This disclosure relates generally to surgical sutures and, more particularly, to a multi-component expanded polytetrafluoroethylene (PTFE) surgical suture.
Surgical sutures are known for binding body tissues together or binding medical appliances to body tissue. Various materials, including natural materials and synthetic materials, for example, may compose a surgical suture. Further, surgical sutures may include various structures, such as a monofilament structure or a multi-filament structure, for example.
Canadian Patent Publication 2,087,903 (“the '903 publication”), entitled “Multicolored Surgical Braid,” purports to address the problem of non-uniform tensile stress distribution across a cross section of a surgical suture. The '903 publication describes a braided surgical suture with different types of braids that can be distinguished by different multicolored patterns. However, the braided structures described in the '903 publication may provide low tensile strength and may present external surface roughness and cross sectional non-uniformity characteristic of the braid pattern applied. Further, the braided sutures described in the '903 publication may include interstices between the braided fibers, which can trap and retain moisture prior to use.
U.S. Patent Publication 2013/0123839 (“the '839 publication”), entitled “Chemical Knots for Sutures,” purports to address the problem of increasing knot profile with increasing knot security (i.e., resistance to loosening and/or slipping of the knot). The '839 publication describes surface activated surgical sutures capable of forming chemically bonded knots. Further, the '839 publication states that a first reactive group may be positioned on a first portion of the suture surface and a second complimentary reactive group may be positioned on a second portion of the suture surface, such that the first and second portions of the suture surface may come in contact and during the knot-tying process and form a chemical bond therebetween. However, the '839 publication does not describe how to make high tensile strength sutures, or sutures having a color pattern indicative of a characteristic of the suture.
U.S. Patent Publication 2011/0277249 (“the '249 publication”), entitled “Method of Producing Colored High-Strength Fibers,” purports to address the problem of successfully dyeing polyolefins. The '249 publication describes a process for producing colored high-strength fibers of ultra-high-molecular-weight polyolefins by pretreating at least a portion of the high-strength fiber with at least one etching agent, prior to applying a dye to the etched fiber. However, the multi-step process for forming a fiber, etching the fiber, and then dyeing the fiber may be complex and expensive.
Accordingly, there is a need for an improved surgical suture having high tensile strength, low cost, and a multi-colored pattern for identifying a characteristic of the suture.
In one aspect, the disclosure describes a method for making an expanded PTFE monofilament. The method includes forming a first paste by mixing a PTFE powder with a hydrocarbon solvent, the first paste including less than about 16% of the hydrocarbon solvent by weight; curing the first paste by exposing the first paste to a first temperature for a first time duration; forming an extrusion preform by pressing the first paste into a form; forming a green monofilament by extruding the first paste through a die; expanding the green monofilament by exposing the green monofilament to a second temperature for a second time duration, the second time duration occurring after the first time duration; stretching the green monofilament substantially along a longitudinal axis of the green monofilament, the stretching the green monofilament occurring after the expanding the green monofilament; and sintering the green monofilament after the stretching the green monofilament.
In another aspect, the disclosure describes a monofilament. The monofilament including a plurality of expanded PTFE materials including a first PTFE material in contact with a second PTFE material along a first longitudinal interface of the monofilament, the first PTFE material defining a first outer surface of the monofilament, the second PTFE material defining a second outer surface of the monofilament, a color of the first PTFE material being different from a color of the second PTFE material.
Throughout the drawings, like reference numbers refer to like elements, unless otherwise specified.
A periphery of the transverse profile 106 of the filament 100 may be a generalized cylinder defined by an intersection of a plane extending in the radial direction 108 with an outer surface 110 of the filament 100. The generalized cylindrical cross section of the filament 100 could include a circular cross section, a polygonal cross section, an elliptical cross section, a lobed cross section, an irregular cross section, or other filament cross section known to persons having ordinary skill in the art. According to one aspect of the disclosure, the generalized cylindrical cross section of the filament 100 is substantially constant along the entire length 102 of the filament 100. Alternatively, according to another aspect of the disclosure, the transverse profile 106 of the filament 100 may vary along the longitudinal axis 104 of the filament 100.
The filament 100 includes a first composition 112 in contact with a second composition 114 along a longitudinal interface 116. The first composition 112 may differ from the second composition 114 by color, molecular weight, polymeric composition, bioactivity, or other suture material characteristic known to persons having ordinary skill in the art. According to one aspect of the disclosure, the first composition 112 differs from the second composition 114 only in color. According to another aspect of the disclosure, a color of first composition 112 is a natural color of a polymer composing at least a portion of the first composition 112. According to yet another aspect of the disclosure, a color of the first composition 112 is different from a natural color of a polymer composing at least a portion of the first composition 112.
The color of either the first composition 112 or the second composition 114 may be varied by addition of dyes, pigments, powders, or other colorants known to persons having ordinary skill in the art. A colorant may be either a dye or a pigment based on its solubility. Some inorganic pigments may be advantageous for coloring PTFE products because they provide high temperature resistance, for example, during sintering.
Referring now to
The longitudinal interface 116 may extend through the entire transverse profile 106 of the filament 100, such that the longitudinal interface 116 intersects the outer surface 110 of the filament 100 at a first point 118 and a second point 120. In turn, the first composition 112 may define a portion of the outer surface 110 extending from the first point 118 to the second point 120, and the second composition 114 may define another portion of the outer surface 110 extending from the first point 118 to the second point 120.
According to an aspect of the disclosure, the longitudinal interface 116 is a planar surface extending through the filament 100, such that the longitudinal interface 116 appears as a substantially straight line in radial cross section. Alternatively, it will be appreciated that the longitudinal interface 116 may appear as an arc, an irregular line, or any other line known to persons having ordinary skill in the art.
According to another aspect of the disclosure, a profile of the longitudinal interface 116 in radial cross section remains substantially constant along the longitudinal axis 104 of the filament 100. According to yet another aspect of the disclosure, a profile of the longitudinal interface 116 in radial cross section varies along the longitudinal axis 104 of the filament 100.
As shown in
As shown in
According to one aspect of the disclosure, the first sector 126 is about 120 degrees. According to another aspect of the disclosure the second sector 128 is also about 120 degrees. However, it will be appreciated that the first sector 126 and the second sector 128 could occupy any advantageous extent of the transverse profile 106.
The second composition 114 may contact the third composition 130 along a second longitudinal interface 132. Further, the third composition 130 may contact the first composition 112 along a third longitudinal interface 134. The first longitudinal interface 116, the second longitudinal interface 132, and the third longitudinal interface 134 may all intersect along a line through the filament 100 that appears as the point 136 in
The third composition 130 may differ from the first composition 112 and the second composition 114 by color, molecular weight, polymeric composition, bioactivity, or other suture material characteristic known to persons having ordinary skill in the art. According to one aspect of the disclosure, the third composition 130 differs from the first composition 112 and the second composition 114 only in color.
The first sector 126 may extend about 90 degrees, and the second sector 138 may also extend about 90 degrees. Further, the second composition 114 may compose the balance of the transverse profile 106. However, it will be appreciated that the first sector 126 and the second sector 138 may each occupy any advantageous extent of the transverse profile 106.
In
The first composition 112, the second composition 114, and the fourth composition 146 may extend over a first sector 126, a second sector 128, and a third sector 152, respectively. Further, the third composition 130 may compose the balance of the transverse profile 106. The first sector 126, the second sector 128, and the third sector 152 may each extend over about 90 degrees. However, it will be appreciated that the first sector 126, the second sector 128, and the third sector 152 may each occupy any advantageous extent of the transverse profile 106.
The second composition 114 may contact the third composition 130 at a second longitudinal interface 140, and the third composition 130 may contact the fourth composition 146 at a third longitudinal interface 148. Further, the fourth composition 146 may contact the first composition 112 at a fourth longitudinal interface 150.
Although
Although
The PTFE resin may have a high molecular weight, for example, a molecular weight greater than 2,000,000, and in some embodiments greater than 7,000,000. Non-limiting examples of PTFE resins that may be used according to aspects of the disclosure include Daikin F131, Daikin F104U, Daikin F107, Daikin F201, Daikin F205, or other similar PTFE resins known to persons having ordinary skill in the art. Further, the PTFE resins may be supplied in a powder form for forming the paste in step 220. Some metrics that may be relevant to selecting a particular PTFE resin include material quality at extrusion and strength after drawing.
Examples of the lubricant that could be used in forming the paste in step 220 include isopar-E, isopar-H, isopar-M, kerosene, naphtha, petroleum ether, or other similar hydrocarbon liquid known to persons having ordinary skill in the art. The lubricant mixed with the PTFE resin may facilitate extrusion during the step 204. It will be appreciated that a plurality of paste batches may be formed according to step 220, where each batch includes a different colorant additive.
According to an aspect of the disclosure, the paste formed in step 220 includes PTFE resin powder mixed with about 12 to 20% lubricant by weight. According to another aspect of the disclosure, the paste formed in step 220 includes PTFE resin powder mixed with about 15% lubricant by weight. According to yet another aspect of the disclosure, the paste formed in step 220 includes Daikin F-131 PTFE resin powder mixed with about 15% isopar by weight. However, it will be appreciated that other paste compositions may be used.
The paste raw materials may be mixed in a mixer for about ten to twenty minutes, or until the paste raw materials are thoroughly mixed. A temperature of the paste raw materials may be advantageously controlled between about 50 degrees Fahrenheit and about 60 degrees Fahrenheit during the mixing process to prevent damage to the resin powder.
Next, in step 222 the paste is cured. The paste is cured at a temperature and time duration to ensure the lubricant fully migrates into the paste powder. According to an aspect of the disclosure, the paste is cured for not less than twenty-four hours. According to another aspect of the disclosure, the past is cured at a temperature ranging from about 68 degrees Fahrenheit to about 78 degrees Fahrenheit.
In step 224, a preform mold is assembled. The preform mold may include an outer tube with dividers disposed within the tube. The tube and dividers may be fabricated from stainless steel or other similar material known to be compatible with the paste mixture formed in step 220.
In step 226, paste is delivered into the preform mold. The dividers within the mold tube may define discrete volumes within the mold that are configured to accept different compositions of paste. For example a divider having a wedge shape may be used to separate the first composition 112 from the second composition 114 to compose a preform transverse profile such as that shown in
After delivering the cured paste to the preform mold, the dividers may be removed from the preform in step 228. Then in step 230, the paste within the mold may be compressed in a preform machine. According to an aspect of the disclosure, the preform is compressed during step 230 at a pressure ranging from about 150 psig to about 190 psig.
In step 246, an end of the extrudate, downstream of the sizing die, may be coupled to a spool, where the spool is driven to rotate a predetermined speed to roll the green PTFE filament onto the spool. Between the extruder and the spool, the extrudate may pass through a heater, as shown in step 244. The heating step 244 may diffuse a portion of the lubricant from the extrudate. According to one aspect of the disclosure, a temperature within the heater during step 244 is not greater than about 500 degrees Fahrenheit. According to another aspect of the disclosure, a temperature within the heater during step 244 is about 400 degrees Fahrenheit. According to still yet another aspect of the disclosure, the extrudate does not undergo significant sintering during the heating step 244. It will be appreciated that a residence time of the extrudate through the heater during step 244 may be varied based on a length of the heater and a speed of the extrudate traveling through the heater.
During the winding step 246, the end of the extrudate coupled to the spool may be rotated substantially about a longitudinal axis of the extrudate extending from the spool, thereby imparting a helical twist to the extrudate as shown in any one of
Referring now to
According to an aspect of the disclosure, a residence time of the green filament in contact with the heated plate ranges from about 0.1 to about 0.5 seconds. According to another aspect of the disclosure, the heated plate has a length in the direction of travel of the green filament of about 3 inches.
Different from expansion of untwisted green filaments, it will be appreciated that green filaments that embody a helical twist may simultaneously and advantageously experience expansion in multiple directions during the expansion step 206.
In step 208 the green filament is stretched to reduce a transverse dimension of the green filament while maintaining a transverse profile of the filament. According to an aspect of the disclosure, a density of the green monofilament is increased to about 0.8 to about 1.5 g/cc during the stretching step 208. Alternatively, a transverse dimension of the green monofilament may be reduced during the stretching step 208 while maintaining a substantially constant density.
According to another aspect of the disclosure, the green monofilament experiences a stretch ratio ranging from about 5 to about 50 during the stretching step 208. It will be appreciated that the stretching step 208 could include a plurality of stretching steps performed in series on the same green monofilament.
Roundness of the green filament may be maintained through the stretching step 208 by using multiple passes from one godet to another godet within one draw stand to hold the green monofilament in place without using nip rolls. Further, orienting the green filament in a vertical direction, with gravity, may also promote preservation of the green filament shape through the stretching step 208.
According to some aspects of the disclosure, the expansion step 206 and the stretching step 208 can occur simultaneously or nearly simultaneously. According to other aspects of this disclosure the expansion step 206 and the stretching step 208 need not be done simultaneously or nearly simultaneously and may be done in any order.
In step 210, the green filament is sintered. According to one aspect of the disclosure, the sintering step 210 includes stretching the green filament while exposing the green filament to an environmental temperature greater than about 700 degrees Fahrenheit. It will be appreciated that various combinations of sintering temperatures and residence times at the sintering temperature may be employed to effect the desired level of filament sintering. For example, the same degree of sintering may be achieved by lower temperature with longer residence times, or higher temperatures with shorter residence times.
According to an aspect of the disclosure, the final sintered filament has a tensile strength not less than about 100,000 psi. According to another aspect of the disclosure, the final sintered filament has a density between about 0.8 and about 1.5 g/cc.
The present disclosure is applicable to filaments in general and to a filament for use as a surgical suture. Aspects of the disclosure provide a high-strength, expanded PTFE monofilament suture to users, which may include medical equipment developers or end users. The monofilament sutures may provide enhanced visual recognition properties by incorporating one or more pigment additives into the monofilament sutures. The pigment additives may be distributed throughout the suture material, or may be advantageously isolated to localized areas of the suture material to effect color patterns, including unique spiral patterns, for example. Further, radiopaque additives may be incorporated into monofilament sutures so that the sutures may be seen in X-ray images or other fluoroscopy images.
Tensile strength and visual recognition are important properties of a suture. Although conventional approaches for making expanded PTFE sutures may provide sufficient handling and abrasion resistance, Applicants identified that the conventional approaches may provide low tensile strength and may pose difficulty distinguishing the natural white color of PTFE against light or white backgrounds. In turn, Applicants identified improvements to suture tensile strength in combination with pigment additives that could improve the marketability of sutures so produced.
The colors and/or patterns incorporated in to the suture can be used to identify a suture characteristic, such as a cross sectional dimension of the suture such as a diameter or the presence or absence of other additives such as bioactive additives. Further, the colors incorporated into the suture may help users distinguish the suture against a white or light colored background, where a plain white PTFE suture would be difficult to see. Moreover, it will be appreciated that enhanced visibility of the suture material may benefit knot tying procedures.
It will be appreciated that the high-strength and/or colored expanded PTFE filament could be used alone as a monofilament suture, or alternatively, combined in a plurality of fibers as a braided suture. For example, the strength and lubricity of the expanded PTFE filament could be combined with ultra-high molecular weight polyethylene (UHMWPE) fibers to create a braid that has high strength, high lubricity, and improved abrasion resistance. Further, if the expanded PTFE filament has radiopacity, then a braided suture incorporating the expanded PTFE element may be visible during X-ray or fluoroscope imaging.
Combinations of the expanded PTFE filament with other polymer filaments, such as, polyester, polypropylene or other non-absorbable suture materials known to persons having ordinary skill in the art may be advantageous. Alternatively, expanded PTFE filaments could be combined with absorbable (i.e., absorbable by an organism) or slow-absorbing materials to make a composite braided suture that exhibited high strength, but could be at least partly absorbed by an organism, leaving just the expanded PTFE filament when it is desirable to minimize long-term implantation or to minimize the long-term profile of the device and/or repair.
It will be appreciated that the foregoing description provides examples of the disclosed apparatus and method. However, it is contemplated that other implementations of the disclosure may differ in detail from the foregoing examples. All references to the disclosure or examples thereof are intended to reference the particular example being discussed at that point and are not intended to imply any limitation as to the scope of the disclosure more generally. All language of distinction and disparagement with respect to certain features is intended to indicate a lack of preference for those features, but not to exclude such from the scope of the disclosure entirely unless otherwise indicated.
Recitation of ranges of values herein are merely intended to serve as a shorthand method of referring individually to each separate value falling within the range, unless otherwise indicated herein, and each separate value is incorporated into the specification as if it were individually recited herein. All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context.
This application is a divisional of U.S. patent application Ser. No. 14/471,716, filed Aug. 28, 2014 and entitled “High Strength Multi-Component Suture”, which claims priority to U.S. Provisional Patent Application No. 61/871,709, filed on Aug. 29, 2013 and entitled “High Strength Multi-Component Suture”, the disclosures of which are hereby incorporated by reference in their entireties.
Number | Name | Date | Kind |
---|---|---|---|
3398219 | Kelly et al. | Aug 1968 | A |
4370114 | Okamoto et al. | Jan 1983 | A |
4381274 | Kessler et al. | Apr 1983 | A |
4482516 | Bowman et al. | Nov 1984 | A |
4743480 | Campbell et al. | May 1988 | A |
5007922 | Chen et al. | Apr 1991 | A |
5024797 | Anderheggen et al. | Jun 1991 | A |
5162074 | Hills | Nov 1992 | A |
5167890 | Sasshofer et al. | Dec 1992 | A |
5227109 | Allen, III et al. | Jul 1993 | A |
5281475 | Hollenbaugh, Jr. et al. | Jan 1994 | A |
5288552 | Hollenbaugh, Jr. et al. | Feb 1994 | A |
5344297 | Hills | Sep 1994 | A |
5364699 | Hollenbaugh, Jr. et al. | Nov 1994 | A |
5429869 | McGregor et al. | Jul 1995 | A |
5462781 | Zukowski | Oct 1995 | A |
5562987 | Shimizu | Oct 1996 | A |
5686033 | Shimizu | Nov 1997 | A |
5718251 | Gray et al. | Feb 1998 | A |
5718926 | Dambrine et al. | Feb 1998 | A |
5733308 | Daugherty et al. | Mar 1998 | A |
5827611 | Forbes | Oct 1998 | A |
5845652 | Tseng et al. | Dec 1998 | A |
5848600 | Bacino et al. | Dec 1998 | A |
5869181 | Kent et al. | Feb 1999 | A |
5878758 | Bacino et al. | Mar 1999 | A |
5888651 | Hoyt et al. | Mar 1999 | A |
6238605 | Wimmer | May 2001 | B1 |
6506197 | Rollero et al. | Jan 2003 | B1 |
6551353 | Baker et al. | Apr 2003 | B1 |
6767498 | Talley, Jr. et al. | Jul 2004 | B1 |
6803102 | Talley et al. | Oct 2004 | B1 |
6833104 | Berger | Dec 2004 | B2 |
6861142 | Wilkie et al. | Mar 2005 | B1 |
6977231 | Matsuda | Dec 2005 | B1 |
6994763 | Austin | Feb 2006 | B2 |
7371253 | Leung et al. | May 2008 | B2 |
7445843 | Lutz et al. | Nov 2008 | B2 |
7524445 | Duran et al. | Apr 2009 | B2 |
7615282 | Lutz et al. | Nov 2009 | B2 |
7736576 | Walter | Jun 2010 | B2 |
7736739 | Lutz et al. | Jun 2010 | B2 |
7737060 | Strickler et al. | Jun 2010 | B2 |
7740020 | Lutz et al. | Jun 2010 | B2 |
7857829 | Kaplan et al. | Dec 2010 | B2 |
7871425 | Jones et al. | Jan 2011 | B2 |
8038712 | van der Burg et al. | Oct 2011 | B2 |
8048111 | Lutz et al. | Nov 2011 | B2 |
8048440 | Chang et al. | Nov 2011 | B2 |
8142475 | Viola | Mar 2012 | B2 |
8262694 | Widomski et al. | Sep 2012 | B2 |
20010016625 | Lahijani | Aug 2001 | A1 |
20020031628 | Zumbrum et al. | Mar 2002 | A1 |
20030082323 | Venditti et al. | May 2003 | A1 |
20040267316 | Powell et al. | Dec 2004 | A1 |
20050053783 | Almeida Neto | Mar 2005 | A1 |
20060135995 | Ruff et al. | Jun 2006 | A1 |
20060269754 | Hayashi et al. | Nov 2006 | A1 |
20080021501 | Schmieding | Jan 2008 | A1 |
20080086170 | Jones et al. | Apr 2008 | A1 |
20080243183 | Miller et al. | Oct 2008 | A1 |
20080272327 | Almeida Neto | Nov 2008 | A1 |
20090012560 | Hunter et al. | Jan 2009 | A1 |
20090032470 | Bacino et al. | Feb 2009 | A1 |
20090099597 | Isse | Apr 2009 | A1 |
20090105753 | Greenhalgh et al. | Apr 2009 | A1 |
20090143819 | D'Agostino | Jun 2009 | A1 |
20090151745 | Padinger et al. | Jun 2009 | A1 |
20100298875 | Leung et al. | Nov 2010 | A1 |
20100298876 | Leung et al. | Nov 2010 | A1 |
20100318124 | Leung et al. | Dec 2010 | A1 |
20110277249 | Abuzaina et al. | Nov 2011 | A1 |
20110282386 | Friedrich et al. | Nov 2011 | A1 |
20120109193 | Primavera et al. | May 2012 | A1 |
20120116449 | Kirsch et al. | May 2012 | A1 |
20120130406 | Odermatt et al. | May 2012 | A1 |
20120136388 | Odermatt et al. | May 2012 | A1 |
20120150194 | Odermatt et al. | Jun 2012 | A1 |
20120179198 | Schmieding et al. | Jul 2012 | A1 |
20120232588 | Stocchero et al. | Sep 2012 | A1 |
20130123839 | Sargeant et al. | May 2013 | A1 |
Number | Date | Country |
---|---|---|
2087903 | Jul 1993 | CA |
2010-110686 | May 2010 | JP |
1995001190 | Jan 1995 | WO |
1997024078 | Jul 1997 | WO |
2001012073 | Feb 2001 | WO |
2004030705 | Apr 2004 | WO |
2004113050 | Dec 2004 | WO |
2007053866 | May 2007 | WO |
Entry |
---|
Aybek et al. “Seven years' experience with suture annuloplasty for mitral valve repair” Surgery for acquired Cardiovascular Disease, 2006, 131, pp. 99-106. |
Chandler-Temple et al. “Expanded poly(tetrafluoroethylene): from conception to biomedical devices” Chemistry in Australia, 2008, 75(8), pp. 3-6. |
David et al. “Chordal replacement with polytetrafluoroethylene sutures for mitral valve repari: A 25-year experience” Journal of Thoracic and Cardiovascular Surgery, [available online Jun. 17, 2012], Corrected Proof. |
Hertweck et al. “Tensile characteristics of PTFE sutures” Biomaterials, 1988, 9(5), pp. 457-459. |
Hiruma et al. “Ion beam modification of ePTFE for improving the blood compatibility” Surface & Coatings Technology, 2011, 206, 905-910. |
Joseph et al. “Randomised Controlled Trial to Evaluate the Efficacy of TachoComb H Patches in Controlling PTFE Suture-hole Bleeding” Eur J Vasc Endovasc Surg, 2004, 27, pp. 549-552. |
Minatoya et al. “Pathologic aspects of polytetrafuoroethylene sutures in human heart” The Annals of Thoracic Surgery, 1996, 61(3), pp. 883-887. |
International Search Report dated Nov. 28, 2014 for PCT/US2014/053118 filed Aug. 28, 2014. |
European Search Report issued in European Patent Application No. 14839555.1, dated Oct. 4, 2016. |
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20180250003 A1 | Sep 2018 | US |
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61871709 | Aug 2013 | US |
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Parent | 14471716 | Aug 2014 | US |
Child | 15974247 | US |