Detailed Description
Example embodiments will now be described more fully with reference to the accompanying drawings. Example embodiments may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein. Rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the concept of example embodiments to those skilled in the art. The same reference numerals in the drawings denote the same or similar structures, and thus their repetitive description will be omitted.
Fig. 1 is a schematic view of apipetting system 100 according to an embodiment of the invention, and fig. 2 is a schematic view of apipetting device 120 in thepipetting system 100. Referring to fig. 1 and 2, thepipetting system 100 includes aturntable 110, apipetting device 120, and aslide rail 130. Thecarousel 110 is provided with apipette replacement zone 112, apipetting zone 114, and areagent placement zone 116. Thepipetting device 120 is capable of performing a pipetting operation in cooperation with the rotation of theturntable 110.
Referring to fig. 2, thepipetting device 120 is used to load afirst pipette 122 and asecond pipette 124, wherein thefirst pipette 122 has a first transfer capacity and thesecond pipette 124 has a second transfer capacity, and the first transfer capacity is different from the second transfer capacity.
Referring to fig. 2, theslide rail 130 is connected to thepipetting device 120, and thepipetting device 120 is used to drive thefirst pipette 122 and thesecond pipette 124 to move along theslide rail 130 to a designated position in cooperation with theturntable 110, for example, thefirst pipette 122 and thesecond pipette 124 can move back and forth between thepipette replacement area 112, thepipetting area 114 and thereagent placement area 116 to perform a pipetting operation. Referring to FIG. 1, a plurality oftest tubes 142, 144 are disposed in thepipetting zone 114 for receiving a blood sample for testing.
One embodiment of pipetting is outlined below. First, thepipetting device 120 moves to thereagent placement area 116 to aspirate a first dose of reagent and add the first dose of reagent to thefirst test tube 142 in thepipetting area 114, and then thepipetting device 120 moves to thepipette replacement area 112 to replace a different pipette and moves to thereagent placement area 116 to aspirate a second dose of reagent and add the second dose of reagent to thefirst test tube 142 in thepipetting area 114. Thepipetting device 120 then moves to thereagent placement area 116 to aspirate a third dose of reagent and add the third dose of reagent to thefirst tube 142 in thepipetting area 114. Subsequently, thepipetting device 120 aspirates the mixed liquid containing the first dose of reagent, the second dose of reagent, and the third dose of reagent, filters the mixed liquid through the filtration system, and adds the filtered mixed liquid to thesecond test tube 144 in thepipetting zone 114. Finally, thepipetting device 120 aspirates a fourth dose of reagent and adds the fourth dose of reagent to thefirst tube 142, and aspirates the mixed fluid containing the fourth dose of reagent through the filtration system and into thesecond tube 144.
In order to precisely control the dosage of the respective reagents, a first dosage of reagent is aspirated, for example, with afirst pipette 122, and a second dosage of reagent is aspirated, for example, with a furtherfirst pipette 122, the first dosage and the second dosage being identical or different. Furthermore, a third dose of reagent is aspirated, for example, with asecond pipette 124, and a fourth dose of reagent is aspirated, for example, with anothersecond pipette 124, the third dose and the fourth dose may be the same or different.
Thefirst pipette 122 and thesecond pipette 124 have different transfer capacities, and the transfer capacity of thefirst pipette 122 is, for example, 1 milliliter (ml) or less, and the transfer capacity of thesecond pipette 124 is, for example, more than 1 milliliter (ml) but 5 milliliters (ml) or less. Thefirst pipette 122 is used to aspirate a smaller amount of reagent, and thesecond pipette 124 is used to aspirate a larger amount of reagent, and thepipetting device 120 can use either thefirst pipette 122 or thesecond pipette 124 according to the amount of the required volume to be aspirated. 1 milliliter (ml) may be converted to 1000 microliters (μ l).
Thepipetting device 120 is not limited to having only onefirst pipette 122 and onesecond pipette 124, and may have two or three pipettes with transfer capacities, for example, when the amount of pipettes is greater than 5 milliliters (ml), a pipette with a larger transfer capacity may be loaded on thepipetting device 120.
In one embodiment, thefirst pipette 122 with a smaller transfer capacity can suck a first dose of reagent of 0.02 milliliters (ml) and a second dose of reagent of 0.04 milliliters (ml), so that the error of the transfer capacity can be controlled to be about 2.5%, and the accuracy requirement of less than 10% is met. If thesecond pipette 124 with a larger transfer capacity is used to suck the first dose of 0.02 milliliters (ml) of reagent and the second dose of 0.04 milliliters (ml) of reagent, the error of the transfer capacity is about 26% and 15%, and the accuracy requirement of less than 10% cannot be met.
The following table shows an example of the transfer amount error of a 20 microliter (μ l) dose drawn by thefirst pipette 122 and thesecond pipette 124, and it is obvious that the transfer amount error of thefirst pipette 122 can be controlled to about 2.5%, and the transfer amount error of thesecond pipette 124 is about 26% when thesecond pipette 124 with a large transfer capacity is used to take a liquid.
Further, by sucking the reagent of the third dose of 2 milliliters (ml) and the reagent of the fourth dose of 5 milliliters (ml) with thesecond pipette 124 having a large transfer capacity, the error of the transfer amount can be controlled to about 2.5%, and the accuracy requirement of less than 10% can be met. If thefirst pipette 122 with a smaller transfer capacity is used to aspirate the third dose of 2 milliliters (ml) of reagent and the fourth dose of 5 milliliters (ml) of reagent, the transfer capacity is limited to 1 ml, which cannot be taken out at one time, and the reagent must be pipetted several times, thereby wasting time and affecting the reaction effect of the reagent.
As can be seen, the conventional pipette operation using a pipette with a single transfer volume is affected by the limited transfer volume or insufficient accuracy requirement of the pipette, and if a pipette with a small extraction amount is used, high accuracy can be maintained, and if a pipette with a large extraction amount is used, accuracy is degraded, and if the accuracy is degraded or the extraction amount is insufficient, a subsequent operation error or erroneous judgment of an analysis result is caused. In addition, in the case of an instrument requiring high precision, if only a pipette with a small amount of extraction is used to perform an experiment, the waste of repeated extraction time and the influence on the reaction of reagents are caused.
Compared to the conventional pipetting operation with a single transfer volume pipette, thepipetting system 100 of the present embodiment uses afirst pipette 122 and asecond pipette 124 with different transfer volumes. Since the amount of reagent added is different during pipetting, thefirst pipette 122 is used to aspirate a small amount of reagent and thesecond pipette 124 is used to aspirate a large amount of reagent, thereby solving the problems of reduced accuracy and insufficient pipetting amount.
Please refer to fig. 3 and fig. 4, which are schematic diagrams of a pipetting operation performed by thepipetting device 120 in fig. 2. Thefirst pipette 122 and thesecond pipette 124 are both mounted on theslide rail 130 and can move synchronously along theslide rail 130. In addition, thefirst pipette 122 and thesecond pipette 124 are respectively mounted on two independentvertical slide rails 132, 134 and can respectively move along thevertical slide rails 132, 134 in the vertical direction. Therefore, thepipetting device 120 can move thefirst pipette 122 or thesecond pipette 124 to the right above the test tube according to the required amount of the pipetted dose.
In addition, thefirst pipette 122 and thesecond pipette 124 with different transfer volumes can be moved vertically at the same time to aspirate different doses of the first reagent and the second reagent, so as to increase the speed of liquid taking.
Please refer to fig. 1 to fig. 5, wherein fig. 5 is a flowchart illustrating the determining steps of the pipetting method, which is outlined below. First, in step S110, a target reagent to be aspirated is determined according to a detection flow, and in step S120, thepipette device 120 moves the pipette along theslide rail 130 to above the target test tube/reagent in cooperation with theturntable 110. In step S130, the required amount of liquid to be sucked is determined, and if the required amount of liquid to be sucked is less than or equal to 1 milliliter (ml), steps S132 and S134 are performed, the height of liquid to be taken for movement is calculated, thefirst pipette 122 with smaller transfer capacity performs a liquid taking action along thevertical slide rail 132, and the original position is returned after the liquid taking is completed; if the required suction dosage is larger than 1 milliliter (ml), steps S136 and S138 are performed to calculate the liquid-taking height required to move, so that thesecond pipette 124 with larger transfer capacity performs the liquid-taking action along thevertical slide rail 134, and returns to the original position after the liquid-taking action is completed. Next, in step S140, thepipetting device 120 moves to above the test tube in thepipetting zone 114 in cooperation with theturntable 110 to perform injection, so as to complete one pipetting operation. In step S142, it is determined whether or not the liquid transfer operation is to be continued, and if the next liquid transfer operation is required, the process returns to step S110 until all the liquid transfer operations are completed.
In summary, although the present invention has been described with reference to the above embodiments, the present invention is not limited thereto. Those skilled in the art can make various changes and modifications without departing from the spirit and scope of the invention. Therefore, the protection scope of the present invention should be determined by the contents defined in the appended claims.