EP0132376B1 - Faserige Strukturen - Google Patents
Faserige Strukturen Download PDFInfo
- Publication number
- EP0132376B1 EP0132376B1 EP84304891A EP84304891A EP0132376B1 EP 0132376 B1 EP0132376 B1 EP 0132376B1 EP 84304891 A EP84304891 A EP 84304891A EP 84304891 A EP84304891 A EP 84304891A EP 0132376 B1 EP0132376 B1 EP 0132376B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- filaments
- polymeric composition
- composition
- portions
- fibrous structure
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 230000006872 improvement Effects 0.000 title description 2
- 239000000203 mixture Substances 0.000 claims abstract description 52
- 238000000034 method Methods 0.000 claims abstract description 15
- 238000004519 manufacturing process Methods 0.000 claims abstract description 6
- 230000007704 transition Effects 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 2
- 230000000704 physical effect Effects 0.000 claims description 2
- 230000008569 process Effects 0.000 abstract description 6
- 238000005421 electrostatic potential Methods 0.000 abstract description 2
- 239000000835 fiber Substances 0.000 abstract description 2
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 description 30
- 229920002635 polyurethane Polymers 0.000 description 10
- 239000004814 polyurethane Substances 0.000 description 10
- 230000002792 vascular Effects 0.000 description 9
- 239000000243 solution Substances 0.000 description 7
- 230000008859 change Effects 0.000 description 5
- 238000010041 electrostatic spinning Methods 0.000 description 5
- 230000008901 benefit Effects 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 230000018109 developmental process Effects 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 238000010926 purge Methods 0.000 description 3
- 238000009987 spinning Methods 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 241000282465 Canis Species 0.000 description 1
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 210000001772 blood platelet Anatomy 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- KAQKFAOMNZTLHT-VVUHWYTRSA-N epoprostenol Chemical compound O1C(=CCCCC(O)=O)C[C@@H]2[C@@H](/C=C/[C@@H](O)CCCCC)[C@H](O)C[C@@H]21 KAQKFAOMNZTLHT-VVUHWYTRSA-N 0.000 description 1
- 229960001123 epoprostenol Drugs 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 229960002897 heparin Drugs 0.000 description 1
- 229920000669 heparin Polymers 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- -1 polytetrafluorethylene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Images
Classifications
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/70—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres
- D04H1/72—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged
- D04H1/728—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged by electro-spinning
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
- D04H3/08—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating
- D04H3/16—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating with bonds between thermoplastic filaments produced in association with filament formation, e.g. immediately following extrusion
Definitions
- the invention relates to fibrous structures, for example fibrous mats or fibrous tubular structures. More particularly but not exclusively, the invention relates to fibrous synthetic vascular grafts.
- different polymeric composition is intended to cover a variation of the composition of the filaments where the polymer itself does not change across the structure but, for example, an additive is present in the composition at one side of the structure but not present at the opposite side of the structure.
- the structure may comprise a transition area between the sides of the structure, and the portions of the filaments in the transition area may have a polymeric composition comprising a mixture of the first and second polymeric compositions.
- the polymeric composition of the filaments may vary progressively between the two sides of the structure, and the composition of the portions of the filaments in the transition area adjacent the one side of the structure may contain a large proportion of the first polymeric composition and the portions of the filaments adjacent the opposite side of the structure may contain a large proportion of the second polymeric composition.
- the composition of the filaments may change abruptly to provide distinct layers within the structure having different polymeric compositions. There may be more than two layers in the structure.
- the structure may be in the form of a mat, or may be a tubular member.
- the portions of the filaments at the inner surface of the tubular member are preferably of the first polymeric composition to provide compatibility with material with which the inner surface will come into contact, and the portions of the filaments at the outer surface of the tubular member are preferably of the second polymeric composition to provide desirable strength characteristics and other physical properties to the tubular member.
- the tubular member may be cut to provide one or more segmental elements from the tubular wall. If the internal diameter of the tubular member is large enough, for example a few centimetres, the segmental element or elements will tend towards being planar, and may be used as pledgets.
- the invention further provides a method of forming an integral fibrous structure according to the invention, which method comprises the steps of directing filaments of a first polymeric composition at a surface to start building up a fibrous structure of the first polymeric composition, and altering the composition of the filaments during production thereof such that the portions of the filaments at the side of the structure remote from the surface is of the second polymeric composition.
- composition of the filaments may be changed abruptly or may be varied gradually across the structure.
- Figure 1 shows diagrammatically apparatus for electrostatically spinning a synthetic vascular graft.
- Polymer solution is ejected from capillary needles 10 towards an electrostatically charged mandrel 11 rotating at several thousand revolutions per minute, for example 5000 r.p.m.
- the mandrel 11 is at a potential of -12kV with respect to the needles 10.
- polymer solution leaves the needles 10 polymer filaments form and these filaments are attracted to the rotating electrostatically charged mandrel 11 to form a fibrous structure around the mandrel.
- the structure is removed from the mandrel to provide a fibrous tube.
- Mechanical properties of the tubular fibrous structure formed on the mandrel 11 can be controlled by variation of the speed of rotation of the mandrel, the type of polymer used and by altering, the potential of auxiliary electrodes 12.
- the capillary needles 10 are supplied with polymer solution from a manifold 13, the manifold 13 being supplied by tubes 14and 15 meeting in a T connector 16. Both tubes 14 and 15 include a flexible coil 17 and 18 respectively.
- the tube 14 has a valve 19 and the tube 15 has a valve 20 to enable the respective tubes to be closed. Control lines 21 and 22 control opening and closing of the valves 19 and 20.
- the tube 14 is supplied from a first air-ram driven syringe 23 and the tube 15 is fed from a second air-ram driven syringe 24 and the apparatus enables polymer solution from either syringe 23 or syringe 24 to be ejected from the needles 10 towards the mandrel 11.
- a purge line 25 including a closure valve 26 allows purging of the manifold 13.
- the apparatus of Figure 1 allows formation of an integral, uninterrupted fibrous structure of continuous polymeric filaments around the surface of the mandrel 11, the portions of the filaments at the inside surface having a different polymeric composition from the portions of the filaments of the outside surface of the fibrous structure.
- This can be advantageous when the tubular fibrous structures are used for, for example, synthetic vascular grafts.
- different polymers have different haemocompatibilities and that different polymers have different strength characteristics.
- one polyurethane has advantageous haemocompatibility but poor elastic properties, exhibiting high creep.
- a second polyurethane having a higher Young's modulus has satisfactory strength properties but poor haemocompatibility.
- the apparatus of Figure 1 allows production of a synthetic vascular graft having a thin inner lining of the first polyurethane on a wall of the second polyurethane, the graft, however, being formed of fibres spun continuously, with individual fibres changing composition between their ends to provide an integral, uninterrupted, fibrous structure.
- polymers can be used in the electrostatic spinning process.
- polyurethanes such as polyurethanes, polyamides and polyacrylonitrile, all of which can be spun from solution, and polytetrafluorethylene and polyesters which may be spun from dispersion.
- Water soluble polymers such as polyvinyl alcohol, polyvinyl pyrrolidone and polyethylene oxide may be spun from aqueous solution.
- the constraint on the fibrous structure and method of production according to the invention is that the two or more polymers used to vary the composition of the filaments during the spinning process must be either dispersible or alternatively soluble in the same solvent system.
- the two or more polymers used to vary the composition of the filaments during the spinning process must be either dispersible or alternatively soluble in the same solvent system.
- a silicone lubricant could be added to a polyurethane polymer and spun as the inner surface of a graft, the outer surface of the graft being the same polyurethane without the silicone lubricant. Such an example is included in the scope of the invention.
- the advantage of the embodiments of grafts hereinbefore described are that the different layers can be optimised for particular properties, either in its morphology (e.g. porosity, pore shape, fibre size) or in its chemistry (e.g. type of polymer, presence of drug.
- a drug such as heparin or prostacyclin may be included in the inner layer to improve the property with regard to contacting blood). If such layers are built up discontinuously, lines of weakness exist between the contiguous surfaces and delamination is likely to occur at quite low mechanical stresses.
- the advantage of the method hereinbefore described is that it builds different layers into an integrally formed fibrous structure so that the successive wall components are merged in a well controlled way.
- tubular fibrous structures for use as vascular grafts
- the invention is equally applicable to planar fibrous structures such as mats and that such alternative structures would have wide applications.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Artificial Filaments (AREA)
- Multicomponent Fibers (AREA)
- Materials For Medical Uses (AREA)
- Prostheses (AREA)
- Inorganic Fibers (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Nonwoven Fabrics (AREA)
- Medicinal Preparation (AREA)
- Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
Claims (13)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT84304891T ATE40424T1 (de) | 1983-07-21 | 1984-07-18 | Faserige strukturen. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8319727 | 1983-07-21 | ||
| GB08319727A GB2145443B (en) | 1983-07-21 | 1983-07-21 | Improvements in fibrous structures |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| EP0132376A2 EP0132376A2 (de) | 1985-01-30 |
| EP0132376A3 EP0132376A3 (en) | 1986-10-01 |
| EP0132376B1 true EP0132376B1 (de) | 1989-01-25 |
Family
ID=10546086
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP84304891A Expired EP0132376B1 (de) | 1983-07-21 | 1984-07-18 | Faserige Strukturen |
Country Status (12)
| Country | Link |
|---|---|
| EP (1) | EP0132376B1 (de) |
| JP (1) | JPS60190947A (de) |
| AT (1) | ATE40424T1 (de) |
| AU (1) | AU558207B2 (de) |
| BR (1) | BR8403634A (de) |
| CA (1) | CA1248720A (de) |
| DE (1) | DE3476432D1 (de) |
| DK (1) | DK357184A (de) |
| ES (1) | ES534506A0 (de) |
| GB (1) | GB2145443B (de) |
| HK (2) | HK67187A (de) |
| SG (2) | SG6887G (de) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111317594A (zh) * | 2020-02-28 | 2020-06-23 | 广州迈普再生医学科技股份有限公司 | 一种人工血管自动化生产装置 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2195251A (en) * | 1986-09-02 | 1988-04-07 | Ethicon Inc | Improvements in synthetic vascular grafts |
| US7780973B2 (en) * | 2003-12-15 | 2010-08-24 | Ethicon Endo-Surgery, Inc. | Method and device for minimally invasive implantation of biomaterial |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1530990A (en) * | 1974-08-05 | 1978-11-01 | Ici Ltd | Electrostatically spun tubular product |
| GB1527592A (en) * | 1974-08-05 | 1978-10-04 | Ici Ltd | Wound dressing |
| DE2806030C2 (de) * | 1978-02-14 | 1984-02-02 | B. Braun Melsungen Ag, 3508 Melsungen | Verfahren zur Herstellung einer schlauchförmigen Blutgefäßprothese |
-
1983
- 1983-07-21 GB GB08319727A patent/GB2145443B/en not_active Expired
-
1984
- 1984-07-18 AT AT84304891T patent/ATE40424T1/de not_active IP Right Cessation
- 1984-07-18 JP JP59147749A patent/JPS60190947A/ja active Pending
- 1984-07-18 DE DE8484304891T patent/DE3476432D1/de not_active Expired
- 1984-07-18 EP EP84304891A patent/EP0132376B1/de not_active Expired
- 1984-07-19 CA CA000459285A patent/CA1248720A/en not_active Expired
- 1984-07-20 AU AU30924/84A patent/AU558207B2/en not_active Ceased
- 1984-07-20 ES ES534506A patent/ES534506A0/es active Granted
- 1984-07-20 BR BR8403634A patent/BR8403634A/pt unknown
- 1984-07-20 DK DK357184A patent/DK357184A/da not_active Application Discontinuation
-
1987
- 1987-02-02 SG SG68/87A patent/SG6887G/en unknown
- 1987-09-17 HK HK671/87A patent/HK67187A/xx not_active IP Right Cessation
-
1989
- 1989-04-14 SG SG256/89A patent/SG25689G/en unknown
- 1989-08-24 HK HK684/89A patent/HK68489A/en not_active IP Right Cessation
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111317594A (zh) * | 2020-02-28 | 2020-06-23 | 广州迈普再生医学科技股份有限公司 | 一种人工血管自动化生产装置 |
| CN111317594B (zh) * | 2020-02-28 | 2023-10-20 | 广州迈普再生医学科技股份有限公司 | 一种人工血管自动化生产装置 |
Also Published As
| Publication number | Publication date |
|---|---|
| ATE40424T1 (de) | 1989-02-15 |
| JPS60190947A (ja) | 1985-09-28 |
| SG6887G (en) | 1987-06-05 |
| DK357184A (da) | 1985-01-22 |
| CA1248720A (en) | 1989-01-17 |
| DE3476432D1 (en) | 1989-03-02 |
| AU558207B2 (en) | 1987-01-22 |
| BR8403634A (pt) | 1985-07-02 |
| SG25689G (en) | 1989-07-14 |
| ES8603776A1 (es) | 1986-01-01 |
| GB2145443B (en) | 1986-07-23 |
| EP0132376A3 (en) | 1986-10-01 |
| GB8319727D0 (en) | 1983-08-24 |
| HK67187A (en) | 1987-09-25 |
| HK68489A (en) | 1989-09-01 |
| DK357184D0 (da) | 1984-07-20 |
| AU3092484A (en) | 1985-01-24 |
| EP0132376A2 (de) | 1985-01-30 |
| GB2145443A (en) | 1985-03-27 |
| ES534506A0 (es) | 1986-01-01 |
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| STAA | Information on the status of an ep patent application or granted ep patent |
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