WO2001034214A1 - Utilisation de derives de cellulose solubles rendus difficilement solubles dans l'eau et methode de preparation de ces derives - Google Patents
Utilisation de derives de cellulose solubles rendus difficilement solubles dans l'eau et methode de preparation de ces derives Download PDFInfo
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- WO2001034214A1 WO2001034214A1 PCT/JP2000/005564 JP0005564W WO0134214A1 WO 2001034214 A1 WO2001034214 A1 WO 2001034214A1 JP 0005564 W JP0005564 W JP 0005564W WO 0134214 A1 WO0134214 A1 WO 0134214A1
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- water
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- soluble
- soluble cellulose
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/14—Macromolecular materials
- A61L27/20—Polysaccharides
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
- A61L15/28—Polysaccharides or their derivatives
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L31/00—Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
- A61L31/04—Macromolecular materials
- A61L31/042—Polysaccharides
Definitions
- a tissue-coating medical material formed from a water-insoluble soluble cellulose derivative obtained by treating the derivative with an acid and (2) a group obtained by freezing and thawing an acidic aqueous solution of the soluble cellulose derivative.
- the present invention relates to a manufacturing method for providing a woven covering medical material.
- carboxymethylcellulose into which a carboxymethyl group is introduced (hereinafter, carboxymethylcellulose refers to sodium carboxymethylcellulose according to a general name) is a typical one, Utilizing its viscoelasticity, it is widely used in the food field and water-absorbing materials, and its use extends to the medical field.
- JP-A-11-132,615 discloses carboxymethylcellulose and fibrin
- JP-A-7-109220 describes carboxymethylcellulose.
- German Patent No. 1,397,893 disclose a wound healing agent comprising carboxymethylcellulose and an anti-inflammatory agent.
- Japanese Patent Application Laid-Open No. Hei 8-550258 and European Patent No. 47647 disclose wound dressings using crosslinked carboxymethylcellulose. All of these use soluble carboxymethylcellulose or carboxymethylcellulose cross-linked with a chemical cross-linking agent, etc., as in the case of the anti-adhesion material. No agent use is disclosed.
- Japanese Patent Application Laid-Open No. 62-39506 discloses a porous material obtained by crosslinking chitin with a drug.
- a sponge is disclosed.
- JP-A-3-23864 discloses a block-like composite material composed of collagen sponge and polylactic acid
- JP-A-7-550643 describes a sponge.
- An excellent bone substitute consisting of hyaluronic acid ester having biocompatibility and bioabsorbability has been disclosed.
- the porous sponge is non-absorbable in vivo and is not completely replaced by bone itself.Therefore, there is a risk of infection and the risk of detachment of the material itself. Had a problem that collagen of the mouth had some antigenicity.
- the method of obtaining carboxymethyl cellulose which has become hardly water-soluble includes a method in which an acidic solution of carboxymethylcellulose is allowed to stand (Encyclopedia of Polymer Science & Technology, Vol. 3, 520-539 (1965)). A method in which a strong acid is added to calepo or xymetyl recellulose in the presence of methyl alcohol or ethyl alcohol (Colloid Polym. Sci., Vol. 267, 226-236 (1989)); And a method using an exchange resin (US Pat. No. 2,617,800). Also, a method of concentrating the acidic solution in the carboxymethyl cell mouth by ultracentrifugation or the like can be used.
- the present inventors have diligently studied the physicochemical properties of the soluble cellulose derivative itself and its effects on living organisms in order to achieve the above object.
- the soluble cellulose derivative hardly soluble in water obtained by acid treatment, which has been reported so far, has a high effect as a tissue covering medical material such as an anti-adhesion material and a wound dressing material. I found it.
- the material produced by freezing and thawing a soluble cellulose derivative aqueous solution under acidic conditions which has not been studied so far, may cause fibrous or filled fine particles due to the effect of ice crystals formed during freezing. It was found to have a fine structure.
- the water-insoluble soluble cellulose derivative obtained by freezing and thawing is more sheet-like than the water-insoluble soluble cellulose derivative prepared by a conventionally known acid treatment method. Not only is it easy to form into a film, sponge, etc., but also into a sheet, film, tube, etc. after being crushed using ultrasonic waves or a mixer. It is clear that the material has excellent material properties as a medical material, such as obtaining a uniform and uniform form.
- the present invention provides: (1) a tissue-covering medical material for use for the purpose of being implanted in a body or pasting to a tissue, comprising (1) a water-insoluble soluble cellulosic derivative; (1) The method for producing a tissue-coating medical material according to (1), wherein the method comprises freezing and thawing an acidic solution of the soluble cellulose derivative. (3) The soluble cellulose derivative concentration is adjusted to 5% by mass or more. A tissue-coating medical material according to (1), wherein a water-insoluble soluble cellulose derivative obtained by mixing with an acid solution and leaving the mixture at a non-freezing temperature is used.
- Tissue-coating medical material according to (1) characterized in that a water-insoluble soluble cellulose derivative obtained by allowing an acidic solution of the soluble cellulose derivative to stand is used.
- the tissue-coated medical material according to 1 or 2 wherein (10) the solubility of the soluble cellulose derivative in a neutral aqueous solution at 60 ° C for 3 hours is 50% or less.
- tissue-coating medical material described in (1) (11) the method for producing a tissue-coated medical material described in (2), wherein the solubility of the water-insoluble soluble cellulose derivative is controlled. 1 2) Soluble cellulose derivative with poor water solubility (1)
- the soluble cellulose derivative according to any one of (1) to (12), (14) the tissue-covering medical material is an adhesion preventing material.
- tissue covering medical material according to (1) or (12), and (15) the tissue covering medical material is a wound covering material, wherein the tissue covering property according to (1) or (12) is characterized.
- FIG. 1 shows carboxymethyl cellulose which has been made hardly water soluble by freeze-thaw treatment
- FIG. 2 shows carboxymethyl cellulose which has been made hardly water soluble by aging treatment with an acidic aqueous solution.
- tissue refers to a tissue such as a mucous membrane, a blood vessel, a bone, a tendon, an organ such as a stomach or an intestine, or a skin on a body surface. It means that it is applied to the skin and mucous membrane. For example, it applies to surgical damage caused by general surgery, physical damage such as fracture, Achilles tendon rupture or bedsore, or chemical damage such as burns caused by chemicals.
- the tissue-covering medical material means a biocompatible material used for coating a damaged or damaged tissue or organ, inside or outside the body.
- the ability to use, as a soluble cellulose derivative, methylcellulose, ethylcellulose, hydroxyshethylcellulose, hydroxypropylcellulose, carboxymethylcellulose, carboxymethylethylcellulose, etc., at an industrial level The most preferred is readily available and inexpensive dexamethasyl cellulose.
- the molecular weight of the soluble cellulose derivative used in the present invention is not particularly limited, and is preferably in the range of about 1 ⁇ 10 1 to about 5 ⁇ 10 5 daltons.
- the degree of etherification which is another parameter of the soluble cellulose derivative, those having a range in which hardly water-soluble is caused by the following treatment can be used.
- the soluble cellulose derivative referred to in the present invention is used in a concept that includes a metal salt of alkali metal, for example, a salt of sodium, potassium, and lithium.
- modification as used in the present invention means to introduce a chemical crosslink or perform a chemical modification in order to make a water-soluble soluble cellulose derivative hardly water-soluble.
- controlling the solubility refers to a method for controlling the solubility of a soluble cell in a phosphate buffered saline solution having a pH of 7.4 at 60 ° C., as described in Examples below. This means that the ratio of the soluble cellulosic derivative eluted in phosphate buffered saline after a certain period of time when the derivative is placed.
- any acid can be used as long as it can adjust the pH to 3.5 or less.
- a strong acid for example, hydrochloric acid, nitric acid, sulfuric acid and the like.
- the pH of the acidic aqueous solution is selected based on the molecular weight of the soluble cellulose derivative used, the degree of etherification, the physical properties of the desired water-insoluble soluble cellulose derivative, and more preferably the pH. 2 or less.
- Freezing and thawing are performed by placing an acidic aqueous solution of a soluble cell derivative in an optional container, freezing it at a predetermined temperature, and thawing at a predetermined temperature after freezing. Is also performed once.
- the temperature and time for freezing and thawing are determined by the size and size of the container and the temperature and time for freezing and thawing the acidic aqueous solution of the soluble cellulose derivative, depending on the volume of the aqueous solution. Thaw temperatures above freezing are preferred.
- a freezing temperature of 15 ° C or less and a thawing temperature of 5 ° C or more are selected because the freezing and thawing times can be shortened.
- the time is not particularly limited as long as it is equal to or longer than the time at which freezing and thawing is completed at that temperature.
- the number of repetitions of the operation of freezing and then thawing the adjusted acidic aqueous solution of the soluble cellulose derivative depends on the molecular weight of the soluble cellulose derivative to be used, the concentration of the aqueous solution, the pH of the aqueous solution, the temperature and time of freezing and thawing, and the production time. It is appropriately determined according to various properties such as the strength of the water-insoluble soluble cellulose derivative. Usually it is preferable to repeat at least once. The temperature and time of freezing and thawing may be changed each time the freezing and thawing operations are repeated.
- the solubility of the resulting water-insoluble soluble cellulose derivative can be easily controlled by appropriately selecting the molecular weight of the soluble cellulose derivative to be used, the pH of the aqueous solution, the freezing temperature and time, and the like.
- U beam dissolved in earthenware pots by to 1% by weight in distilled water
- the pH of the aqueous solution is set to 1.5, and the resulting solution is frozen at ⁇ 20 ° C. and thawed at room temperature, the longer the freezing time, the more difficult it is to dissolve.
- an aqueous solution of sodium carboxymethylcellulose prepared at the same concentration and having a different molecular weight at pH 1.5 was frozen at 120 ° C for a certain period of time, and further thawed at room temperature. The higher the molecular weight of the rim, the less water-soluble carboxymethylcellulose that is less soluble is obtained.
- any acid can be used for mixing.
- a strong acid for example, hydrochloric acid, nitric acid, sulfuric acid and the like.
- Mixing and standing are as follows: After placing the soluble cellulose derivative and the acid solution in an arbitrary container, mixing them until they are sufficiently uniform, and after mixing, leave the mixture at a predetermined temperature. Do it twice. Is the temperature and time for mixing and standing determined by the size and capacity of the container? Generally, mixing temperatures below room temperature are preferred. Further, the leaving time is not particularly limited as long as the operation is completed or longer.
- a conventionally known method of allowing a soluble cellulose derivative acidic solution to stand is to dissolve the soluble cellulose derivative in water and acidify the aqueous solution by adding hydrochloric acid, nitric acid, sulfuric acid, or the like. Any method can be used as long as an acidic aqueous solution of a soluble cellulose derivative can be obtained, such as a method of dissolving a soluble cellulose derivative.
- the content is preferably 5% by mass or less, and more preferably 1% by mass or less.
- the pH of the acidic aqueous solution is selected from the molecular weight of the soluble cellulose derivative used, the degree of etherification, the physical properties of the desired water-insoluble soluble cellulose derivative, etc., and is preferably pH 3.5 or less. Preferably it is pH 2 or less.
- the ability to obtain a water-insoluble soluble cellulose derivative by allowing the prepared acidic solution of the soluble cellulose derivative to stand still ⁇ ', and the standing time is the same as the pH of the acidic solution.
- the degree of etherification, the degree of etherification, the physical properties of the water-soluble soluble cellulose derivative desired to be hardly soluble, and the like are selected.
- the temperature at the time of standing is not particularly limited as long as the above operation is completed, but is generally preferably room temperature or lower, and more preferably 5 ° C or lower. This is the temperature at which the derivative acidic aqueous solution does not freeze.
- the poorly water-soluble soluble cellulose derivative can be obtained by mixing an acidic aqueous solution of the soluble cellulose derivative with a polar organic solvent such as methanol or ethanol.
- concentration of the soluble cellulose derivative in the acidic solution is not particularly limited, but is preferably 5% by mass or less, more preferably 1% by mass or less.
- the pH is 5 ', preferably pH 3.5 or less, which is selected from the molecular weight of the soluble cellulose derivative used, the degree of etherification, the physical properties of the desired water-insoluble soluble cellulose derivative, and the like. More preferably, it is pH 2 or less.
- Polar organic solvents are polar solvents that are completely compatible with water, and that a mixed solvent of the polar organic solvent and water can dissolve the soluble cellulose derivative at room temperature or above room temperature to form a solution.
- a water-soluble organic compound having the formula:
- the polar organic solvent used in the present invention is not particularly limited as long as a soluble cellulose derivative hardly soluble in water can be obtained.
- a lower alcohol-based solvent such as methanol and ethanol, glycerin / ethylene glycol and the like can be used.
- Alcoholic solvents, ketone solvents such as acetone and methylethyl ketone, ether solvents such as dioxane and tetrahydrofuran, formamide, N, N-dimethylformamide Solvents such as amides, sulfoxide solvents such as dimethyl sulfoxide and tetrahydrothiophene-11, and amide solvents such as hexamethylphosphoric triamide. , Acetonitrile, etc.
- the polar organic solvent may be used alone or in combination of two or more. These polar organic solvents may be added at once, or may be a water-insoluble soluble solvent. It may be further added to the acidic solution after recovering the hydrophilic cellulose derivative, and the method of addition is not limited at all. Alternatively, an acidic aqueous solution of the soluble cellulose derivative may be prepared, and an appropriate amount of a polar organic solvent may be added to the aqueous solution.However, after dissolving the soluble cellulose derivative powder directly in a mixed solvent of the polar organic solvent and water, May be acidified.
- a column filled with a strong ionic ion exchange resin is used.
- concentration of the soluble cellulose derivative is selected depending on the molecular weight, the degree of etherification, and the like of the soluble cellulose derivative, but is preferably 1% by mass or less, and more preferably 0.5% by mass or less.
- the ion exchange resin to be used is not particularly limited as long as it has a capability of exchanging sodium of a soluble cellulose derivative with hydrogen, and a strong ionizable cation exchange resin having a sulfon group and 5 'is preferable.
- examples of the concentrating method include ultracentrifugation, ventilation drying, drying under reduced pressure, and freeze drying.
- the concentration of the soluble cellulose derivative in the acidic aqueous solution before the concentration is preferably 5% by mass or less, more preferably 1% by mass or less, because it is easy to handle.
- the forming process of a soluble cellulose derivative that has been made hardly water-soluble when it is applied as a medical material will be described. First, it is necessary to remove and wash the acid used for adaptation to the living body.
- the acid is removed by replacing the liquid around the soluble cellulose derivative that has been rendered poorly water-soluble with a neutral buffer, and if the mixing of buffer components becomes inconvenient, replacement with purified water is performed to remove the acid. A soluble cellulose derivative is obtained.
- the neutral buffer used is not particularly limited, as long as it does not impair the function of the soluble cellulose derivative hardly soluble in water.
- a pharmacologically acceptable phosphate buffer is used.
- the neutralization method is not particularly limited, but usually, a batch method, a filtration method, a method of filling a column or the like and passing the solution, or the like is used.
- These neutralization conditions include conditions such as the amount of the neutralization solution, the number of times, etc. If so, it can be appropriately selected depending on the form and use of the soluble cellulose derivative which has been rendered hardly water-soluble.
- the water-insoluble soluble cellulose derivative thus obtained may be subjected to treatment such as immersion in a solvent, wet state containing a solvent, ventilation drying, drying under reduced pressure or freeze drying, depending on the purpose of use. It is provided in a dry state after passing through.
- Processing such as molding of the water-insoluble soluble cellulose derivative may be performed in the form of a sheet by selecting the soluble cellulosic derivative and the prepared soluble cellulosic acid acidic aqueous solution container or method at the time of preparation. It is possible to prepare a water-insoluble soluble cellulose derivative in a desired form in the form of a film, a crush, a sponge, a lump, a fiber, and a tube. Examples of processing after the production of the water-insoluble soluble cellulose derivative include fine crushing by mechanical pulverization, film formation by rolling, and spinning.
- a square or circular sheet, film, sponge, or other water-insoluble soluble cellulose derivative can be obtained by freezing, for example, by using a square or circular container. be able to.
- the water-insoluble soluble cellulose derivative obtained once is crushed by a mixer or the like in distilled water or physiological saline, etc. to form a water-insoluble water-soluble soluble cellulose derivative suspension or a suspension. It can be dried in various containers to form sheets, films, or blocks.
- the soluble cellulose derivative made hardly soluble in water by the freeze-thaw method has a fibrous or film-like structure, the suspension is sufficiently fine to capture the soluble cellulose derivative made hardly soluble in water. It can be easily formed into a uniform sheet or film by spreading it on a filter having holes and drying it.
- a polymer compound can be mixed with the water-insoluble soluble cellulose derivative according to the present invention.
- the polymer compound can be used regardless of a natural polymer compound, a synthetic polymer compound, a water-soluble polymer compound, or a water-insoluble polymer compound. There is no restriction if you do not have one. These are soluble cell mouths that have been made hardly water soluble.
- it may be mixed with an acidic solution of the soluble cellulose derivative, or may be mixed with the prepared soluble cellulose derivative having poor water solubility. There is no particular limitation as long as the method does not hinder solubilization.
- polysaccharides selected from the group consisting of polysaccharides, proteins, nucleic acids, and synthetic polymers, but are not limited thereto.
- polysaccharides include glycosaminoglycans other than hyaluronic acid or hyaluronate (eg, heparin, heparan sulfate, dermatan sulfate), and chondroitin sulfate (eg, And keratin sulfate, arginic acid and its biologically acceptable salts, cellulose, chitin, chitosan, dextran, starch, amylose, polylactic acid, carrageenan, etc. Is mentioned.
- glycosaminoglycans other than hyaluronic acid or hyaluronate eg, heparin, heparan sulfate, dermatan sulfate
- chondroitin sulfate eg, And keratin sulfate, arginic acid and its biologically acceptable salts, cellulose, chitin, chitosan, dextran, starch, am
- proteins include collagen, gelatin, albumin, elastin, various globulins, casein, gluten, and the like, and biologically acceptable synthetic derivatives thereof.
- Examples of the synthetic polymer include polyvinyl alcohol, polyethylene glycol, polyglycolic acid, polyacrylic acid, polymer acrylic acid, polylactic acid, copolymers thereof, and acrylic acid. Derivatives such as poly (uric acid or hydroxymethyl) ester, poly (acrylic amide), polyvinyl alcohol, and copolymers of maleic acid and fumaric acid. .
- the present invention is not limited to these polymer compounds.
- the sterilization treatment required for medical devices is described. Since the sugar chain structure of soluble cellulose derivatives is relatively stable to heat, radiation, etc., tissue-coated medical materials composed of soluble cellulose derivatives that have been rendered sparingly soluble in water are sterilized by y-ray, electron beam, and ethylene oxide gas. Various sterilization methods such as plasma gas sterilization can be adopted. A phenomenon in which the solubility of the soluble cell mouth derivative, which has become poorly water-soluble due to such harsh treatment, is confirmed to change. The force is more stable in advance by changing the manufacturing conditions such as the freezing time in the freeze-thaw method. Manufactures the best materials It is also possible to control the in-vivo storage.
- the anti-adhesion material of the soluble cellulose derivative hardly water-soluble obtained in the present invention may be in the form of sheet, film, crushed, sponge, lump, fibrous, fluid, or tubular. Can be used for surgery. It is preferable to apply it directly to the surgical site in the form of a film or a sheet, or to use it in the form of a finely crushed or flowing fluid using a syringe or the like. It is preferably applied to It can also be used for laparoscopic surgery.
- the wound dressing material of the water-insoluble soluble cellulose derivative obtained in the present invention may be in the form of sheet, film, crushed, sponge, lump, fibrous, fluid, tube or the like. Used.
- the form to be used can be appropriately selected depending on the force 'which is preferably applied directly to the affected part as a film or sheet, and the shape and size of the wound.
- Example 2 After mixing with 1 N nitric acid at room temperature to cormorants it'll become a carboxymethyl chill cellulose used in Example 1 to 2 0 mass 0/0, and stored in a refrigerator at 4 ° C for 3 days. Thereafter, neutralization was carried out with water and a phosphate buffer (pH 6.8) having a concentration of 100 mM to obtain a lumpy water-insoluble carboxymethyl cellulose. The water-insoluble carboxymethylcellulose is stretched by applying a pressure of about 30 NZ cm 2 and dried at about 50 ° C. to obtain about 1.5 mg Z cm 2 . The film was included.
- a phosphate buffer pH 6.8
- the poorly water-soluble carboxymethylcellulose is suspended in physiological saline, and the suspension is then poly- After casting in a styrene container, it was dried at about 50 ° C. to obtain a film containing about 1.5 mg / cm 2 .
- Example 5 Was dissolved in earthenware pots by becomes 0.3 mass 0/0 in distilled water carboxymethylcellulose used in Example 1.
- TSKgel SP-Toyono packed in a glass column approximately 5 cm id, approximately 15 cm long packed with 550 ml and equilibrated with 0.5 mm o 1/1 phosphoric acid did.
- the prepared carboxymethylcellulose solution was injected into the ion-exchange column using a liquid chromatograph pump P-500, and 0.5 mm 01-phosphate was added at a flow rate of 0.5 ml / min. The solution was passed through to obtain a viscous carboxymethylcellulose solution made hardly soluble in water.
- a water-insoluble carboxymethylcellulose solution obtained after sufficient dialysis against water and a phosphate buffer (pH 6.8) at a concentration of 100 mM was added to a polystyrene container.
- a phosphate buffer pH 6.8
- An anesthetic (ketamine solution) was intramuscularly injected into the rat (SD, female, 9 weeks of age or older), anesthetized, fixed on the back, disinfected the abdominal skin with isodine, and then shaved.
- the rat abdominal muscle was opened along the midline, the cecum was removed from the abdominal cavity, and the cecum was fixed with a perforated (? 5 16 mm) tephron sheet.
- a rotating rod (13 mm) covered with gauze was pressed against the cecal part exposed from the hole, and rubbed about 120 times (two places on one side).
- Example 8 Microscopic Observation of Carboxymethyl Cellulose Made Insoluble in Water
- the carboxymethyl cellulose made hardly soluble in water obtained in Examples 1 to 4 was mixed with water and a phosphate buffer (pH 6. After being neutralized by 8), it was dried at about 50 ° C.
- Digital microscope (Ki-en) (VH-70000 type, manufactured by K.K.). As a result, a fibrous structure or a film-like structure was recognized only in the water-insoluble carboxymethyl cellulose obtained in Example 1.
- the figure (photograph) of the hardly water-soluble carboxymethylcellulose obtained in Example 1 and the poorly water-soluble carboxymethylcellulose obtained in Example 3 as a control is shown.
- the obtained water-insoluble carboxymethylcellulose is slurried in distilled water by crushing with a microhomogenizer (NISSEI EXCEL AUTO HOMOGENIZAER), then spread on a screen for printing and dried. Into a film shape. A uniform film was obtained with the poorly water-soluble carboxymethyl cellulose obtained in Example 1 in Fig. 1, whereas the other poorly water-soluble carboxymethyl cellulose was obtained as shown in Fig. 2. Lumuka? It became uneven.
- the pH of the aqueous solution thus prepared was adjusted to 1.5 with 1N nitric acid, and 15 ml of the acidic aqueous solution was placed in a 30 ml polystyrene container and set at 120 ° C. Into a freezer. After allowing to stand for 1 day, it was thawed at 25 ° C. Thereafter, neutralization was carried out with water and a phosphate buffer (pH 6.8) at a concentration of 100 mM to obtain a carboxymethyl cellulose in the form of a water-insoluble sponge.
- a phosphate buffer pH 6.8
- Example 1 1 The standing period at 120 ° C. in Example 10 was set to 3 days to obtain a carboxymethyl cellulose in the form of a sponge which was made hardly water-soluble.
- Example 1 the aqueous solution of carboxymethylcellulose was left without acidification. As a result, carboxymethylcellulose made hardly soluble in water was not obtained. This aqueous solution was freeze-dried to form a sponge.
- Example 10 the aqueous solution of carboxymethylcellulose was left without acidification. As a result, carboxymethyl cellulose made hardly soluble in water was not obtained. This aqueous solution was freeze-dried to form a sponge.
- Example 12 Solubility test of carboxymethyl cellulose made hardly soluble in water A phosphate buffered saline having a pH of 7.4 and having the following composition was prepared.
- the concentration of carboxymethylcellulose in phosphate buffered saline was determined from the peak area of the differential refractive index detector using GPC. That is, phosphate buffered saline collected over time was filtered through a 0.45 m filter and injected into GPC.
- Example 10 The storage period at 120 ° C. in Example 10 was set to one day to obtain a carboxymethyl cellulose in the form of a water-insoluble sponge. This poorly water-soluble carboxymethylcellulose was lyophilized into a sheet containing about 2.0 mg / cm 2 .
- Example 15 The water-insoluble carboxymethylcellulose sheet obtained in Example 13 was sterilized at 25 kGy with a cobalt 60 as a radiation source.
- Example 15 The water-insoluble carboxymethylcellulose sheet obtained in Example 13 was sterilized at 25 kGy with a cobalt 60 as a radiation source.
- Example 10 The standing period at 120 ° C. in Example 10 was set to 7 days to obtain a carboxymethyl cellulose in the form of a water-insoluble sponge. About 2 Ri by the sparingly water-solubilized mosquito Le ball carboxymethylcellulose to lyophilization. After the O mg / cm 2 a includes sheet-like, of 2 5 k G y of the cobalt 6 0 the radiation source A-line sterilization was performed.
- Example 17 After Example 1 0 freeze carboxymethylcellulose were poorly water-soluble reduction obtained in forming dry by Ri about 2 to. 0 mg / cm 2 sheet shape comprising, for the Le bets 6 0 the radiation source A 25 kG y line sterilization was performed.
- Example 17
- Example 11 The water-insoluble carboxymethyl cellulose obtained in Example 11 was freeze-dried to form a sheet containing about 2.0 mg / cm 2 , and then Kovar 60 was used as a radiation source. Y-ray sterilization of 25 kG y was performed.
- Example 1 Water-insoluble carboxymethyl cell mouth subjected to 7-line sterilization
- Example 12 a solubility test was performed on the carboxymethyl cellulose sheet obtained in Examples 13 to 16, which had been subjected to sterilization by aerial radiation and made hardly water-soluble. Table 3 shows the results.
- Example 11 Steam water was added to the poorly water-soluble carboxymethylcellulose obtained in Example 11 so that the carboxymethylcellulose concentration became 1%, and then the mixture was treated with a microhomogenizer (NISSEI EXCEL AUTO HOMOGENIZAER). The slurry was crushed to obtain a slurry of carboxymethylcellulose that had become hardly water-soluble. The slurry was spread on a printing screen and dried at about 40 ° C to make it hardly water-soluble. It was made into a film containing about 2.0 mg / cm 2 of carboxymethyl cellulose. Further, this film was subjected to 25 kGy y-ray sterilization using a control 60 as a radiation source.
- a microhomogenizer NISSEI EXCEL AUTO HOMOGENIZAER
- Example 20 Anti-adhesion test of hardly water-soluble dextrin cellulose obtained by freeze-thaw method
- Example 7 the sheet or film obtained in Example 13, Example 16, or Example 19 was subjected to an adhesion prevention test.
- a commercially available sepra film manufactured by Jenzym was used. Table 4 shows the results.
- Example 2 3 A saline solution was added to the poorly water-soluble carboxymethylcellulose obtained in Example 15 so that the carboxymethylcellulose concentration became 1% by mass, followed by crushing with a microhomogenizer (NISSEI EXCEL AUTO HOMOGENIZAER). A slurry containing about 3% by mass of solubilized carboxymethyl cellulose was obtained.
- Example 22 and Example 23 were subjected to the following tests.
- As a control an untreated group to which only physiological saline was administered was set.
- Example 23 The group was treated with the slurry and the untreated group. Implantation was performed by cutting the hair of the rabbit's head, creating a bone defect (5 mm in diameter) using a microdrill on the skull under ether anesthesia, and applying various water-insoluble carboxymethyl cellulose to the bone. It was performed by filling and suturing the defect.
- Example 1 The carboxymethylcellulose used in Example 1 and chondroitin 6—sulfuric acid (manufactured by Seikagaku Corporation) having a molecular weight of about 3.5 ⁇ 10 4 daltons were added to distilled water in amounts of 0.5 mass. was dissolved in a jar'll become to 0/0. The pH of the prepared aqueous solution was adjusted to pH 1.5 with 1 N nitric acid, and 15 ml of this acidic aqueous solution was placed in a 30 ml polystyrene container, and a freezer set at 20 ° C was used. Put in. After standing for 5 days, it was thawed at 25 ° C. Thereafter, neutralization was carried out with water and a phosphate buffer (pH 6.8) having a concentration of 100 mM to obtain a carboxymethylcellulose sponge-like hardly water-soluble composition.
- a phosphate buffer pH 6.8
- the carboxymethylcellulose and polyvinyl alcohol (polymerization degree: 1500, manufactured by Wako Pure Chemical Industries) used in Example 10 were dissolved in distilled water so as to be 0.5% by mass and 10% by mass, respectively. . Adjust the pH of the prepared aqueous solution with 1 N nitric acid. The pH was adjusted to HI.5, and 15 ml of this acidic aqueous solution was placed in a 30 ml polystyrene container, and then placed in a freezer set at 20 ° C. After standing for 5 days, it was thawed at 25 ° C. Thereafter, neutralization was carried out with water and a phosphate buffer (pH 6.8) having a concentration of 100 mM to obtain a sponge-like hardly water-soluble ruboxymethylcellulose composition.
- a phosphate buffer pH 6.8 having a concentration of 100 mM
- Example 0 The carboxymethylcellulose and sodium alginate (manufactured by Funakoshi) used in Example 0 were dissolved in distilled water so as to be 0.5% by mass.
- the pH of the prepared aqueous solution was adjusted to 1.5 with 1N nitric acid, and 15 ml of this acidic aqueous solution was placed in a 30 ml polystyrene container, and the temperature was raised to 20 ° C. Placed in the set freezer. After standing for 7 days, it was thawed at 25 ° C. Thereafter, neutralization was performed with water and a phosphate buffer (pH 6.8) having a concentration of 100 mM to obtain a carboxymethylcellulose composition having a water-insoluble and sponge shape.
- a phosphate buffer pH 6.8 having a concentration of 100 mM
- the carboxymethylcellulose and chitosan (manufactured by Wako Pure Chemical Industries) used in Example 10 were dissolved in distilled water so as to be 1.0% by mass and 0.1% by mass, respectively.
- the pH of the prepared aqueous solution is adjusted to pH 1.5 with 1N nitric acid, and 15 ml of this acidic aqueous solution is placed in a 30 ml polystyrene container and set at 20 ° C. And put them in a freezer. After standing for 5 days, it was thawed at 25 ° C. Thereafter, neutralization was carried out with water and a phosphate buffer (pH 6.8) having a concentration of 100 mM to obtain a carboxymethylcellulose composition in the form of a sponge, which was made hardly soluble in water.
- a phosphate buffer pH 6.8 having a concentration of 100 mM
- Example 29 Cytotoxicity test of carboxymethyl cellulose made water-insoluble in water The water-solubility obtained in Examples 1 to 6, Example 9, Example 11, and Examples 14 to 17 was obtained. Cytotoxicity tests were carried out on carboxymethyl cellulose and the water-insoluble water-soluble propyloxymethyl cellulose compositions obtained in Examples 25 to 28.
- Water insolubilization obtained by the present invention in fibroblast cultures derived from normal human skin The non-contacted lipoxymethylcells were coexisted, and their cytotoxicity was evaluated by observing the cell growth behavior.
- the preparation was immersed in phosphate buffered saline and then freeze-dried. Twenty mg of the freeze-dried product was mechanically pulverized, placed in a Falcon Cell Culture Insert (pore size: 3 m), and immersed in a medium in which cells were seeded. The culture in the absence of carboxymethylcellulose, which was made hardly water-soluble, was used as a control.
- Seeding cell number 1 X 1 0 4 or Z Ueru
- a poorly water-soluble soluble cell mouth derivative comprising a soluble cellulose derivative can be obtained without using any chemical crosslinking agent or chemical modifier. It is useful for medical materials because it avoids the adverse effects on biocompatibility caused by the use of chemical cross-linking agents and chemical modifiers and easily controls solubility.
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Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002390556A CA2390556C (en) | 1999-11-09 | 2000-08-18 | Use of soluble cellulose derivative having been made hardly soluble in water and method for producing it |
EP00953516A EP1228771A4 (en) | 1999-11-09 | 2000-08-18 | USE OF SOLUBLE CELLULOSE DERIVATIVES MADE DIFFICULTLY SOLUBLE IN WATER AND METHOD OF PREPARING SUCH DERIVATIVES |
AU65970/00A AU782519B2 (en) | 1999-11-09 | 2000-08-18 | Use of soluble cellulose derivative having been made hardly soluble in water and process for producing the same |
KR1020027005853A KR20020062301A (ko) | 1999-11-09 | 2000-08-18 | 수난용성화된 가용성 셀룰로오스 유도체의 용도 및 그제조방법 |
US10/129,751 US7514097B1 (en) | 1999-11-09 | 2000-08-18 | Use of soluble cellulose derivative having been made hardly soluble in water and process for producing the same |
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JP11/318587 | 1999-11-09 | ||
JP31858799 | 1999-11-09 | ||
JP2000/39244 | 2000-02-17 | ||
JP2000039244 | 2000-02-17 |
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WO2001034214A1 true WO2001034214A1 (fr) | 2001-05-17 |
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PCT/JP2000/005564 WO2001034214A1 (fr) | 1999-11-09 | 2000-08-18 | Utilisation de derives de cellulose solubles rendus difficilement solubles dans l'eau et methode de preparation de ces derives |
Country Status (7)
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US (1) | US7514097B1 (ja) |
EP (1) | EP1228771A4 (ja) |
KR (1) | KR20020062301A (ja) |
CN (1) | CN100379462C (ja) |
AU (1) | AU782519B2 (ja) |
CA (1) | CA2390556C (ja) |
WO (1) | WO2001034214A1 (ja) |
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JP2005000512A (ja) * | 2003-06-13 | 2005-01-06 | Yasuharu Noisshiki | 管腔形成誘導性材料 |
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JP2006525836A (ja) * | 2003-05-09 | 2006-11-16 | ブリストル−マイヤーズ スクイブ カンパニー | 褥瘡治療における創傷被覆材の使用 |
WO2007015579A1 (ja) | 2005-08-04 | 2007-02-08 | Teijin Limited | セルロース誘導体 |
JP2008013510A (ja) * | 2006-07-07 | 2008-01-24 | Seikagaku Kogyo Co Ltd | 水難溶性組成物並びにその製造方法及び用途 |
JP2010285440A (ja) * | 2002-08-06 | 2010-12-24 | Mytogen Inc | 治療複合物 |
WO2011121858A1 (ja) | 2010-03-31 | 2011-10-06 | 株式会社ホギメディカル | 癒着防止材 |
JP2017036235A (ja) * | 2015-08-10 | 2017-02-16 | 日立化成株式会社 | ナノ薄膜転写シート及びその製造方法 |
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Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2617800A (en) * | 1949-06-10 | 1952-11-11 | Phillips Petroleum Co | Purification of carboxymethyl cellulose by ion exchange resins |
JPS62183768A (ja) * | 1986-02-10 | 1987-08-12 | テルモ株式会社 | 生体適合性材料およびその製造方法 |
US5017229A (en) * | 1990-06-25 | 1991-05-21 | Genzyme Corporation | Water insoluble derivatives of hyaluronic acid |
WO1992020349A1 (en) * | 1991-05-20 | 1992-11-26 | Genzyme Corporation | Water insoluble derivatives of polyanionic polysaccharides |
JPH07179649A (ja) * | 1991-01-23 | 1995-07-18 | Snow Brand Milk Prod Co Ltd | 植物繊維とキトサンの複合多孔質体の調製方法 |
EP0705878A2 (en) * | 1994-10-06 | 1996-04-10 | Genzyme Corporation | Compositions containing polyanionic polysaccharides and hydrophobic bioabsorbable polymers |
US5906997A (en) * | 1997-06-17 | 1999-05-25 | Fzio Med, Inc. | Bioresorbable compositions of carboxypolysaccharide polyether intermacromolecular complexes and methods for their use in reducing surgical adhesions |
JP2000178304A (ja) * | 1998-12-15 | 2000-06-27 | Denki Kagaku Kogyo Kk | ヒアルロン酸ゲルの製造方法 |
Family Cites Families (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US261780A (en) | 1882-07-25 | stevens | ||
DE1397893U (ja) | ||||
US3064313A (en) * | 1960-06-14 | 1962-11-20 | Hercules Powder Co Ltd | Preparation of free acid cellulose ether films |
DE1239284B (de) | 1963-01-23 | 1967-04-27 | Vaessen Schoemaker Holding Bv | Verfahren zur Herstellung von in Wasser leicht gelierbaren Carboxymethylderivaten der Amylose oder der Staerke |
GB1086323A (en) | 1963-07-18 | 1967-10-11 | Courtaulds Ltd | Derivative of carboxy methyl cellulose |
SE430609B (sv) * | 1976-12-21 | 1983-11-28 | Sca Development Ab | Sett att ur cellulosaderivat framstella absorberande material |
EP0010519A1 (fr) | 1978-10-12 | 1980-04-30 | Battelle Memorial Institute | Procédé pour réticuler la carboxyméthyl-cellulose et produits obtenus suivant ce procédé |
FR2489145A1 (fr) | 1980-09-04 | 1982-03-05 | Geistlich Soehne Ag | Compositions pharmaceutiques accelerant la guerison de blessures |
US4521594A (en) | 1983-05-20 | 1985-06-04 | Daicel Chemical Industries, Ltd. | Process for producing sodium carboxymethylcellulose |
JPS6239506A (ja) | 1985-08-14 | 1987-02-20 | Unitika Ltd | 抜歯窩充填物 |
SE452469B (sv) | 1986-06-18 | 1987-11-30 | Pharmacia Ab | Material bestaende av en tverbunden karboxylgrupphaltig polysackarid och forfarande vid framstellning av detsamma |
JP2538213B2 (ja) | 1986-07-31 | 1996-09-25 | ダイセル化学工業株式会社 | 高吸水性組成物 |
GB8708960D0 (en) * | 1987-04-14 | 1987-05-20 | Shell Int Research | Preparation of polymer-grafted cellulose fibres |
US5705485A (en) | 1987-09-18 | 1998-01-06 | Ethicon, Inc. | Gel formulations containing growth factors |
IT1219942B (it) | 1988-05-13 | 1990-05-24 | Fidia Farmaceutici | Esteri polisaccaridici |
IT1219587B (it) | 1988-05-13 | 1990-05-18 | Fidia Farmaceutici | Polisaccaridi carbossiilici autoreticolati |
JPH01301624A (ja) | 1988-05-31 | 1989-12-05 | Nippon Zeon Co Ltd | 癒着防止材 |
FI103583B (fi) | 1989-02-10 | 1999-07-30 | Alko Yhtioet Oy | Vesiliukoisesta karboksimetyyliselluloosasta entsymaattisesti valmiste ttu hydrolysaatti |
JP2805086B2 (ja) | 1989-06-20 | 1998-09-30 | グンゼ株式会社 | 生体組織用充填材 |
IT1259090B (it) | 1992-04-17 | 1996-03-11 | Fidia Spa | Biomaterialli per protesi d'osso |
GB9219457D0 (en) | 1992-09-15 | 1992-10-28 | Fisons Plc | Reducing interferences in plasma source mass spectrometers |
GB9301258D0 (en) | 1993-01-22 | 1993-03-17 | Courtaulds Plc | Use of absorbent fibre |
GB2276819B (en) | 1993-03-23 | 1996-12-11 | Johnson & Johnson Medical | Aqueous wound treatment composition comprising a polysaccharide and hexylene glycol |
JPH0790121A (ja) | 1993-09-22 | 1995-04-04 | Dai Ichi Kogyo Seiyaku Co Ltd | カルボキシメチルセルロースナトリウム塩のゲル状物の製造方法 |
DK0892863T3 (da) | 1996-04-12 | 2001-09-24 | Bristol Myers Squibb Co | Sammensatte fibre, forbindinger indeholdende sådanne fibre og fremgangsmåde til fremstilling deraf |
GB2318577B (en) * | 1996-10-28 | 2000-02-02 | Johnson & Johnson Medical | Solvent dried polysaccharide sponges |
JP3792824B2 (ja) | 1997-03-07 | 2006-07-05 | 第一工業製薬株式会社 | 水性ゲル基材の製法およびそれによって得られた水性ゲル基材 |
AU7908798A (en) * | 1997-07-02 | 1999-01-25 | Coloplast A/S | A method for preparing a non-fibrous porous material |
JP3981448B2 (ja) | 1997-10-03 | 2007-09-26 | ダイセル化学工業株式会社 | 新規なカルボキシメチルセルロースナトリウム塩含有水性ゲル組成物及びその製造法 |
JP3578627B2 (ja) | 1998-05-15 | 2004-10-20 | 株式会社ホギメディカル | 創傷患部の治癒を促進する組織シーラント |
NZ513517A (en) * | 1999-02-19 | 2003-08-29 | Denki Kagaku Kogyo Kk | Hyaluronic acid gel composition containing a polymer for use as a wound dressing |
-
2000
- 2000-08-18 CA CA002390556A patent/CA2390556C/en not_active Expired - Fee Related
- 2000-08-18 AU AU65970/00A patent/AU782519B2/en not_active Ceased
- 2000-08-18 US US10/129,751 patent/US7514097B1/en not_active Expired - Fee Related
- 2000-08-18 EP EP00953516A patent/EP1228771A4/en not_active Withdrawn
- 2000-08-18 KR KR1020027005853A patent/KR20020062301A/ko not_active Application Discontinuation
- 2000-08-18 CN CNB008182973A patent/CN100379462C/zh not_active Expired - Fee Related
- 2000-08-18 WO PCT/JP2000/005564 patent/WO2001034214A1/ja active IP Right Grant
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2617800A (en) * | 1949-06-10 | 1952-11-11 | Phillips Petroleum Co | Purification of carboxymethyl cellulose by ion exchange resins |
JPS62183768A (ja) * | 1986-02-10 | 1987-08-12 | テルモ株式会社 | 生体適合性材料およびその製造方法 |
US5017229A (en) * | 1990-06-25 | 1991-05-21 | Genzyme Corporation | Water insoluble derivatives of hyaluronic acid |
JPH07179649A (ja) * | 1991-01-23 | 1995-07-18 | Snow Brand Milk Prod Co Ltd | 植物繊維とキトサンの複合多孔質体の調製方法 |
WO1992020349A1 (en) * | 1991-05-20 | 1992-11-26 | Genzyme Corporation | Water insoluble derivatives of polyanionic polysaccharides |
EP0705878A2 (en) * | 1994-10-06 | 1996-04-10 | Genzyme Corporation | Compositions containing polyanionic polysaccharides and hydrophobic bioabsorbable polymers |
US5906997A (en) * | 1997-06-17 | 1999-05-25 | Fzio Med, Inc. | Bioresorbable compositions of carboxypolysaccharide polyether intermacromolecular complexes and methods for their use in reducing surgical adhesions |
JP2000178304A (ja) * | 1998-12-15 | 2000-06-27 | Denki Kagaku Kogyo Kk | ヒアルロン酸ゲルの製造方法 |
Non-Patent Citations (2)
Title |
---|
HAKERT H. ET AL.: "Rheological and electron microscopic characterization of aquerous carboxymethyl cellulose gels part I: Rheological aging of aquerous gels of carboxymethyl cellulose in the free acid form(HCMC)", COLLOID & POLYM. SCI., vol. 267, 1989, pages 226 - 229, XP002934246 * |
MUELLER T. ET AL.: "Rheological and electron microscopic characterization of aquerous carboxymethyl cellulose gels part II: Visualization of the gel structure by freeze-fracturing", COLLOID & POLYM. SCI., vol. 267, 1989, pages 230 - 236, XP002934247 * |
Cited By (13)
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JP2010285440A (ja) * | 2002-08-06 | 2010-12-24 | Mytogen Inc | 治療複合物 |
JP4759703B2 (ja) * | 2003-05-09 | 2011-08-31 | コンバテック・テクノロジーズ・インコーポレイテッド | 褥瘡治療における創傷被覆材の使用 |
JP2006525836A (ja) * | 2003-05-09 | 2006-11-16 | ブリストル−マイヤーズ スクイブ カンパニー | 褥瘡治療における創傷被覆材の使用 |
JP2005000512A (ja) * | 2003-06-13 | 2005-01-06 | Yasuharu Noisshiki | 管腔形成誘導性材料 |
JPWO2005000374A1 (ja) * | 2003-06-30 | 2006-08-03 | 電気化学工業株式会社 | 脊椎・脊髄手術用癒着防止材 |
US20090226503A1 (en) * | 2003-06-30 | 2009-09-10 | Hirotaka Haro | Adhesion inhibiting material for vertebral/spinal operation |
WO2005000374A1 (ja) * | 2003-06-30 | 2005-01-06 | Denki Kagaku Kogyo Kabushiki Kaisha | 脊椎・脊髄手術用癒着防止材 |
JP4690892B2 (ja) * | 2003-06-30 | 2011-06-01 | 電気化学工業株式会社 | 脊椎・脊髄手術用癒着防止材 |
WO2007015579A1 (ja) | 2005-08-04 | 2007-02-08 | Teijin Limited | セルロース誘導体 |
US8378091B2 (en) | 2005-08-04 | 2013-02-19 | Teijin Limited | Cellulose derivative |
JP2008013510A (ja) * | 2006-07-07 | 2008-01-24 | Seikagaku Kogyo Co Ltd | 水難溶性組成物並びにその製造方法及び用途 |
WO2011121858A1 (ja) | 2010-03-31 | 2011-10-06 | 株式会社ホギメディカル | 癒着防止材 |
JP2017036235A (ja) * | 2015-08-10 | 2017-02-16 | 日立化成株式会社 | ナノ薄膜転写シート及びその製造方法 |
Also Published As
Publication number | Publication date |
---|---|
US7514097B1 (en) | 2009-04-07 |
CA2390556C (en) | 2009-05-19 |
KR20020062301A (ko) | 2002-07-25 |
CN100379462C (zh) | 2008-04-09 |
CN1423568A (zh) | 2003-06-11 |
EP1228771A1 (en) | 2002-08-07 |
AU782519B2 (en) | 2005-08-04 |
AU6597000A (en) | 2001-06-06 |
CA2390556A1 (en) | 2001-05-17 |
EP1228771A4 (en) | 2003-01-29 |
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