US3110549A - Method of preparing formed collagen - Google Patents

Method of preparing formed collagen Download PDF

Info

Publication number
US3110549A
US3110549A US112213A US11221361A US3110549A US 3110549 A US3110549 A US 3110549A US 112213 A US112213 A US 112213A US 11221361 A US11221361 A US 11221361A US 3110549 A US3110549 A US 3110549A
Authority
US
United States
Prior art keywords
collagen
pulp
heating
fibers
sheets
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 - Lifetime
Application number
US112213A
Inventor
Cohen Jerome
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Armour and Co
Original Assignee
Armour and Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Armour and Co filed Critical Armour and Co
Priority to US112213A priority Critical patent/US3110549A/en
Priority to FR7411A priority patent/FR1322010A/en
Priority to ES277559A priority patent/ES277559A1/en
Priority to BE617977A priority patent/BE617977A/en
Priority to AT423362A priority patent/AT248599B/en
Priority to GB19899/62A priority patent/GB949424A/en
Priority to NL278815D priority patent/NL278815A/xx
Application granted granted Critical
Publication of US3110549A publication Critical patent/US3110549A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B60VEHICLES IN GENERAL
    • B60RVEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
    • B60R1/00Optical viewing arrangements; Real-time viewing arrangements for drivers or passengers using optical image capturing systems, e.g. cameras or video systems specially adapted for use in or on vehicles
    • B60R1/12Mirror assemblies combined with other articles, e.g. clocks
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08HDERIVATIVES OF NATURAL MACROMOLECULAR COMPOUNDS
    • C08H1/00Macromolecular products derived from proteins
    • C08H1/06Macromolecular products derived from proteins derived from horn, hoofs, hair, skin or leather
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L89/00Compositions of proteins; Compositions of derivatives thereof
    • C08L89/04Products derived from waste materials, e.g. horn, hoof or hair
    • C08L89/06Products derived from waste materials, e.g. horn, hoof or hair derived from leather or skin, e.g. gelatin
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F4/00Monocomponent artificial filaments or the like of proteins; Manufacture thereof
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01KMEASURING TEMPERATURE; MEASURING QUANTITY OF HEAT; THERMALLY-SENSITIVE ELEMENTS NOT OTHERWISE PROVIDED FOR
    • G01K1/00Details of thermometers not specially adapted for particular types of thermometer
    • G01K1/14Supports; Fastening devices; Arrangements for mounting thermometers in particular locations
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B60VEHICLES IN GENERAL
    • B60RVEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
    • B60R1/00Optical viewing arrangements; Real-time viewing arrangements for drivers or passengers using optical image capturing systems, e.g. cameras or video systems specially adapted for use in or on vehicles
    • B60R1/12Mirror assemblies combined with other articles, e.g. clocks
    • B60R2001/123Mirror assemblies combined with other articles, e.g. clocks with thermometers

Definitions

  • native collagen which has been reduced by mechanical means to the form of discrete fibers. This can be accomplished in various wa s.
  • the native collagen can be subjected to a preliminary treatment in a paper beating machine in much the same way as cellulose is treated to form a fibrous pulp. If desired,'the beaten collagen can be dewatered, and store-d prior to use in the present process. It will be understood that in preparing collagen fibers from animal hides, such as cattle hides, that the grain layer and the flesh layer are preferably separated from the coriurn, which is the collagen-containing layer.
  • an aqueous pulp of collagen fibers is heated at a substantially neutral pH.
  • the pulp should be in the form of a soft pasty mass.
  • discrete fibers of native collagen are mixed with sufiicient water to form a doughy pulp containing from 10 to 25% solids by weight. Since the pulp is to be heated at a substantially neutral pH, there will normally be no need to add any acidic or basic reagents to the pulp.
  • the doughy, substantially neutral pulp of fibrous collagen is heated at a temperature within the. range from 40 to 65 C. It is desirable to control the heating step to solubilize a portion of the collagen without appreciably shrinking the collagen fibers.
  • the collagen in the fibers begins to melt and to be extracted into the solution as gelatin rather than as reconstituta-ble collagen.
  • temperatures above 62 C. this undesirable conversion may occur to some extent, and at temperatures above 65 C., it is almost certain to occur to an objectionably large extent;
  • the temperature of the heating is too low, the desired con version to reconstitutable collagen proceeds too slowly.
  • the optimum temperature of heating is within the range from 54 to 62 C. At temper occurring within this range there is little fiber shrinkage and formation of gelatin. At the same time, however, the conversion of a portion of the fibrous collagen to solubilized but reconstitutable collagen is facilitated.
  • the pulp will contain 12 to 18% solids and will be at a pH of approximately 6.0. This pulp is then heated at a temperature of 55 to 60 C. until 10 to 12% of the collagen has been solubilized.
  • the desired solubilization can usually be obtained in approximately one hour. It will be understood, of course, can be varied considerably, and that the time lWlll usually vary inversely with thetemperature.
  • the pulp can be observed to see whether the shrinkage of the fibers is being avoided, and samples can be taken and subjected to vacuum filtration to measure the percent of collagen which has been solubilized.
  • the solubilized collagen willpass through the filter, which upon being separated from the water by drying, can be compared on a weight basis with the dried insolubleresidue.
  • the doughy pulp is formed into the desired shape.
  • the pulp may be extruded to form sheets or filaments.
  • the dough is forced under pressure through a die.
  • the die will provide a horizontally extending slit corresponding to the desired width of the sheet. provide one or more orifices to the diameter of the filaments.
  • the dough can fall upon a moving conveyor belt which is timed to permit the continuity of the sheets or filaments to be maintained.
  • uniform sheets or films of any desired thickness maybe produced. The thickness will usually correspond to that of natural leather.
  • the diameters of the filaments can also be varied as desired. For some purposes, it may be advantageous to form the collagen. dough in a mold to produce solid or hollow bodies,
  • the forming or extrusion step is preferably carried out while the pulp is still atan elevated temperature.
  • temperatures of to are suitable, and parcorresponding in diameter ticularly good results are obtained at a temperature of around 50 C.
  • the temperature is not particularlycritical providing the dough is sufficiently fluid to permit it to be satisfactorily formed by extrusion or other forming procedure.
  • the sheets may be fixed In this step, the
  • temperature of the sheets should usually be reduced below 20 C. More specifically, temperatures in the range of 2 to 10 C. are suitable.
  • the chilling may be accomplished in various ways, such as by passing the sheets over chilled rollers.
  • the ammonium sulfate solution may be injected into the formed collagen at spaced This procedure is believed to increase the strength of the formed collagen by encouraging the precipitation of the solubilized collagen.
  • the sheets or filaments may also be subjected to other procedures which are well-known in the processing of leather.
  • the sheets may be tanned with various standard tanning solutions, such as an aqueous solution containing 1% chromic oxide and 2% sodium formats.
  • the starting material was native collagen fibers Whi had been prepared from the corium layer of fresh unlimed cattle skins by mechanically subdividing the coriuin into discrete fibers by means of a paper beater.
  • the cerium was treated in an aqueous slurry in the beater, and the resulting fiberswere subsequently dewatered and dried to provide the starting material.
  • the doughy pulp was formed into a sheet by a hand rolling procedure.
  • the sheet was cold set at 4 C. for ten minutes, and then immersed in a bath of half saturated ammonium sulfate (plldil). After one hour the sheet was examined and found to be exceedingly strong.
  • the sheet was then tanned according to standard procedures, using a chrome tanning reagent.
  • a method of preparing formed collagen comprising mixing discrete fibers of native collagen with water to form a doughy pulp, said pulp having a substantially neutral pH, heating said pulp at a temperature within the range from 40 to 65 C. to solubilize a portion of the collagen therein without appreciably shrinking said fibers, continuing said heating until at least 5% by weight of the collagen in said pulp has been solubilized while the major portion of the said collagenremains infibrillar form, and thereatter forming said pulp.
  • a method of preparing formed collagen comprising mixing discrete fibers of native collagen with water to form a doughy pulp, said pulp having'a pH above 5.0 but below 8.0 and containing from to solids by Weight, heating said pulp at a temperature within the range from to 65 C. to solubilize a portion of the collagen therein without appreciably shrinking said fibers, continuing said heating until from 8 to 30% by l weight of the collagen in said pulp has been solubilized, and thereafter forming said pulp.
  • said pulp having a pH above 5.0 but below 8.0 and being in the form of a soft pasty mass
  • said heating step being controlled to transform from 8 to 30% by weight of the fibrous collagen in said pulp to solubilized collagen without appreciable shrinkage of the collagen fibers, termi- 'd heating step while the major portion of said collagen remains in fibrous form, extruding the heated pulp to a predetermined form, and chilling the formed collagen.
  • aqueous pulp of collagen fibers said pulp having a pH of from 5.0 to 7.0 and being in the form of a soft pasty mass, said heating step being controlled to transform from 8 to 15% by Wei ht of the fibrous collagen in said pulp to solubilized collagen without appreciable shrinkage of the collagen fibers, extruding the heated pulp to form sheets, and chilling said sheets.
  • a method of preparing collagen sheets comprising heating an aqueous pulp of collagen fibers, said pulp having a pH of from 5.5 to 7.0 and being in the form of a soft pasty mass, said heating'step being controlled to transform at least 8 to 15% by weight of the fibrous collagen in said pulp to solubilized collagen without appreciable shrinkage of the collagen fibers, said heating being carried out at a temperature of substantially from '54 to 62 C. and being terminated While the major portion of said collagen remains in fibrous form, extruding the heated pulp to form sheets, and chilling said sheets.

Description

United States Patent 3,110,549 METHOD OF PREPARINQ FORMED CGLLAGEN .leronie Cohen, Chicago, ill., assignor to Armour and Company, Chicago, lllL, a corporation of Belt-1W3; No Drawing. Filed May 24, 1961, Ser. No. 112,213 7 Claims. (Cl. 18-57) to Obtain a product of satisfactory quality while fully utilizing the starting material. The present invention provides for the achievement of this objective.
In practicing the method of the present invention, the.
preferred starting material is native collagen which has been reduced by mechanical means to the form of discrete fibers. This can be accomplished in various wa s. For example, the native collagen can be subjected to a preliminary treatment in a paper beating machine in much the same way as cellulose is treated to form a fibrous pulp. If desired,'the beaten collagen can be dewatered, and store-d prior to use in the present process. It will be understood that in preparing collagen fibers from animal hides, such as cattle hides, that the grain layer and the flesh layer are preferably separated from the coriurn, which is the collagen-containing layer.
In accordance with the present invention, an aqueous pulp of collagen fibers is heated at a substantially neutral pH. The pulp should be in the form of a soft pasty mass. In one preferred embodiment, discrete fibers of native collagen are mixed with sufiicient water to form a doughy pulp containing from 10 to 25% solids by weight. Since the pulp is to be heated at a substantially neutral pH, there will normally be no need to add any acidic or basic reagents to the pulp.
Preferably, the doughy, substantially neutral pulp of fibrous collagen is heated at a temperature within the. range from 40 to 65 C. It is desirable to control the heating step to solubilize a portion of the collagen without appreciably shrinking the collagen fibers. At the temperature where appreciable shrinkage begins to occur, as can be determined visually and by a standardized test procedure, the collagen in the fibers begins to melt and to be extracted into the solution as gelatin rather than as reconstituta-ble collagen. At temperatures above 62 C., this undesirable conversion may occur to some extent, and at temperatures above 65 C., it is almost certain to occur to an objectionably large extent; When the temperature of the heating is too low, the desired con version to reconstitutable collagen proceeds too slowly. On the basis of present knowledge, it is believed that the optimum temperature of heating is within the range from 54 to 62 C. At temperautres within this range there is little fiber shrinkage and formation of gelatin. At the same time, however, the conversion of a portion of the fibrous collagen to solubilized but reconstitutable collagen is facilitated.
It is preferred to terminate the. heating step while the major portion of the collagen remains in fibrous form. It the pH is below 5.0 or above 8.0, it is difiicult to control the heating step, and it is therefore desirable to avoid pronounced acidic or basic conditions during the heating. Optimum results are believed to be achieved at a pH within the range from 5.5 to 7.0. v
To achieve the benefits of the present invention, the heating should be continued until at least 5% by weight of the fibrous collagen in the pulp is transformed to "ice solubilized collagen. Best results are believed to be ob tained when from 8 to 15% by weight of the collagen is solubilized, although higher percentages up to may be achieved under certain conditions. The relative proportions between the solubilized collagen and the collagen fibers can also be varied by adding. additional fibers or native collagen to the pulp during or subsequent to the heating step.
In one preferred embodiment, the pulp will contain 12 to 18% solids and will be at a pH of approximately 6.0. This pulp is then heated at a temperature of 55 to 60 C. until 10 to 12% of the collagen has been solubilized. In this particular embodiment, the desired solubilization can usually be obtained in approximately one hour. It will be understood, of course, can be varied considerably, and that the time lWlll usually vary inversely with thetemperature. During the heating, the pulp can be observed to see whether the shrinkage of the fibers is being avoided, and samples can be taken and subjected to vacuum filtration to measure the percent of collagen which has been solubilized. The solubilized collagen willpass through the filter, which upon being separated from the water by drying, can be compared on a weight basis with the dried insolubleresidue.
Following the heating step the doughy pulp is formed into the desired shape. This may be done by various procedures. For example, the pulp may be extruded to form sheets or filaments. In this procedure, the dough is forced under pressure through a die. In accordance with known procedures, if sheets are desired the die will provide a horizontally extending slit corresponding to the desired width of the sheet. provide one or more orifices to the diameter of the filaments. Upon being extruded, the dough can fall upon a moving conveyor belt which is timed to permit the continuity of the sheets or filaments to be maintained. By this procedure, uniform sheets or films of any desired thickness maybe produced. The thickness will usually correspond to that of natural leather. The diameters of the filaments can also be varied as desired. For some purposes, it may be advantageous to form the collagen. dough in a mold to produce solid or hollow bodies,
The forming or extrusion step is preferably carried out while the pulp is still atan elevated temperature. For example, temperatures of to are suitable, and parcorresponding in diameter ticularly good results are obtained at a temperature of around 50 C. In this step, the temperature is not particularlycritical providing the dough is sufficiently fluid to permit it to be satisfactorily formed by extrusion or other forming procedure.
Following the forming step, or set by subjecting them to chilling.
the sheets may be fixed In this step, the
temperature of the sheets should usually be reduced below 20 C. More specifically, temperatures in the range of 2 to 10 C. are suitable. The chilling may be accomplished in various ways, such as by passing the sheets over chilled rollers.
The formed collagen produced in the manner described above can be subjected to further processing steps in order to improve its appearance, strength, and other properties. For example, the sheets may be subjected to needlin'g. In this procedure, the porosity of the sheets is increased by pressing a die. or roller providing a plurality of needles against the sheets. As described in copending application, Serial No. 141,956, filed October 2, 1961, entitled Method of Increasing Strength of Formed Collagen, the formed and set collagen may be subjected to the action of a protein precipitating agent, such asan aqueous solution of ammonium sulfate. For example, the sheets or filaments may be passed through a bath of half saturated aqueous ammonium sulfate having a pH that the time of heating For filaments, the die will intervals.
of around 6.0. As an alternative, the ammonium sulfate solution may be injected into the formed collagen at spaced This procedure is believed to increase the strength of the formed collagen by encouraging the precipitation of the solubilized collagen. The sheets or filaments may also be subjected to other procedures which are well-known in the processing of leather. For example, the sheets may be tanned with various standard tanning solutions, such as an aqueous solution containing 1% chromic oxide and 2% sodium formats.
The following example provides a more specific illustration of the method of this invention.- The starting material was native collagen fibers Whi had been prepared from the corium layer of fresh unlimed cattle skins by mechanically subdividing the coriuin into discrete fibers by means of a paper beater. The cerium was treated in an aqueous slurry in the beater, and the resulting fiberswere subsequently dewatered and dried to provide the starting material. In the experiment, 60
grams of the collagen fibers were dispersed in 240 cc. of
Water. The pH was 6.0 and the solids concentration was 20%. The temperature of the Water was raised to 50 C. before the fiber was metered in. Heating was continued until a maximum of 60 was reached at which time blending was started. Blending was continued during the entire heating period of one hour. At the conclusion of the heating, the doughy pulp was formed into a sheet by a hand rolling procedure. The sheet was cold set at 4 C. for ten minutes, and then immersed in a bath of half saturated ammonium sulfate (plldil). After one hour the sheet was examined and found to be exceedingly strong. The sheet was then tanned according to standard procedures, using a chrome tanning reagent.
While in the foregoing specification'this invention has been described in relation to certain specific embodiment thereof and many details have been set forth for pur-.
pose of illustration, it will be apparent to those skilled in the art that the invention is susceptible to additional embodiments and that certain of the details described herein can be varied considerably without departing from the basic principles of the invention.
I claim:
1; I In a method of preparing formed collagen, the steps comprising mixing discrete fibers of native collagen with water to form a doughy pulp, said pulp having a substantially neutral pH, heating said pulp at a temperature within the range from 40 to 65 C. to solubilize a portion of the collagen therein without appreciably shrinking said fibers, continuing said heating until at least 5% by weight of the collagen in said pulp has been solubilized while the major portion of the said collagenremains infibrillar form, and thereatter forming said pulp.
2. In a method of preparing formed collagen, the steps comprising mixing discrete fibers of native collagen with water to form a doughy pulp, said pulp having'a pH above 5.0 but below 8.0 and containing from to solids by Weight, heating said pulp at a temperature within the range from to 65 C. to solubilize a portion of the collagen therein without appreciably shrinking said fibers, continuing said heating until from 8 to 30% by l weight of the collagen in said pulp has been solubilized, and thereafter forming said pulp.
3. in a method of preparing formed collagen, the steps comprising mixing discrete fibers of native collagen with Water to form a doughy pulp, said pulp having a pH of from 5. 5 to 7.0 and containing from 10 to 25% solids by Weight, 1 eating said pulp at a temperature of from 54 to 62 C., continuing said heating until from 8 to 15 by weight of the collagen in said pulp has been solubilized While the major portion of the said collagen remains in fibrillar form, and thereafter forming said pulp.
4-. in a method of preparing collagen sheets, the steps comprising heating an aqueous pulp of collagen fibers, said pulp having a substantially neutral pH and being in the form of a soft pasty mass, said heating steps being controlled to transform at least 5% by weight of the fibrous collagen in said pulp to solubilized collagen with out appreciable shrinkage of the collagen fibers, terminating said heating step While the major portion of said collagen remains in fibrous form, extruding the heated pulp to a predetermined form, and chilling the formed collagen.
5. In a method of preparing formed collagen, the steps comprising heating an aqueous pulp, of collagen fibers;
said pulp having a pH above 5.0 but below 8.0 and being in the form of a soft pasty mass, said heating step being controlled to transform from 8 to 30% by weight of the fibrous collagen in said pulp to solubilized collagen without appreciable shrinkage of the collagen fibers, termi- 'd heating step while the major portion of said collagen remains in fibrous form, extruding the heated pulp to a predetermined form, and chilling the formed collagen.
6. in a method of preparing collagen sheets, the steps comprising heating an aqueous pulp of collagen fibers, said pulp having a pH of from 5.0 to 7.0 and being in the form of a soft pasty mass, said heating step being controlled to transform from 8 to 15% by Wei ht of the fibrous collagen in said pulp to solubilized collagen without appreciable shrinkage of the collagen fibers, extruding the heated pulp to form sheets, and chilling said sheets.
7. In a method of preparing collagen sheets, the steps comprising heating an aqueous pulp of collagen fibers, said pulp having a pH of from 5.5 to 7.0 and being in the form of a soft pasty mass, said heating'step being controlled to transform at least 8 to 15% by weight of the fibrous collagen in said pulp to solubilized collagen without appreciable shrinkage of the collagen fibers, said heating being carried out at a temperature of substantially from '54 to 62 C. and being terminated While the major portion of said collagen remains in fibrous form, extruding the heated pulp to form sheets, and chilling said sheets.
References Cited in the file of this patent UNITED STATES PATENTS

Claims (1)

  1. 4. IN A METHOF OF PREPARING COLLAGEN SHEETS, THE STEPS COMPRISING HEATING AN AQUEOUS PULP OF COLLAGEN FIBERS, SAID PULP HAVING A SUBSTANTIALLY NEUTRAL PH AND BEING IN THE FORM OF A SOFT PASTY MASS, SAID HEATING STEPS BEING CONTROLLED TO TRANSFORM AT LEST 5% BY WEIGHT OF THE FIBROUS COLLAGEN IN SAID PULP TO SOLUBILIZED COLLAGEN WITHOUT APPRECIABLE SHRINKAGE OF THE COLAGEN FIBERS, TERMINATING SAID HEATING STEP WHILE THE MAJOR PORTION OF SAID COLLAGEN REMAINS IN FIBROUS FORM, EXTRUDING THE HEATED PULP TO A PREDETERMINED FORM, AND CHILLING THE FORMED COLLAGEN.
US112213A 1961-05-24 1961-05-24 Method of preparing formed collagen Expired - Lifetime US3110549A (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
US112213A US3110549A (en) 1961-05-24 1961-05-24 Method of preparing formed collagen
FR7411A FR1322010A (en) 1961-05-24 1962-05-16 Process for the preparation of shaped collagen
ES277559A ES277559A1 (en) 1961-05-24 1962-05-22 Method of collagen preparation configured (Machine-translation by Google Translate, not legally binding)
BE617977A BE617977A (en) 1961-05-24 1962-05-23 Process for the preparation of molded collagen
AT423362A AT248599B (en) 1961-05-24 1962-05-23 Process for the production of synthetic fiber leather
GB19899/62A GB949424A (en) 1961-05-24 1962-05-23 Improved method of preparing formed collagen
NL278815D NL278815A (en) 1961-05-24 1962-05-24

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US112213A US3110549A (en) 1961-05-24 1961-05-24 Method of preparing formed collagen

Publications (1)

Publication Number Publication Date
US3110549A true US3110549A (en) 1963-11-12

Family

ID=22342691

Family Applications (1)

Application Number Title Priority Date Filing Date
US112213A Expired - Lifetime US3110549A (en) 1961-05-24 1961-05-24 Method of preparing formed collagen

Country Status (7)

Country Link
US (1) US3110549A (en)
AT (1) AT248599B (en)
BE (1) BE617977A (en)
ES (1) ES277559A1 (en)
FR (1) FR1322010A (en)
GB (1) GB949424A (en)
NL (1) NL278815A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4014971A (en) * 1973-05-11 1977-03-29 Perkins Rodney C Method for making a tympanic membrane prosthesis
CN108367101A (en) * 2015-11-10 2018-08-03 医疗美容解决方案祖韦拉克医生公司 Method for producing the biocompatible matrix with targeting structure design
EP3583255B1 (en) * 2017-02-15 2023-08-23 Ecco Sko A/S Method and apparatus for manufacturing a staple fiber based on natural protein fiber and a raw wool based on the staple fiber.

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1656681A (en) * 1925-08-07 1928-01-17 Samuel Jacob Method of manufacturing artificial sausage skins
US2631942A (en) * 1951-05-01 1953-03-17 United Shoe Machinery Corp Methods of forming fibers from collagen
US2838363A (en) * 1954-10-19 1958-06-10 Armour & Co Method of preparing filaments and sheets from procollagen
US2927345A (en) * 1955-06-13 1960-03-08 American Cyanamid Co Apparatus for casting gelatin upon a cooled drum including drum warp compensating means
US3034852A (en) * 1960-01-26 1962-05-15 Japan Leather Mfg Co Ltd Solubilization of insoluble collagen fibers and reconstitution thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1656681A (en) * 1925-08-07 1928-01-17 Samuel Jacob Method of manufacturing artificial sausage skins
US2631942A (en) * 1951-05-01 1953-03-17 United Shoe Machinery Corp Methods of forming fibers from collagen
US2838363A (en) * 1954-10-19 1958-06-10 Armour & Co Method of preparing filaments and sheets from procollagen
US2927345A (en) * 1955-06-13 1960-03-08 American Cyanamid Co Apparatus for casting gelatin upon a cooled drum including drum warp compensating means
US3034852A (en) * 1960-01-26 1962-05-15 Japan Leather Mfg Co Ltd Solubilization of insoluble collagen fibers and reconstitution thereof

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4014971A (en) * 1973-05-11 1977-03-29 Perkins Rodney C Method for making a tympanic membrane prosthesis
CN108367101A (en) * 2015-11-10 2018-08-03 医疗美容解决方案祖韦拉克医生公司 Method for producing the biocompatible matrix with targeting structure design
US20180326116A1 (en) * 2015-11-10 2018-11-15 Medskin Solutions Dr. Suwelack Ag Method for producing a biocompatible matrix with targeted structural design
US11369715B2 (en) * 2015-11-10 2022-06-28 Medskin Solutions Dr. Suwelack Ag Method for producing a biocompatible matrix with targeted structural design
EP3583255B1 (en) * 2017-02-15 2023-08-23 Ecco Sko A/S Method and apparatus for manufacturing a staple fiber based on natural protein fiber and a raw wool based on the staple fiber.
EP3583256B1 (en) * 2017-02-15 2023-11-01 Ecco Sko A/S A filament and yarn produced on the basis of a natural protein

Also Published As

Publication number Publication date
ES277559A1 (en) 1962-10-16
BE617977A (en) 1962-09-17
FR1322010A (en) 1963-03-22
AT248599B (en) 1966-08-10
GB949424A (en) 1964-02-12
NL278815A (en) 1964-11-10

Similar Documents

Publication Publication Date Title
US3123481A (en) Tanned edible collagen casing and method of producing same
US3622353A (en) Sausage preparation process
US3071477A (en) Process of forming collagen articles
US3123482A (en) R lieberman
US2598608A (en) Preparation of collagenous materials
US2747228A (en) Production of collagen strands
US4455206A (en) Shaped article of collagen and process for preparing same
US2374201A (en) Gelatin filaments and preparation thereof
US2114220A (en) Manufacture of artificial sausage skins or casings
US3194865A (en) Acid depilation and extrudable fibril production from hide corium
US3110549A (en) Method of preparing formed collagen
US3620775A (en) Edible collagen casing
US3627542A (en) Edible collagen casing containing monoglyceride or acetylated monoglyceride softener
US4021522A (en) Method of forming collagen dispersions
US3178301A (en) Reconstitutable acid solubilized collagen
US3126433A (en) Benzoic acid treatment of collagen
US3123483A (en) Edible collagen casing and method
US3894132A (en) Method of forming collagen dispersions
US3505084A (en) Method of preparing a collagen sausage casing
US3433864A (en) Methods of extruding collagen
US3634561A (en) Collagen products
US3374103A (en) Collagen fibril and neutral salt composition
US3297459A (en) Process of preparing formed collagen bodies
US3579358A (en) Method of preparing an edible tubular collagen casing
US3932677A (en) Collagen casings from limed hide collagen