- Open Access
Permanent magnet actuation for magnetic bead-based DNA extraction
© The Author(s) 2018
- Published: 6 November 2018
Recently, automatic molecular diagnostic devices to extract DNA have been extensively developed using magnetic beads. While various methods can be applied to the control of the beads, the efficiency of the control when incorporated in automatic devices has not been studied. This paper proposes a compact magnet actuation method for the control of magnetic beads for DNA extraction, and compares the efficiency to the already available magnetic bead-based DNA extraction device. A permanent magnet was preferred for its compactness, while an electro-magnet provides easy operation. After investigating various methods to actuate the magnet with perspective to the size, circuit complexity, and power requirement, we determined the solenoid actuation method to be most efficient. To further reduce the dimension of the overall actuation device, direct actuation of the permanent magnet to control the hold/release of the beads was employed in this paper. The proposed method was compared with the conventional solenoid actuator with a metal plunger. An experimental fluidics device was set up with a fluidic channel and a syringe pump. The bead holding performance against the fluid speed was tested while a fixed amount of beads was loaded into the center of the channel. The group velocity of the beads was analyzed via image processing to determine whether the magnet was sufficient to hold the beads. The required power and space was analyzed and compared qualitatively and quantitatively.
The proposed direct actuation method was capable of holding the beads at faster fluidic speed than the conventional solenoid actuator. The required power was comparable contemplating the high initial power of the solenoid actuator, and required much smaller space since no plunger was needed.
The direct actuation of the permanent magnet using a solenoid coil showed enhanced performance in holding the beads via permanent magnet, with less complexity of the actuation circuit and space. The proposed method therefore can efficiently improve the overall performance of the bead-based DNA extraction.
- DNA extraction
- Magnetic bead
- Permanent magnet
- Solenoid actuator
- Solenoid coil
Molecular diagnostics is widely adapted in various fields such as disease detection and health monitoring. This method evaluates the nucleic acids (e.g., DNA, RNA, or a variation of both) for human samples as well as bacteria or virus which are the causes of many diseases [1–6]. The process examines the nucleic acids to determine the status of diseases and investigate the agent responsible for the infections. Molecular diagnostics follows four basic steps of sample collection, gene extraction from the collected sample, gene amplification by polymerase chain reaction (PCR), and analysis. The gene amplification step enables the diagnosis to be extremely accurate with high sensitivity and specificity.
The gene extraction from the sample is one of the most critical steps in the vast majority of recently developed automated DNA analysis devices [4, 7–14]. Accordingly, various studies have focused on methods to improve the efficiency of gene extraction, including the magnetic-bead based DNA extraction [3, 7, 8, 15]. Many automatic equipments for DNA analysis purpose adopted this technique due to its advantages of automation and application. Magnetic beads are widely used not only in DNA analysis, but also in diverse biochemical analysis using fluidics owing to the facile control of magnet beads with a magnetic force [4, 10, 12, 16–20].
In most researches, a permanent magnet is placed in close proximity to the region of interest in the microfluidic pathway to generate magnetic force to control the magnet beads [3, 16]. For the magnetic bead based extraction to be employed in automated devices, an electromagnet or a permanent magnet with an actuator is required to enable the binary operation of hold/release of the beads. Following the interest of end users that requests biochemical analysis equipments to be more compact and portable, we determined that a permanent magnet to be more suitable in improving the devices. An electromagnet is disadvantageous in regards to dimension since it becomes larger to produce the magnetic force comparable to a permanent magnet. By placing the permanent magnet in proximity to the beads by utilizing a motor or a solenoid actuator will efficiently decrease the size of the device. Although servo or stepper motors can be considered as an alternative, it has no advantage over a solenoid actuator with respect to the system complexity and the required space. For motors to be employed in a magnetic bead based extraction equipment, it requires an additional step for setting the home position upon assembly, and the control software of a stepper motor is also relatively complicated, when only the binary operation such as the hold/release of magnetic beads is required. Hence, this study focuses on the solenoid actuation methods for compact and portable analysis equipments.
While commercial solenoid actuators embed metal plungers, a permanent magnet can provide more advantages such as a relatively larger magnetic force and faster response [21, 22]. This paper proposes a direct actuation of the permanent magnet using a solenoid coil without the need of a metal plunger. Since the permanent magnet will be the plunger of the solenoid actuator, this method will reduce the space required to a great extent. However, the performance of the permanent magnet actuation via solenoid coil needs to be determined since the interaction between the permanent magnet and exposed magnetic force of the solenoid coil might effect the generated magnetic field that controls the magnetic beads.
The solenoid actuator with a metal plunger (solenoid actuator from hereafter) generates the largest force when the metal plunger is completely inserted . Therefore, the power consumption can be minimized by inserting the metal plunger completely when holding the beads and removing it completely for release. This can be realized with a push-type solenoid actuator where the metal plunger is out of the solenoid coil using a spring in the release position. However, this type of solenoid actuator requires initial high current when actuated to the hold position due to the low force generated when the plunger is out of the solenoid coil. Consequently, a two-step circuit that can lower the initial current and prevent the solenoid actuator from being heated when the plunger is inserted to reach the hold position is required. In contrast, if a permanent magnet is driven directly with a solenoid coil, this two-step circuit is not required and can be implemented with a simple switch.
The distribution of the magnetic field can be analyzed through simulation or measurement to investigate the interaction of the permanent magnet and the solenoid coil [21, 24]. This study focuses on comparing the bead-holding performances of the two methods through a fluidic channel emulator . The bead movement according to the fluidic velocity is analyzed using image processing to determine to what speed the magnetic force can efficiently hold the beads. We also performed a visual inspection of the bead movement to verify the image processing results. The experimental results indicate that directly actuating a permanent magnet with a solenoid coil is more advantageous over a solenoid actuator.
The beads and permanent magnet used in this study were obtained from a commercial DNA extraction kits (MagAttract Suspension G, Qiagen, Germany). The procedure was repeated for various fluidic speeds. Since this study aimed to assess the bead-holding performances when the permanent magnet was actuated by the solenoid actuator to that of an independent solenoid coil, the solenoid coil used in the proposed method was obtained by disassembling the control subject (i.e., solenoid actuator, M060160H, Shindengen, Japan). The experiment procedure was as follows: loading the 9 μl bead solution at the channel center while the silicon channel is placed on the acrylic base; assembling the cover and the aluminum plates; and recording the bead movement using an industrial video camera (Chameleon, Point Grey Research, Inc., USA) while pumping the fluids with the syringe at a given velocity.
The initial release position was determined to be 10 mm away from the acrylic base of the fluidic emulator, which is twice as far from the distance where the fluidic emulator showed no influence on the magnetic beads at the fluid speed of 100 mm/s.
The consumption power of the solenoid actuator and the solenoid coil to maintain the magnet at the hold position (10 mm from the actuators) was measured, and the solenoid coil consumed more power by 25%, with 144 mW and 180 mW for the solenoid actuator and the solenoid coil, respectively. However, taking into consideration that the solenoid actuator was twice as long, the power consumption of the solenoid coil is comparable to the actuator with twice more windings of coil. In electromagnet theory, the magnetic field and force generated by a solenoid is correlative to the length and number of windings a solenoid has. Therefore the power required for the solenoid coil to maintain the holding distance can be further reduced by increasing the winding of the coil.
The linear relationship between the motor jogging speed and the fluidic velocity was investigated to ensure that the acceleration of the motor drive did not influence the velocity of the fluid. The coefficient of determination (R2) of 0.9975 was obtained verifying the linearity of the motor jogging speed and fluid velocity, and that the number of the missing steps and the accelerating time of the stepper motor could be ignored.
In this study, we discovered that directly actuating a permanent magnet with a solenoid coil was more efficient in holding magnetic beads in position than the conventional solenoid actuator. The magnetic force generated by the solenoid coil seemed to bring a synergistic effect with the magnetic force of the permanent magnet. In contrast, the solenoid actuator lost its performance efficiency due to the housing of the metal plunger that interrupted the magnetic force generated by the coil.
To confirm that the electromagnet needs more space as stated in the instruction, the bead holding performance of the electromagnet tested by locating the solenoid coil at the bottom of fluidic emulator and driving it with the allowed maximum power (4 W). But it could not hold the bead even at the velocity of 100 mm/s.
The proposed method in this study will aid significantly in the improvement of not only the magnetic bead based DNA extraction devices, but also any magnetic bead based microfluidic devices, by simplifying and reducing the size of the equipment as well as reducing the cost since it does not require a solenoid actuator. The image processing analysis employed in our study can also be applied to any bead-based biochemical application.
This study qualitatively and quantitatively compared the permanent magnet-driving methods used to extract DNA using magnetic beads. We compared the existing method of using a metal plunger paired with a solenoid coil and the proposed method of directly actuating the magnet with a solenoid coil through image processing. The experimental results showed that the solenoid coil had higher performance in holding the magnetic beads in position compared to the solenoid actuator. From our study, it can be concluded that the actuation of the magnet using a solenoid coil is advantageous in terms of the complexity of actuation circuits, required space, and holding performance than the conventional solenoid actuator.
Authors’ contributions CP and YP carried out the studies. YK, HS, JK participated in its design and coordination and helped to draft the manuscript. JK conceived the study. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Availability of data and materials
All data analyzed during this study are included in this published article.
Consent for publication
Ethics approval and consent to participate
This material is based upon work supported by the Ministry of Trade, Industry & Energy (MOTIE, Korea) under Industrial Technology Innovation Program. No. 10052106, ‘Development of CMOS/MEMS hybrid biosensor array platform, and the publication charge was also funded by this program.
About this supplement
This article has been published as part of BioMedical Engineering OnLine Volume 17 Supplement 2, 2018: Proceedings of the International Conference on Biomedical Engineering Innovation (ICBEI) 2016. The full contents of the supplement are available online at https://biomedical-engineering-online.biomedcentral.com/articles/supplements/volume-17-supplement-2.
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