|Publication number||US3738914 A|
|Publication date||Jun 12, 1973|
|Filing date||Oct 6, 1969|
|Priority date||Oct 6, 1969|
|Also published as||CA941701A, CA941701A1, DE2046813A1|
|Publication number||US 3738914 A, US 3738914A, US-A-3738914, US3738914 A, US3738914A|
|Inventors||K Knudson, G Thorne, O Wood|
|Original Assignee||Baxter Laboratories Inc|
|Export Citation||BiBTeX, EndNote, RefMan|
|Referenced by (100), Classifications (7)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent [191 Theme et a1.
[ June 12, 1973 221 Filed:
[ APPARATUS FOR PRESERVATION OF ORGANS  lnventors:' Gale H. Thorne, Bountiful; Orin Lew Wood, Salt Lake City; Kay L. Knudson, Murray, all of Utah  Assignee: Baxter Laboratories, Inc., Morton Grove, Ill.
21 Appl. No; 863,869
 References Cited UNITED STATES PATENTS 12/1970 Swenson et a1. 195/127 OTHER PUBLICATIONS Eisman et al., Surgery, Vol. 60, No. 6, pp. 1183-1186, Dec. 1966 Primary ExaminerRichard L. Huff Attorney-W. Garrettson Ellis  ABSTRACT Apparatus and method of preserving life organs, the apparatus having an organ container in which the organ may be subjected to elevated pressure, a pump pulsatilely delivering perfusate into the organ and an oxygenator to oxygenate the perfusate effluent from the organ. A constant pressure bias maintains a minimum pressure on the perfusate between pulses. A fluid flow control system delivers driving fluid in a pulsed manner to the pump at a selected rate and at selected pulse duration. The method includes delivering pulsed oxygenated perfusate to the organ and uniformly conducting perfusate away from the organ and providing a constant pressure bias on the perfusate. Loss or gain of liquid volume caused by waste secretion by the organ is compensated for.
8 Claims, 4 Drawing Figures PMENIEU JUN I 21975 sum 1 or 3' INVENTORS. GALE H. THORNE ORIN LEW WOOD KAY L. KNUDSON 1 APPARATUS FOR PRESERVATION OF ORGANS BACKGROUND I. Field of the Invention The present invention relates to treatment of organs and more particularly to the clinical and laboratory preservation and perfusion of life organs. I
2. The Prior Art The preservation of life organs for purposes such as surgical transplant and the like have become increas: ingly important. Of particular importance is the preservation of the organ in the state which closely approximates the natural physiological state in order to best preserve the organ and to avoid trauma in the organ.
Prior art, having to do with life organ perfusion, has primarily consisted of electric motor-driven, positive displacement rotary pumping systems. The mentioned prior art systems utilize the convenience of electricity but have not been completely satisfactory clue to the non-pulsatile nature of the perfusate flow and pressure. Thus, the organ perfusion is non-physiologic and the flow of perfusate into the organ is constant regardless of the pressure. The pressure is thereforea function of organ resistance and the organ can be easily damaged if it physiologically restricts itself and is subject to increased pressures. I
Also, the use of electricity in known prior art systems presents a potential danger'that the organ will be inadvertently shocked or exposed to driving electrical cur rent.
BRIEF SUMMARY AND OBJECTS or THE INVENTION The present invention provides versatile apparatus and method for life organ perfusion and preservation. The invention provides pulsatile flow of the perfnsate through an organ in a fashion closely simulating natural physiological blood flows and pressures. Also, a novel flow control system accommodates selected regulation BRIEF DESCRIPTION or THE FIGURES FIG. 1 is a schematic representation of one presently preferred system according to the present invention;
FIGS. 2 and 3 are schematic circuit diagrams, each illustrating a presently preferred control uniewhich may respectively comprise part of the system of FIG. 1;
- and FIG. 4 is a schematic circuit diagram of another presently preferred control unit which may also be used in r the system in FIG. 1..
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS FIG. 1
Referring now to FIG. 1, the organ preservation system, generally designated 20, is powered by a pneumatic source 22 which is preferably compressed oxygen.
ing of the compressed oxygen communicated through the line 24. Also, the control unit 26 pulses the input oxygen and communicates the pulsed oxygen to the output 32 of the unit 26. Significantly, dials 34 and 36 may be used to control the pulse rate and period of systole, respectively, of the output of the control unit. An on off switch 27 and gauge switches I34 and 138 are also provided. A more detailed discussion of the structure and operation of the control unit 26 will be subsequently more fully described in connection with FIG. 2.
The pulsed output pressure, termed systolic pressure, from the control unit 26 is communicated through line 38 to a pump 40. One suitable embodiment of the pump 40 includes a cylindrical flexible pump bladder (not shown) fitted with silicone rubber tricuspid type check valves (not shown) in both ends to insure flow only in the desired direction. The rigid pump housing 46 encloses the bladder and seals the bladder at both ends, the pulsating pneumatic pressures from the control unit 26 being communicated between the pump bladder and the interior of the pump housing 46.
Perfusate, such as whole blood, disposed within the bladder of the pump 40, is communicated through the conduit 42 to the simulated aorta 44 with each high pressure pulse through the line 38. The simulated aorta 44 is a perfusate or blood-receiving chamber and has a tubular silicone bladder (not shown) enclosed in a rigid cylindrical housing 48. The interior of the cylindrical housing 48 is in communication with a constant biasing pressure through line 50 which is, in turn, coupled with the control unit 26. The pressure in line 50 has a pre-selected magnitude which exerts a biasing force upon the blood in the aorta 44. The bias pressure is preferably selectively adjustable in a range of about 0 to 200 millimeters of mercury above ambient. Thus, the forward bias pressure on the blood will serve as a minimum or diastolic pressure.
The blood forced through the aorta 44 by the pump 40 is communicated through line 52 to a temperature bath 54. Although any suitable temperature bath could be used, one suitable type includes a coil of line 52 disposed within a constant temperature water bath.
Blood, emitted from the temperature bath 54 is then communicated through a port 56 to the interior of an organ container 58. Organ container 58 is preferably formed of transparent material such as, for example, acrylic plastic so that the organ (not shown) therein may be readily visually observed without disrupting the environment. The container 58 is constructed so as to accommodate elevated internal pressures such as on the order of about three atmospheres (45 p.s.i.g.). Also, the interior of the container 58 is preferably regulated in temperature with conventional heat exchange apparatus 238 (FIG. 4). Thus, the container 58 secures an organ (not shown) in a selected temperature and pressure environment.
Preferably, a tube 60 is connected to the organ (not shown) so as to receive excreted waste or by-products of the organ perfusion, such as urine or bile (when the After the pulsed blood has been circulated through the organ, the blood is then carried away from the organ through line 64 to an oxygenator 66. The oxygenator 66 may be of any suitable conventional type, for example, amembrane oxygenator. Fresh oxygen is communicated to the oxygenator 66 through line 68 from the control unit 26. In the oxygenator 66, carbon dioxide in the blood is exchanged for oxygen, carbon dioxide rich fluid being communicated away from the oxygenator 66 through line 70 to the control unit 26.
The oxygenated blood effluent from the oxygenator 66 is conducted by line 72 to simulated atrium 74. Significantly, an additional supply of blood or other perfusate is also in communication with the atrium 74 through line 76. The supply is maintained in a reservoir 78 to compensate for any reduction in blood volume in the system resulting from secretion of fluids through the line 60 to the accumulator 62. Also, it should be appreciated that the container 58 is disposed at a greater vertical height than the oxygenator 66 and the oxygenator 66 is, in turn, disposed at a greater height than the atrium 74. Thus, the flow of blood from the organ in the container 58 through the oxygenator 66 and to the atrium 74 is gravity flow.
Atrium 74 is a flexible silicone rubber receiver or chamber for receiving the blood or other perfusate from the oxygenator 66 and the reservoir 78. Atrium 74 carries a substantial supply of blood and, therefore, insures a non-interrupted venous inflow of blood to the pump 40 and also provides a relatively uniform pressure head for passive filling of the pump 40. Thus, the
atrium 74 cooperates with the pump 40 to closely simulate natural physiologic conditions.
Briefly summarizing the method of preserving an organ in the container 58, the system is primed with perfusate such as whole blood and purged of all air or gas in the blood circulatory system. Pneumatic pressure, such as compressed oxygen, is pulsed by the control unit 26 which, in turn, actuates the pump 40 forcing blood into the aorta 44 and, thereafter, through the temperature control bath 54 into the organ (not shown). A bias pressure on the aorta 44 regulated through the control unit 26 insures a minimum diastolic pressure in the system.
Any liquid waste or like product created by the organ in the container 58 during perfusion and preservation is delivered by the organ secretion ducts to the tube 60 at a greater vertical height than the oxygenator 66, oxygenator 66 being in turn at a greater vertical height than atrium 74. The developed pressure head is sufficient to drive the blood through the oxygenator 66. Also, the control system 26 is manually set to regulate and control the rate of oxygenation as required by the organ.
The oxygenated blood entering the atrium 74 is made available to the pump 40 in a continuous uninterrupted manner so that the pump 40 may be efficiently filled with blood when the pneumatic line 38 is vented to ambient pressure, as between successive systolic pressure pulses. When the pneumatic line 38 is vented to ambient pressure, the pressure head in the atrium 74 opens the upper pump valve (not shown) and allows the pump to be refilled preparatory to initiation of another cycle of pumping.
The Control Unit Embodiment of FIG. 2
Referring to FIG. 2, the control unit 26 comprises a pressure source 22 which, as above described, may be compressed oxygen. It is presently preferred that the pressure from source 22 enter the control unit 26 at about 20 p.s.i.g. (pounds per square inch gauge). The pressure from the source 22 is communicated through line to an oscillator circuit 92. Oscillator circuit 92 has an or/nor gate 94 one side of which is in communication with lines 90. The other side of the or/nor gate 94 is in communication through line 96 with a pneumatic capacitor 98. A needle valve 100 controls the flow of fluid from the capacitor 98 to a fixed resistor 102 and also to or/nor gate 104.
The regulated pressure supplied to the gate 94 passes freely through the gate until sufficient control pressure builds up in the capacitor 98 to switch the gate 94 off. When the gate 94 is off, the capacitor 104 discharges through the needle valve 100 and vents through the restrictor 102. When the pressure in pneumatic capacitor 98 reaches a predetermined minimum level, the gate 94 switches on again to conduct the 20 p.s.i.g. pressure through line 106 to the gate 104. Thus, 20 p.s.i.g. pressure is alternately conducted to the gate 104 and vented through the resistor 102. The rate of alternation is termed the pulse rate" and the pulse rate is determined by the setting on the needle valve 100, needle valve 100 controlling the rate of charge and discharge of the capacitor 98. The needle valve 100 may be manually set by turning knob 34 (FIG. 1).
A pressure regulator 108 reduces the 20 p.s.i.g. input pressure to 10 p.s.i.g. and thereafter conducts the reduced pressure through line 110 to the gate 104. A high pressure pulse in the line 106 switches the gate 104 to the on" position so that the 10 p.s.i.g. pressure through line 110 is conducted through line 112 as a pulse to the switching valve or fluid valve 116.
Fluid valve 116 responds to the pressure pulse from gate 104 by opening communication between line 118 and the output 32 of the control unit 26 (see also FIG. 1). Line 118 communicates pressure from the source 22, a regulator 120 being interposed into the lines to accommodate selective regulation of the pressure to the pump 40 (FIG. 1).
When gate 104 is switched off, i.e. when the oscillator 92 vents through the fixed resistor 102, the fluid valve 116 will be operated to vent the increased pressure developed in the pump 40. Fluid valve 116 is biased toward the vent position by fluid pressure existing in line 122. A pressure regulator 124 is disposed in the line 122 and controls the amount of pressure delivered to the right side of the fluid valve 1 16. Thus, the setting on regulator 120 determines the pressure which is necessary to move the valve 116 from the extreme left position to the extreme right position to communicate driving fluid pressure to the output 32. The time period during which driving fluid is communicated through the output 32 is increased by increasing the pressure setting on the regulator 124. Hence, regulator 124 determines the period or duration of the systolic pressure.
A pneumatic capacitor 126 is interposed between the regulator 124 and the pressure source 22 to dampen minor fluctuations in the pressure line caused by the oscillator circuit 92.
Fluid pressure 'from the source 22 is communicated through line 128 to the aorta 44 (FIG. 1) as above de-' scribed; A regulator 130 controlled by knob 28 (FIG. 1) is disposed in the line 128 and is adjustable to set the bias fluid pressure in line 128 to a predetermined minimum diastolic pressure.
Pressure gauge 30 is coupled to a switch 134 (see also FIG. 1) disposed in line 136. When switch 134 is in one position, the driving pressure to the pump 40 is registered on the gauge 30. When the switch is placed in the other position, the bias pressure to the aorta 44 is indicated on the gauge 30. The other gauge 31 is coupled to a switch 138 which is disposed in line 140. In
' one position the switch 138 causes the gauge 31 to reg- The Embodiment of FIG. 3
The control unit embodiment generally designated 144 and best illustrated in FIG. 3 is, in many respects, substantially identical to the control unit 26, like parts having like numerals throughout. The control unit 144 has a fluid valve control subsystem generally designated 149 and including a fluid valve 146 which is biased by spring 148 toward the vent position. Thus, in the absence of a high pressure systolic pulse at the lefthand side of the fluid valve 146, the pump 40 (FIG. 1) will be vented through the valve 146. The spring bias eliminates the requirement for a regulated fluid pressure source to switch the fluid valve to vent (i.e. to terminate the systole output).
The period of systole output is controlled by the or/- nor gates 150 and 152 and the needle valve 154 as will now be described. The pulse signals of the oscillator 92 switch the gate 150 to the on condition, causing fluid in line 156 to be conducted through the gate 150 and through restrictor 158 to the input 160 of gate 152. It should be observed that the fluid in line 156 is communicated from a pneumatic capacitor 162 which is, in turn, connected to input line 164. Capacitor 162 provides a more constant pressure to the oscillator circuit 92. Input line 164 is in communication with the fluid supply 22 when switch 166 is in the illustrated on" position. Switch 166 permits regulation of the supply pressure prior to placing the control unit 144 in the on condition. The pressure regulation is accommodated by regulator 168. Fluid from the pressure source is initially filtered through filter 170 and, when switch 166 is in the illustrated closed position, the regulated fluid pressure is conducted through line 164 to the capacitor 162 and made available to the gate 150.
When gate 150 is in the on condition, as above described, a pressure pulse will appear at gate 152 switching gate 152 to the on condition. Thus, the gate 150 isolates the systole control subsystem 149 from the oscillator circuit 92.
When gate 152 is in the on condition, the fluid in line 156 is communicated through line 172 to the lefthand side of fluid valve 146 causing the valve to communicate the fluid pressure in line 118 to the pump at output 32 (see FIG. 1). Significantly, the amount of pressure required to place gate 152 in the on condition is governed by the needle valve 154. Thus, the needle valve 154 is adjusted to regulate the period of systolic output of the fluid valve 146. When gate 152 is again switched to the of condition, the spring 148 will return the fluid valve 146 to the vent position, fluid in the left-hand side of the valve 146 being vented through resistor 174.
It should be appreciated in the control unit 144 that the gauge 31 and the switch 138 are connected so that in one position gauge 31 monitors the pressure as regulatcd prior to placing the switch 166 in the on" condition and, in the opposite position, monitors the pressure as supplied to the oscillator circuit. The control unit 144 has the advantage of more positive control of the switching action of the fluid valve 146.
The Control Unit Embodiment of FIG. 4
The control unit illustrated in FIG. 4 and generally designated 180 is similar to the control units 26 and 144 above described, like parts having like numerals throughout. The control unit 180 differs in that it provides a parallel circuit operating and controlling two fluidic pumps simultaneously. Also, the unit 180 is constructed for operation under hyperbaric conditions.
Most of the components of the control unit 180 are carried within a hyperbaric chamber 182 which may be formed of acrylic plastic and which is constructed so as to maintain a hyperbaric environment. The chamber 182 also contains the organ container 58 (not shown in FIG. 4).
The unit 180 comprises an oscillator circuit 184 which is substantially similar to the oscillator circuit 92 above described, circuit 184 comprising a gate 94, a fluidic capacitor 98 and a needle valve 100. The control unit 180 differs from control unit 92 in that a restrictor 186 is disposed between the line 106 and restrictor 102. Restrictor 186 minimizes the volume of pneumaticfluid required by the unit 180 and allows the size of the capacitor 98 to be minimized. The operation of oscillator 184 is essentially identical to the operation of oscillator 92 above described.
The output of oscillator 184 in line 106 is simultaneously communicated to each of two fluid valve controlsubsy'stems 149 which may be substantially identical to the fluid valve control subsystem 149 above described and illustrated in FIG. 3. The subsystems 149 are connected in parallel and relate one with another with line 192 which equalizes the fluid pressure between gates and also with line 194 which communicates fluid in line 156 to gates 152 simultaneously. Eachof the fluid' valves 146 is connected to a separate pump 196 and 198.
With continued reference to FIG. 4, fluid from the source 22 is communicated through the filter to the regulator 168 as above described (FIG. 3). The system is operated when the switch 166 is moved from the of position illustrated in FIG. 4 to the on position opposite the position illustrated in FIG. 4. In the on position the oscillator 184 is energized and a pulsatile signal is developed by the subcircuits 149 to drive the pumps 196 and 198. The input pressure through the regulator 168 is also communicated through line 200 to switch 202 so that gauge 204 measures the pressure communicated through line 206 to the oxygenator 66. A restrictor 208 dampens pressure fluctuation in the line servicing the pressure gauge 204 protecting it from shock damage.
The pressure from the supply 22 is also conducted to regulators 210 and 212 which control the pumping pressure to pumps 198 and 196 respectively. A switch 214 is provided to selectively turn the pump 198 on or off so that a single pump may be operated if desired. Also, switch 216, in one position, allows the pressure available to pump 196 to be registered on the gauge 218 and, in the opposite position, allows the pressure in pump 198 to be monitored on gauge 218.
Gauge 218 is connected to switch 220 which in the illustrated position monitors the pressure on the selected one of the pumps 198 or 196 and, in the opposite position, monitors the pressure to the aorta. A regulator 222 controls the pressure supplied to the oxygenator 66 and a flow meter 224 monitors and controls the rate of flow to the oxygenator. Diodes 226 and 228 prevent application of negative pressure on the gauge 218 to avoid damaging the gauge.
A regulator 230 sets and controls the pressure in the hyperbaric chamber 182 and relief valve 232 functions as a safety valve to avoid overpressurizing the chamber 182. The pressure in the chamber 182 is monitored by a gauge 234 which is protected from pressure fluctuation by a restrictor 236.
If desired, as illustrated in FIG. 4, the hyperbaric chamber 182 may be provided with a heat exchanger 238 to maintain a constant predetermined temperature within the chamber 182 and/or of the perfusate.
The operation of the control circuit 180 is substantially similar to the operation of the control circuit 144 (FIG. 3) above. However, the unit 180 simultaneously drives two pumps which may be connected to the same or different organs. The system accommodates preservation of an organ in a manner closely approaching actual physiological conditions and accommodates a wide variety of controls to achieve maximum preservative effect.
The invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The present embodiments are, therefore, to be considered in all respects as illustrative dicated by the appended claims rather than by the foregoing description, and all changes which come within the meaning and range of equivalency of the claims are therefore to be embraced therein.
What is claimed and desired to be secured by United States Letters Patent is:
I. In an artificial organ perfusion apparatus including container means for receiving an organ, means for delivering perfusate to the organ within the container, and means for developing a pulsatile pressure in the perfusate delivered to the organ, the improvement comprising aorta means for imposing a minimum pressure bias on perfusate circulated through the organ between pressure pulses, said aorta means including a housing having a tubular bladder enclosed therein, and means for pressurizing the interior of said housing to a predetermined pressure to develop said minimum pressure bias on the perfusate.
2. Artificial organ perfusion apparatus as defined in claim 1 in which said container means are disposed within chamber means for maintaining a selected temperature and pressure to accommodate hyperbaric perfusion.
3. Artificial organ perfusion apparatus as defined in claim 1 having means for regulating the temperature of perfusate prior to delivery thereof to the organ.
4. Artificial organ perfusion apparatus as defined in claim 3 which includes means for oxygenating the perfusate.
5. Artificial organ perfusion apparatus of claim 4 in which the oxygenating means is disposed at a vertical height lower than the vertical height of the container means for receiving an organ, whereby perfusate in the oxygenating means is under gravity-generated hydrostatic pressure.
6. Artificial organ perfusion apparatus of claim 5 in which the portions thereof intended for contacting said perfusate are atraumatic to whole blood.
7. Artificial organ perfusion apparatus of claim 1 in which said means for imposing a minimum pressure bias is adjustable to provide a variable predetermined pressure of O to 200 mm. of mercury above ambient pressure.
8. The perfusion apparatus of claim 7 in which said bladder of the aorta means is silicone.
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US3935065 *||Aug 29, 1973||Jan 27, 1976||Roland Karl Doerig||Procedure for conservation of living organs and apparatus for the execution of this procedure|
|US4395492 *||Jun 3, 1981||Jul 26, 1983||Res-Del Group Ltd.||Perfusion chamber|
|US5141847 *||Feb 20, 1990||Aug 25, 1992||Kureha Chemical Industry Co., Ltd.||Method and apparatus for producing pulsation|
|US5338662 *||Sep 21, 1992||Aug 16, 1994||Bio-Preserve Medical Corporation||Organ perfusion device|
|US5494822 *||Jul 29, 1994||Feb 27, 1996||Bio-Preserve Medical Corporation||Organ perfusion device|
|US5786136 *||Jun 6, 1994||Jul 28, 1998||Mayer; Berndt||Method and device for conserving organs, body extremities and pieces of body tissue|
|US6046046 *||Apr 3, 1998||Apr 4, 2000||Hassanein; Waleed H.||Compositions, methods and devices for maintaining an organ|
|US6100082 *||Sep 23, 1997||Aug 8, 2000||Hassanein; Waleed H.||Perfusion apparatus and method including chemical compositions for maintaining an organ|
|US6490880 *||Oct 26, 2000||Dec 10, 2002||Islet Technology Inc.||Regulated organ containment shipping system using dual-layer preservation liquid|
|US6673594||Aug 25, 2000||Jan 6, 2004||Organ Recovery Systems||Apparatus and method for maintaining and/or restoring viability of organs|
|US6881569 *||Jan 25, 2002||Apr 19, 2005||Children's Medical Center Corporation||Apparatus and method for evaluating tissue engineered biological material|
|US7572622||Aug 14, 2003||Aug 11, 2009||Transmedic, Inc.||Heart preservation chamber|
|US7651835||Jan 26, 2010||Transmedics, Inc.||Method of timing pulsatile flow of normothermic perfusate to the heart|
|US7678563||Apr 2, 2004||Mar 16, 2010||Organ Recovery Systems, Inc.||Method and apparatus for controlling air pressure in an organ or tissue container|
|US7691622||Apr 6, 2010||Lifeline Scientific, Inc.||Method and apparatus for transferring heat to or from an organ or tissue container|
|US7749693||Feb 2, 2004||Jul 6, 2010||Lifeline Scientific, Inc.||Method of determining that an organ is not suitable for transplantation and using it for testing substances|
|US7824848||Jul 11, 2003||Nov 2, 2010||Lifeline Scientific, Inc.||Apparatus and method for maintaining and/or restoring viability of organs|
|US7897327||Jun 2, 2003||Mar 1, 2011||Organ Recovery Systems, Inc.||Method and apparatus for pressure control for maintaining viability of organs|
|US7998725||Aug 16, 2011||Organ Recovery Systems||Method and apparatus for holding a plurality of tubes connectible to an organ or tissue container|
|US8097449||Feb 16, 2010||Jan 17, 2012||Organ Recovery Systems||Method and apparatus for transferring heat to or from an organ or tissue container|
|US8128740||Apr 2, 2004||Mar 6, 2012||Organ Recovery Systems, Inc.||Device for separating gas from a liquid path|
|US8268547||Oct 25, 2005||Sep 18, 2012||Lifeline Scientific, Inc.||Method of transporting and storing a kidney|
|US8268612||Sep 18, 2012||Lifeline Scientific, Inc.||Apparatus and method for maintaining and/or restoring viability of organs|
|US8304181||Nov 6, 2012||Transmedics, Inc.||Method for ex-vivo organ care and for using lactate as an indication of donor organ status|
|US8318415||Oct 22, 2010||Nov 27, 2012||Lifeline Scientific, Inc.||Method of determining transport and/or storage parameters for maintaining viability of an organ|
|US8323954||Dec 4, 2012||Lifeline Scientific, Inc.||Apparatus and method for maintaining and/or restoring viability of organs|
|US8349551||Nov 5, 2010||Jan 8, 2013||Lifeline Scientific, Inc.||Method for controlling perfusion of an organ|
|US8389271||Dec 31, 2009||Mar 5, 2013||Organ Recovery Systems, Inc.||Method and apparatus for controlling air pressure in an organ or tissue container|
|US8409846||Apr 2, 2013||The United States Of America As Represented By The Department Of Veteran Affairs||Compositions, methods and devices for maintaining an organ|
|US8420380||Apr 16, 2013||Transmedics, Inc.||Systems and methods for ex vivo lung care|
|US8420381||Nov 5, 2010||Apr 16, 2013||Lifeline Scientific, Inc.||Apparatus and method for maintaining and/or restoring viability of organs|
|US8431385||Jan 21, 2011||Apr 30, 2013||Lifeline Scientific, Inc.||Apparatus and method for maintaining and/or restoring viability of organs|
|US8445260||Aug 10, 2011||May 21, 2013||Lifeline Scientific, Inc.||Apparatus and method for maintaining and/or restoring viability of organs|
|US8465970||Oct 7, 2005||Jun 18, 2013||Transmedics, Inc.||Systems and methods for ex-vivo organ care|
|US8535934||Apr 19, 2007||Sep 17, 2013||Transmedics, Inc.||Systems and methods for ex vivo organ care|
|US8585380||Oct 7, 2005||Nov 19, 2013||Transmedics, Inc.||Systems and methods for ex-vivo organ care|
|US8609400||May 12, 2010||Dec 17, 2013||Lifeline Scientific, Inc.||Apparatus and method for maintaining and/or restoring viability of organs|
|US8822203||Sep 28, 2010||Sep 2, 2014||Transmedics, Inc.||Systems and methods for ex vivo organ care|
|US8962303||Aug 10, 2011||Feb 24, 2015||Lifeline Scientific, Inc.||Apparatus and method for maintaining and/or restoring viability of organs|
|US8986978||Feb 29, 2008||Mar 24, 2015||Lifeline Scientific, Inc.||Perfusion regulation|
|US9055740||Oct 7, 2005||Jun 16, 2015||Transmedics, Inc.||Systems and methods for ex-vivo organ care|
|US9078428||Oct 7, 2005||Jul 14, 2015||Transmedics, Inc.||Systems, methods, compositions and solutions for perfusing an organ|
|US9215867||Oct 7, 2005||Dec 22, 2015||Transmedics, Inc.||Systems and methods for ex-vivo organ care|
|US9247728||Apr 8, 2008||Feb 2, 2016||Transmedics, Inc.||Systems and methods for ex vivo lung care|
|US9301519||Oct 7, 2005||Apr 5, 2016||Transmedics, Inc.||Systems and methods for ex-vivo organ care|
|US20030143519 *||Jan 25, 2002||Jul 31, 2003||Perry Tjorvi Ellert||Apparatus and method for evaluating tissue engineered biological material|
|US20040171138 *||Aug 14, 2003||Sep 2, 2004||Transmedics, Inc.||Heart preservation chamber|
|US20040221719 *||Apr 2, 2004||Nov 11, 2004||Organ Recovery Systems, Inc.||Device for separating gas from a liquid path|
|US20040224298 *||Feb 2, 2004||Nov 11, 2004||John Brassil||Apparatus and method for determining effects of a substance of an organ|
|US20040224299 *||Apr 2, 2004||Nov 11, 2004||Organ Recovery Systems||Method and apparatus for transferring heat to or from an organ or tissue container|
|US20040235142 *||Apr 2, 2004||Nov 25, 2004||Organ Recovery Systems||Method and apparatus for holding a plurality of tubes connectible to an organ or tissue container|
|US20040241634 *||Jun 2, 2003||Dec 2, 2004||Organ Recovery Systems||Method and apparatus for pressure control for maintaining viability of organs|
|US20050147958 *||Feb 17, 2005||Jul 7, 2005||Waleed Hassanein||Compositions, method and devices for maintaining an organ|
|US20060063142 *||Oct 25, 2005||Mar 23, 2006||Organ Recovery Systems, Inc.||Apparatus and method for maintaining and/or restoring viability of organs|
|US20060148062 *||Oct 7, 2005||Jul 6, 2006||Transmedics, Inc.||Systems and methods for ex-vivo organ care|
|US20060154357 *||Oct 7, 2005||Jul 13, 2006||Transmedics, Inc.||Systems and methods for ex-vivo organ care|
|US20060154358 *||Oct 7, 2005||Jul 13, 2006||Transmedics, Inc.||Systems and methods for ex-vivo organ care|
|US20060154359 *||Oct 7, 2005||Jul 13, 2006||Transmedics, Inc.||Systems and methods for ex-vivo organ care|
|US20060160204 *||Oct 7, 2005||Jul 20, 2006||Transmedics, Inc.||Systems and methods for ex-vivo organ care|
|US20060292544 *||Oct 7, 2005||Dec 28, 2006||Transmedics, Inc.||Systems, methods, compositions and solutions for perfusing an organ|
|US20070190636 *||Oct 7, 2005||Aug 16, 2007||Transmedics, Inc.||Systems and methods for ex-vivo organ care|
|US20070275364 *||Apr 25, 2007||Nov 29, 2007||Waleed Hassanein||Systems and methods for ex-vivo organ care and for using lactate as an indication of donor organ status|
|US20080017194 *||Apr 19, 2007||Jan 24, 2008||Transmedics, Inc||Systems and methods for ex vivo organ care|
|US20080234768 *||Jul 6, 2007||Sep 25, 2008||Transmedics, Inc||Systems for monitoring and applying electrical currents in an organ perfusion system|
|US20090197241 *||Apr 8, 2008||Aug 6, 2009||Transmedics, Inc||Systems and methods for ex vivo lung care|
|US20090197292 *||Apr 8, 2008||Aug 6, 2009||Transmedics, Inc||Systems and methods for ex vivo lung care|
|US20090197325 *||Apr 8, 2008||Aug 6, 2009||Transmedics, Inc||SYSTEMS AND METHODS FOR Ex vivo LUNG CARE|
|US20100028850 *||Feb 29, 2008||Feb 4, 2010||Lifeline Scientific, Inc.||Perfusion regulation|
|US20100112542 *||Dec 31, 2009||May 6, 2010||Organ Recovery Systems, Inc.||Method and apparatus for controlling air pressure in an organ or tissue container|
|US20100151559 *||Feb 16, 2010||Jun 17, 2010||Lifeline Scientific, Inc.||Method and apparatus for transferring heat to or from an organ or tissue container|
|US20100221696 *||Sep 2, 2010||Organ Recovery Systems, Inc.||Apparatus and method for maintaining and/or restoring viability of organs|
|US20110039253 *||Feb 17, 2011||Lifeline Scientific, Inc.||Apparatus and method for maintaining and/or restoring viability of organs|
|US20110053256 *||Nov 5, 2010||Mar 3, 2011||Lifeline Scientific, Inc.||Apparatus and method for maintaining and/or restoring viability of organs|
|US20110059429 *||Nov 5, 2010||Mar 10, 2011||Lifeline Scientific, Inc.||Apparatus and method for maintaining and/or restoring viability of organs|
|US20110129908 *||Jan 21, 2011||Jun 2, 2011||Lifeline Scientific, Inc.||Apparatus and method for maintaining and/or restoring viability of organs|
|US20110136096 *||Jun 9, 2011||Transmedics, Inc.||Systems and Methods for Ex Vivo Organ Care|
|DE4201258A1 *||Jan 18, 1992||Jul 22, 1993||Sachs Elektronik Kg Hugo||Perfusionseinrichtung|
|EP2258175A2||Aug 27, 2001||Dec 8, 2010||Organ Recovery Systems, Inc.||Apparatus for maintaining and/or restoring viability of organs|
|EP2258176A2||Aug 27, 2001||Dec 8, 2010||Organ Recovery Systems, Inc.||Method for maintaining and/or restoring viability of organs|
|EP2301334A2||Aug 27, 2001||Mar 30, 2011||Organ Recovery Systems, Inc.||Method of transporting and storing an organ|
|EP2301335A2||Aug 27, 2001||Mar 30, 2011||Organ Recovery Systems, Inc.||Apparatus for holding an organ|
|EP2301336A2||Aug 27, 2001||Mar 30, 2011||Organ Recovery Systems, Inc.||Method of transporting and storing an organ|
|EP2301337A2||Aug 27, 2001||Mar 30, 2011||Organ Recovery Systems, Inc.||Apparatus for holding an organ|
|EP2301338A2||Aug 27, 2001||Mar 30, 2011||Organ Recovery Systems, Inc.||Apparatus for perfusing organs|
|EP2301339A2||Aug 27, 2001||Mar 30, 2011||Organ Recovery Systems, Inc.||Method for maintaining and/or restoring viability of organs|
|EP2301340A2||Aug 27, 2001||Mar 30, 2011||Organ Recovery Systems, Inc.||Portable apparatus for transporting organs|
|EP2301341A2||Aug 27, 2001||Mar 30, 2011||Organ Recovery Systems, Inc.||Apparatus for holding organs|
|EP2301342A2||Aug 27, 2001||Mar 30, 2011||Organ Recovery Systems, Inc.||Method for controlling operation of a transporter|
|EP2308291A2||Aug 27, 2001||Apr 13, 2011||Organ Recovery Systems, Inc.||Method for holding an organ|
|EP2308292A2||Aug 27, 2001||Apr 13, 2011||Organ Recovery Systems, Inc.||Apparatus for holding an organ|
|EP2308293A2||Aug 27, 2001||Apr 13, 2011||Organ Recovery Systems, Inc.||Method for maintaining and/or restoring viability of organs|
|EP2308294A2||Aug 27, 2001||Apr 13, 2011||Organ Recovery Systems, Inc.||Method for maintaining and/or restoring viability of organs|
|EP2308295A2||Sep 29, 1999||Apr 13, 2011||Organ Recovery Systems, Inc.||Apparatus for transporting an organ|
|EP2308296A2||Sep 29, 1999||Apr 13, 2011||Organ Recovery Systems, Inc.||System and method for holding an organ|
|WO1996029865A1 *||Mar 27, 1996||Oct 3, 1996||Organ, Inc.||Organ evaluation and resuscitation device and method|
|WO2004089235A2||Apr 2, 2004||Oct 21, 2004||Organ Recovery Systems, Inc.||Methods and apparatus for perfusion, diagnosis, storage and/or transport of an organ or tissue|
|WO2012078968A2||Dec 9, 2011||Jun 14, 2012||Lifeline Scientific, Inc.||Machine perfusion with complement inhibitors|
|WO2012148685A1||Apr 12, 2012||Nov 1, 2012||Lifeline Scientific, Inc.||Living donor cannula|
|WO2012148687A1||Apr 12, 2012||Nov 1, 2012||Lifeline Scientific, Inc.||Cannula|
|WO2014011534A2||Jul 8, 2013||Jan 16, 2014||Lifeline Scientific, Inc.||Cannula|
|U.S. Classification||435/284.1, 137/14, 137/624.11|
|International Classification||A01N1/00, A61M1/32|