WO2010128418A1 - Arrangement and method for heating of a magnetic material - Google Patents
Arrangement and method for heating of a magnetic material Download PDFInfo
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- WO2010128418A1 WO2010128418A1 PCT/IB2010/051699 IB2010051699W WO2010128418A1 WO 2010128418 A1 WO2010128418 A1 WO 2010128418A1 IB 2010051699 W IB2010051699 W IB 2010051699W WO 2010128418 A1 WO2010128418 A1 WO 2010128418A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/05—Detecting, measuring or recording for diagnosis by means of electric currents or magnetic fields; Measuring using microwaves or radio waves
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/05—Detecting, measuring or recording for diagnosis by means of electric currents or magnetic fields; Measuring using microwaves or radio waves
- A61B5/0515—Magnetic particle imaging
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/40—Applying electric fields by inductive or capacitive coupling ; Applying radio-frequency signals
- A61N1/403—Applying electric fields by inductive or capacitive coupling ; Applying radio-frequency signals for thermotherapy, e.g. hyperthermia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N2/00—Magnetotherapy
- A61N2/02—Magnetotherapy using magnetic fields produced by coils, including single turn loops or electromagnets
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01R—MEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
- G01R33/00—Arrangements or instruments for measuring magnetic variables
- G01R33/12—Measuring magnetic properties of articles or specimens of solids or fluids
- G01R33/1276—Measuring magnetic properties of articles or specimens of solids or fluids of magnetic particles, e.g. imaging of magnetic nanoparticles
Definitions
- the present invention relates to an arrangement and a corresponding method for heating of a magnetic material located in the centre region of an inscribed sphere within a region of action. Further, the present invention relates to a computer program.
- An arrangement of this kind is known from WO 2004/018039 Al, which particularly describes a system and method for the local heating of a target region of an object by varying the magnetization of magnetic or magnetizable substances.
- a magnetic field is generated whose magnetic field strength varies in space in such a manner that a first sub-region of low magnetic field strength and a second sub-region which encloses the first sub-region and has a higher magnetic field strength are formed in the target region (also called region of action).
- the position in space of the two sub-regions in the target region is varied with a given frequency for so long that the particles are heated to a desired temperature due to frequent variation of the magnetization.
- MPI Magnetic Particle Imaging
- Gleich, B. and Weizenecker, J. (2005) "Tomographic imaging using the nonlinear response of magnetic particles” in Nature, vol. 435, pp. 1214-1217.
- the arrangement and method for magnetic particle imaging (MPI) described in that publication takes advantage of the non- linear magnetization curve of small magnetic particles. Signals are recorded which are dependent on the magnetization in the examination zone, which magnetization has been influenced by the shift in the position in space of the sub-zones, and information concerning the spatial distribution of the magnetic particles in the examination zone is extracted from these signals, so that an image of the examination zone can be formed.
- Such an arrangement has the advantage that it can be used to examine arbitrary examination objects - e. g.
- Magnetic hyperthermia stands for a local heating effect that can lead to apoptosis of tumor cells (thermoablation) if the local temperature exceeds the window 42-45 0 C.
- thermalablation apoptosis of tumor cells
- local moderate heating may result in an increase in efficacy of the combined method.
- Local heating can be realised due to the presence of magnetic nanoparticles in tumor cells or in close vicinity thereof. Magnetic nanoparticles are usually administered intratumorally.
- an arrangement for heating of a magnetic material located in the centre region of an inscribed sphere within a region of action is presented that comprises:
- - selection means for generating a magnetic selection field having a pattern in space of its magnetic field strength such that a first sub-zone having a low magnetic field strength and a second sub-zone having a higher magnetic field strength are formed in the region of action
- - drive means for changing the position in space of the two sub-zones in the region of action by means of a magnetic drive field so that the magnetization of the magnetic material changes locally
- - control means for controlling the drive means to change the position in space of the first sub-zone along a sequence of locations around said inscribed sphere for so long and with such a frequency that the centre region of said inscribed sphere is heated.
- a computer program comprising program code means for causing a computer to control an arrangement according to the present invention to carry out the steps of the method according to the present invention when said computer program is carried out on the computer.
- the present invention is based on the following considerations and recognitions.
- Typical values used in hyperthermia experiments are: particle size 10-25 nm, frequency 400 kHz, amplitude 10 kA/m
- hyperthermia is its compatibility with magnetic particle imaging with an operational base frequency of 25 kHz.
- a first option is to move to higher frequency to generate more heat per unit time.
- MPI to scale to higher frequency which results in a loss of signal generation due to the necessity of a lower effective anisotropy in relevant particles.
- a second option would be to move to higher amplitude, however it is known that for the frequency range of MPI, i.e. 25 kHz, there is a strong contribution of Brownian motion in the complex susceptibility, which does not increase as soon as a minimal field amplitude threshold is overcome.
- magnetic hyperthermia looses its ability to be a focal technology for too high an amplitude. It is to be noted that 10 rnT is the envisioned full field swing in a complete imaging volume. Hence field values should be reduced rather than increased.
- the present invention relies primarily on the Brownian rotational degree of freedom of suspended magnetic particles.
- a sequence of the spatial positions of the field free point (FFP; corresponds to the first sub-zone having a low magnetic field strength) as a function of time can be defined, that is able to rotate the cumulative magnetic vector in a particular area, in particular in the centre region, in a concerted way.
- FFP field free point
- Such a fundamental sequence is revolving around the defined area in which magnetic particles are present and where eventually the heating effect will be focused. Heating power will scale with the revolving frequency of the particles.
- a family of revolving focal heating sequences (in particular for MPI, whereby receiving means for signal detection and processing means for image generation from said detection signals are not necessarily required) are proposed that allow for a very local heating, for instance for focal cancer therapy.
- a revolving sequence is defined as the spatial position of the field free point as function of time. Suppose that this position is located on a sphere with the magnetic material in its origin. In 3D space the field free point 'spins' around the magnetic material in a fashion comparable to an electron spinning around its nucleus. Due to the fact that the magnetic material is now exposed to a constant magnetic field that is continuously changing its direction, i.e. in the direction opposite to the field free point, the magnetization vector will (try to) align to this field.
- the effective magnetic field strenght is a function of the gradient field in MPI and the radius of the revolving sphere.
- magnetic particle assays are optimised to favour Brownian particle rotation, either from chemical synthesis or physical fractionation. This is preferably achieved by nanoparticles that are thermally blocked.
- superparamagnetism is the fundamental effect behind e.g. MRI contrast agents. If the magnetic core diameter and/or magnetic anisotropy increases, which is physically equivalent to an increase of the "energy" equal to the product K. V to be compared to the thermal energy k.T, the magnetization may become thermally blocked. In fact, this means that Neel internal realignment is no longer possible and
- MPI has been turned into an excellent method to provide and focus optimal heating conditions locally by revolving sequence design. This prevents a high degree of fractionation in the treatment to be delivered, which is essential for optimal workflow.
- control means is adapted for controlling the drive means to change the position in space of the first sub-zone along a two-dimensional sequence of locations, in particular along a circle, around said inscribed sphere.
- control means is adapted for controlling the drive means to change the position in space of the first sub-zone along a three-dimensional sequence of locations, in particular over a sphere, around said inscribed sphere.
- One main advantage of a two-dimensional trajectory is a simple control scheme with only two currents.
- One main advantage of a three-dimensional trajectory is that the circular revolution can be modulated over the third dimension.
- control means is adapted for controlling the drive means to change the position in space of the first sub-zone with constant angular velocity.
- the magnetization vector would be continuously rotating with constant angular velocity, which leads to optimal heating efficiency.
- control means is adapted for controlling the drive means to change the position in space of the first sub-zone with a frequency in the range from 1 to 100 kHz, in particular in the range from 10 to 30 kHz.
- frequencies will be used that match MPI imaging so that a system can be switched from imaging mode to heating mode.
- the characteristic time constant will be in the order of tens of micro-seconds which limits the frequency to tens of kHz.
- a frequency in the region of 25 kHz is a good compromise.
- the presence of the magnetic particles can be imaged or monitored before and/or after the heating experiment by the provision of receiving means for acquiring detection signals and processing means for reconstructing an image, as conventionally provided in an MPI arrangement.
- Instrumentational aspects such as operational frequency, field gradients and field amplitudes in MPI and hyperthermia treatment can now be comparable, so that all functions can be performed by use of the same arrangement.
- Preferred magnetic material comprises monodomain magnetic nanoparticles, in particular colloidally stabilised monodomain magnetic nanoparticles. Further preferred is that the monodomain magnetic nanoparticles, in particular the colloidally stabilised monodomain magnetic nanoparticles, are encapsulated into liposomes, polymersomes or vesicles having an inner volume of with viscosity equal or similar to that of water separated by a hydrophobic membrane, wherein the magnetic particles are arranged in the inner volume.
- Fig. 1 shows a schematic view of the principle layout of a magnetic particle imaging (MPI) arrangement
- Fig. 2 shows an example of the field line pattern produced by an arrangement according to the present invention
- Fig. 3 shows an enlarged view of a magnetic particle present in the region of action
- Figs. 4a and 4b show the magnetization characteristics of such particles
- Fig. 5 shows a block diagram of an embodiment of the apparatus according to the present invention
- Fig. 6 shows a diagram of an example of a two-dimensional sequence
- Fig. 7 shows a diagram of an example of a three-dimensional sequence
- Fig. 8 shows a diagram of another example of a three-dimensional sequence
- Fig. 9 shows a diagram illustrating a Gaussian distribution of a polydisperse material
- Fig. 10 shows a diagram illustrating power generation as function of magnetic core diameter.
- Fig. 1 shows an arbitrary object to be examined by means of a MPI arrangement 10.
- the reference numeral 350 in Fig. 1 denotes an object, in this case a human or animal patient, who is arranged on a patient table 351, only part of the top of which is shown.
- magnetic particles 100 Prior to the application of the method according to the present invention, magnetic particles 100 (not shown in Fig. 1) are arranged in a region of action 300 of the inventive arrangement 10.
- the magnetic particles 100 are positioned in the region of action 300, e.g. by means of a liquid (not shown) comprising the magnetic particles 100 which is injected into the body of the patient 350.
- an arrangement 10 is shown in Fig. 2 comprising a plurality of coils forming a selection means 210 whose range defines the region of action 300 which is also called the region of treatment 300.
- the selection means 210 is arranged above and below the patient 350 or above and below the table top.
- the selection means 210 comprise a first pair of coils 210', 210", each comprising two identically constructed windings 210' and 210" which are arranged coaxially above and below the patient 350 and which are traversed by equal currents, especially in opposed directions.
- the first coil pair 210', 210" together are called selection means 210 in the following.
- direct currents are used in this case.
- the selection means 210 generate a magnetic selection field 211 which is in general a gradient magnetic field which is represented in Fig. 2 by the field lines. It has a substantially constant gradient in the direction of the (e.g. vertical) axis of the coil pair of the selection means 210 and reaches the value zero in a point on this axis. Starting from this field- free point (not individually shown in Fig. 2), the field strength of the magnetic selection field 211 increases in all three spatial directions as the distance increases from the field- free point.
- first sub-zone 301 or region 301 which is denoted by a dashed line around the field- free point the field strength is so small that the magnetization of particles 100 present in that first sub-zone 301 is not saturated, whereas the magnetization of particles 100 present in a second sub- zone 302 (outside the region 301) is in a state of saturation.
- the field-free point or first sub-zone 301 of the region of action 300 is preferably a spatially coherent area; it may also be a punctiform area or else a line or a flat area.
- the magnetic field strength is sufficiently strong to keep the particles 100 in a state of saturation.
- the (overall) magnetization in the region of action 300 changes.
- information about the spatial distribution of the magnetic particles in the region of action can be obtained.
- a further magnetic field, the so-called magnetic drive field 221 is superposed to the selection field 211 in the region of action 300 or at least in a part of the region of action 300.
- Fig. 3 shows an example of a magnetic particle 100 of the kind used together with an arrangement 10 of the present invention.
- a spherical substrate 101 for example, of glass which is provided with a soft-magnetic layer 102 which has a thickness of, for example, 5 nm and consists, for example, of an iron-nickel alloy (for example, Permalloy).
- This layer may be covered, for example, by means of a coating layer 103 which protects the particle 100 against chemically and/or physically aggressive environments, e.g. acids.
- the magnetic field strength of the magnetic selection field 211 required for the saturation of the magnetization of such particles 100 is dependent on various parameters, e.g. the diameter of the particles 100, the used magnetic material for the magnetic layer 102 and other parameters.
- a magnetic field of approximately 800 A/m (corresponding approximately to a flux density of 1 mT) is then required, whereas in the case of a diameter of 100 ⁇ m a magnetic field of 80 A/m suffices.
- Even smaller values are obtained when a coating 102 of a material having a lower saturation magnetization is chosen or when the thickness of the layer 102 is reduced.
- Another suitable material is, for instance, described in EP 1738773 and EP 1738774 where magnetic nanoparticles optimised for MPI have been described, i.e. colloidal Fe oxide based SPIO (i.e. superparamagnetic nanoparticles).
- Other suitable material comprises monodomain magnetic nanoparticles, in particular colloidally stabilised monodomain magnetic nanoparticles. Further preferred is that the monodomain magnetic nanoparticles, in particular the colloidally stabilised monodomain magnetic nanoparticles, are encapsulated into liposomes, polymersomes or vesicles having an inner volume of with viscosity equal or similar to that of water separated by a hydrophobic membrane, wherein the magnetic particles are arranged in the inner volume.
- the size of the first sub-zone 301 is dependent on the one hand on the strength of the gradient of the magnetic selection field 211 and on the other hand on the field strength of the magnetic field required for saturation.
- the first sub-zone 301 in which the magnetization of the particles 100 is not saturated has dimensions of about 1 mm (in the given space direction).
- a further magnetic field - in the following called a magnetic drive field 221 - is superposed on the magnetic selection field 210 (or gradient magnetic field 210) in the region of action 300
- the first sub-zone 301 is shifted relative to the second sub-zone 302 in the direction of this magnetic drive field 221; the extent of this shift increases as the strength of the magnetic drive field 221 increases.
- the superposed magnetic drive field 221 is variable in time, the position of the first sub-zone 301 varies accordingly in time and in space. It is advantageous to receive or to detect signals from the magnetic particles 100 located in the first sub-zone 301 in another frequency band (shifted to higher frequencies) than the frequency band of the magnetic drive field 221 variations. This is possible because frequency components of higher harmonics of the magnetic drive field 221 frequency occur due to a change in magnetization of the magnetic particles 100 in the region of action 300 as a result of the non-linearity of the magnetization characteristics.
- the second coil pair 220' generates a component of the magnetic drive field 221 which extends in the direction of the coil axis of the first coil pair 210', 210" or the selection means 210, i.e. for example vertically.
- the windings of the second coil pair 220' are traversed by equal currents in the same direction.
- the effect that can be achieved by means of the second coil pair 220' can in principle also be achieved by the superposition of currents in the same direction on the opposed, equal currents in the first coil pair 210', 210", so that the current decreases in one coil and increases in the other coil.
- the temporally constant (or quasi constant) selection field 211 also called gradient magnetic field
- the temporally variable vertical magnetic drive field are generated by separate coil pairs of the selection means 210 and of the drive means 220.
- the two further coil pairs 220", 220'" are provided in order to generate components of the magnetic drive field 221 which extend in a different direction in space, e.g. horizontally in the longitudinal direction of the region of action 300 (or the patient 350) and in a direction perpendicular thereto.
- third and fourth coil pairs 220", 220'" of the Helmholtz type like the coil pairs for the selection means 210 and the drive means 220
- these coil pairs would have to be arranged to the left and the right of the region of treatment or in front of and behind this region, respectively. This would affect the accessibility of the region of action 300 or the region of treatment 300.
- the third and/or fourth magnetic coil pairs or coils 220", 220'" are also arranged above and below the region of action 300 and, therefore, their winding configuration must be different from that of the second coil pair 220'.
- Coils of this kind are known from the field of magnetic resonance apparatus with open magnets (open MRI) in which an radio frequency (RF) coil pair is situated above and below the region of treatment, said RF coil pair being capable of generating a horizontal, temporally variable magnetic field. Therefore, the construction of such coils need not be further elaborated herein.
- This embodiment of the arrangement 10 according to the present invention further comprise receiving means 230 that are only schematically shown in
- the receiving means 230 usually comprise coils that are able to detect the signals induced by magnetization pattern of the magnetic particles 100 in the region of action 300. Coils of this kind, however, are known from the field of magnetic resonance apparatus in which e.g. a radio frequency (RF) coil pair is situated around the region of action 300 in order to have a signal to noise ratio as high as possible. Therefore, the construction of such coils need not be further elaborated herein.
- RF radio frequency
- receiving means 230 are not necessarily required to perform the desired method of the present invention. Only, if imaging in addition to the heating of a magnetic material 100 is desired, such receiving means 230 are to be provided in the arrangement.
- the selection means 210 shown in Fig. 1 permanent magnets (not shown) can be used to generate the gradient magnetic selection field 211. In the space between two poles of such (opposing) permanent magnets (not shown) there is formed a magnetic field which is similar to that of Fig. 2, that is, when the opposing poles have the same polarity.
- the selection means 210 comprise both at least one permanent magnet and at least one coil 210', 210" as depicted in Fig. 2.
- the frequency ranges usually used for or in the different components of the selection means 210, drive means 220 and receiving means 230 are roughly as follows:
- the magnetic field generated by the selection means 210 does either not vary at all over the time or the variation is comparably slow, preferably between approximately 1 Hz and approximately 100 Hz.
- the magnetic field generated by the drive means 220 varies preferably between approximately 25 kHz and approximately 100 kHz.
- the magnetic field variations that the receiving means are supposed to be sensitive are preferably in a frequency range of approximately 50 kHz to approximately 10 MHz.
- Figs. 4a and 4b show the magnetization characteristic, that is, the variation of the magnetization M of a particle 100 (not shown in Figs.
- Fig. 4a illustrates the effect of a sinusoidal magnetic field H(t) at the location of the particle 100 where the absolute values of the resulting sinusoidal magnetic field H(t) (i.e. "seen by the particle 100") are lower than the magnetic field strength required to magnetically saturate the particle 100, i.e. in the case where no further magnetic field is active.
- the magnetization of the particle 100 or particles 100 for this condition reciprocates between its saturation values at the rhythm of the frequency of the magnetic field H(t).
- the resultant variation in time of the magnetization is denoted by the reference M(t) on the right hand side of Fig. 4a. It appears that the magnetization also changes periodically and that the magnetization of such a particle is periodically reversed.
- the dashed part of the line at the centre of the curve denotes the approximate mean variation of the magnetization M(t) as a function of the field strength of the sinusoidal magnetic field H(t).
- the magnetization extends slightly to the right when the magnetic field H increases from -H c to +H C and slightly to the left when the magnetic field H decreases from +H C to -H c .
- This known effect is called a hysteresis effect which underlies a mechanism for the generation of heat.
- the hysteresis surface area which is formed between the paths of the curve and whose shape and size are dependent on the material, is a measure for the generation of heat upon variation of the magnetization.
- Fig. 5 shows a block diagram of the apparatus 10 shown in Fig. 1.
- the selection means 210 is shown schematically in Fig. 5.
- the selection means 210 are provided with three magnetic selection field generation means, in particular either coils, permanent magnets or a combination of coils and permanent magnets.
- Said three magnetic selection field generation means are preferably arranged such that for each spatial direction one magnetic selection field generation means is provided. If in an embodiment coil pairs are provided as magnetic selection field generation means, the coil pairs are supplied with a DC current from a controllable current source 32, said current source 32 being controlled by the control means 76.
- an overlaid current is overlaid to at least one of coil pairs, wherein the overlaid current of opposed coils is oppositely oriented.
- the control means 76 furthermore controls that the sum of the field strength and the sum of the gradient strength of all three spatial fractions of the selection field 211 is maintained at a predefined level. If in an embodiment permanent magnets are provided as magnetic selection field generation means instead of coil pairs, the current source 32 need to be exchanged by an actuation means 32', e.g. an electro motor, which is able to mechanically move the permanent magnets in order to set the gradient strength in the desired direction according to the control signals provided by the control means 76.
- an actuation means 32' e.g. an electro motor
- the control means 76 is in turn connected to a computer 12 which is coupled to a monitor 13 for displaying the distribution of magnetic particles in the examination area and an input unit 14, for example a keyboard.
- a user is therefore able to set the desired direction of the highest resolution and in turn receives the respective image of the region of action on the monitor 13. If the critical direction, in which the highest resolution is needed, deviates from the direction set first by the user, the user can still vary the direction manually in order to produce a further image with an improved imaging resolution.
- This resolution improvement process can also be operated automatically by the control means 76 and the computer 12.
- the control means 76 in this embodiment sets the gradient field in a first direction which is automatically estimated or set as start value by the user. The direction of the gradient field is then varied stepwise until the resolution of the thereby received images, which are compared by the computer 12, is maximal, respectively not improved anymore. The most critical direction can therefore be found respectively adapted automatically in order to receive the highest possible resolution.
- the coil pairs (second magnetic means) 220', 220", 220'” are connected to current amplifiers 41, 51, 61, from which they receive their currents.
- the current amplifiers 41, 51, 61 are in turn in each case connected to an AC current source 42, 52, 62 which defines the temporal course of the currents Ix, Iy, Iz to be amplified.
- the AC current sources 42, 52, 62 are controlled by the control means 76.
- the - not necessarily required - receiving coil (receiving means) is also shown schematically in Fig. 5.
- the signals induced in the receiving coil 230 are fed to a filter unit 71, by means of which the signals are filtered.
- the aim of this filtering is to separate measured values, which are caused by the magnetization in the examination area which is influenced by the change in position of the two part-regions (301, 302), from other, interfering signals.
- the filter unit 71 may be designed for example such that signals which have temporal frequencies that are smaller than the temporal frequencies with which the coil pairs 220', 220", 220"' are operated, or smaller than twice these temporal frequencies, do not pass the filter unit 71.
- the signals are then transmitted via an amplifier unit 72 to an analog/digital converter 73 (ADC).
- ADC analog/digital converter
- the digitalized signals produced by the analog/digital converter 73 are fed to an image processing unit (also called reconstruction means) 74, which reconstructs the spatial distribution of the magnetic particles from these signals and the respective position which the first part-region 301 of the first magnetic field in the examination area assumed during receipt of the respective signal and which the image processing unit 74 obtains from the control means 76.
- the reconstructed spatial distribution of the magnetic particles is finally transmitted via the control means 76 to the computer 12, which displays it on the monitor 13.
- the magnetization must be changed several times.
- the necessary number of changes that is, the frequency within a given time interval, and the associated temperature rise of the medium surrounding the particles in the heating region is dependent on the particle concentration, on the production of heat per change (which itself is dependent on the particle structure and the speed of the magnetic reversal), and the dissipation of heat in the regions surrounding the heating region.
- the control means 76 for controlling the drive means 220 are arranged to change the position in space of the first sub-zone 301 (FFP) along a sequence of locations around an inscribed sphere for so long and with such a frequency that the centre region of said inscribed sphere is heated.
- FFP first sub-zone 301
- Fig. 6 shows a two-dimensional continuous revolving sequence 400 of locations of the FFP 301 around the centre region 401 in which, for instance, a tumor is located and in which magnetic material 100 is placed.
- the inscribed sphere preferably has the same diameter as the circular sequence 400, but can also have a smaller diameter (but no larger diameter).
- the revolving sequence 400 is generated as function of time by a selection field with its field free point located at the position of in the magnetic material, superposed with AC fields.
- the combination of frequency and effective field Heff can be optimised according to a particular magnetic particle assay for maximum heat generation. Frequency and effective field can be tuned for maximum heat generation in a particular magnetic particle assay. The other way around, tuning the chemistry to make those particles, would be most difficult.
- the effective field is set by the gradient fields in the system and the diameter of the inscribing sphere along which the field free point is moved around. This effective field should be as large as possible but will be practically limited to ⁇ 5 - 10 - 20 mT.
- a continuous 3D sequence is used.
- More complex sequences can be used in 2D or 3D, as long as the inscribing feature corresponds to a the circle or sphere, respectively.
- Two examples include parametric 2D and 3D time paths 410, 420 as depicted in Figs. 7 and 8.
- the frequencies involved in the parametric path are preferably limited to a couple of base frequencies that only differ slightly (compare to COi and CO 2 mentioned above) as to not complicate design aspects in the instrumentation such as transmit and receive filters.
- the effective torque (or more generally speaking manipulation) of the magnetization vector of the magnetic particles 100 in the centre 401 is now modulated by a modulation in effective magnetic field in that location.
- This degree of freedom gives an additional parameter for optimization of frequency and effective field for maximum heat generation. It is to be noted once more that maximum heat generation is essential to maintain the implicit focus that has been created by the local presence of magnetic material.
- Effective duty-cycling as described here may be appropriate for magnetic particle assays that do not entirely match a particular operational frequency for MPI imaging.
- the common characteristic of all trajectories is that they comprise an inscribed sphere that is formed around the location of the tumor.
- the magnetization of any magnetic material in that location will have a revolving character.
- frequencies will be used that match MPI imaging so that a system can be switched from imaging mode to heating mode.
- the characteristic time constant will be in the order of tens of micro-second which limits the frequency to tens of kHz. Therefore 25 kHz is a good compromise.
- a specific example here could be the use of two contrast agents simultaneously.
- the first agent could be a standard blood pool agent for MPI in imaging mode, injected intravenously, whereas the second one is e.g. administered intratumorally, for treatment.
- the first agent will be present and may even slightly accumulate in or in the vicinity of the tumor, to highlight the position of the tumor, whereas the second one is within the time frame of the treatment fixed within the tumor. It is important in this case that any heating due to material of the first agent is kept to a minimum. It is preferred that the magnetic particles should essentially be unbound.
- Fig. 10 shows a diagram illustrating power generation as function of magnetic core diameter.
- X-axis shows the magnetic core diameter D; the Y-axis shows the fractional power loss per unit density Pi oss , calculated from the product of the power loss per unit density (W/g) and the intensity of distribution for a given magnetic core diameter.
- the integral under the curve gives the total power loss per unit density (W/g) for a material.
- the three curves correspond to Neel-only, Brown-only and a combination thereof (average). The term average relates to the weighing of the time
- volume V 1 is indicative for the magnetic core volume on which a magnetic torque is exerted.
- the magnetic anisotropy K, viscosity ⁇ and a hydrodynamic volume Vh 1 including dimensions of the magnetic core and the coating.
- the present invention can be favourably applied in magnetic hyperthermia or thermoablation for treatment of different cancers in e.g. prostate, breast or head/neck. It can also be applied in combination with other cancer treatment options such as brachy, chemo, radiation etc.
- hyperthermia where two fundamental modes exist. Either one aims for moderate heating at elevated temperature of 41°-43°C, during which hyperthermia is primarily meant to assist other treatment for better efficacy, or one aims for thermo-ablation at 45°-47°C, resulting in direct cell death or apoptosis with the risk of heating surrounding healthy tissue. Therefore for the latter case a fast temperature transient would be most appropriate.
- the simple answer on 'how long' would be as long as the treatment does require this elevated temperature. For instance, to support local brachytherapy (prostate) 1-hour fractions were used, to be repeated weekly.
- a sequence can be designed that is able to rotate the cumulative magnetic vector in a particular area in a concerted way.
- Such a fundamentally 3D sequence must be revolving around the defined area in which magnetic particles are present and where eventually the heating effect will be focused. Heating power will scale with the revolving frequency of the particles.
- a computer program may be stored/distributed on a suitable medium, such as an optical storage medium or a solid-state medium supplied together with or as part of other hardware, but may also be distributed in other forms, such as via the Internet or other wired or wireless telecommunication systems.
- a suitable medium such as an optical storage medium or a solid-state medium supplied together with or as part of other hardware, but may also be distributed in other forms, such as via the Internet or other wired or wireless telecommunication systems.
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- Magnetic Treatment Devices (AREA)
- Electrotherapy Devices (AREA)
- Thermotherapy And Cooling Therapy Devices (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
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CN201080020045.5A CN102421359B (en) | 2009-05-08 | 2010-04-19 | Arrangement and method for heating of a magnetic material |
US13/319,351 US9451900B2 (en) | 2009-05-08 | 2010-04-19 | Arrangement and method for heating of a magnetic material |
JP2012509119A JP5750098B2 (en) | 2009-05-08 | 2010-04-19 | Apparatus and method for heating magnetic materials |
RU2011149781/14A RU2536700C2 (en) | 2009-05-08 | 2010-04-19 | Assembly and method for heating magnetic material |
EP10717814A EP2427108A1 (en) | 2009-05-08 | 2010-04-19 | Arrangement and method for heating of a magnetic material |
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EP09159802 | 2009-05-08 | ||
EP09159802.9 | 2009-05-08 |
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WO2010128418A1 true WO2010128418A1 (en) | 2010-11-11 |
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PCT/IB2010/051699 WO2010128418A1 (en) | 2009-05-08 | 2010-04-19 | Arrangement and method for heating of a magnetic material |
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US (1) | US9451900B2 (en) |
EP (1) | EP2427108A1 (en) |
JP (1) | JP5750098B2 (en) |
CN (1) | CN102421359B (en) |
RU (1) | RU2536700C2 (en) |
WO (1) | WO2010128418A1 (en) |
Families Citing this family (8)
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KR101772686B1 (en) | 2016-02-02 | 2017-08-29 | 연세대학교 원주산학협력단 | Nanoparticle drug delivery apparatus and method for controlling the same |
EP4085827A1 (en) | 2016-07-12 | 2022-11-09 | Magnetic Insight, Inc. | Magnetic particle imaging |
TWI711425B (en) * | 2017-10-13 | 2020-12-01 | 謝振傑 | Device for non-invasive thermal ablation |
EP3545835B1 (en) * | 2018-03-29 | 2022-03-30 | Julius-Maximilians-Universität Würzburg | System and method for generating a traveling field free line |
US11554269B2 (en) * | 2019-02-01 | 2023-01-17 | Weinberg Medical Physics, Inc. | Method, system and components for selective magnetic particle motion |
US11890488B2 (en) | 2019-03-13 | 2024-02-06 | Magnetic Insight, Inc. | Magnetic particle actuation |
CN110354392B (en) * | 2019-08-02 | 2024-07-19 | 北京大学第三医院(北京大学第三临床医学院) | Coil mechanism, heating device and thermal therapy equipment for thermal therapy |
CN111013019A (en) * | 2019-10-30 | 2020-04-17 | 南京逐路电子科技有限公司 | Magnetic induction thermotherapy temperature control device |
Citations (6)
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EP0913167A2 (en) * | 1997-10-29 | 1999-05-06 | Paragon Medical Limited | Improved targeted hysteresis hyperthermia as a method for treating tissue |
US6470220B1 (en) * | 1999-03-29 | 2002-10-22 | The Regents Of The University Of California | Diagnosis and treatment of cancers using in vivo magnetic domains |
DE10238853A1 (en) * | 2002-08-24 | 2004-03-04 | Philips Intellectual Property & Standards Gmbh | Process for local heating with magnetic particles |
WO2004091386A2 (en) * | 2003-04-15 | 2004-10-28 | Philips Intellectual Property & Standards Gmbh | Arrangement and method for the spatially resolved determination of state variables in an examination area |
WO2004091393A1 (en) * | 2003-04-15 | 2004-10-28 | Philips Intellectual Property & Standards Gmbh | Arrangement for influencing magnetic particles |
WO2006035359A2 (en) * | 2004-09-28 | 2006-04-06 | Philips Intellectual Property & Standards Gmbh | Method of determining a spatial distribution of magnetic particles |
Family Cites Families (9)
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RU2034548C1 (en) * | 1993-04-29 | 1995-05-10 | Андрей Георгиевич Маленков | Method for destroying malignant neoplasms |
DE10151778A1 (en) | 2001-10-19 | 2003-05-08 | Philips Corp Intellectual Pty | Method for determining the spatial distribution of magnetic particles |
AU2003281213A1 (en) * | 2002-07-03 | 2004-01-23 | Schering Corporation | 1-amido-4-phenyl-4-benzyloxymethyl-piperidine derivatives and related compounds as neurokinin-1(nk-1) antagonists for the treatment of emesis, depression, anxiety and cough |
US7758622B2 (en) * | 2003-04-15 | 2010-07-20 | Koninklijke Philips Electronics N.V. | Method and apparatus for influencing magnetic particles |
RU2295933C2 (en) * | 2005-06-17 | 2007-03-27 | ООО "Перспективные магнитные технологии и консультации" | Method for carrying out malignant neoplasm magnetic therapy |
EP1738773A1 (en) | 2005-06-29 | 2007-01-03 | Schering AG | Composition comprising magnetic iron oxide particles and use thereof in medical imaging |
EP1738774A1 (en) | 2005-06-29 | 2007-01-03 | Schering AG | Compositions comprising magnetic iron oxide particles and use thereof in medical imaging |
EP2091419A2 (en) * | 2006-12-20 | 2009-08-26 | Philips Intellectual Property & Standards GmbH | Arrangement and method for influencing and/or detecting magnetic particles in a region of action |
CN101896225A (en) * | 2007-12-13 | 2010-11-24 | 皇家飞利浦电子股份有限公司 | Arrangement and method for influencing and/or detecting magnetic particles in a region of action |
-
2010
- 2010-04-19 RU RU2011149781/14A patent/RU2536700C2/en not_active IP Right Cessation
- 2010-04-19 WO PCT/IB2010/051699 patent/WO2010128418A1/en active Application Filing
- 2010-04-19 CN CN201080020045.5A patent/CN102421359B/en not_active Expired - Fee Related
- 2010-04-19 US US13/319,351 patent/US9451900B2/en active Active
- 2010-04-19 EP EP10717814A patent/EP2427108A1/en not_active Withdrawn
- 2010-04-19 JP JP2012509119A patent/JP5750098B2/en not_active Expired - Fee Related
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EP0913167A2 (en) * | 1997-10-29 | 1999-05-06 | Paragon Medical Limited | Improved targeted hysteresis hyperthermia as a method for treating tissue |
US6470220B1 (en) * | 1999-03-29 | 2002-10-22 | The Regents Of The University Of California | Diagnosis and treatment of cancers using in vivo magnetic domains |
DE10238853A1 (en) * | 2002-08-24 | 2004-03-04 | Philips Intellectual Property & Standards Gmbh | Process for local heating with magnetic particles |
WO2004091386A2 (en) * | 2003-04-15 | 2004-10-28 | Philips Intellectual Property & Standards Gmbh | Arrangement and method for the spatially resolved determination of state variables in an examination area |
WO2004091393A1 (en) * | 2003-04-15 | 2004-10-28 | Philips Intellectual Property & Standards Gmbh | Arrangement for influencing magnetic particles |
WO2006035359A2 (en) * | 2004-09-28 | 2006-04-06 | Philips Intellectual Property & Standards Gmbh | Method of determining a spatial distribution of magnetic particles |
Non-Patent Citations (1)
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Also Published As
Publication number | Publication date |
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CN102421359A (en) | 2012-04-18 |
JP2012525900A (en) | 2012-10-25 |
CN102421359B (en) | 2014-10-29 |
RU2011149781A (en) | 2013-06-20 |
US20120058441A1 (en) | 2012-03-08 |
JP5750098B2 (en) | 2015-07-15 |
EP2427108A1 (en) | 2012-03-14 |
US9451900B2 (en) | 2016-09-27 |
RU2536700C2 (en) | 2014-12-27 |
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