Patent Application
20190292567
The present invention relates to a piezo-driven microinjection system with force feedback suitable for use in biological cell micromanipulation. The invention may also find use in injection of material into other pierceable microstructure targets, such as viruses when used with injectors of appropriate dimensions.
Biological cell micromanipulation involves the operation of gripping, injection, cutting, etc. for biological cells. Cell injection is the process of delivering exogenous materials into cells, which is a common operation in biological experiments. Cell injection has been widely applied in genetic engineering, intracytoplasmic sperm injection (ICSI), DNA therapy or other biomedical areas. Comparison study of the human reference genome shows that approximately 70% of human genes have at least one obvious zebrafish orthologue [1], which leads to the widespread use of zebrafish embryo in disease study and drug testing. With advantages of flexibility and efficiency, micropipette injection method has been extensively used in traditional manual cell manipulations. However, the cell injection process requires precision control of the pipette to execute accurate puncturing, injecting, and retracting tasks. It usually requires a long training time for human operators while results in low success rate. The reason lies in that human operators suffer from fatigue problems for the injection of large batch of cells. To overcome such weakness, automated injection technologies have been widely investigated over the last few decades. For example, a microrobotic system with a hybrid visual servo control for automatic cell injection has been developed in [2], which greatly reduces the manipulation time and improves the injection success rate. Optical tweezers have been introduced to conduct cell patterning for the execution of the required operation [3]. A comprehensive review of recent automated microinjection systems has been presented in [4].
There are two main criteria in cell injection, i.e. success rate and survival rate. Image-based visual servo is the dominant control method in existing automatic cell injection systems [5-7]. However, the pipette location, which is extracted by an image processing algorithm, is not absolutely synchronous with the cell status due to the time delay induced by the image acquisition and processing procedure. The vision-based feedback is difficult to identify whether the pipette has pierced in or slipped off the cell during the operation. As a result, a low success rate of cell injection is caused. Meanwhile, it has been reported that a higher success rate will be achieved with force feedback intervened [8]. In the literature, the cell force model has been developed by bulk-scale methods, which rely on the average value of hundreds or thousands of cells. But the individual cell's characteristics would be obscure among the cell group [9]. For an accurate measurement of the exerted force, a microinjection prototype with the integration of a piezoresistive micro-force sensor was developed for zebrafish embryos [10]. It can synchronize the position control with force profile during the injection process. In addition, PVDF (Polyvinylidene Fluoride) films have been used for force sensing during cell injection [11,12].
To improve the cell survival rate, it is necessary to minimize the adverse effect of deformation for the zebrafish embryos induced by the injection force. To cope with this problem, piezoelectric actuators (PZTs) with the advantages of the fast response, high acceleration and precision positioning resolution can be adopted [13]. Piezo-driven micropipette was first introduced into cell injection by Kimura [14], in which the pipette was driven by a serial of piezo-pules to execute mouse oocytes injection. A survival rate of 80% was achieved in that experiment, while only 16% of the oocytes survived with conventional method. Afterwards, several remarkable research works have been conducted with piezo-driven cell injection system [15-20]. However, all of these works are conducted based on the vibration character of PZTs. It means that the PZT acts like a vibration drill and it is combined with the other actuators to perform the cell injection tasks. Thus, the PZTs' high resolution of displacement is not effectively exploited in these cases.
Commercially available piezoelectric actuators (PZTs) can only provide a limited output displacement (32 μm in this work). It is not large enough to pierce zebrafish embryos with diameter of 600-1200 μm. Hence, a displacement amplifier is required to meet the motion range requirement. Moreover, the injector pipette should experience a pure in-plane translation by avoiding lateral movement, because the latter can induce extra damage to the penetrated cells.
In the literature, piezo displacement amplifiers have been researched extensively [21] and are mainly used for micro/nano manufacturing, atomic force microscopy (AFM), and so on. In this work, a piezo-driven flexure-based injector is designed with a bridge-type displacement amplifier, as shown in
Referring to
Assume that each flexure hinge offers a one-degree-of-freedom (1-DOF) rotational compliance which arises from the bending deformation, and other elements are rigid bodies. The displacement output in the injection direction can be calculated by [22]:
Δy=lpsinα−√{square root over (lp2sin2α−Δx2−2lpcosαΔx)} (1)
Then, the amplification ratio of the bridge-based amplifier can be derived as:
As a case design, the main parameters of the injector mechanism are selected as shown in Table 1. With a driving displacement of 32 μm, analytical model predicts an output displacement of 350 μm. Finite-element analysis (FEA) is conducted with ANSYS software, the configuration and simulation result can be found in
To make full use of the ultrahigh displacement resolution of PZT, the PZT is adopted as linear actuator with a flexure guiding mechanism to drive the pipette directly for executing cell injection in this work. However, up to now, it is unknown to what extent that the force control performs better than the position control in biological cell injection manipulation. In this work, a piezoelectric actuator with a displacement amplifier is designed to drive the injection pipette. Both position and force sensors are integrated into the device to achieve a higher compactness. Comparative studies with position control and force control have been carried out by experimental injection of 100 zebrafish embryos, and some remarkable conclusions are derived. To the knowledge of the author, no such work has been conducted before in the literature.
Accordingly, from a first aspect, the present invention provides a device, for example for use with a micro injection pipette, said device comprising a linear actuator with position and force strain gauge sensors. Such actuator may be a piezoelectric actuator with a displacement amplifier and the strain gauge sensors may be semiconductor strain gauge sensors.
From a second aspect, the invention provides a microinjection system combining such device and a microinjection pipette. Typically such a system includes a flexure guiding mechanism for driving the pipette to its intended location and for ensuring withdrawal of the pipette with minimal damage to the target. Microinjection pipettes for use in the invention will be chosen with appropriate dimensions based on the nature of the pierceable microstructure target such that when the target is, for example a virus, a pipette with a smaller tip may be used than in the case where the target is a cell or embryo.
The microinjection system of the present invention features low cost, convenient installation, and easy maintenance. A flexure-based displacement amplifier is designed to enlarge the stroke of PZT. With the integration of strain gage sensors, the position and force status of the injected embryos is monitored in real time. This system enables a high operation speed, confident success rate, and high survival rate.
From a third aspect the invention provides a method for microinjection of a substance into a pierceable microstructure such as a biological cells, nuclear envelopes and viral capsids and envelopes using such a piezoelectric actuator.
Such methods may be used in genetic engineering to introduce DNA into a nucleus or virus, including gene therapy, for example in treatment of cancer, in vitro fertilization of an ova, cloning techniques and insertion of cells, such as stem cells, into an embryo.
Microinjection has two main requirements namely that the injection needle is aligned with the target and that the needle remains within the target while the desired material is being injected into the target.
The present invention provides a new injector system with both position and force sensors. Such system typically further includes a micromanipulator and optical microscope to assist in aligning the injector with the target.
Suitable piezoelectric actuators for use in the present invention include piezoelectric stacks in rectangular, parallelepiped or cylindrical shapes.
Suitable displacement amplifiers include bridge-type and compound bridge type flexure-based amplifiers.
Suitable integrated position sensors include resistance based and capacitive-based sensors.
Suitable force sensors include resistance-based and capacitive-based sensors. Suitable injection pipettes include glass micropipettes and metal micropipettes.
The components of the system are configured so that the piezoelectric actuator provides an accurate location of the target for injection such as a biological cell, for example by use of a bridge-type displacement amplifier of the type shown in
Operation of the system of the present invention may conveniently be carried out on accordance with the flow chart shown in
Two half-bridge circuits are constructed by semiconductor strain gages (model: TP-3.8-350, from Bengbu Tianguang Sensor, Ltd.), which are adopted to measure the output displacement of this stage and applied force on the injection needle. The laser sensor (model: LK-H055, from Keyence Corp.) and load cell (model: GSO-10, from Transducer Technology, Inc.) are used for the calibration of the position and force sensing strain gages, respectively. A thick-walled glass capillary (borosilicate glass B100-50-10 from Sutter Instrument Co.) was pulled using micropipette puller (P-1000, Sutter Instrument Co.) to get an appropriate outer diameter (3 μm) of the injection needle. The inverted microscope (model: IX81, from Olympus, Inc.) has an XY stage for positioning the petri dish. Zebrafish embryos are placed in parallel V-grooves, which are made from the 1.5% agarose gel in a petri dish. The injector can move in plane for the embryos in each groove, which simplifies 3D movement to plane motion in each groove. The calibration and experiments with zebrafish embryos are conducted at the room temperature of 24° C.
The cell injection control algorithm is implemented on Natural Instruments (NI) cRIO-9022 real-time controller integrated with cRIO-9118 reconfigurable chassis, which contains a Field-Programmable Gate Array (FPGA) module. In addition, NI-9263 analog output module with 16-bit resolution and NI-9237 bridge analog input module with 24-bit resolution are employed to produce the excitation voltage and obtain the strain gage sensor signals, respectively. The sampling rate of the system is selected as 4 kHz.
In cell injection, majority of force sensors are designed with Polyvinylidene Fluoride (PVDF) film [8,11,12,23], which have a remarkable dynamic force detection ability. However, the dynamic sensor is not suitable for the sensing of quasi-static signals. Alternatively, with the advantages of higher unit resistance and sensitivity, semiconductor strain gages are used as force sensor in this work. It works based on the piezoresistive effects of silicon and measures the change in resistance due to the accompanied strain.
Two strain gages are mounted on a cantilever-beam mylar (see
To construct a half-bridge circuit for the position measurement, two strain gages are mounted on the flexure of displacement amplifier, as shown in
By inspecting the results in
The measurement range and sampling rate of position and force sensors are limited by the equipment used. For example the NI-9237 bridge module, has ±25 mV analog input range and 50 Ks/s sampling rate. Hence, although a force measurement range with ±355 mN and position measurement range with ±360 μm can be achieved in theory, these ranges may be more limited in due to the initial installing deformation.
To compare the performances of cell injection system with the traditional position control and position/force control during cell puncturing process, the same controller structure is adopted. In particular, owing to its popularity and model-free nature, the incremental PID controller is employed as the position and force controllers for cell injection system. By defining e(t)=x(t)−xr(t) as the position/force tracking error, the control action is derived as follows.
u(t)=u(t−T)+Kp[e(t)−e(t−T)]+Kie(t)+Kd[e(t)−2e(t−T)+e(t−2T)] (3)
where x is position/force variable, xr denotes the desired position/force trajectory, T is the sampling time interval, and u(t−T) denotes the control variable in the previous time step, Kp, Ki and Kd are the positive gains to be tuned.
For cell microinjection testing, the fabricated injector is mounted on an XYZ micromanipulator (model: MP-285, from Sutter Instrument Corp) to develop an automatic cell injection system. In the experimental study, a batch of zebrafish embryos are immobilized on the V-groove agarose gel in a petri dish, which is placed on the platform of an inverted microscope. The injector tip can move in plane for embryos in each V-groove. After the initialization and calibration of the CCD camera, the relative position between the pipette and target embryo can be recognized with computer vision algorithm. The micropipette moves from the initial position to the target cell controlled by the XYZ micromanipulator first. Once the pipette needle contacts with the embryo, which can be detected by the integrated force sensor, the coarse movement of micromanipulator is switched to the precision control of the piezo-driven injector. Two control schemes are realized in this work, i.e. (a) the traditional injection sequence with position control and (b) the improved operation flow with force control intervened.
A predefined position/force trajectory is used as a reference based on the trigger value for pipette puncturing until a dramatic force drop is detected. Then, a time interval is reserved to execute practical injection task, i.e. injecting the desired material. After that, a gentle retracting movement is applied under the precise position control to avoid throwing out the injected material by the retracting pipette. Finally, when the piezoelectric actuator returns to its home position, the micromanipulator translates back with a safe distance to prevent the pipette needle from crashing into the embryo during moving to the next embryo. When the next embryo comes into camera view, the above injection process is repeated. The motion sequence is shown in
Experimental Study and Results
In this section, experimental study on cell injection is carried out using the developed injector with the foregoing control schemes.
Cell Injection Experiments
In practice, majority of unsuccessful cell injections are caused by the fact that, the computer believes that the target cell had been punctured while the pipette needle did not do that in reality. Actually, it is difficult to distinguish with the visual feedback whether the target embryo has contacted with micropipette or just slipped over.
For example, two injection scenarios are depicted in
The collected embryos are spread on the V-grooves and aligned with manual assist carefully. A total of 100 zebrafish embryos are divided into to two equal groups, which are continuously injected using the proposed injection system with position and force control, respectively. The average injection time for each embryo is reduced to less than 3 s, which is better than that of a proficient human operator. The injection speed is set as 2 mm/s and 20 mN/s for position and force control, respectively. A gentle retracting speed is set as 220 μm/s. The force trigger threshold from coarse to fine movement is 500 μN, the punctured force velocity trigger is −10 mN/s. In addition, once the embryo is pierced, a period of 500 ms is reserved to inject the desired material. The safe distance of coarse movement is set as 5 mm. By trial and error, the parameters of PID position controller are tuned as Kp=2×10−3, Ki=6×10−4, and Kd=1.5×10−3. The parameters of PID force controller are adjusted as Kp=6×10−3, Ki=9×10−4, and Kd=1×10−3.
It is found that the change rate of the temperature drift is quite low (≤10 mN/s). In practice, an efficient and quick manipulation behavior (˜20 mN/s) during the cell injection is preferred. Hence, the velocity of variation between the noise and working force can be differentiated conveniently. In this work, a change rate limit of 10 mN/s is used to extract the force signal from noise during algorithm implementation, which means that only a rapid change signal (i.e. puncturing force) can pass this gate while the noise is resisted.
To reduce the temperature drift of strain-gage force sensor further, the motion sequence of the automatic cell injection system is specifically designed. The force output is set as zero before the signal value reaches contact force threshold. The puncturing time is quite short (˜0.1 s), which reduces the drift impact further. The force is reset to zero again after each cell membrane is punctured.
Results
The experimental results of position and force control are shown in
The survival rate is defined as the ratio between the number of injected embryos that are capable of developing into larva and the total number of embryos injected. It essentially represents the severity and frequency of cell damage due to the injection. Based on the 100 injected zebrafish embryos with position control and force control, the survival rates are calculated as 82 and 86%, respectively.
The survival rates obtained by the existing approaches are compared as shown in Table 2. It is observed that the force control produces a higher survival rate than conventional position control in the same operation environment. With force control involved, the achieved survival rate of 86% is better than majority of existing works. It is notable that the survival rate can be further improved with more delicate care during the embryo culturing and precision control algorithm design. Even so, it is better than the survival rate of 50-70% in manual operation which is caused by the proficiency difference and fatigue problems. The improvement of survival rate with force control is dominantly contributed by the smoother force interaction and the greatly reduced embryo deformation.
With the force-controlled injection system, another remarkable improvement is the injection speed. With the advantages of force feedback and PZTs, quick response and assured pierced state are achieved without time delay and misjudgment. Injection time of 3 s per embryo can be achieved, i.e. 20 embryos/min. The injection speed is much quicker than the manual injection speed of about 8-15 embryos/min. In common practical experiments, the cell number to be processed generally is about 300-500. The improvement of the cell manipulation speed can reduce the individual difference effectively for practical applications, such as drug development and gene therapy.
Further improvement of the proposed injection system will be focused on higher-throughput automatic cell injection and force sensor resolution.
Experimental results confirm the superiority of the force control vs. conventional position control in the cell injection system. Despite the difference size between the commonly used objects in biological injection experiments, this proposed system can be easily applied to other cell injection applications, such as mouse oocytes, graine, and other types of suspended cells.
To demonstrate the superiority of the developed system over skilled human operator, practical experimental studies have been conducted. Different from the previous experimental study which mimics the material delivery process, the sgRNA and Cas9 mixture is injected into Zebrafish embryos for gene editing. In this work, the drug dose of 2.2 nL is injected to every cell. Zebrafish embryos are placed in parallel V-grooves in a petri dish, and the V-grooves are made from the 1.5% agarose gel. The petri dish is mounted on an XY stage, which is used along with the microscope. The tip diameter of the adopted injector is around 1 μm and the depth of injection is set as 700 μm.
In each experimental setup, a batch of 69 cells are injected by the automated microinjection system. For more convincing comparison, the same operation is also conducted by a skilled human operator who has more than three years' manual injection experience. The experiment has been repeated by 5 times. Results indicate that the developed microinjection system provides the average injection speed of 3.55 s per cell, which is 42% slower than the skilled manual speed of 2.50 s per cell. On the other hand, the results reveal that the automated system achieves the average cell viability of 46.0%, which is 18% higher than the manual operation result of 39.0%. Moreover, concerning the cell viability, the standard deviation of the microinjection system's result is 0.37, which has been reduced by 91% in comparison with the manual operation result of 4.24.
Considering that the injection speed of the automated system can be greatly enhanced by employing multiple machines working in parallel, the developed microinjection system is superior to manual manipulation in terms of consistency and viability of the injected cells, which are the key indicators of the cell injection quality. Therefore, the experimental results confirm the effectiveness of the developed force-sensing microinjection system for multi-cell injection task. It is notable that the injection speed of the system can be improved by employing more advanced image acquisition and processing hardware.
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This application claims priority from provisional application 62/647947 filed on Mar. 26, 2018.
| Number | Date | Country | |
|---|---|---|---|
| 62647947 | Mar 2018 | US |
