Estimation of Vibration Amplitude and Elastic Properties of Extra-capillary Tissue with Ultrasound Driven Vibration of Intra-capillary Gas Bubbles
20230112529 · 2023-04-13
Inventors
- Seyednaseh AMINI (Trondheim, NO)
- Bjorn Angelsen (Trondheim, NO)
- STIAN SOLBERG (Florvåg, NO)
- YAMEN ZAZA (Trondheim, NO)
Cpc classification
G01S7/52039
PHYSICS
A61B8/485
HUMAN NECESSITIES
A61B8/4461
HUMAN NECESSITIES
A61B8/4483
HUMAN NECESSITIES
A61B8/5207
HUMAN NECESSITIES
A61B8/481
HUMAN NECESSITIES
International classification
Abstract
Estimation of vibration amplitude of intra-capillary micro-bubbles driven to vibrate with an incident ultrasound wave with amplitude and frequency to adjust the drive amplitude of the incident wave to obtain specified vibration amplitude of extra-capillary tissue. Estimation uses transmission of M groups of pulse complexes having low frequency pulse (LF) at bubble drive frequency, and high frequency (HF) pulse with angular frequency ω.sub.H> ~ 5 ω.sub.L, and pulse duration shorter than π/4ω.sub.L along HF beam. The phase between HF and LF pulses is ω.sub.Lt.sub.m for each group, where t.sub.m varies between the groups. Within each group, LF pulse varies between pulse complexes in amplitude and/or, where the LF pulse can be zero for a pulse complex, and LF pulse is different from zero for pulse complex within each group. HF receive signals are processed to obtain a parameter relating to bubble vibration amplitude when the HF pulse hits bubble.
Claims
1. A method for estimating parameters related to the surface or volume displacement vibration amplitude of at least one micro-bubble brought to vibration by an ultrasound wave of amplitude P.sub.L and angular frequency ω.sub.L transmitted along a LF beam with a given propagation direction along the unit vector e.sub.L, comprising a) transmitting towards said at least one micro-bubble at least two high frequency (HF) pulses with ω.sub.H > 5ω.sub.L along one HF beam along the unit vector e.sub.H at different times, b) directing at least one HF receive beam towards the region of the at least one micro-bubble with a direction e.sub.HR, the LF transmit and the HF transmit and receive beams are arranged so that they overlap at least in an observation region that includes said at least one micro-bubble, c) arranging the transmit timing of each of the transmitted HF pulses so that the pulses hits said at least one micro-bubble at different phases the LF oscillation, d) receiving at least two HF receive signals scattered from each said at least two transmitted HF pulses, and e) processing the at least two HF receive signals, to for each said at least one micro-bubble to produce an estimate of a bubble vibration parameter that gives one or both of the relative vibration of one or both of i) the bubble volume vibration relative to the resting bubble volume, and ii) a parameter related to relative bubble volume vibration.
2. The method according to claim 1, where the HF transmit beam is directed in close to the same direction as the LF transmit beam and the LF transmit and HF transmit and HF receive beams are positioned so that the three beams overlap in a region around said at least one micro-bubble, to produce estimates of said bubble vibration parameter for each said at least one micro-bubble.
3. The method according to claim 2, where a) a set S.sub.N of N≥1 groups G.sub.n of combined LF and HF pulse complexes are transmitted, each group G.sub.n comprising at least two pulse complexes, where for each group the LF pulse amplitude can be zero for one pulse complex, and the LF pulse amplitude is non-zero for at least one pulse complex, and at least one of the polarity, amplitude, or phase of the LF pulse varies between pulse complexes, and where b) for each group G.sub.n the HF pulse is transmitted with a timing relative t.sub.n to the LF pulse so that the HF pulses hit said at least one micro-bubble with a phase relation of ω.sub.Lt.sub.n relative to the transmitted LF oscillation, where the time t.sub.n is different for different groups G.sub.n, and c) the processing includes combining the HF receive signals from the scattered HF pulses from said at least two HF transmit pulses for each group G.sub.n to produce a detection parameter D.sub.n for group G.sub.n and each said at least one micro-bubble, and d) for each said at least one micro-bubble, the detection parameter D.sub.m for the group G.sub.m that gives maximal detection parameter for all G.sub.n ∈ S.sub.N is used as an estimate to obtain an estimate of the amplitude of said bubble vibration parameter.
4. The method according to claim 2, where a) a long LF pulse of duration T.sub.L is transmitted towards said at least one micro-bubble, where T.sub.L is longer than T.sub.R, preferably longer than N*TR, where T.sub.R is the propagation time from HF transmit transducer to said at least one micro-bubble, and b) a set S.sub.N of N ≥ 1 groups G.sub.n, comprising two HF pulses are transmitted at a reference time t.sub.n for each group, and internal timing within each group is selected so that at least two pulse complexes hits the bubble at opposite polarities of the LF oscillation, and c) the processing includes combining the scattered HF pulses from said at least two HF pulses for each group G.sub.n to produce a detection parameter D.sub.n for group G.sub.n and each said at least one micro-bubble, and d) for each said at least one micro-bubble, the detection parameter D.sub.m for the group G.sub.m, that gives maximal detection parameter for all G.sub.n ∈ S.sub.N is used as an estimate to obtain an estimate of the amplitude of said bubble vibration parameter.
5. The method according to claim 2, where the HF receive signals are compensated by one or both of i) a nonlinear propagation delay, and ii) a nonlinear pulse form distortion in the processing chain to produce estimates of said bubble vibration parameter for each said at least one micro-bubble.
6. The method according to claim 1, for an adequately dense group of micro bubbles, where a) the HF transmit beam defined by e.sub.H, is directed at an angle to the direction of the LF transmit beam defined by e.sub.L, and b) at least one HF receive beam are positioned together with the LF and HF transmit beams so that the three beams overlap at the region of said dense group of micro-bubbles, and c) transmitting a single group G.sub.n comprising at least two HF pulses at a reference time t.sub.n, and one of ci) the LF pulse polarity is switched between at least two of the HF pulses within the group, and cii) internal timing of the pulses within the group is selected, so that at least two HF pulse complexes hits at least one bubble within said group of micro-bubbles at opposite polarities of the LF oscillation, and d) processing that includes combining the received HF signal from said at least two HF pulses to produce a detection parameter D.sub.n for each bubble n in said group of micro-bubbles, and e) selecting estimate of a bubble vibration parameter the detection parameter D.sub.m for the bubble n = m that has the highest value.
7. The method according to claim 1, where said parameter related to relative bubble volume vibration is the average surface normal vibration amplitude relative to a radius of the bubble.
8. The method according to claim 7, where the value of the average surface normal is used to set the transmit amplitude of the LF wave.
9. The method according to claim 1, where the LF beam is focused onto in the therapeutic region.
10. The method according to claim 1, where the HF beam is broad with width less than the LF beam in the observation region, and several multi-focused parallel HF receive beams are generated to provide spatial resolution in the estimates of said bubble vibration parameter for a group of micro-bubbles.
11. The method according to claim 1, where scanning in 2 or 3 dimensions of one or more of i) the HF receive beam direction, and ii) the HF transmit beam direction, and iii) the LF beam direction to produce images of vibrating micro bubbles and the vibration amplitudes of the bubbles for a given transmitted amplitude of the LF wave.
12. The method according to claim 3, where the phase of the 2.sup.nd order transfer function between incident LF pressure oscillation and the amplitude bubble volume vibration is estimated from the timing t.sub.m that gives the maximal detection parameter D.sub.m.
13. The method according to claim 12, where the maximal detection parameter D.sub.m is obtained for at least two different frequencies of the LF beam, and estimates of the following parameters of the 2.sup.nd order approximation to the transfer function from incident pressure amplitude to bubble volume vibration i) the angular resonance frequency ω̂.sub.0 of the bubble ii) the absorption coefficient
14. The method according to claim 13, where for a bubble filling parts of a vessel estimates of at least one of the following vibration parameters for the surrounding tissue is obtained i) the ratio of the tissue shear wave velocity c.sub.s to the vessel radius a.sub.v is obtained from the estimate of the angular resonance frequency ω̂.sub.0 of the bubble, ii) for a known radius of the vessel the real part of tissue shear stiffness is obtained from the estimate of the angular resonance frequency ω̂.sub.0 of the bubble, iii) for a known radius of the vessel the imaginary part of tissue shear stiffness is obtained from the estimate of the angular resonance frequency ω̂.sub.0 of the bubble.
15. An instrument for obtaining estimates of parameters related to the surface or volume displacement vibration amplitude of at least one micro-bubble brought to vibration by an ultrasound wave of amplitude P.sub.L and angular frequency ω.sub.L, comprising a) means for transmitting towards said at least one micro-bubble ai) at least one LF pulse along a LF transmit beam with a transmit beam direction along a unit vector e.sub.L, and aii) at least two high frequency (HF) pulses with ω.sub.H> 5ω.sub.L along a HF beam along the unit vector e.sub.H at different times, and iii) means for arranging the transmit timing of each of the transmitted HF pulses so that the pulses hit said at least one micro-bubble at different phases the LF oscillation, and b) means for receiving that includes i) means for directing at least one HF receive beam with direction e.sub.HR to produce an overlap region (OR) with the LF and HF transmit beams that includes the at least one micro-bubble, and ii) means for receiving at least two HF receive signals scattered from each said at least one micro-bubble from said at least two transmitted HF pulses, and c) means for processing the at least two HF receive signals, to for each said at least one micro-bubble to produce an estimate of a bubble vibration parameter that gives one or both of the relative vibration of one or both of i) the bubble volume vibration relative to the resting bubble volume, and ii) a parameter related to relative bubble volume vibration.
16. The instrument according to claim 15, where a) said means for transmitting include means for transmitting said HF transmit beam in close to the same direction as the LF transmit beam, and b) said means for receiving include means for directing the HF receive beam so that the LF transmit and HF transmit and HF receive beams overlap at the position of said at least one micro-bubble.
17. The instrument according to claim 16, where a) said means for transmitting includes i) means for transmitting a set S.sub.N of N≥1 groups G.sub.n of combined LF and HF pulse complexes, each group G.sub.n comprising at least two pulse complexes, where for each group the LF pulse amplitude can be zero for one pulse complex, and the LF pulse amplitude is non-zero for at least one pulse complex, and ii) means for varying at least one of the polarity, amplitude, or phase of the LF pulse between pulse complexes, and iii) means that for group G.sub.n for sets the transmit time t.sub.n of the HF pulse relative to the LF pulse so that the HF pulses hit said at least one micro-bubble with a phase relation of ω.sub.Lt.sub.n relative to the LF pulse oscillation when the HF pulse hits the at least one micro-bubble, where the time t.sub.n is different for different groups G.sub.n. and b) said means for processing includes i) means for combining the scattered HF pulses from said at least two HF pulses for each group G.sub.n to produce a detection parameter D.sub.n for group G.sub.n and each said at least one micro-bubble, and ii) means for selecting for each said at least one micro-bubble, the detection parameter D.sub.m for the group G.sub.m, that gives maximal detection parameter for all G.sub.n ∈ S.sub.N, said D.sub.m is used as a basis to obtain an estimate of the amplitude of said bubble vibration parameter.
18. The instrument according to claim 16, where a) said means for transmitting include ai) means for transmitting a long LF pulse of duration T.sub.L towards said at least one micro-bubble, where T.sub.L is long, preferably longer than NT.sub.R where T.sub.R is the propagation time from HF transmit transducer to said at least one micro-bubble, and ii) a set S.sub.N of N ≥ 1 groups G.sub.n comprising two HF pulses transmitted at a reference time t.sub.n for each group, and selecting internal timing within each group so that at least two pulse complexes hits the bubble at opposite polarities of the LF oscillation, and b) said means for processing includes bi) means for combining the received scattered HF pulses from said at least two HF transmit pulses for each group G.sub.n to produce a detection parameter D.sub.n for group G.sub.n and each said at least one micro-bubble, and bii) means for selecting for each said at least one micro-bubble the detection parameter D.sub.m for group G.sub.m, that gives maximal detection parameter for all G.sub.n ∈ S.sub.N, Said G.sub.m is used to obtain an estimate of the amplitude of said bubble vibration parameter for each said at least one micro-bubble.
19. The instrument according to claim 16, where said processing means include means for compensating the HF receive signals by one or both of i) a nonlinear propagation delay, and ii) a nonlinear pulse form distortion in the processing chain to produce estimates of said bubble vibration parameter for each said at least one micro-bubble.
20. The instrument according to claim 15, for an adequately dense group of micro bubbles, where a) said means for transmitting includes ai) means for directing the HF transmit beam defined by e.sub.H, at an angle to the direction of the LF transmit beam defined by e.sub.L, and aii) means for transmitting a single group G.sub.n comprising at least two HF pulses at a reference time t.sub.n, and one of a) the LF pulse polarity is switched between at least two of the HF pulses within the group, and ii) internal timing of the pulses within the group is selected, so that at least two HF pulse complexes hits at least one bubble within said group of micro-bubbles at opposite polarities of the LF oscillation, and b) said means for receiving includes means for directing at least one HF receive beam together with the LF and HF transmit beams so that the three beams overlap at a region of said dense group of micro-bubbles, and c) said means for processing includes ci) means combining the received HF signal from said at least two HF pulses to produce a detection parameter D.sub.n for each bubble n in said group of micro-bubbles, and cii) means for selecting the detection parameter D.sub.m for the bubble n = m that has the highest value, and use D.sub.m in the processing chain to produce and estimate of a bubble vibration parameter.
21. The instrument according to claim 15, where the LF beam is focused onto in the therapeutic region.
22. The instrument according to claim 15, where the HF transmit beam is broad with width less than the LF beam in the observation region, and several multi-focused parallel HF receive beams are generated to provide spatial resolution in the estimates of said bubble vibration parameter for a group of micro-bubbles.
23. The instrument according to claim 15, where said parameter related to relative bubble volume vibration is the average surface normal vibration amplitude relative to a radius of the bubble.
24. The instrument according to claim 23, comprising means to use the value of the average surface normal to set the transmit amplitude of the LF wave.
25. The instrument according to claim 15, where said transmit and receive means comprises means for scanning in 2 or 3 dimensions of one or more of i) the HF receive beam direction, and ii) the HF transmit beam direction, and iii) the LF beam direction to produce images of vibrating micro bubbles and the vibration amplitudes of the bubbles for a given transmitted amplitude of the LF wave.
26. The instrument according to claim 17, where said processing means include means to estimate the phase of the 2.sup.nd order transfer function between incident LF pressure oscillation and the amplitude bubble volume vibration from the timing t.sub.m that gives the maximal detection parameter D.sub.m.
27. The instrument according to claim 26, where the processing means includes a) means for detection of the maximal detection parameter D.sub.m for at least two different frequencies of the LF beam, and b) means for estimating the following parameters of the 2.sup.nd order approximation to the transfer function from incident pressure amplitude to bubble volume vibration i) the angular resonance frequency ω̂.sub.0 for the bubble ii) the absorption coefficient
28. The instrument according to claim 27, where the processing means comprises means to estimate at least one of the following vibration parameters for the tissue surrounding a bubble that is filling a part of a vessel i) the ratio of the tissue shear wave velocity c.sub.s to the vessel radius a.sub.v from estimates of the angular resonance frequency ω̂.sub.0 of the bubble, and ii) the real part of tissue shear stiffness for a known radius of the vessel from estimates of the angular resonance frequency ω̂.sub.0 of the bubble, and iii) the imaginary part of tissue shear stiffness for a known radius of the vessel from the estimate of the angular resonance frequency ω̂.sub.0 of the bubble .
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION OF EMBODIMENTS
[0030] This section gives a more detailed description of example embodiments of the invention, where the examples by no means represents limitations of the invention, which in its broadest aspect is defined by the claims appended hereto.
A. Fundamental Bubble Vibration
[0031] The invention presents methods and instrumentation for extracting information about ultrasound driven vibrations of micro-bubbles in tissue, and also to use this information for estimation of tissue properties, such as elastic properties, and properties relating to elastic properties.
[0032] The invention is relevant for micro-bubbles with diameter less than the capillaries, and also bubbles that in large arteries have a spherical shape with radius a ~ 5 - 30 .Math.m that gives a bubble volume V.sub.b = 4πα.sup.3/3, while in capillaries with radii a.sub.v ~ 3 - 5 .Math.m the larger bubbles fill at least part of the capillary. Examples of the larger bubbles are shown in
[0033] There is spatially distributed elasticity and mass density of the tissue, the blood, and the gas, that implies wave propagation with reflection at boundaries. The tissue and the blood have both a high volume compression stiffness λ.sub.t = 1/κ.sub.t(κ.sub.t- volume compressibility) that upholds pressure waves with propagation velocity c.sub.p ≈1500 m/s for both tissue and blood. The tissue has in addition a low shear/deformation stiffness .Math..sub.t that produces tissue shear/deformation waves with no volume compression and low propagation velocity c.sub.s ~ 2 - 20 m/s. The blood and the gas have negligible shear stiffness, and hence no shear waves. The bubble gas has a low volume compression stiffness, but the mass density is also so low that the gas pressure can be approximated as constant across the bubble volume. The bubble gas pressure depends on the bubble volume and its variation as
where P.sub.0 ~100 kPa is the environmental pressure, V.sub.b is the equilibrium bubble volume, δV is the change in bubble volume, C.sub.p and C.sub.vare the heat capacities at constant pressure and volume. Typical gases have large molecules that makes C.sub.p ≈ Cv and γ≈ 1. The volume-pressure relation is inherently nonlinear for larger changes in the volume, but we shall in our work use the approximate linear variation with δV/V.sub.b, to study fundamental aspects of the bubble vibration.
[0034] The low tissue shear stiffness allows large deformations of the cylindrical bubble surface 111, with large amplitude, short-range shear deformation of the surrounding tissue with comparatively low volume compression. The large vibration amplitude of the close surrounding tissue produces an outward acoustic radiation force (ARF) that has interesting applications for drug transport both across the capillary wall, through the interstitial space between the tissue cells, and across membranes of the cells and other tissue structures. In this context it is important to obtain adequate bubble/tissue vibration amplitude (~ 1 .Math.m) and one target of this invention is to use ultrasound scattering from vibrating bubbles to measure the bubble vibration amplitude produced by an incident ultrasound wave. The invention further uses the measured bubble vibration amplitude to set the amplitude of the incident vibration wave to achieve desired bubble vibration amplitude in the surrounding tissue to achieve the desired therapeutic effect.
[0035] A bubble in a large vessel, as 101 in 100, has a practically spherical shape with a spherical vibration pattern. A drive pressure P.sub.d that is the difference between the gas pressure P.sub.g and the pressure P.sub.∞ at a point so distant from the bubble that one can neglect the tissue shear vibration, produces a complex volume vibration amplitude □V.sub.c of the bubble as [1]
where ρ.sub.b and η.sub.b are the mass density and coefficient of viscosity of the surrounding blood, and E.sub.st is the Youngs module of the blood/gas surface layer. We refer to H.sub.d as the direct drive transfer function, and ω.sub.d as the direct drive angular resonance frequency produced by the interaction between the co-oscillating mass of the surrounding blood and the elasticity of the blood/gas surface layer. Viscous friction in the blood and the surface layer is given by η.sub.b.
[0036] An incident acoustic wave with pressure amplitude P.sub.i and angular frequency ω produces a variation in the bubble volume and the gas pressure that produces drive pressure amplitude P.sub.d as
which gives the complete transfer function H.sub.V(ω) from the incident pressure amplitude P.sub.i to the complex relative volume amplitude as
[0037] With the 2.sup.nd order form of the H.sub.d(ω) in Eq.(2), we get the following form of H.sub.V(ω)
[0038] For a bubble that partially fills a capillary with a large cylindrical region as 111 in
[0039] The
[0040]
[0041] Eqs.(12,13,19) shows that for a bubble with dimensions adequately smaller than the incident wavelength the scattered signal is determined by the bubble volume V.sub.b and bubble volume compressibility κ.sub.b. We note from
where 2 L is the length of a cylindrical bubble in a capillary with the same volume V.sub.b. The vibrating area of the cylindrical bubble is
[0042] We notice that Ac is
which is ⅓ of the surface area of the end spheres. However, the effect of this error is reduced because the displacement of the semi-spherical end surfaces is less than the radial vibration of the cylinder surface as shown in
[0043] Analysis of vibration and scattering from the cylindrical bubble is carried through in Appendix A. We note from 210 in
from Eq.(A10, A12) of Appendix A for 1.sub.c/a.sub.v=5. The dotted lines show the magnitude |Ĥ.sub.v(ω)| (302) and the phase θ̂v(ω) (303) of the 2.sup.nd order approximation |Ĥ.sub.v(ω)| of Eq.(A14). The approximation of the 2.sup.nd order function to Eq.(A12) is done in the following steps: [0044] 1. Re{H.sub.v(ω.sub.0)}=0 of Eq.(A14) gives the angular resonance frequency ω.sub.0. [0045] 2. ζ is determined from the differential of the ohase of H.sub.V as in Eq.(25). [0046] 3. ω.sub.m and K.sub.V is determined from Eq.(27)
[0047] In the example in
[0048] To observe the LF vibration amplitude of a bubble driven by the incident LF wave with angular frequency ω.sub.L , the invention presents methods and instrumentation building on U.S. Pat. 8,550,998; 9,291,493; 9,939,413; 10,578,725 and 7,727,156; 10,879,867.
[0049] An LF pulse shown by example as 401 or 405 in
[0050] In many situations, for example trans-abdominal and trans-costal applications, the access window to the therapeutic region is limited, and it is desirable to have a HF transmit and receive beam arrangement with the same direction as the LF beam as illustrated in
[0051] With adequate ultrasound access windows, it can be useful to use crossing multi/depth focused HF receive beams exemplified by 514 and the dots 515 in
[0052] In a particular solution, one transmits a set S.sub.N of N≥ 1 groups G.sub.n pulse complexes where one for each group G.sub.n transmits at least two pulse complexes comprising a LF manipulation pulse and a HF observation pulse where the LF pulse varies in one of amplitude, and polarity, and phase between each pulse complexes, where the LF pulse might be zero for one pulse complex, and the LF pulse is non-zero for at least one pulse complex. The LF pulses 401 and 405 in
[0053] The time between transmit of the HF pulses is determined so that it is larger than the round trip propagation time T.sub.R from HF transmit transducer to the micro-bubble and to the HF receive transducer. In particular solutions where one wants long duration LF transmit vibration of the bubble we can use LF pulses with long duration time T.sub.L, for example longer than NT.sub.R where N is the the number of groups G.sub.n. Several groups G.sub.n of HF transmit pulses are then transmitted with time distance larger than T.sub.R and t.sub.n defining the detailed phase relation between the HF pulse and the LF oscillation of the bubble when the HF pulse hits the bubble.
[0054] It is also interesting the use a HF transmit beam 513 that crosses the LF beam 501 in the same direction as the set of HF receive beams 514/515.
[0055] For therapy we generally drive the bubble with the low frequency (LF) pressure wave with angular frequency ω.sub.L, typically in the neighborhood of the bubble resonance frequency to produce large therapeutic cylindrical radius vibration amplitude (~ 1 .Math.m). The LF pulse has an amplitude envelope pP.sub.Le(t), where p is a polarity parameter of the LFwave. p = 1 implies positive LF amplitude (e.g. 401), p = -1 implies inverted LF amplitude (e.g. 405), while p = 0 implies zero LF amplitude. Other values/sequences of the polarity parameter can be used to enhance the signal processing, where the cited patents show examples of p = 0, ±1; p = ±1, ±2, for example to improve suppression of tissue noise and/or compensate for bubble movements between the HF pulses.
[0056] The LF pulse produces a vibration in bubble volume as
[0057] Where θ(ω.sub.L)=∠H(ω.sub.L) is the phase of H(ω.sub.L), and τ.sub.e(ω.sub.L)≈θʹ(ω.sub.L) is an approximate delay of the envelope produced by the transfer function H(ω) for an adequately narrow band HF pulse. The last approximation of δV.sub.Le(t) assumes that he envelope varies slowly relative to the ω.sub.L oscillation. To measure the bubble vibration amplitude we transmit HF observation pulses as described in
[0058] The scattered pressure field of an incident ultrasound pressure wave with angular frequency ω and amplitude P.sub.i from a bubble with volume V.sub.b and adequately less extension than the incident wavelength λ, is by the Born approximation obtained as
where [0059] r is the radial distance from the bubble center of mass, [0060] k is the wave vector magnitude of both the incident and scattered wave, and λ = 2π/k is the wave length of both the incident and scattered waves. [0061] e.sub.i is the unit direction vector of the incident wave approximated as plane wave across the bubble with amplitude P.sub.i, [0062] e.sub.s is the unit direction vector of the observed scattered wave, [0063] c.sub.p is the pressure wave propagation velocity, [0064] δV.sub.b is the vibration amplitude of the bubble volume, V.sub.b, and δV.sub.t is the vibration amplitude of the surrounding tissue volume, V.sub.t, both produced by the incident wave, [0065] κ.sub.b (ω) is the bubble volume compressibility, and [0066] κ.sub.t (ω) is the volume compressibility of the surrounding material.
[0067] The term κ.sub.b/κ.sub.t represents scattering due to the deviation of the bubble volume compressibility from the tissue volume compressibility, and the term e.sub.se.sub.i represents scattering due the relative difference between the bubble mass density (≈ 0) and the tissue mass density ρ.sub.t. In a typical situation |κ.sub.b(ω)/κ.sub.t|>>|e.sub.se.sub.i|, and the term e.sub.se.sub.i can be neglected. Using
we modify Eq.(6) to
[0068] Both for contrast agent bubbles and bubbles for therapy, we are generally interested in vibrating the bubbles in the low frequency (LF) range Ω.sub.0 around the bubble volume vibration resonance frequency, where the 2.sup.nd order transfer functions of Eqs.(5,A14) are useful. To measure the bubble vibration amplitude at ω.sub.L we transmit in addition high frequency (HF) observation pulses with angular center frequency ω.sub.H ~10ω.sub.L >> ω.sub.0 as illustrated in
[0069] Spherical Bubble:
[0070] Cylindrical Bubble:
where it is shown the major dependencies of the receive signal Y(D;ω) on the bubble dimensions D. For the spherical bubble D is the bubble radius a, while for the bubble filling parts of the capillary D is (a.sub.v,L) or (a.sub.v, a) by Eq.(7). A change in the bubble dimension/volume at the HF/LF time reference t.sub.m when the HF pulse hits the bubble, produces a change in the amplitude of the HF receive signal. For polarity p of the LF pulse the major change in bubble dimensions are
[0071] The spatial average
where c.sub.0 is the low amplitude linear propagation velocity, P.sub.L is the pressure of the low frequency wave at the location of the HF pulse, β is a nonlinearity parameter of the tissue bulk compression, and p is a scaling parameter defined in relation to Eqs.(10,11). This nonlinear propagation effect gives a non-linear propagation delay (NPD) to the HF pulse, pτ.sub.n(r), and a weaker pulse form distortion (PFD) that increases with the propagation distance r is before scattering, as described in the cited patents. When the transmitted HF pulse is at the crest or through of the LF wave, the NPD has a larger effect than the PFD that generally can be neglected. When the transmitted HF pulse is at a zero crossing of the LF wave, the PFD has a larger effect than the NPD that generally can be neglected.
[0072] The back scattered HF signal will generally in addition to the scattering from the bubbles contain considerable scattering from tissue surrounding the bubble, and it is devised to suppress the tissue signal, for example by correcting the received signal for adequate NPD and/or PFD according to the methods in the cited patents, or using the 2.sup.nd harmonic component of the received HF signal, or a combination of both. We notice, however that the transmitted LF amplitude to vibrate bubbles is generally lower than for imaging, and both the NPD and the PFD have less effect, and corrections for NPD and/or PFD can in many cases be neglected. Before further processing, we assume that the received HF signals are adequately corrected with the NPD and PFD, as described in the cited patents, and in the notation for the received HF signals below, we assume that that adequate correction have been done.
[0073] For illustration of a simplest form, we linearize the receive signals and form a detection signal D.sub.m with p = ±1 as
where the subscript n indicates the time point t.sub.n in
[0074] Components for Y.sub.s and Y.sub.c in Eqs.(14,15) that have low variation with bubble dimension variations are shorted in the ratio of D.sub.m. In particular has H.sub.b low sensitivity to variations in bubble dimensions that are small compared to the wave length. H.sub.b(K) is the Fourier transform of the bubble volume with Fourier vector K=k(e.sub.i-e.sub.s). The largest magnitude K.sub.max=2ke.sub.i=4π/λ)e.sub.i is found for back-scattering where e.sub.s= –e.sub.i, which the situation in
[0075] We notice that for the sphere we have for back scattering Ka=(4πa/c.sub.p).Math.f where f is the frequency and c.sub.p ≈ 1500 m/s is the propagation velocity of the pressure wave.
[0076] Scattering from the cylindrical bubble in
[0077] ΔH.sub.b/H.sub.b0 is analyzed in
[0078] For this situation ΔH.sub.b/H.sub.b0<0.02 is obtained for f = 2.5 and 5 MHz. Reducing □a.sub.v to 0.5 □m we have ΔH.sub.b/H.sub.b0<0.02 up to 7.5 MHz for all situations.
[0079] We expect capillaries and hence also bubbles to have random position within the tumor, and if we select the bubbles with the strongest back-scatter, i.e. incident wave normal to the capilary length and φ close to ± π/2 eg , we can assume that the variation of H.sub.b for the variations of the bubble dimension produced by the LF pulse is negligible for all the given bubble lengths and frequencies HF < 15 MHz.
[0080] We note that when the incident HF beam hits close to the short axis of the bubble, both H.sub.b0 and ΔH.sub.β/H.sub.b0 are approximately independent of the dimension variations for HF < 15 MHz When we can neglect the changes in H.sub.b with the bubble dimension variations produced by the polarity change in the incident LF pulse, H.sub.b is essentially canceled in the fraction of D.sub.m in Eq.(18). Neglecting H.sub.b in the expression for Y.sub.s, Y.sub.c in Eq.(14,15) we see that D.sub.m of Eq.(18) gives
where K.sub.pH(L/a.sub.v) is given in Eq.(15, A17). We note that ψ.sub.cm is the spatial average of the normal displacement ψ.sub.r for the cylinder, as shown in Eq.(A12), while ψ.sub.sm is the maximal displacement of the spherical bubble radius, as the bubble displacement is constant across the bubble surface. A.sub.cm as a function of l.sub.c/a.sub.v is shown as 700 in
[0081] The relative volume variation δV/V.sub.b can be approximated from the relative displacement for the spherical and cylindrical bubbles with the linear approximations as
[0082] Considering measurements errors and relative displacement magnitudes, these approximate expressions have good practical value. More accurate nonlinear expressions between δV/V.sub.b and the displacements can be calculated by anyone skilled in the art.
[0083] For the 2.sup.nd order transfer functions in Eqs.(5,A14) it is possible to measure/estimate the three major parameters, w.sub.0, ζ, and K.sub.V, for example in the following way. We get a phase estimate θ(ω.sub.L)=∠H(ω.sub.L) of the transfer function at ω.sub.L for the t.sub.n = t.sub.m that gives maximum of δV.sub.b in Eq.(11), i.e.
[0084]
[0085] Measuring θ̂(ω.sub.L1) and θ̂(ω.sub.L2) from Eq.(22) for two low frequencies ω.sub.L1 and ω.sub.L2 where we get the maximal detection signal for t.sub.m1 and t.sub.m2, we can for example though linear interpolation, indicated as 703 in
[0086] At the resonance frequency □.sub.0 we shall have θ(ω.sub.0) = -π/2 which gives an estimated resonance frequency from Eq.(23) as
[0087] Matching the differential of the phase in Eq.(5,A14) at ω= ω.sub.0 to Eq.(24) we get an estimate for the absorption losses in the tissue vibrations as
[0088] Another estimate of the absorption factor ζ is from Eq.(5) also found for a single low frequency ω.sub.L as
[0089] The parameter K.sub.V can for example be found by the angular frequency ω.sub.m that gives maximal amplitude of H.sub.V(ω). From the estimates of ω̂.sub.0 and ζ̂ we can obtain an estimate of
where we measure |H.sub.V| at the estimated angular frequency ω.sub.m. If we do not have an estimate of ζ̂, we can search for the ω.sub.m that gives max|H.sub.V| and do the following calculations
[0090] Estimating the phases θ̂.sub.n = θ̂(ω.sub.Ln) at more than two frequencies ω.sub.Ln, n=1, 2, ... , N, we can improve the estimate of ω̂.sub.0 with more complex interpolations, as known by any-one skilled in the art. By example, for n = 1, ... , N we the set of measured frequencies by the vector ωL = {ω.sub.L1,...ω.sub.Ln,...ω.sub.LN} and the set of estimated phases by ωL = {ω.sub.L1,...ω.sub.Ln,...ω.sub.LN}, we can then form an estimate of ω̂.sub.0 and ζ̂ω̂.sub.0 through minimization of a mean square functional as
[0091] Other forms of functionals for minimization, also including added information, can be formed by any-one skilled in the art.
[0092] From Eq.(5-7) we notice that for θ̂(ω.sub.L)+ω.sub.Lt.sub.m≈ 0 the amplitude of the received HF signal takes the form
[0093] and we can for example include the amplitude of the received signal ~|H.sub.v(ω.sub.Ln)| for the different {ω.sub.L1,...ω.sub.Ln} in addition to the phase in the functional for parameter estimation in Eq.(29).
[0094] The extra capillary tissue is determined by the mass density, ρ.sub.t, and the real and imaginary part, .Math..sub.tr and .Math..sub.ti of the complex shear stiffness of the tissue, as shown in Eq.(A6, A7). We can approximate ρ.sub.t≈ 1100 kg/m.sup.3 for most solid tumor tissues, and hence it is .Math..sub.tr and .Math..sub.ti which are the most sought after tissue parameters. From the measured/estimated ω̂.sub.0 and k̂.sub.v, we see from Eq.(A18) that we can obtain an estimate of ω̂.sub.d as
where γ ≈ 1 and P.sub.0 ≈ 101 kPa.
[0095] From F.sub.d(x) in Eq.(A11) we obtain estimated x.sub.d(l.sub.c/a.sub.v) from Re{F.sub.d(x.sub.d)=0.
which allows us to calculate
[0096]
[0097] The power dissipated by the surface vibration at a surface area element d.sup.2r is
[0098] We assume P.sub.i approximately constant across the bubble surface, and integrated across the whole bubble surface gives the following power dissipation that provides a heating energy per unit time
Inserting the transfer function from Eq.(5), we get
[0099] Hence, from estimation of ω.sub.0 and ζ and assessment of the bubble volume and the incident pressure amplitude, we can assess the dissipated power from the bubble on the surrounding tissue at ω= ω.sub.L. Because ω.sub.L is low, we can estimate the low frequency amplitude P.sub.i = P.sub.L using an assessment of the low absorption. From the ultrasound image (2D or 3D) we can automatically estimate the number of bubbles N per unit volume and assess the total heat generation as
that can be used to estimate temperature increase in the tissue to avoid uncontrollable results.
[0100]
[0101] For 3D scanning of the ultrasound beams, the linear array 901 can in this example embodiment be rotated around the long axis 904 that provides a mechanical scanning of the LF/HF beam in an elevation direction, indicated by the arrows 905. For each elevation position of the array, one does electronic scanning of LF/HF transmit beams in an azimuth direction indicated by the arrows 906, through electronic selection of transmitting LF and HF elements, and transmitting combined LF/HF pulse complexes for example as shown in
[0102] At least two pulse complexes with different LF pulses, for example as illustrated in
[0103] Two versions of the instrument are useful, where the first version 903 comprises beam former for HF receive cross-beams, illustrated as 914 in the 2D scan plane 908, and HF back scatter receive beams with the same axis as the HF transmit beam 907, shown in further detail in
[0104] The processor 911 typically comprises at least one multicore central processing unit (CPU) and at least one graphics processor unit (GPU) that are SW programmable, according to known methods. The processor receives user inputs from a user/operator input unit 913 that operates according to known methods, and displays image data and other information necessary for communication with the user/operator through a combined display and audio unit 912, according to known methods.
[0105] In the second version of the instrument, the digital HF receive signals from each HF receive elements and each transmitted pulse complex are via the high-speed bus 910 transferred to the processor 911 for storage and further processing. For 2D imaging in the second version, a SW program in the processor unit 911 combines HF receive signals from multiple HF receive elements to produce both HF backscatter receive beams and HF receive cross-beams crossing each HF transmit beam in the 2D set, for example as shown as 914 and in more detail in
[0106] One use of the cross-beam (914) HF receive signals is to estimate the nonlinear propagation delay at a multitude of depths along the HF transmit beam with low influence of multiple scattered noise, as described in U.S. Pat. Appl. 2020/0405268. A set of cross beams is also useful to provide better suppression of signal from tissue, that is noise for detecting bubbles, vibration amplitudes, and tissue parameters. When we have imaging situations where the level of multiple scattering noise in the back-scatter HF receive signal is low compared to the 1st order scattered signals, the nonlinear propagation delay at multitude of depths along the HF transmit beam (907) can be obtained from the back-scatter HF receive signal, as described in the above cited US Patents, and the beam former for HF receive cross-beams, has less importance and can be omitted.
[0107] The processor 911 further comprises means, for example implemented as SW programs, to carry through the processing as described above to estimate [0108] i) the relative variation of the bubble volume or displacement amplitude when driven by the LF signal, as for example described in Eqs.(19,21) and following equations, and [0109] ii) the bubble vibration resonance frequency and absorption, as for example described in Eqs.(22-25, 30) and related equations, and [0110] iii) parameters of shear elasticity of the extravascular tissue, for example as shown in
[0111] The method and instrument is useful for estimating vibration amplitudes of bubbles of any dimension at an angular frequency we define as the low frequency, ω.sub.L. For spherical bubbles we have a good analytic relationship of a 2.sup.nd order transfer function, Eq.(5) between the bubble radius and the scattered wave over a large frequency range from well below to well above the resonance frequency. For Bubbles that fill a capillary, like in
[0112] Thus, while there have shown and described and pointed out fundamental novel features of the invention as applied to preferred embodiments thereof, it will be understood that various omissions and substitutions and changes in the form and details of the devices illustrated, and in their operation, may be made by those skilled in the art without departing from the spirit of the invention.
[0113] It is also expressly intended that all combinations of those elements and/or method steps which perform substantially the same function in substantially the same way to achieve the same results, are within the scope of the invention. Moreover, it should be recognized that structures and/or elements and/or method steps shown and/or described in connection with any disclosed form or embodiment of the invention may be incorporated in any other disclosed or described or suggested form or embodiment as a general matter of design choice. It is the intention, therefore, to be limited only as indicated by the scope of the claims appended hereto.
APPENDIX A
[0114] For the vibration field outside the cylindrical capillary from the vibrating bubble in
where λ = 2πc.sub.p/ω is the wavelength of the pressure wave with propagation velocity c.sub.p. The particle vibration displacement ψ and the pressure P in the co-oscillating mass are obtained from A as
[0115] Fourier transform along the z-axis gives
[0116] Setting x = k.sub.zr and A(r,k.sub.z) .sub.= y(k.sub.zr) we get the modified Bessel equation with the solution K.sub.0(x)
[0117] With A defined for r= a.sub.v and a tissue mass density ρ, we get the following field amplitudes in the tissue outside the capillary
[0118] Inside the co-oscillating mass the incompressible tissue deformation produces shear stresses, which balances to zero inside the tissue, but at the boarder to the bubble at the capillary wall we get a stress contribution to the tissue surface as
where .Math..sub.t = .Math..sub.tr + i.Math..sub.ti = .Math..sub.tr(1 +iη) is the complex shear stiffness of the tissue where the imaginary component produces absorption of oscillation power. At the bubble-tissue surface interface this stress adds to the pressure in Eq.(A5) to the following pressure from the cylindrical bubble surface towards the tissue
[0119] When the bubble cylindrical length 2/.sub.c is adequately larger than the capillary radius a.sub.v, we can approximate the bubble with semi-spherical end surfaces with radius a.sub.v with a cylinder with length 2L as shown in Eqs.(7, 8) above. P.sub.d (a.sub.v,k.sub.z is the z-Fourier transform of a spatially constant drive pressure amplitude P.sub.d relative to infinity in the interval (- L, L), and zero outside
[0120] The ψ.sub.r vibration amplitude at the cylindrical part of the bubble amplitude, gives a volume change of the cylinder
[0121] Changing integration coordinates q = k.sub.za.sub.v, k.sub.z = q/a.sub.v , dk.sub.z = dq/a.sub.v we get the direct drive transfer function H.sub.d as
where c.sub.s is the shear wave velocity and ω.sub.s is the shear wave angular frequency. Introducing x = ω/ ω.sub.s we obtain the scaled direct drive transfer function F.sub.d as
[0122] Note that for the cylindrical bubble in a capillary we have above put the surrounding tissue real shear stiffness .Math..sub.tr outside H.sub.d and F.sub.d. This gives F.sub.d the nice property that it does not depend on .Math..sub.tr and ω.sub.s, only on η. We assume a linear variation η with frequency, i.e. η = 2αx. The resonance frequency of F.sub.d is defined as the value x.sub.d that gives the real part of F.sub.d equal zero, i.e. Re{Fd(xd;L/av}.
[0123] Including gas elasticity according to Eq.(3) we get the complete transfer function from incident pressure to relative volume amplitude
[0124]
[0125] Due to the frequency variation of the displacement along the bubble surface as shown in 212 of
[0126] With the 2.sup.nd order approximation of H.sub.v in Eq.(A14) we can from Eq.(13) approximate the scattered field in the low frequency range as
[0127] For detection of the low frequency LF vibration amplitude we transmit a high frequency (HF) pulse, HF ~ 10*LF or more, i.e. ω>> ω.sub.0, as described in relation to Eqs.(12-19) and
[0128] Inserted into Eq.(13) we then get the approximation to the scattered field for the Ω.sub.H frequency range as
[0129] The received HF amplitude is then proportional to
[0130] With the 2.sup.nd order approximation of H.sub.v in Eq.(A14) the angular frequency ω.sub.m for max|H.sub.v (ω)| is given by
REFERENCES
[0131] 1. Lars Hoff: “Acoustic Characterization of Contrast Agents for Medical Ultrasound Imaging” Springer Science + Business Media. 2001