Laparoscopic device

Information

  • Patent Grant
  • 9649125
  • Patent Number
    9,649,125
  • Date Filed
    Tuesday, October 7, 2014
    10 years ago
  • Date Issued
    Tuesday, May 16, 2017
    7 years ago
Abstract
A medical instrument includes a tubular cutter extending along an axis and having a windowed outer sleeve and a moveable inner cutting sleeve. An ultrasound transducer is operatively coupled to the inner cutting sleeve in order to induce motion in the inner cutting sleeve to enhance cutting or resection of tissue by the inner cutting sleeve as it is reciprocated or otherwise moved past the cutting window. The instrument typically will include a motor drive configured to reciprocate and/or rotate the inner cutting sleeve relative to the windowed outer sleeve, usually at a reciprocation rate between 1 and 10 Hz.
Description
BACKGROUND OF THE INVENTION

1. Field of the Invention


The present invention relates devices and methods for cutting and removal of tissue from the interior of a patient's body, typically in a laparosopic procedure.


Laparoscopic and other minimally invasive tissue cutters are known, some of which operate by advancing a tubular blade past an open window in an outer housing to resect or sever intruding tissue. Optionally the cutter may be rotated as it is axially advanced past the window to enhance cutting. Although quite effective, such cutters cannot always adequately cut difficult tissue structure, and it would therefore be advantageous to provide improved devices and methods for laparoscopic and other minimally invasive tissue resection,


2. Description of the Background Art


Reciprocating and rotational tissue cutters are described in U.S. Published Patent Applications 20130267937; 20130172870; and 20120330292. Atherectomy catheters having ultrasound imaging transducers on the cutting blades are described in U.S. Pat. No. 5,429,136.


SUMMARY OF THE INVENTION

In a first aspect, the present invention provides a medical instrument comprising a tubular cutter extending along an axis and having a windowed outer sleeve and a moveable inner cutting sleeve. An ultrasound transducer is operatively coupled to the inner cutting sleeve in order to induce motion in the inner cutting sleeve to enhance cutting or resection of tissue by the inner cutting sleeve as it is reciprocated or otherwise moved past the cutting window. The instrument typically will include a motor drive configured to reciprocate and/or rotate the inner cutting sleeve relative to the windowed outer sleeve, usually at a reciprocation rate between 1 and 10 Hz.


The ultrasound transducer is typically configured to cause at least one of axial motion and rotational motion in the distal end of the inner cutting sleeve. Usually, the inner cutting sleeve will have a cutting edge at is distal end so that the tissue may be effected by axially advancing the blade in a distal direction. Rotational and/or oscillatory motion may be superimposed on the axial reciprocation to enhance cutting with the ultrasonic motion being further superimposed to further enhance cutting. In other embodiments, the inner cutting sleeve may have an axially oriented cutting edge so that cutting is provided primarily by rotation of the sleeve about the axis. In that case, axial oscillation may be superimposed to enhance cutting together with the ultrasonic motion. In all cases, a dimension between the ultrasound transducer and the distal end of the inner sleeve may be selected to optimize at least one of axial motion and rotational motion in the distal end of the inner cutting sleeve.


In some embodiments, the instrument may further comprise at least a second ultrasound transducer, wherein first and second ultrasound transducers are configured to cause axial and rotational motion in the distal end of the inner sleeve. The ultrasound transducer may be removably secured to a handle portion of the tubular cutter.


The instruments of the present invention may further comprise a negative pressure source coupled to a tissue extraction lumen in the tubular cutter. The instrument of the present invention may still further comprise a pressurized fluid source, either liquid, gas, or a mixed fluid, coupled to an inflow lumen in the cutter, and the inflow lumen may extend to an outlet in a distal portion of the cutter.


The instruments of the present invention may further comprise a controller coupled to the tubular cutter for controlling operating parameters of the ultrasound transducer, the motor drive, the negative pressure source, and/or the pressurized fluid source. In such cases, the instruments may still further comprise a sensor configured to send signals to the controller indicating the position of the inner sleeve relative to the window in the outer sleeve, and the controller may be adapted or configured to modulate activation of the ultrasound transducer in response to the sensor signals that indicate the position of the inner sleeve. The controller may activate the ultrasound transducer when the inner sleeve moves toward a window-closed position to cut tissue and de-activates the ultrasound transducer when the inner sleeve moves toward a window-open position. In particular, the controller may activate the pressurized fluid source when the inner sleeve is in a window-closed position and/or may de-activate the pressurized fluid source when the inner sleeve is in a window-open position.


In a second aspect, the present invention provides a medical instrument comprising a tubular assembly extending along an axis with a windowed outer sleeve and a moveable inner cutting sleeve. The inner cutting sleeve has a tissue-extraction passageway. A seal in the tissue-extraction passageway in the inner cutting sleeve has a first condition that closes the passageway and second condition that permits a tissue chip to pass through the seal. The tubular assembly typically has a flow channel terminating in a distal outlet in a region of the assembly that is distal to the seal, where the flow channel is in communication with a fluid source or a negative pressure source.





BRIEF DESCRIPTION OF DRAWINGS


FIG. 1 is a schematic view of a tissue resecting device and block diagram of operating components corresponding to the invention in a laparoscopic resection procedure.



FIG. 2A is a cut-away view of a handle portion of a resecting device of the invention with a detachable ultrasound component de-coupled from the device.



FIG. 2B is a cut-away view of the resecting device handle as in FIG. 2A with the ultrasound component coupled to the resecting device to provide vibratory motion to the inner sleeve.



FIG. 3 is a perspective view of the ultrasound component de-coupled from the resecting device illustrating a plurality of piezoelectric elements carried therein.



FIG. 4 is a perspective view of the working end of a shaft portion of the resecting device showing the assembly of the outer and inner sleeves.



FIG. 5 is a perspective view of the working end of a resecting device showing a sensor for sensing tissue contact.



FIG. 6 is a perspective view of another working end of a resecting device showing a plurality of sensors for sensing tissue contact.



FIG. 7 is a perspective view of another working end of a resecting device showing a rotating inner sleeve that can be coupled to an ultrasound source.



FIG. 8A is a step of a method of cutting and extracting a tissue chip in a laparoscopic resection procedure using a tubular cutter as shown in FIGS. 1-4, with FIG. 8A being a sectional view of a resecting device working end illustrating the activation of a negative pressure source to suction tissue into a window of the cutter.



FIG. 8B is another step of the method following the step of FIG. 8A illustrating the activation of motor drive to reciprocate the inner cutting sleeve and actuating an ultrasound component to provide vibratory motion at the inner sleeve edge to resect tissue drawn into the window of the cutter.



FIG. 8C is another step following the step of FIG. 8B illustrating a resected tissue chip captured in an interior passageway of the cutting sleeve.



FIG. 8D is another step depicting actuation of a pressurized fluid flow through an inflow channel and outward from a flow outlet distal to an interior seal to eject the tissue chip through the seal in a proximal direction in the interior passageway of the inner sleeve.



FIG. 8E is a further step after the pressurized fluid flow of FIG. 8D pushes the tissue chip through the seal in the interior passageway.



FIG. 8F depicts a further step of the invention wherein another pressurized fluid flow outward from an outlet proximal of the seal to pushes the tissue chip further in the proximal direction in the interior passageway.



FIG. 9 is a perspective view of another working end of a resecting device showing a plurality of seals in the tissue extraction lumen and flow outlets for providing independent fluid flows distal of each seal to assist in expelling tissue through each seal.



FIG. 10 is a perspective view of another resecting device working end showing an independent fluid channel with a port proximate the window in the outer sleeve for suctioning tissue into the window.





DETAILED DESCRIPTION OF THE INVENTION


FIGS. 1, and 2A-2B illustrate a tissue resecting system 10 that includes a hand-held single-use tissue resection device 50. The device 50 has a handle portion 102 that is coupled to a shaft portion 105 having an outer diameter ranging from about 3 mm to 20 mm. The shaft portion 105 extends along axis 106 and can have a length suitable for introducing directly into a body space, for introducing though a trocar in a laparoscopic procedure or for introducing through a working channel of an endo scope. A hand-held device corresponding to the invention as depicted in FIGS. 1 and 2A-2B is adapted for laparoscopic resection procedures such as in a hysterectomy. FIG. 1 schematically illustrates the tissue resecting device 50 introduced through a trocar sleeve or port 52 in a body wall 54 to an insufflated working space 55, which, for example, can be an abdominal cavity. An endoscope 60 is introduced through a second port 62 to allow viewing of the tissue volume 65 targeted for resection and extraction. An additional port can be provided for a tissue grasping instrument (not shown) that may be used in the resection procedure. In another embodiment, a similar elongate resecting device can be configured for resecting tissue in other body tracts and spaces utilizing any type of endoscope to allow endoscopic viewing of the working space.


Referring to FIGS. 1, 2A-2B and 3, the resecting device 50 has a shaft portion 105 and working end 112 that comprises an assembly of a first or outer sleeve 115 extending along axis 106 to a distal end 116 having a window 118 therein for receiving tissue. A second or inner sleeve 125 with a distal blade edge 126 and distal opening 128 is dimensioned to reciprocate in bore 132 of outer sleeve 115. The outer and inner sleeves, 115 and 125, are typically fabricated of thin-wall stainless steel but any other suitable materials can be used. As can be understood from FIG. 4, reciprocation of the inner sleeve 125 will cut tissue captured in the window 118 of the outer sleeve. FIG. 4 shows the working end 112 or the assembly of outer sleeve 115 and inner sleeve 125 with the inner sleeve in a partially window-open position.


The resecting device 50 of FIGS. 1-2B includes subsystems operatively coupled to handle 102 and inner sleeve 125 to enhance the cutting and removal of tissue from a working space in the interior of a patient's body. FIG. 2A is a cut-away view of handle 102 of the resecting device showing outer sleeve 115 fixed to collar portion 160 of the handle. The handle 102 typically consists of a molded plastic two-part handle shell with a hollow interior. In one variation shown in FIGS. 1 and 2A, the reciprocatable inner sleeve 125 extends partly through the interior of handle 102 and has a proximal sleeve end 162 that is received in bore 164 of cylindrical fixed member 165 that is fixed to support brackets 172 in shell 144 of handle 102. As will be described below, the inner sleeve 125 is reciprocated by DC electrical motor 148 in handle portion 102 (see FIGS. 2A-2B).


In one embodiment, the DC motor 148 is housed within the handle with motor shaft 185 having a pulley 186 that carries one or more flexible belts 188. The belts 188 can be fabricated of rubber, Viton® or a similar material and are adapted to rotate the cylindrical drive member 190 which in turn converts rotational motion to axial motion to thereby reciprocate the inner sleeve 125. A gear system instead of belts 188 also can be used to rotate the drive member 190. The drive member 190 is rotatable and secured in the handle 102 at rotation-permitting collars 192a and 192b at ends of the drive member. The inner sleeve 125 extends through the drive member 190 and has a projecting first pin 194 that engages the inner surfaces 195 of arcuate slot 196 in drive member 190. The DC motor is geared (together with pulleys 186 and 198) to rotate the drive member 190 at suitable speed to reciprocate the inner sleeve 125 within a range of 1 Hz to 10 Hz. The DC motor 148 has an electrical cable 202 extending to the controller 210 and a DC electrical source 215.


Referring to FIGS. 2A, 2B and 3, the resecting device 10 may be part of a system that includes a vibratory or ultrasound component 220 that is re-useable and removable from the resecting device 50. As can be seen in FIG. 3, the ultrasound component 220 has an elongate slot 222 therein that is configured to allow the component to slide axially over cylindrical fixed member 165 and the inner sleeve 125. Component 220 carries a vibrating mechanism such as at least one piezoelectric element 225 for applying vibratory motion to the inner sleeve 125 and more particularly to the distal blade edge 126 of the inner sleeve 125. In one variation shown in FIGS. 2A-3, three piezoelectric elements 225 are shown. An electrical source 235 is coupled to the piezoelectric elements 225 (see FIGS. 1 and 3) through electrical cable 236 and electrical leads (not shown) in the ultrasound component 220 to drive the piezoelectric elements. As can be seen in FIGS. 2A-3, the ultrasound component 220 has a J-lock 242 that engages second pin 244 of the inner sleeve 125 for securely locking the component 220 to the inner sleeve. The piezoelectric elements 225 are locked to inner sleeve 125 and are adapted to transmit energy to flange 238 of inner sleeve 125 and to its distal blade edge 126 (see FIGS. 2A-2B and 4). In one variation, the dimension between the piezoelectric element 225 and the distal blade edge 126 (see FIG. 4) of inner sleeve 125 is selected to optimize motion in the blade edge. The dimension D relates to the length of a standing wave caused by the piezoelectric element in the material of sleeve 125 as is known in that art of utilizing ultrasound to activate the working end of medical instruments. It should be appreciated that any suitable locking feature can be used to detachably couple the ultrasound component 220 to the inner sleeve 125 such as a threaded connector, a clamp, catches, magnets or the like. It should further be appreciated that independent electrical cable 236 that is directly coupled to the ultrasound component 220 can be eliminated. Instead, the electrical power for the ultrasound component 220 can be provided with electrical cable 202 and a slidable electrical contact (not shown) between handle 102 and the ultrasound component 220 can deliver current to the piezoelectric elements 225.


As can be seen in FIGS. 1, 2A-2B, and 4, the resecting device 10 may be part of a system that includes a negative pressure source 240 operatively coupled to a tissue extraction channel 252 in the device which is in part the passageway in the inner sleeve 125. As can be understood from FIGS. 1 and 2A, a flexible outflow tube 254 can extend from the negative pressure source 240 to a quick-connect fitting 255 at the end of the fixed member 165. The tissue extraction channel 252 extends through inner sleeve 125 and handle 102 to the cylindrical fixed member 165 (FIG. 2A). In one variation, the negative pressure source 240 is a peristaltic pump but any other source such as hospital wall suction may be used. In another variation, the extraction channel 252 in the combination of inner sleeve 125 and fixed member 165 can transition from a smaller cross-section to a larger cross-section to facilitate the extraction of cut tissue chips. The controller 210 is adapted to control the negative pressure source 240 as indicated in FIG. 1. A tissue catch structure 258 is provided in outflow tube 254 to collect tissue chips.


In FIGS. 1, 2A-2B, and 4, it can be seen that the resecting device 10 may be part of a system that includes a fluid source 260 that includes positive pressure mechanism for providing a pressurized fluid flow through an inflow lumen 265 in the resecting device shaft 105 which is used to assist in applying pressure to expel captured tissue chips from the instrument's working end 112. In one variation, the fluid source 260 can comprise a reservoir containing saline solution and the pressurization mechanism can be a peristaltic pump. In another variation, the fluid source can be a hospital source of an insufflation gas such as CO2. The fluid is delivered by tubing 268 to the quick-connect fitting 270 in handle 102. The flow pathway 272 in the quick-connect 270 extends through tubing 275 in the handle 102 to inflow lumen 265 in the shaft portion of the resecting device 50. As can be seen in FIG. 4, the inflow lumen 265 has a small cross section, e.g., a diameter from 0.05″ to 0.25″, and can be formed in the wall 276 of outer sleeve 115 or can be provided in a hypotube affixed to the outer sleeve 115. In one aspect of the invention, the inflow lumen 265 extends to an outlet 277 that is proximate to or distal to the window 118 to allow a fluid flow from the outlet in the window-closed position to apply proximally-directed fluid pressure on a tissue chip (not shown) captured in the extraction channel 252. In one variation shown in FIG. 4, the inflow lumen 275 has a distal region 278 that includes a 180° turn to provide a flow from outlet 277 that is aligned with the axis 106 of the shaft 105.


Referring to FIGS. 2A-2B, the system further includes a sensor 285 in the handle that is adapted to determine the rotational position of drive member 190 and to send a signal to the controller 200 that indicates the drive member position. As can be easily understood from FIGS. 2A-2B and 4, the rotational position of drive member 190 determines the axial position of the inner sleeve and thus can indicate a fully window-open position, a window-closed position or any intermediate window-open position. In one embodiment, the sensor 285 is a Hall effect sensor that is actuated when a magnet 288 in the drive member 190 passes the sensor. In another variation, the sensor can be a mechanically-actuated switch that is actuated by an indent or projection carried by the drive member 190. In other embodiments, any sensor known it the art can be used and the sensor can be activated by either rotation of the drive member 190 or axial movement of the inner sleeve 125 in the handle 102.


Referring back to FIG. 1, the controller 210 of system 10 is adapted to receive signals from sensor 285 and in response can control operating parameters of the ultrasound transducer, the negative pressure source and the pressurized fluid source in relation to a window-open or window-closed position of the cutter. In one embodiment, a footswitch 290 is utilized to actuate the resecting device 50, but a finger-operated switch in the handle 102 also may be used (not shown). In one variation, the controller includes algorithms that activate the piezoelectric element 225 only when the inner sleeve 125 is moving forward or in distal direction from the fully window-open position to the window-closed position. In this variation, the piezoelectric element 225 is de-activated on the return or proximal stroke from the window-closed position to the window-open position. Thus, the ultrasonic or vibratory effect at the blade edge 126 of the inner sleeve 125 is only activated when tissue is being cut on the forward stroke of the inner sleeve.


Still referring to FIG. 1, the controller 210 can further control the pressurized fluid source 260 in response to signals from sensor 285 and the window-open or window-closed position of the inner sleeve 125. In one variation, the controller 210 has an algorithm that activates the fluid source 260 for a selected time interval only when the inner cutting sleeve 125 is in a fully window-closed position. Thus, at the moment the inner cutting sleeve 125 cuts and captures a tissue chip in the extraction channel 252, the controller 210 can provide a high pressure flow through the inflow lumen 275 and outlet 277 to push the tissue chip proximally in the extraction channel 252. In one embodiment, the controller 200 can have an algorithm that de-activates the motor 148 to thereby stop reciprocation of inner sleeve 125 in the window-closed position for a time interval to allow a longer pressurized flow from the fluid source 260 to push a captured tissue chip through the extraction lumen 252. For example, the inner sleeve 125 may be stopped for a time interval ranging from 0.1 second to 2 seconds.


Referring to FIG. 1, the controller 210 can include algorithms to modulate the negative pressure source 240 in response to signals from a sensor and the corresponding window-open or window-closed condition of the resecting device. In one variation of working end 112 shown in FIG. 5, the at least one sensor 302 is provided proximate the window 118 to sense tissue contact with the window. For example, the sensor 302 can be a capacitance sensor that is configured to send a signal to the controller when the sensor contacts tissue. It can be easily understood that the capacitance reading from the sensor 302 when in contact with tissue would differ greatly from a capacitance reading in the absence of tissue contact. Any similar type sensor 302 could be used, such as an impedance sensor, pressure sensor and the like. As can be seen in FIG. 6, another variation of working end 212′ can have a plurality of sensors 302 and 304 and can be used to modulate the negative pressure source 240. In one variation, the controller 210 can activate the negative pressure source 240 only when a sensor 302 and/or 304 (FIGS. 5 and 6) is in contact with tissue which then provides suction force to suction tissue into the window 118. At other times, for example when the physician is re-positioning the working end relative to tissue targeted for resection, the negative pressure source 240 would be de-activated to thus prevent insufflation gas from being withdrawn from the working space 55 (see FIG. 1).


In another aspect of the invention, the controller 210 can include an algorithm adapted to move the inner cutting sleeve 125 to a predetermined position relative to the window 118 each time the physician de-activates the device. In one variation, when the physician lifts his or foot from the footswitch, or lifts finger from a trigger, a “stop-reciprocation” signal is sent to controller 210 which in turn determines the location of the inner sleeve 125 relative to the window 118 by means of a timer and the next signal (or previous signal) from the position sensor 285 that determines the rotational position of drive member 190. The controller 210 then can calculate the time interval needed to stop the drive member 190 and sleeve 125 at a predetermined location based on a library of known time intervals following de-activation of the motor 148 to allow the inner sleeve 125 to coast (overcome momentum) to the predetermined position. In one embodiment, the predetermined position can be a fully window-open condition, which would then allow the physician to position the open window 118 against the targeted tissue to commence resection. In one variation, the edge of window 118 and the tissue-contact sensor 302 would contact tissue which then cause the controller 210 to activate the negative pressure source 240 to suction tissue into the window and also actuate reciprocation and the piezoelectric elements 225. It should be appreciated that the controller algorithm may be programmed to activate the negative pressure source 240 and reciprocation simultaneously or the reciprocation may be actuated in a sequence, for example 0.1 seconds to 2 seconds after the negative pressure. Alternatively, the device may be provided with a two stage trigger, with a first trigger actuation movement activating the negative pressure source and an additional second trigger movement activating the reciprocation and piezoelectric element 225.


Referring back to FIGS. 3 and 4, it can be seen that the piezoelectric elements 225 are configured to cause axial motion in the distal end of the inner sleeve 125. In another variation, the piezoelectric elements can be oriented to cause rotational motion in a keyed flange 138 (see FIGS. 2A-2B) to rotationally vibrate the blade edge 126 of the inner sleeve. In another variation, a plurality of piezoelectric elements can be provided to cause both axial and rotational motion in the distal end of the inner sleeve. Such motion can be sequential or contemporaneous. The blade edge 126 can have any suitable configuration such as being smooth or having teeth, etc.



FIG. 7 illustrates another variation of a working end 405 corresponding to the invention in which an inner sleeve 410 is configured to rotate relative to outer sleeve 415 rather that reciprocating as in the embodiment of FIGS. 1-5. It can be easily understood that a handle similar to that of FIG. 2A can use an appropriately geared motor to rotate the inner sleeve 415 at a selected speed or rotate the sleeve 415 sequentially in clockwise and counter-clockwise directions. Contemporaneously, the at least one piezoelectric element can be used to vibrate the inner sleeve 415 in the manner described previously. As can be seen in FIG. 7, the window 418 of inner sleeve 415 has sharp teeth 422 at its edge 424, and the combination of rotation and ultrasonic or vibratory movement of edge 424 will assist is cutting or sawing tougher tissues. In one variation, the controller can include an algorithm that will sequentially rotate the inner sleeve from a window-open start position in clockwise direction from 5° to 30°, then back past the start position and then 5° to 30°, in a counter-clockwise direction followed by one or more increased sequential angular rotation to cut a tissue chip. After successive cutting by such sequential rotations, the inner sleeve 415 can be rotated to the fully window closed position to capture the tissue in the extraction lumen 440 of the inner sleeve. In one variation, an inflow channel 265 as shown in FIG. 4 can be provided in the device of FIG. 7 to allow proximally directed fluid flow to push the tissue chip in the proximal direction in the extraction channel.


In general, the controller 210 can control all operating parameters of the ultrasound component, the motor drive that reciprocates or rotates the inner sleeve, the negative pressure source and the pressurized fluid source, as well as responding to signals from sensors to provide sequential actuation of different component as well as to provide interlocks between various operations and functions of the resecting devices and systems of the present invention.



FIGS. 8A-8F illustrate another resecting device 500 of the invention that has a working end 512 including an outer sleeve 515 with window 518 and a reciprocating, ultrasound-actuated inner cutting sleeve 525. The resecting device 500 has at least one deformable seal 540 or valve in the tissue extraction channel 544 which allows a cut tissue chip to pass thru the seal 540. The seal 540 is configured to close to its repose state to prevent the loss of insufflation gas after tissue passes through the seal. More in particular, FIGS. 8A-8F schematically illustrate one variation of resecting device 500 and a sequence of operating the pressurized fluid source 260 and the negative pressure source 240 to assist in cutting and extraction of tissue chips in a laparoscopic procedure.


In FIG. 8A, the working end 512 of the resecting device is positioned so that the window 518 is in contact with a targeted tissue volume 545. As described above, the controller 210 has algorithms that stop the inner sleeve in a window-open position of FIG. 8A. At this point in time, none of the operational mechanisms (ultrasound component, motor drive, negative pressure source and pressurized fluid source) are activated, thus no insufflation gas is lost though the device. The insufflation pressure is maintained automatically by an independent insufflator system as is known in the art. In one variation, the physician then partially actuates a trigger switch 290 (see FIG. 1) which signals the controller 210 to activate the negative pressure source 240. In FIG. 8A, the negative pressure source thus suctions a portion of the targeted tissue 545 into the window 518. In FIG. 8B, the physician further actuates the trigger switch 290 which maintains activation of the negative pressure source 240 and activates the motor 148 (FIG. 2B) to cause reciprocation of the inner sleeve 525 and simultaneously activates the ultrasound component. As can be seen in FIG. 8B, the distal movement of the inner sleeve 525 begins to cut tissue. FIG. 8C illustrates the inner sleeve 525 at the distal end of its stroke which captures a tissue chip 548 in the extraction channel 544 of the inner sleeve.


In FIG. 8D, the position of inner sleeve 525 at the distal end of its stroke can cause a controller algorithm to optionally terminate the ultrasound component and optionally halt reciprocation for a brief interval as described above. With the inner sleeve 525 in the window closed position in FIG. 8D, the controller 210 causes the fluid source 260 to provide a high pressure fluid flow through first inflow channel 552 and outward from outlet 555 to thus push the tissue chip 548 through the seal 540 in extraction channel 544 as depicted in FIG. 8E. The controller 210 can control the fluid volume, pressure and duration of the flow to optimize the expulsion of the tissue chip through the seal 540. An instant after the fluid flow has applied proximally-directed forces to the tissue chip, FIG. 8E shows the controller has activated the motor 148 to thereby move the inner sleeve 525 to the window open position.



FIG. 8F illustrates another step in the sequence of resecting tissue wherein the controller 210 causes the fluid source 260 to provide another high pressure fluid flow through a second inflow channel 562 and outward from outlet 565 to push tissue chip 548 further outward (proximally) through the extraction channel 544. It can be seen that the inflow channel 562 is within wall of outer sleeve 515 which has an outlet 568 that is aligned with port 565 in the inner sleeve 525 to thus permit a high pressure flow to reach the extraction channel 544 in the inner sleeve. In order to provide the fluid flows sequentially through the first inflow channel 552 and then the second inflow channel 562, the controller 210 can control solenoid valves 570a and 570b as shown schematically in FIGS. 8A-8F. Following the step of using the fluid flow to expel tissue as depicted in FIG. 8F, the sequence of steps 8A-8F can automatically be repeated to rapidly resect the targeted tissue volume. It should be appreciated that the inner sleeve 525 may reciprocate at a constant rate and the controller 210 can actuate the fluid source 260 at selected intervals to provide the sequential fluid flows through the first and second inflow channels 552 and 562. Further, the system can be configured to cause the pressurized fluid flow through the second inflow channel 562 with the inner sleeve 525 in any axial position relative to window 518.


In another variation, referring to FIG. 9, the inner sleeve 525 may be configured with a plurality of seals, for example seals 540 and 540′ with inflow ports 565 and 565′ (which can be elongated slots) to allow for a plurality of flow pulses in different axial locations to push and expel tissue chips through the extraction channel 544. The flow pulses can be contemporaneous or sequential through inflow ports 565 and 565′ from a single inflow channel 562 and outlets 568 and 568′ or can be sequenced through a plurality of independent inflow channels each in communication with an inflow ports 565 and 565′. In various embodiments, the number of seals 540 and corresponding inflow ports 565 can range from 1 to 10.


In any embodiment, the passageway seal 540 can be any type of flexible leaflet-type seal, hinged-door seal, duckbill-type seal or the like that is adapted to close the passageway in a repose condition.



FIG. 10 illustrates another resecting device 570 that is similar to that of FIGS. 8A-8F except that outer sleeve 515 carries an independent passageway 575 coupled to negative pressure source 240 that is controlled independently by controller 210 to provide suction forces in the interior of window 518. More in particular, the independent passageway 575 in outer sleeve 515 extends to a distal opening 577 in a distal region of the bore 580 of sleeve 515 proximate window 518. Thus, the controller 210 can actuates the negative pressure source 240 to suction tissue into the window independent of suction force provided through the tissue extraction channel 544 of the inner sleeve 525. Further, the controller 210 can use an algorithm to modulate suction pressure through passageway 575 and opening 577 during different portions of the stroke of the inner sleeve 515 to optimize suction for pulling tissue into the window and to minimize loss of insufflation gas. The controller 210 can operate solenoid valves 590a and 590b to control negative pressure in the channels 544 and 575. In one variation, the inner sleeve 515 can have a slot or notch 585 that is axially aligned with opening 577 so that the opening is not covered by the inner sleeve 515 during a distal region of the sleeve's reciprocation. Thus, suction forces can be applied to tissue throughout reciprocation of the inner sleeve 515.


In the various embodiments described above, the inflows from fluid source have been described as any suitable fluid or flow media. It should be appreciated the flow media can be a liquid (e.g., saline or sorbital) or a gas such as CO2. Either a liquid or gas can be used to assist in expelling tissue, with each having its advantages. The use of a incompressible liquid could apply greater expelling forces to a captured tissue chip. The use of an insufflation gas can reduce the complexity of the system. In a variation, the system could use a gas media to expel a just-cut tissue chip from the region of the window through the seal 540 in the step shown in FIG. 8D and then use a liquid flow in the step depicted in FIG. 8F. In such a variation, pulse liquid flows can operate continuously or intermittently during operation of the device.


It should be appreciated that the features described in the system embodiments of FIGS. 8A-10 including seals 540 and independent suction passageway 570 can be provided in a “rotating” inner cutting sleeve as illustrated in FIG. 7.


In another variation, a plurality of piezoelectric element can each be coupled to a separate elongated member or component that is a part of an assembly that comprises the reciprocating or rotating cutting sleeve. Thus each piezoelectric element can drive a member that has a selected length to cooperate with a standing wave in the material caused by the piezoelectric element to optimize the tissue effect at the distal end of the cutting sleeve. Each elongated member can have an axial or spiral configuration.


Although particular embodiments of the present invention have been described above in detail, it will be understood that this description is merely for purposes of illustration and the above description of the invention is not exhaustive. Specific features of the invention are shown in some drawings and not in others, and this is for convenience only and any feature may be combined with another in accordance with the invention. A number of variations and alternatives will be apparent to one having ordinary skills in the art. Such alternatives and variations are intended to be included within the scope of the claims. Particular features that are presented in dependent claims can be combined and fall within the scope of the invention. The invention also encompasses embodiments as if dependent claims were alternatively written in a multiple dependent claim format with reference to other independent claims.

Claims
  • 1. A medical instrument comprising: a tubular cutter extending along an axis and having a windowed outer sleeve and a moveable inner cutting sleeve;a first ultrasound transducer operatively coupled to the inner cutting sleeve; andat least a second ultrasound transducer, wherein first and second ultrasound transducers are configured to cause axial and rotational motion in the distal end of the inner sleeve.
  • 2. The instrument of claim 1 further comprising a motor drive configured to reciprocate the inner cutting sleeve relative to the windowed outer sleeve.
  • 3. The instrument of claim 2 wherein the motor drive reciprocates the inner cutting sleeve at a reciprocation rate between 1 and 10 Hz.
  • 4. The instrument of claim 1 wherein the ultrasound transducer is configured to cause at least one of axial motion and rotational motion in the distal end of the inner cutting sleeve.
  • 5. The instrument of claim 4 wherein a dimension between the ultrasound transducer and the distal end of the inner sleeve is selected to optimize at least one of axial motion and rotational motion in the distal end of the inner cutting sleeve.
  • 6. The instrument of claim 1 wherein the ultrasound transducer is removably secured to a handle portion of the tubular cutter.
  • 7. The instrument of claim 1 further comprising a negative pressure source coupled to a tissue extraction lumen in the tubular cutter.
  • 8. The instrument of claim 7 further comprising a pressurized fluid source coupled to an inflow lumen in the cutter.
  • 9. The instrument of claim 8 wherein the inflow lumen extends to an outlet in a distal portion of the cutter.
  • 10. The instrument of claim 8 wherein the pressurized fluid source comprises a liquid source.
  • 11. The instrument of claim 8 wherein the pressurized fluid source comprises a gas source.
  • 12. The instrument of claim 7 further comprising a controller coupled to cutter for controlling operating parameters of the ultrasound transducer, the motor drive, the negative pressure source and the pressurized fluid source.
  • 13. The instrument of claim 12 further comprising a sensor configured to send signals to the controller indicating the position of the inner sleeve relative to the window in the outer sleeve.
  • 14. The instrument of claim 13 wherein the controller is adapted to modulate activation of the ultrasound transducer in response to the sensor signals that indicate the position of the inner sleeve.
  • 15. The instrument of claim 14 wherein the controller activates the ultrasound transducer when the inner sleeve moves toward a window-closed position to cut tissue and de-activates the ultrasound transducer when the inner sleeve moves toward a window-open position.
  • 16. The instrument of claim 13 wherein the controller activates the pressurized fluid source when the inner sleeve is in a window-closed position.
  • 17. The instrument of claim 13 wherein the controller de-activates the pressurized fluid source when the inner sleeve is in a window-open position.
  • 18. A medical instrument comprising: a tubular assembly extending along an axis with a windowed outer sleeve and a moveable inner cutting sleeve, wherein the inner cutting sleeve has a tissue-extraction passageway; anda seal in the tissue-extraction passageway in the inner cutting sleeve, the seal having a first condition that closes the passageway and a second condition that is configured to permit a tissue chip to pass through the seal.
  • 19. The instrument of claim 18 wherein the tubular assembly has a flow channel terminating in a distal outlet in a region of the assembly that is distal to the seal, wherein the flow channel is in communication with a fluid source.
  • 20. The instrument of claim 18 wherein the tubular assembly has a flow channel terminating in a distal outlet in a region of the assembly that is distal to the seal, wherein the flow channel is in communication with a negative pressure source.
  • 21. A medical instrument comprising: a tubular cutter extending along an axis and having a windowed outer sleeve and a moveable inner cutting sleeve;an ultrasound transducer operatively coupled to the inner cutting sleeve;a negative pressure source coupled to a tissue extraction lumen in the tubular cutter;a pressurized fluid source coupled to an inflow lumen in the cutter;a motor drive configured to reciprocate the inner cutting sleeve relative to the windowed outer sleeve;a controller coupled to the tubular cutter for controlling operating parameters of the ultrasound transducer, the motor drive, the negative pressure source, and the pressurized fluid source; and a sensor configured to send signals to the controller indicating the position of the inner sleeve relative to the window in the outer sleeve;wherein the controller is adapted to modulate activation of the ultrasound transducer in response to the sensor signals that indicate the position of the inner sleeve.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Application No. 61/891,288, filed Oct. 15, 2013, the entire content of which is incorporated herein by reference.

US Referenced Citations (272)
Number Name Date Kind
3903891 Brayshaw Sep 1975 A
4428748 Peyman Jan 1984 A
4949718 Neuwirth et al. Aug 1990 A
4979948 Geddes et al. Dec 1990 A
5045056 Behl Sep 1991 A
5078717 Parins Jan 1992 A
5084044 Quint Jan 1992 A
5191883 Lennox et al. Mar 1993 A
5197963 Parins Mar 1993 A
5242390 Goldrath Sep 1993 A
5248312 Langberg Sep 1993 A
5277201 Stern Jan 1994 A
5282799 Rydell Feb 1994 A
5324254 Phillips Jun 1994 A
5344435 Turner et al. Sep 1994 A
5374261 Yoon Dec 1994 A
5401272 Perkins Mar 1995 A
5401274 Kusunoki Mar 1995 A
5429136 Milo et al. Jul 1995 A
5441498 Perkins Aug 1995 A
5443470 Stern et al. Aug 1995 A
5496314 Eggers Mar 1996 A
5501681 Neuwirth et al. Mar 1996 A
5505730 Edwards Apr 1996 A
5558672 Edwards Sep 1996 A
5562703 Desai Oct 1996 A
5562720 Stern et al. Oct 1996 A
5575788 Baker et al. Nov 1996 A
5584872 LaFontaine et al. Dec 1996 A
5647848 Jørgensen Jul 1997 A
5653692 Masterson et al. Aug 1997 A
5662647 Crow et al. Sep 1997 A
5672174 Gough et al. Sep 1997 A
5681308 Edwards et al. Oct 1997 A
5697281 Eggers Dec 1997 A
5697882 Eggers Dec 1997 A
5713942 Stern et al. Feb 1998 A
5733298 Berman Mar 1998 A
5769846 Edwards et al. Jun 1998 A
5769880 Truckai et al. Jun 1998 A
5779662 Berman Jul 1998 A
5800493 Stevens et al. Sep 1998 A
5810802 Panescu et al. Sep 1998 A
5827273 Edwards Oct 1998 A
5843020 Tu et al. Dec 1998 A
5846239 Swanson et al. Dec 1998 A
5860974 Abele Jan 1999 A
5876340 Tu et al. Mar 1999 A
5879347 Saadat Mar 1999 A
5891094 Masterson et al. Apr 1999 A
5891134 Goble et al. Apr 1999 A
5891136 McGee Apr 1999 A
5902251 vanHooydonk May 1999 A
5904651 Swanson et al. May 1999 A
5925038 Panescu et al. Jul 1999 A
5954714 Saadat et al. Sep 1999 A
5964755 Edwards Oct 1999 A
5976129 Desai Nov 1999 A
5980515 Tu Nov 1999 A
5997534 Tu et al. Dec 1999 A
6024743 Edwards Feb 2000 A
6026331 Feldberg et al. Feb 2000 A
6041260 Stern et al. Mar 2000 A
6053909 Shadduck Apr 2000 A
6057689 Saadat May 2000 A
6086581 Reynolds et al. Jul 2000 A
6113597 Eggers Sep 2000 A
6139570 Saadat et al. Oct 2000 A
6146378 Mikus et al. Nov 2000 A
6149620 Baker et al. Nov 2000 A
6228078 Eggers et al. May 2001 B1
6254599 Lesh et al. Jul 2001 B1
6283962 Tu et al. Sep 2001 B1
6296639 Truckai et al. Oct 2001 B1
6302904 Wallsten et al. Oct 2001 B1
6315776 Edwards et al. Nov 2001 B1
6366818 Bolmsjo Apr 2002 B1
6387088 Shattuck et al. May 2002 B1
6395012 Yoon et al. May 2002 B1
6409722 Hoey et al. Jun 2002 B1
6416508 Eggers et al. Jul 2002 B1
6416511 Lesh et al. Jul 2002 B1
6443947 Marko et al. Sep 2002 B1
6508815 Strul et al. Jan 2003 B1
6551310 Ganz et al. Apr 2003 B1
6589237 Woloszko et al. Jul 2003 B2
6602248 Sharps et al. Aug 2003 B1
6607545 Kammerer et al. Aug 2003 B2
6622731 Daniel et al. Sep 2003 B2
6635054 Fjield et al. Oct 2003 B2
6635055 Cronin Oct 2003 B1
6663626 Truckai et al. Dec 2003 B2
6673071 VanDusseldorp et al. Jan 2004 B2
6699241 Rappaport et al. Mar 2004 B2
6726684 Woloszko et al. Apr 2004 B1
6736811 Panescu et al. May 2004 B2
6746447 Davison et al. Jun 2004 B2
6758847 Maguire Jul 2004 B2
6780178 Palanker et al. Aug 2004 B2
6802839 Behl Oct 2004 B2
6813520 Truckai et al. Nov 2004 B2
6814730 Li Nov 2004 B2
6832996 Woloszko et al. Dec 2004 B2
6837887 Woloszko et al. Jan 2005 B2
6837888 Ciarrocca et al. Jan 2005 B2
6840935 Lee Jan 2005 B2
6872205 Lesh et al. Mar 2005 B2
6896674 Woloszko et al. May 2005 B1
6905497 Truckai et al. Jun 2005 B2
6923805 LaFontaine et al. Aug 2005 B1
6929642 Xiao et al. Aug 2005 B2
6949096 Davison et al. Sep 2005 B2
6951569 Nohilly et al. Oct 2005 B2
6954977 Maguire et al. Oct 2005 B2
6960203 Xiao et al. Nov 2005 B2
7074217 Strul et al. Jul 2006 B2
7083614 Fjield et al. Aug 2006 B2
7087052 Sampson et al. Aug 2006 B2
7108696 Daniel et al. Sep 2006 B2
7118590 Cronin Oct 2006 B1
7175734 Stewart et al. Feb 2007 B2
7179255 Lettice et al. Feb 2007 B2
7186234 Dahla et al. Mar 2007 B2
7192430 Truckai et al. Mar 2007 B2
7238185 Palanker et al. Jul 2007 B2
7270658 Woloszko et al. Sep 2007 B2
7276063 Davison et al. Oct 2007 B2
7278994 Goble Oct 2007 B2
7294126 Sampson et al. Nov 2007 B2
7297143 Woloszko et al. Nov 2007 B2
7326201 Fijeld et al. Feb 2008 B2
7331957 Woloszko et al. Feb 2008 B2
RE40156 Sharps et al. Mar 2008 E
7371231 Rioux et al. May 2008 B2
7371235 Thompson et al. May 2008 B2
7381208 van der Walt et al. Jun 2008 B2
7387628 Behl et al. Jun 2008 B1
7407502 Strul et al. Aug 2008 B2
7419500 Marko et al. Sep 2008 B2
7452358 Stern et al. Nov 2008 B2
7462178 Woloszko et al. Dec 2008 B2
7500973 Vancelette et al. Mar 2009 B2
7512445 Truckai et al. Mar 2009 B2
7530979 Ganz et al. May 2009 B2
7549987 Shadduck Jun 2009 B2
7556628 Utley et al. Jul 2009 B2
7566333 Van Wyk et al. Jul 2009 B2
7572251 Davison et al. Aug 2009 B1
7604633 Truckai et al. Oct 2009 B2
7625368 Schechter et al. Dec 2009 B2
7674259 Shadduck Mar 2010 B2
7678106 Lee Mar 2010 B2
7708733 Sanders et al. May 2010 B2
7717909 Strul et al. May 2010 B2
7736362 Eberl et al. Jun 2010 B2
7749159 Crowley et al. Jul 2010 B2
7824398 Woloszko et al. Nov 2010 B2
7824405 Woloszko et al. Nov 2010 B2
7846160 Payne et al. Dec 2010 B2
7879034 Woloszko et al. Feb 2011 B2
7918795 Grossman Apr 2011 B2
7985188 Felts et al. Jul 2011 B2
8197476 Truckai Jun 2012 B2
8197477 Truckai Jun 2012 B2
8372068 Truckai Feb 2013 B2
8382753 Truckai Feb 2013 B2
8486096 Robertson Jul 2013 B2
8500732 Truckai et al. Aug 2013 B2
8540708 Truckai et al. Sep 2013 B2
8690873 Truckai et al. Apr 2014 B2
8821486 Toth et al. Sep 2014 B2
8998901 Truckai et al. Apr 2015 B2
20020022870 Truckai et al. Feb 2002 A1
20020058933 Christopherson et al. May 2002 A1
20020068934 Edwards et al. Jun 2002 A1
20020082635 Kammerer et al. Jun 2002 A1
20030130655 Woloszko et al. Jul 2003 A1
20030153905 Edwards et al. Aug 2003 A1
20030171743 Tasto et al. Sep 2003 A1
20030176816 Maguire et al. Sep 2003 A1
20030208200 Palanker et al. Nov 2003 A1
20030216725 Woloszko et al. Nov 2003 A1
20040002702 Xiao et al. Jan 2004 A1
20040010249 Truckai et al. Jan 2004 A1
20040087936 Stern et al. May 2004 A1
20040215180 Starkebaum et al. Oct 2004 A1
20040215182 Lee Oct 2004 A1
20040215296 Ganz et al. Oct 2004 A1
20040230190 Dahla et al. Nov 2004 A1
20050075630 Truckai et al. Apr 2005 A1
20050165389 Swain et al. Jul 2005 A1
20050182397 Ryan Aug 2005 A1
20050192652 Cioanta et al. Sep 2005 A1
20050228372 Truckai et al. Oct 2005 A1
20050240176 Oral et al. Oct 2005 A1
20050251131 Lesh Nov 2005 A1
20060009756 Francischelli et al. Jan 2006 A1
20060052771 Sartor et al. Mar 2006 A1
20060084969 Truckai et al. Apr 2006 A1
20060089637 Werneth et al. Apr 2006 A1
20060189971 Tasto et al. Aug 2006 A1
20060189976 Karni et al. Aug 2006 A1
20060224154 Shadduck et al. Oct 2006 A1
20060259025 Dahla Nov 2006 A1
20070021743 Rioux et al. Jan 2007 A1
20070083192 Welch Apr 2007 A1
20070161981 Sanders et al. Jul 2007 A1
20070213704 Truckai et al. Sep 2007 A1
20070282323 Woloszko et al. Dec 2007 A1
20070287996 Rioux Dec 2007 A1
20070288075 Dowlatshahi Dec 2007 A1
20070293853 Truckai et al. Dec 2007 A1
20080058797 Rioux Mar 2008 A1
20080097242 Cai Apr 2008 A1
20080097425 Truckai Apr 2008 A1
20080125765 Berenshteyn et al. May 2008 A1
20080125770 Kleyman May 2008 A1
20080154238 McGuckin Jun 2008 A1
20080183132 Davies et al. Jul 2008 A1
20080208189 Van Wyk et al. Aug 2008 A1
20080221567 Sixto, Jr. Sep 2008 A1
20080249518 Warnking et al. Oct 2008 A1
20080281317 Gobel Nov 2008 A1
20090048593 Ganz et al. Feb 2009 A1
20090054888 Cronin Feb 2009 A1
20090054892 Rioux et al. Feb 2009 A1
20090076494 Azure Mar 2009 A1
20090105703 Shadduck Apr 2009 A1
20090131927 Kastelein et al. May 2009 A1
20090149846 Hoey et al. Jun 2009 A1
20090163908 MacLean et al. Jun 2009 A1
20090209956 Marion Aug 2009 A1
20090306654 Garbagnati Dec 2009 A1
20100004595 Nguyen et al. Jan 2010 A1
20100036372 Truckai et al. Feb 2010 A1
20100042095 Bigley et al. Feb 2010 A1
20100042097 Newton et al. Feb 2010 A1
20100049190 Long et al. Feb 2010 A1
20100100091 Truckai Apr 2010 A1
20100100094 Truckai Apr 2010 A1
20100106152 Truckai et al. Apr 2010 A1
20100114089 Truckai et al. May 2010 A1
20100121319 Chu et al. May 2010 A1
20100125269 Emmons et al. May 2010 A1
20100137855 Berjano Zanon et al. Jun 2010 A1
20100137857 Shiroff et al. Jun 2010 A1
20100152725 Pearson et al. Jun 2010 A1
20100185191 Carr et al. Jul 2010 A1
20100198214 Layton et al. Aug 2010 A1
20100204688 Hoey et al. Aug 2010 A1
20100217256 Strul et al. Aug 2010 A1
20100228239 Freed Sep 2010 A1
20100228245 Sampson et al. Sep 2010 A1
20100286680 Kleyman Nov 2010 A1
20110004205 Chu et al. Jan 2011 A1
20110060391 Unetich et al. Mar 2011 A1
20110112524 Stern et al. May 2011 A1
20110282340 Toth et al. Nov 2011 A1
20120041434 Truckai Feb 2012 A1
20120041437 Truckai Feb 2012 A1
20120116384 Truckai May 2012 A1
20120130361 Toth et al. May 2012 A1
20120330292 Shadduck et al. Dec 2012 A1
20130172870 Germain et al. Jul 2013 A1
20130267937 Shadduck et al. Oct 2013 A1
20130345705 Truckai et al. Dec 2013 A1
20140012249 Truckai et al. Jan 2014 A1
20140303611 Shadduck et al. Oct 2014 A1
20140336632 Toth et al. Nov 2014 A1
20150119916 Dietz Apr 2015 A1
20150182281 Csaba et al. Jul 2015 A1
20160095615 Orczy-Timko et al. Apr 2016 A1
Foreign Referenced Citations (13)
Number Date Country
101198288 Jun 2008 CN
1236440 Sep 2002 EP
1595507 Nov 2005 EP
2349044 Aug 2011 EP
2493407 Sep 2012 EP
WO 0053112 Sep 2000 WO
WO 2005122938 Dec 2005 WO
WO 2006001455 Jan 2006 WO
WO 2008083407 Jul 2008 WO
WO-2010048007 Apr 2010 WO
WO 2011053599 May 2011 WO
WO-2011060301 May 2011 WO
WO 2014165715 Oct 2014 WO
Non-Patent Literature Citations (49)
Entry
Office action dated Dec. 16, 2014 for U.S. Appl. No. 13/281,805.
Co-pending U.S. Appl. No. 15/008,341, filed Jan. 27, 2016.
Office action dated Feb. 4, 2016 for U.S. Appl. No. 13/857,068.
Co-pending U.S. Appl. No. 14/657,684, filed Mar. 13, 2015.
Notice of allowance dated Feb. 25, 2015 for U.S. Appl. No. 13/975,139.
Office action dated May 22, 2015 for U.S. Appl. No. 14/657,684.
Office action dated Jun. 5, 2015 for U.S. Appl. No. 13/857,068.
Office action dated Jul. 23, 2015 for U.S. Appl. No. 13/281,805.
Co-pending U.S. Appl. No. 14/864,379, filed Sep. 24, 2015.
Office action dated Sep. 24, 2015 for U.S. Appl. No. 13/236,471.
U.S. Appl. No. 13/938,032, filed Jul. 9, 2013, Truckai et al.
U.S. Appl. No. 13/975,139, filed Aug. 23, 2013, Truckai et al.
U.S. Appl. No. 14/341,121, filed Jul. 25, 2014, Toth et al.
European search report and search opinion dated Apr. 16, 2013 for EP Application No. 09822443.
European search report and search opinion dated Jul. 10, 2013 for EP Application No. 10827399.
International search report and written opinion dated Feb. 2, 2011 for PCT/US2010/056591.
International search report and written opinion dated Dec. 10, 2009 for PCT/US2009/060703.
International search report and written opinion dated Dec. 14, 2010 for PCT/US2010/054150.
Notice of allowance dated Jan. 9, 2014 for U.S. Appl. No. 13/938,032.
Notice of allowance dated Mar. 5, 2012 for U.S. Appl. No. 13/281,846.
Notice of allowance dated Mar. 5, 2012 for U.S. Appl. No. 13/281,856.
Notice of allowance dated Mar. 29, 2013 for U.S. Appl. No. 12/605,546.
Notice of allowance dated May 9, 2014 for U.S. Appl. No. 12/944,466.
Notice of allowance dated May 24, 2013 for U.S. Appl. No. 12/605,929.
Notice of allowance dated Nov. 15, 2012 for U.S. Appl. No. 12/541,043.
Notice of allowance dated Nov. 15, 2012 for U.S. Appl. No. 12/541,050.
Notice of allowance dated Dec. 2, 2014 for U.S. Appl. No. 13/975,139.
International Search Report dated Sep. 10, 2014 for PCT/US2014/032895.
Office action dated Jan. 28, 2013 for U.S. Appl. No. 12/605,546.
Office action dated Mar. 12, 2012 for U.S. Appl. No. 12/541,043.
Office action dated Mar. 12, 2012 for U.S. Appl. No. 12/541,050.
Office action dated Apr. 24, 2014 for U.S. Appl. No. 13/975,139.
Office action dated Jun. 18, 2012 for U.S. Appl. No. 12/605,546.
Office action dated Sep. 22, 2014 for U.S. Appl. No. 13/281,805.
Office action dated Sep. 28, 2012 for U.S. Appl. No. 12/541,043.
Office action dated Sep. 28, 2012 for U.S. Appl. No. 12/541,050.
Office action dated Sep. 28, 2012 for U.S. Appl. No. 12/605,929.
Office action dated Oct. 9, 2014 for U.S. Appl. No. 13/857,068.
Office action dated Oct. 24, 2014 for U.S. Appl. No. 13/975,139.
Office action dated Nov. 6, 2013 for U.S. Appl. No. 13/938,032.
Office action dated Dec. 4, 2014 for U.S. Appl. No. 13/236,471.
Office action dated Dec. 6, 2011 for U.S. Appl. No. 13/281,846.
Office action dated Dec. 22, 2011 for U.S. Appl. No. 13/281,856.
Notice of Allowance dated Aug. 2, 2016 for U.S. Appl. No. 13/281,805.
Office Action dated Mar. 31, 2016 for U.S. Appl. No. 13/281,805.
Office Action dated Apr. 22, 2016 for U.S. Appl. No. 14/657,684.
Office Action dated Jul. 5, 2016 for U.S. Appl. No. 13/236,471.
Office Action dated Sep. 7, 2016 for U.S. Appl. No. 13/857,068.
Office Action dated Nov. 2, 2016 for U.S. Appl. No. 14/657,684.
Related Publications (1)
Number Date Country
20150105791 A1 Apr 2015 US
Provisional Applications (1)
Number Date Country
61891288 Oct 2013 US