An apparatus and method for minimally invasive treatment of deep subcutaneous fat deposits in lieu of cosmetic surgery is disclosed. The apparatus comprises a high voltage pulse generator connected to two or more needle electrodes at least one of which is configured for placement deeply under the skin in a treatment site of the patient's body. high voltage pulses, delivered to the electrodes, create an electric field that kills subcutaneous fat cells.

Patent
   RE43009
Priority
Aug 17 2000
Filed
Oct 01 2009
Issued
Dec 06 2011
Expiry
Aug 17 2021
Assg.orig
Entity
Large
87
153
all paid
18. A method for reducing the number of subcutaneous fat cells in a predetermined treatment zone by electroporation of the cells in the treatment zone, said method comprising:
disposing at least a first electrode in the treatment zone;
disposing a second electrode on the patient's skin in close proximity to the first electrode; and
applying high voltage electric field pulses via the first and second electrodes with an amplitude sufficient to cause death to subcutaneous fat cells by electroporation.
10. Apparatus for reduction of subcutaneous fat deposits in a predetermined treatment zone beneath a predetermined area of a patient's skin by electroporation, said apparatus comprising:
a plurality of electrodes, wherein at least one of said electrodes is a subcutaneous electrode configured for placement under the skin and within the treatment zone and wherein at least one of said electrodes is a patch electrode applied to the patient's skin;
a generator of high voltage pulses for applying a pulsed electric field to the treatment zone via said electrodes, wherein the applied pulses generate an electric field above the upper electroporation limit for subcutaneous fat cells in the treatment zone, and
connectors connecting said generator of high voltage electrical pulses with said electrodes.
7. An apparatus for reducing deep subcutaneous fat deposits in a predetermined treatment volume beneath a predetermined area of a patient's skin by electroporation, said apparatus comprising:
a set of needle electrodes, wherein said set of electrodes comprises:
an array of electroporation needle electrodes, said electroporation needle electrodes being provided for applying a pulsed electric field to the subcutaneous volume of tissues, wherein said needle electrodes are arrayed such that each needle electrode is adjacent to at least one needle electrode having the opposite polarity and wherein the needle electrodes include proximal and distal insulated portions and a central uninsulated portion configured to insulate the skin and dispose the uninsulated portion in the subcutaneous fat deposit;
a generator of high voltage pulses for applying a pulsed electric field to the predetermined area via said electrode set, said pulses generating an electric field above the upper electroporation limit for subcutaneous fat cells in the volume of the subcutaneous tissue to be treated, and
connectors connecting said generator of high voltage electrical pulses with corresponding electroporation electrodes.
1. An apparatus for reducing subcutaneous fat deposits by electroporation comprising:
an applicator comprising a plurality of needle electrodes adapted for penetrating the skin of a patient and applying a high amplitude pulsed electric field to the area of the subcutaneous volume of fat tissue to be treated by electroporation, at least one of said plurality of needle electrodes includes insulated portions and a pair of uninsulated needle portions axially separated along said needle electrode, wherein
said uninsulated needle portions form axially separate electrodes of opposite polarity; and
said insulated portions include proximal, distal, and central insulated portions, said proximal insulated portion being provided for insulating the skin of the patient during an electroporation treatment, said distal insulated portion being provided to avoid spark discharges to an adjacent needle electrode and said central insulated portion separating said electrodes, wherein said electrodes are disposed on said needle electrode such that they are disposed within the subcutaneous fat deposit during treatment;
a generator of high voltage pulses for applying pulsed electric field to the electrodes, said pulses generating an electric field above the upper electroporation limit for subcutaneous fat cells in the volume of subcutaneous fat tissue to be treated; and
connectors connecting said generator of high voltage electrical pulses with corresponding needle electrodes placed under the skin.
6. A method for reducing deep subcutaneous fat deposits by electroporation comprising:
providing an applicator comprising a set of high voltage needle electrodes adapted for penetrating the skin of a patient and applying a high amplitude pulsed electric field to the area of the subcutaneous volume of tissues to be treated by electroporation, at least one of said plurality of needle electrodes including insulated portions and a pair of uninsulated needle portions axially separated along said needle electrode, wherein
said uninsulated needle portions form axially separated electrodes of opposite polarity; and
said insulated portions include proximal, distal, and central insulated portions, said proximal insulated portion being provided for insulating the skin of the patient during an electroporation treatment, said distal insulated portion being provided to avoid spark discharges to an adjacent needle electrode and said central insulated portion separating said electrodes, wherein said electrodes are disposed on said needle electrode such that they are disposed within the subcutaneous fat deposit during treatment;
providing a generator of high voltage pulses for applying pulsed electric field to the electrodes, said pulses generating an electric field above the upper electroporation limit for subcutaneous fat cells in the volume of the subcutaneous tissue to be treated;
connecting said generator of high voltage electrical pulses with corresponding needle electrodes placed in the deep subcutaneous fat tissue; and
applying high voltage pulses via said set of needle electrodes with an amplitude sufficient to cause death to subcutaneous fat cells.
2. An apparatus according to claim 1 wherein said high voltage pulses have a duration in a range of about 10 microseconds to about 10 millisecond.
3. An apparatus according to claim 1 wherein the amplitude of the electric field applied to the treated volume falls in a range of about 20 Volt/mm to about 2000 Volt/mm.
4. An apparatus according to claim 1 wherein high voltage pulses are electrically balanced in such a manner that in average no direct current is passing through the treatment volume.
5. An apparatus according to claim 1 wherein high voltage pulses are rectangularly balanced.
8. An apparatus according to claim 7 wherein high voltage pulses are electrically balanced in such a manner that in average no direct current is passing through the treatment volume.
9. An apparatus according to claim 7 wherein high voltage pulses are rectangular rectangularly balanced.
11. An apparatus according to claim 10 wherein said subcutaneous electrode is a needle electrode adapted for penetrating the skin of a patient, said needle electrode including insulated portions and a pair of uninsulated needle portions axially separated alone said needle electrode, wherein
said uninsulated needle portions form axially separate electrodes of opposite polarity; and
said insulated portions include proximal, distal, and central insulated portions, said proximal insulated portion being provided for insulating the skin of the patient during an electroporation treatment, said distal insulated portion being provided to avoid spark discharaes to an adjacent needle electrode and said central insulated portion separating said electrodes, wherein said electrodes are disposed on said needle electrode such that they are disposed within the subcutaneous fat deposit during treatment.
12. An apparatus according to claim 10 wherein said apparatus includes at least a pair of subcutaneous electrodes.
13. An apparatus according to claim 12 wherein each of said at least one pair of subcutaneous electrodes is formed on a needle comprising proximal and distal insulated portions and wherein said subcutaneous electrode is formed therebetween said insulated portions on each needle.
14. An apparatus according to claim 10 and further including plurality of subcutaneous electrodes and wherein said plurality of subcutaneous electrodes comprises an array of electrodes each configured for placement under the skin and within the treatment zone, said electrodes being provided with alternating positive and negative polarities.
15. An apparatus according to claim 10 wherein the high voltage pulses are electrically balanced in such a manner that in average no direct current is passing through the treatment zone.
16. An apparatus according to claim 10 wherein the high voltage pulses are rectangularly balanced.
17. An apparatus according to claim 10 wherein said high voltage pulses have a duration in a range of about 10 microseconds to about 10 millisecond.
19. A method according to claim 18 wherein said at least one treatment zone electrode is a needle including an electrode.
20. A method according to claim 18 and further including a needle, wherein said plurality of electrodes comprises a pair of spaced apart electrodes disposed on said needle.
21. A method according to claim 18 wherein the high voltage pulses are electrically balanced in such a manner that in average no direct current is passing through the treatment zone.
22. An apparatus according to claim 17 wherein the amplitude of the electric field applied to the treated volume falls in a range of about 20 Volt/mm to about 2000 Volt/mm.
23. An apparatus according to claim 18 wherein said high voltage pulses have a duration in a range of about 10 microseconds to about 10 millisecond.
24. An apparatus according to claim 23 wherein the amplitude of the electric field applied to the treated volume falls in a range of about 20 Volt/mm to about 2000 Volt/mm.

The present application claims priority from and is a continuation-in-part of U.S. patent application Ser. No. 09/931,672, filed Aug. 17, 2001, entitled Apparatus and Method for Reducing Subcutaneous Fat Deposits, Virtual Face Lift and Body Sculpturing by Electroporation, now U.S. Pat. No. 6,892,099, the specification and drawings of which are incorporated herein in their entirety by reference, which claims the benefit of U.S. Provisinal Application Ser. No. 60/267,106 filed Feb. 8, 2001 and U.S. Provisional Application Ser. No. 60/225,775, filed Aug. 17, 2000. The present application also claims priority from U.S. Provisional Patent Application Serial No. 60/358,443, filed Feb. 22, 2002, and entitled Apparatus and Method for Reducing Subcutaneous Fat Deposits by Electroporation, the specification and drawings of which are incorporated herein in their entirety by reference.

The present invention relates generally to electroporation in-vivo and specifically to apparatus and method for reducing subcutaneous fat deposits and/or for performing virtual face lifts and/or body sculpturing.

“Cosmetic surgery” is a phrase used to describe broadly surgical changes made to a human body with the usual, though not always, justification of enhancing appearance. This area of medical practice constitutes an ever-growing industry around the world. Obviously, where such a procedure fails to deliver an enhanced appearance, the procedure fails to meet the desired goal. One of the reasons that the majority of current procedures fail to deliver upon their promise is that, for the most part, current procedures are invasive, requiring incisions and suturing, and can have serious and unpleasant side effects, including but not limited to scarring, infection, and loss of sensation.

One of the more common forms of cosmetic surgery is the “face-lift.” A face-lift is intended to enhance facial appearance by removing excess facial skin and tightening the remaining skin, thus removing wrinkles. A face-lift is traditionally performed by cutting and removing portions of the skin and underlying tissues on the face and neck. Two incisions are made around the ears and the skin on the face and neck is separated from the subcutaneous tissues. The skin is stretched, excess tissue and skin are removed by cutting with a scissors or scalpel, and the skin is pulled back and sutured around the ears. The tissue tightening occurs after healing of the incisions because less skin covers the same area of the face and neck and also because of the scars formed on the injured areas are contracting during the healing process.

Traditional face-lift procedures are not without potential drawbacks and side effects. One drawback of traditional cosmetic surgery is related to the use of scalpels and scissors. The use of these devices sometimes leads to significant bleeding, nerve damage, possible infection and/or lack of blood supply to some areas on the skin after operation. Discoloration of the skin and alopecia (baldness) are other possible side effects of the standard cosmetic surgery. The overall quality of the results of the surgery is also sometimes disappointing to the patients because of possible over-corrections, leading to undesired changes in the facial expression. Additionally, face-lift procedures require a long recovery period before swelling and bruising subside.

The use of lasers to improve the appearance of the skin has been also developed. Traditional laser resurfacing involves application of laser radiation to the external layer of the skin—the epidermis. Destruction of the epidermis leads to rejuvenation of the epidermis layer. The drawback of the laser resurfacing procedure is possible discoloration of the skin (red face) that can be permanent.

Another laser procedure involves using optical fibers for irradiation of the subcutaneous tissues, such as disclosed in U.S. Pat. No. Re36,903. This procedure is invasive and requires multiple surgical incisions for introduction of the optical fibers under the skin. The fibers deliver pulsed optical radiation that destroys the subcutaneous tissues as the tip of the fiber moves along predetermined lines on the face or neck. Debulking the subcutaneous fat and limited injury to the dermis along the multiple lines of the laser treatment results in contraction of the skin during the healing process, ultimately providing the face lift. The drawback of the method is its high price and possibility of infection.

Electrosurgical devices and methods utilizing high frequency electrical energy to treat a patient's skin, including resurfacing procedures and removal of pigmentation, scars, tattoos and hairs have been developed lately, such as disclosed in U.S. Pat. No. 6,264,652. The principle drawback of this technology is collateral damage to the surrounding and underlying tissues, which can lead to forming scars and skin discoloration.

Other forms of cosmetic surgery are also known. One example is liposuction, which is an invasive procedure that involves inserting a suction device under the skin and removing fat tissues. As with other invasive surgical procedures, there is always a risk of infection. In addition, because of the invasive nature of the procedure, physicians usually try to minimize the number of times the procedure must be performed and thus will remove as much fat tissue as possible during each procedure. Unfortunately, this procedure has resulted in patient deaths when too much tissue was removed. Assuming successful removal of excess fat tissue, further invasive surgery may be required to accomplish desired skin tightening.

The prior art to date, then, does not meet the desired goal of performing cosmetic surgery in a non-invasive manner while causing minimal or no scarring of the exterior surface of the skin and at the same time resulting in the skin tightening.

The term “electroporation” (EP) is used herein to refer to the use of a pulsed electric field to induce microscopic pores in the biological membranes, also commonly called a cell wall, of living cells. The cell membrane separates the inner volume of a cell, or cytosol, from the extracellular space, which is filled with lymph. This membrane performs several important functions, not the least of which is maintaining gradients of concentration of essential metabolic agents across the membrane. This task is performed by active protein transporters, built in the membrane and providing transport of the metabolites via controlled openings in the membrane. Normally, the active protein transporters, or pumps, which routinely provide transport of various metabolic agents, especially proteins, across the cell membrane, use either the energy of positive ions (hydrogen or sodium ions) passing from the positive potential of the intracellular space to the negative potential of the cytosol, or the energy of negative ions (chlorine ions) for movement across the membrane in the opposite direction. This energy supply for the protein transporters is provided by maintaining the potential difference across the membrane, which, in turn, is linked to the difference in concentrations of sodium and potassium ions across the membrane. When this potential difference is too low, thousands of the active transporters find themselves out of power.

Inducing relatively large pores in the cell membrane by electroporation creates the opportunity for a fluid communication through the pores between the cytosol and the extracellular space that may lead to a drastic reduction of these vitally important gradients of concentrations of the metabolic agents and thus a reduction in the potential difference across the membrane. Uncontrolled exchange of metabolic agents, such as ions of sodium, potassium, and calcium between a living cell and the extracellular space imposes on the cell intensive biochemical stress.

When a cell is undergoing biochemical stresses the major biochemical parameters of the cell are out of equilibrium and the cell cannot perform its routine functions. Invasion of very high concentration of calcium ions through membrane pores from the interstitial space between cells, where the calcium ion concentration is about 100 times higher than in the cytosol, can create such stresses by reducing the potential difference across the membrane. In an attempt to repair itself, the cell starts working in a damage control mode: an emergency production of actin filaments is triggered that extend across the large pores in the membrane in an attempt to bridge the edges of the pores, pull the edges together, and thereby seal the membrane. In muscle cells the calcium ion invasion may cause lethal structural damage by forcing the cell to over-contract and rupture itself. Small pores in the membrane created by a relatively short electric pulse can reseal themselves spontaneously and almost instantaneously after the removal of electric field. No significant damage to the cell is done in this case. Contrary to that, larger pores may become meta-stable with very long life time and cause irreversible damage. It can be said that, depending on the number, effective diameter -and life time of pores in the membrane, electroporation of the cell may result in significant metabolic or structural injury of the cell and/or its death. The cause of cell death after electroporation is believed to be an irreversible chemical imbalance and structural damage resulted from the fluid communication of the cytosol and the extracellular environment.

Below a certain limit of the electric field no pores are induced at all. This limit, usually referred to as the “lower EP limit” of electroporation, is different for different cells, depending, in part, on their sizes in an inverse relationship. That is, pores are induced in larger cells with smaller electric fields while smaller cells require larger electric fields. Above the lower EP limit the number of pores and their effective diameter increase with both the amplitude and duration of the electric field pulses.

Removing the electric field pulses enables the induced pores to reseal. This process of resealing of the pores and the ability of the cell to repair itself, discussed briefly above, currently is not well understood. The current understanding is that there is a significant range of electric field amplitudes and pulse durations in which cells survive electroporation and restore their viability thereafter. An electroporated cell may have open pores for as long as many minutes and still survive. The range of electric field amplitudes and pulse durations in which cells survive is successfully used in current biomedical practice for gene transfer and drug delivery inside living cells.

Nevertheless, the survivability of electroporated cells is limited As the electric field amplitude and/or duration of pulses, increases, this limit, usually referred to as the “upper EP limit” of electroporation, is inevitably achieved. Above the upper EP limit, the number and sizes of pores in the cellular membrane become too large for a cell to survive. Multiple pulses cause approximately the same effect on the cells as one pulse with a duration equal to the total duration of all applied pulses. After application of an electrical pulse above the upper electroporation limit the cell cannot repair itself by any spontaneous or biological process and dies. The upper EP limit is defined by the combinations of the amplitudes of electric field and pulse durations that cause cellular death.

The vulnerability of cells to electroporation depends on their size: the larger the cell, the lower the electric field and duration of a pulse capable of killing it. If cells of different sizes are exposed to the same electric field, the largest cells will die first. Thus, this ability of electroporation to discriminate cells by their sizes may be used to selectively kill large cells in the human body.

In the previously referred to application for U.S. patent application entitled “Apparatus and Method for Reducing Subcutaneous Fat Deposits, Virtual Face Lift and Body Sculpting by Electroporation”, Ser. No. 09/931,672, filed Aug. 17, 2001, an apparatus and method for performing non-invasive treatment of the human face and body by electroporation in lieu of cosmetic surgery is disclosed. The apparatus comprises a high voltage pulse generator and an applicator having two or more electrodes utilized in close mechanical and electrical proximity with the patient's skin to apply electrical pulses thereto. The applicator may include at least two electrodes with one electrode having a sharp tip and another having a flat surface. High voltage pulses delivered to the electrodes create at the tip of the sharp electrode an electric field high enough to cause death of relatively large subcutaneous fat cells by electroporation. Moving the electrode tip along the skin creates a line of dead subcutaneous fat cells, which later are metabolized by the body. Multiple applications of the electrode along predetermined lines on the face or neck create shrinkage of the skin and the subcutaneous fat reduction under the treated area.

The electroporation in-vivo, employed in the disclosed method is a non-invasive treatment of subcutaneous fat, which, as was previously described before, involves application of high amplitude electric pulses between external electrodes to cause death by electroporation of the subcutaneous fat cells. Fat cells, being typically larger than other cells of the body, are more easily killed by electroporation treatment than are smaller lean muscle cells. The electric field, applied to the external electrodes, is efficient for cell killing in the subcutaneous layer of fat tissue directly under the skin. However, the amplitude of the field significantly decreases with increasing the depth of the deposits of fat cells. The deeper penetration of the electric field may be achieved by increasing the distance between electrodes with simultaneous increase in the operating voltage. This approach, though, leads to concomitant increase of the volume that is treated by electroporation. Occasionally, during such cosmetic and body sculpting procedures as described above, a small volume of deep subcutaneous fat deposit must be treated. The non-invasive method of treating subcutaneous tissue by electroporation as described in the earlier referenced patent application, in which the high voltage pulses are applied to the external electrodes, is sometimes difficult to apply to deep fat deposits especially when a fine spatial resolution is required

It would be desirable to have available an apparatus and a method for electroporation treatment to reduce deep fat deposits by allowing deep localized application of the electroporation pulses that can provide high spatial resolution of the body sculpting. Preferably, such apparatus and methods would also be minimally invasive.

The present invention provides an apparatus and method for creation of a controlled electroporation injury to deep subcutaneous fat tissues that, with the healing that follows, leads to permanent loss of the fat cells in the treated tissue. According to present invention an electric field capable of killing fat cells in deep subcutaneous deposits may be applied by a set of needle electrodes, configured for placement deeply under the skin. An apparatus according to the current invention comprises a voltage pulse generator, an applicator with two or multiple electrodes of different shapes and sizes, and a cable connecting the electrodes to the pulse generator. The pulse generator produces a sequence of high voltage pulses of predetermined amplitude, duration and number to cause necrosis in a treated area of the subcutaneous tissue.

A method of weight loss and body sculpturing in accord with the present invention comprises application of electrical pulses to the electrodes positioned under the skin in a treatment area of the subcutaneous fat tissue. The amplitude, duration and number of applied pulses are selected to cause necrosis of fat cells at a predetermined distance around the needles in the subcutaneous tissue. During the treatment a number of sites in a predetermined pattern are exposed to electroporation. Later, during the healing process the treated area contracts as the electroporated cells die and are metabolized by the body, thus reducing volume of fat tissue and providing desired change of body contours. The injury to the tissues made by electroporation is very selective, targeting only large fat cell and not damaging the epidermis, the most external layer of the skin. As a matter of fact, in accordance with the current invention, the electrical field is applied only to the deep subcutaneous fat deposits, no electric field is applied to the skin of the patient.

The present invention, as well as its various features and advantages, will become evident to those skilled in the art when the following description of the invention is read in conjunction with the accompanying drawings as briefly described below and the appended claims. Throughout the drawings, like numerals refer to similar or identical parts.

FIG. 1 is a schematic illustration of an electroporation system for treatment of deep subcutaneous fat deposits.

FIG. 2 shows time diagrams for high voltage pulses during EP treatment wherein FIG. 2a illustrates unipolar pulsing and FIG. 2b illustrates bipolar pulsing.

FIG. 3 illustrates a one-needle applicator with two electrodes.

FIG. 4 illustrates an embodiment of an applicator comprising one needle in combination with an external patch electrode wherein FIG. 4a provides a plan view and FIG. 4b provides a cross-sectional view taken along viewing plane 4b—4b.

FIG. 5 illustrates an embodiment of the applicator comprising an array of needle electrodes.

FIG. 6 illustrates in orthogonal views in FIGS. 6a and 6b an embodiment of the applicator comprising needle electrodes without insulated parts.

FIG. 1 shows schematically an electroporation system 100 for in-vivo treatment of deep subcutaneous fat deposits. The system 100 includes a high voltage electroporation pulse generator 101 connected by an appropriate connector 102 to an applicator 103. Applicator 103 may include a handle 104 and a pair of needle 120 and 122 extending therefrom. Handle 104 may be used by the operator for the safe and efficacious placement of the needles 120 and 122 in a selected-for-treatment anatomical site. Needles 120 and 122 may include proximal insulated portions 124 and 126, respectively, central uninsulated portions 128 and 130, respectively, and distal insulated portions 132 and 134. Preferably, distal portions 132 and 134 includes sharpened ends or tips 136 and 138, respectively.

As illustrated in the Figure, an operator of system 100 will use handle 104 to push the tips 136 and 138 through the skin 150 of the patient into a deep subcutaneous fat deposit 152. The sharpened tips 136 and 138 facilitate penetration of the skin 150 and fat tissue 152 while minimizing pain or serious discomfort to the patient. Insulated proximal portions 124 and 126 of needles 120 and 122, respectively, provide electrical insulation from the skin 150 during an EP treatment. That is, this insulation prevents a current flow from the needles 120 and 122 through the skin and with it an associated discomfort of the patient. Similarly, the insulated distal portions 132 and 134 of needles 120 and 122 helps to avoid spark discharges between the tips during high voltage electroporation pulsing.

Central portions 128 and 130 form the electrodes for the system 10, which as noted are uninsulated. The electrodes 128 and 130 are in close electrical contact with the surrounding tissue 152 and provide a pulsed electrical field, as indicated by shown by arrows 160, to the treatment zone 162 between and around electrodes 128 and 130, as indicated by dotted line 162. It will be understood that the treatment zone is actually a three dimensional zone extending in all directions from the electrodes 128 and 130.

The larger the diameter of the cells or the higher applied voltage, the larger treatment zone 162 will be where the cells are actually killed. It should be mentioned that not all cells die at any point of the treatment zone. The smaller fat cells will survive. As was mentioned early, cell killing by electroporation is selective on the cell size and the upper EP limit is higher for small cells. Small fat cells, for which applied electric field is below the upper electroporation limit, will survive any reasonable number of electric pulses without any morphological or functional damage and will stay in the tissue. Also, there is no electroporation treatment for the tissues interfacing the insulated parts of the needles.

A computer 170 connected by an appropriate connector 172 to EP generator 101, may be provided to control the whole procedure of EP treatment: the predetermined amplitude, duration, and number of EP pulses supplied to the electrodes 128 and 130. The EP pulses may be applied with a repetition rate of about 1 to about 50 Hz and may have a current peak of about 0.5 to about 10 A depending on the size and shape of electrodes. Generally, the voltage of the EP pulses can be in the range of about 50 V to about 5000 V with a duration from about 10 microseconds to about 10.0 milliseconds depending on the location of the treated segment of the body, the sizes and shapes of the electrodes, and the distance between the electrodes. Regardless of the possible configuration of the electrodes and the voltages applied to the treatment volume, the voltage applied to an individual subcutaneous fat cell should fall in the range of about 2 to about 10 V per cell to be able to kill it.

To achieve successful cell killing by electroporation the electric field applied to the treated volume of cells must be above the upper EP limit for the cells. The probability of cell killing increases if longer or multiple pulses are employed.

According to present invention high voltage pulses of different waveforms may be used for the EP treatment. The pulses may be rectangular or exponential in shape, be unipolar (positive or negative only) or bipolar (positive and negative). Bipolar rectangular pulses are known to be very efficient in cell killing by electroporation. This is because both directions of the electrical field, positive and negative, are equally efficient in creating pores in cellular membranes, and the electric field strength, contrary to the exponential pulses, stays high during the whole pulse. The efficiency results because electroporation is a process related to the difference in the energy of the porous and non-porous membrane in the presence of an electric field. The energy difference depends on the square of the amplitude (or strength) of the electric field (i.e., E2) and does not depend on the sign or polarity (+ or −) of the electric field.

From a practical stand point, however, applying balanced pulses during in-vivo electroporation treatment has one important advantage. Contrary to unipolar pulsing, that carries a direct current component into the treated tissue and creates undesired electrolytic effects on the interface of the electrodes and tissues, bipolar pulsing is free from these drawbacks. With bipolar pulsing of the field, problems such as metal depositions from the electrodes or chemical decomposition of tissue during treatment are largely if not completely avoided.

These advantageous properties of balanced pulses, namely, high efficiency in cell killing and freedom from electrolytic effects, make using rectangular bipolar balanced pulses a preferred mode for electroporation pulsing in the current invention. Technically, balancing of two pulses of the opposite polarities may be easily achieved by using a pulse generator having a direct current blocking capacitor electrically coupled in series to the needle electrodes.

In FIGS. 2a and 2b plots of high voltage EP pulses against time are shown. In FIG. 2a the upper curve shows a plot of rectangular balanced pulses, the preferred embodiment and the lower curve shows exponential balanced pulses. FIG. 2b depicts rectangular and exponential unipolar pulses in the upper and lower curves, respectively.

In FIG. 3 another embodiment 300 of the needle applicator is shown. Needle applicator 300 comprises a single needle 310 with two axially separated electrodes 328 and 330 of opposite polarity insulated from each other and separated by insulator 308. The needle may be made of a hollow tube carrying inside two conductors connecting electrodes 328 and 330 via cable 302 to the output of the EP generator, not shown in the figure. Proximal end 325 of the needle 310 is covered with an insulation layer to protect the skin of the patient during treatment from an electric current and discomfort associated with it. To avoid sparking from the distal end 333 of the applicator the needle 310 may be made of insulating material or of a metal piece electrically insulated from the electrodes 328 and 330. Additionally, distal end 333 may have a sharp tip 337.

The electric field between electrodes 328 and 330 is shown by lines 360. Dotted lines 362 delineate the treatment zone, where the electric field is the highest and where actual killing cells by electroporation occurs.

Yet another embodiment 400 of the needle applicator is shown in FIG. 4 in two substantially orthogonal views, namely FIGS. 4a and 4b. Applicator 400 comprises a needle 410 with an electrode 428 combined with a patch electrode 430. Patch electrode 430 is placed on the skin 450 of the patient near the treatment site, which is delineated by a dotted line 462. Needle 410 may include a sharp tip 436 and insulated proximal and distal portions 442 and 433 on either side of electrode portion 428 of needle 410. The electrical field lines generated between electrodes 428 and 430 are indicated by lines 460. High voltage EP pulses during treatment are delivered to the electrodes 428 and 430 via appropriate conductors 454 and 455, respectively, which are connected to the connector 402 coupled to the output of the EP generator 101, not shown in the FIG. 4.

During use of the needle applicator 400, the electroporation leading to cellular death occurs only around the conductive surface, i.e., electrode 428, of the needle placed in the tissue. No electroporation takes place near the patch electrode 430 on the skin because the value of the electric field near its surface is less than the upper EP limit. FIG. 4b shows cross section of the applicator. Dotted line 462 delineates the treatment zone around the electrode 428 where the fat cells are killed.

FIG. 5 shows yet another implementation 500 of a needle applicator in accord with the present invention. Applicator 500 comprises a handle 504 supporting a needle frame 505. Needle frame 505 supports a plurality of needles 520 of one polarity (positive) and a plurality of needles 522 including an electrode of the other polarity (negative), with each needle of one polarity being adjacent to one or more needles of the other polarity. Handle 504 is connected via connector 502 to the output of the EP generator 101 (not shown in the Figure). The needles 520 and 522 in the needle array alternately have positive and negative polarity. The needles 520 and 522 may include a proximal insulated portion 524 and 526, central electrode portions 528 and 530, and distal insulated portions 536 and 538 respectively. Each needle 520 and 522 will also preferably include sharp tip 536 and 538. For EP treatment of subcutaneous deposits the needles are placed preferably normally to the skin. One of benefits of this configuration is that the tissue electroporation occurs in thin cylindrical layers around the electrodes and later, during healing process, macrophages from nearby blood vessels will travel a shorter distance to the damaged cells. Thus, this configuration may accelerate the disposal of the dead fat cells.

Yet another implementation of the needle applicator is shown in FIG. 6. Applicator 600 may include a handle 604 and a pair of needle 620 and 622 extending therefrom. Handle 604 may be used by the operator for the safe and efficacious placement of the needles 620 and 622 in a selected-for-treatment anatomical site. The sharpened tips 636 and 638 facilitate penetration of the skin 650 and fat tissue 652 while minimizing pain or serious discomfort to the patient. In this implementation of the current invention the whole needles 620 and 622 perform function of electrodes; that is, the needles 620 and 622 do not include insulated portions as in the previously described embodiments. Via an appropriate connector 602 needles 620 and 622 are connected to the EP generator (not shown in the Figures) providing high voltage pulses during treatment. Electric field lines between electrodes 620 and 622 are shown by arrows 660. Dotted line 662 shows the treatment area of the fat tissue 652 where electroporation actually kills fat cells.

Needle electrode diameters may fall in a range of about 0.3 mm to about 1.0 mm, which corresponds to the standard of minimally invasive size. The distance between adjacent needles may be in a range of several mm to several cm. Applied voltage, depending on the distance between needles and the size of the fat cells to be killed, may vary in a wide range from about 100 V to several hundreds and even thousands of volts. In any case the resultant electric field applied to the treated fat cells must be above their upper electroporation limit, or about 2 to about 10 V per cell. The electroporation pulses during treatment may be applied simultaneously to all electrodes or in a sequence of sets of two to several electrodes throughout the whole treated area. The number of pulses per treatment of a selected site may vary from several pulses to several tens of pulses. Preferred duration of the pulses is from about 10 microseconds to about 10 milliseconds.

A method for electroporation treatment of deep subcutaneous fat deposits comprises providing a high voltage pulse generator for generation EP pulses and a needle applicator. The needle applicator or needle applicator and pad electrode may be placed by a physician in an anatomically selected site of treatment under ultrasound or other type of imaging guidance. After the needle placement a sequence of high voltage EP pulses is applied to the electrodes. The electrodes may be placed in plurality of treatment sites in accordance with a treatment plan developed by a physician. Sequences of the high voltage EP pulses are repeatedly applied to the electrodes. After a session of electroporation treatment the remnants of fat cells and released lips will be metabolized and removed by the patient's body over about a two week period. A subsequent electroporation treatment can then be performed with new treatment sites selected for the electroporation treatment. In this manner, then, a patient's body can be sculpted as desired.

The present invention has been described in language more or less specific as to the apparatus and method features. It is to be understood, however, that the present invention is not limited to the specific features described, since the apparatus and method herein disclosed comprise exemplary forms of putting the present invention into effect. For example, while the needles have been described as having sharp tips, blunted end needles may also be used. Additionally, as indicated in the Figures, insulation may be used on the needles in some embodiments, but not others. The invention is, therefore, claimed in any of its forms or modifications within the proper scope of the appended claims appropriately interpreted in accordance with the doctrine of equivalency and other applicable judicial doctrines.

Chornenky, Victor I., Jaafar, Ali

Patent Priority Assignee Title
10092346, Jul 20 2010 Zeltiq Aesthetics, Inc. Combined modality treatment systems, methods and apparatus for body contouring applications
10117707, Apr 29 2008 Virginia Tech Intellectual Properties, Inc System and method for estimating tissue heating of a target ablation zone for electrical-energy based therapies
10154874, Apr 29 2008 Virginia Tech Intellectual Properties, Inc Immunotherapeutic methods using irreversible electroporation
10201380, Jan 31 2014 ZELTIQ AESTHETICS, INC Treatment systems, methods, and apparatuses for improving the appearance of skin and providing other treatments
10238447, Apr 29 2008 Virginia Tech Intellectual Properties, Inc System and method for ablating a tissue site by electroporation with real-time monitoring of treatment progress
10245098, Apr 29 2008 Virginia Tech Intellectual Properties, Inc Acute blood-brain barrier disruption using electrical energy based therapy
10245105, Apr 29 2008 Virginia Tech Intellectual Properties, Inc. Electroporation with cooling to treat tissue
10272178, Apr 29 2008 Virginia Tech Intellectual Properties, Inc Methods for blood-brain barrier disruption using electrical energy
10286108, Apr 29 2008 Virginia Tech Intellectual Properties, Inc. Irreversible electroporation to create tissue scaffolds
10292755, Apr 09 2009 Virginia Tech Intellectual Properties, Inc. High frequency electroporation for cancer therapy
10292859, Sep 26 2006 Zeltiq Aesthetics, Inc. Cooling device having a plurality of controllable cooling elements to provide a predetermined cooling profile
10383787, May 18 2007 Zeltiq Aesthetics, Inc. Treatment apparatus for removing heat from subcutaneous lipid-rich cells and massaging tissue
10448989, Apr 09 2009 Virginia Tech Intellectual Properties, Inc High-frequency electroporation for cancer therapy
10470822, Apr 29 2008 Virginia Tech Intellectual Properties, Inc System and method for estimating a treatment volume for administering electrical-energy based therapies
10471254, May 12 2014 Virginia Tech Intellectual Properties, Inc Selective modulation of intracellular effects of cells using pulsed electric fields
10524956, Jan 07 2016 ZELTIQ AESTHETICS, INC Temperature-dependent adhesion between applicator and skin during cooling of tissue
10537379, Apr 29 2008 Virginia Tech Intellectual Properties, Inc. Irreversible electroporation using tissue vasculature to treat aberrant cell masses or create tissue scaffolds
10555831, May 10 2016 ZELTIQ AESTHETICS, INC Hydrogel substances and methods of cryotherapy
10568759, Aug 19 2014 ZELTIQ AESTHETICS, INC Treatment systems, small volume applicators, and methods for treating submental tissue
10575890, Jan 31 2014 ZELTIQ AESTHETICS, INC Treatment systems and methods for affecting glands and other targeted structures
10675176, Mar 19 2014 ZELTIQ AESTHETICS, INC Treatment systems, devices, and methods for cooling targeted tissue
10675178, Aug 21 2007 ZELTIQ AESTHETICS, INC Monitoring the cooling of subcutaneous lipid-rich cells, such as the cooling of adipose tissue
10682297, May 10 2016 ZELTIQ AESTHETICS, INC Liposomes, emulsions, and methods for cryotherapy
10694972, Dec 15 2014 Virginia Polytechnic Institute and State University; Virginia Tech Intellectual Properties, Inc Devices, systems, and methods for real-time monitoring of electrophysical effects during tissue treatment
10702326, Jul 15 2011 Virginia Tech Intellectual Properties, Inc Device and method for electroporation based treatment of stenosis of a tubular body part
10702337, Jun 27 2016 GALVANIZE THERAPEUTICS, INC Methods, apparatuses, and systems for the treatment of pulmonary disorders
10765552, Feb 18 2016 ZELTIQ AESTHETICS, INC Cooling cup applicators with contoured heads and liner assemblies
10806500, Jan 31 2014 Zeltiq Aesthetics, Inc. Treatment systems, methods, and apparatuses for improving the appearance of skin and providing other treatments
10828085, Apr 29 2008 Virginia Tech Intellectual Properties, Inc Immunotherapeutic methods using irreversible electroporation
10828086, Apr 29 2008 Virginia Tech Intellectual Properties, Inc Immunotherapeutic methods using irreversible electroporation
10912599, Jan 31 2014 Zeltiq Aesthetics, Inc. Compositions, treatment systems and methods for improved cooling of lipid-rich tissue
10935174, Aug 19 2014 ZELTIQ AESTHETICS, INC Stress relief couplings for cryotherapy apparatuses
10939958, Jun 27 2016 GALVANIZE THERAPEUTICS, INC Methods, apparatuses, and systems for the treatment of pulmonary disorders
10952891, May 13 2014 ZELTIQ AESTHETICS, INC Treatment systems with adjustable gap applicators and methods for cooling tissue
10959772, Apr 29 2008 Virginia Tech Intellectual Properties, Inc. Blood-brain barrier disruption using electrical energy
11076879, Apr 26 2017 ZELTIQ AESTHETICS, INC Shallow surface cryotherapy applicators and related technology
11154418, Oct 19 2015 ZELTIQ AESTHETICS, INC Vascular treatment systems, cooling devices, and methods for cooling vascular structures
11179269, Sep 26 2006 Zeltiq Aesthetics, Inc. Cooling device having a plurality of controllable cooling elements to provide a predetermined cooling profile
11219549, Sep 26 2006 Zeltiq Aesthetics, Inc. Cooling device having a plurality of controllable cooling elements to provide a predetermined cooling profile
11224536, Apr 30 2009 Zeltiq Aesthetics, Inc. Device, system and method of removing heat from subcutaneous lipid-rich cells
11254926, Apr 29 2008 Virginia Tech Intellectual Properties, Inc. Devices and methods for high frequency electroporation
11272979, Apr 29 2008 Virginia Tech Intellectual Properties, Inc. System and method for estimating tissue heating of a target ablation zone for electrical-energy based therapies
11291606, May 18 2007 Zeltiq Aesthetics, Inc. Treatment apparatus for removing heat from subcutaneous lipid-rich cells and massaging tissue
11311329, Mar 13 2018 Virginia Polytechnic Institute and State University; Virginia Tech Intellectual Properties, Inc; VIRGINA POLYTECHNIC INSTITUTE AND STATE UNIVERSITY Treatment planning for immunotherapy based treatments using non-thermal ablation techniques
11369433, Jun 27 2016 GALVANIZE THERAPEUTICS, INC Methods, apparatuses, and systems for the treatment of pulmonary disorders
11382681, Apr 09 2009 Virginia Tech Intellectual Properties, Inc. Device and methods for delivery of high frequency electrical pulses for non-thermal ablation
11382790, May 10 2016 ZELTIQ AESTHETICS, INC Skin freezing systems for treating acne and skin conditions
11395760, Nov 09 2006 Zeltiq Aesthetics, Inc. Tissue treatment methods
11406820, May 12 2014 Virginia Tech Intellectual Properties, Inc Selective modulation of intracellular effects of cells using pulsed electric fields
11446175, Jul 31 2018 ZELTIQ AESTHETICS, INC Methods, devices, and systems for improving skin characteristics
11452634, Apr 30 2009 Zeltiq Aesthetics, Inc. Device, system and method of removing heat from subcutaneous lipid-rich cells
11453873, Apr 29 2008 Virginia Tech Intellectual Properties, Inc. Methods for delivery of biphasic electrical pulses for non-thermal ablation
11583438, Aug 21 2007 ZELTIQ AESTHETICS, INC Monitoring the cooling of subcutaneous lipid-rich cells, such as the cooling of adipose tissue
11607271, Apr 29 2008 Virginia Tech Intellectual Properties, Inc. System and method for estimating a treatment volume for administering electrical-energy based therapies
11607537, Dec 05 2017 Virginia Tech Intellectual Properties, Inc Method for treating neurological disorders, including tumors, with electroporation
11638603, Apr 09 2009 Virginia Tech Intellectual Properties, Inc Selective modulation of intracellular effects of cells using pulsed electric fields
11655466, Apr 29 2008 Virginia Tech Intellectual Properties, Inc. Methods of reducing adverse effects of non-thermal ablation
11707629, May 28 2009 AngioDynamics, Inc. System and method for synchronizing energy delivery to the cardiac rhythm
11723710, Nov 17 2016 AngioDynamics, Inc. Techniques for irreversible electroporation using a single-pole tine-style internal device communicating with an external surface electrode
11737810, Apr 29 2008 Virginia Tech Intellectual Properties, Inc Immunotherapeutic methods using electroporation
11779395, Sep 28 2011 AngioDynamics, Inc. Multiple treatment zone ablation probe
11819257, Jan 31 2014 Zeltiq Aesthetics, Inc. Compositions, treatment systems and methods for improved cooling of lipid-rich tissue
11890046, Apr 29 2008 Virginia Tech Intellectual Properties, Inc System and method for ablating a tissue site by electroporation with real-time monitoring of treatment progress
11903690, Dec 15 2014 Virginia Tech Intellectual Properties, Inc. Devices, systems, and methods for real-time monitoring of electrophysical effects during tissue treatment
11925405, Mar 13 2018 Virginia Tech Intellectual Properties, Inc Treatment planning system for immunotherapy enhancement via non-thermal ablation
11931096, Oct 13 2010 AngioDynamics, Inc. System and method for electrically ablating tissue of a patient
11950835, Jun 28 2019 AngioDynamics, Inc Cycled pulsing to mitigate thermal damage for multi-electrode irreversible electroporation therapy
11952568, Apr 29 2008 Virginia Tech Intellectual Properties, Inc. Device and methods for delivery of biphasic electrical pulses for non-thermal ablation
11957405, Jun 13 2013 AngioDynamics, Inc. Methods of sterilization and treating infection using irreversible electroporation
8676338, Jul 20 2010 ZELTIQ AESTHETICS, INC Combined modality treatment systems, methods and apparatus for body contouring applications
8702774, Apr 30 2009 Zeltiq Aesthetics, Inc.; ZELTIQ AESTHETICS, INC Device, system and method of removing heat from subcutaneous lipid-rich cells
9314368, Jan 25 2010 ZELTIQ AESTHETICS, INC Home-use applicators for non-invasively removing heat from subcutaneous lipid-rich cells via phase change coolants, and associates devices, systems and methods
9375345, Sep 26 2006 Zeltiq Aesthetics, Inc. Cooling device having a plurality of controllable cooling elements to provide a predetermined cooling profile
9408745, Aug 21 2007 ZELTIQ AESTHETICS, INC Monitoring the cooling of subcutaneous lipid-rich cells, such as the cooling of adipose tissue
9545523, Mar 14 2013 ZELTIQ AESTHETICS, INC Multi-modality treatment systems, methods and apparatus for altering subcutaneous lipid-rich tissue
9598691, Apr 29 2008 Virginia Tech Intellectual Properties, Inc Irreversible electroporation to create tissue scaffolds
9655770, Jul 13 2007 Zeltiq Aesthetics, Inc. System for treating lipid-rich regions
9737434, Dec 17 2008 Zeltiq Aestehtics, Inc. Systems and methods with interrupt/resume capabilities for treating subcutaneous lipid-rich cells
9757196, Sep 28 2012 AngioDynamics, Inc. Multiple treatment zone ablation probe
9844460, Mar 14 2013 ZELTIQ AESTHETICS, INC Treatment systems with fluid mixing systems and fluid-cooled applicators and methods of using the same
9844461, Jan 25 2010 ZELTIQ AESTHETICS, INC Home-use applicators for non-invasively removing heat from subcutaneous lipid-rich cells via phase change coolants
9861421, Jan 31 2014 ZELTIQ AESTHETICS, INC Compositions, treatment systems and methods for improved cooling of lipid-rich tissue
9861520, Apr 30 2009 Zeltiq Aesthetics, Inc. Device, system and method of removing heat from subcutaneous lipid-rich cells
9867652, Apr 29 2008 Virginia Tech Intellectual Properties, Inc Irreversible electroporation using tissue vasculature to treat aberrant cell masses or create tissue scaffolds
9888956, Jan 22 2013 AngioDynamics, Inc Integrated pump and generator device and method of use
9895189, Jun 13 2013 AngioDynamics, Inc. Methods of sterilization and treating infection using irreversible electroporation
D777338, Mar 20 2014 ZELTIQ AESTHETICS, INC Cryotherapy applicator for cooling tissue
Patent Priority Assignee Title
1653819,
4016886, Nov 26 1974 The United States of America as represented by the United States Energy Method for localizing heating in tumor tissue
4226246, May 27 1977 Carba Societe Anonyme Apparatus for maintaining the negative potential of human, animal, and plant cells
4262672, Jan 02 1978 Acupuncture instrument
4407943, Dec 16 1976 MILLIPORE INVESTMENT HOLDINGS LIMITED, A CORP OF DE Immobilized antibody or antigen for immunoassay
4810963, Apr 03 1984 Public Health Laboratory Service Board Method for investigating the condition of a bacterial suspension through frequency profile of electrical admittance
4907601, Jun 15 1988 Etama AG Electrotherapy arrangement
4946793, May 08 1987 Electropore, Inc.; ELECTROPORE, INC , A DE CORP Impedance matching for instrumentation which electrically alters vesicle membranes
5019034, Jan 21 1988 MASSACHUSETTS INSTITUTE OF TECHNOLOGY, THE, A CORP OF MA Control of transport of molecules across tissue using electroporation
5052391, Oct 22 1990 R F P , INC High frequency high intensity transcutaneous electrical nerve stimulator and method of treatment
5058605, Feb 22 1989 Ceske vysoke uceni technicke Method and device for the controlled local, non-invasive application of DC pulses to human and animal tissues
5098843, Jun 04 1987 Apparatus for the high efficiency transformation of living cells
5134070, Jun 04 1990 ALLAN PIASETZKI, GREGORY Method and device for cell cultivation on electrodes
5173158, Jul 22 1991 Apparatus and methods for electroporation and electrofusion
5193537, Jun 12 1990 ZOLL Medical Corporation Method and apparatus for transcutaneous electrical cardiac pacing
5273525, Aug 13 1992 GENETRONICS, INC Injection and electroporation apparatus for drug and gene delivery
5283194, Jul 22 1991 Apparatus and methods for electroporation and electrofusion
5318563, Jun 04 1992 RUTH MALIS, REPRESENTATIVE , ESTATE OF LEONARD I MALIS, DECEASED Bipolar RF generator
5328451, Aug 15 1991 Board of Regents, The University of Texas System Iontophoretic device and method for killing bacteria and other microbes
5389069, Jan 21 1988 Massachusetts Institute of Technology Method and apparatus for in vivo electroporation of remote cells and tissue
5403311, Mar 29 1993 Boston Scientific Scimed, Inc Electro-coagulation and ablation and other electrotherapeutic treatments of body tissue
5425752, Nov 25 1991 Method of direct electrical myostimulation using acupuncture needles
5439440, Apr 01 1993 OncoSec Medical Incorporated Electroporation system with voltage control feedback for clinical applications
5458625, May 04 1994 Transcutaneous nerve stimulation device and method for using same
5533999, Aug 23 1993 REFRACTEC INC Method and apparatus for modifications of visual acuity by thermal means
5536240, Aug 12 1992 VENTURE LENDING & LEASING, INC Medical probe device and method
5575811, Jul 08 1993 PROJECT TROJAN INTELLECTUAL PROPERTY ACQUISITION, LLC; AUSLO RESEARCH LLC Benign prostatic hyperplasia treatment catheter with urethral cooling
5626146, Dec 18 1992 British Technology Group Limited Electrical impedance tomography
5634899, Aug 20 1993 VENTION MEDICAL ADVANCED COMPONENTS, INC Simultaneous cardiac pacing and local drug delivery method
5674267, Mar 30 1993 Centre National de la Recherche Scientifique Electric pulse applicator using pairs of needle electrodes for the treatment of biological tissue
5702359, Apr 01 1993 OncoSec Medical Incorporated Needle electrodes for mediated delivery of drugs and genes
5720921, Mar 10 1995 MaxCyte, Inc Flow electroporation chamber and method
5778894, Apr 18 1996 FD MANAGEMENT, INC Method for reducing human body cellulite by treatment with pulsed electromagnetic energy
5782882, Nov 30 1995 Koninklijke Philips Electronics N V System and method for administering transcutaneous cardiac pacing with transcutaneous electrical nerve stimulation
5800378, Aug 12 1992 Vidamed, Inc. Medical probe device and method
5810762, Apr 10 1995 OncoSec Medical Incorporated Electroporation system with voltage control feedback for clinical applications
5836905, Jun 20 1994 Apparatus and methods for gene therapy
5843026, Aug 12 1992 Vidamed, Inc. BPH ablation method and apparatus
5873849, Apr 24 1997 Ichor Medical Systems, Inc. Electrodes and electrode arrays for generating electroporation inducing electrical fields
5919142, Jun 22 1995 BTG International Limited Electrical impedance tomography method and apparatus
5947889, Jan 17 1995 Balloon catheter used to prevent re-stenosis after angioplasty and process for producing a balloon catheter
5983131, Aug 11 1995 Massachusetts Institute of Technology Apparatus and method for electroporation of tissue
5991697, Dec 31 1996 CALIFORNIA, UNIVERSITY OF, REGENTS OF THE, THE Method and apparatus for optical Doppler tomographic imaging of fluid flow velocity in highly scattering media
5999847, Oct 21 1997 Apparatus and method for delivery of surgical and therapeutic agents
6009347, Jan 27 1998 OncoSec Medical Incorporated Electroporation apparatus with connective electrode template
6010613, Dec 08 1995 CELLECTIS S A Method of treating materials with pulsed electrical fields
6016452, Mar 19 1996 Dynamic heating method and radio frequency thermal treatment
6041252, Jun 07 1995 ICHOR MEDICAL SYSTEMS, INC Drug delivery system and method
6055453, Aug 01 1997 OncoSec Medical Incorporated Apparatus for addressing needle array electrodes for electroporation therapy
6068650, Aug 01 1997 OncoSec Medical Incorporated Method of Selectively applying needle array configurations
6085115, May 22 1997 Massachusetts Institute of Technology Biopotential measurement including electroporation of tissue surface
6090106, Jan 09 1996 Gyrus Medical Limited Electrosurgical instrument
6102885, Aug 08 1996 CURVE MEDICAL, LLC Device for suction-assisted lipectomy and method of using same
6106521, Aug 16 1996 United States Surgical Corporation Apparatus for thermal treatment of tissue
6109270, Feb 04 1997 NATIONAL AERONAUTICS AND SPACE ADMINISTRATION, ADMINISTRATOR OF THE Multimodality instrument for tissue characterization
6122599, Feb 13 1998 JONES JAIN, LLP Apparatus and method for analyzing particles
6132419, May 22 1992 Genetronics, Inc. Electroporetic gene and drug therapy
6159163, May 07 1998 Cedars-Sinai Medical Center System for attenuating pain during bone marrow aspiration and method
6208893, Dec 07 1998 OncoSec Medical Incorporated Electroporation apparatus with connective electrode template
6210402, Nov 22 1995 Arthrocare Corporation Methods for electrosurgical dermatological treatment
6212433, Jul 28 1998 Boston Scientific Scimed, Inc Method for treating tumors near the surface of an organ
6216034, Aug 01 1997 OncoSec Medical Incorporated Method of programming an array of needle electrodes for electroporation therapy of tissue
6219577, Apr 14 1998 GMP DRUG DELIVERY, INC Iontophoresis, electroporation and combination catheters for local drug delivery to arteries and other body tissues
6241702, Aug 12 1992 Vidamed, Inc. Radio frequency ablation device for treatment of the prostate
6261831, Mar 26 1999 The United States of America as represented by the Secretary of the Air; GOVERNMENT OF THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY OF THE AIR FORCE, THE Ultra-wide band RF-enhanced chemotherapy for cancer treatmeat
6278895, Apr 27 1997 Ichor Medical Systems, Inc. Electrodes and electrode arrays for generating electroporation inducing electrical fields
6300108, Jul 21 1999 Regents of the University of California, The Controlled electroporation and mass transfer across cell membranes
6326177, Aug 04 1999 OLD DOMINION UNIVERSITY RESEARCH FOUNDATION Method and apparatus for intracellular electro-manipulation
6347247, May 08 1998 OncoSec Medical Incorporated Electrically induced vessel vasodilation
6349233, Feb 22 1993 ELA MEDICAL, S A Neuro-stimulation to control pain during cardioversion defibrillation
6351674, Nov 23 1998 Synaptic Corporation Method for inducing electroanesthesia using high frequency, high intensity transcutaneous electrical nerve stimulation
6387671, Jul 21 1999 REGENTS OF THE UNIVERSITY OF CALIFORNIA,THE Electrical impedance tomography to control electroporation
6403348, Jul 21 1999 Regents of the University of California, The Controlled electroporation and mass transfer across cell membranes
6470211, Jun 03 1997 UAB Research Foundation Method and apparatus for treating cardiac arrhythmia
6482619, Jul 21 1999 The Regents of the University of California Cell/tissue analysis via controlled electroporation
6493592, Dec 01 1999 MEAGAN MEDICAL, INC Percutaneous electrical therapy system with electrode position maintenance
6500173, Jul 18 1996 Arthrocare Corporation Methods for electrosurgical spine surgery
6526320, Nov 16 1998 United States Surgical Corporation Apparatus for thermal treatment of tissue
6562604, Jul 21 1999 The Regents of the University of California Controlled electroporation and mass transfer across cell membranes
6607529, Jun 19 1995 VIDAMED, INC Electrosurgical device
6611706, Nov 09 1998 Syneron Medical Ltd Monopolar and bipolar current application for transdermal drug delivery and analyte extraction
6613211, Aug 27 1999 Monogram Biosciences, Inc Capillary electrokinesis based cellular assays
6627421, Apr 13 1999 CEREVAST THERAPEUTICS, INC Methods and systems for applying multi-mode energy to biological samples
6653091, Sep 30 1998 Lifescan IP Holdings, LLC Method and device for predicting physiological values
6669691, Jul 18 2000 Boston Scientific Scimed, Inc Epicardial myocardial revascularization and denervation methods and apparatus
6678558, Mar 25 1999 GENETRONICS, INC Method and apparatus for reducing electroporation-mediated muscle reaction and pain response
6692493, Feb 11 1998 Cosman Company, Inc.; The General Hospital Corporation Method for performing intraurethral radio-frequency urethral enlargement
6697669, Jul 13 1998 GENETRONICS, INC Skin and muscle-targeted gene therapy by pulsed electrical field
6697670, Aug 17 2001 AngioDynamics, Inc Apparatus and method for reducing subcutaneous fat deposits by electroporation with improved comfort of patients
6702808, Sep 28 2000 Syneron Medical Ltd Device and method for treating skin
6795728, Aug 17 2001 AngioDynamics, Inc Apparatus and method for reducing subcutaneous fat deposits by electroporation
6801804, May 03 2002 ACIONT, INC Device and method for monitoring and controlling electrical resistance at a tissue site undergoing iontophoresis
6865416, May 08 1998 OncoSec Medical Incorporated Electrically induced vessel vasodilation
6892099, Feb 08 2001 AngioDynamics, Inc Apparatus and method for reducing subcutaneous fat deposits, virtual face lift and body sculpturing by electroporation
6912417, Apr 05 2002 ICHOR MEDICAL SYSTEMS, INC Method and apparatus for delivery of therapeutic agents
6927049, Jul 21 1999 Regents of the University of California, The Cell viability detection using electrical measurements
6962587, Jul 25 2000 AngioDynamics, Inc Method for detecting and treating tumors using localized impedance measurement
6972014, Jan 04 2003 Varian Medical Systems, Inc Open system heat exchange catheters and methods of use
6994706, Aug 13 2001 AngioDynamics, Inc Apparatus and method for treatment of benign prostatic hyperplasia
7053063, Jul 21 1999 The Regents of the University of California Controlled electroporation and mass transfer across cell membranes in tissue
7063698, Jun 14 2002 Atricure, Inc Vacuum coagulation probes
7130697, Aug 13 2002 AngioDynamics, Inc Apparatus and method for the treatment of benign prostatic hyperplasia
7211083, Mar 17 2003 AngioDynamics, Inc Apparatus and method for hair removal by electroporation
7267676, Mar 17 2003 AngioDynamics, Inc Method for hair removal by electroporation
20010044596,
20020010491,
20020055731,
20020077676,
20020099323,
20020138117,
20020193831,
20030009110,
20030060856,
20030088189,
20030130711,
20030170898,
20030208200,
20030225360,
20040019371,
20040059389,
20040146877,
20040153057,
20040243107,
20040267189,
20050043726,
20050049541,
20050165393,
20050171523,
20050171574,
20050182462,
20050261672,
20050288730,
20060015147,
20060025760,
20060079883,
20060121610,
20060212078,
20060217703,
20060264752,
20070043345,
20070118069,
20080052786,
DE4000893,
DE863111,
EP378132,
EP935482,
WO20554,
WO107583,
WO107584,
WO107585,
WO181533,
WO4037341,
WO9639531,
//////////
Executed onAssignorAssigneeConveyanceFrameReelDoc
Oct 01 2009AngioDynamics, Inc.(assignment on the face of the patent)
May 22 2012AngioDynamics, IncJPMORGAN CHASE BANK, N A , AS ADMINISTRATIVE AGENTSECURITY AGREEMENT0282600329 pdf
Sep 19 2013AngioDynamics, IncJPMORGAN CHASE BANK, N A , AS ADMINISTRATIVE AGENTSECURITY AGREEMENT0313150720 pdf
Sep 19 2013JPMORGAN CHASE BANK N A , AS ADMINISTRATIVE AGENTAngioDynamics, IncRELEASE BY SECURED PARTY SEE DOCUMENT FOR DETAILS 0313150361 pdf
Nov 07 2016AngioDynamics, IncJPMORGAN CHASE BANK, N A , AS ADMINISTRATIVE AGENTSECURITY INTEREST SEE DOCUMENT FOR DETAILS 0406130049 pdf
Nov 07 2016JPMORGAN CHASE BANK, N A , AS ADMINISTRATIVE AGENTAngioDynamics, IncRELEASE BY SECURED PARTY SEE DOCUMENT FOR DETAILS 0406880540 pdf
Jun 03 2019AngioDynamics, IncJPMORGAN CHASE BANK, N A , AS ADMINISTRATIVE AGENTCONFIRMATORY GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS0493710657 pdf
Aug 30 2022AngioDynamics, IncJPMORGAN CHASE BANK, N A , AS ADMINISTRATIVE AGENTSECURITY INTEREST SEE DOCUMENT FOR DETAILS 0613600668 pdf
Aug 30 2022JPMORGAN CHASE BANK, N A , AS ADMINISTRATIVE AGENTAngioDynamics, IncRELEASE BY SECURED PARTY SEE DOCUMENT FOR DETAILS 0613630446 pdf
Jun 08 2023JPMORGAN CHASE BANK, N A , AS ADMINISTRATIVE AGENTAngioDynamics, IncRELEASE BY SECURED PARTY SEE DOCUMENT FOR DETAILS 0639400362 pdf
Date Maintenance Fee Events
May 07 2012REM: Maintenance Fee Reminder Mailed.
Aug 22 2012M1552: Payment of Maintenance Fee, 8th Year, Large Entity.
Aug 22 2012M1555: 7.5 yr surcharge - late pmt w/in 6 mo, Large Entity.
Mar 09 2016M1553: Payment of Maintenance Fee, 12th Year, Large Entity.


Date Maintenance Schedule
Dec 06 20144 years fee payment window open
Jun 06 20156 months grace period start (w surcharge)
Dec 06 2015patent expiry (for year 4)
Dec 06 20172 years to revive unintentionally abandoned end. (for year 4)
Dec 06 20188 years fee payment window open
Jun 06 20196 months grace period start (w surcharge)
Dec 06 2019patent expiry (for year 8)
Dec 06 20212 years to revive unintentionally abandoned end. (for year 8)
Dec 06 202212 years fee payment window open
Jun 06 20236 months grace period start (w surcharge)
Dec 06 2023patent expiry (for year 12)
Dec 06 20252 years to revive unintentionally abandoned end. (for year 12)