The invention relates to the field of intravascular medical devices, and more particularly to an improved balloon for a catheter.
In percutaneous transluminal coronary angioplasty (PTCA) procedures, a guiding catheter is advanced until the distal tip of the guiding catheter is seated in the ostium of a desired coronary artery. A guidewire, positioned within an inner lumen of a dilatation catheter, is first advanced out of the distal end of the guiding catheter into the patient's coronary artery until the distal end of the guidewire crosses a lesion or obstruction to be dilated. The dilatation catheter having an inflatable balloon on the distal portion thereof is then advanced into the patient's coronary anatomy, over the previously introduced guidewire, until the balloon of the dilatation catheter is properly positioned across the lesion or obstruction. Once properly positioned, the dilatation balloon is inflated with liquid one or more times to a predetermined size at relatively high pressures (e.g., greater than 8 atmospheres) so that the stenosis is compressed against the arterial wall and the wall expanded to open up the passageway. Generally, the inflated diameter of the balloon is approximately the same diameter as the native diameter of the body lumen being dilated so as to effect the dilatation without over-expanding the arterial wall. Substantial, uncontrolled expansion of the balloon against the vessel wall can cause trauma to the vessel wall. After the balloon is finally deflated, blood flow may resume through the dilated artery and the dilatation catheter can be withdrawn from the patient.
In such angioplasty procedures, there may be restenosis of the artery, i.e. reformation of the arterial blockage, or obstructions that cannot be resolved by inflation of the balloon alone. These conditions often necessitate either another angioplasty procedure, or some other method of repairing, strengthening, or unblocking the dilated area. To reduce the restenosis rate and to strengthen or unblock the dilated area, physicians frequently implant an intravascular prosthesis, generally called a stent, inside the artery at the site of the lesion. Stents may also be used to repair vessels having an intimal flap or dissection or to generally strengthen a weakened section of a vessel. Stents are usually delivered to a desired location within a coronary artery in a contracted condition on a balloon of a catheter which is similar in many respects to a balloon angioplasty catheter and expanded to a larger diameter by expansion of the balloon. The balloon is deflated to remove the catheter and the stent left in place within the artery at the site of the dilated lesion.
Catheter balloons are typically manufactured independently of the catheter itself and then secured to the catheter with an adhesive or other bonding method. In standard balloon manufacture, a polymer tube is blown biaxially under the action of axial tension, internal pressure, and heat within a mold. The polymer tube may either be simultaneously stretched in the radial and axial directions, or sequentially by first stretching axially and then radially. The starting dimensions of the polymer tube and the finished dimensions of the blow-molded balloon within the mold are a measure of the degree to which the polymeric material has been stretched and oriented during balloon blowing, and affect important characteristics of the finished balloon such as rupture pressure and compliance. The blow-up-ratio (BUR) refers generally to the ratio of the diameter of the blown balloon to the diameter of the undeformed polymer tube. Above a critical BUR for a selected polymer, the balloon blowing process becomes unstable and the polymer tubing will rupture or tear before a balloon is fully formed.
In the standard blow molding process, an initiated air bubble in the polymer tube rapidly expands until the polymer tube forms a balloon that is eventually constrained by the mold wall. The hoop stress in the wall of the tubing, as it grows into a balloon, may be approximated by the expression:
σh=(P·R)/δ
where P is the inflation pressure, R is the mean radius of the polymeric tube at any time during the inflation and δ is the wall thickness of the tubing. To form a balloon from the tubing, the inflation pressure P should be such that the wall hoop stress exceeds the material resistance (typically the yield stress) to stretching at the blowing temperature. Once a balloon begins to form from the tubing, it grows rapidly in size until it touches the mold wall. As the balloon expands, its radius R increases and its wall thickness δ decreases. This results in a rapid increase in the wall hoop stress σh during constant pressure blowing. If the wall hoop stress of the growing balloon exceeds the ultimate hoop strength of the material, rupture will occur. This phenomena limits the maximum attainable BUR for a given polymeric material forming the balloon layer.
In the design of catheter balloons, balloon characteristics such as strength, flexibility and compliance must be tailored to provide optimal performance for a particular application. Angioplasty and stent delivery balloons preferably have high strength for inflation at relatively high pressure, and high flexibility and softness for improved ability to track the tortuous anatomy and cross lesions. The balloon compliance is chosen so that the balloon will have the required amount of expansion during inflation. Compliant balloons, for example balloons made from materials such as polyethylene, exhibit substantial stretching upon the application of internal pressure. Noncompliant balloons, for example balloons made from materials such as PET, exhibit relatively little stretching during inflation, and therefore provide controlled radial growth in response to an increase in inflation pressure within the working pressure range. However, noncompliant balloons generally have relatively low flexibility and softness, making it challenging to provide a low compliance balloon with high flexibility and softness for enhanced catheter trackability. A compromise is typically struck between the competing considerations of softness/flexibility and noncompliance, which, as a result, has limited the degree to which the compliance of catheter balloons can be further lowered.
As a balloon is formed by the process described above where an extruded tube is expanded into a mold cavity, the balloon's wall always exhibits a gradient in circumferential orientation of the polymer molecules within. Moreover, the highest degree of orientation occurs at the inner surface and the outer surface experiences the lowest degree of orientation. The gradient is nonlinear, and arises because the percent change in circumference at the inner surface is always greater than that at the outer surface.
There have been attempts to develop methods to raise the overall degree of orientation within the wall of a balloon during expansion. One method employs extruded tubing containing multiple layers of different durometer materials, with the material possessing the highest elongation (typically the lowest durometer) as the innermost layer to enable an increase in the “blow-up ratio” at the balloon's inner surface. Another method utilizes a two-stage expansion process, in which the extruded tubing is first expanded into a mold cavity of intermediate size before being subsequently expanded again into a final, larger mold. This so-called “double-blow” method helps to make the initiation event during balloon expansion less severe and enables the processing of balloons possessing a greater overall BUR value at their innermost surface.
When extruded tubing is expanded circumferentially into a balloon mold, invariably some degree of axial elongation also occurs. The actual degree of axial elongation can be calculated using measured values of initial, “as-extruded” inner diameter (ID) and outer diameter (OD), as well as the final balloon OD, and final balloon double-wall thickness. The calculated value, known as the “area draw-down ratio” (or ADDR) is the ratio of the extrusion's original cross-sectional area to the final balloon's cross-sectional area. The value of ADDR is mathematically equivalent to the ratio of the final length to the original length of the material which comprises the balloon's working length. Higher values of ADDR represent greater axial elongation during the balloon's formation.
The current design and processing approach for balloons purposely involves imparting a substantial amount of axial elongation during balloon expansion. A target ADDR value of 3.0 is common, which means that the material within the wall of the balloon's working length is stretched to 3 times its original length. This amount of axial elongation must be accounted for in the design of the extruded tubing. The extrusion's ID is already made as small as possible by the need to maximize the blow-up ratio, so it is necessary to account for the high degree of axial stretch by increasing the extrusion's OD. Geometric calculations are routinely performed to ensure that the correct final wall thickness will result when a proposed extruded tube is expanded into the desired balloon mold size with an ADDR value of about 3.0. To help control the lot-to-lot variability in axial flow behavior of the extruded tube, a specification exists for the tube's as-extruded elongation to failure (nominally 225% elongation to failure, which translates to an ADDR value of 3.25). Additionally, the amount of externally applied tension may be varied in order to help control the lot-to-lot variability in the axial elongation and thus wall thickness.
The present invention enhances a catheter balloon's performance by improving compliance and rupture properties for a given wall thickness, or by maintaining targeted balloon performance levels while reducing wall thickness. In the former instance, a balloon possessing more robust properties are made with properties similar to more non-compliant balloons with little or no loss in flexibility or deliverability. In the latter instance, either a more robust or non-compliant balloon are made thinner and thus more flexible and deliverable. Additionally, the present invention reduces the compacted or folded balloon profiles by reducing the wall thickness of balloon tapers and shafts.
The method of the invention purposely reduces the outer diameter of the as-extruded tube and correspondingly reduces the target value of ADDR during balloon expansion so that the resulting wall thickness is either unchanged (for improved balloon compliance and rupture performance without increasing wall thickness) or decreased (for comparable balloon compliance and rupture performance using thinner walls). Reducing the as-extruded tube's OD naturally raises the blow-up ratio at the outer surface of the final balloon. The blow-up ratio of underlying material within the balloon wall is also raised. The overall effect of reducing the as-extruded tube's OD is to shift the final balloon wall's BUR gradient upwards everywhere except at the innermost surface. It is further shown that a 10-20% increase in “integrated average” BUR can be attained, in theory, by the present invention. It has been confirmed experimentally that improved balloon performance, notably in rupture strength and “compliance modulus” results from the present invention.
One approach for implementing the present invention is to use a small 1st-stage mold during the double-blow process. By thus limiting the extruded tube's radial growth during the 1st stage, the axial load imparted by the 1st stage inflation pressure is also minimized. This is because the axial load during balloon expansion is related to the inflation pressure multiplied by the cross-sectional area of the just-formed balloon, and that small 1st stage molds serve to minimize this cross-sectional area. By so limiting the axial elongation during the 1st stage expansion and then transferring to a 2nd stage mold of equivalent length, the ADDR of the final balloon after 2nd stage can be substantially reduced. Experiments of this nature on 3.0 mm balloons have led to final ADDR values of approximately 2.0, a significant reduction from the values near 3.0 associated with conventional balloon processing.
A second approach is to controllably reduce the as-extruded tube's elongation to failure. All else being equal, extrusions possessing a high elongation to failure (say, 225% nominal, which translates to an ADDR of 3.25) naturally tend to axially elongate to a greater degree during balloon expansion than extrusions having lower elongation to failure. Thus, targeting an ADDR of 2.0 in the present invention would warrant extrusions possessing an elongation to failure more closely matched (say, 125 or 150% nominal, which translates to ADDR values of 2.25 or 2.5). In such manner, the extruded tubing would be axially deformed to an extent nearer its axial deformation limit and thus be more greatly oriented in the axial direction. The advantage of suitably reducing the as-extruded tube's elongation to failure, rather than controlling ADDR mainly through the judicious selection of 1st stage balloon mold diameter, is that single-stage balloon expansion is possible via the former approach and the resulting ADDR during expansion tends to be self-limited by the balloon tubing.
The byproduct of reducing the as-extruded tubing's % elongation to failure is the increased likelihood of circumferential balloon ruptures, which may be addressed by modifying the balloon's post-expansion “beat set” treatment so as to promote that material change which has been shown to enhance the material's axial strength. The “enhanced heat set” approach offers the potential benefit of also increasing circumferential strength and thereby further enhancing balloon performance in terms of rupture strength and compliance modulus.
In addition, to improving performance within a balloon's working length, this invention could be also used to reduce thickness within a balloon's tapers and shafts. Consequently, a balloon's folded profile could be improved by reducing wall thickness within its tapers, which often possess the greatest profile on the larger angioplasty balloon sizes. Further, the profile of its seals could be improved by reducing wall thickness within its shafts, particularly at the proximal seal where balloon shaft drilling is not presently performed.
These and other advantages of the invention will become more apparent from the following detailed description of the invention and the accompanying exemplary drawings.
In the illustrated embodiment, the shaft comprises an outer tubular member 19 defining the inflation lumen, and an inner tubular member 20 defining the guidewire lumen 22 and positioned in the outer tubular member 19 such that the inflation lumen is the annular space between the inner surface of the outer tubular member 19 and the outer surface of the inner tubular member 20 as best shown in
Although not illustrated, the balloon 14 of the invention typically has a deflated configuration with wings wrapped around the balloon to form a low profile configuration for introduction and advancement within a patient's body lumen. As a result, the balloon inflates to a nominal working diameter by unfolding and filling the molded volume of the balloon.
Balloon 14 has a first layer 30, and a second layer which is an inner layer relative to the first layer 30. In the illustrated embodiment, the second layer 31 is on an inner surface of the balloon 14 with the first layer 30 defining an outer surface of the balloon 14 and the second layer 31 defining an inner surface of the balloon 14. However, the balloon 14 of the invention can alternatively have one or more additional layers (not shown). Additional layer(s) increase the dimensions of the tube/balloon formed therefrom to a desired value, and/or can be used to provide an inner or outer surface of the balloon with a desired characteristic. Therefore, it should be understood that the balloon 14 of the invention discussed below has at least two layers, and optionally includes one or more additional layers, unless otherwise noted as having a specified set number of layers.
The first (outer) layer 30 is formed of a first polymeric material, and the second (inner) layer 31 is formed of a second polymeric material that can be expanded to a higher BUR than the first polymeric material. The second (inner) layer 31 is at a BUR which is typically about 15% to about 25% greater than the BUR of the first (outer) layer 30. Each layer 30, 31 is preferably at its maximum BUR, so that the balloon has layers of highly oriented material and, consequently, a very low compliance.
A variety of suitable materials can be used to form the first and second layers 30, 31. In a presently preferred embodiment, the first and second polymeric materials are elastomers providing a relatively low flexural modulus for balloon flexibility, although nonelastomers can alternatively be used. Presently preferred materials are from the same polymeric family/class such as polyamides including nylons and polyether block amides (PEBAX). Forming the layers of compatible polymeric materials allows for heat fusion bonding the layers together. The layers can alternatively be formed of different polymer classes which are not sufficiently compatible to fusion bond together, in which case a tie layer is typically provided between the outer and inner layers 30, 31 to bond the balloon layers together. For example, a PET inner layer and a PEBAX outer layer typically have a tie layer of an adhesive polymer such as Primacor (a functionalized polyolefin) therebetween.
The balloon 14 is formed by a method in which the layers of material that can be expanded to higher BURs are the inner layers of the balloon tubing, and lower BUR materials are the outer layers, and the balloon is blow-molded such that the innermost layer is optimized for radial orientation. By judicious selection of layer thickness, the other layer(s) can be optimized for radial orientation as well. The resulting balloon has an increased resistance to radial expansion at increasing inflation pressures.
The balloon 14 is blow-molded from a multilayered tube which has the first layer 30, and second layer 31 as an inner layer relative to the first layer 30. However, as discussed above, a balloon of the invention may have one or more additional layers, so that the tubing used to blow-mold the balloon would similarly be formed with the additional layer(s). The tube is typically formed by coextrusion, although a variety of suitable methods may be used. For example, in one embodiment, a multilayered tube is formed by coextruding at least two layers, and one or more additional layers are added to the coextruded tube by heat shrinking, adhesive or fusion bonding, or frictionally engaging the layer(s) to the coextruded tube.
The multilayered tube is then radially expanded in a balloon mold to form the balloon 14.
The materials and dimensions of the multilayered tube 40 and balloon mold 41 are selected so that each layer of the balloon has been radially expanded to substantially its maximum possible amount, expressed as the BUR of the balloon layers. In a presently preferred embodiment, the outer layer 30 has a higher Shore durometer hardness than the one or more inner layers. The percentage of elongation to break of the inner layer is approximately 350%, whereas the percentage to break of the outer layer is more in the range of 220-250%. The key driver between BUR differences that can be achieved is the difference between the ultimate elongations of the material. Pebax 63D is used in a preferred embodiment as the inner layer and Pebax 70D or 72D is used as the outer layer. Pebax 63D has an elongation at break of around 350% whereas the Pebax 70D or 72D is approximately 220-250%. See U.S. Patent Publication No. 2007/0142771, incorporated herein by reference in its entirety, for further discussion of these materials.
The dimensions of catheter 10 are determined largely by the size of the balloon and guidewire to be employed, the catheter type, and the size of the artery or other body lumen through which the catheter must pass or the size of the stent being delivered. Typically, the outer tubular member 14 has an outer diameter of about 0.025 to about 0.04 inch (0.064 to 0.10 cm), usually about 0.037 inch (0.094 cm), and the wall thickness of the outer tubular member 14 can vary from about 0.002 to about 0.008 inch (0.0051 to 0.02 cm), typically about 0.003 to 0.005 inch (0.0076 to 0.013 cm). The inner tubular member 16 typically has an inner diameter of about 0.01 to about 0.018 inch (0.025 to 0.046 cm), usually about 0.016 inch (0.04 cm), and a wall thickness of about 0.004 to about 0.008 inch (0.01 to 0.02 cm). The overall length of the catheter 10 may range from about 100 to about 150 cm, and is typically about 143 cm. Preferably, balloon 24 has a length about 0.8 cm to about 6 cm, and an inflated working diameter of about 2 to about 5 mm.
The various components may be joined using conventional bonding methods such as by fusion bonding or use of adhesives. Although the shaft is illustrated as having an inner and outer tubular member, a variety of suitable shaft configurations may be used including a dual lumen extruded shaft having a side-by-side lumens extruded therein. Similarly, although the embodiment illustrated in
The present invention examines the BUR gradient of the expanded balloon as it undergoes a biaxial deformation. The extent of axial deformation occurring during balloon expansion, or Area Draw-Down Ratio (“ADDR”), is the ratio of the as-extruded tube's cross-sectional area to the balloon's as-expanded cross-sectional area. When determining the ADDR associated with a particular balloon, the calculation yields a single result. The formula for ADDR requires only the extruded material's initial OD & ID and the balloon's final OD & ID. The resulting value defines the amount of axial deformation that has occurred at every position throughout the wall of the balloon during expansion.
When calculating the BUR for a particular balloon, this also involves the material's initial and final diameters. However, the BUR formula provides a different value for every radial position within the final balloon wall. That is, for any expanded hollow cylinder, an increasing gradient in BUR from its inner surface to its outer surface will naturally occur. The precise calculation of BUR for material at any given location within a balloon wall requires that material's original radial position within the extruded tubing. Consequently, BUR values have traditionally been calculated only at the wall's inner and outer surfaces, because only there are the material's original and final radial position directly measurable or readily calculable.
Because of the unavoidable BUR gradient within the wall of any expanded balloon, it is desirable to have a single value which represents the overall extent of the circumferential deformation and thus the induced molecular orientation. The most convenient approach is to simply take the average the two BUR values corresponding to the balloon's inner and outer surfaces. However, the BUR gradient within an expanded hollow cylinder is not linear, so a simple high/low average may not be the most representative single value to describe its circumferential deformation.
A more accurate value of BUR can be determined as follows. An initial length of tubular material is internally pressurized and heated such that it expands both radially and axially into a balloon mold. Axial tension may be applied to the ends to induce additional axial deformation and thus increase ADDR, as needed. The tubular material remains pressurized while the mold is subsequently cooled. Afterward the balloon is removed from the mold cavity.
Typically the balloon's as-expanded OD is measured by laser micrometer while lightly pressurized. The balloon's double-wall thickness (DWT) is typically measured by a drop gage or snap gage when deflated. The balloon's ID can then be readily calculated by subtracting the DWT value from the OD measurement.
ODo=Original outer diameter of extruded material
IDo=Original inner diameter of extruded material
Lo=Original length of material which will be formed into a balloon
ODf=Final outer diameter after balloon expansion
IDf=Final inner diameter after balloon expansion
Lf=Final length of the formed material after expansion
Mid-Wall Dimensional Variables
N=Number of nested, thin-walled cylindrical elements the tube is divided into
To=Original single-wall thickness of every element before expansion
ODo1 (=ODo)=Original outer diameter of element 1
ODo2=Original outer diameter of element 2
ODo3=Original outer diameter of element 3
ODon=Original outer diameter of element n
IDo1 (=ODo2)=Original inner diameter of element 1
IDo2 (=ODo3)=Original inner diameter of element 2
IDo3 (=ODo4)=Original inner diameter of element 3
IDon (=ODo)=Original inner diameter of element 1
Tf1=Final single-wall thickness of element 1 after balloon expansion
Tf2=Final single-wall thickness of element 2 after balloon expansion
Tf3=Final single-wall thickness of element 3 after balloon expansion
Tfn=Final single-wall thickness of element n after balloon expansion
ODf1 (=ODf)=Final outer diameter of element 1
ODf2=Final outer diameter of element 2
ODf3=Final outer diameter of element 3
ODfn=Final outer diameter of element n
IDf1 (=ODf2)=Final inner diameter of element 1
IDf2 (=ODf3)=Final inner diameter of element 2
IDf3 (=ODf4)=Final inner diameter of element 3
IDfn (=IDf)=Final inner diameter of element n
Blow Up Ratios
BURSimpleAve=Average of two BUR values, at only the outer and inner surfaces
BURIntegAve=Average BUR, integrated across the balloon's final wall thickness
ADDR, Length Ratio, and % Elongation:
The volume of material in that span of material which participates in the balloon expansion process is conserved. For a length of hollow cylindrical material of initial length Lo that elongates to some final length Lf:
(Pi/4)*(Lo)*(ODo2−IDo2)=(Pi/4)*(Lf)*(ODf2−IDf2) [constant cyl. volume] [1]
[Pi/4)*(ODo2−IDo2]/[(Pi/4)*(ODf2−IDf2)]=Lf/Li [rearranging] [2]
As set forth above, Area Draw-Down Ratio, “ADDR”, is defined as the ratio of final cross sectional area to original cross section area, which is the left side of Equation 2. Thus:
ADDR=[Pi/4)*(ODo2−IDo2)/[(Pi/4)*(ODf2−IDf2)]=Lf/Li [definition] [3]
ADDR=(ODo2−IDo2)/(ODf2−IDf2)=Lf/Li [simplifying] [4]
The right side of Equations 2, 3 and 4, here referred to as Length Ratio, is related to percent elongation as follows:
% Elongation=100*[(Lf−Li)/Li] [definition] [5]
% Elongation=100*[(Lf/Li)−1] [rearranging] [6]
Lf/Li=1+(% Elongation)/100 [rearranging] [7]
Surface BUR Simple Average BUR Values:
By definition, the Blow Up Ratio or “BUR” is the ratio of the balloon material's final expanded diameter to its original as-extruded diameter. At the outer surface:
BUROD=(ODf)/(ODo) [definition] [8]
Similarly, at the inner surface:
BURID=(IDf)/(IDo) [definition] [9]
Original Dimensions of Thin-Walled Cylindrical Elements:
To determine the Blow-Up Ratio for a material's position somewhere within the wall of the tubing, its position must be known within both the initial extrusion and the final balloon wall. This can be done by first dividing the initial extrusion into numerous elements of the identical wall thickness. Collectively, they comprise a nested set of ultra-thin cylinders. After they have all been expanded, both in the axial and circumferential directions, to produce the balloon's final dimensions, each of their wall thickness will be thinner but no longer identical. The outermost element will have been circumferentially expanded the least amount and will therefore be thickest. Conversely, the innermost element will have been circumferentially expanded the most and will thus be thinnest. Note that the extent of the axial expansion (ADDR or Length Ratio) is the same for every element and depends only upon the expanded material's original and final lengths.
Prior to expansion, the original single-wall wall thickness (To) of every element is the as-extruded single-wall wall thickness divided by the number of elements (N):
To=[(ODo−IDo)/2]/N [12]
The original OD of the outermost element (ODo1) is identical to the original outer diameter of the extruded material (ODo). The original ID of the element (IDo1) is, of course, less than OD by its double-wall thickness:
ODo1=ODo [13]
IDo1=ODo−2*To [14]
The original OD of the next element inward (ODo2) is the same as the original ID of the previous element (IDo1). Its original ID is, again, less than its OD by its double-wall thickness:
ODo2=IDo1 [15]
IDo2=ODo2−2*To [16]
Similar formulas apply for all subsequent elements. For the innermost element:
ODon=IDo(n-1) [17]
IDon=ODon−2*To=IDo [18]
Final Dimensions of Thin-Walled Cylindrical Elements:
The final OD of the outermost element (ODfl) is identical to the final balloon OD (ODf) so it is directly measurable after expansion. The final ID of this element can be calculated based on its original OD and ID, its final OD, and the Area Draw-Down Ratio. The pertinent formula is the same as Equation 4:
ADDR=(ODo12−IDo12)/(ODf12−IDf12) [customization of Eq. 4]
(ODf12−IDf12)=(ODo12−IDo12)/ADDR [rearranging]
IDf12=ODf12−(ODo12−IDo12)/ADDR [rearranging]
IDf1=[ODf12−(ODo12−IDo12)/ADDR]1/2 [rearranging]
IDf1=[ODf2−(ODo2−IDo12)/ADDR]1/2 [substituting Eq. 13] [19]
Equation 19 gives the final ID of the 1st element in terms of the tube's original and final outside diameter, the original ID of that element, and the ADDR. The formula for calculating the final ID of the 2nd element is similar to equation 19. However, because all elements are nested both before and after expansion, the final OD of the 2nd element (ODf2) is identical to the final ID of the 1st element (IDf1), and the original OD of the 2nd element (ODo2) is identical to the original ID of the 1st element (IDo1). Making appropriate substitutions into Equation 19 yields:
IDf2=[IDf12−(IDo12−IDo22)/ADDR]1/2 [20]
Similar formulas can be used to calculate the final ID's of all remaining elements. For the innermost element, note that the original ID is IDo and the final ID is IDf.
IDfn=[IDf2−(IDo(n-1)2−IDo2)/ADDR]1/2 [21]
Interior BUR Values:
Using the final ID values calculated using Equations 19 and 20, and the original ID values calculated via the examples provided by Equations 14 and 16, the Blow Up Ratio for any element, regardless of its position, can be calculated as follows:
BUR1=IDf1/IDo1 [definition of BUR] [22]
BUR2=IDf2/IDo2 [definition of BUR] [23]
BURn=IDfn/IDon [definition of BUR] [24]
Integrated Average BUR:
Because Blow Up Ratio varies from one element to another, with the highest value at the inner surface and the lowest at its outer surface, when BUR is plotted vs. position within the balloon's final wall a curve is produced. Finding the area under this curve enables an “integrated average” BUR value to be obtained. The area under the curve is readily calculated by numerical integration. This involves multiplying each element's BUR by its final wall thickness and summing:
Area Under Curve=Σ[BUR1*(ODf−IDf1)/2]+[BUR2*(ODf2−IDf2)/2]+ . . . [BURn*(ODfn−IDfn)/2] [25]
It turns out that every individual product of BUR*thickness (each bracketed term in equation 25) approaches the same numerical value as the number of elements is increased. This is because any element's final thickness is inversely proportional to its extent of circumferential strain, whereas its Blow Up Ratio is directly proportional to circumferential strain; the change in one value balances the change in the other. To calculate the area under the curve, it is therefore only necessary to compute the BUR and final thickness for one element, calculate their product, and then multiply this product by the number of elements. The outermost element is the obvious choice in this endeavor, because its original and final OD are directly measurable. Thus:
Area Under Curve=N*[BUR1*(ODf−IDf1)/2] [26]
Substituting equation 22 in equation 26 produces:
Area Under Curve=N*[(IDf1/IDo1)*(ODf−IDf1)/2] [27]
where IDf1=[ODf2−(ODo2−IDo12)/ADDR]1/2 [Eq. 19]
and IDo1=ODo−2*To [Eq. 14]
and To=[(ODo−IDo)/2]/N [Eq. 12]
For any numerical integration, the accuracy tends to improve as the number of elements increases. Due to the convenient simplification represented in equation 26 or 27, the number of terms that must be computed and summed does not depend on the number of elements. Thus, there is no workload penalty for selecting as many as 100, or even 1000 elements to improve accuracy.
The area under the curve obtained via equation 26 or 27 happens to be in units of BUR*in or BUR*mm, depending on the unit of measure used for diameter. Dividing the area under the curve by the balloon's final single-wall thickness results in an “integrated average” BUR value that is dimensionless. Thus:
BURIntegAve=N*[BUR1*(ODf−IDf1)/2]/(ODf1−IDf1)/2]=N*BUR1 [28]
BURIntegAve=N*[IDf1−IDo1)] [29]
where IDf1=[ODf2−(ODo2−IDo12)/ADDR]1/2 [Eq. 19]
and IDo1=ODo−2*To [Eq. 14]
and To=[(ODo−IDo)/2]/N [Eq. 12]
Due to the nature of the curve of BUR vs. position within a balloon's final wall thickness (concave upward), the value of BURIntegAve will always be less than the value of BURSimpleAve.
Note that the “integrated average” BUR is always less than the simple “high/low” average BUR, but that they increase and become closer together as the initial tube OD is decreased and the ADDR is correspondingly reduced. Thus, in order to raise the extent of the circumferential orientation throughout the balloon wall and, consequently, to reduce balloon compliance and increase rupture strength, the as-extruded tube OD should be reduced and the ADDR correspondingly diminished. In effect, this would raise circumferential orientation at the expense of axial orientation. However, there is a practical limit: an ADDR below 1.0 means that the material must be axially compressed during expansion, which seems unlikely if not impossible by traditional methods.
However, blowing the balloon in two multiple stages (“double blow”) allows the overall ADDR to be reduced and thus enable the use smaller as-extruded OD's. This, of course, would also help to reduce wall thickness within balloon tapers and balloon shafts.
A variety of experiments have been performed using 3.0 mm 2nd stage balloon molds, dual-layer balloon tubing (Pebax 63D inner, Pebax 72D outer) and the double-blow process with various 1st-stage balloon mold sizes. The highest degree of success is attained by extruding balloon tubing to the same ID as conventional tubing, but with a smaller OD, and correspondingly reducing the area draw down ratio (ADDR) resulting from a 2nd stage balloon expansion so that the wall thickness within the working length matches that of a conventional 3.0 mm balloon.
The target range for % elongation to failure of conventional as-extruded balloon tubing (ca. 225%) does not work well for the present invention. Consequently, the actual ADDR's resulting from 2nd stage balloon expansion were too high in initial experiments, which led to inadequate wall thickness and abnormally low rupture values. However, analysis of the balloon compliance test data showed that, despite undesirably low ruptures, these balloons exhibited unusually high values of compliance modulus (the rate of change of hoop stress with respect to the change in hoop strain as balloon inflation pressure is ramped upward). For a given balloon size and double-wall thickness, higher compliance modulus values are generally associated with flatter balloon compliance curves and higher rupture strengths.
Next, the target % elongation to failure of as-extruded tubing was reduced so that less axial stretch would naturally occur during balloon expansion, thereby lowering the actual ADDR and increasing the final balloon wall thickness so that it matched that of conventional 3.0 mm balloons. This had the desired effect of raising the rupture strength, to the extent that the mean rupture strength and rated burst pressure (RBP), when normalized for wall thickness, exceeded that of conventional 3.0 mm balloons. However the majority of samples failed circumferentially (radial rupture) rather than longitudinally (axial rupture). For product safety reasons, it is much preferred that balloon ruptures in the longitudinal direction, and the majority of conventionally-processed balloons fail in the longitudinal mode.
To pinpoint the reason for the change in balloon rupture mode, previous balloon tubing tensile test data was analyzed. The tensile data represented nineteen different Pebax 72d balloon tubing extrusion runs involving various puller speeds, air gap distances, melt temperatures, and draw-down ratios. The groups exhibited a variety of average % elongation values, as expected. The trend is depicted graphically in
The observed decrease in tensile break load with increasing rate of cooling from the melt is possibly caused by the higher cooling rates inhibiting crystallization within the material's “hard” segments. Pebaxes are block copolymers comprised of largely amorphous “soft” segments interspersed with semi-crystalline “hard” segments. Thus, a more rapid cooling rate during extrusion lowered the % elongation via enhanced axial orientation within both segment types, but may have lowered the overall tensile strength by reducing the percent crystallinity primarily within the hard segment. Heating the extruded material to temperatures below but near the melting point enhances molecular mobility and enables additional crystallization to occur, thereby raising the tensile strength.
This was supported by heat treating low-elongation dual-layer balloon tubing at various temperatures ranging from 100° C. to 160° C. for times of 15 and 60 minutes.
Efforts to reduce or eliminate circumferential ruptures involve heat treatments that are similar but are performed after balloon expansion. For example, balloons subject to a heat set heat treatment at approximately 60° C. for about fifteen minutes while lightly pressurized to preserve dimensions. That time/temperature combination is thought to be insufficient to bring about substantial improvement in axial strength. Higher temperatures and longer times have brought about a boost in axial strength comparable to as-extruded balloon tubing. It has been found that radial containment of the balloons is preferable so their diameters do not creep to unacceptably large values during the requisite heating and pressurization.
The byproduct of reducing the as-extruded tubing's % elongation to failure is the increased likelihood of circumferential balloon ruptures, which may be addressed by modifying the balloon's post-expansion “heat set” treatment so as to promote that material change which has been shown to enhance the material's axial strength. The “enhanced heat set” approach offers the potential benefit of also increasing circumferential strength and thereby further enhancing balloon performance in terms of rupture strength and compliance modulus.
In addition, to improving performance within a balloon's working length, this invention could be also used to reduce thickness within a balloon's tapers and shafts. Consequently, a balloon's folded profile could be improved by reducing wall thickness within its tapers, which often possess the greatest profile on the larger angioplasty balloon sizes. Further, the profile of its seals could be improved by reducing wall thickness within its shafts.
While the present invention is described herein in terms of certain preferred embodiments, those skilled in the art will recognize that various modifications and improvements may be made to the invention without departing from the scope thereof. Moreover, although individual features of one embodiment of the invention may be discussed herein or shown in the drawings of the one embodiment and not in other embodiments, it should be apparent that individual features of one embodiment may be combined with one or more features of another embodiment or features from a plurality of embodiments.
This application is a continuation of U.S. patent application Ser. No. 14/204,885, entitled “Method For Forming Catheter Balloon” filed Mar. 11, 2014, which issued as U.S. Pat. No. 9,352,135 on May 31, 2016, which is a continuation of U.S. patent application Ser. No. 12/881,733, entitled “Catheter Balloon and Method of Forming Same,” filed Sep. 14, 2010, which issued as U.S. Pat. No. 8,703,260 on Apr. 22, 2014; to both of which priority is claimed and the contents of both of which are incorporated herein in their entireties.
Number | Name | Date | Kind |
---|---|---|---|
4941877 | Montano, Jr. | Jul 1990 | A |
4952357 | Euteneuer | Aug 1990 | A |
4963313 | Noddin et al. | Oct 1990 | A |
RE33561 | Levy | Mar 1991 | E |
5041125 | Montano, Jr. | Aug 1991 | A |
5087394 | Keith | Feb 1992 | A |
5112304 | Barlow et al. | May 1992 | A |
5195969 | Wang et al. | Mar 1993 | A |
5195970 | Gahara | Mar 1993 | A |
5207700 | Euteneuer | May 1993 | A |
5254091 | Aliahmad et al. | Oct 1993 | A |
5270086 | Hamlin | Dec 1993 | A |
5290306 | Trotta et al. | Mar 1994 | A |
5330428 | Wang et al. | Jul 1994 | A |
5342386 | Trotta | Aug 1994 | A |
5348538 | Wang et al. | Sep 1994 | A |
5358486 | Saab | Oct 1994 | A |
5403340 | Wang et al. | Apr 1995 | A |
5447497 | Sogard et al. | Sep 1995 | A |
5478320 | Trotta | Dec 1995 | A |
5499980 | Euteneuer | Mar 1996 | A |
5500181 | Wang et al. | Mar 1996 | A |
5512051 | Wang et al. | Apr 1996 | A |
5556383 | Wang et al. | Sep 1996 | A |
5587125 | Roychowdhury | Dec 1996 | A |
5613979 | Trotta et al. | Mar 1997 | A |
5620649 | Trotta | Apr 1997 | A |
5647848 | Jorgensen | Jul 1997 | A |
5679817 | Sakai et al. | Oct 1997 | A |
5755690 | Saab | May 1998 | A |
5769817 | Burgmeier | Jun 1998 | A |
5792415 | Hijlkema | Aug 1998 | A |
5797887 | Rosen et al. | Aug 1998 | A |
5807327 | Green et al. | Sep 1998 | A |
5833657 | Reinhardt et al. | Nov 1998 | A |
5853389 | Hijlkema | Dec 1998 | A |
5879369 | Ishida | Mar 1999 | A |
5908406 | Ostapchenko et al. | Jun 1999 | A |
6004289 | Saab | Dec 1999 | A |
6004339 | Wijay | Dec 1999 | A |
6024722 | Rau et al. | Feb 2000 | A |
6059751 | Ostapchenko et al. | May 2000 | A |
6086556 | Hamilton et al. | Jul 2000 | A |
6124007 | Wang et al. | Sep 2000 | A |
6132824 | Hamlin | Oct 2000 | A |
6136258 | Wang et al. | Oct 2000 | A |
6146356 | Wang et al. | Nov 2000 | A |
6171278 | Wang et al. | Jan 2001 | B1 |
6242063 | Ferrera et al. | Jun 2001 | B1 |
6270522 | Simhambhatla et al. | Aug 2001 | B1 |
6328925 | Wang et al. | Dec 2001 | B1 |
6336936 | Simhambhatla et al. | Jan 2002 | B2 |
6358227 | Ferrera et al. | Mar 2002 | B1 |
6416494 | Wilkins | Jul 2002 | B1 |
6495090 | Wilkins | Dec 2002 | B1 |
6500148 | Pinchuk et al. | Dec 2002 | B1 |
6585688 | Ferrera et al. | Jul 2003 | B2 |
6620127 | Lee et al. | Sep 2003 | B2 |
6620128 | Simhambhatla | Sep 2003 | B1 |
6645422 | Jung et al. | Nov 2003 | B2 |
6673302 | Wang et al. | Jan 2004 | B2 |
6679860 | Stiger | Jan 2004 | B2 |
6695809 | Lee | Feb 2004 | B1 |
6732734 | Ogushi et al. | May 2004 | B2 |
6756094 | Wang et al. | Jun 2004 | B1 |
6796960 | Cioanta et al. | Sep 2004 | B2 |
6835189 | Musbach et al. | Dec 2004 | B2 |
6866650 | Stevens et al. | Mar 2005 | B2 |
6875197 | Simhambhatla et al. | Apr 2005 | B1 |
6896842 | Hamilton et al. | May 2005 | B1 |
6911038 | Mertens et al. | Jun 2005 | B2 |
6942640 | Kokish | Sep 2005 | B2 |
6946092 | Bertolino et al. | Sep 2005 | B1 |
6949112 | Sridharan et al. | Sep 2005 | B1 |
6951675 | Chin et al. | Oct 2005 | B2 |
7008438 | O'brien | Mar 2006 | B2 |
7026026 | Ferrera et al. | Apr 2006 | B2 |
7029732 | Wang et al. | Apr 2006 | B2 |
7074206 | Lee et al. | Jul 2006 | B2 |
7112357 | Miller et al. | Sep 2006 | B2 |
7147817 | Lim et al. | Dec 2006 | B1 |
7195638 | Sridharan et al. | Mar 2007 | B1 |
7335185 | Tang et al. | Feb 2008 | B2 |
7781038 | Hamilton et al. | Aug 2010 | B2 |
7815628 | Devens, Jr. | Oct 2010 | B2 |
7828766 | Durcan et al. | Nov 2010 | B2 |
7906066 | Wilson et al. | Mar 2011 | B2 |
7942847 | Stupecky et al. | May 2011 | B2 |
8388575 | Durcan et al. | Mar 2013 | B2 |
8394055 | Durcan et al. | Mar 2013 | B2 |
8535596 | Durcan | Sep 2013 | B2 |
8703260 | Simpson | Apr 2014 | B2 |
9095689 | Durcan | Aug 2015 | B2 |
9132259 | Lin et al. | Sep 2015 | B2 |
9211392 | Durcan | Dec 2015 | B2 |
9352135 | Simpson et al. | May 2016 | B2 |
20020018866 | Lee et al. | Feb 2002 | A1 |
20020068953 | Kokish | Jun 2002 | A1 |
20020087165 | Lee et al. | Jul 2002 | A1 |
20020118866 | Breeuwer et al. | Aug 2002 | A1 |
20020160134 | Ogushi et al. | Oct 2002 | A1 |
20020165523 | Chin et al. | Nov 2002 | A1 |
20020171180 | Simhambhatla | Nov 2002 | A1 |
20040096606 | Lee et al. | May 2004 | A1 |
20040170782 | Wang et al. | Sep 2004 | A1 |
20040173935 | Lim et al. | Sep 2004 | A1 |
20040191443 | Hamlin | Sep 2004 | A1 |
20040207127 | Hamlin | Oct 2004 | A1 |
20050015107 | O'Brien | Jan 2005 | A1 |
20050043679 | Devens et al. | Feb 2005 | A1 |
20050124976 | Devens, Jr. et al. | Jun 2005 | A1 |
20050124978 | Kim | Jun 2005 | A1 |
20050186370 | Hamilton et al. | Aug 2005 | A1 |
20050228428 | Ali et al. | Oct 2005 | A1 |
20050228429 | Burgmeier et al. | Oct 2005 | A1 |
20050238833 | Wang et al. | Oct 2005 | A1 |
20050277878 | Lee | Dec 2005 | A1 |
20060165926 | Weber | Jul 2006 | A1 |
20070060863 | Goeken et al. | Mar 2007 | A1 |
20070142771 | Durcan | Jun 2007 | A1 |
20070142772 | Deshmukh et al. | Jun 2007 | A1 |
20070167973 | Stupecky et al. | Jul 2007 | A1 |
20070250101 | Horn et al. | Oct 2007 | A1 |
20080045928 | Simpson et al. | Feb 2008 | A1 |
20080065188 | Pallazza | Mar 2008 | A1 |
20090156998 | Arana et al. | Jun 2009 | A1 |
20090171336 | Weber | Jul 2009 | A1 |
20100010470 | Bates | Jan 2010 | A1 |
20100042198 | Burton | Feb 2010 | A1 |
20100042199 | Burton | Feb 2010 | A1 |
20100076539 | Klocke et al. | Mar 2010 | A1 |
20110022150 | Durcan et al. | Jan 2011 | A1 |
20120065718 | Simpson et al. | Mar 2012 | A1 |
20120145317 | Durcan et al. | Jun 2012 | A1 |
20120203324 | Durcan | Aug 2012 | A1 |
20130172817 | Durcan et al. | Jul 2013 | A1 |
20140142505 | Lin et al. | May 2014 | A1 |
20140190630 | Simpson et al. | Jul 2014 | A1 |
20150290434 | Lin et al. | Oct 2015 | A1 |
20150290435 | Durcan | Oct 2015 | A1 |
20150343180 | Lin et al. | Dec 2015 | A1 |
Number | Date | Country |
---|---|---|
0 420 488 | Apr 1991 | EP |
0 485 903 | May 1992 | EP |
0 592 885 | Apr 1994 | EP |
0 611 576 | Aug 1994 | EP |
0 768 097 | Apr 1997 | EP |
H05-305146 | Nov 1993 | JP |
H06-507101 | Aug 1994 | JP |
20011029450 | Feb 2001 | JP |
2005-167638 | Jun 2005 | JP |
2007000157 | Jan 2007 | JP |
WO 9208512 | May 1992 | WO |
WO 9518647 | Jul 1995 | WO |
WO 0151115 | Jul 2001 | WO |
WO 02056930 | Jul 2002 | WO |
WO 2005021083 | Mar 2005 | WO |
WO 2005065735 | Jul 2005 | WO |
WO 20060126311 | Nov 2006 | WO |
Entry |
---|
U.S. Appl. No. 11/313,041, Oct. 4, 2010 Issue Fee payment. |
U.S. Appl. No. 11/313,041, Jul. 2, 2010 Notice of Allowance. |
U.S. Appl. No. 11/313,041, Jun. 4, 2010 Request for Continued Examination (RCE). |
U.S. Appl. No. 11/313,041, Apr. 6, 2010 Notice of Allowance. |
U.S. Appl. No. 11/313,041, Mar. 1, 2010 Amendment and Request for Continued Examination (RCE). |
U.S. Appl. No. 11/313,041, Oct. 27, 2009 Final Office Action. |
U.S. Appl. No. 11/313,041, Jun. 22, 2009 Response to Non-Final Office Action. |
U.S. Appl. No. 11/313,041, Apr. 17, 2009 Examiner Interview Summary. |
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U.S. Appl. No. 11/313,041, Feb. 21, 2008 Non-Final Office Action. |
U.S. Appl. No. 12/881,733, Dec. 4, 2013 Notice of Allowance. |
U.S. Appl. No. 12/881,733, Oct. 30, 2013 Response to Non-Final Office Action. |
U.S. Appl. No. 12/881,733, Oct. 17, 2013 Applicant-Initiated Interview Summary. |
U.S. Appl. No. 12/881,733, Sep. 24, 2013 Applicant-Initiated Interview Summary. |
U.S. Appl. No. 12/881,733, May 30, 2013 Non-Final Office Action. |
U.S. Appl. No. 12/881,733, Mar. 12, 2013 Response to Restriction Requirement. |
U.S. Appl. No. 12/881,733, Feb. 12, 2013 Restriction Requirement. |
U.S. Appl. No. 12/881,733, Mar. 4, 2014 Issue Fee Payment. |
U.S. Appl. No. 12/897,202, Feb. 7, 2013 Issue Fee payment. |
U.S. Appl. No. 12/897,202, Nov. 7, 2012 Notice of Allowance. |
U.S. Appl. No. 13/397,140, Aug. 16, 2013 Issue Fee Payment. |
U.S. Appl. No. 13/397,140, May 17, 2013 Notice of Allowance. |
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U.S. Appl. No. 13/447,635, Feb. 5, 2013 Issue Fee payment. |
U.S. Appl. No. 13/447,635, Nov. 5, 2012 Notice of Allowance. |
U.S. Appl. No. 13/680,299, Nov. 10, 2014 Response to Restriction Requirement. |
U.S. Appl. No. 13/680,299, Sep. 8, 2014 Restriction Requirement. |
U.S. Appl. No. 13/680,299, Aug. 7, 2015 Issue Fee Payment. |
U.S. Appl. No. 13/680,299, May 8, 2015 Notice of Allowance. |
U.S. Appl. No. 13/680,299, Feb. 24, 2015 Response to Non-Final Office Action. |
U.S. Appl. No. 13/680,299, Nov. 26, 2014 Non-Final Office Action. |
U.S. Appl. No. 13/775,724, Nov. 20, 2014 Non-Final Office Action. |
U.S. Appl. No. 13/775,724, Feb. 20, 2015 Response to Non-Final Office Action. |
U.S. Appl. No. 13/775,724, Feb. 26, 2015 Applicant Initiated Interview Summary. |
U.S. Appl. No. 13/775,724, Mar. 24, 2015 Noticed of Allowance. |
U.S. Appl. No. 13/775,724, Jun. 24, 2015 Issue Fee Payment. |
U.S. Appl. No. 13/775,724, Aug. 5, 2015 Notice of Allowance. |
U.S. Appl. No. 13/775,724, Oct. 6, 2015 Non-Final Office Action. |
U.S. Appl. No. 13/775,752, Nov. 5, 2015 Issue Fee Payment. |
U.S. Appl. No. 13/775,752, Aug. 5, 2015 Notice of Allowance. |
U.S. Appl. No. 14/204,885, Apr. 29, 2016 Issue Fee Payment. |
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U.S. Appl. No. 14/204,885, Jan. 6, 2016 Response to Non-Final Office Action. |
U.S. Appl. No. 14/204,885, Oct. 6, 2015 Non-Final Office Action. |
(“Hytrel” data sheet) including Hytrel TPC-ET, 94 pages (date not available). |
“Cleartuf 8006”, Shell Chemical Company (date not available). |
“Comparison of Arnitel EL 740 with Hytrel 7246”, retrieved from co-pending application U.S. Appl. No. 11/313,041, filed Apr. 1, 2013. |
Affidavit of Dr. John Chen regarding the measurements for Traytuf 7357 mentioned in Material Testing analysis & Characterization of Traytuf 7357 (2009). |
Ahearne, et al., “Mechanical characterisation of hydrogels for tissue engineering applications,” Topics in Tissue Engineering, 4 (Chapter 12): 3-16 (2008). |
Concise Encyclopedia of Polymer Science and Engineering, p. 759, 815 (1990). |
Data sheet Aurum PL450C (2 sheets), received Oct. 19, 2009. |
Data Sheets of Hytrel grades 2 pages (date not available). |
DuPont Engineering Polymers, “From concept to commercialisation,” (40 ppages) Sep. 1996. |
DuPont Product and Properties Guide, “Hytrel polyester elastomer” Nov. 1999. |
DuPont Product Information, “Hytrel polyester elastomer”, Nov. 1993. |
DuPont Product Information, Injection Molding Guide, “Hytrel polyester elastomer”, Oct. 1996. |
Extract from Wikipedia, “Polyimide” (2 sheets) 2009 (Accessed on Oct. 9, 2009). |
International Search Report dated Jul. 23, 2014 in PCT/US2013/070540. |
Mat Web Information for Plexar (25 pages). (Accessed Oct. 20, 2008). |
Material Testing Analysis & Characterization of Traytuf 7357, 5 pages (2007). |
Nylon Plastics Handbook, Melvin I. Kohan, pp. 298-302 (1995). |
Oudshoorn et al., “Synthesis and characterization of hyperbranched polyglycerol hydrogels,” Biomaterials, 27:5471-5479, Jul. 2006. |
Table “Hytrel grades available before Oct. 1996” (date not available). |
Technical data sheet “Selar PT 4368” Oct. 31, 1990. |
Technical data sheet “Traytuf® 7357 Polyester Resin”, (date not available). |
Thesis for the Degree of Master of Science by Samantha Garramone, 65 pages (May 2001). |
Number | Date | Country | |
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20160243342 A1 | Aug 2016 | US |
Number | Date | Country | |
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Parent | 14204885 | Mar 2014 | US |
Child | 15145620 | US | |
Parent | 12881733 | Sep 2010 | US |
Child | 14204885 | US |