|Publication number||USRE40570 E1|
|Application number||US 10/406,354|
|Publication date||Nov 11, 2008|
|Filing date||Apr 3, 2003|
|Priority date||Jul 29, 1994|
|Publication number||10406354, 406354, US RE40570 E1, US RE40570E1, US-E1-RE40570, USRE40570 E1, USRE40570E1|
|Inventors||Sophie Carpentier, Alain F. Carpentier, Lillian J. Quintero, Victor S. Packham, Jong H. Wang, Stefan G. Schreck|
|Original Assignee||Edwards Lifesciences Corporation|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (38), Non-Patent Citations (2), Referenced by (14), Classifications (21), Legal Events (2)|
|External Links: USPTO, USPTO Assignment, Espacenet|
The present application is a divisional of U.S. application Ser. No. 08/874,180, filed Jun. 13, 1997, now U.S. Pat. No. 5,931,969, entitled “Methods and Apparatuses for Treating Biological Tissue to Mitigate Calcification,” which is a continuation-in-part of U.S. application Ser. No. 08/812,506, filed Mar. 7, 1997, now abandoned, which is a continuation of U.S. application Ser. No. 08/282,358, filed Jul. 29, 1994, now abandoned.
Notice: More than one reissue application has been filed for the reissue of U.S. Pat. No. 6,210,957. The reissue applications are application Ser. Nos. 10/406,354 (the present application), and 10/834,399, all of which are divisional reissues of U.S. Pat. No. 6,210,957.
The present invention pertains generally to apparatuses for preparing biomedical materials, and more particularly to an apparatus for preparing preserved biological tissue, such as bovine pericardium, for implantation in a mammalian body that induces relative treatment fluid/tissue motion.
The prior art has included numerous methods for preserving or fixing biological tissues, to enable such tissues to be subsequently implanted into mammalian bodies. Examples of the types of biological tissues that have heretofore been utilized for surgical implantation include cardiac valves, vascular tissue, skin, dura mater, pericardium, ligaments and tendons.
The term “grafting” as used herein is defined as the implanting or transplanting of any living tissue or organ (See Dorlands Illustrated Medical Dictionary, 27th Edition, W.B. Saunders Co. 1988). Biological tissues which are grafted into the body of a mammal may be xenogeneic (i.e., a xenograft) or allogeneic (i.e., an allograft). The term “bioprosthesis” defines many types of biological tissues chemically pretreated before implantation (Carpentier—See Ionescu (editor), Biological Tissue in Heart Valve Replacement, Butterworths, 1972). As opposed to a graft, the face of a bioprosthesis is based upon the stability of the chemically treated biological material and not upon cell viability or host cell ingrowth. Chemical pretreatment includes the “fixing” or tamning of the biological tissue. Such fixing or tanning of the tissue is accomplished by exposing the tissue to one or more chemical compounds capable of cross-linking collagen molecules within the tissue.
Various chemical compounds have been utilized to fix or cross-link biological tissues including formaldehyde, glutaraldehyde, dialdehyde starch, hexamethylene diisocyanate and certain polyepoxy compounds.
In particular, glutaraldehyde has proven to be relatively physiologically inert and suitable for fixing various biological tissues for subsequent surgical implantation (Carpentier, A., J. Thorac. Cardiovasc. Surg. 58:467-68 (1969)). In particular, examples of the types of biological tissues which have heretofore been subjected to glutaraldehyde fixation include porcine bioprosthetic heart valves and bovine pericardial tissues.
Clinical experience has revealed that glutaraldehyde-fixed bioprosthetic tissues may tend to become calcified. Such calcification of glutaraldehyde-fixed bioprosthetic tissues has been reported to occur most predominantly in pediatric patients see, Carpentier et al. and “Continuing Improvements in Valvular Bioprostheses, J. Thorac Cardiovasc. Surg. 83:27-42, 1982. Such calcification is undesirable in that it may result in deterioration of the mechanical properties of the tissue and/or tissue failure. In view of this, surgeons have opted to implant mechanical cardiovascular valves into pediatric patients, rather than to utilize glutaraldehyde-preserved porcine valves. However, pediatric patients who receive mechanical valve implants require long term treatment with anticoagulant medications and such anticoagulation is associated with increased risk of hemorrhage.
The mechanism by which calcification occurs in glutaraldehyde-fixed bioprosthetic tissue has not been fully elucidated. However, factors which have been thought to influence the rate of calcification include:
Methods for treating fixed biological tissue so as to inhibit calcification thereof following implantation in a mammalian body tend to substantially increase the usable life of such tissue subsequent to implantation in a mammalian body, thereby mitigating the requirements for subsequent tissue replacement. As those skilled in the art will appreciate, such tissue replacement frequently causes substantial trauma to the patient, occasionally resulting in the patient's death. As such, it greatly beneficial to be able to either avoid or postpone the need for the replacement of implanted biological tissue.
Various efforts have been undertaken to find ways to mitigating calcification of glutaraldehyde fixed bioprosthetic tissue. Included among these calcification mitigation techniques are the methods described in U.S. Pat. No. 4,885,005 (Nashef et al.) SURFACTANT TREATMENT OF IMPLANTABLE BIOLOGICAL TISSUE TO INHIBIT CALCIFICATION; U.S. Pat. No. 4,648,881 (Carpentier et al.) IMPLANTABLE BIOLOGICAL TISSUE AND PROCESS FOR PREPARATION THEREOF; U.S. Pat. No. 4,976,733 (Girardot) PREVENTION OF PROSTHESIS CALCIFICATION; U.S. Pat. No. 4,120,649 (Schechter) TRANSPLANTS; U.S. Pat. No. 5,002,2566 (Carpentier) CALCIFICATION MITIGATION OF BIOPROSTHETIC IMPLANTS; EP 103947A2 (Pollock et al.) METHOD FOR INHIBITING MINERALIZATION OF NATURAL TISSUE DURING IMPLANTATION; WO84/01879 (Nashef et al.) SURFACTANT TREATMENT OF IMPLANTABLE BIOLOGICAL TISSUE TO INHIBIT CALCIFICATION; U.S. Pat. No. 5,595,571 (Jaffe) BIOLOGICAL MATERIAL PRE-FIXATION TREATMENT; and WO 95/11047 (Levy et. al.) METHOD OF MAKING CALCIFICATION-RESISTANT BIOPROSTHETIC TISSUE.
Although some researchers believe that glutaraldehyde actually increases the risk of calcification, it is still the most accepted fixation solution. For example, the Levy patent application noted above utilizes an alcohol treatment for mitigating calcification, in addition to a glutaraldehyde fixation
There is significant research occurring into the extent the mechanisms mentioned above cause calcification. Many processes are believed to mitigate calcification, without their proponents knowing exactly why. Indeed, the Levy patent does not offer a mechanism why alcohol is effective in calcification mitigation, other than it is preferred over aldehydes.
A number of tests are conventionally used to gauge the efficiacy of various calcification mitigation treatments. The most reliable test is actual implantation into a living organisms, preferably a human. Of course, such host studies are by their nature long-term and the results somewhat skewed by the variations present in each individual host. Researchers are therefore constrained to predict the ultimate calcification mitigation benefits of a particular treatment by using laboratory tests on treated tissue, such as calcium uptake studies. Ultimately, there is a substantial amount of extrapolation from the empirical data of such laboratory tests, and to date there is no one predominant mechanism recognized for multigrating calcification.
There remains a need for the development of new methods for inhibiting or mitigrating calcification of chemically fixed biological tissue.
These, as well as other advantages of the present invention will be more apparent from the following description and drawings. It is understood that changes in the specific structure shown and the described may be made within the scope of the claims without departing from the spirit of the invention.
The present invention provides a method for treating at least partially fixed biological tissue to inhibit calcification of the tissue following implantation in mammalian body, comprising immersing the tissue in a treatment solution, inducing relative and repeated tissue/solution movement, and beating the solution during the step of inducing. The step of inducing may comprise flowing treatment fluid across the tissue and restraining the immersed tissue from gross movement, or enclosing the treatment solution in a container and either shaking the container or stirring the solution within the container, with the immersed tissue floating free or being restrained from gross movement within the container. The step of heating may be applying beat to the outside of the container to indirectly heat the solution therein, or placing the treatment container in an enclosure and heating the enclosure. Alternatively, the step of heating may comprise applying heat directly to the treatment solution.
The present invention also includes a method for treating at least partially fixed biological tissue to inhibit calcification of the tissue following implantation in a mammalian body, comprising positioning the tissue in a flow container; restraining the tissue from gross movement within the container, flowing treatment solution through the flow container into contact with the tissue, and heating the solution during the step of flowing. The step of restraining may comprise mounting the tissue in a planar configuration substantially parallel to the direction of flow of the flowing solution. The tissue may be positioned within a flow container having a cross-section oriented substantially normal to the direction of flow of the flowing solution, the tissue being positioned downstream of a baffle to create a substantially uniform downstream flow profile over the cross-section. In one embodiment, treatment solution is supplied to an inlet of the flow container from a reservoir, and fluid is expelled from an outlet of the flow container to the reservoir. The treatment solution may be heated in the reservoir. Preferably, the treatment fluid flows upward through the flow container from the inlet to the outlet and into contact with the tissue.
In accordance with the invention, an apparatus for treating at least partially fixed biological tissue to inhibit calcification of the tissue following implantation in a mammalian body is provided. The apparatus comprises a flow container, a supply of treatment fluid, a fluid input to the container, a fluid output from the container, a tissue mount for positioning the at least partially fixed biological tissue within the container between the input and output and restrain its gross movement therein, and means for heating the fluid. The flow container is preferably divided into at least two sections in series separated by perforated baffles, with at least one tissue mount in each section. The flow container may be an elongated tube and the baffles circular. The tissue mount may be configured to mount the tissue in a planar configuration substantially parallel to the direction of flow of the solution flowing through the container. The apparatus may additionally include at least one baffle positioned in the flow container and upstream of the tissue mount, the baffle being configured to create a substantially uniform downstream flow profile over a cross-section of the flow container.
The detailed description set forth below in connection with the appended drawings is intended as a description of the presently preferred embodiment of the invention, and is not intended to represent the only form in which the present invention may be constructed or utilized. The description sets forth the functions and sequence of steps for constructing and operating the invention in connection with the illustrated embodiment. It is to be understood, however, that the same or equivalent functions and sequences may be accomplished by different embodiments that are also intended to be encompassed within the spirit and scope of the invention.
One method for treating glutaraldehyde fixed biological tissue to inhibit calcification thereof following implantation in a mammalian body is illustrated in
Referring now to
After harvesting, the biological tissue is carried in saline solution, typically for a period of 1-6 hours 12.
The tissue is next fixed using a buffered glutaraldehyde solution of adequate concentration, for example between 0.2% and 0.8%, at room temperature for at least 3 hours 14. As is well known, glutaraldehyde effects cross-linking of the proteins, e.g., collagen, within the tissue. Such cross-linking tends to make the tissue more durable and effects preservation thereof. It is known that cross-linked protein exhibits increased resistance to proteolytic cleavage and further that one of the major processes by which circulating blood may destroy tissue is via enzymatic activity which involves unfolding of the protein substrate in order to facilitate enzymatic hydrolysis. Cross-linking of the protein of a tissue makes the tissue resistant to such unfolding, and consequently tends to prevent deterioration thereof due to the enzymatic activity of blood.
The tissue is next sterilized, preferably with an alcohol/formaldehyde solution for 2 hours at room temperature 16. The preferred solution for effecting sterilization of the tissue comprises approximately 12 ml/l of Tween 80; approximately 2.65 gms/l of MgCl2.H2O; approximately 108 ml/l of formaldehyde (37%); approximately 220 ml/l of ethyl alcohol (100%) and approximately 4.863 gms/l of HEPES buffer. The balance of the solution comprises double filtered H2O. The pH of the solution is typically adjusted to 7.4 via the addition of NaOH. Those skilled in the art will recognize various other sterilization solutions are likewise suitable.
Antimineralization treatment 18 is optionally performed so as to inhibit the accumulation of mineral deposits upon the biological tissue after implantation of a mammalian body. As those skilled in the art will recognize, various different antimineralization treatments are utilized so as to prevent the deposition of various different minerals upon the biological tissue.
The tissue is trimmed and any non-biological components are then added thereto 20. For example, it is common to sew a heart valve to a valve holder which aids in the handling thereof and which may additionally function as a mount for the valve when implanted into a mammalian body.
Next, the biological tissue is once again sterilized 22, preferably in an alcohol/formaldehyde solution as discussed above. Since preparation of the biological tissue is substantially complete and the biological tissue will next likely be stored for an extended period of time, a more rigorous sterilization procedure from that previously utilized is typically employed. At this stage, the biological tissue is typically sterilized for approximately 9 hours at 34-38° C.
After sterilization, the biological tissue is stored in glutaraldehyde at room temperature 24.
Tissue Treatment Using Heat
Referring now to
The treatment fluid should be heated to a temperature greater than body temperature (37° C.) but not high enough to damage either the tissue or the treatment fluid. Thus, the preferred heat range is between 35-75° C. However, the temperature affects the amount of calcification mitigation, and the process time, and is preferably between 45° C. and 55° c., and more preferably between 50° C.±1° C.
Heating of the biological tissue may be performed at any time after harvesting the tissue from the animal or human cadaver and prior to implanting the tissue within a mammalian body. However, heating of the biological tissue is preferably performed at a point in the process for preparing the biological tissue when the biological tissue is already disposed within a bath of glutaraldehyde solution, as occurs at various stages of the process according to the prior art. Thus, the method for treating glutaraldehyde fixed biological tissues according to the present invention is preferably performed either during fixing thereof with a glutaraldehyde solution, immediately after fixing thereof with the glutaraldehyde solution, or alternatively just prior to or after being stored in a glutaraldehyde solution.
As a further alternative, a method for treating glutaraldehyde fixed biological tissues may be performed during antimineralization treatment by adding glutaraldehyde to the antimineralization solution and heating the solution, preferably to approximately 35-75° C. for approximately 4-22 weeks. More preferably, the tissue is heat treated at 50° C.±1° C. for a period of a few days to 22 weeks.
For example, after fixing tissue using a buffered glutaraldehyde solution of adequate concentration, for example between 0.2% and 0.8%, at room temperature for at least 3 hours 14, the biological tissue may be heat treated in either the same or different glutaraldehyde solution, preferably at approximately 35-75° C. for a few days to 22 weeks 15.
As one of the alternative discussed above, the biological tissue is fixed and heat-treated simultaneously 13 in the 0.2-0.8% glutaraldehyde solution, again preferably at approximately 35-75° C. for approximately a few days to 22 weeks. Another alternative is to heat the tissue in saline 17 prior to fixation 21.
As the other alternative discussed above, the biological tissue may simultaneously undergo antimineralization treatment and heat treatment 19. Glutaraldehyde is added to the antimineralization solution so as to effect the inhibition of calcification of the tissue following implantation in a mammalian body.
Tissue Treatment Using Relative Tissue/Fluid Movement
The solution 24 is preferably a buffered glutaraldehyde, but may be any chemical solution, such as Denacol® or others, which performs substantially the same in this context. The shaking and/or heat may be applied during fixation or after. The tissue is preferably at least partially fixed prior to being subjected to the calcification mitigation treatment described herein, and more preferably the tissue is fully fixed prior to the treatment. The treatment thus can be designed to complete the fixation process. In a preferred embodiment, tissue that has been fixed for a period of between thirty minutes to fourteen days is placed in the container 25 with a buffered clutaraldehyde solution of adequate concentration, for example between 0.2% and 0.8%. The solution is then shaken for thirty minutes after which the container 25 remains static for fourteen days.
The tissue 22 may be sheets of bovine pericardium tissue, precut leaflets, or fully formed porcine heart valves. One potential disadvantage of using precut leaflets or porcine heart valves is the tissue's nonuniform capacity for shrinkage during calcification mitigation treatment. It can be difficult, though not impossible, to consistently and accurately compensate for this phenomenon. A detailed map of the fiber orientation, thickness and other properties of each individual leaflet may be required to predict the final form of the leaflet after treatment. Therefore, the preferred procedure is to place sheets or pieces of tissue in the container and subject it to the shaking and/or heat. Afterwards, the leaflets are cut from the treated tissue.
It will be noted that the tissue 22 within the solution 24 may be allowed to move about freely. In another embodiment, and as will be described below with respect to the embodiment of
In another variation on the shaking, a treatment system 30 is shown in
In another version of shaking, multiple flasks or containers holding the treatment fluid and tissue samples are clamped to a rotating ferris-wheel apparatus. The apparatus includes a wheel rotating about a tilted axis so that the flasks follow a tilted circular trajectory. In this manner, the fluid within the flasks gently washes over the tissue pieces as the wheel rotates.
The containers 25 and 34 in
Relative movement between the tissue and the treatment fluid is believed to enhance calcification mitigation. A mechanism for this result has not been fully formulated, although mass transport of the fluid surrounding the tissue may be relevant. Indeed, one theory is that certain cell material, for example, proteins, is extracted or removed from the tissue by the treatment fluid, which removal is enhanced relative to static treatment methods by the movement of the fluid. In other words, the relative movement of the tissue within the fluid repeatedly replenishes the fluid surrounding any one portion of tissue. Test results shown in
The solution is heated indirectly through the surrounding air, such as with the radiant heaters 28 shown in
Tissue Treatment Using Relative Tissue/Fluid Flow
The system 40 comprises a flow container 42 within which tissue 44 is placed. A number of conduits 46 connect one end of the flow container 42 to a pump 50 and then to a solution reservoir 48. Conduit 47, shown in dashed line, may be coimected between the other end of the flow container 42 and the reservoir 48 to complete a closed circulation loop. The pump propels treatment solution through the system 40 in the direction shown by the arrows 52. The tissue 44 is preferably restrained within the flow container 42 using means schematically illustrated at 56. Resistance heaters 54 are illustrated surrounding the reservoir 48. If immersion heaters are used, they must be able to withstand the extended exposure to sometimes caustic treatment fluid. Of course, one or both of the resistance heating elements 54 may be removed from around the reservoir, or alternative heating devices may be used. For example, treatment system 40, and the system 20 or 30 shown in
The basic elements of a method for treating tissue using the system 40 are illustrated in FIG. 7. Initially, the tissue is harvested, rinsed, fixed and cut into pieces, preferably squares or rectangles, from which leaflets may be formed. The tissue (or leaflets in some instances) may be placed within the flow container 42 and subjected to flow during or after fixation. In a preferred embodiment, the tissue 44 is at least partially fixed before being subjected to the flow within the system 40, and more preferably the tissue is fully fixed prior to the treatment. The pieces of tissue are then placed in the treatment container, and the solution caused to flow therethrough, initiating relative movement between the tissue pieces and surrounding treatment medium which is continued for a predetermined time. The solution is heated directly outside of the container, or indirectly by heating the container. Finally, the tissue pieces are removed from the container, rinsed and stored for later use. Of course, rather than storing the tissue, it may be formed directly into leaflets and assembled into a heart valve directly after the treatment process.
With reference to
In an alternative method of treating tissue in the system 40, the treatment time is between thirty and sixty days. The flow rate is approximately 7.4 gallons per minute (28 lpm) on average, and is uniform throughout a cross section normal to the flow within the flow container 42. The tissue 44 is preferably a rectangle of bovine pericardium of about 2 inches by 4 inches in dimension. This size of tissue sample may be used to form one or two leaflets after treatment.
Those with skill in the art will recognize that variations to the above mentioned systems and processes for moving the fluid and/or heating the tissue are available. For example, the flow of solution past the tissue may be combined with a vibrational or shaking motion of the flow container 42 to enhance any calcification mitigation benefits derived from either method. Additionally, though the system 40 is shown as a closed circulation device, fresh solution may be pumped to the flow container 42 and discharged after passing through the container (thus the conduit 47 is shown as optional). Of course, this will require a significant amount of treatment solution which may be prohibitively expensive. Nevertheless, one of the theoretical mechanisms for the beneficial aspects of the present treatment method including flow is that the solution is constantly replenished in the region surrounding the tissue so that a maximum mass transport of chemicals and/or biological material such as protein is realized from the tissue to the solution. Thus, a system which inputs fresh treatment solution, rather than recycling it through a reservoir, would theoretically be more effective in this regard.
Flow Column Apparatus
As mentioned above, the solution within the reservoir 74 is preferably directly heated to the desired treatment temperature. Although not illustrated, the reservoir is desirably provided with one or more immersion resistance heaters. A thermocouple 77 senses the temperature of the reservoir and is preferably connected to feedback electronics for controlling the immersion heater so that the solution temperature does not rise too high to a level which might be detrimental to the tissue. The temperature within the flow container is monitored using a thermocouple 78 both as a safety, and to record the precise temperature profile of the treatment fluid. Excessive temperatures can detrimentally affect the treatment solution itself, and thus the heating must be done gradually and with a heater having good temperature control.
The vertical flow column or cylinder 60 is segmented into a plurality of vertical sections 80 (seen enlarged in
The baffles 82 are commonly mounted on a vertical support rod 84 extending along the axis of the cylinder 60. The support rod 84 contacts the lower ceiling cap 62b and extends upward into close proximity to the upper cap 62a. As seen at the lower end of
As mentioned above, the baffles 82 divide the cylinder 60 into a plurality of vertical sections 80. In this respect, the vertical sections 80 include the region between two baffles 82. In the illustrated embodiment, there are eight such vertical sections 80 having a height of between seven and eight inches (17.8-20.3 cm). The entire height of the column 60 is approximately 6 feet (1.8 m), and thus there is some space left above the top baffle and below the bottom baffle. The baffles 82 are slidably mounted on the support rod 84 to enable adjustment of the spacing therebetween, if desired. Furthermore, the tissue pieces 82 can be easily mounted when the baffles 82 are removed from the system, whereupon the baffles are slid over the support rod which is then positioned within the tube 61. The tissue pieces to be treated are mounted in a particular manner in a circumferential array about the support rod 84, as will be apparent from the description of
At the top of the cylinder 60 a vertical space is created between the upper baffle and the upper cap 62a, in which the central support rod 84 terminates. The space is needed to insure that the flow passing through upper baffle 82 is not unduly disturbed so that the flow within the upper vertical section 80 remains uniform in a horizontal cross section. Indeed, the uniformity of flow across any horizontal cross section between the baffles is important in the present configuration to insure that the flow past any one piece of tissue is equal to the flow past other tissues. The primary mechanism for insuring such uniform flow is the baffles 82 themselves. Preferably, the perforations 83 are sufficiently numerous and have a sufficient diameter so that the cross-sectional area of the baffles 82 has less structural material than open flow channels. The baffles 82 are thus designed to maintain a uniform, non-laminar upward flow stream through each flow section 80.
At the lower end of the cylinder 60, below the lowest baffle 82, a flow straightener 92 is positioned just above a velocity reducer plate 94. Inlet flow through the aperture 90 thus passes upward through the velocity reducer plate 94 and flow straightener 92 to impinge on the lowest baffle 82. The velocity reducer plate 94 is a disc like plate having a plurality of apertures 96 formed therein. The apertures are relatively widely spaced in the plate 94 to create a drag on the flow and slow its velocity. The flow straightener 92 resembles a honeycomb structure with a relatively densely spaced number of individual flow channels, and has a vertical dimension greater than the velocity reducer plate 94 or baffles 82. Flow enters the column 60 through the aperture 90 and continues upward through the velocity reducer plate 94 and straightener 92. After flow passes through the straightener 92, it impinges on the lowest baffle 82. The treatment solution flows upward through each baffle 82 into each successive section 80 and out the top of the column 60. The column 60 is initially filled with air which is forced out as the surface of the upwardly advancing treatment solution flow passes upward through the column.
Now with reference to
Rectangular tissue pieces 108 are attached to the mounts with sutures or other similar expedient. In the illustrated embodiment, a lower edge 110 of each tissue piece 108 loops around the bridge portion of the U-shaped member 102 and is sewn to the main body of the tissue piece along line 112. In this way, the leading edge of the tissue piece 108 in the upward flow stream is rounded, and thus protected from friction induced tearing or wear. One or more sutures 114 connect the upper corners of the tissue piece 108 to the upper ends of the legs of the U-shaped members 112. Preferably the tissue piece 108 is only connected at one or two locations along its vertical length to prevent gross movement or flapping of the tissue, while allowing the maximum freedom for the tissue to shrink. An O-ring 116 or other such device placed on each leg of the member 112 prevents the sutures 114 from sliding down the leg. The upward flow 118 of treatment solution also assists in maintaining the generally planar configuration of each tissue piece 108.
Mounting the tissue pieces 108 in a planar configuration substantially parallel to the direction of flow of the solution ensures that an even amount of solution contacts both sides of the tissue. That is, is the tissue pieces were canted with respect to the flow, the backsides would be exposed to less direct flow, and eddy currents and the like might be set up, further making the fluid exposure nonuniform. In addition, the preferred parallel orientation minimizes any stretching of the tissue during the extensive treatment period, such as might occur if the fluid was directed to one face of the tissue or the other.
The radial orientation of the plane of each tissue piece 108 desirably ensures uniform contact with treatment solution during flow through the column 60. Ideally, the baffles 82 include perforations 120, seen in
There are preferably eight vertical sections 80 in which six tissue pieces 108 are mounted for a total of forty-eight tissue pieces being treated at once. Of course, other numbers of sections and tissue pieces per section are possible. The present flow column is extremely well-suited for consistently manufacturing high quality treated bioprosthetic tissue. The segmented flow column with uniform flow, and vertical orientation of each tissue piece 108 provides high uniformity of treatment. The modular nature of the column with the entire support rod 84 having all of the baffles 82 attached thereto is a significant advantage in manufacturing. One batch of tissues may be treated, and then removed so that after flushing the system a new batch can be ready for installation and treatment. Furthermore, the flow column lends itself to a high degree of control over the system parameters such as the relative tissue/fluid velocity and the temperature. Significantly, there are no large stagnant zones of flow within the column, and especially not within each vertical segment 80.
Rat Subcutaneous Studies
Group 1 on the left is a control and shows results for two subgroups of 7 and 4 samples each. The control samples were treated for 2 months in 0.6% HEPES-glutaraldehyde at a pH of 7.4 with no heat or movement. Each sample was implanted in 16 day old rats, and left implanted for a period of between 3 and 4 months before being removed to test for calcium.
Groups 4-6 in the middle were all heat treated at 50° C. in the same treatment solution as group 1 for the same period. The differences between the treatment regimen for groups 2-6 are the methods used to induce relative tissue/fluid movement. The methods are shown graphically below each group. Group 2-7 includes two subgroups of 7 and 8 samples each subjected to reciprocal orbital shaking. Group 3-7 includes two subgroups of 2 and 11 samples each placed in a flask with a magnetic stirring bar in the bottom. Group 4 is the same method as group 3 but with two subgroups of 8 samples each placed on a filter instead of being allowed to float around the flask. Group 5 included two subgroups of 12 samples each placed in a first container and subjected to a rolling motion, using a tilted ferris wheel arrangement. Group 6 included two subgroups of 20 and 12 samples each placed in a second container and also subjected to a rolling motion.
Groups 7-9 on the right were all heat treated at 42° C. in the same treatment solution as groups 1-8 and for the same period. Again, the differences between the treatment regimen for groups 7-9 are the methods used to induce relative tissue/fluid movement, shown graphically below each group. Group 7 includes two subgroups of 8 and 4 samples each subjected to reciprocal orbital shaking. Group 8 includes two subgroups of 8 and 11 samples each placed in a flask with a magnetic stirring bar in the bottom. Group 9 is the same method as group 8 but with two subgroups of 8 samples each placed on a filter instead of being allowed to float around the flask.
It is apparent from these tests that the shaking and heat treatment reduced calcium intake over the control group, as well as over the heat treatment alone. Also, treatment at 50° C. was substantially more effective than treatment at 42° C. Comparisons of the different shaking/stirring methods indicates that stirring with a magnetic rod within the flask produced the least amount of calcium uptake, regardless of temperature, although perhaps not by a significant margin at 50° C.
It is understood that the exemplary methods and apparatuses for treating glutaraldehyde fixed biological tissue described herein and shown in the drawings represent only presently preferred embodiments of the present invention. Indeed, various modifications and additions may be made to such embodiments without departing from the spirit and scope of the invention. For example, various fixing agents, such as Denacol® or aldehydes other than glutaraldehyde, may exhibit properties similar to those glutaraldehyde so as to make them suitable for use in the present invention and, thus, may likewise be utilized. Accordingly, these and other modifications and additions may be obvious to those skilled in the art and may be implemented to adapt the present invention for use in a variety of different applications. Furthermore, the scope of the invention should be determined with reference to the appended claims.
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|2||Sealed Information Submission Under MPEP § 724.|
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|U.S. Classification||435/284.1, 435/297.1, 435/289.1, 435/303.1, 623/23.72, 623/2.13, 435/307.1, 435/297.2, 8/94.10R, 623/915, 435/297.5, 600/36, 8/94.11|
|International Classification||A61L27/36, A01N1/00, A61F2/04|
|Cooperative Classification||A61L2400/02, A61L27/3691, A61L27/3687|
|European Classification||A61L27/36H2, A61L27/36H4|
|May 4, 2010||CC||Certificate of correction|
|Oct 3, 2012||FPAY||Fee payment|
Year of fee payment: 12