|Publication number||US3878830 A|
|Publication date||Apr 22, 1975|
|Filing date||May 31, 1973|
|Priority date||May 31, 1973|
|Publication number||US 3878830 A, US 3878830A, US-A-3878830, US3878830 A, US3878830A|
|Inventors||Haim I Bicher|
|Original Assignee||Mediscience Technology Corp|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (9), Referenced by (57), Classifications (8), Legal Events (3)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent 1191 Bicher 1 Apr. 22, 1975 CATHETER SYSTEM FOR BLOOD GAS MONITORING  lnventor: .Haim I. Bicher, Charleston, S.C.
221 Filed: May 31,1973
211 App]. No.: 365,431
 US. Cl 128/2 E; 128/2 L; 204/195 B  Int. Cl A611) 5/00  Field of Search 128/2 E, 2 L, 2.1 E;
204/195 B, 195 P, 195 S, 195 W  Reierences Cited UNITED STATES PATENTS 3,259,124 7/1966 Hillier et al.., 204/195 X 3,278,408 10/1966 Leonard et al. 204/195 P 3,334,039 8/1967 Vlasak 204/195 P 3,380,905 4/1968 Clark, Jr 204/195 P 3,400,054 9/1968 Ruka et a1. 204/195 S 3,406,109 10/1968 Molloy 204/195 P 3,533,403 10/1970 Woodson.... 128/2.06 3.682.159 8/1972 lmredy et a1... 128/2 E 3,791,376 2/1974 Rybak 128/2 E OTHER PUBLICATIONS Niedrach, L. W. et al.. Jou'rn. of Assoc. for Advanc. of
Med. Instr., Vol. 6, No. 2, Mar.-Apr., 1972, pp. 121-125.
Primary Examiner-Kyle L. Hlowell Attorney, Agent, or Firm-Jacob Trachtman [5 7] ABSTRACT A catherter system for blood gas monitoring comprising a polarographic sensing means having a body, first and second conductors supported by the body and each respectively having an exposed conducting surface at a region of the body, electrolytic material supported by the body at said region in contact with the exposed surfaces at the first and second conductors, and a membrane supported by the body extending over the region of said body covering the electrolytic material. The membrane is pervious to oxygen in the fluid system and semi-pervious to water. The electrolytic material is anhydrous prior to use of the device and is activated by immersing in a aqueous solution just before use. The sensing means is at the end of a cable carrying the conductors which cable has its other end joined to the connector end of a terminal or transport unit. The end opposite the connector end of the unit has a securing means for attaching the unit to the hub end of a catherer through which the sensing means and cable are receivable.
15 Claims, 10 Drawing Figures CATHETER SYSTEM FOR BLOOD GAS MONITORING The invention relates to a catheter system for blood gas monitoring and particularly a system for monitoring and measuring the partial pressure of oxygen in the blood system which provides a sensing head with a dry electrolyte for long shelf life which can be activated prior to use by emersion in an aqueous solution.
The constant monitoring of respiratory gas tensions in the circulating blood is vital for determining patient responses during anesthesia, certain surgical proce dures and the treatment of the heart, pulmonary and metabolic diseases, as well as for assisting positive pressure breathing and during many medical emergencies including shock or trauma. I-Ieretofore, no device has been available for fulfilling such needs in a practical, reproducable, and economical manner. The present invention provides such a catheter system which is readily implantable and has a disposable catheter and sensing means for determining gas tension in the blood, particularly the partial pressure of oxygen and can be implanted in the vein or artery, or in the tubing attached to a heart-lung machine or to any similar profusion apparatus.
It is therefore a principal object of the invention to provide a new and improved catheter system for blood gas monitoring which is highly reliable and may easily be implanted in the region where the blood system is to be monitored.
Another object of the invention is to provide a new and improved catheter system which may be inexpensively produced and has a disposable catheter and sensing unit.
Another object of the invention is to provide a new and improved catheter system for monitoring the partial pressure of oxygen in the blood system in-situ or at a selective point or location in the circulatory system with desirable accuracy over an extended period of time.
Another object of the invention is to provide a new and improved catheter system for blood gas monitoring which provides a relatively long shelf life and may be readily activated just before use byimmersion in an aqueous solution.
Another object of the invention is to provide a new and improved catheter system for blood gas monitoring which allows a sensing head to be threaded through a catheter or cannula already in place in the patient without disturbing other catheter functions.
Another object of the invention is to provide a new and improved catheter system for blood gas monitoring which may readily be calibrated in-situ, provides for obtaining blood samples and for infusing fluids therethrough without interfering with the monitoring and measuring functions.
Another object of the invention is to provide a new and improved catheter system for blood gas monitoring which includes a delivery or transport unit for being secured with a catheter and controlling the placement of the sensing head selectively within the catheter or extending beyond the catheter into the circulatory system.
Another object of the invention is to provide a new and improved catheter system for blood gas monitoring which permits the sensing head to be implanted with the insertion of a catheter or after a catheter has been implanted, and also allows the removal of the sensing means without requiring the removal or disturbing of the implanted catheter.
Another object of the invention is to provide a new and improved catheter system for blood gas monitoring which is highly reliable in operation, provdes good stability over an extended period of time, and may readily be calibrated to provide accurate read-out information.
The above and other objects of the invention are achieved by providing a catheter system for blood gas monitoring which has a polarographic sensing means or head comprising a body, first and second conductors supported by the body and each respectively having an exposed conducting surface at a region of the body, electrolytic material supported by the body at said region in contact with the exposed surfaces of the first and second conductors, and a membrane supported by the body extending over the region of said body and covering the electrolytic material. The membrane is provided with an inner layer which is pervious to oxygen in the fluid system and semi-pervious to water, and a gas pervious outer layer which is compatible with the blood system into which it is placed.
Prior to use of the sensing head, the electroytic material is anhydrous or of crystalline form for providing long shelf life with minimized deterioration. The electrolytic material is activated by immersing the sensing head in an aqueous solution, which may be a saline solution, prior to use. In the particular form illustrated, the electrolytic material is potassium chloride, and the inner layer of the membrane is made of polyvinyl formal with an outer layer of silicone elastomer.
The pair of conductors of the head each comprising a copper wire having a silver coating. Oneof the conductors is chlorinated to provide a silver chloride, copper chloride surface in contact with the postassium chloride electrolyte as one electrode, while the other electrode is formed by the silver clad copper wire, also in contact with the electrolyte. The pair of conductors of the sensing head are provided by one end of a cable which has an insulating coating of a flexible material such as Teflon." The cable is connected at its other end to a terminal or transport unit which provides a connector for electrically detachably joining the wires of the cable to read-out equipment which may digitally indicate information derived from the sensing head, and also provide the bias potential utilized for operation of the sensing head.
The transport unit also has a first end providing a connector for threadedly engaging the hub of a cannula or catheter through which the cable and sensing head are threaded, and a cavity for communicating through the opening of the catheter to the circulatory system. The terminal unit is also provided with a plunger or piston which is received within the chamber and may be longitudinally moved for extending the sensing head from within the catheter to a position beyond the end of the catheter for making measurements in-situ. The piston when it is in its retracted position may be, locked to avoid movement of the sensing head.
The terminal unit is also provided with a port communicating with its chamber which allows the drawing of blood samples through the catheter, and also for the infusion of fluids into the circulatory system as may be required.
The method of making the sensing means of the invention includes the steps of forming a body with first and second spaced electrodes providing exposed surfaces at a region of the body, affixing an anhydrous electrolytic material over the exposed surfaces of the electrodes on the body, securing with the body a mem brane which is semi-pervious to water, enclosing the electrolytic material and the exposed surfaces of the electrodes. The anhydrous electrical material is affixed over the exposed surfaces of the electrodes by applying a wet electrolytic material on the body over the electrodes and allowing it to dry prior to enclosing the electrolytic material by the membrane. The wet electrolytic material is comprised of potassium chloride gel which is dried to crystalline form. The membrane is formed by applying a solution of polyvinyl formal to the body over the anhydrous electrolytic material and drying same to form a coating which is semi-pervious to water and pervious to oxygen in an aqueous solution. An outer coating for the membrane is formed by the additional'step of applying a silicone solution over the polyvinyl formal coating and allowing same to dry.
The method for forming the body of the sensing means with first and second spaced electrodes includes providing a cylindrical mold having an opening along its longitudinal axis and positioning in spaced axial extending relationship therein the first and second conductors, filling the opening of the mold about the conductors with an epoxy material in unset form and per mitting the epoxy material to set and harden, severing the mold, the epoxy material and conductors extending therethrough, along a plane perpendicular to the longitudinal axis of the mold, providing the conductors with an exposed surface at a flat surface region of the body, and removing the remaining mold from about the body.
The method also includes the step of applying an aqueous solution to the outside of the membrane for activating the electrolytic material of the sensing means by passage of water through the membrane, prior to the utilization of the sensing means for blood gas monitor- The foregoing and other objects of the invention will become more apparent when the following detailed description of the invention is read in conjunction with the drawings, in which:
FIG. 1 is an elongated perspective view of a catheter system for blood gas monitoring embodying the invention,
FIG. 2 is a sectional view of reduced size taken on the line 22 of FIG. 1,
FIG. 3 is an end elevational view taken on the line 3-3 of FIG. 2,
FIGS. 4, 5, 6, 7 and 8 are enlarged sectional views illustrating the method of making the sensing head of the invention,
FIG. 8a is an enlarged portion of FIG. 8, and
FIG. 9 is an enlarged sectional view of the sensing head similar to that shown in FIG. 8 after the electrolytic material has been activated by immersing the head in an aqueous solution.
Like numerals designate like parts throughout the several views.
Referring to the figures, the catheter system of the invention comprises a sensing means 10 having a sensing head 12 at the end 14 of a flexible cable 16 including double parallel insulated lines 18 and 20 with wire conductors 22 and 24. The cable 16 may have an outer insulating wall 26 of a plastic material which is compatible with the blood system, such as that commercially known as Teflon. The conductors 22 and 24, may be made of any suitable conducting material, and in the specific embodiment disclosed comprises copper wire which is silver plated. Such a cable having AWG size 36 wires is commercially available from Phoenix Wire, Inc. as catalog number 36TDQ.
The conductors 22 and 24 at the other end 28 of the cable 16 are secured with and electrically connected to the posts 30, 32 of a male connector 34 which is located at the rear end 36 of a terminal or transport unit 40. The front end 42 of the transport unit 40 provides an opening 46 and internal threads 44 for engaging the connecting end or hub 48 of a catheter 51. The opening 46 of the transport unit 40 communicates with a chamber 52 therewithin. The chamber 52 communicates with the opening 54 of the catheter 51 which opening 54 extends from the connector end or hub 48 to the distal end 56 thereof. The chamber 52 of the transport unit 40 extends in the longitudinal direction within a cylinder portion 58 of the transport unit 40.
The end 36 of the unit 40 is provided with a plunger or piston 60 which extends into the chamber 52 and is movable therein in the longitudinal direction. The end of the piston 60 is provided with a rubber seal 62 for preventing leakage of fluid from the chamber 52. The cable 16 passes axially and in the longitudinal direction through the center of the seal 62 and a central opening 64 in the piston 60 to the connector 34. The cable 16 extends in the opposite direction through the chamber 52 and out of the opening 46 of the unit 40 to the sensing head 12 at its other end 14. The sensing head 12 may be threaded through the opening 54 of a catheter 51 after which the connector end 48 of the catheter is threadedly engaged with the end 42 of the unit 40 as illustrated in FIGS. 1 and 2.
As also illustrated in FIG. 1, when the unit 40 is in its extended position, the head 12 is moved toward the end 42 of the unit, while when the unit 40 is in its compressed condition with the piston 60 fully received into the chamber 52, the sensing head 12 is extended away from the end 42 of the unit 40. This relative movement of the head 12 may be seen from the illustrations of FIG. 1, which shows the sensing head 12 within the opening 54 of the catheter 51, and FIG. 2 which shows the sensing head 12 extending from the end 56 of the catheter 51 so that it is positioned external to the catheter 51.
The terminal or transport unit 40 is provided with a radially extending portion providing a port 68, proximate to its connector end 42 which has a radially extending opening 66 communicating with the chamber 52. The port 68 may be closed by a stop plug 70 when not in use, as illustrated, and may be used for delivering or removing fluid through the catheter 51 when such use is desired.
The rear end 36 may be enlarged over the piston 60 to provide ease of handling and a stop abutment when the piston 60 is fully received into the chamber 52 of the cylinder 58. The unit 40 is also provided with a locking means 72 in the form of a pin 74 extending radially from the piston 60 proximate to the rear end 36 and a J-shaped groove 76 in the cylindrical portion 58 for receiving the pin in the axially direction and locking same by relative rotation of the piston 60 and cylinder 58. Such locking action is important for preventing the relative movement of the piston 60 with respect to the cylinder 58 and in turn preventing the movement of the sensing head 12, especially when the chamber 52 is subjected to high fluid pressure.
""12 is produced at the end 14 of the cable 16 in a manner illustrated by FIGS. 4 to 8 inclusive. The end 14 of the cable 16 is placed into the end of a tube 78. The tube 78 may be made of plastic material, such as poly- .:ethylene, forming a casting mold as shown in FIG. 4. Epoxy material 80 in its plastic state is placed within the opening of the tube 78 about theend 14 of the cable 16. The positioning the epoxy 80 within the tube 78 may be assisted by using a hypodermic syringe needle at the rear of the tube to suck up the epoxy mate rial. After the epoxy has set and hardened and has dried for at least 8 hours, the tube 78, epoxy material 80 and the cable 16 are severed along a plane indicated by the dashed line 82 of FIG. 4. The plane along which the cut is made provides a surface 84 which is perpendicular to the extending direction of the cable 16.
The tube 78 is now removed leaving an epoxy cast or plug 86 at the end 14 of the cable 16 with a flat end surface 84. The end surface 84, as seen in FIG. 6, provides exposed perpendicular cross sections of the conductors 22 and 24 of the cable 16 each of which is respectively ,surrounded by an insulation layer 88, 89 which may be of Teflon and bound to each other by the intermediate joining plastic material 93 which may also be Teflon. Surrounding the cable 16 is the epoxy cast or plug 86. The plastic covering 88 of the cable 16 may be provided with a red coloring to distinguish the conductor 22 from the conductor 24 which is covered by a plastic material 89 which is colored green'or any other distinguisting color.
The end .14 of the cable 16 with its cast epoxy body 86 and exposed conductors 22, 24 is immersed in a 0.05 HCl aqueous solution for 2 minutes while an elec trical potential of 1 volt is applied at the other end of the cable 16 between-the conductors 22, 24. The positive potential is applied to the conductor 22, while the ;negative potential is supplied to the conductor 24. This results in providing a silver chloride coating at the silyer plated surface of the conductor 22 and copper fchloride coating at the exposed copper surface to form the reference electrode. The silver' plated copper conductor 24 is not affected by the chlorination operation thus performed and provides the other electrode of the head 12. The flat end surface 84 of the plug 86 is positioned to face upwardly and a drop of wet electrolyte 90 is placed thereon making certain the electrolyte 90 is not received over the cylindrical side wall 85 of the plug 86. The electrolyte 90 is allowed to dry to form a dry electrolyte layer 90 for approximately 2 hours. The electrolyte 90 applied is potassium chloride gel such as that commercially available from Beckman Instruments, Inc. as P Electrolyte No. 326590. Upon drying, the potassium chloride electrolyte crystallizes to provide a layer of electrolyte on the surface 84 extending over and between, and in contact with the exposed chlorinated end of the conductor 22 and the exposed metallic end of the conductor 24 (see FIG. 7).
The plug 86 is dipped into a solution of 0.25% Formvar in ethylene dichloride. The Formvar utilized is Formvar l/95E, a polyvinyl formal which has an average molecualr weight of 24,000 to 40,000, a solution viscosity (15% by wt.) of 3,000 to 4,500 cp., a resin viscosity of 37 to 53 cp., a specific gravity (23/23) of 1.227, a hydroxyl content expressed as polyvinyl alcohol of 5.0 to 6.0 (Dl396-58), an acetate content expressed as polyvinyl acetate of 9.5 to 13.0 (D1 396-58) and a formal content expressed as polyvinyl formal of about 82. This product is sold by Monsanto Chemical Co. and is described in detail in the Monsanto Technical Bulletin No. 6070A.
It has been found desirable to repeat the dipping process by double dipping the plug 86 in the solution, at one minute intervals between double dippings, and holding the plug 86 in the upward direction and alternately in a downward direction between dippings. The coated material is allowed to dry for from 5 to 10 minutes to provide the inner layer 92 of the membrand 94. The layer 92 extends over the entire outside surface of the epoxy material 86 and where the end surface 84 is covered by the dried electrolyte layer 90, it extends overand encloses the electroyte 90 as shown in FIGS. 8 and 8a.
After the inner layer 92 is dried, the plug 86 is double dipped in a solution of 0.2 gram of Silastic to each cc of xylene and allowed to air dry for 24 hours. The Silastic used is commercially available from Dow Corning Corp. as Silastic Medical Adhesive-Sicicone, Type A, Stock No. 891. This forms a second or outer layer 96 of the membrane 94. The outer layer 96 extends completely over the inner layer 92 and provides a surface which is compatible with the blood system into which the sensor head 12 is to be received for making measurements.
In operation, the sensor head 12 is activated just prior to its use by immersing it. in an aqueouos solution, which may be a saline solution. With the passage through the membrane 94 of water, the crystallized potassium chloride electrolyte 90 is transformed into the electrolyte 91 in its active liquid state. This transformation causes the expansion of electrolyte 90 to provide the wet electrolyte 91 as shown in FIG. 9. In the ex- .panded form, the member 94 is stretched to provide In the form illustrated, the sensing means 10 provides a intra-arterial catheter with a polarographic head 12 for, measuring in-vivo, the partial pressure of oxygen in the blood. The sensing head 12 is provided with an outside diameter of 0.5 mm so that it may easily fit through a 20 gauge Teflon arterial canulla. The sensing head 12 may be placed in an artery by utilizing a catheter which had previously been implanted in the subject, or by positioning an arterial canulla or catheter with its implanted end at the location at which in-vivo measurements are to be taken.
Thus, for example, with the catheter 51 positioned in the artery as required, the cable 16 with the head 12 at its leading end 14 is threaded through the opening 54 of the catheter 51 by entering its terminal end or hub 48. At this time, the transport means 40 is positioned with its plunger 60 in its withdrawn or extended condition as shown in FIG. 1. After the cable 16 has been fully threaded through the catheter 51, its sensing head 12is positioned as indicated by the dashed lines in FIG. 1 and the end 42 of the transport unit 40 is proximate to the threaded end or hub 48 of the catheter 51. The end 48 of the catheter 51 and. the end 42 of the transport unit are threadedly engaged so that the protruding male portion 45 of the transport unit 40 is received into and securely sealed with the catheter 51 to provide communication .between its chamber 52 and the opening 54 of the catheter 51.
The end 36 of the transport unit 40 may now be moved to its contracted position shown in FIG. 2 and locked. The inward movement of the piston or plunger 60 results in the advancement of the sensing head 12 so that it extends out of the end 56 of the catheter 51 and into the blood system in which measurements of partial pressure of oxygen are to be obtained and monitored. An electrical measuring apparatus (not shown) is electrically joined to the connector 34 of the terminal 36 and provides a bias voltage potential to the conductors and electrodes 22, 26 of the sensing head 12 of 0.6 volt. 7
Since the membrane 94 is pervious to oxygen in the blood system, the oxygen passes therethrough to the electrolyte 91 resulting in polarographic action. As well known, the presence of oxygen at the polarographic sensing head 12 produces a current which may be calibrated to show the partial pressure of oxygen. Such current flow is delivered to an indicating means (not shown) providing output readings which may be calibrated by reference to measurements taken of blood samples by means of a conventional gas analyzer.
The catheter system for blood gas monitoring has been most effective and useful during and after major cardiovascular and pulmonary operations by providing continuous indications of oxygen tension in the blood correlated to within 12% of the values obtained by conventional gas analyzers. Such indications have followed faithfully stepwise changes in oxygen tension of inspired gas. It has been found that the catheter system could be left in-situ in patients for periods of 24 hours and more, proving the system to be of value for monitoring arterial partial oxygen pressure during and after major cardiovascular and pulmonary surgery and providing helpful information for the controlling of artificial ventilation.
The system provides a great advantage over prior art, by having a polarographic sensing head with an extended shelf life. This is achieved by providing the head with its electrolyte in a dry condition when not in use, while the head may be readily activated for use by placing same in a saline solution. The sensing head 12 can also be activated by placing same in the blood system, although the preactivation by immersion in the saline solution is preferred.
The in-situ calibration is also advantageous in that it permits making allowance for flow, temperature, and positioning artifacts. Calibration is readily accomplished by withdrawing blood samples through the catheter 51 by a syringe attached to the port 68 of the transport unit 40. In addition to removing such blood samples, other desirable fluids may be infused through the port 68, so that the catheter system does not inter- I invention disclosed may find wide application with appropriate modification to meet individual design circumstances, but without substantial depature from the essence of the invention.
What is claimed is:
l. A polarographic sensing means for a fluid system comprising a body, first and second electrical conductors insulated from each other and supported by said body and each respectively having an exposed conducting surface at a region of said body, a deactivated electrolytic material supported by said body at said region in contact with the exposed surfaces of said first and second conductors, and a membrane supported by said body extending over the region of said body and covering said electrolytic material, said membrane being pervious to oxygen in the fluid system and semi-pervious to water. v
2. The sensing means of claim 1 in which the electrolytic material is anhydrous, and the electrolytic material of said sensing means is activated by immersing said sensing means in an aqueous solution prior to use.
3. The sensing means of claim 2 in which the electrolytic material is crystalline potassium chloride.
4. The sensing means of claim 2 in which the membrane comprises a layer of polyvinyl formal.
5. The sensing means of claim 2 in which the electrolytic material is potassium chloride, the membrane is a layer of polyvinyl formal, said first conductor providing an exposed silver surface in contact with said electolytic material said second conductor providing a silver chloride surface in contact with said electrolytic material.
6. The sensing means of claim 4 in which said membrane includes an outer layer of silicone over the layer of polyvinyl formal.
7. the sensing means of claim 6 in which said first and second conductors are elongated wires encased in a flexible plastic material and extending from said body to a terminal end.
8. The sensing means of claim 7 including a terminal unit having a connector with a pair of contacts respectively electrically engaging the said first and second wires at said terminal end.
9. The sensing means of claim 8 in which said body has a head of substantially cylindrical configuration with an end providing a flat surface, said wires extend through said body and have an end providing said exposed conducting surfaces at said flat surface, said electrolytic material being supported on the flat surface of said head, and said membrane extending over the end of said head and covering said electrolytic material.
10. The sensing means of claim 9 in which said terminal unit has a first end and a second end and a cavity therein extending through said first end, the connector of said unit being secured at its second end with the wires of said first and second conductors extending therefrom through the cavity and opening in the first end of said unit to said head. i
11. The sensing means of claim 10 in which the first end of said unit includes securing means for attachment to the end of a catheter through which the head and extending conductors are receivable.
' 12. The sensing means of claim 11 including a catheter having a first end removably attached to the first end of said terminal unit and a second end, said catheter having a longitudinal opening therein communicating with the cavity of said unit and receiving said head and extending conductors therewithin.
13. The sensing means of claim 12 in which said unit has a scalable port communicating with its cavity for withdrawing fluid from and infusing fluid into said fluid system through said catheter.
The sensing means of claim 12 in which the first end of said unit has a cylinder containing said cavity and said second end includes a piston received within said cavity and movable between a first extended position and a second compressed position, said head being positioned within the opening of said catheter when ter is an elongated plastic tube.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3259124 *||Jul 19, 1963||Jul 5, 1966||Beckman Instruments Inc||Catheter transducer for in vivo measurements|
|US3278408 *||Dec 19, 1962||Oct 11, 1966||Beckman Instruments Inc||Electrochemical cell|
|US3334039 *||Jan 6, 1964||Aug 1, 1967||Abbott Lab||Electrode construction in oxygen sensor|
|US3380905 *||Oct 11, 1963||Apr 30, 1968||Leland C. Clark Jr.||Electrolytic sensor with anodic depolarization|
|US3400054 *||Mar 15, 1966||Sep 3, 1968||Westinghouse Electric Corp||Electrochemical method for separating o2 from a gas; generating electricity; measuring o2 partial pressure; and fuel cell|
|US3406109 *||Jul 20, 1964||Oct 15, 1968||Yellow Springs Instr||Polarographic sensor|
|US3533403 *||May 10, 1967||Oct 13, 1970||Woodson Riley D||Combination heart catheter and electrode|
|US3682159 *||Apr 6, 1970||Aug 8, 1972||Us Catheter & Instr Corp||Catheter electrode for oxygen polarography|
|US3791376 *||Dec 14, 1970||Feb 12, 1974||B Rybak||Microsonde for catheter use, for the continuous measurement of partial oxygen pressure|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US3981297 *||Mar 3, 1975||Sep 21, 1976||Sorenson Research Co., Inc.||Gas sampling catheter assembly and method|
|US4016866 *||Dec 18, 1975||Apr 12, 1977||General Electric Company||Implantable electrochemical sensor|
|US4120292 *||Jan 14, 1977||Oct 17, 1978||General Electric Company||Implantable electrochemical sensor having an external reference electrode|
|US4176659 *||Jul 19, 1977||Dec 4, 1979||Peter Rolfe||Catheter with measurement electrodes|
|US4265250 *||Jul 23, 1979||May 5, 1981||Battle Research And Development Associates||Electrode|
|US4339317 *||Nov 5, 1980||Jul 13, 1982||Instituto Sieroterapico E Vaccinogeno Toscano "Sclavo" S.P.A.||Device for performing measurements on fluids, directly in the sample container|
|US4783250 *||Feb 12, 1987||Nov 8, 1988||Pons B Stanley||Immobilized electrochemical cell devices and methods of manufacture|
|US4830013 *||Jan 30, 1987||May 16, 1989||Minnesota Mining And Manufacturing Co.||Intravascular blood parameter measurement system|
|US4934369 *||Mar 23, 1989||Jun 19, 1990||Minnesota Mining And Manufacturing Company||Intravascular blood parameter measurement system|
|US4951669 *||Aug 8, 1988||Aug 28, 1990||Minnesota Mining And Manufacturing Company||Blood parameter measurement system|
|US4989606 *||Aug 8, 1988||Feb 5, 1991||Minnesota Mining And Manufactoring Company||Intravascular blood gas sensing system|
|US5048525 *||Jun 18, 1990||Sep 17, 1991||Minnesota Mining And Manufacturing Company||Blood parameter measurement system with compliant element|
|US5109850 *||Aug 12, 1991||May 5, 1992||Massachusetts Institute Of Technology||Automatic blood monitoring for medication delivery method and apparatus|
|US5175016 *||Mar 20, 1990||Dec 29, 1992||Minnesota Mining And Manufacturing Company||Method for making gas sensing element|
|US5195963 *||Jan 14, 1992||Mar 23, 1993||Minnesota Mining And Manufacturing Company||Method and system for monitoring of blood constituents in vivo|
|US5284775 *||Sep 21, 1992||Feb 8, 1994||Minnesota Mining And Manufacturing Company||Gas sensing element and method for making same|
|US5316647 *||Aug 26, 1992||May 31, 1994||Martell Medical Products, Inc.||Portable oxygen analyzer|
|US5322609 *||Sep 24, 1992||Jun 21, 1994||Becton, Dickinson And Company||Device for detecting electrolytes in liquid samples|
|US5335658 *||Jun 29, 1992||Aug 9, 1994||Minnesota Mining And Manufacturing Company||Intravascular blood parameter sensing system|
|US5345932 *||Jan 15, 1993||Sep 13, 1994||Minnesota Mining And Manufacturing Company||Method and system for monitoring of blood constituents in vivo|
|US5390671 *||Mar 15, 1994||Feb 21, 1995||Minimed Inc.||Transcutaneous sensor insertion set|
|US5421328 *||May 20, 1994||Jun 6, 1995||Minnesota Mining And Manufacturing Company||Intravascular blood parameter sensing system|
|US5462052 *||Apr 27, 1993||Oct 31, 1995||Minnesota Mining And Manufacturing Co.||Apparatus and method for use in measuring a compositional parameter of blood|
|US5568806 *||Feb 16, 1995||Oct 29, 1996||Minimed Inc.||Transcutaneous sensor insertion set|
|US5586553 *||Feb 16, 1995||Dec 24, 1996||Minimed Inc.||Transcutaneous sensor insertion set|
|US7036224 *||May 12, 2003||May 2, 2006||Mamac Systems, Inc.||Method of making fluid sensor probe|
|US7048716 *||Nov 24, 1999||May 23, 2006||Stanford University||MR-compatible devices|
|US7291131||Apr 23, 2004||Nov 6, 2007||Physicians Industries, Inc.||Infusion syringe|
|US7351223||Jan 30, 2004||Apr 1, 2008||Physicians Industries, Inc.||Infusion syringe with integrated pressure transducer|
|US7662133||Feb 16, 2010||Smith & Nephew, Inc.||Spinal fluid introduction|
|US7740746||Jun 22, 2010||Delta Electronics, Inc.||Disposable electrochemical sensor strip|
|US8187446 *||Apr 19, 2005||May 29, 2012||Chun-Mu Huang||Method of manufacturing a disposable electrochemical sensor strip|
|US9084539 *||Feb 2, 2012||Jul 21, 2015||Volcano Corporation||Wireless pressure wire system with integrated power|
|US9097756 *||Sep 24, 2008||Aug 4, 2015||MRI Interventions, Inc.||Control unit for MRI-guided medical interventional systems|
|US9226999 *||May 25, 2012||Jan 5, 2016||Maquet Cardiopulmonary Ag||Use of nonionic esters in a coating for surfaces coming in contact with blood|
|US9398876||Dec 13, 2012||Jul 26, 2016||Pharmacophotonics, Inc.||Renal function analysis method and apparatus|
|US20040193045 *||Feb 23, 2004||Sep 30, 2004||Nelson Scarborough||Spinal fluid introduction|
|US20040227636 *||May 12, 2003||Nov 18, 2004||Mamac Systems, Inc.||Method of making fluid sensor probe|
|US20040260238 *||Jan 30, 2004||Dec 23, 2004||Call Evan W.||Infusion syringe|
|US20050004518 *||Apr 23, 2004||Jan 6, 2005||Call Evan W.||Infusion syringe|
|US20050187097 *||Apr 19, 2005||Aug 25, 2005||Chun-Mu Huang||Method of manufacturing a disposable electrochemical sensor strip|
|US20060196768 *||May 2, 2006||Sep 7, 2006||Chun-Mu Huang||Disposable electrochemical sensor strip|
|US20060229533 *||Jun 2, 2004||Oct 12, 2006||Joachim Hoenes||Integrated test element|
|US20070156035 *||Jan 3, 2006||Jul 5, 2007||Salus Corporation D/B/A Icp Medical||Catheter operable to deliver IV fluids and provide blood testing capabilities|
|US20070219438 *||Jun 12, 2007||Sep 20, 2007||Salus Corporation D/B/A Icp Medical||Catheter operable to deliver iv fluids and provide blood testing capabilities|
|US20090082783 *||Sep 24, 2008||Mar 26, 2009||Surgi-Vision, Inc.||Control unit for mri-guided medical interventional systems|
|US20090285761 *||Apr 17, 2009||Nov 19, 2009||Pharmacophotonics, Llc D/B/A Fast Diagnostics||Renal Function Analysis Method and Apparatus|
|US20100094229 *||Dec 7, 2009||Apr 15, 2010||Smith & Nephew, Inc.||Spinal fluid introduction|
|US20120238771 *||Sep 20, 2012||Maquet Cardiopulmonary Ag||Use of nonionic esters in a coating for surfaces coming in contact with blood|
|US20130204111 *||Feb 2, 2012||Aug 8, 2013||Axsun Technologies, Inc.||Wireless Pressure Wire System with Integrated Power|
|EP0276977A2 *||Jan 26, 1988||Aug 3, 1988||Minnesota Mining And Manufacturing Company||Intravascular blood parameter measurement system|
|EP0307162A2 *||Sep 6, 1988||Mar 15, 1989||C.R. Bard, Inc.||Apparatus for positioning a sensor in vivo|
|EP0479341A2 *||Jan 26, 1988||Apr 8, 1992||Minnesota Mining And Manufacturing Company||Intravascular blood parameter measurement system|
|EP0485118A1 *||Oct 31, 1991||May 13, 1992||Puritan-Bennett Corporation||Intravascular blood parameter sensor apparatus|
|EP0536808A1 *||Jan 26, 1988||Apr 14, 1993||Minnesota Mining And Manufacturing Company||Intravascular blood parameter measurement system|
|WO2009140026A2 *||Apr 17, 2009||Nov 19, 2009||Pharmacophotonics, Llc D/B/A Fast Diagnostics||Renal function analysis method and apparatus|
|WO2009140026A3 *||Apr 17, 2009||Jan 21, 2010||Pharmacophotonics, Llc D/B/A Fast Diagnostics||Renal function analysis method and apparatus|
|U.S. Classification||600/360, 204/403.13, 204/415|
|Cooperative Classification||A61B5/14542, A61B5/1473|
|European Classification||A61B5/1473, A61B5/145N|
|Oct 10, 1996||AS||Assignment|
Owner name: MALLINCKRODT SENSOR SYSTEMS, INC., MICHIGAN
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:MALLINCKRODT MEDICAL, INC.;REEL/FRAME:008048/0732
Effective date: 19960930
|Oct 10, 1996||AS02||Assignment of assignor's interest|
Owner name: MALLINCKRODT MEDICAL, INC.
Effective date: 19960930
Owner name: MALLINCKRODT SENSOR SYSTEMS, INC. 1590 EISENHOWER
|Mar 11, 1991||AS||Assignment|
Owner name: MALLINCKRODT MEDICAL, INC., 675 MCDONNELL BOULEVAR
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:MALLINCKRODT, INC., A CORP. OF DE;REEL/FRAME:005635/0379
Effective date: 19910227