This application claims the priority benefit of China application serial no. 202310232473.3, filed on Mar. 6, 2023 and China application serial no. 202310232480.3, filed on Mar. 6, 2023. The entirety of each of the above-mentioned patent applications is hereby incorporated by reference herein and made a part of this specification.
The disclosure belongs to the technical field of magnetic robotics and capsule robotics, and in particular, relates to a magnetically driven capsule robot with controllable drug administration and sampling functions and a fabrication method thereof.
The gastrointestinal (GI) tract, a major hormone-producing organ in the body, is implicated in various clinical disorders including inflammation, ulcers, hemorrhage, and cancers. However, the most commonly used flexible endoscopy faces significant limitations necessitating urgent innovative solutions: while it allows for both diagnosis and treatment integration, it often causes intense discomfort and has contraindications.
Integrating traditional capsules with energy-driven micro-robotics, particularly using magnetic actuation, offers promising solutions for diagnostic and therapeutic challenges. This method has significant advantages such as non-contact, high controllability, and good penetration performance, making it one of the safest and most efficient options for capsules.
An encouraging advancement in this area for GI disease diagnosis is magnetic capsule endoscopy, which has bolstered confidence in the development and biomedical applications of magnetically driven capsules. However, current magnetic capsule endoscopy is limited as it primarily focuses on image acquisition and transmission without additional diagnostic or treatment capabilities.
While certain progress has been made in developing new magnetically driven capsules for drug delivery or sampling purposes, the inherent constraints of the capsule's narrow spatial structure and the complex environment of the GI tract give rise to several ongoing challenges. These include issues such as limited active mobility, complex structure and control, and constrained medical functionalities.
In view of the defects found in the related art, the disclosure aims to provide a magnetically driven capsule robot with both controllable drug administration and sampling functions and a fabrication method thereof, so as to solve the problems of limited medical functions, low administration efficiency, complex capsule structure, and complex control found in a magnetically driven capsule robot provided by the related art.
To achieve the above, the disclosure provides a magnetically driven capsule robot including a robot body and a magnetic field-driven control module.
The robot body includes a capsule shell, and two ends of the capsule shell are provided with hollow air chambers. A carrier chamber is disposed between the hollow air chambers, and the carrier chamber and the hollow air chambers are isolated from each other.
A substance transfer channel, a magnetic lock disposed around the substance transfer channel, and a soft switch valve matched with the magnetic lock are disposed on a side wall of the carrier chamber. The soft switch valve is a magnetized magnetic soft switch valve. The substance transfer channel is provided to allow transfer or exchange of substances between the carrier chamber and the external environment when the magnetic soft switch valve is opened. The magnetic lock and the magnetized magnetic soft switch valve are matched through a magnetic attraction force to keep the magnetic soft switch valve in a closed state, so as to ensure that the carrier chamber is isolated from the external environment when the magnetically driven capsule robot is not working.
The magnetic field-driven control module is configured to apply a magnetic torque to the magnetized magnetic soft switch valve under an action of an external magnetic field excitation source to open or close the magnetic soft switch valve.
Preferably, the substance transfer channel is one or a plurality of openings located on a side wall of the capsule shell and protruding toward the inside or outside of a capsule. A magnetic lock recess is formed between a periphery of the opening and the side wall of the capsule shell, and the magnetic lock recess is provided to fix the magnetic lock. When the magnetic soft switch valve is in a closed state, the magnetic soft switch valve covers surfaces of the magnetic lock and the substance transfer channel and is configured to close the substance transfer channel to isolate the carrier chamber from the external environment. The magnetic soft switch valve is able to deform when being controlled by the magnetic field-driven control module to cause the substance transfer channel to reach an open state and to allow transfer or exchange of substances between the carrier chamber and the external environment.
Preferably, a magnetization direction of the magnetized magnetic soft switch valve is unidirectional magnetization or symmetrical magnetization with both ends in opposite directions. During use, a magnetic torque is applied to the magnetized magnetic soft switch valve under the action of the external magnetic field excitation source, so that the magnetized magnetic soft switch valve is deformed under an action of a magnetic torque, and that the magnetic soft switch valve is opened.
Preferably, the external magnetic field excitation source is a permanent magnet or an electromagnetic coil (such as Helmholtz coil).
Preferably, the carrier chamber includes two or more independent and mutually isolated sub-carrier chambers. A side wall of each of the sub-carrier chambers is provided with the substance transfer channel, the magnetic lock disposed around the substance transfer channel, and the magnetic soft switch valve matched with the magnetic lock, so that multi-channel transfer or exchange of substances is achieved.
According to another aspect of the disclosure, the disclosure further provides a fabrication method of the magnetically driven capsule robot, and the method includes the following steps.
To sum up, the above technical solutions provided by the disclosure have the following beneficial effects compared with the related art.
In order to make the objectives, technical solutions, and advantages of the disclosure clearer and more comprehensible, the disclosure is further described in detail with reference to the drawings and embodiments. It should be understood that the specific embodiments described herein serve to explain the invention merely and are not used to limit the invention.
The disclosure provides a magnetically driven capsule robot including a robot body and a magnetic field-driven control module. Herein, the robot body includes a capsule shell, and two ends of the capsule shell are provided with hollow air chambers. A carrier chamber is disposed between the hollow air chambers disposed on the two ends, and the carrier chamber and the hollow air chambers are isolated from each other. A substance transfer channel, a magnetic lock disposed around the substance transfer channel, and a magnetic soft switch valve matched with the magnetic lock are disposed on a side wall of the carrier chamber. The magnetic soft switch valve is a magnetized magnetic soft switch valve. The substance transfer channel is provided to allow transfer or exchange of substances between the carrier chamber and the external environment when the magnetic soft switch valve is opened. The magnetic lock and the magnetized magnetic soft switch valve are matched through a magnetic attraction force to keep the magnetic soft switch valve in a closed state, so as to ensure that the carrier chamber is isolated from the external environment when the magnetically driven capsule robot is not working.
The magnetic field-driven control module is configured to apply a magnetic torque to the magnetized magnetic soft switch valve under an action of an external magnetic field excitation source to open or close the magnetic soft switch valve. When working, when the magnetic soft switch valve is opened, transfer or exchange of substances may be carried out between the carrier chamber and the external environment through the substance transfer channel.
In some embodiments, the capsule shell is fabricated using light-curing 3D printing technology, and various printing methods may be used. For instance, the capsule shell may be divided into two parts: a base and a top cover, which are printed separately and then are obtained through assembly. The capsule shell is made of medical rubber, medical plastic, and other materials that exhibit good biological safety and are not affected by gastrointestinal environments such as gastric acid. For instance, MED610, transparent non-fluorescent resin materials, etc. may be used.
In the magnetically driven capsule robot provided by the disclosure, the robot body includes the capsule shell, and the two ends of the capsule shell are provided with the hollow air chambers. The carrier chamber is disposed between the hollow air chambers disposed on the two ends, and both the carrier chamber and the hollow air chambers are isolated. The carrier chamber is located inside the capsule shell. When the magnetic soft switch valve is in a closed state, the carrier chamber is a closed space, and this space is used either for the storage of drug solutions or for storing sampling tissue. The substance transfer channel disposed the magnetically driven capsule robot provided by the disclosure acts as a drug or tissue fluid exchange window between the internal carrier chamber and the external environment. In this way, when the magnetic soft switch valve is opened, a drug in the carrier chamber may reach a lesion area through the substance transfer channel, or the tissue fluid in a target area may enter the carrier chamber to achieve the function of sampling.
In some embodiments, the substance transfer channel is one or a plurality of openings located on a side wall of the capsule shell and protruding toward the inside or outside of a capsule. A magnetic lock recess is formed between a periphery of the opening and the side wall of the capsule shell, and the magnetic lock recess is provided to fix the magnetic lock. When the magnetic soft switch valve is in a closed state, the magnetic soft switch valve covers surfaces of the magnetic lock and the substance transfer channel and is configured to close the substance transfer channel to isolate the carrier chamber from the external environment. The magnetic soft switch valve is able to deform when being controlled by the magnetic field-driven control module to cause the substance transfer channel to reach an open state and to allow transfer or exchange of substances between the carrier chamber and the external environment.
In some embodiments, a magnetization direction of the magnetized magnetic soft switch valve is unidirectional magnetization or symmetrical magnetization with both ends in opposite directions, so as to facilitate the control of opening and closing of the magnetic soft switch valve. During use, a magnetic torque is applied to the magnetized magnetic soft switch valve under the action of the external magnetic field excitation source, so that the magnetized magnetic soft switch valve is deformed under an action of a magnetic torque, and that the magnetic soft switch valve is opened.
In some embodiments, when the magnetization direction is unidirectional magnetization in one direction, the deformation is a side opening with one end tilted. When the magnetization direction is symmetrical magnetization with opposite directions at both ends, the deformation is curling from both ends to the middle.
In some embodiments, a pulse magnetization module is used to magnetize the magnetic soft switch valve, and the pulse magnetization module may include a pulse power supply, a magnetizing coil, a discharge capacitor, a discharge switch, a freewheeling circuit, and a magnetization mold. Herein, the pulse power supply is configured to provide oscillation attenuation or a sinusoidal half-wave pulse current for the magnetizing coil. The magnetizing coil is configured to magnetize the magnetic soft switch valve. The discharge capacitor is configured to store electrical energy. The discharge switch is configured to trigger and turn on a discharge circuit, so that a pulse current provided by the discharge capacitor is able to flow into the magnetizing coil. The freewheeling circuit includes a freewheeling diode and a freewheeling resistor for adjusting a current waveform. The magnetization mold is configured to fix the magnetic soft switch valve. When the pulse magnetization module is working, the magnetization mold provided with the magnetic soft switch valve is disposed inside the magnetizing coil. When oscillation attenuation or a sinusoidal half-wave pulse current is introduced into the magnetizing coil, a strong pulse magnetic field is generated in an internal space of the magnetizing coil, so that the magnetic soft switch valve arranged inside the magnetization mold is subjected to non-oscillating magnetizing or oscillating de-magnetizing. Herein, when the freewheeling resistance is small (can be as low as 0), a discharge current has a non-oscillating waveform, and after flowing into the coil, the discharge current can generate a non-oscillating magnetic field for magnetizing the magnetic soft switch valve. The magnetic lock and the magnetic soft switch valve constitute a switch of the magnetically driven capsule robot of the disclosure, and both of them are made of magnetic materials.
The magnetic soft switch valve is made of a permanent magnet material at the micron scale and below (e.g., NdFeB, CrO2 and other magnetic particles) and a soft material (e.g., silica gel, a TPE material, hydrogel, and other materials with elastic modulus below GPa), and is a magnetic soft composite material. The magnetic lock is made of a permanent magnet material at the micron scale and below and a non-magnetic material (e.g., silica gel, a TPE material, hydrogel, etc.). Since the magnetic lock does not require to be deformed, the selection range of both the permanent magnet material and the non-magnetic material is wider. In addition to NdFeB magnetic particles, the permanent magnet material may also be ferromagnetic particles. The non-magnetic material may be a soft material or a hard material. In some embodiments, a pre-prepared mixed solution of the magnetic lock is evenly added to a magnetic lock mold, placed in a constant temperature oven at 70° C. for solidification, and demoulded after it is completely solidified, and the fabricated magnetic lock is thus obtained. The fabrication of the magnetic soft switch valve is the same.
In the magnetically driven capsule robot of the disclosure, the magnetic lock is fixedly disposed in the magnetic lock recess on a periphery of the substance transfer channel. The surface of the magnetic lock is flush with the surface of the substance transfer channel, and the magnetic soft switch valve covers the surfaces of the magnetic lock and the substance transfer channel. The two are sealed and bonded together through magnetic attraction, thus sealing the substance transfer channel and isolating the carrier chamber from the external environment. There are two magnetic attraction modes between the magnetic lock and the magnetic soft switch valve. The magnetic lock can be magnetized or not. For instance, when the magnetic lock is made of a permanent magnet material, the magnetic lock does not need to be magnetized, so that a magnetic attraction force similar to an iron magnet may be formed between the magnetic lock and the magnetic soft switch valve. In a preferred embodiment, in order to further enhance the attraction force of the magnetic lock and the magnetic soft switch valve, the magnetic lock containing a magnetic material can be magnetized, so that an attraction effect similar to that of a permanent magnet is produced between the magnetic lock and the magnetized magnetic soft switch valve.
In some embodiments, the magnetizing coil is wound by flat copper wire, with a reinforcing material provided on its periphery, and the central area of its coil frame is hollow. In this way, when the pulse current flows through the magnetizing coil, a relatively uniform axial pulse magnetic field is generated in the central area to magnetize the magnetic soft switch valve.
In some embodiments, when symmetrically-reverse magnetization is performed on both ends of the magnetic soft switch valve through a mold method, the following steps are specifically included. The processed magnetic soft switch valve is folded symmetrically first, and then the folded magnetic soft switch valve is placed into a prefabricated magnetization mold groove. Finally, the entire magnetizing mold carrying the magnetic soft switch valve is placed in the magnetizing coil for overall axial magnetizing.
In some embodiments, the external magnetic field excitation source is a permanent magnet or an electromagnetic coil (such as Helmholtz coil).
In some embodiments, the external magnetic field excitation source applies a magnetic torque of 50 Hz or below and 100 mT or below to the magnetized magnetic soft switch valve, so that the magnetized magnetic soft switch valve is deformed under an action of a magnetic torque, and that the magnetic soft switch valve is opened.
In some embodiments, the carrier chamber includes two or more independent sub-carrier chambers. A side wall of each of the sub-carrier chambers is provided with the substance transfer channel, the magnetic lock disposed around the substance transfer channel, and the magnetic soft switch valve matched with the magnetic lock, so that multi-channel transfer or exchange of substances is achieved.
In a preferred embodiment, the carrier chamber includes sub-carrier chambers disposed symmetrically up and down and thus is symmetrically provided with the substance transfer channels, the magnetic locks disposed around the substance transfer channels, and the magnetic soft switch valves matched with the magnetic locks. In this way, bilateral transfer or exchange of substances may be achieved, making it possible to mix multiple drugs.
The disclosure further provides a fabrication method of the magnetically driven capsule robot, and the method includes the following steps.
In some embodiments, the magnetic lock is embedded into the magnetic lock recess formed by the periphery of the substance transfer channel and the side wall of the capsule shell to be fixed. To be specific, in the magnetically driven capsule robot provided by the disclosure, the substance transfer channel disposed on the capsule shell may be one or a plurality of openings located on the side wall of the carrier chamber of the capsule shell and protruding toward the inside of the capsule or may be one or a plurality of openings located on the side wall of the carrier chamber protruding toward the outside of the capsule. When the opening is configured to protrude inwards, the periphery of the opening and an inner wall of the capsule shell form the magnetic lock recess, and the magnetic lock is embedded into the magnetic lock recess formed by the periphery of the substance transfer channel and the inner wall of the capsule shell to be fixed. When the opening is configured to protrude outwards, the periphery of the opening and an outer wall of the capsule shell form the magnetic lock recess, and the magnetic lock is embedded into the magnetic lock recess formed by the periphery of the substance transfer channel and the outer wall of the capsule shell to be fixed.
In some embodiments, in step (2), the discharge capacitor in the pulse magnetization module is charged first, and then the discharge switch is triggered to discharge the magnetizing coil. A uniform axial magnetic field is generated in the central area of the coil to axially fully magnetize the folded magnetic soft switch valve placed in the magnetization mold, and a magnetic soft switch valve with reversely symmetrical magnetization distribution at both ends is thus obtained.
In some embodiments, in order to improve the controllability of the magnetic soft switch valve, the magnetizing voltage of the pulse power supply may be increased to ensure that the magnetized magnetic soft switch valve has higher residual magnetization characteristics, so that the breaking capacity of the magnetic soft switch valve is improved.
A method of using the magnetically driven capsule robot provided by the disclosure to perform controllable drug administration specifically includes the following steps. When the magnetically driven capsule robot containing a drug reaches the lesion, the drug is not released due to the magnetic attraction force of the magnetic lock to the magnetic soft switch valve. Herein, the external magnetic field excitation source is used to apply a magnetic field outside the human body, so that both ends of the magnetic soft switch valve are acted upon by the magnetic torque. The magnetic soft switch valve opens to release the drug solution to the lesion for administration. When the drug release is completed or the drug reaches the released amount, the magnetic field is reversed and drug administration is stopped. Further, the magnetic soft switch valve may also be repeatedly closed and opened by repeatedly changing the magnetic field direction of the external magnetic field excitation source in the magnetic field-driven control module, and the full release of the drug is thereby accelerated.
A method of sampling using the magnetically driven capsule robot provided by the disclosure includes the following steps. When the magnetically driven capsule robot reaches a sampling target area, the external magnetic field excitation source is used to apply a magnetic field outside the human body, causing both ends of the magnetic soft switch valve to bend and deform inward under the action of the magnetic torque. The substance transfer channel is opened, allowing tissue fluid in a designated area to enter the carrier chamber. When sufficient tissue fluid is extracted from the carrier chamber, the magnetic field of the magnetic field-driven control module is reversed, so that the magnetic soft switch valve is closed, and the sampling function of the designated area is thereby completed.
In the disclosure, when the magnetically driven capsule robot is used for controllable drug administration, the substance transfer channel is an administration channel, and the carrier chamber is a drug-carrying chamber. The magnetic soft switch valve provided therein is used to release the drug inside the magnetically driven capsule robot and is disposed between the administration channel and the drug-carrying chamber. When the magnetic soft switch valve is in a closed state, that is, the magnetic soft switch valve is affected by a magnetic attraction force of the magnetic lock, thereby ensuring that the drug inside the magnetically driven capsule does not exchange with the outside. When the external magnetic field of the magnetic field-driven control module acts, the magnetic torque experienced by the magnetic soft switch valve is greater than the magnetic attraction force generated by the magnetic lock. At this time, the magnetic soft switch valve changes from the closed state to an open state, so the drug in the drug-carrying chamber may reach the lesion area in the human body through the administration channel. Further, in order to accelerate the release of drugs within human tissues, the magnetic soft switch valve may be closed and opened by repeatedly changing the magnetic field direction of the magnetic field-driven control module. The flapping effect of the valve is used to accelerate the exchange of drug solution and internal tissue fluid of the human body, so that administration efficiency is improved to a significant extent.
On the other hand, if the magnetically driven capsule robot is used for active sampling, the function of the magnetic soft switch valve is to open the substance transfer channel when the magnetically driven capsule reaches the lesion area, tissue fluid in the designated area is thereby extracted. When the magnetic field-driven control module is not working, the magnetic soft switch valve is affected by the magnetic attraction force of the magnetic lock, thereby ensuring that the interior of the carrier chamber is isolated from the external environment. When the magnetic field-driven control module applies an external magnetic field, the magnetic soft switch valve bends and deforms inward due to the effect of magnetic torque, and the substance transfer channel opens, thereby allowing the tissue fluid in the designated area to enter the carrier chamber. When sufficient tissue fluid is extracted from the carrier chamber, the external magnetic field of the magnetic field-driven control module is reversed, so that the magnetic soft switch valve is closed, and the sampling function of the designated area is thereby completed.
In the disclosure, the methods used by the magnetically driven capsule robot to achieve site-specific administration and sampling may be achieved by using imaging equipment assistance, magnetic positioning, or gastrointestinal motility timing monitoring, and other methods conventionally used in the art to achieve site-specific administration.
In the disclosure, the internal system structure and the method of regulating the magnetically driven capsule are simple. The on-demand and targeted administration and sampling functions of the magnetically driven capsule are cleverly achieved through the bidirectional magnetic control of the magnetic attraction force and the magnetic torque. Further, the administration progress may be accelerated and slowed down by controlling the amplitude and frequency of the external excitation field current. Besides, the double-sided administration channel design provides the possibility of window opening in any magnetic field direction and on-demand mixed administration of multiple drugs. Combined with the advantages of strong magnetic control penetrating ability and unrestricted area of action, the magnetically driven capsule robot provided by the disclosure provides a new technical path for the multi-functionalization of the capsule robots.
In some embodiments, as shown in
As shown in (a) of
In some embodiments, the pulse magnetization module as shown in
The structural schematic diagram of the magnetically driven capsule robot fabricated in the experiment before releasing the drug and after releasing the drug is respectively shown in (c) and (d) of
In some embodiments, the external magnetic field 8 used in the magnetic field-driven control module to open and close the magnetic soft switch valve is generated by the electromagnetic coil. Preferably, when the magnetically driven capsule robot reaches the designated location and needs to release the drug, a sinusoidal pulse current is introduced into the electromagnetic coil, an oscillating magnetic field with alternating directions is thereby generated to repeatedly open and close the magnetic soft switch valve. At the same time, the repeated oscillation of the magnetic soft switch valve causes the surrounding liquid to accelerate the flow, and the drug release efficiency is thereby further accelerated.
In some embodiments, the magnetically driven capsule robot is further designed into a double-sided administration channel. That is, in addition to providing the administration channel, the magnetic lock, and the magnetic soft switch valve on the base of the capsule shell, a corresponding set is also provided on the upper top cover. In
In some other embodiments, in order to verify the practicability of the magnetically driven capsule robot, its simulated administration experiment diagram is shown in
In some other embodiments, the abovementioned magnetically driven capsule robot is used for active sampling. When the magnetically driven capsule robot reaches the sampling target area, the external magnetic field excitation source is used to apply a magnetic field outside the human body, causing both ends of the magnetic soft switch valve to bend and deform inward under the action of the magnetic torque. The substance transfer channel is opened, allowing the tissue fluid in the designated area to enter the carrier chamber. When sufficient tissue fluid is extracted from the carrier chamber, the magnetic field of the magnetic field-driven control module is reversed, so that the magnetic soft switch valve is closed, and the sampling function of the designated area is thereby completed.
The above results fully prove that in the disclosure, through the bidirectional magnetic control of the magnetic attraction force and the magnetic torque, the on-demand and site-specific administration and sampling functions of the magnetically driven capsule can be achieved. The structure of the administration device is simple and lightweight. The magnetically driven capsule may be opened and closed remotely and repeatedly through an alternating magnetic field. Advantages such as wireless driving and strong controllability are provided, so the disclosure exhibits potential medical values.
A person having ordinary skill in the art should be able to easily understand that the above description is only preferred embodiments of the disclosure and is not intended to limit the disclosure. Any modifications, equivalent replacements, and modifications made without departing from the spirit and principles of the disclosure should fall within the protection scope of the disclosure.
Number | Date | Country | Kind |
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202310232473.3 | Mar 2023 | CN | national |
202310232480.3 | Mar 2023 | CN | national |