GB1564957A - Coil dialyzer - Google Patents
Coil dialyzer Download PDFInfo
- Publication number
- GB1564957A GB1564957A GB41683/76A GB4168376A GB1564957A GB 1564957 A GB1564957 A GB 1564957A GB 41683/76 A GB41683/76 A GB 41683/76A GB 4168376 A GB4168376 A GB 4168376A GB 1564957 A GB1564957 A GB 1564957A
- Authority
- GB
- United Kingdom
- Prior art keywords
- outlet
- blood
- membrane
- core
- jack
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000012528 membrane Substances 0.000 claims description 110
- 239000008280 blood Substances 0.000 claims description 94
- 210000004369 blood Anatomy 0.000 claims description 94
- 239000000385 dialysis solution Substances 0.000 claims description 46
- 230000017531 blood circulation Effects 0.000 claims description 9
- 239000012530 fluid Substances 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 7
- 238000004804 winding Methods 0.000 claims description 4
- 238000004891 communication Methods 0.000 claims description 3
- 238000007789 sealing Methods 0.000 claims description 3
- 230000000712 assembly Effects 0.000 claims description 2
- 238000000429 assembly Methods 0.000 claims description 2
- 238000005452 bending Methods 0.000 claims description 2
- 230000008878 coupling Effects 0.000 claims 1
- 238000010168 coupling process Methods 0.000 claims 1
- 238000005859 coupling reaction Methods 0.000 claims 1
- 239000002699 waste material Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920000298 Cellophane Polymers 0.000 description 3
- DDRJAANPRJIHGJ-UHFFFAOYSA-N creatinine Chemical compound CN1CC(=O)NC1=N DDRJAANPRJIHGJ-UHFFFAOYSA-N 0.000 description 2
- 210000003734 kidney Anatomy 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000002093 peripheral effect Effects 0.000 description 2
- 206010020772 Hypertension Diseases 0.000 description 1
- 208000001953 Hypotension Diseases 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 230000036772 blood pressure Effects 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229940109239 creatinine Drugs 0.000 description 1
- 239000013536 elastomeric material Substances 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 208000012866 low blood pressure Diseases 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 239000002991 molded plastic Substances 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D63/00—Apparatus in general for separation processes using semi-permeable membranes
- B01D63/10—Spiral-wound membrane modules
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D61/00—Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
- B01D61/24—Dialysis ; Membrane extraction
- B01D61/28—Apparatus therefor
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2313/00—Details relating to membrane modules or apparatus
- B01D2313/02—Specific tightening or locking mechanisms
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Urology & Nephrology (AREA)
- Engineering & Computer Science (AREA)
- Water Supply & Treatment (AREA)
- External Artificial Organs (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
Description
(54) COIL DIALYZER
(71) We, BAXTER TRAVENOL LABORA
TORIES INC., a Corporation organised and existing under the laws of the State of
Delaware, United States of America, of One
Baxter Parkway, Deerfield, Illinois 60015,
United States of America, do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement: This invention relates to coil dialyzers of the type which include a semipermeable membrane; and more particularly, to dialyzers of the type used in artificial kidney systems.
Artificial kidney systems are used to treat a patient's blood so as to remove waste products therefrom. One type of dialyzer used in such systems is commonly referred to as a coil dialyzer. It includes a flattened, tubularly-shaped, semipermeable membrane of a material, such as Cellophane (Registered
Trade Mark) or polycarbonate, which along with an appropriate support member, is wound or coiled about a center core and enclosed in a cylindrical housing. Blood from a patient enters the dialyzer through an inlet in the core, flows through the dialyzer inside the membrane and exists the dialyzer through an outlet. Dialysis solution flows in a crosswise direction through the housing and between the wound support and membrane.
The dialysis solution contacts the membrane, and due to the difference in waste product concentration between the blood and the dialysis solution, the waste products, such as urea and creatinine, diffuse from the blood through the membrane and into the dialysis solution.
During treatment of blood in a dialyzer, water is removed from the blood by virtue of a process known as ultrafiltration. The amount of water which is removed is related to the difference in blood pressure and dialysis solution pressure on opposite sides of the membrane. Existing dialyzers operate at relatively high blood pressure levels which is related to the size and shape of the membrane and the membrane support. This high pressure may result in undesirably high and/or variable levels of water removal.
In existing dialyzers the conduits which carry blood to and from the dialyzer may become kinked where they enter and exit the dialyzer. Further, in existing constructions dialysis solution exits from the top of the dialyzer. This results in an aesthetically displeasing "sloshing" sound.
The Cellophane (R.T.M.) membrane is relatively fragile and may rupture or tear during assembly of the dialyzer when the membrane is sealed and is connected to the blood conduits.
Furthermore, existing dialyzers are relatively expensive to manufacture.
The dialyzer described hereafter avoids or reduces these problems.
The present invention provides a coil dialyzer comprising a hollow core, a blood inlet conduit, a flattened tubular semipermeable membrane coupled adjacent one end to said core for communication via a passageway in a wall of said core with said inlet conduit, a support member positioned to engage said membrane and wound about said core with said membrane, an outlet connector assembly coupled to the said membrane adjacent the other end thereof, a blood outlet conduit connected to said outlet connector assembly for receiving flow from said membrane, a housing having a body within which said core, said membrane and said support member are positioned, and said housing including a bottom portion having a dialysis solution outlet and a dialysis solution inlet, a first flow path being defined for dialysis solution between the membrane and the support member and means adjacent the upper end of the dialyzer connecting the first flow path with the hollow core such that dialysis solution entering the fluid inlet passes upwardly through said first flow path and then downwardly through said core to said dialysis solution outlet.
Reference is now made to the accompanying drawings, wherein: FIGURE 1 is a perspective view of a dialyzer made in accordance with the invention;
FIGURE 2 is a fragmentary longitudinal cross-sectional view taken substantially along line 2-2 of FIGURE 1;
FIGURE 3 is a transverse cross-sectional view taken substantially along line 3-3 of
FIGURE 1,
FIGURE 4 is an exploded perspective view of an inlet jack assembly for use in the dialvzer; FIGURE 5 is a top plan view of a blood button connector for use with the inlet jack assemblv:
FIGURE 6 is a lonvitudinal cross-sectional view taken substantially along line 6-6 of
FIGURE 5;
FIGURE 7 is an exploded, fragmentary sectional view showing the connection between the inlet jack assembly and semipermeable membrane:
FIGURE 8 is a fragmentary perspective view of a support member and a membrane for use in the dialyzer;
FIGURE 9 is a sectional view of the support member taken substantially along line 9-9 of FIGURE 8: FIGURE 10 is a sectional view similar to FIGURE 8 but showing an alternative supnort member configuration;
FIGURE 11 is a plan view of a support member of the type shown in FIGURES 9 and 10:
FIGURE 12 is a sectional view taken substantiallv along line 12-12 of FIGURE 8; FIGURE 13 is an exploded perspective view of an outlet jack assembly for use in the dialvzer showing the inner side of the outlet iack:
FIGURE 14 is a perspective view of the outer sirle of the outlet jack;
FIGURE 15 is a transverse cross-sectional view taken substantially along line 15-15 of FT < TIJRE 13:
FIGURE 16 is a perspective view of a top csn for use in the dialvzer;
FIGURE 17 is a frarnentarv and exploded perspective view showing a portion of the dialyzer housing and core assembly; and
FIGURE 18 is a perspective view of a bottom cap for use in the dialyzer.
DESCRIPTION OF THE PREFERRED
EMBODIMENT
General
Referring now to the drawings, and more particularly FIGURES 1-3, there is shown a dialyzer 10 having an outer casing which includes a hollow, elongated, pear-shaped, transparent, plastics housing 12, an upper or top end cap 14 and a lower or bottom end cap 16. The dialyzer also includes: a centrally-positioned, cylindrical, core as sembly 18; an elongated plastics support member 20 and an elongated membrane 22, which are wound about the core assembly; and an outlet jack assembly 24. An inner centrally-positioned, flexible, plastics blood inlet tube 26 extends through the upper cap 14 and cooperates in directing blood entering the dialyzer into the membrane 22. An outer blood outlet tube 28 extends through the upper cap and directs blood exiting the membrane to a point outside the dialyzer.
The lower end cap 16 also includes a dialysis solution inlet 30 and a dialysis solution outlet 32.
Generally speaking, blood from a patient who is being treated enters the dialyzer throuh the blood inlet tube 26, flows through the coiled tubular membrane 22, and exits the dialyzer through blood outlet tube 28. The dialysis solution enters the dialyzer through the inlet port 30, flows upwardly between the windings of the membrane and the membrane support, contacts the membrane so as to receive metabolic waste products and water from the blood, and exits the dialyzer through the outlet 32.
The Core Assembly
The inner core assembly 18 as shown in
FIGURES 2, 3 and 17, includes an elongated, C-shaped core 34, which is extruded from a plastics, such as polystyrene, and a separate inlet jack assembly 35. The core 34 is shaped to provide an offset somewhat
U-shaped membrane retaining slot 36 and a smaller offset support member retaining slot 38. Both of these slots extend inwardly toward the center of the core and open outwardly toward the outside of the core. The facing edges 40 and 42 of the core each includes a semicircular jack-receivinn slot 44 or 46 and define an elongated inlet-jackreceiving gap.
The inlet jack assembly 35, as shown in FIGURES 3. 4 and 7, includes the blood inlet tube 26, an inlet elbow 48, and an elongated molded inlet jack member 50. The jack member is constructed to fit within the gap defined by the core edges 40 and 42 and be bonded to the core 34. The lack member has a curved central body portion 52 and a pair of side flanges 54 and 56, which slidably and sealingly engage the jack receiving slots 44 and 46. The outer surface of the central body portion of the jack is curved in a manner complementary to the curvature of the core so as to form a generally cylindrical core assembly.
A short, integral, boss-like structure 58 is centrally positioned between the ends of the jack member on the back side thereof and extends toward the center of the core assembly. A tapered passageway 60 extends transversely through the body portion 56 and through the boss 58. An integrallymolded, countersunk, O-ring-receiving, recess 62 is formed in the body portion 56 and surrounds the outer terminal end of the passageway 60 and a plurality of molded blood distribution grooves, such as 63 and 64, extend radially from the O-ring recess.
A tapered internal, annular snap-lock shoulder 65 extends inwardly into the passageway adjacent the other end of the passageway.
The elbow 48 is bonded to outlet end of the blood inlet tube 26 and also telescopically engages and is bonded to the boss 58 so as to direct incoming blood flow from the tube 26 into the passageway 60.
The Membrane and The Support Member
Referring now to FIGURES 3, 8-12 and 17, the membrane 22 is an elongated, flattened tube of a semipermeable material, such as Cellophane (R.T.M.) or a cellulose derivative sold under the Registered Trade
Mark Cuprophan. The membrane is coiled or wound about the core assembly and serves as a conduit for the passage of blood through the dialyzer from the core assembly 18 to the outlet jack assembly 24. This membrane separates the blood and dialysis solution but permits blood waste products and water to pass from the blood into the dialysis solution contacting the membrane. It also permits preselected substance placed in the dialysis solution to pass through it and into the blood.
The support member is longer and wider than the membrane and may be of the conventional open mesh screen type as disclosed in U.S. Reissue Patent No. 27,510 or of an embossed type, such as is disclosed in U.S.
Patent No. 3,687,293. Such an embossed support includes an imperforate center web having equal-height, membrane-engaging ribs in each side of the web.
The member 20 shown in FIGURES 9 and 10 is embossed and is wound about the core along with the membrane 22 so as to space the convolutions or windings of the membrane from each other to assure that dialysis solution flows between the convolutions, and that the solution contacts the membrane walls or surfaces. The support member 20 as shown herein is a fluid impermeable sheet of an appropriate material which has been embossed, on both sides, with an appropriate pattern of supporting and channel forming ribs. The support member 20 includes a central web 66 having, on each side, a plurality of elongated ribs, such as 68, 70, 72, 74, 76 and 78, that extend angularly across the web from one longitudinal edge to the other.
The ribs on each side form an acute angle of about 60 degrees to the longitudinal edge of the web. However, the ribs on opposite sides extend in opposite directions. This causes the ribs to overlap in a diamond-like pattern, where the obtuse or included angle formed is preferably about 120 degrees.
However, that angle may be between about 60 degrees and 140 degrees. The rib patterns on each side of the member are identical, except for direction, and repeat in a pattern of one large rib and four smaller roundedtip ribs.
The preferred support member 20, as shown in FIGURE 8, is fabricated of a soft, low-modulus-of-elasticy material, such as medium density polyethylene. In the preferred rib pattern, the larger or high ribs 68 and 78 are flat-topped, have a trapezoidal cross-section, are spaced about 0.323 inches apart and are about .021 inches tall. The smaller or low ribs 70, 72, 74 and 76 are triangularly-shaped, have rounded membrane-engaging tips, are each about .012 inches tall, and are substantially equally spaced between the high ribs. The total thickness of the support member is about .047 inches. The rib height and spacing have been selected to form an appropriate blood path in the membrane which assures a low blood pressure and substantially equal dialysis solution flow rates in the channels defined by the ribs and membrane.
Referring now to FIGURE 10, there is shown an alternative support member 80, which has a different rib pattern or configuration. In this support member all of the ribs 82, 84, 86, 88, 90 and 92 are triangularly shaped and have slightly rounded membraneengaging tips. The two large or high ribs 82 and 92 are each about .023 inches tall and are spaced apart, on centers, about .323 inches. The ribs 84 and 90 which are adjacent the high ribs are each about .016 inches high and the innermost ribs 86 and 88 are about .012 inches tall. The lower ribs are substantially equally spaced between the high ribs 82 and 92. The total thickness of the member 80 is about .050 inches.
This particular member is fabricated from a stiffer, higher modulus material, such as high density polyethylene.
As can be seen, the rib configuration can be varied so as to provide multi-rib levels which permit a wide range of control over blood path geometry.
From FIGURE 12 it will be seen that when wound, the support member engages the membrane on opposite sides and due to the angular attitude of the supporting ribs, the large ribs, such as 68 and 78, overlap so as to form substantially a plurality of point contacts which grasp and hold the membrane therebetween. Since the ribs are angularly disposed, the overlapping ribs cannot interfit between one another (otherwise known as interdigitation) which could prevent or inhibit flow of blood and/or dialysis solution.
The angle ribs in either of the support members provide a clear flow channel for the dialysis solution to flow angularly from one longitudinal edge of the support member to the other. The shorter supporting ribs engage the membrane in a manner so as to define substantially equal flow channels and to prevent the membrane from contacting the web.
The inner end of the support member 20 is secured to the core assembly by fitting its inner transverse edge into the support member receiving slot 38.
Membrane End Seal
The membrane 22 is a flattened tubular member which must be sealed at each end in order to provide a leak-free conduit between the blood inlet tube 26 and blood outlet tube 28. Referring to FIGURES 3, 8 and 17, a particularly effective end seal is achieved by forming end flaps, such as 22a, and folding the flaps against the body of the membrane. Such a fold forms a transverse fold line 22b which extends from one lonai- tudinal edge of the membrane to the other longitudinal edge thereof. Preferably the fold line is substantially perpendicular to the longitudinal edges of the membrane.
At the core assembly end, the membrane 22 is folded so as to form the flap 22a which is folded outwardly onto the membrane body so as to form the inner fold line 22b. The fold is then positioned in the wedge-receiving groove 36 for maintaining the fold line.
An elongated wedge 94 is pressed into the groove 36 so as to securely retain the fold and to secure the membrane end in position on the core as it is wound. The wedge 94 matingly fits within the groove and includes a shaped outer surface 94a, which conforms to the outer configuration of the core.
Blood Button Connector
A molded plastics inlet blood button connector 100 (as shown in FIGURES 4-7), connects the inlet jack passageway 60 with the membrane interior for directing blood entering the dialyzer into the membrane.
The inlet blood button connector 100 is a hollow, rivet-shaped member having a convex crown or cap portion 102 and a tapered body or barrel portion 104 having a bore or passage 105 which extends through the barrel and cap. The barrel includes a reduced diameter section or recess 106 and a tapered retaining lip 108 adjacent the end of the barrel opposite the cap. The lip and reduced diameter section define a snap-lock groove which cooperates with the inlet jack aperture shoulder 65 for snappingly engaging and securing the blood button connector to the inlet jack.
Six radial blood distributing grooves, such as 110 and 112, are provided in the cap for cooperation with the membrane in distributing blood radially outwardly from the passageway 105.
An O-ring seal 114 is seated in the recess or groove 62 surrounding the passageway 60. The O-ring 114 is an elastomeric sealing member which cooperates in providing a leak-free connection between the passageway and membrane and which is compressed when assembled so as to resiliently engage: the membrane adjacent the underside of the blood button cap 102 and hold it against the cap; the jack; and the blood button barrel 104. The O-ring 114 is of a non-aging, resilient, creep-resistant, elastomeric material, such as silicone, which minimizes seal leakage.
In order to install the inlet blood button connector 100, a small, round aperture 116, is cut into a side wall of the membrane 22 adjacent the inner end thereof and approximately centered between the membrane edges.
The blood button is then slipped into the membrane from an open end, before the end is sealed, and the barrel 104 is inserted through the aperture 116 so that the cap 102 is positioned against the inside wall of the membrane 22 and the barrel extends outwardly therefrom. The blood button is then urged inwardly and snap-locks with the shoulder 65 in the jack bore. The blood button cap firmly holds the portion of the membrane contacting the underside of the cap against the inlet jack and against the O-ring so as to minimize seal leakage.
With the end seal secured by the inlet jack wedge 94, a substantially leak-free seal and conduit system is provided for blood flowing through the inlet tube 26, the inlet elbow 48, the inlet jack passageway 60 and the blood button connector 100.
An advantage to the connector 100 is that the membrane 22 is held against the core assembly 18 and any force applied to the inlet tube is transmitted to the core assembly 18 rather than directly to the membrane 22.
With the membrane end sealed, the blood button 100 secured to the inlet jack 50, and the support member 20 positioned in the support member recess 38, the member 20 and membrane 22 are wound together about the core until the predetermined length of the support member and membrane are exhausted. Normally, the support member 20 is both longer and wider than membrane 22. The support member 20 and membrane 22 are then secured to the outlet jack assembly 24. Furthermore with both the membrane and support secured to the core assembly, relative movement between the membrane and member is reduced which further minimizes possible damage to the membrane.
Outlet Jack Assembly
The outlet jack assembly 24, as shown in
FIGURES 2 and 3, includes an elongated molded outlet jack member 120, as shown in FIGURES 13-15. The jack has a concave inner face 122, which is constructed to fit against the outermost winding of the membrane 22. The inner face includes several longitudinally extending sections for cooperation with the membrane which it contacts.
The first section 124 is a blood inlet path defining section which includes a plurality of spaced parallel ribs, such as 126 and 128, which extend inwardly from the leading edge of the jack. These ribs 126 and 128 serve to direct blood flow in the membrane further along the inner face of the outlet jack.
A recessed blood flow collection path or channel 130 is positioned adjacent the blood path section 124 and extends for the full length of the jack. A blood button receiving bore and blood flow passageway 132 is centrally positioned in the blood flow channel.
A countersunk O-ring receiving recess 136 surrounds the bore and faces toward the inside of the dialyzer. The bore 132 extends through an outwardly extending boss 134 on the back side of the outlet jack. An elbow 138, which is bonded to the inlet end of the outlet tube 28, telescopically engages and is bonded to the boss 134, and directs blood flowing from the passageway 132 to the blood outlet tube 28.
An inwardly facing fold-retaining and wedge-receiving groove 140 is positioned on the side of the blood flow channel 130 opposite the blood directing ribs 126 and 128.
The bottom end of the jack is defined by a bottom fin or plate 142, which extends rearwardly or outwardly from the inner face 122. A top plate or fin 144 extends across the top of the jack, but it will be noted that the top plate is recessed at a position above the boss 134 for cooperation in positioning the blood outlet tube 28. A pair of elongated rigidifying ribs 146 and 148 on the outer side of the jack connect the top and bottom fins. Top and bottom locating pins 150 and 152 project from the fins 144 and 142, respectively.
The membrane 22 is connected to the outlet jack 24 with an outlet blood button connector 154, which is substantially identical with the previously described inner blood button connector 100.
An O-ring 156, similar to the O-ring used with the inlet jack assembly, is positioned in the O-ring groove 136 and the outlet blood button connector is snap-locked to the outlet jack to hold the membrane to the outlet jack in the same manner as the inlet jack.
The membrane is end-sealed by a fold seal of the type described in connection with the inlet jack with the main difference being that the outer flap is positioned on the inner side of the membrane. The outlet jack wedge
157 retains and holds the end seal in position. In the assembly, the outer end of the support member thereof is positioned back behind the inner face of the outlet jack.
Housing and Assembly
As seen in FIGURES 2-3 and 16--18, once the core assembly 18, support member 20 and membrane 22 and outlet jack 24 are assembled, the housing 12 is slipped over the assembly so as to retain it in position with the outlet jack positioned within the protruding portion 12a which extends along the side of the housing 12. The top and bottom caps 14 and 16 are mounted to and sealingly engage the ends of the housing.
The top cap 14 is molded so as to provide a centrally positioned blood inlet tube aperture 170 and an offset blood outlet aperture
172. The blood inlet tube 26 extends through and sealingly engages the inlet aperture 170, and the blood outlet tube 28 passes through and sealingly engaging the outlet aperture 172. The cap 14 also includes the spaced parallel outer and inner walls 174 and 176, which define a groove 178 therebetween for sealingly engaging the top edge of the housing 12.
Three cap ribs 180, 182 and 184 extend inwardly from the cylindrical portion of inner wall 176 toward the blood inlet tube aperture 170. Each of the ribs includes a tapered and notched inner edge or shoulder 186, which is adapted to engage the top edge of the core assembly for centrally positioning the core assembly in the housing.
The lower surface, such as 181, of each rib engages the top edge of the wound membrane and support so as to prevent telescoping or upward movement of the membrane and support.
A small curved, outlet-jack engaging wall 188 is molded across the protruding portion of the cap for general alignment with the inner face 122 of the outlet jack. A pinreceiving socket 190 is also molded adjacent the wall and is for receiving the top pin 150 on the top end of the outlet iack.
The bottom cap 16 includes parallel outer and inner peripheral walls 192 and 194, which together define a peripheral groove 196 for cooperative sealing engagement with the bottom edge of the housing 12. A small, curved outlet jack engaging wall 198 is molded across the protruding portion of the cap and is generally shaped to conform to the inner face of the outlet jack. An outlet jack pin-receiving socket 200 is molded along the wall for receiving the outlet jack bottom pin 152.
A tubular inlet 202 is molded to the outer and underside of the bottom cap and includes a bore 204 which communicates with the inlet 30. The outlet 32 is formed by a large aperture in the cap. The aperture is surrounded by a core assembly locating and receiving shoulder 206 and collar 208. It should be noted that the inlet bore 204 is positioned between the collar 208 and wall 198.
With the housing 12 in place, the inlet tube 26 and outlet tube 28 are then passed through the upper cap and the upper cap is fitted downwardly against the top edge of the housing, the top of the core assembly and the top of the outlet jack. In a similar manner, the bottom cap is fitted against the bottom edge of the housing and against the core assembly and the outlet jack. It will be noted that with such an assembly both the blood inlet tube 26 and blood outlet tube 28 extend in a generally parallel and axial arrangement whereby kinking and bending of the tubes are minimized.
Once the core assembly 18 and outlet jack assembly 24 are fixed in position in the housing by the top cap 14 and bottom cap 16, any forces applied to the tubes 26 or 28 are transmitted through the core or jack assemblies to the caps and housing. Thus, those forces are not applied directly to the membrane and membrane rupture is reduced.
Operation
As seen in FIGURE 2, incoming dialysis solution flows, as indicated by arrow 210, upwardly through the inlet 30. The dialysis solution then flows around the core assembly locating collar and upwardly through the wound membrane and support member into the center of the core assembly 18 as indicated by arrows 216 and 218. From there the dialysis solution flows downwardly and exits the dialyzer through the outlet 32. Thus the dialysis solution flow path forms a generally inverted U-shape.
Blood entering the dialyzer through the tube 26 flows downwardly through tube 26, as indicated by arrow 220, through the elbow into the inlet jack and through the blood button bore into the membrane 22. Blood then flows inside the membrane in a spiral path around the core until it reaches the outlet jack assembly 24. At the outlet jack assembly. the blood is directed by the blood directing ribs, such as 126 and 128, into the blood flow channel 130 and hence to the blood button connector 154. Blood entering the blood button connector 154 flows through the outlet jack passageway 132 into the outlet elbow 138 and from there through the tube 28.
The blood is prevented from flowing out of the end seals by virtue of the folded-andlocked end seal arrangements, both at the inlet jack and outlet jack. The possibilities of blood leak have been minimized by the selection of the support materials and rib structure. Dialysis solution flow into the outlet jack area is minimized by the engagement of the arcuate walls 188 and 198 with the outlet jack. However, some dialysis solution flow into the outlet jack area can be tolerated.
Performance of the invention described above involves use of the invention as described and claimed in patent specifications
Nos. 7,902,413 (Serial No. 1,564,958); 7,902414 (Serial No. 1,564,959) and 7,902,415 (Serial No. 1,564,960).
WHAT WE CLAIM IS:- 1. A coil dialyzer comprising a hollow core, a blood inlet conduit, a flattened tubular semipermeable membrane coupled adjacent one end to said core for communication via a passageway in a wall of said core with said inlet conduit, a support member positioned to engage said membrane and wound about said core with said membrane, an outlet connector assembly coupled to the said membrane adjacent the other end thereof, a blood outlet conduit connected to said outlet connector assembly for receiving flow from said membrane, a housing having a body within which said core, said membrane and said support member are positioned, and said housing including a bottom portion having a dialysis solution outlet and a dialysis solution inlet, a first flow path being defined for dialysis solution between the membrane and the support member and means adjacent the upper end of the dialyzer connecting the first flow path with the hollow core such that dialysis solution entering the fluid inlet passes upwardly through said first flow path and then downwardly through said core to said dialysis solution outlet.
2. A dialyzer as in Claim 1, wherein the dialysis solution outlet is aligned
Claims (13)
- **WARNING** start of CLMS field may overlap end of DESC **.196 for cooperative sealing engagement with the bottom edge of the housing 12. A small, curved outlet jack engaging wall 198 is molded across the protruding portion of the cap and is generally shaped to conform to the inner face of the outlet jack. An outlet jack pin-receiving socket 200 is molded along the wall for receiving the outlet jack bottom pin 152.A tubular inlet 202 is molded to the outer and underside of the bottom cap and includes a bore 204 which communicates with the inlet 30. The outlet 32 is formed by a large aperture in the cap. The aperture is surrounded by a core assembly locating and receiving shoulder 206 and collar 208. It should be noted that the inlet bore 204 is positioned between the collar 208 and wall 198.With the housing 12 in place, the inlet tube 26 and outlet tube 28 are then passed through the upper cap and the upper cap is fitted downwardly against the top edge of the housing, the top of the core assembly and the top of the outlet jack. In a similar manner, the bottom cap is fitted against the bottom edge of the housing and against the core assembly and the outlet jack. It will be noted that with such an assembly both the blood inlet tube 26 and blood outlet tube 28 extend in a generally parallel and axial arrangement whereby kinking and bending of the tubes are minimized.Once the core assembly 18 and outlet jack assembly 24 are fixed in position in the housing by the top cap 14 and bottom cap 16, any forces applied to the tubes 26 or 28 are transmitted through the core or jack assemblies to the caps and housing. Thus, those forces are not applied directly to the membrane and membrane rupture is reduced.Operation As seen in FIGURE 2, incoming dialysis solution flows, as indicated by arrow 210, upwardly through the inlet 30. The dialysis solution then flows around the core assembly locating collar and upwardly through the wound membrane and support member into the center of the core assembly 18 as indicated by arrows 216 and 218. From there the dialysis solution flows downwardly and exits the dialyzer through the outlet 32. Thus the dialysis solution flow path forms a generally inverted U-shape.Blood entering the dialyzer through the tube 26 flows downwardly through tube 26, as indicated by arrow 220, through the elbow into the inlet jack and through the blood button bore into the membrane 22. Blood then flows inside the membrane in a spiral path around the core until it reaches the outlet jack assembly 24. At the outlet jack assembly. the blood is directed by the blood directing ribs, such as 126 and 128, into the blood flow channel 130 and hence to the blood button connector 154. Blood entering the blood button connector 154 flows through the outlet jack passageway 132 into the outlet elbow 138 and from there through the tube 28.The blood is prevented from flowing out of the end seals by virtue of the folded-andlocked end seal arrangements, both at the inlet jack and outlet jack. The possibilities of blood leak have been minimized by the selection of the support materials and rib structure. Dialysis solution flow into the outlet jack area is minimized by the engagement of the arcuate walls 188 and 198 with the outlet jack. However, some dialysis solution flow into the outlet jack area can be tolerated.Performance of the invention described above involves use of the invention as described and claimed in patent specifications Nos. 7,902,413 (Serial No. 1,564,958); 7,902414 (Serial No. 1,564,959) and 7,902,415 (Serial No. 1,564,960).WHAT WE CLAIM IS:- 1. A coil dialyzer comprising a hollow core, a blood inlet conduit, a flattened tubular semipermeable membrane coupled adjacent one end to said core for communication via a passageway in a wall of said core with said inlet conduit, a support member positioned to engage said membrane and wound about said core with said membrane, an outlet connector assembly coupled to the said membrane adjacent the other end thereof, a blood outlet conduit connected to said outlet connector assembly for receiving flow from said membrane, a housing having a body within which said core, said membrane and said support member are positioned, and said housing including a bottom portion having a dialysis solution outlet and a dialysis solution inlet, a first flow path being defined for dialysis solution between the membrane and the support member and means adjacent the upper end of the dialyzer connecting the first flow path with the hollow core such that dialysis solution entering the fluid inlet passes upwardly through said first flow path and then downwardly through said core to said dialysis solution outlet.
- 2. A dialyzer as in Claim 1, wherein the dialysis solution outlet is aligned with the hollow core, which is centrally positioned in the housing, and the dialysis solution inlet is offset with respect to the outlet and aligned with the wound membrane and support member.
- 3. A dialyzer as in Claim 2, wherein said housing further includes: a top cap having an inlet-conduit-receiving-aperture aligned with said core, through which said inlet conduit extends and with which a fluidtight seal is formed; and an outlet-conduitreceiving-aperture offset from said inlet conduit aperture through which said outlet extends and with which a fluid-tight seal is formed.
- 4. A dialyzer according to Claim 1 or 2 further comprising means for maintaining said blood inlet conduit and blood outlet conduit in a substantially kink-free disposition.
- 5. A dialyzer according to Claim 3 including conduit connecting means comprising rigid elbows each having one end connected to the core and outlet connector assembly respectively and the other end connected to said conduits, and being generally aligned with the inlet and outlet apertures in said top cap.
- 6. A dialyzer according to any preceding Claim including an inlet connector assembly connecting the blood inlet conduit to the core, wherein said housing includes a substantially smooth exterior surface encasing said inlet connector assembly and said outlet connector assembly.
- 7. A dialyzer as in any preceding Claim, wherein said housing further includes means for positioning said core and outlet connector assembly in generally axial alignment with said housing.
- 8. A dialyzer as in any preceding Claim, wherein said core includes an elongate inlet jack, said jack having a fluid passageway extending transversely through said jack and means defining a plurality of fluid distribution grooves extending from said passageway.
- 9. A dialyzer as in any preceding Claim, wherein said outlet connector assembly is a jack assembly including a concave inner face for engaging the outermost winding of said wound membrane, and said face includes a recessed blood flow channel having a fluid passageway extending transversely through said assembly for providing fluid coupling between said membrane and said passageway.
- 10. A dialyzer as in Claim 9, wherein said passageway is centrally positioned in said channel.
- 11. A dialyzer as in Claim 9 or 10, wherein said outlet jack assembly includes a first longitudinal section having a plurality of flow directing ribs along one edge of said face for engaging said membrane and for directing flow within said membrane inwardly from said edge.
- 12. A dialyzer as in any preceding Claim, wherein said oulet connector assembly and said core are secured to said housing for preventing movement of the connector assembly and core relative to said housing.
- 13. A dialyzer as in Claim 3 or any one of Claims 7 to 12 as appendant to Claim 3, wherein said top cap includes a plurality of inwardly extending ribs, each having shoulder defining means at the inner edge thereof, said ribs adapted to prevent upward movement of the top edge of said support member and said shoulder means adapted to engage and cooperate in positioning said core.
Applications Claiming Priority (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US62054375A | 1975-10-08 | 1975-10-08 | |
US62061775A | 1975-10-08 | 1975-10-08 | |
US62061675A | 1975-10-08 | 1975-10-08 | |
US62061375A | 1975-10-08 | 1975-10-08 | |
US05/620,541 US4009107A (en) | 1975-10-08 | 1975-10-08 | Multi-level support member for use with semipermeable membrane |
US05/620,619 US4028253A (en) | 1975-10-08 | 1975-10-08 | Dialyzer connector system |
US05/620,542 US4035305A (en) | 1975-10-08 | 1975-10-08 | Support member construction for semipermeable membrane |
US05/620,546 US4008157A (en) | 1975-10-08 | 1975-10-08 | End seal construction for semipermeable membrane |
US05/620,618 US4006088A (en) | 1975-10-08 | 1975-10-08 | Snap-lock button-type fluid connector with recess |
US05/620,614 US4009108A (en) | 1975-10-08 | 1975-10-08 | Dialyzer construction |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1564957A true GB1564957A (en) | 1980-04-16 |
Family
ID=27581298
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2413/79A Expired GB1564958A (en) | 1975-10-08 | 1976-10-07 | Coil dialyzer |
GB2414/79A Expired GB1564959A (en) | 1975-10-08 | 1976-10-07 | Connector for coil dialyzer |
GB41683/76A Expired GB1564957A (en) | 1975-10-08 | 1976-10-07 | Coil dialyzer |
GB2415/79A Expired GB1564960A (en) | 1975-10-08 | 1976-10-07 | Coil dialyzer |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2413/79A Expired GB1564958A (en) | 1975-10-08 | 1976-10-07 | Coil dialyzer |
GB2414/79A Expired GB1564959A (en) | 1975-10-08 | 1976-10-07 | Connector for coil dialyzer |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2415/79A Expired GB1564960A (en) | 1975-10-08 | 1976-10-07 | Coil dialyzer |
Country Status (8)
Country | Link |
---|---|
JP (1) | JPS5279597A (en) |
AU (1) | AU506263B2 (en) |
CH (1) | CH617855A5 (en) |
DE (1) | DE2645516A1 (en) |
FR (5) | FR2345188A1 (en) |
GB (4) | GB1564958A (en) |
IL (1) | IL50623A (en) |
IT (1) | IT1077060B (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2532736C2 (en) * | 1975-07-22 | 1991-05-08 | Etablissements François Salomon et Fils, 74011 Annecy, Haute-Savoie | Ski brake attached to a sole retainer for releasing ski bindings |
JPS5621397Y2 (en) * | 1976-10-20 | 1981-05-20 | ||
SE405550B (en) * | 1977-05-13 | 1978-12-18 | Gambro Ab | DIFFUSION DEVICE PREFERREDLY INTENDED FOR DIALYSIS |
SE408998B (en) * | 1977-11-18 | 1979-07-23 | Gambro Ab | DEVICE FOR CONNECTING THE END OF A PLANT COMPRESSED HOSE OF A THIN MEMBRANE MATERIAL |
SE408999B (en) * | 1977-11-18 | 1979-07-23 | Gambro Ab | SEALING DEVICE |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE558724A (en) * | 1956-07-25 | |||
US2969150A (en) * | 1957-01-25 | 1961-01-24 | Baxter Laboratories Inc | Artificial kidney system |
US3077268A (en) * | 1959-05-06 | 1963-02-12 | Univ Pennsylvania | Dialyzer |
US3417870A (en) * | 1965-03-22 | 1968-12-24 | Gulf General Atomic Inc | Reverse osmosis purification apparatus |
GB1203582A (en) * | 1966-10-10 | 1970-08-26 | Nat Res Dev | Improvements in or relating to dialysers |
BE514578A (en) * | 1967-05-22 | |||
DE1792305A1 (en) * | 1968-08-16 | 1971-07-08 | Siegfried Klusch | Dialyzer use preferably for hemodialysis |
US3508662A (en) * | 1969-01-21 | 1970-04-28 | Extracorporeal Med Spec | Disposable,low-prime,spirally wound,artificial kidney |
BE758435A (en) * | 1969-11-05 | 1971-04-16 | Avon Rubber Co Ltd | IMPROVEMENTS TO HEMODIALYSIS EQUIPMENT |
US3668837A (en) * | 1970-02-13 | 1972-06-13 | Pall Corp | Separator of the semipermeable membrane type |
US3650404A (en) * | 1970-02-27 | 1972-03-21 | Antonio A Versaci | Disposable dialysis apparatus |
US3712474A (en) * | 1970-04-08 | 1973-01-23 | Baxter Laboratories Inc | Artifical kidney apparatus |
US3712475A (en) * | 1970-08-31 | 1973-01-23 | Baxter Laboratories Inc | Positive pressure lid for dialyzer apparatus |
US3741395A (en) * | 1971-03-11 | 1973-06-26 | Vernitron Medical Prod Inc | Disposable human blood dialysis device |
US3738495A (en) * | 1971-04-13 | 1973-06-12 | W Esmond | Exchange device |
IT955923B (en) * | 1972-05-26 | 1973-09-29 | Bellco Spa | ROLL DIALUZZATRICE CARTRIDGE PARTICULARLY FOR EXTRA BODY ARTIFICIAL KIDNEYS |
IT956374B (en) * | 1972-06-08 | 1973-10-10 | Dasco Spa | DEVICE FOR CONNECTING MEMBRANE FLEXIBLE HOSES WITH INLET OR OUTLET DUCTS IN ROLL DIALYZERS |
US3853769A (en) * | 1973-04-05 | 1974-12-10 | Extracorporeal Med Spec | Rigid casing for dialyzer coil |
FR2287256A1 (en) * | 1974-10-09 | 1976-05-07 | Rhone Poulenc Ind | Support elements in exchangers with semi-permeable membranes - has spaced (non) continuous projections as point supports for membrane |
-
1976
- 1976-10-06 IL IL50623A patent/IL50623A/en unknown
- 1976-10-07 GB GB2413/79A patent/GB1564958A/en not_active Expired
- 1976-10-07 GB GB2414/79A patent/GB1564959A/en not_active Expired
- 1976-10-07 AU AU18460/76A patent/AU506263B2/en not_active Ceased
- 1976-10-07 IT IT28110/76A patent/IT1077060B/en active
- 1976-10-07 GB GB41683/76A patent/GB1564957A/en not_active Expired
- 1976-10-07 GB GB2415/79A patent/GB1564960A/en not_active Expired
- 1976-10-08 FR FR7630294A patent/FR2345188A1/en not_active Withdrawn
- 1976-10-08 JP JP51121764A patent/JPS5279597A/en active Pending
- 1976-10-08 DE DE19762645516 patent/DE2645516A1/en not_active Withdrawn
- 1976-10-08 CH CH1275576A patent/CH617855A5/en not_active IP Right Cessation
-
1977
- 1977-06-28 FR FR7719759A patent/FR2345191A1/en not_active Withdrawn
- 1977-06-28 FR FR7719758A patent/FR2345190A1/en not_active Withdrawn
- 1977-06-28 FR FR7719760A patent/FR2345192A1/en not_active Withdrawn
- 1977-06-28 FR FR7719757A patent/FR2345189A1/en not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
JPS5279597A (en) | 1977-07-04 |
FR2345191A1 (en) | 1977-10-21 |
IL50623A (en) | 1981-07-31 |
FR2345190A1 (en) | 1977-10-21 |
FR2345192A1 (en) | 1977-10-21 |
FR2345189A1 (en) | 1977-10-21 |
GB1564960A (en) | 1980-04-16 |
GB1564958A (en) | 1980-04-16 |
GB1564959A (en) | 1980-04-16 |
FR2345188A1 (en) | 1977-10-21 |
DE2645516A1 (en) | 1977-04-21 |
CH617855A5 (en) | 1980-06-30 |
AU506263B2 (en) | 1979-12-20 |
IT1077060B (en) | 1985-04-27 |
AU1846076A (en) | 1978-04-13 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed [section 19, patents act 1949] | ||
PCNP | Patent ceased through non-payment of renewal fee |