The subject matter relates to handling of samples, and more particularly, to a liquid transfer device.
Molecular diagnosis, morphological detection, and immunological detection are mostly carried out in laboratories. Detection processes are time-consuming, complex, inefficient, and inflexible, and detection devices are generally not portable. Transferring of a sample usually need to be done in a laboratory. Therefore, the detection cannot be carried out anytime and anywhere, especially at home.
Implementations of the present technology will now be described, by way of example only, with reference to the attached figures.
It will be appreciated that for simplicity and clarity of illustration, where appropriate, reference numerals have been repeated among the different figures to indicate corresponding or analogous components. In addition, numerous specific details are set forth in order to provide a thorough understanding of the embodiments described herein. However, it will be understood by those of ordinary skill in the art that the embodiments described herein can be practiced without these specific details. In other instances, methods, procedures, and components have not been described in detail so as not to obscure the related relevant feature being described. Also, the description is not to be considered as limiting the scope of the embodiments described herein. The drawings are not necessarily to scale, and the proportions of certain parts may be exaggerated to better illustrate details and features of the present disclosure.
The term “comprising,” when utilized, means “including, but not necessarily limited to”; it specifically indicates open-ended inclusion or membership in the so-described combination, group, series, and the like.
In an embodiment, the transfer unit 10, the reaction chamber 20, and the collecting unit 30 are detachably fixed with each other, so that the liquid transfer device 1000 can be switched among a first state, a second state, and a third state. The first state is that the transfer unit 10 is disposed and fixed above the collecting unit 30. The second state is that the transfer unit 10 is disposed and fixed above the reaction chamber 20. The third state is that the reaction chamber 20 is disposed and fixed between the transfer unit 10 and the collecting unit 30.
When the liquid transfer device 1000 is in the first state, the piston assembly 11 can move away from the collecting unit 30 along the central axis of the pipette 12. Therefore, the pipe 12 is deformed to absorb the sample solution in the collecting unit 30. When the liquid transfer device 1000 is in the second state, the piston assembly 11 can move close to the reaction chamber 20 along the central axis of the pipette 12. Therefore, the pipe 12 is deformed to release the sample solution in the reaction chamber 20. The reagent adding unit 13 is used to add the reagent in the reaction chamber 20. The reagent is mixed with the sample solution to form a mixed solution. The piston assembly 11 can move away from the reaction chamber 20 along the central axis of the pipette 12. Therefore, the pipe 12 is deformed to intake the mixed solution. Then the mixed solution in the pipe 12 can be added in a nucleic acid detection device (not shown). The third state of the liquid transfer device 1000 is a resting state. The reaction chamber 20 is disposed and fixed between the transfer unit 10 and the collecting unit 30 for easy storage.
Referring to
Referring to
In an embodiment, referring to
Referring to
Referring to
In an embodiment, the reagent tube portion 132 has two tubes 1321, able to receive two kinds of regents. The two tubes 1321 are disposed side by side in the reagent tube portion 132. The inserting member 133 includes two inserting rods 1331 corresponding to the two tubes 1321 in the reagent tube portion 132. The two inserting rods 1331 insert into the two tubes 1321 to release the reagents in the reagent tube portion 132 together. The reagent tube portion 132 can receive two different reagents, which allows a reaction in the reaction chamber 20 to be more convenient. There is no need to open the liquid transfer device 1000 to add sample and reagents into the reaction chamber 20, this avoids contamination of the reaction affecting a detection result.
Referring to
In an embodiment, the second housing 21 includes two elastic sheets 211, a protrusion 212 disposed on an inner sidewall of each elastic sheet 211, and a second pressing head 213 disposed on an outer sidewall of each elastic sheet 211. When the reaction chamber 20 is connected to the transfer unit 10, the two protrusions 212 are aligned with the two first latching grooves 118 on the first housing 111. The second pressing head 213 can be pressed to bend the elastic sheet 211 inward. Therefore, the protrusion 212 can press the latching blocks 117 to exit from the first latching grooves 118.
In an embodiment, the connector 23 defines two through holes 231 corresponding to the pipette 12 and the reagent adding unit 13 respectively. The collector 22 is connected to the cuvette 24 through the two through holes 231. A baffle 232 is disposed in each through hole 231. Before the pipette 12 or the reagent adding unit 13 is inserted into the reaction chamber 20, the baffle 232 is closed and seals the cuvette 24. When sampling is required, the pipette 12 or the reagent adding unit 13 can pass through the baffle 232 and be inserted into the cuvette 24. Referring to
In an embodiment, the cuvette 24 is substantially a conical cup which is conducive to the transfer of a trace sample.
In an embodiment, the collecting unit 30 includes a third housing 31, at least one third latching groove 32 disposed on a sidewall of the third housing 31, a collection cup 33 disposed inside the third housing 31, and a puncture portion 34 disposed in the collection cup 33. Each of the transfer unit 10 and the reaction chamber 20 corresponding to the third latching groove 32 includes at least one clamping position 35. The collecting unit 30 is connected to the transfer unit 10 or the reaction chamber 20 through the clamping of the clamping positions 35 with the third latching groove 32.
Referring to
In an embodiment, the reagent box 36 includes a reagent adding opening 361, a gasket 362 disposed below the reagent adding opening 361, and a reagent package 363 disposed below the gasket 362 and connected to the reagent adding opening 361. A material of the reagent package 363 is such that it may be easily pierced, such as tin foil paper or plastic film.
Referring to
Initially, the liquid transfer device 1000 is in the third state. When in use, the collecting unit 30 and the transfer unit 10 are removed from the reaction chamber 20. Then, the sample solution to be tested is placed in the collecting unit 30. The liquid transfer device 1000 is switched to the first state. The piston assembly 11 moves away from the collecting unit 30 relative to the pipette 12, so that the pipette 12 absorbs the sample solution. Then, the liquid transfer device 1000 is switched to the second state. The piston assembly 11 moves towards the reaction chamber 20 relative to the pipette 12, so that the pipette 12 discharges the sample solution into the reaction chamber 20. The reagents in the reagent adding unit 13 are added in the reaction chamber 20 to mix with the sample solution to form the mixed solution. The piston assembly 11 moves away from the reaction chamber 20 relative to the pipette 12 to make the pipette 12 absorb the mixed solution in the reaction chamber 20. Finally, the transfer unit 10 transfers the mixed solution to a nucleic acid detection device for example, for detection.
Referring to
At step one, the second pressing head 213 on the sidewall of the transfer unit 10 is pressed to push the latching blocks 117 to exit from the first latching grooves 118. An elastic restoring force of the elastic member 115 drives the piston 113 to move downward, and the latching blocks 117 are inserted in the second latching grooves 119 to discharge the air in the pipette 12.
At step two, the clamping position 35 on the transfer unit 10 is clamped into the third latching groove 32 on the collecting unit 30, so as to lock the transfer unit 10 on the collecting unit 30. Therefore, the pipette 12 extends into the collection cup 33 of the collecting unit 30.
At step three, the pushing mechanism 114 is pressed to make the latching blocks 117 exit from the second latching grooves 119 and move upward to clamp into the first latching grooves 118. At this time, the piston 113 is driven to move upward to make the pipette 12 absorb a quantified amount of the sample solution in the collection cup 33.
At step four, the transfer device 10 is separated from the collecting unit 30 and locked with the reaction chamber 20. The pipette 12 is inserted into the reaction cup 24 through the collector 22 and one through hole 231 on the connector 23. The regent adding unit 13 is inserted into the reaction cup 24 through the collector 22 and another through hole 231 on the connector 23.
At step five, the second pressing head 213 is pressed again, and the latching blocks 117 exit from the first latching grooves 118. The elastic restoring force of the elastic member 115 drives the piston 113 downward. Therefore, the latching blocks 117 are inserted into the second latching grooves 119 to inject the sample solution in the pipette 12 into the cuvette 24.
At step six, the pressuring rods 131 on the reagent adding unit 13 are pressed to push the inserting members 133 downward, so as to pierce the sealing films 135 at the bottom end of the reagent tube portion 132. Therefore, the reagents in the reagent tube portion 132 can enter the cuvette 24.
The liquid transfer device 1000 provided by the present disclosure can be used to transfer a variety of liquids. For example, samples of the liquid may be, but are not limited to, a biological sample, a veterinary sample, or an environmental sample.
The liquid transfer device 1000 provided by the present disclosure can be used to collect and prepare volumes of 1 μl˜5 ml (such as 1 μl, 2 μl, 4 μl, 5 μl, 10 μl, 20 μl, 50 μl. 100 μl, 200 μl, 500 μl. 1 ml, 2 ml, and 5 ml of liquid), and volumes in between.
The liquid transfer device 1000 has the advantages of simple overall structure, low cost, and convenient operation.
The disassembly and assembly of the transfer unit 10, the reaction chamber 20, and the collecting unit 30 of the liquid transfer device 1000 are simple and convenient. The piston assembly 11 and the reagent adding unit 13 are received in the transfer unit 10, which avoids opening the liquid transfer device 1000 to add samples during the reaction process. Therefore, the sealing performance of the liquid transfer device 1000 is improved to avoid contamination of the reaction. Thus, the liquid transfer device 1000 has a simple structure, which is portable, flexible, and convenient, and can be used at home.
The embodiments shown and described above are only examples. Even though numerous characteristics and advantages of the present technology have been set forth in the foregoing description, together with details of the structure and function of the present disclosure, the disclosure is illustrative only, and changes may be made in the detail, including in matters of shape, size and arrangement of the parts within the principles of the present disclosure, up to and including the full extent established by the broad general meaning of the terms used in the claims.
Number | Date | Country | Kind |
---|---|---|---|
202110277711.3 | Mar 2021 | CN | national |