6) is positioned on the cooler case (2) and the tissues are placed in the tissue divisions (6.1), it is positioned in the slot (5.2) of a transport cabin (5). The tissue handling unit (6) provides the storage of portioned tissues for different analysis processes. It is ensured that the user does not come into contact with the cooler case (2) with the help of the handle (5.1) on the transport cabin (5). Thus, the samples are not exposed to the body heat of the user as an external factor. In addition, there is no discomfort or burning in the user's hand since the user will not be in direct contact with the dry ice-containing environment during transportation, As in the tissue handling unit (6), the samples added to the spore body (4) used are also transported with the transport cabin (5), the details of which are shown in Figure-8. After the biochemistry tubes are positioned in the spore housings (4.1) of the spore body (4) on the cooler case (2) where the cooling material is added, the device is taken to the transport cabin (5) at the end of the process.

All kinds of samples are both easily storable and ensure the preservation of the required temperature for long-term storage of tissues or biochemistry samples during transportation with the help of the transport cabin (5). In addition, tissue samples on the tissue handling unit (6) located in the slot (5.2) of the transport cabin (5) and blood or serum samples in the spore slots (4.1) of the spore body (4) to be transferred to the relevant analysis unit without the need for an additional cooler can be transported for at least 3 hours without any thermal degradation. Furthermore, these devices, which are made of PLA material and have a thermal conductivity coefficient of 0.13 W/m.K, provide the opportunity to carry them to distances of 5 hours or more with the addition of dry ice. The heat dissipation at every point of the total volume does not make much difference than +/- 10% with the dry ice supplement. For example; portions or biochemistry samples transported with a temperature of -20°C lose a maximum of 2 degrees after 3 hours of transport and become -18°C. The whole structure of the spore body (4) has 3mm walls.

Cooler case (2), inner compartment (3) tissue cutting bench (1), tissue transport unit (6) and spore body (4), and all other structures used in the cold processing assembly made of PLA material has sufficient mechanical strength and flexibility in the operating range of - 80°C and - 20°C.

However, the heat dissipation in the entire volume is homogeneous. For example; the fresh tissue sample taken at 37°C shows a maximum 10% temperature difference after 3 hours, regardless of which slot it is placed in the dry ice cooler case (2). That is to say, the temperature of the portion in the middle of the tissue handling unit (6) positioned on the cooler case (2) is measured as -16°C, while the internal temperature of the tissue in the farthest division is measured as -14.4°C. The cold processing device described above is made of PLA material and the basic structure walls are 3mm and in long-term transports of 5 hours or more, 3 cm thick styrofoam transport container is used.