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US3450502A - Method of operating heart-lung apparatus - Google Patents

Method of operating heart-lung apparatus
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US3450502A
US3450502AUS670395AUS3450502DAUS3450502AUS 3450502 AUS3450502 AUS 3450502AUS 670395 AUS670395 AUS 670395AUS 3450502D AUS3450502D AUS 3450502DAUS 3450502 AUS3450502 AUS 3450502A
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ethylene oxide
molecular weight
heart
solution
weight
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US670395A
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Alan C Hymes
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Wyandotte Chemicals Corp
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Wyandotte Chemicals Corp
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United States Patent U.S. Cl. 23-258.5 4 Claims ABSTRACT OF THE DISCLOSURE Isotonic solutions of certain ethylene oxide-polypropylene glycol condensation products have been found to be extremely effective as priming agents in the heart-lung apparatus.
The present invention relates to an improved method of operating the heart-lung apparatus. More particularly, the present invention relates to the use of certain solutions of ethylene oxide-polypropylene glycol condensation products as priming agents in the heart-lung apparatus.
The heart-lung apparatus is an instrument which permits surgeons to by-pass both the heart and the lungs during operations. The instrument comprises two essential components, a pump and an oxygenator. The function of the instrument is to oxygenate and withdraw carbon dioxide from blood and to pump this blood into the arteries, thus substituting for both the heart and the lungs. Prior to patient hook-up, the heart-lung apparatus is primed with enough fluid to fill all working chambers, reservoirs, and tubing in the patient. Historially, blood plasma was employed as a priming agent for the heartlung apparatus. However, because of the high cost, scarcity and storage problems of blood plasma, the art has long been in need of a material which will perform as a substitute therefor. To be useful as a blood plasma substitute, a material must possess the following properties: 1) it must retain a sufficient molecular size to remain in the blood space, thus creating an osmotic pres sure great enough to retain the solvent (water) within the circulation, (2) it must be miscible with blood, (3) it must be non-antigenic, non-toxic, and non-pyretogenic, (4) it must not draw water from the cellular area of the body, (5) it must be readily available and stable under prolonged storage conditions, and (6) when no longer needed, it must be readily discharged from the body circulation. With such formidable requirements, it is little wonder that the art has not heretofore found any material which satisfactorily performs as a blood plasma substitute. This is so notwithstanding the fact that various materials such as salt solutions, gelatin derivatives, various proteins and derivatives thereof, mannitol, starch and dextrans have been investigated as blood plasma substitues. However, these materials all lack one or more of the above requirements, thereby rendering them not totally acceptable as blood plasma substitutes.
Now, in accordance with the present invention, it has been determined that certain solutions of ethylene oxidepolypropylene glycol condensation products may be effectively employed as priming agents in the heart-lung apparatus. It has been determined that by the process of the present invention, prolonged extracorporeal circulation may be carried out without any significant adverse effects. Thus, the process of the present invention comprises the improvement in the operation of the heartlung apparatus which comprises employing as a priming agent therefor an isotonic (isosmotic) solution containing from 0.375 to 1.5 millimoles/liter of a compound of the formula wherein a is an integer such that the hydrophobe base represented by (C H O) has a molecular weight of at least 950 and b is an integer such that the hydrophile portion represented by (C H O) constitutes from about 50% to 90% by weight of the compound. By the phrase isotonic or isosmotic solution is meant a solution having the same osmotic pressure as blood. This phrase is well known in the art. Illustrative soliutions which may be employed in the preparation of the blood plasma substitutes employed in the process of the present invention include saline (a solution of sodium chloride, containing 8.5 to 9.5 grams of salt in 1000 cc. of purified water), Ringers solution, Ringers lactated solution, Krebs- Ringers solution, and various sugar solutions.
As stated above, critical amounts of certain ethylene oxide-polypropylene glycol condensation products must be employed in the preparation of the blood plasma substitutes useful in the present invention. Generally, the isotonic solutions useful in the present invention will comprise from 0.375 to 1.5 millimoles/liter of the abovementioned ethylene oxide-polypropylene glycol condensation products. Compositions comprising amounts of products outside of the above-cited range have been found to be unacceptable blood plasma substitutes.
The condensation products which are operable in the present invention are prepared by condensing ethylene oxide with polypropylene glycol. A more detailed discussion of the preparation of these products is found in U.S. 2,674,619. To be useful in the present invention, the products must contain at least 50% by weight of ethylene oxide. Furthermore, the polyproylene glycol base must have a molecular weight of at least 950. It has been determined that products outside of these limits are not satisfactory blood plasma substitutes for various reasons. For example, a product containing less than 50% ethylene oxide is not sufficiently non-toxic to be useful whereas a product containing a hydrophobic base molecular Weight of less than about 950 has completely different physio-a1 properties, particularly with regard to solubility, than the products useful in the present invention.
Illustrative ethylene oxide-polypropylene glycol condensation products which may be employed in the preparation of the isotonic solutions useful in the present invention include:
(1) 4750 molecular weight polyol containing approximately by weight ethylene oxide,
(2) 3500 molecular weight polyol containing approximately 5 0% by weight ethylene oxide,
(3) 7800 molecular weight polyol containing approximately 80% by weight ethylene oxide,
(4) 7500 molecular weight polyol containing approxi mately 70% by weight ethylene oxide,
(5) 16,250 molecular weight polyol containing approximately 80% by weight ethylene oxide,
6) 13,330 molecular weight polyol containing approximately 70% by Weight ethylene oxide,
(7) 9500 molecular weight polyol containing approximately by weight ethylene oxide.
The following examples illustrate the nature of the invention. All parts are by weight unless otherwise stated.
Example I An isotonic solution was prepared by dissolving 0.4% by weight of a 7800 molecular weight polyol prepared by condensing ethylene oxide with a polypropylene glycol having a molecular weight of 1750, said polyol containing approximately 80% ethylene oxide in Ringers lactated (0.513 millimoles/liter). Ringers lactated is a solution of 570 to 630 mg. sodium chloride, 290 to 330 mg. sodium lactate, 18 to 22 mg. calcium chloride, and 27 to 33 mg. potassium chloride in each 100 cc. of distilled water. The solution was then employed as a priming agent in the heart-lung apparatus in the manner described in an article by A. C. Hymes, N. Norimotf, and A. P. Thal, entitled A Comparison Between Mannitol Solutions and Low Molecular Weight Dextran as a Perfusate in Extracorporeal Circulation, Surgery, 59: 414-420, March 1966.
Of the 29 dogs perfused with the above solution, 27 survived (93% survival) without complications. Perfusion flow rates were high, and arterial blood pH one hour postperfusion was normal (7.33:0.06). Urine production was unimpaired during and following perfusion. Plasma hemoglobin was low and averaged 30 mg. percent. Fifteen minutes post-perfusion blood volume was only 8% greater than the initial blood volume before perfusion. Following this procedure, all of the fluid within the heartlung apparatus (now mixed with blood) was returned to the animal. The high flow rates during perfusion indicate that the osmotic pressure of the solute (polyol) was great enough to retain the solvent (water) within the vascular space during the procedure.
Example H A solution containing 1.0 millimole/liter of a polyol having a molecular weight of about 16,250 and containing approximately 80% ethylene oxide prepared by the reaction of ethylene oxide with a polypropylene glycol having a molecular weight of 3250 was prepared by dissolving 16.25 grams of said polyol in liters of saline solution containing 9 grams of sodium chloride in 1000 cc. of water. The solution was then employed as a priming agent in the heart-lung apparatus as described in Example I. Of the ten dogs treated, nine survived. In addition, no adverse effects were noticed in the surviving dogs.
What is claimed is:
1. The improvement in the method of operating the heart-lung apparatus which comprises employing as priming agent therefor, an isotonic solution containing from 0.375 to 1.5 millimoles/liter of a compound of the formula wherein a is an integer such that the hydrophobe base represented by (C H O) has a molecular weight of at least compound of the formula wherein a is an integer such that the hydrophobe base represented by (C H O) has a molecular weight of from 1750 to 4000 and b is an integer such that the hydrophile portion represented by (CZHQO) constitutes by weight of the compound.
3. The method of claim 1 wherein the isotonic solution comprises from 0.375 to 1.5 millimoles per liter of lactated Ringers solution of a compound of the formula wherein a is an integer such that the hydrophobe base represented by (C H O) has a molecular weight of at least 950 and b is an integer such that the hydrophile portion represented by (C H O) constitutes from about 50% to by weight of the compound.
4. The method of claim 1 wherein the isotonic solution comprises from 0.375 to 1.5 millimoles per liter of saline solution of a compound of the formula 2 4 )b( a s )a( 2 4. )b wherein a is an integer such that the hydrophobe base represented by (C H O) has a molecular weight of at least 950 and b is an integer such that the hydrophile portion represented by (C H.,O) constitutes from about 50% to 90% by weight of the compound.
References Cited MORRIS O. WOLK, Primary Examiner.
BARRY S. RICHMAN, Assistant Examiner.
US. Cl. X.R.
US670395A1967-09-251967-09-25Method of operating heart-lung apparatusExpired - LifetimeUS3450502A (en)

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Cited By (47)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US3839314A (en)*1971-06-291974-10-01Baxter Laboratories IncClarification of blood serum and plasma using block copolymers of ethylene oxide and polyoxypropylene
US3880989A (en)*1973-01-301975-04-29Baxter Laboratories IncProduction of antisera comprising fractionating plasma or serum with an ethylene oxide-polyoxypropylene block copolymer
US3893991A (en)*1973-04-051975-07-08Baxter Laboratories IncClarification of blood serum and plasma using block copolymers of ethylene oxide and polyoxypropylene
US3893990A (en)*1973-04-051975-07-08Baxter Laboratories IncClarification of blood serum and plasma using a block copolymer of ethylene oxide and polyoxypropylene
US3956259A (en)*1973-01-301976-05-11Baxter Laboratories, Inc.Fractionation of blood using block copolymer of ethylene oxide and polyoxypropylene polymer to recover fraction suitable for organ perfusate
US4025500A (en)*1974-06-061977-05-24Baxter Laboratories, Inc.Preparation of albumin by fractionation of blood plasma or serum
US4073886A (en)*1973-01-301978-02-14Baxter Travenol Laboratories, Inc.Blood fractionation process using block copolymers of ethylene oxide and polyoxypropylene
US4164524A (en)*1974-05-311979-08-14Ward Charles ATreatment of blood containing vessels
US4506018A (en)*1982-12-301985-03-19Becton, Dickinson And CompanyBlood diluent
US4801452A (en)*1986-05-151989-01-31Hunter Robert LFibrinolytic composition
US4837014A (en)*1986-05-151989-06-06Emory UniversityAn improved method of treating sickle cell anemia
US4873083A (en)*1986-05-151989-10-10Emory UniversityFibrinolytic composition
US4879109A (en)*1986-05-151989-11-07Emory UniversityMethod for treating burns
US4897263A (en)*1986-05-151990-01-30Emory UniversityMethods and compositions for treatment of pathological hydrophobic interactions in biological fluids
US4937070A (en)*1986-05-151990-06-26Emory UniversityMethods and compositions for treatment of pathological hydrophobic interactions in biological fluids
US4938961A (en)*1989-04-281990-07-03Geoffrey CollinsOrgan preservation solution containing pokyethylene gycol and method of performing cardioplegia
US4997644A (en)*1986-05-151991-03-05Emory UniversityMethod of treating adult respiratory distress syndrome
US5017370A (en)*1986-05-151991-05-21Emory UniversityImproved method of performing angioplasty procedures
US5028599A (en)*1986-05-151991-07-02Emory UniversityMethod of treating mycardial damage
US5030448A (en)*1986-05-151991-07-09Emory UniversityMethod of delivering drugs to damaged or diseased tissue
US5032394A (en)*1986-05-151991-07-16Emory UniversityMethod of treating burns
US5039520A (en)*1986-05-151991-08-13Emory UniversityPlasma extender
US5041288A (en)*1986-05-151991-08-20Emory UniversityMethod of treating tissue damaged by reperfusion injury
US5047236A (en)*1986-05-151991-09-10Emory UniversityMethod of treating stroke
US5064643A (en)*1986-05-151991-11-12Emory UniversityMethod for treating sickle cell disease
US5071649A (en)*1986-05-151991-12-10Emory UniversityMethod of preventing blockage in catheters
US5078995A (en)*1986-05-151992-01-07Emory UniversityFibrionolytic composition
US5080894A (en)*1986-05-151992-01-14Emory UniversityMethod and composition for reducing tissue damage
US5089260A (en)*1986-05-151992-02-18Emory UniversityMethod of treating ischemic tissue
US5152979A (en)*1986-05-151992-10-06Emory UniversityMethod for treating vascular obstructions caused by abnormal cells
US5182106A (en)*1986-05-151993-01-26Emory UniversityMethod for treating hypothermia
US5198211A (en)*1986-05-151993-03-30Emory UniversityMethod of treating myocardial damage
US5240701A (en)*1986-05-151993-08-31Emory UniversityMethod of performing angioplasty procedures
US5250294A (en)*1986-05-151993-10-05Emory UniversityImproved perfusion medium for transplantation of organs
WO1995012310A1 (en)*1993-11-021995-05-11Emory UniversityComposition for tissue and organ transplantation preservation
US5523492A (en)*1991-03-191996-06-04Cytrx CorporationPolyoxypropylene/polyoxyethylene copolymers with improved biological activity
US5536427A (en)*1991-10-231996-07-16Sodick Co., Ltd.Non-flammable electric discharge machining fluid including a block copolymer
US5622649A (en)*1991-06-271997-04-22Emory UniversityMultiple emulsions and methods of preparation
US5648071A (en)*1986-05-151997-07-15Emory UniversityMethod of treating tumors
US5658560A (en)*1994-01-181997-08-19Serikov; Vladimir B.Method of treating endotoxemia by administering tyloxapol
US5674911A (en)*1987-02-201997-10-07Cytrx CorporationAntiinfective polyoxypropylene/polyoxyethylene copolymers and methods of use
US5696298A (en)*1991-03-191997-12-09Cytrx CorporationPolyoxypropylene/polyoxyethylene copolymers with improved biological activity
US5811088A (en)*1987-02-201998-09-22Emory UniversityAntiinfective compounds and methods of use
USRE38558E1 (en)1991-03-192004-07-20Cytrx CorporationPolyoxypropylene/polyoxyethylene copolymers with improved biological activity
US20040248833A1 (en)*1991-03-192004-12-09Emanuele R MartinTherapeutic delivery compositions and methods of use thereof
US6933286B2 (en)1991-03-192005-08-23R. Martin EmanueleTherapeutic delivery compositions and methods of use thereof
US7202225B1 (en)1993-10-152007-04-10Emanuele R MartinTherapeutic delivery compositions and methods of use thereof

Citations (3)

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US2674619A (en)*1953-10-191954-04-06Wyandotte Chemicals CorpPolyoxyalkylene compounds
US2677700A (en)*1951-05-311954-05-04Wyandotte Chemicals CorpPolyoxyalkylene surface active agents
US3396849A (en)*1966-05-101968-08-13Univ MinnesotaMembrane oxygenator-dialyzer

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US2677700A (en)*1951-05-311954-05-04Wyandotte Chemicals CorpPolyoxyalkylene surface active agents
US2674619A (en)*1953-10-191954-04-06Wyandotte Chemicals CorpPolyoxyalkylene compounds
US3396849A (en)*1966-05-101968-08-13Univ MinnesotaMembrane oxygenator-dialyzer

Cited By (55)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US3839314A (en)*1971-06-291974-10-01Baxter Laboratories IncClarification of blood serum and plasma using block copolymers of ethylene oxide and polyoxypropylene
US3880989A (en)*1973-01-301975-04-29Baxter Laboratories IncProduction of antisera comprising fractionating plasma or serum with an ethylene oxide-polyoxypropylene block copolymer
US3956259A (en)*1973-01-301976-05-11Baxter Laboratories, Inc.Fractionation of blood using block copolymer of ethylene oxide and polyoxypropylene polymer to recover fraction suitable for organ perfusate
US4073886A (en)*1973-01-301978-02-14Baxter Travenol Laboratories, Inc.Blood fractionation process using block copolymers of ethylene oxide and polyoxypropylene
US3893991A (en)*1973-04-051975-07-08Baxter Laboratories IncClarification of blood serum and plasma using block copolymers of ethylene oxide and polyoxypropylene
US3893990A (en)*1973-04-051975-07-08Baxter Laboratories IncClarification of blood serum and plasma using a block copolymer of ethylene oxide and polyoxypropylene
US4164524A (en)*1974-05-311979-08-14Ward Charles ATreatment of blood containing vessels
US4025500A (en)*1974-06-061977-05-24Baxter Laboratories, Inc.Preparation of albumin by fractionation of blood plasma or serum
US4506018A (en)*1982-12-301985-03-19Becton, Dickinson And CompanyBlood diluent
US5071649A (en)*1986-05-151991-12-10Emory UniversityMethod of preventing blockage in catheters
US5047236A (en)*1986-05-151991-09-10Emory UniversityMethod of treating stroke
US4873083A (en)*1986-05-151989-10-10Emory UniversityFibrinolytic composition
US4879109A (en)*1986-05-151989-11-07Emory UniversityMethod for treating burns
US4897263A (en)*1986-05-151990-01-30Emory UniversityMethods and compositions for treatment of pathological hydrophobic interactions in biological fluids
US4937070A (en)*1986-05-151990-06-26Emory UniversityMethods and compositions for treatment of pathological hydrophobic interactions in biological fluids
US4837014A (en)*1986-05-151989-06-06Emory UniversityAn improved method of treating sickle cell anemia
US5250294A (en)*1986-05-151993-10-05Emory UniversityImproved perfusion medium for transplantation of organs
US4997644A (en)*1986-05-151991-03-05Emory UniversityMethod of treating adult respiratory distress syndrome
US5017370A (en)*1986-05-151991-05-21Emory UniversityImproved method of performing angioplasty procedures
US5028599A (en)*1986-05-151991-07-02Emory UniversityMethod of treating mycardial damage
US5030448A (en)*1986-05-151991-07-09Emory UniversityMethod of delivering drugs to damaged or diseased tissue
US5032394A (en)*1986-05-151991-07-16Emory UniversityMethod of treating burns
US5039520A (en)*1986-05-151991-08-13Emory UniversityPlasma extender
US5041288A (en)*1986-05-151991-08-20Emory UniversityMethod of treating tissue damaged by reperfusion injury
US5648071A (en)*1986-05-151997-07-15Emory UniversityMethod of treating tumors
US5064643A (en)*1986-05-151991-11-12Emory UniversityMethod for treating sickle cell disease
US4801452A (en)*1986-05-151989-01-31Hunter Robert LFibrinolytic composition
US5078995A (en)*1986-05-151992-01-07Emory UniversityFibrionolytic composition
US5080894A (en)*1986-05-151992-01-14Emory UniversityMethod and composition for reducing tissue damage
US5089260A (en)*1986-05-151992-02-18Emory UniversityMethod of treating ischemic tissue
US5152979A (en)*1986-05-151992-10-06Emory UniversityMethod for treating vascular obstructions caused by abnormal cells
US5182106A (en)*1986-05-151993-01-26Emory UniversityMethod for treating hypothermia
US5240701A (en)*1986-05-151993-08-31Emory UniversityMethod of performing angioplasty procedures
US5198211A (en)*1986-05-151993-03-30Emory UniversityMethod of treating myocardial damage
US5811088A (en)*1987-02-201998-09-22Emory UniversityAntiinfective compounds and methods of use
US5674911A (en)*1987-02-201997-10-07Cytrx CorporationAntiinfective polyoxypropylene/polyoxyethylene copolymers and methods of use
WO1990013307A1 (en)*1989-04-281990-11-15Waters Instruments, Inc.Organ preservation solution and method
US4938961A (en)*1989-04-281990-07-03Geoffrey CollinsOrgan preservation solution containing pokyethylene gycol and method of performing cardioplegia
US5691387A (en)*1991-03-191997-11-25Cytrx CorporationPolyoxypropylene/polyoxyethylene copolmers with improved biological activity
USRE38558E1 (en)1991-03-192004-07-20Cytrx CorporationPolyoxypropylene/polyoxyethylene copolymers with improved biological activity
US6933286B2 (en)1991-03-192005-08-23R. Martin EmanueleTherapeutic delivery compositions and methods of use thereof
US20040248833A1 (en)*1991-03-192004-12-09Emanuele R MartinTherapeutic delivery compositions and methods of use thereof
US5523492A (en)*1991-03-191996-06-04Cytrx CorporationPolyoxypropylene/polyoxyethylene copolymers with improved biological activity
US6747064B2 (en)1991-03-192004-06-08Cytrx CorporationPolyoxypropylene/polyoxyethylene copolymers with improved biological activity
US5696298A (en)*1991-03-191997-12-09Cytrx CorporationPolyoxypropylene/polyoxyethylene copolymers with improved biological activity
US6359014B1 (en)1991-03-192002-03-19Cytrx CorporationPolyoxypropylene/polyoxyethylene copolymers with improved biological activity
US5990241A (en)*1991-03-191999-11-23Cytrx, CorporationPolyoxypropylene/polyoxyethylene copolymers with improved biological activity
USRE36665E (en)*1991-03-192000-04-18Cytrx CorporationPolyoxypropylene/polyoxyethylene copolymers with improved biological activity
USRE37285E1 (en)1991-03-192001-07-17Cytrx CorporationPolyoxypropylene/polyoxyethylene copolmers with improved biological activity
US5622649A (en)*1991-06-271997-04-22Emory UniversityMultiple emulsions and methods of preparation
WO1993003738A1 (en)*1991-08-141993-03-04Emory UniversityMethod for treating vascular obstructions caused by abnormal cells
US5536427A (en)*1991-10-231996-07-16Sodick Co., Ltd.Non-flammable electric discharge machining fluid including a block copolymer
US7202225B1 (en)1993-10-152007-04-10Emanuele R MartinTherapeutic delivery compositions and methods of use thereof
WO1995012310A1 (en)*1993-11-021995-05-11Emory UniversityComposition for tissue and organ transplantation preservation
US5658560A (en)*1994-01-181997-08-19Serikov; Vladimir B.Method of treating endotoxemia by administering tyloxapol

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