US20180296312A9

US20180296312A9 - Absorbable/biodegradable composite yarn constructs and applications thereof

Info

Publication number: US20180296312A9
Application number: US14/262,845
Authority: US
Inventors: Shalaby W. Shalaby; Shawn Peniston; Scott Taylor; Douglas D. Greene
Original assignee: Poly Med Inc
Current assignee: Poly Med Inc
Priority date: 2005-04-26
Filing date: 2014-04-28
Publication date: 2018-10-18
Also published as: US20140309667A1; US10085826B2; JP2009022728A; US10098722B2; EP2016956A2; US10856960B2; CN101348972A; EP2016956B1; US20090024162A1; CN101348972B; US20210128288A1; US8709023B2; EP2016956A3; US20150305848A1; JP5336061B2; US20190083222A1

Abstract

Absorbable composite medical devices such as surgical meshes and braided sutures, which display two or more absorption/biodegradation and breaking strength retention profiles and exhibit unique properties in different clinical settings, are made using combinations of at least two types of yarns having distinctly different physicochemical and biological properties and incorporate in the subject construct special designs to provide a range of unique properties as clinically useful implants.

Description

This is a continuation-in-part of PCT Application Serial No. 2006014939 filed on Apr. 20, 2006, which claimed the benefit of a prior provisional application U.S. Ser. No. 60/674,826 filed on Apr. 26,2005.

FIELD OF THE INVENTION

This invention relates to composite warp knitted and braided constructs, each comprising two types of yams having significantly different absorption/biodegradation and strength retention profiles to produce warp-knitted meshes and braided sutures exhibiting bimodular changes in their properties when used as surgical implants.

BACKGROUND OF THE INVENTION

Blending of non-absorbable fibers having distinctly different individual physicochemical properties is a well-established practice in the textile industry and is directed toward achieving unique properties based on the constituent fibers in such blends. The most commonly acknowledged examples of these blends include combinations of (1) wool staple yarn and polyethylene terephthalate (PET) continuous multifilament yarn to produce textile fabrics which benefit from the insulating quality of wool and high tensile strength of the polyester; (2) cotton staple yarn and PET continuous multifilament yarn to produce water-absorbing, comfortable (due to cotton), strong (due to PET) fabrics; (3) nylon continuous multifilament yam and cotton staple yam to achieve strength and hydrophilicity; and (4) cotton staple yarn and polyurethane continuous monofilament yarn to yield water-absorbing, comfortable elastic fabrics. The concept of blending non-absorbable and absorbable fibers was addressed to a very limited extent in the prior art relative to combining polypropylene (PP) with an absorbable polyester fiber in a few fibrous constructs, such as hernial meshes, to permit tissue ingrowth in the PP component of these meshes and reducing long-term implant mass, as the absorbable fibers lose mass with time. However, the use of totally absorbable/biodegradable blends of two or more yams to yield fibrous properties that combine those of the constituent yarns is heretofore unknown in the prior art, This provided the incentive to pursue this invention, which deals with totally absorbable/biodegradable composite yarns having at least two fibrous components and their conversion to medical devices, such as sutures and meshes, with modulated, integrated physicochemical and biological properties derived from the constituent yarns and which can be further modified to exhibit specific clinically desired properties.
A key feature of having an absorbable/biodegradable surgical implant comprising at least two differing fibrous components, which, in turn exhibit different absorption and strength retention profiles has been disclosed in the present parent application PCT Serial No. 2006014939. However, these applications did not describe any specifically new construct design of devices such as surgical sutures and hernial meshes, which are responsible for achieving novel clinical properties. Accordingly, this invention is directed to novel construct designs made of fully absorbable/biodegradable surgical sutures, especially those used in slow-healing tissues and surgical meshes such as those used in hernial repair and vaginal tissue reconstruction.

SUMMARY OF THE INVENTION

Generally, the present invention is directed to warp knitted composite meshes and braided composite sutures comprising slow-absorbable/biodegradable and fast-absorbable/biodegradable components, specially sized and constructed to produce surgical devices having unique properties.
One major aspect of this invention is directed to a warp-knitted composite mesh with a minimum area density of 50 g/m², which includes (a) a slow absorbing/biodegradable multifilament yarn component having individual filament diameter of less than 20 micron; and (b) a fast-absorbing multifilament yarn component having individual filament diameter exceeding 20 micron, wherein the slow-absorbing/biodegradable multifilament component is a segmented copolymer made of molecular chains comprising at least 80 percent of l-lactide-based sequences and the fast-absorbing multifilament component is a segmented polyaxial copolymer made of molecular chains comprising at least 70 percent of glycolide-derived sequences, and wherein the slow-absorbing multifilament component is knitted in a 2-bar sand-fly net pattern and the fast-absorbing multifilament component is knitted in a standard 2-bar marquisette pattern, with all guide bars threaded 1-in and 1-out, using a warp knitting machine. Alternatively, the slow-absorbing multifilament component is knitted in 2-bar full tricot pattern and the fast-absorbing multifilament component yarn is knitted in a standard 2-bar marquisette pattern with all guide bars threaded 1-in and 1-out, using a warp knitting machine.
A clinically important aspect of this invention is the provision of a composite mesh having an area weight of about 130 g/m²and exhibiting a maximum burst force of at least 250 N and a maximum elongation of less than 10 percent under a 16 N force per cm of mesh width, and when incubated in buffered solution at pH 7.2 and 50° C. for about 2 weeks retains more than 20 percent of its maximum burst force and undergoes at least 12 percent elongation under a force of 16 N per cm of mesh width.
Alternatively, the slow-absorbing/biodegradable multifilament yarn component of the mesh comprises a poly-3-hydroxyalkanoate made of molecular chains consisting of at least 50 percent of 3-hydroxybutyric acid-derived sequences.
This invention also deals with a warp-knitted composite mesh with a minimum area density of 50 g/m², comprising (a) a slow absorbing/biodegradable multifilament yarn component having individual filament diameter of less than 20 micron; and (b) a fast-absorbing multifilament yarn component having individual filament diameter exceeding 20 micron, wherein said mesh is coated with an absorbable polymer at a coating add-on of at least 0.1 percent based on the uncoated mesh weight. Optionally, the coating comprises a polyaxial copolyester made of molecular chains comprising about 95/5 ϵ-caprolactone-/glycolide-derived sequences, wherein the coating contains at least I bioactive agent selected from those groups known for their antineoplastic, anti-inflammatory, antimicrobial, anesthetic and cell growth-promoting activities.
Another major aspect of this invention deals with a braided composite suture comprising (a) a slow-absorbing/biodegradable multifilament yarn component having individual filament diameter of less than 20 micron, and capable of retaining at least 20 percent of its initial breaking strength when tested individually as a braid and incubated in a phosphate buffer at pH 7.2 and 50° C. for about 2 weeks; and (b) a fast-absorbing/biodegradable multifilament yarn component capable of retaining at least 20 percent of its initial breaking strength when tested individually as a braid and incubated in a phosphate buffer at pH 7.2 and 50° C. for about I day. In one embodiment the slow-absorbing/biodegradable and fast-absorbing/biodegradable multifilament components constitute the core and sheath of the braid, respectively. Alternatively, the slow-absorbing/biodegradable and fast-absorbing/biodegradable multifilament components constitute the sheath and core of the braid, respectively.
In terms of the chemical composition of the composite suture, in one embodiment the slow-absorbing/biodegradable multifilament component comprises a segmented copolymer made of the molecular chains consisting of at least 80 percent of l-lactide-derived sequences and the fast-absorbing/biodegradable multifilament component comprises a segmented polyaxial copolymer made of molecular chains consisting of at least 70 percent of glycolide-derived sequences. Alternatively, the slow absorbable/biodegradable multifilament component comprises silk, or a poly-3-hydroxyalkanoate made of a molecular chain consisting of at least 50 percent of 3-hydroxybutyric acid-derived sequences.
Additional aspects of this invention deal with a braided composite suture as described above coated with an absorbable polymer at a coating add-on of at least 0.1 percent based on the uncoated suture weight. Optionally, the coating comprises a polyaxial copolyester made of molecular chains comprising about 95/5 ϵ-caprolactone-/glycolide-derived sequences, wherein the coating contains at least one bioactive agent selected from those groups known for their antineoplastic, anti-inflammatory, antimicrobial, anesthetic and cell growth-promoting activities.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

During the first one to two days of introducing an implant in living tissue, an acute inflammation prevails at the implant site. This is manifested as redness, heat, swelling and pain. After about day three, any persistent local inflammatory response to the implant subsides. When a non-absorbable material is implanted, the acute inflammation persists for less than a week and the development of a fibrous connective tissue around the implant progresses for about a month, leading to a generally static, fibrous capsule. A long-term separation of the non-absorbable implant from surrounding tissues by the capsule can lead to complications. Depending on the type of implant site, these complications may (1) increase the risk of infection and (2) interfere with the integration of the implant components with surrounding tissue leading to mechanical instability, as in the case of hernial meshes. On the other hand, if the implant material biodegrades/absorbs over time, the inflammation can be restimulated, incrementally, during the implant residence time period at the site, a feature which can be most desirable in certain applications. These include surgical meshes used in hernial repair, where an incremental restimulation of inflammation can result in controlled and persistent collagen deposition and mechanical integration with the fibrous components of the mesh leading to critically needed mechanical stability. Obviously, one should not expect this to terminate after the first three or four weeks following implantation leading to catastrophic mechanical failure of the mesh. Additionally, the incremental restimulation of inflammation and controlled collagen deposition can be achieved through (1) movement of the mesh components and/or at the mesh-tissue interface; (2) providing continually increased porosity in the mesh to permit progressively increasing facile fibroblast migration; and (3) having structurally stable mesh construction that resists tear and unraveling under dynamic mechanical stresses. And, optimally, the mesh components should be designed to (I) exhibit at least two absorption/strength retention profiles, one that prevails during the first two to four weeks and a second which will be responsible for continued restimulation beyond four weeks; (2) display sufficient mechanical strength and stiffness in the first three to four weeks during which collagen is deposited and the mechanical load at the site commences to be shared between the mesh and surrounding tissue without experiencing premature deformation; (3) accommodate the biomechanical events associated with wound healing and tissue shrinkage, as well as incremental dynamic stresses due to regular motions of active patients, through an incremental increase in the engineering compliance of the mesh; and (4) have a carefully warp-knitted construction that accommodates mechanical changes at the implant site while resisting tearing and breaking/unraveling at the tissue-mesh interface and/or within the mesh construct itself.
In concert with the aforementioned discussion, the present invention addresses the requirements set forth for an optimal mesh. Similarly, it addresses the requirements of an optimum suture that is expected to provide an effective ligation for three to four weeks as well as up to a few months following implantation, as would be required for wound repairs of compromised and slow-healing tissues.
A key general aspect of this invention is directed to a warp-knitted composite mesh with minimum density of 50 g/m²to ensure having adequate mass and strength to allow anchoring to the natural tissue, using a suture and/or absorbable adhesive, without tearing, unraveling, and/or breaking immediately after placement and during the first few weeks of functional performance. This is to prevent mechanical failure at the tissue-mesh interface or within the mesh components. For anchoring the mesh to the biological site, an absorbable suture of choice will be expected to maintain a strength retention profile that parallels that of a long-lasting component of the composite mesh. Meanwhile, the composite mesh is expected to comprise (1) a slow-absorbing/biodegradable, multifilament yarn component having individual filament diameter of less than 20 micron and preferably less than 15 micron as the main, relatively more flexible matrix of the mesh, which retains a measurable breaking strength for at least six weeks and preferably for more than eight weeks; (2) a fast-absorbing/biodegradable, multifilament yarn component having individual filament diameter of more than 20 micron and preferably exceeding 25 micron, as the minor, relatively less flexible component of the mesh that will be responsible for providing adequate initial rigidity of the mesh, and facile anchoring to the surrounding tissues, while exhibiting a brief breaking strength profile of about two to four weeks—this is to allow the slow-absorbing flexible matrix to become progressively more extensible at about two to four weeks following implantation; and (3) a slow- and fast-absorbing multifilament components in specially designed warp-knitted construction to ensure their mechanical interdependence in terms of load-bearing contributions and ability to anchor to the surrounding tissue using an absorbable tissue adhesive, absorbable suture, or a combination, for example, of an absorbable cyanoacrylate-based adhesive and an absorbable suture—a useful illustration of such warp-knit construction entails knitting the slow-absorbing multifilament component in a 2-bar, sand-fly net pattern and the fast-absorbing component in a standard 2-bar marquisette pattern, with all guide bars threaded 1-in and 1-out in 18 gauge using preferably a Raschel or tricot knitting machine. An alternative composite mesh construction entails knitting the slow-absorbing component using a 2-bar full tricot pattern and the fast-absorbing component using a standard 2-bar marquisette pattern, with all guide bars threaded 1-in and 1-out in 18 gauge. The warp construction can be achieved using other patterns. To improve the initial burst strength of the composite mesh through minimizing the fiber-to-fiber friction coefficient and hence minimize the fraying of the mesh structure, a lubricant coating is applied to the mesh at a level of 0.1 to 10 percent based on the mesh uncoated weight. The absorbable coating can also be used as a carrier for the controlled release of one or more bioactive agents belonging to one or more group of drugs known for their antimicrobial, anti-adhesion, and growth-promoting agents. The ideal coating system can be a crystalline, easy-to-apply, lubricious polymeric system that provides surface lubricity and its composition can be controlled to assist in modulating the absorption/biodegradation profile of the fast-absorbing component at least in the first two weeks following implantation.
Although slow- and fast-absorbable/biodegradable components of the composite are, so far, described as multifilament yarns, which are warped independently, other alternative approaches can be used entailing (I) plying the fast- with the slow-absorbable/biodegradable yarns prior to warping; (2) using one or more additional yarns with a moderate or fast absorption/biodegradation profile; (3) using the fast-absorbing component as a single or two-ply monofilament; (4) using a yarn component based on an elastomeric polymer—this can be in the form of a fast-, moderate- or faster-absorbing monofilament, 2-ply monofilament or multifilament. The use of elastomeric components is expected to accommodate any transient change in stress at the application site at the initial period of implantation when inflammation-induced swelling is encountered. To further modulate the performance of the composite mesh, enzymatically biodegradable, multifilament yarn can be used as the slow-biodegrading component. Such yarns include those based on silk fibroin, poly-4-hydroxyalkanoate, casein, chitosan, soy protein, and similar naturally derived materials with or without chemical modification to modulate their biodegradation and breaking strength retention profiles.
Another key general aspect of this invention is directed to a braided suture comprising at least two absorbable/biodegradable monofilament and/or multifilament yarn components having a range of absorption/biodegradation and breaking strength retention profiles. The rationale for invoking such a diversity in the components constituting the composite braid is practically similar to that noted above for composite mesh, with the exception of the fact that in constructing the braid, there is an additional degree of freedom, namely, having a core and sheath as the basic structural components of the braid. Meanwhile, the braid construction may entail (1) using variable ratios of the core-to-sheath without encountering core popping; (2) having slow-absorbable/biodegradable, multifilament yam as the core or sheath with the balance of braid consisting of a fast-absorbable/biodegradable multifilament yarn; (3) using elastomeric monofilament, plied monofilament or multifilament yarn as part of the braid construct and preferably in the core at variable levels to impart a controlled level of elasticity—this is to accommodate site swelling during the first few days following suture implantation. The composite suture can be coated to (1) improve its tie-down and handling properties; (2) possibly prolong the breaking strength retention profile; and (3) function as an absorbable carrier for the controlled release of one or more bioagent selected from the groups known for their antimicrobial, anti-adhesion, antithrombogenic, antiproliferative, antineoplastic, anti-inflammatory, and cell growth-promoting activities. The coating can also be used to allow the controlled and timely delivery of anesthetic agents to mediate pains following surgery. A useful feature of using a coating with an antineoplastic agent allows the use of the composite suture in cancer patients to minimize the likelihood of metastasis. Another useful feature is the use of the composite suture in anchoring synthetic vascular graft and perivascular wrap where (1) having two or more absorption/biodegradation profiles can allow accommodating physicomechanical changes at the suture line due to prevailing biological events; and (2) using antithrombogenic and/or antiproliferative agents can be beneficial in maintaining the long-term patency of the graft.
A clinically important aspect of this invention deals with bioactive meshes comprising a coating containing an antineoplastic, anti-inflammatory, and/or antiproliferative agent that allows the use of the composite mesh as vascular wrap in the management of vascular embolism.
Further illustrations of the present invention are provided by the following examples:

EXAMPLE 1

Preparation of Yarns I and H For Composite Mesh Construction

A segmented l-lactide copolymer (P1) prepared by the copolymerization of a mixture of an 88/12 (molar) l-lactide/trimethylene carbonate [following the general polymerization methods described in U.S. Pat. No. 6,342,065 (2002)] was melt-spun using a 20-hole die to produce multifilament Yarn I—this is used as the slow-absorbable/biodegradable component of certain composite meshes. The extruded multifilament yarn was further oriented using a one-stage drawing over a heated Godet at about I00-120° C. prior to its use for knitted mesh construction. Typical properties of Yarn I are shown below, For producing Yarn II, the fast-absorbing/biodegradable component of the composite mesh, a polyaxial, segmented glycolide copolymer (P2), made by ring-opening polymerization of a combination of an 88/7/5 (weight) glycolide/trimethylene carbonate/l-lactide [using the general polymerization method described in U.S. Pat. No. 7,129,319 (2006)] was melt-spun using a 10-hole die and oriented by in-line drawing. Typical properties of Yarn II and the form used in knitting are shown below.

- Key properties of Yarns I and II:
- Yarn I (2-ply natural yarn)
  - Fiber Count: 43
  - Denier Range: 80-100 g/9000 m
  - Tenacity Range: 1.8 to 4.5 g/denier
  - Ultimate Elongation: 20-30%
- Yarn II (1-ply natural yarn)
  - Fiber Count: 10
  - Denier Range: 120-170 g/9000 m
  - Tenacity Range: 3.5-5.5 g/denier
  - Ultimate Elongation: 40-70%

EXAMPLE 2

General Method For Composite Mesh Construction

Compositions consisting of Yarns I and II which possess different degradation profiles (one relatively fast degrading and one slow degrading) were constructed using various knitting patterns to construct the desired warp-knitted meshes. Knit constructions were produced using a two-step process of warping yarn onto beams and constructing meshes using a typical Raschel or tricot knitting machine. Various knitting patterns and weight ratios of I to H can and were varied to modulate mechanical properties of the specific mesh. Knit constructions can be made from multifilament yarn, monofilament yarn, or combinations thereof. Knit mesh was heat set or annealed at 120° C. for 1 hour while under constant strain in the wale and course directions. Coating can be applied following annealing to modify the in vivo and/or in vitro characteristics.

EXAMPLE 3

Knitting Process of Mesh Pattern A

The knitting process utilized two warped beams of Yarn 1, threaded on bars 1 and 2, and two warped beams of Yarn II threaded on bars 3 and 4. The knitting machine was equipped with 18-gauge needles. Yarn II was knitted in a 2-bar marquisette pattern and Yarn I was knitted in a 2-bar sand-fly net pattern with all guide bars for each pattern threaded 1-in and 1-out in 18 gauge.

- Pattern A (28 courses per inch)
- Bar 1—1-0/1-212-3/2-1//2x (1-in, 1-out)
- Bar 2—2-3/2-1/1-0/1-2112x (1-in, 1-out)
- Bar 3—1-0/0-1//4x (1-in, 1-out)
- Bar 4—0-0/3-3//4x (1-in, 1-out)

EXAMPLE 4

Knitting Process of Mesh Pattern-B

The knitting process utilized two warped beams of Yarn I threaded on bars 1 and 2 and two warped beams of Yarn II, threaded on bars 3 and 4. The knitting machine was equipped with 18-gauge needles. Yarn II was knitted in a 2-bar marquisette pattern and Yarn I was knitted in a 2-bar full tricot pattern with all guide bars for each pattern threaded 1-in and 1-out in 18 gauge.

- Pattern B (19 courses per inch)
- Bar 1—1-0/2-3//4x (1-in, 1-out)
- Bar 2—2-3/1-0//4x (1-in, 1-out)
- Bar 3—1-0/0-1//4x (1-in, 1-out)
- Bar 4—0-0/3-3//4x (1-in, 1-out)

EXAMPLE 5

Characterization and In Vitro Evaluation of Typical Composite Meshes From Example 3

Testing Methods For Meshes from Example 3
Mechanical properties were characterized using the ball burst testing apparatus with physical characteristics based on the ASTM D3787-01 guideline for the fixture geometry (25.4 mm polished steel ball, 4.445 cm diameter inside opening). The mesh was clamped in the fixture without any applied tension and the ball was positioned in the center of the 4.445 mm diameter opening. The ball is then brought down to a position on the mesh such that a 0.1N force is applied. The test is initiated and the ball travels at 2.54 cm/min until failure characterized by the point of maximum load. For each test the following three characteristics were recorded with standard deviation values for n=4 sample sizes:

1) Maximum burst force obtained during the test (N)
2) The extension at the maximum load (mm)
3) The extension at 71N load (mm)

The extension at 71N is used to determine the 16N/cm elongation. The value of 71N is derived from the diameter of the opening (4.445 cm×16N/cm=71N). Initially the mesh has a 44.45 mm diameter and is all in one plane. As the test progresses the ball pushes the mesh downward and creates a cone like shape with the radius of the ball as the tip. Using CAD and curve fitting software a mathematical expression which relates the linear travel of the ball to the change in length of a line that passes under the center of the ball and up to the original 44.45 mm diameter (radial distension) was developed. From this information the percent elongation was determined
In vitro conditioned burst strength retention [BSR=(max. load at time point/initial max. load)*100] was conducted using a MTS MiniBionix Universal Tester (model 858) equipped with a burst test apparatus as detailed in ASTM D3787-01. Samples were tested initially, after in vitro conditioning using a 0.1M solution of buffered sodium phosphate at a 12.0pH in 50 mL tubes for 10 days, and after conditioning using a 0.1M solution of buffered sodium phosphate at a 7.2pH in 50 mL tubes for multiple time points of interest. Tubes were placed in racks and incubated at 50° C. under constant orbital-agitation. Samples were removed at predetermined time points for mechanical properties testing (n=3).

Physical Properties of a Typical Warp-knit Composite Mesh From Example 3

TABLE I

Pattern A Warp Knit Composite Mesh Physical Properties

Knitting	Area Weight	Yarn II Content
Patterrn	(g/m²⁾	(weight %)

Pattern A	132	40

Mechanical Properties of Meshes From Example 3

TABLE II

Pattern A Warn Knit Com osite Mesh Initial Burst Properties

		Elongation	Elongation
Sample	Max. Burst	at Max	at 71 N	Elongation at
Description	Force (N)	Force (mm)	Force (mm)	16 N/cm (%)

Pattern A	356	14.6	6.8	5.2

TABLE III

Properties of Pattern A Warp Knit Composite Mesh
Following Accelerated In Vitro Conditioning 12 H, 50° C., 10 days

		Elongation	Elongation
Sample	Max. Burst	at Max	at 71 N	Elongation at
Description	Force (N)	Force (mm)	Force (mm)	16 N/cm (%)

Pattern A	194	21.5	15.8	25.6

TABLE IV

Properties of Pattern A Warp Knit Composite Mesh Due to Accelerated In
Vitro A in (7.2 pH, 50° C.

		Max.
In Vitro	BSR	Burst	Elongation at	Elongation at	Elongation at
Duration	(%)	Force	Max Force	71 N Force	16 N/cm Force

0 days	—	352	14.29	6.52	4.76
3 days	106.3	374	14.71	6.84	5.28
7 days	44.9	158	14.24	7.92	7.14
11 days	59.1	208	18.89	13.13	18.38
14 days	55.7	196	19.63	14.31	21.46
18 days	52.6	185	17.98	13.20	18.56
21 days	55.4	195	18.44	13.21	18.59
35 days	51.4	181	17.88	13.54	19.43
56 days	36.9	130	16.37	14.01	20.66

EXAMPLE 6

Characterization and In Vitro Evaluation of Typical Composite Meshes From Example 4

Testing Methods For Meshes From Example 4

Mechanical properties testing was conducted using a MTS MiniBionix Universal Tester (model 858) equipped with a burst test apparatus as detailed in ASTM 1)3787-01. Samples were tested initially and after being conditioned using a 0.1M solution of buffered sodium phosphate at a 12.0pI-1 in 50 mL tubes for 10 days. Tubes were placed in racks and incubated at 50° C. under constant orbital-agitation. Samples were removed at predetermined time points for mechanical properties testing (n=3).

Physical Properties of a Typical Warp-knit Composite Mesh From Example 4

TABLE V

Pattern B Warp Knit Composite Mesh Tabulated Physical Properties

Knitting		Yarn B Content
Pattern	Area Weight (g/m)²	(weight %)

Pattern B	135	31

Mesh Resultant Mechanical Properties From Example 4

TABLE VI

Pattern B Warp Knit Composite Mesh Initial Burst Properties

		Elongation at	Elongation at	Elongation at
Sample	Max. Burst	Max Force	71 N Force	16 N/cm
Description	Force (N)	(mm)	(mm)	(°/0)

Pattern B	436	16.3	7.1	5.7

TABLE VII

Properties of Pattern B Warp Knit Composite Mesh Following
Accelerated In Vitro Conditioning 12 H, 50° C., 10 days,

		Elongation	Elongation
Sample	Max. Burst	at Max	at 71 N	Elongation at
Description	Force (N)	Force (mm)	Force (mm)	16 N/cm (/0)

Pattern B	240	19.4	13.2	18.5

EXAMPLE 7

Preparation of Yarn III For Composite Braid Construction

The same polymer precursor, P2, described in Example 1 was used in preparing multifilament Yarn III. The polymer was melt-spun using a 20-hole die to produce multifilament Yarn III, which was further oriented using one-stage drawing over a heated Godet at about 100-120° C., prior to its use in braid construction.

EXAMPLE 8

Construction of Composite Braid SM1-1 Comprising a Yarn I-Core and Yarn III-Sheath

Braid SM1-1 was prepared using a 4-carrier core of Yarn I as single ply and 8-carrier Yarn III as 3-ply. The braid was hot-stretched to about 5-10 percent of its initial length using heated air at about 90° C. to tighten the braid construction. The strained braid was then annealed at 110° C. for 1 hour to yield a braided suture having about 110 ppi and a diameter of about 0.35 MM.

EXAMPLE 9

Construction of Composite Braid SM1-2 Comprising a Yarn III-Core and Yarn I-Sheath

Braid SM1-2 was prepared using a 6-carrier core of Yarn III as single ply and 16-carrier sheath of Yarn I as single ply. The braid was hot stretched and annealed as described in Example 8 to yield a braided suture having about 50 ppi and a diameter of about 0.36.

EXAMPLE 10

In Vitro and In Vivo Evaluation of Braids SM1-1 and SM1-2 Suture Properties

The braids were sterilized with ethylene oxides and tested for their (1) initial physical properties; (2) accelerated in vitro breaking strength retention profile at pH 7.2 and 50° C.; and (3) in vivo breaking strength retention using a subcutaneous rat model. The results of the in vitro and in vivo evaluation are summarized in Table VIII.

TABLE VIII

In Vitro and In Vivo Properties of Composite Braids SMI-1 and SMI-2

Experiment	Braid SMI-1	Braid SMI-2

Physical Properties:
Diameter, mm	0.35	0.36
Initial Strength, Kpsi (N)	54.4 (36.1)	52.4 (36.7)
Elongation, %	45	41
Knot Max. Load, N	24.7	23.7
In vitro Breaking Strength Retention (BSR)	85, 50, 24	81, 80, —
at

In-Vivo BSR at Percent at	Weeks 1 and 2	21, 19	76, 76
	Weeks 2 and 3	43, 25	81, 77

Preferred embodiments of the invention have been described using specific terms and devices. The words and terms used are for illustrative purposes only. The words and terms are words and terms of description, rather than of limitation. It is to be understood that changes and variations may be made by those of ordinary skill art without departing from the spirit or scope of the invention, which is set forth in the following claims. In addition it should be understood that aspects of the various embodiments may be interchanged in whole or in part. Therefore, the spirit and scope of the appended claims should not be limited to descriptions and examples herein.

Claims

1-19. (canceled)

20. An absorbable/biodegradable surgical implant comprising at least first and second fibrous components, the fibrous components having differing absorption profiles and differing strength retention profiles in the biological environment, the first and second fibrous components form a knitted mesh; and

wherein the first and second fibrous components comprise an absorbable copolyester derived from cyclic monomers selected from the group consisting of glycolide, l-lactide, e-caprolactone, trimethylene carbonate, p-dioxanone, 1,5-dioxepan-2-one, and morpholine-2,5-dione, or mixtures of same;

wherein the first individual fibrous component further comprises a slow absorbing copolyester and the second fibrous component comprises a fast absorbing copolyester.

21. An absorbable/biodegradable surgical implant as set forth in claim 20 wherein the fast absorbing copolyester comprises glycolide.

22. An absorbable/biodegradable surgical implant as set forth in claim 20 wherein the slow absorbing copolyester comprises l-lactide.

23. An absorbable/biodegradable surgical implant as set forth in claim 20 in the form of a braided suture.

24. An absorbable/biodegradable surgical implant as set forth in claim 20 in the form of a knitted mesh construct for use in hernial repair.

25. An absorbable/biodegradable surgical implant as set forth in claim 1 in the form of a woven mesh construct.

26. An absorbable/biodegradable surgical implant as set forth in claim 23 wherein the suture further comprises a coating, the coating comprising an absorbable polymer to improve tie-down properties and minimize tissue drag.

27. An absorbable/biodegradable surgical implant as set forth in claim 24 wherein the mesh further comprises a surface coating, the coating comprising an absorbable polymer to modulate the construct permeability to biological fluids and tissue ingrowth into the construct.

28. An absorbable/biodegradable surgical implant as set forth in claim 25 wherein the mesh further comprises a surface coating, the coating comprising an absorbable polymer to modulate the construct permeability to biological fluids and tissue ingrowth into the construct.

29. An absorbable/biodegradable surgical implant as set forth in claim 20 in the form of a device for use as a tissue-engineered hernial repair patch.

30. An absorbable/biodegradable surgical implant as set forth in claim 20 in the form of a device for use as a tendon, ligament, or vascular graft.

31. An absorbable/biodegradable surgical implant as set forth in claim 20 in the form of a tubular knitted mesh.

32. An absorbable/biodegradable surgical implant as set forth in claim 31 wherein the mesh further comprises a thin absorbable film insert.

33. An absorbable/biodegradable surgical implant as set forth in claim 32 wherein the mesh and the film insert are in the form of a compressed, three-layer sheet construct for use in hernial repair.

34. An absorbable/biodegradable surgical implant as set forth in claim 33 wherein the three-layer sheet construct further comprises an absorbable coating.

35. An absorbable/biodegradable surgical implant as set forth in claim 20 further comprising an absorbable polyester coating comprising a bioactive agent, the bioactive agent selected from the group consisting of antimicrobial agents, analgesic agents, antineoplastic agents, anti-inflammatory agents, and cell growth promoters.

36. An absorbable/biodegradable surgical implant as set forth in claim 20 wherein the fibrous components comprise at least two differing yarns, at least one comprising a multifilament and at least one comprising a monofilament yarns, each comprising a different polyester made from at least one monomer selected from the group consisting of glycolide, l-lactide, ϵ-caprolactone, p-dioxanone, trimethylene carbonate, l,5-dioxepan-2-one, and a morpholinedione or mixtures thereof, by ring-opening polymerization in the presence of an organometallic catalyst and an organic initiator.

37. An absorbable/biodegradable surgical implant as set forth in claim 36 in the form of a coated or uncoated jersey knit mesh.

38. An absorbable/biodegradable surgical implant as set forth in claim 36 in the form of a coated or uncoated warp knit mesh.

39. An absorbable/biodegradable surgical implant as set forth in claim 36 in the form of a coated or uncoated woven mesh.

40. An absorbable/biodegradable surgical implant as set forth in claim 36 in the form of a device for hernial repair, vascular tissue repair, producing vascular grafts or tissue engineering.

41. An absorbable/biodegradable surgical implant as set forth in claim 36 in the form of a coated or uncoated suture comprising a monofilament core and a braided sheath.

42. An absorbable/biodegradable surgical implant as set forth in claim 36 further comprising a coating comprising an absorbable polyester having a melting temperature of less than 100° C.

43. An absorbable/biodegradable surgical implant as set forth in claim 42 wherein the coating comprises at least one bioactive agent selected from the group consisting of antimicrobial agents, anti-inflammatory agents, antineoplastic agents, anesthetic agents, and growth promoting agents.

44. An absorbable/biodegradable surgical implant comprising at least first and second components, the components having differing absorption profiles and differing strength retention profiles in the biological environment, the first and second components form a knitted mesh; and

wherein the first and second components comprise an absorbable copolyester derived from cyclic monomers selected from the group consisting of glycolide, l-lactide, -caprolactone, trimethylene carbonate, p-dioxanone, 1,5-dioxepan-2-one, and morpholine-2,5-dione, or mixtures of same;

wherein the first individual component comprises a slow absorbing copolyester comprising l-lactide and the second component comprises a fast absorbing copolyester comprising glycolide.