The present invention relates to an analytical sample preparation apparatus, and more particularly, to an apparatus, which can prepare analytical samples with oscillation and centrifugal coupling.
The analytical sample preparation process typically involves extraction and clean-up steps: the purpose of the extraction is to transfer components of a sample to a liquid as much as possible to obtain the so-called extract; and the clean-up is to separate the to-be-analyzed components from other components in the extract. The most basic clean-up step is to remove the remaining samples in the extract, which is usually done in a centrifugal manner. The most important step in the extraction process is to thoroughly mix the solids and the liquid to transfer components from the solids to the liquid. The mixing can be achieved in many ways, such as ultrasonic extraction, microwave extraction, and mechanical oscillatory extraction, wherein the mechanical oscillation is the most widely used. The centrifugation method uses high-speed rotation and the centrifugal forces to achieve separation, which is also a purely mechanical method. In most cases, the oscillation and centrifugation involve very different operations, which require different devices, and would not only increase cost, but also require very inconvenient sample transfer. If the two functions can be jointly implemented in a same mechanical device, the analysis sample preparations may be greatly simplified, and their efficiency substantially increased.
At present, there has been report about the use of stepper motor to accomplish oscillation and centrifugal functions. The implementation method includes using a stepper motor as a driving source to produce reciprocating actions at a certain frequency and amplitudes to achieve oscillation, and one-way rotations to achieve centrifugation. This method can only achieve planar oscillations, with their frequencies and angles significantly limited by the performance of the stepper motors, resulting in insufficient vibrations. In addition, the stepper motors have small load capacities, low one-way rotation speed. As a result, the sample processing and the centrifugal speeds cannot fully satisfy the requirements for preparing analytical samples.
In view of the technical problems existing in the conventional technologies, the present disclosure provides a new device for oscillation and centrifugal coupling, which can accomplish oscillation and centrifugal coupling in the same mechanical device, which greatly simplifies the preparation process of analysis samples and greatly improves the efficiency.
The present invention includes the following technical features:
An analytical sample preparation device, includes a base 1, an elastic connection body 5, a group of a synchronous unidirectional bearing inner ring 41 and a synchronous unidirectional bearing outer ring 42, a group of an eccentric unidirectional bearing inner ring 61 and an eccentric unidirectional bearing outer ring 62, and a synchronous fixed ring 2 and a motor 31 on the base 1, wherein the motor 31 is positioned within a synchronous fixed ring 2, wherein one end of the synchronous fixed ring 2 is fixed to the synchronous unidirectional bearing inner ring 41, wherein the synchronous unidirectional bearing outer ring 42 is connected to a lower end of the elastic connection body 5, wherein the eccentric unidirectional bearing inner ring 61 is connected with an eccentric shaft 32 extending from a motor 31, wherein the eccentric unidirectional bearing outer ring 62 is fixed to an eccentric shaft sleeve 9 that is fixed to a sample plate 7 and an upper end of the elastic connection body 5, wherein the eccentric shaft sleeve 9, the eccentric shaft 32, the eccentric unidirectional bearing inner ring 61, and the eccentric unidirectional bearing outer ring 62 have their center of mass disposed on a line extended from the center line of the motor 31, wherein the eccentric unidirectional bearing inner ring 61 and the eccentric unidirectional bearing outer ring 62 can only rotate in direction A, wherein the synchronous unidirectional bearing outer ring 41 and the synchronous unidirectional bearing outer ring 42 can only rotate in a direction opposite to direction A.
Further, the angle between the eccentric shaft 32 and the line extended from the centerline of the motor 31 is between 1° and 10°.
Further, an upper end of the elastic connection body 5 is connected with a lower end of the eccentric shaft sleeve 9, wherein the sample plate 7 is fixedly connected to the upper end of the eccentric shaft sleeve 9.
Further, the direction A can be clockwise or counterclockwise.
A method for preparing analytical samples using the analytical sample preparation device, includes:
1) placing a sample tube containing the samples and extracts into the sample tray 7;
2) setting the motor 31 to rotate in direction A for a first predetermined time, wherein the motor 31 drives the eccentric unidirectional bearing inner ring 61 to rotate relative to the eccentric unidirectional bearing outer ring 62, which causes the elastic connection body 5 to drive the sample tube to oscillate, thereby achieving extraction of the sample by vibration; and
3) when the vibration is finished, setting the motor 31 to rotate in the direction opposite to direction A for a second predetermined time, wherein the motor 31 drives the synchronous unidirectional bearing inner ring 41 to rotate relative to the synchronous unidirectional bearing outer ring 42, which causes the elastic connection body 5 to drive the sample tube to oscillate, thereby achieving separation of the sample from the extract in the sample tube.
Further, the method includes adjusting the first predetermined time and the second predetermined time; and repeating step 2) and step 3) one or more times to achieve sample separation from the extract in the sample tube.
Further, the method includes placing a plurality of sample tubes symmetrically on the sample plate
The presently disclosed device structure is schematically illustrated in
The sample 81 and the extract 82 are placed in the sample tube 8 during operation and placed on the sample tray 7. Thereafter, the starting motor 31 is rotated in direction A (A can be clockwise or counterclockwise) to start the vibration extraction, and the equivalent structure thereof is schematically shown in
Referring to the equivalent structure in
Compared with conventional technologies, the present invention includes the following advantageous effects:
According to the above description, the disclosed structure accomplishes oscillating and centrifuging in an appropriate control mode. The two steps can be continuously operated, which greatly simplifies sample preparation process and greatly improves efficiency. Since the type of the motor 31 is not limited in the process, the motor 31 can be ensured to provide high load and high rotational speed at the same time. Therefore, the effects of the oscillation and centrifugation will be greatly improved, and the requirements for the preparation of the sample are satisfied. Moreover, since no special motor is required, the reliability of the device is significantly increased, maintenance costs significantly reduced, which are other important advantages of the disclosed structure.
Chicken samples each weighted 2.0±0.05 g (accurate to 0.01 g) is placed in the 50 mL centrifuge tube, and are respectively added with appropriate amounts of Amantadine, D15-amantadine, Rimantadine, D4-rosin ethylamine, Chlorpheniramine, D4-chlorobenzene standard working solution, mixed, and let stand for 30 min (using oscillation coupling centrifugation method, directly placing the samples into the 50 mL centrifuge tubes in the outer tube and introducing the standard working solution). Blank samples and samples oscillatory coupling added with 20 μg/L of above described chemicals are respectively prepared in parallel. Both blank samples and the samples added with the chemicals are treated using the following two methods. The samples are then analyzed using machines specified in the national standards for food safety “animal-derived food Amantadine and Rimantadine residues Determination of Liquid Chromatography—Tandem Mass Spectrometry”.
(1) Manual treatment method: adding 20 mL of 1% acetic acid acetonitrile solution, whirlpool oscillation for 3 min, adding 2 g of anhydrous magnesium sulfate, vortex for 30 s, centrifuge at 4000 r/min for 5 min. Take 1 mL of the supernatant, add 50 mg of PSA, vortex for 30 s, and centrifuge at 4000 r/min for 3 min. The resulting supernatant was filtered with a 0.22 μm filter and measured with LC-MS/MS.
(2) Automatic treatment method: add 2 g of anhydrous magnesium sulfate and 20 mL of 1% acetic acid acetonitrile into the 50 mL sample tube in the centrifuge tube, mix; add 150 mg of PSA into the inner tube, the inner tube inserted into the outer tube, then placed them in the centrifuge. Program 1 setting: clockwise rotation to achieve 8-shaped oscillation for 2 min, and then counterclockwise rotation to centrifuge at 5000 rpm for 3 min. Program 2 setting: clockwise rotation to achieve 8-shaped oscillation for 1 min, and then counterclockwise rotation to centrifuge at 500 rpm for 2 min. Run the two programs. After completion, the resulting supernatant was filtered with a 0.22 μm filter and measured with LC-MS/MS.
From the above table we can see that there is no significant difference in the matrix effect between the two methods for Amantadine; based on the external standard method, the absolute recovery rate by the oscillation coupling centrifugation method is basically the same as that of the manual treatment method, both being above 95%. Based on the internal standard method, the automatic method and manual treatment method can obtain relatively good recovery rates and accurate results. For Amantadine, there is no significant difference in the matrix effects between the two methods. Based on the external standard method, the difference in absolute recovery rates between the manual treatment and the oscillation coupling centrifugation method is not significant, both being above 75%, whereas the internal standard method can obtain relatively better recovery rates and more accurate results. According to the isotope internal standard method adopted in the draft version of the national standard for food safety titled “Determination of Amantadine residues in animal food by liquid chromatography—tandem mass spectrometry”, the present experiments can produce similar results using the disclosed sample oscillation coupling centrifugal treatment method and manual treatment method.
Number | Date | Country | Kind |
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201510579053.8 | Sep 2015 | CN | national |
Filing Document | Filing Date | Country | Kind |
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PCT/CN2016/094635 | 8/11/2016 | WO | 00 |