Blood sampling syringe

Claim 2

A syringe assembly for obtaning a blood sample from a patient, said syringe assembly comprising: a syringe barrel having a central bore formed by an inner wall, an open end, a partially closed end forming a floor of said syringe barrel with an opening therein, and a syringe tip, located at said partially closed end of said syringe barrel, having a hypodermic needle detachably secured thereto and having conduit means therethrough for conveying said blood sample from said patient into said syringe barrel; a plunger, slideably mounted within said syringe barrel, having a first end protruding from said open end of said syringe barrel and a second end disposed with said bore: a compressible, elastomeric plunger tip mounted on said second end of said plunger in frictional compression with respect to said inner wall of said syringe barrel to form a slideable seal with said inner wall; said plunger tip having an end face that with said floor and said inner wall of said syringe barrel forms a chamber that varies in size with sliding movement of said plunger in said bore; and means for preventing the inward movement of said plunger beyond a predetermined position to prevent compressive contact of said plunger tip with said floor of said barrel and to provide a minimum size for said chamber, thereby avoiding compression of said plunger tip against said floor by the inward movement of said plunger and thereby avoiding air from being sucked into said syringe barrel upon release of compression; whereby the volume for anti-coagulant and thus the amount of anti-coagulant admixed with said blood sample is controlled; said minimum size of said chamber being such that the volume thereof together with the volume of said conduit means and said hypodermic needle will hold a sufficient amount of said anti-coagulant to prevent coagulation in said blood sample, but less than an amount of said anti-coagulant that would adversely affect the tests to be made on said blood sample; whereby, when air and excess anti-coagulant are expelled from said syringe assembly prior to drawing said blood sample, the correct controlled amount of anti-coagulant remaining in said syringe assembly and needle is insured; said inner wall asserting on said tip a frictional sealing force to permit the pressure of the patient's blood when said needle is inserted into a blood vessel of the patient to move said plunger axially in said barrel away from said floor to draw said sample into said barrel.

Claim 3

The syringe assembly of claim 1, wherein said preventing means comprises an annular ring, attached to said plunger adjacent said first end thereof.

Claim 4

The syringe assembly of claim 1, wherein said preventing means comprises at least one protrusion on said plunger adjacent said first end thereof.

Claim 5

The syringe assembly of claim 1, wherein said syringe barrel is substantially cylindrical and said preventing means comprises a cylindrical member hvaing a first part disposed within said syringe barrel and a second, shoulder part protruding from said open end of said syringe barrel.

Claim 6

The syringe assembly of claim 4, wherein said first part of said cylindrical member comprises means to limit the outward of said plunger at a position where the desired sample volume has been reached.

Claim 7

The syringe assembly of claim 1, wherein said preventing means limits the minimum size of said chamber from about 0.002 to 0.2 milliliter per milliliter of said blood sample.

Claim 8

The syringe assembly of claim 1, wherein said preventing means limits the minimum size of said chamber from about 0.005 to 0.1 milliliter per milliliter of said blood sample.

Claim 9

The syringe assembly of claim 1, wherein said compressible tip comprises a material which has a low coefficient of friction in contact with the material which makes up said barrel.

Claim 10

The syringe assembly of claim 6, wherein said compressible tip comprises a silicone rubber.

Claim 11

The syringe assembly of claim 1, wherein said syringe barrel comprises a material which is substantially impermeable to oxygen and carbon dioxide and inert to the sample to be analyzed.

Claim 12

The syringe assembly of claim 1, wherein said syringe barrel comprises polyethylene.

Claim 13

A syringe assembly for drawing a blood sample directly from a patient into said syringe assembly already containing a controlled amount of an anti-coagulant whereby said blood sample is admixed with said anti-coagulant, said syringe assembly comprising: a barrel having a central bore with an inner wall, an open end, a partially closed end forming a floor of said barrel with an opening therein, and a syringe tip, located at said partially closed end of said barrel, having a hypodermic needle detachably secured thereto and having conduit means therethrough for conveying said blood sample from said patient into said barrel; a plunger, slidably mounted within said barrel, having a first end protruding from said open end of said barrel and a second end disposed within said bore; a compressible, elastomeric plunger tip mounted on said second end of said plunger in frictional sealing compression with respect to said inner wall of said barrel to form a slideable seal with said inner wall; said plunger tip having an end face that with said floor and said inner wall of said barrel forms a chamber that varies in size with sliding movement of said plunger in said bore; means for preventing the movement of said plunger toward said floor of said barrel beyond a predetermined position to prevent compressive contact of said plunger tip with said floor of said barrel and to provide a minimum size for said chamber, thus controlling the amount of said anti-coagulant remaining in said barrel, thereby avoiding compression of said plunger tip against said floor by the inward movement of said plunger during expulsion of excess anti-coagulant and air prior to drawing said blood sample and thereby controlling the amount of said anti-coagulant admixed with said blood sample and avoiding air from being sucked into said barrel upon release of compression; said minimum size of said chamber being such that the volume thereof together with the volume of said conduit means and said hypodermic needle will hold a sufficient amount of said anti-coagulant to prevent coagulation in said blood sample, but less than an amount of said anti-coagulant that would adversely affect the tests to be made on said blood sample; whereby, when air and excess anti-coagulant are expelled from said syringe assembly prior to drawing said blood sample, the correct controlled amount of anti-coagulant remaining in said syringe assembly and needle is insured; said inner wall asserting on said tip a frictional sealing force to permit the pressure of the patient's blood when said needle is inserted into a blood vessel of the patient to move said plunger axially in said barrel away from said floor to draw said sample into said barrel; and means to limit the outward movement of said plunger at a position where a desired sample volume has been reached; whereby said means to limit outward movement cooperates with said means for preventing the movement of said plunger toward said floor to insure that the desired amounts of blood sample and anti-coagulant are admixed.

Claim 14

A syringe assembly for drawing a blood sample directly from a patient into said syringe assembly already containing a controlled amount of an anti-coagulant whereby said blood sample is admixed with said anti-coagulant, said syringe assembly comprising: a barrel having a central bore with an inner wall, an open end, a partially closed end forming a floor of said barrel with an opening therein, and a syringe tip, located at said partially closed end of said barrel, having a hypodermic needle detachably secured thereto and having conduit means therethrough for conveying said blood sample from said patient into said barrel; a plunger, slidably mounted within said barrel, having a first end protruding from said open end of said barrel and a second end disposed within said bore; a compressible, elastomeric plunger tip mounted on said second end of said plunger in frictional sealing compression with respect to said inner wall of said barrel to form a slideable seal with said inner wall; said plunger tip having an end face that with said floor and said inner wall of said barrel forms a chamber that varies in size with sliding movement of said plunger in said bore; means for preventing the movement of said plunger toward said floor of said barrel beyond a predetermined position to prevent compressive contact of said plunger tip with said floor of said barrel and to provide a minimum size for said chamber, thus controlling the amount of said anti-coagulant remaining in said barrel, thereby avoiding compression of said plunger tip against said floor by the inward movement of said plunger during expulsion of excess anti-coagulant and air prior to drawing said blood sample and thereby controlling the amount of said anti-coagulant admixed with said blood sample and avoiding air from being sucked into said barrel upon release of compression; said minimum size of said chamber being such that the volume thereof together with the volume of said conduit means and said hypodermic needle will hold a sufficient amount of said anti-coagulant to prevent coagulation in said blood sample, but less than an amount of said anti-coagulant that would adversely affect the tests to be made on said blood sample; whereby, when air and excess anti-coagulant are expelled from said syringe assembly prior to drawing said blood sample, the correct controlled amount of anti-coagulant remaining in said syringe assembly and needle is insured; said inner wall asserting on said tip a frictional sealing force to permit the pressure of the patient's blood when said needle is inserted into a blood vessel of the patient to move said plunger axially in said barrel away from said floor to draw said sample into said barrel; and means to limit the outward movement of said plunger at a position where a desired sample volume has been reached; whereby said means to limit outward movement cooperates with said means for preventing the movement of said plunger toward said floor to insure that the desired amounts of blood sample and anti-coagulant are admixed.

Claim 15

The syringe assembly of claim 1, wherein said syringe barrel comprises polypropylene.

Claim 16

The syringe assembly of claim 12, wherein said means for preventing the movement of said plunger toward the floor of said barrel comprises an annular ring on said plunger adjacent said first end thereof.

Claim 17

The syringe assembly of claim 12, wherein said means for preventing the movement of said plunger toward the floor of said barrel comprises at least one protrusion on said plunger adjacent said first end thereof.

Claim 18

The syringe assembly of claim 12, wherein said barrel is substantially cylindrical and said means for preventing the movement of said plunger toward said floor of said barrel comprises a cylindrical member having a first part disposed within said barrel and a second part protruding from said open end of said barrel.

Claim 19

The syringe assembly of claim 16, wherein said cylindrical member comprises means to limit the outward movement of said plunger at a position where a desired sample volume has been reached.

Claim 20

The syringe assembly of claim 12, wherein said minimum size of said chamber is such that the volume remaining in said syringe assembly and said hypodermic needle is from 0.002 to 0.2 milliliter per milliliter of said blood sample.

Claim 21

The syringe assembly of claim 18, wherein said minimum size of said chamber is such that the volume remaining in said syringe assembly and said hypodermic needle is from about 0.005 to 0.1 milliliter per milliliter of said blood sample.

Claim 22

A syringe assembly according to claim 12, said barrel having means to stop the outward movement of said plunger by said blood pressure of the patient at a position where the desired volume of blood is withdrawn.

Claim 23

A syringe assembly for obtaining a blood sample from a patient, said syringe assembly comprising: a syringe barrel having a central bore surrounded by an inner wall, an open end, a partially closed end forming a floor of said syringe barrel with an opening therein, and a syringe tip, located at said partially closed end of said syringe barrel, having a hypodermic needle detachably secured thereto and having conduit means therethrough for conveying said blood sample from said patient into said syringe barrel; a plunger, slidably mounted within said syringe barrel, having a first end protruding from said open end of said syringe barrel and a second end disposed within said bore; a compressible, elastomeric plunger tip mounted on said second end of said plunger in a frictional compression with respect to said inner wall of said syringe barrel to form a slidable seal with said inner wall; said plunger tip having an end face that with said floor and said inner wall of said syringe barrel forms a chamber that varies in size with sliding movement of said plunger in said bore; and means for preventing the inward movement of said plunger beyond a predetermined position to prevent contact of said plunger tip with said floor of said barrel and to provide a minimum size for said chamber, which is substantially smaller in volume than the blood sample to be drawn, thereby avoiding compression of said plunger tip against said floor by the inward movement of said plunger and thereby avoiding air from being sucked into said syringe barrel upon release of compression.

Claim 24

A syringe assembly for obtaining a blood sample from a patient, said syringe assembly comprising: a syringe barrel having a central bore surrounded by an inner wall, an open end, a partially closed end forming a floor of said syringe barrel with an opening therein, and a syringe tip, located at said partially closed end of said syringe barrel, having a hypodermic needle detachably secured thereto and having conduit means therethrough for conveying said blood sample from said patient into said syringe barrel; a plunger, slidably mounted within said syringe barrel, having a first end protruding from said open end of said syringe barrel and a second end disposed within said bore; a compressible, elastomeric plunger tip mounted on said second end of said plunger in a frictional compression with respect to said inner wall of said syringe barrel to form a slidable seal with said inner wall; said plunger tip having an end face that with said floor and said inner wall of said syringe barrel forms a chamber that varies in size with sliding movement of said plunger in said bore; and means for preventing the inward movement of said plunger beyond a predetermined position to prevent contact of said plunger tip with said floor of said barrel and to provide a minimum size for said chamber, which is substantially smaller in volume than the blood sample to be drawn, thereby avoiding compression of said plunger tip against said floor by the inward movement of said plunger and thereby avoiding air from being sucked into said syringe barrel upon release of compression.

Claim 25

A syringe assembly according to claim 21 for drawing a blood sample directly from a patient into said syringe assembly already containing a controlled amount of anticoagulant whereby said blood sample is admixed with said anticoagulant said minimum size of said chamber being such that the volume thereof together with the volume of said conduit means and said hypodermic needle will hold a sufficient amount of said anti-coagulant to prevent coagulation of said blood sample, but less than an amount of said anti-coagulant that would adversely affect the tests to be made on the blood sample.

Claim 26

A syringe, which comprises; a cylindrical barrel having a first open end for receiving a plunger and a second open end adapted to mount a needle on the opening thereof; and a plunger slidably mounted in said barrel, said plunger being withdrawable from said barrel through said first open end and said plunger comprising: a. means for receiving a force to move said plunger in or out of said barrel, b. an elastomeric plunger tip adapted to form a sliding seal with the inner walls of said barrel, c. a shank joining said means to said plunger tip, d. means for preventing the plunger tip from moving inwardly beyond a predetermined position to prevent the plunger tip from contacting said barrel second end, thereby avoiding compression of said plunger tip against said second open end by the inward movement of said plunger and thereby avoiding air from being sucked into said syringe barrel upon release of compression, and to provide a chamber defined by said second open end of said barrel and the lower end of said plunger tip when said plunger tip is in said predetermined position, e. an inert fluid disposed in said barrel between the second open end thereof and said plunger tip, in a volume in excess of that required to fill said chamber and the bore of said needle.

Claim 27

A syringe, which comprises; a cylindrical barrel having a first open end for receiving a plunger and a second open end adapted to mount a needle on the opening thereof; and a plunger slidably mounted in said barrel, said plunger being withdrawable from said barrel through said first open end and said plunger comprising: a. means for receiving a force to move said plunger in or out of said barrel, b. an elastomeric plunger tip adapted to form a sliding seal with the inner walls of said barrel, c. a shank joining said means to said plunger tip, d. means for preventing the plunger tip from moving inwardly beyond a predetermined position to prevent the plunger tip from contacting said barrel second end, thereby avoiding compression of said plunger tip against said second open end by the inward movement of said plunger and thereby avoiding air from being sucked into said syringe barrel upon release of compression, and to provide a chamber defined by said second open end of said barrel and the lower end of said plunger tip when said plunger tip is in said predetermined position, e. an inert fluid disposed in said barrel between the second open end thereof and said plunger tip, in a volume in excess of that required to fill said chamber and the bore of said needle.