US3807273A - Method of making pliable, dyed and braided polyester sutures - Google Patents
Method of making pliable, dyed and braided polyester sutures Download PDFInfo
- Publication number
- US3807273A US3807273A US00256401A US25640172A US3807273A US 3807273 A US3807273 A US 3807273A US 00256401 A US00256401 A US 00256401A US 25640172 A US25640172 A US 25640172A US 3807273 A US3807273 A US 3807273A
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- United States
- Prior art keywords
- strand
- thread
- dyed
- hot
- braided
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- Expired - Lifetime
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- 229920000728 polyester Polymers 0.000 title claims abstract description 40
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 239000000463 material Substances 0.000 claims abstract description 19
- 238000004043 dyeing Methods 0.000 claims abstract description 17
- 239000007788 liquid Substances 0.000 claims abstract description 17
- 238000004804 winding Methods 0.000 claims abstract description 15
- 238000009954 braiding Methods 0.000 claims abstract description 14
- 239000011248 coating agent Substances 0.000 claims abstract description 7
- 238000000576 coating method Methods 0.000 claims abstract description 7
- -1 polyethylene terephthalate Polymers 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 24
- 229920001296 polysiloxane Polymers 0.000 claims description 15
- 239000012530 fluid Substances 0.000 claims description 13
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 11
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 11
- 239000002904 solvent Substances 0.000 claims description 10
- 230000001050 lubricating effect Effects 0.000 claims description 7
- 230000009477 glass transition Effects 0.000 claims description 5
- 238000005406 washing Methods 0.000 claims description 5
- QCAHUFWKIQLBNB-UHFFFAOYSA-N 3-(3-methoxypropoxy)propan-1-ol Chemical group COCCCOCCCO QCAHUFWKIQLBNB-UHFFFAOYSA-N 0.000 claims description 3
- 230000001464 adherent effect Effects 0.000 abstract description 5
- 239000000975 dye Substances 0.000 description 37
- 229920000642 polymer Polymers 0.000 description 21
- 239000000835 fiber Substances 0.000 description 15
- 239000002245 particle Substances 0.000 description 9
- 229920002545 silicone oil Polymers 0.000 description 9
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 6
- 230000002776 aggregation Effects 0.000 description 4
- 238000004220 aggregation Methods 0.000 description 4
- 229920002994 synthetic fiber Polymers 0.000 description 4
- 241001589086 Bellapiscis medius Species 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 230000035508 accumulation Effects 0.000 description 3
- 238000009825 accumulation Methods 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 229950011260 betanaphthol Drugs 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 239000012209 synthetic fiber Substances 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- TVRGPOFMYCMNRB-UHFFFAOYSA-N quinizarine green ss Chemical compound C1=CC(C)=CC=C1NC(C=1C(=O)C2=CC=CC=C2C(=O)C=11)=CC=C1NC1=CC=C(C)C=C1 TVRGPOFMYCMNRB-UHFFFAOYSA-N 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- DIZMHOOFCDVUGW-UHFFFAOYSA-N 1,3-bis[(2,3-dimethylphenyl)diazenyl]naphthalen-2-ol Chemical compound C1(=C(C(=CC=C1)C)C)N=NC=1C(=C(C2=CC=CC=C2C1)N=NC1=C(C(=CC=C1)C)C)O DIZMHOOFCDVUGW-UHFFFAOYSA-N 0.000 description 1
- VUSAIZBVVMZCCH-UHFFFAOYSA-N 1-[(2,5-dimethylphenyl)diazenyl]naphthalen-2-ol Chemical compound C1(=C(C=CC(=C1)C)C)N=NC1=C(C=CC2=CC=CC=C12)O VUSAIZBVVMZCCH-UHFFFAOYSA-N 0.000 description 1
- 229940087166 1-phenylazo-2-naphthylamine Drugs 0.000 description 1
- KLCDQSGLLRINHY-UHFFFAOYSA-N 1-phenyldiazenylnaphthalen-2-amine Chemical compound NC1=CC=C2C=CC=CC2=C1N=NC1=CC=CC=C1 KLCDQSGLLRINHY-UHFFFAOYSA-N 0.000 description 1
- 241000837181 Andina Species 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 235000021028 berry Nutrition 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- NOKUWSXLHXMAOM-UHFFFAOYSA-N hydroxy(phenyl)silicon Chemical compound O[Si]C1=CC=CC=C1 NOKUWSXLHXMAOM-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003356 suture material Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- UGCDBQWJXSAYIL-UHFFFAOYSA-N vat blue 6 Chemical compound O=C1C2=CC=CC=C2C(=O)C(C=C2Cl)=C1C1=C2NC2=C(C(=O)C=3C(=CC=CC=3)C3=O)C3=CC(Cl)=C2N1 UGCDBQWJXSAYIL-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Images
Classifications
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04C—BRAIDING OR MANUFACTURE OF LACE, INCLUDING BOBBIN-NET OR CARBONISED LACE; BRAIDING MACHINES; BRAID; LACE
- D04C1/00—Braid or lace, e.g. pillow-lace; Processes for the manufacture thereof
- D04C1/06—Braid or lace serving particular purposes
- D04C1/12—Cords, lines, or tows
-
- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G3/00—Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
- D02G3/44—Yarns or threads characterised by the purpose for which they are designed
- D02G3/448—Yarns or threads for use in medical applications
Definitions
- ABSTRACT Fabricating a pliable, dyed and braided polyester thread which comprises winding a polyester strand loosely around a perforated hollow dyeing element, passing dye under pressure through the winding of said polyester strand, hot-stretching the dyed strand to reduce the elastic memory thereof, coating the hotstretched strand with a liquid, film-forming material adherent but substantially inert to said polyester strand braiding a plurality of said coated filaments into a braided thread, and removing said film-forming materialv 7 Claims, 2 Drawing Figures GOOOOGOOO'O METHOD OF MAKING PLIABLE, DYED AND BRAIDED POLYESTER SUTURES
- the present invention relates to an improved method for the preparation of braided sutures of dyed and hotstretched synthetic polyester filaments or strands.
- polyester fibers There are several synthetic fibers which have been proposed for use as sutures, amongst which are polyester fibers. Polyester fibers have been found to possess certain physical and chemical properties superior to natural fibers such as silk fibers that render them particularly suitable for use as surgical suturing material.
- the monofilament fiber has a cross-section which cannot be varied, i.e., the cross-section is frozen and ina fixed relationship to adjacent cross-sections. Polyfilamentous materials, on the other hand, can have displacement of the fibers, thus accomodating the stress of curvature.
- lt is another object of the invention to remedy the aforementioned problem without adversely affecting the pliability and flexibility characteristics of the final product.
- the liquid film-forming materials contemplated for use in the present invention are those which form adherent films on the polyester strand.
- the liquid filmforming materials allow the loose particles and dyes to come off the polyester strand without aggregation during the braiding operation. Deposition of the loose dye and scuff occurs onto the braiding maching but in the liquid film-forming material which prevents aggregation and formation of the louse.
- the film-forming liquids should be substantially inert to the polyester and substantially non-absorbable thereby.
- suitable film-forming liquids will readily come to the mind of those skilled in the art and include materials such as surface active or wetting agents, oils of lubricating viscosity, antistatic agents and the like.
- a particularly suitable film-forming liquid for use in the present invention are silicone oils'of lubricating viscosity.
- Silicone oils of lubricating viscosity which can be employed in the method of the invention are liquid organic siloxane polymers in which the siloxane structure, Si-OSi, occurs successively along the polymer chain and in which the major number of residual valences of the silicone atoms are not satisfied by the substitution thereon of monovalent organic essentially hy drocarbon'radicals such as aromatic and aliphatic radicals.
- the aliphatic substituents of the polymers are preferably low molecular weight alkyl radicals (i.e., those not having more than about 5 carbon atoms per radical) such as methyl, ethyl and butyl radicals, and the aromatic substituents are preferably phenyl, halogen-substituted phenyl radicals, and alkyl-substituted phenyl radicals in which the alkyl group is halogenated.
- the aromatic siloxane polymers are preferably those in which a major proportion of the silicone atoms are bonded to aliphatic radicals such as methyl radicals, and in which the remaining number of organic radicals are aromatic radicals.
- Typical examples of specific silicone oils which may be use are the dimethyl siloxane polymers having a viscosity of at least 10 centistokes at 25 C. (77 F.) and preferably a viscosity of at least 20 centistokes at 25 C.
- Such methyl-substituted siloxanes are commercially known as the Dow Corning Silicone Type 200 fluids and are mixtures of polymers of the homologous series of trimethyl end-blocked dimethyl siloxane polymers having a viscosity at 25 C. ranging up to about 12,500 centistokes.
- Suitable aliphaticand aromatic-substituted siloxane polymers are the methyl phenyl siloxanes in which the phenyl radical is substituted with halogen such as in methyl-p-bromophenyl siloxane polymer, methyl-pchlorphenyl siloxane polymer, methyl-mtrifluoromethyl phenyl siloxane polymer and methyl 3,4-dichlorophenyl siloxane polymer. It is within the scope of the present invention to employ any admixture of the above-mentioned silicone oils as an ingredient of the presently described novel compositions.
- siloxane poly mer as used herein includes silicone oils having the following general formula:
- R R and R are the same or different hydrocarbon radicals such as straight or branched chain alkyl, aryl, alkaryl, arylalkyl, halogen-substituted aryl or halogen-containing alkyl-substituted aryl radicals and n in an integer of at least 2.
- Such silicones are also referred to in the literature as organo polysiloxanes.
- Dyes suitable for use in the method of the invention have been determined and are well recognized in the suture dyeing art. Generally, the dyes may be defined and classified as oil-soluble or oil-solvent soluble, water-insoluble azo,'quinoline, anthraquinone, thio-indigo and isoxanthene dyes. It is intended that the dyes contemplated by the present invention embrace F. D. A. approved dyes;
- the hot-stretching step of the invention comprises stretching the strand at a temperature above its glass transition temperature, to the softening point thereof which will permit a change in configuration without the introduction of internal stresses.
- the strand may be heated to its softening point.
- Tension is applied to the heated filament such that the filament is stretched, for example, up to its breaking point. Elongation of over 1-0 percent and particularly from about- 20 percent up to about, but not including, the breaking point are suitable to reduce the elastic memory of the strand sufficiently.
- the temperature necessary to reduce or eliminate elasticity and memory is called the heat-setting temperature which is known for the various polyesters. For instance, in the case of polyesters of terephthalic acid, a temperature of 320 F. or above will suffice, although temperatures of about 390 to 450 F. are preferred.
- Coating of the polyester strands with the liquid, filmforming material may be effected in any convenient manner, for instance, by simply immersing the strand in the liquid for a short period of time sufficient to saturate and thoroughly impregnate and coat the strand. Ordinarily, complete saturation is effected in a matter of minutes.
- removal of the liquid filmforming material from the braided thread may be effected by any of the techniques well known to the art such as washing the product with a suitable solvent for the film-forming material.
- Solvents for silicone oil include the alkyl and aryl monoethers of alkylene glycols such as ethylene glycol, propylene glycol, etc. Illustrative'of these solvents are those of the Dowanol series.
- the thread After extraction of the liquid, film-forming material from the braided thread, the thread may be waterw'ashed in any convenient manner and then while still wet impregnated with inert, insoluble synthetic polymeric particles small enough to penetrate into the interstices of the polyfilamentous thread.
- the inert, polymeric particles may be any of those known in the art for endowing polyfilamentous strands with improved softness, knottability and flexibility such as those disclosed in U. S. Pat. Nos. 3,390,681 and 3,322,125, hereby incorporated by reference.
- inert, insoluble synthetic resins which can be used for this purpose include polyolefins such as polyethylene, polypropylene and the like; diolefins such as polymers of butadiene and isoprene; polystyrene; polyamides and silicone waxes such as are disclosed by U. S. Pat. No. 3,187,752, hereby incorporated by reference.
- a particularly preferred particle is polytetrafluoroethylene (Teflon).
- Aqueous dispersions of these materials such as aqueous dispersions of Teflon described in Berry, U. S. Pat. No. 2,478,229, are suitable to incorporate the particles into the thread. Saturated aqueous dispersions are particularly suitable. Ordinarily, the inert particles employed will-have a particle size of up to 1 micron.
- FIG. 1 shows a perforated dye tube
- FIG. 2 shows a dye tube with thread wound thereon in a pressure dye machine.
- the shrunken thread is then loosely wound onto another perforated dye tube and the tube with the winding of thread is refitted onto shaft 4 of the dye machine.
- the wound threads are then dyed by passing under pressure in the same manner as the heating fluid in the shrinking operation an aqueous solution of D & C Green No. 6 dye at a temperature of approximately 270 F.
- the dyed thread is then transferred onto a twister bobbin and in a twist texturing machine given two final twists while hot-stretching the thread percent of its original length at a temperature of 450 F.
- the resulting hot-stretched thread is transferred onto a soft package dye tube and the tube with the winding of thread immersed in a vat of silicone fluid (Dow Corning 710).
- Eight threads thus prepared are then braided on a New England Butt braider.
- the braided thread is washed with Dowanol (dipropylene glycol monomethyl ether) after which it is water-washed and dried
- a method of fabricating a pliable, dyed and braided polyester thread which comprises winding a polyester strand loosely around a perforated hollow dyeing element, passing dye under pressure through the winding of polyester strand, hot-stretching the dyed strand to reduce the elastic memory thereof, coating the hot-stretched strand with a liquid, film-forming material adherent but substantially inert to said polyester strand, braiding a plurality of said coated filaments into a braided thread, and removing said film-forming material.
- liquid, filmforming material is silicone fluid of lubricating viscosity.
- the method of fabricating a pliable dyed and braided polyethylene terephthalate thread which comprises winding a polyethylene terephthalate strand loosely around a perforated hollow dyeing element, passing dye under pressure through the winding of polyethylene terephthalate strand, hot-stretching the dyed strand to reduce the elastic memory thereof, said hot-stretching being conducted at a temperature in the range of from the glass transition temperature thereof to the softening point thereof to elongate the strand in the range of a minimum of 20 percent based on its prestretched length to just below the breaking point, coating the hot-stretched filament with silicone fluid of lubricating viscosity, braiding a plurality of said coated polyethylene terephthalate strands into a braided thread and then removing the silicone fluid by washing the braided thread with a solvent.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Mechanical Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Materials For Medical Uses (AREA)
- Coloring (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Braiding, Manufacturing Of Bobbin-Net Or Lace, And Manufacturing Of Nets By Knotting (AREA)
Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US00256401A US3807273A (en) | 1972-05-24 | 1972-05-24 | Method of making pliable, dyed and braided polyester sutures |
AU49775/72A AU459259B2 (en) | 1972-05-24 | 1972-12-07 | Method of making pliable, dyed & braided polyester sutures |
GB5720472A GB1420613A (en) | 1972-05-24 | 1972-12-12 | Methods for the preparation of braided suttures |
ZA728861A ZA728861B (en) | 1972-05-24 | 1972-12-14 | Method of making pliable,dyed and braided polyester sutures |
IT13098/72A IT969293B (it) | 1972-05-24 | 1972-12-18 | Metodo per la fabbricazione di fili per suture chirurgiche in polie stere flessibili tinti ed intrec ciati |
ES409890A ES409890A1 (es) | 1972-05-24 | 1972-12-21 | Un procedimiento para fabricar un hilo de poliester flexi- ble, tenido y trenzado, preferentemente para usos quirurgi- cos. |
FR7246772A FR2186030A5 (enrdf_load_stackoverflow) | 1972-05-24 | 1972-12-28 | |
JP1712973A JPS5737708B2 (enrdf_load_stackoverflow) | 1972-05-24 | 1973-02-13 | |
CH269573A CH547640A (fr) | 1972-05-24 | 1973-02-23 | Procede de fabrication d'un fil en fibre de polyester, tresse et teint, pour suture chirurgicale. |
DE2325790A DE2325790C3 (de) | 1972-05-24 | 1973-05-22 | Verfahren zur Herstellung eines gefärbten, aus Einzelfäden oder aus Teilgarnen von miteinander verdrillten Einzelfäden geflochtenen Polyesterfadens |
CA172,060A CA981003A (en) | 1972-05-24 | 1973-05-23 | Method of making pliable, dyed and braided polyester sutures |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US00256401A US3807273A (en) | 1972-05-24 | 1972-05-24 | Method of making pliable, dyed and braided polyester sutures |
Publications (1)
Publication Number | Publication Date |
---|---|
US3807273A true US3807273A (en) | 1974-04-30 |
Family
ID=22972107
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00256401A Expired - Lifetime US3807273A (en) | 1972-05-24 | 1972-05-24 | Method of making pliable, dyed and braided polyester sutures |
Country Status (11)
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0475430A1 (en) * | 1990-09-13 | 1992-03-18 | E.I. Du Pont De Nemours And Company | Process for improving the parallel alignment of individual fibers in a fiber bundle |
US5688451A (en) * | 1995-01-03 | 1997-11-18 | American Cyanamid Company | Method of forming an absorbable biocompatible suture yarn |
US6060007A (en) * | 1998-10-20 | 2000-05-09 | Tyco Group S.A.R.L. | Process for forming dyed braided suture |
US20050004601A1 (en) * | 2003-04-29 | 2005-01-06 | Kong James Kam Fu | Coded surgical aids |
EP2145692A1 (en) * | 2008-07-17 | 2010-01-20 | Tyco Healthcare Group LP | Spool dip and overcoat process for medical devices |
US20100075020A1 (en) * | 2008-09-25 | 2010-03-25 | Tyco Healthcare Group Lp | Methods for coating filaments |
CN101927032A (zh) * | 2010-08-04 | 2010-12-29 | 陈启忠 | 狸獭尾筋医用缝合线的染色制备方法 |
JP2015145555A (ja) * | 2015-05-08 | 2015-08-13 | 株式会社アートネイチャー | かつら用毛髪の染色方法、及び、かつらの製造方法 |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2189363B1 (enrdf_load_stackoverflow) * | 1972-06-21 | 1974-10-25 | Rhone Progil | |
DE3030971A1 (de) * | 1980-08-16 | 1982-04-01 | Institute für Textil- und Faserforschung Stuttgart, 7410 Reutlingen | Chirurgischer naehfaden |
DE3030972A1 (de) * | 1980-08-16 | 1982-04-01 | Institute für Textil- und Faserforschung Stuttgart, 7410 Reutlingen | Chirurgischer naehfaden |
US4463652A (en) * | 1980-09-25 | 1984-08-07 | Compagnie Francaise Des Isolants | High-speed braiding |
DE3530936A1 (de) * | 1984-09-25 | 1986-04-17 | Aktiengesellschaft Fr. Mettler's Söhne Maschinenfabrik, Arth am See | Einrichtung zum verarbeiten eines fadens aus synthesefasern, verwendung der einrichtung und verfahren zum herstellen eines gebrauchsfertigen naehzwirnes |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
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US2872356A (en) * | 1955-06-02 | 1959-02-03 | Dow Chemical Co | Lubrication of synthetic cellulose fibers |
US2992940A (en) * | 1957-01-23 | 1961-07-18 | Goodyear Tire & Rubber | Treatment of cellular materials |
US3143561A (en) * | 1960-09-23 | 1964-08-04 | Eastman Kodak Co | Poly-(alkoxy silanes) and their process of preparation |
US3240622A (en) * | 1962-08-27 | 1966-03-15 | Du Pont | Lubricating elastomers with silicate esters |
US3308616A (en) * | 1965-03-08 | 1967-03-14 | Du Pont | Sewing thread |
US3379552A (en) * | 1963-11-15 | 1968-04-23 | Sutures Inc | Impregnation of stretched multifilament polyester suture with polytetrafluoroethylene |
US3379091A (en) * | 1964-05-08 | 1968-04-23 | Sutures Inc | Method of making softened fabrics |
US3418160A (en) * | 1965-05-14 | 1968-12-24 | Du Pont | Process for coating polyester fibers with a mixture of lanolin and an oily silicone |
US3423314A (en) * | 1966-01-19 | 1969-01-21 | Dow Corning | Antistatic lubricant as a process finish for synthetic fibers |
US3434189A (en) * | 1966-08-02 | 1969-03-25 | Klinger Mfg Co Ltd | Method of continuously dyeing and stretching undrawn yarn |
US3717575A (en) * | 1971-05-25 | 1973-02-20 | Union Carbide Corp | Spandex lubricant |
-
1972
- 1972-05-24 US US00256401A patent/US3807273A/en not_active Expired - Lifetime
- 1972-12-07 AU AU49775/72A patent/AU459259B2/en not_active Expired
- 1972-12-12 GB GB5720472A patent/GB1420613A/en not_active Expired
- 1972-12-14 ZA ZA728861A patent/ZA728861B/xx unknown
- 1972-12-18 IT IT13098/72A patent/IT969293B/it active
- 1972-12-21 ES ES409890A patent/ES409890A1/es not_active Expired
- 1972-12-28 FR FR7246772A patent/FR2186030A5/fr not_active Expired
-
1973
- 1973-02-13 JP JP1712973A patent/JPS5737708B2/ja not_active Expired
- 1973-02-23 CH CH269573A patent/CH547640A/fr not_active IP Right Cessation
- 1973-05-22 DE DE2325790A patent/DE2325790C3/de not_active Expired
- 1973-05-23 CA CA172,060A patent/CA981003A/en not_active Expired
Patent Citations (11)
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US2872356A (en) * | 1955-06-02 | 1959-02-03 | Dow Chemical Co | Lubrication of synthetic cellulose fibers |
US2992940A (en) * | 1957-01-23 | 1961-07-18 | Goodyear Tire & Rubber | Treatment of cellular materials |
US3143561A (en) * | 1960-09-23 | 1964-08-04 | Eastman Kodak Co | Poly-(alkoxy silanes) and their process of preparation |
US3240622A (en) * | 1962-08-27 | 1966-03-15 | Du Pont | Lubricating elastomers with silicate esters |
US3379552A (en) * | 1963-11-15 | 1968-04-23 | Sutures Inc | Impregnation of stretched multifilament polyester suture with polytetrafluoroethylene |
US3379091A (en) * | 1964-05-08 | 1968-04-23 | Sutures Inc | Method of making softened fabrics |
US3308616A (en) * | 1965-03-08 | 1967-03-14 | Du Pont | Sewing thread |
US3418160A (en) * | 1965-05-14 | 1968-12-24 | Du Pont | Process for coating polyester fibers with a mixture of lanolin and an oily silicone |
US3423314A (en) * | 1966-01-19 | 1969-01-21 | Dow Corning | Antistatic lubricant as a process finish for synthetic fibers |
US3434189A (en) * | 1966-08-02 | 1969-03-25 | Klinger Mfg Co Ltd | Method of continuously dyeing and stretching undrawn yarn |
US3717575A (en) * | 1971-05-25 | 1973-02-20 | Union Carbide Corp | Spandex lubricant |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0475430A1 (en) * | 1990-09-13 | 1992-03-18 | E.I. Du Pont De Nemours And Company | Process for improving the parallel alignment of individual fibers in a fiber bundle |
US5688451A (en) * | 1995-01-03 | 1997-11-18 | American Cyanamid Company | Method of forming an absorbable biocompatible suture yarn |
US6060007A (en) * | 1998-10-20 | 2000-05-09 | Tyco Group S.A.R.L. | Process for forming dyed braided suture |
US20050004601A1 (en) * | 2003-04-29 | 2005-01-06 | Kong James Kam Fu | Coded surgical aids |
EP2145692A1 (en) * | 2008-07-17 | 2010-01-20 | Tyco Healthcare Group LP | Spool dip and overcoat process for medical devices |
US20100016890A1 (en) * | 2008-07-17 | 2010-01-21 | Steve Tsai | Spool Dip And Overcoat Process For Medical Devices |
EP2535118A1 (en) * | 2008-07-17 | 2012-12-19 | Tyco Healthcare Group, LP | Suture coating and drying tank system |
US20100075020A1 (en) * | 2008-09-25 | 2010-03-25 | Tyco Healthcare Group Lp | Methods for coating filaments |
CN101927032A (zh) * | 2010-08-04 | 2010-12-29 | 陈启忠 | 狸獭尾筋医用缝合线的染色制备方法 |
JP2015145555A (ja) * | 2015-05-08 | 2015-08-13 | 株式会社アートネイチャー | かつら用毛髪の染色方法、及び、かつらの製造方法 |
Also Published As
Publication number | Publication date |
---|---|
FR2186030A5 (enrdf_load_stackoverflow) | 1974-01-04 |
CH547640A (fr) | 1974-04-11 |
GB1420613A (en) | 1976-01-07 |
DE2325790A1 (de) | 1973-11-29 |
ZA728861B (en) | 1973-09-26 |
IT969293B (it) | 1974-03-30 |
CA981003A (en) | 1976-01-06 |
JPS5737708B2 (enrdf_load_stackoverflow) | 1982-08-11 |
JPS4925252A (enrdf_load_stackoverflow) | 1974-03-06 |
AU4977572A (en) | 1974-06-13 |
DE2325790B2 (de) | 1978-02-09 |
AU459259B2 (en) | 1975-03-20 |
DE2325790C3 (de) | 1978-10-05 |
ES409890A1 (es) | 1975-11-16 |
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Legal Events
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AS | Assignment |
Owner name: PFIZER HOSPITAL PRODUCTS GROUP INC. Free format text: CHANGE OF NAME;ASSIGNOR:HOWMEDICA, INC.;REEL/FRAME:004471/0589 Effective date: 19840624 |