WO2015137499A2 - 水素含有生体適用液の製造方法及びそのための外装体 - Google Patents
水素含有生体適用液の製造方法及びそのための外装体 Download PDFInfo
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- WO2015137499A2 WO2015137499A2 PCT/JP2015/057553 JP2015057553W WO2015137499A2 WO 2015137499 A2 WO2015137499 A2 WO 2015137499A2 JP 2015057553 W JP2015057553 W JP 2015057553W WO 2015137499 A2 WO2015137499 A2 WO 2015137499A2
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/18—Antioxidants, e.g. antiradicals
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/12—Ophthalmic agents for cataracts
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
- A61P39/06—Free radical scavengers or antioxidants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/22—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by diffusion
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen; Reversible storage of hydrogen
- C01B3/02—Production of hydrogen; Production of gaseous mixtures containing hydrogen
- C01B3/06—Production of hydrogen; Production of gaseous mixtures containing hydrogen by reaction of inorganic compounds containing electro-positively bound hydrogen with inorganic reducing agents
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen; Reversible storage of hydrogen
- C01B3/02—Production of hydrogen; Production of gaseous mixtures containing hydrogen
- C01B3/06—Production of hydrogen; Production of gaseous mixtures containing hydrogen by reaction of inorganic compounds containing electro-positively bound hydrogen with inorganic reducing agents
- C01B3/08—Production of hydrogen; Production of gaseous mixtures containing hydrogen by reaction of inorganic compounds containing electro-positively bound hydrogen with inorganic reducing agents by reaction of inorganic compounds with metals
- C01B3/10—Production of hydrogen; Production of gaseous mixtures containing hydrogen by reaction of inorganic compounds containing electro-positively bound hydrogen with inorganic reducing agents by reaction of inorganic compounds with metals by reaction of water vapour with metals
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/36—Hydrogen production from non-carbon containing sources, e.g. by water electrolysis
Definitions
- the present invention relates to a method for producing a hydrogen-containing biological fluid and an exterior body therefor.
- a biological application liquid placed in a container having high hydrogen molecule permeability such as a plastic bag, is housed in a portable hydrogen reservoir having low hydrogen molecule permeability, and the hydrogen reservoir is stored in a hydrogen-containing water.
- a non-destructive hydrogen-containing method is known in which a hydrogen application liquid is filled with a liquid or gas containing a hydrogen molecule, such that the hydrogen molecule is contained in a biological application liquid without opening the container. According to this method, hydrogen molecules are dissolved in the biological application liquid, but are blocked by a hydrogen reservoir having a low hydrogen molecule permeability, and are less likely to be lost to the outside world during the distribution process and storage period.
- the problem to be solved by the present invention is to provide a method for producing a hydrogen-containing biological application liquid in which hydrogen molecules do not substantially decrease during the distribution process and storage period, and an exterior body therefor.
- the present invention relates to a container having a water vapor permeability in which a biological application liquid is stored, a hydrogen generation system that generates hydrogen by moisture, and a packaging material having a low hydrogen molecule permeability that covers the container and the hydrogen generation system.
- a hydrogen molecule supply-type exterior body for manufacturing a hydrogen-containing biological application liquid comprising: the packaging material covering the container and a hydrogen generation system located outside the container; and the container.
- a method for producing a hydrogen-containing biological application liquid by supplying hydrogen molecules to a biological application liquid contained in a water vapor permeable container, comprising the container and a hydrogen generation system located outside the container.
- a step of covering with a packaging material having a low hydrogen molecule permeability, a step of increasing the humidity of the space between the container and the packaging material, and the biological application of hydrogen molecules generated from the hydrogen generation system from the outside of the container is solved by a method for producing a hydrogen-containing biological application liquid comprising a step of permeating into the liquid.
- the hydrogen molecules are not decreased during the product distribution process or during the storage period, but conversely, the structure is such that the hydrogen molecules gradually increase.
- a hydrogen-containing bioapplication fluid designed to optimize the concentration can be produced in the factory.
- FIG. 1 is a front view showing a hydrogen molecule supply type exterior body according to an embodiment of the present invention, and the hydrogen molecule supply type exterior body according to the present invention will be described with an example shown in FIG.
- the hydrogen molecule supply-type exterior body 1 of this example includes a water vapor permeable container 12 in which a biological application liquid 11 is stored, a hydrogen generation system 13 that generates hydrogen by moisture, and the container 12 and the hydrogen generation system 13. And a packaging material 14 having low hydrogen molecule permeability (which covers and seals the container 12 and the hydrogen generation system 13).
- the hydrogen generation system 13 is positioned outside the container 12 having water vapor permeability that accommodates the biological application liquid 11, and the hydrogen generation system 13 and the container 12 are covered with a packaging material 14 having low hydrogen molecule permeability.
- the hydrogen molecule supply type exterior body 1 which is one Embodiment of this application is obtained by performing the process which raises the humidity of the space between the container 12 and the packaging material 14.
- the biological application liquid 11 is an injection solution or an oral solution for osmotic adjustment of saline, water, nutrition, electrolyte replenishment, or an injection solution in which a drug is dissolved. Includes physiological saline, liquid drugs, blood transfusion preparations used for blood transfusion (blood for transfusion), autologous blood, enteral fluid, and drinking water.
- organ preservation solution, cell culture solution, cell maintenance solution, biological application solution containing lymphocytes and vaccines used in cancer immunotherapy and vaccine therapy, peritoneal dialysis solution, dialysate prepared for organ preservation May contain myocardial protective drugs and the like.
- the biological application liquid 11 of the present example is a concept that indicates all liquids that are applied to a living organism orally or parenterally for the purpose of maintaining and improving biological functions and preventing or treating diseases and diseases.
- Diseases / diseases that can be applied to the hydrogen-containing biological fluid 11 include digestive diseases such as liver damage caused by drugs and harmful substances, ischemic reperfusion injury, cardiovascular diseases such as arteriosclerosis, gastric ulcer, and gastric mucosal damage.
- Free radicals such as organ system diseases, respiratory diseases, diabetic complications (eg, hypertension, cerebral infarction, myocardial infarction), kidney diseases, cataracts, skin diseases, various inflammatory diseases, neurological diseases, cancer, aging, etc. It includes oxidative stress diseases caused by lipid peroxides, and is particularly suitable for diseases involving acute oxidative stress such as ischemic reperfusion injury, but is not limited thereto.
- the biological application liquid 11 of the present invention may already contain a certain amount of hydrogen molecules prior to the application of the present invention. In that case, the present invention can maintain the dissolved hydrogen concentration by replenishing hydrogen molecules in the biological application liquid 11.
- the container 12 having water vapor permeability is preferably a plastic container made of polyethylene, polypropylene, polyethylene terephthalate, polystyrene, or the like used for an infusion bag or an infusion bag, but is not limited thereto.
- the water vapor permeability of the container 12 having water vapor permeability (g / m 2 / day (40 ° C., 90% RH)) is 0.001 or more, preferably 0.01, more preferably 0.1, more preferably Is preferably 0.5, more preferably 1 or more.
- the water vapor permeable container 12 since hydrogen molecules are transferred into the biological application liquid 11 by allowing hydrogen molecules to permeate from the outside of the water vapor permeable container 12, the water vapor permeable container 12 is provided in advance. Although it is not necessary to open the package, it does not exclude the case where hydrogen molecules are allowed to pass through in the opened state.
- the biological application liquid 11 contained in a container 12 having water vapor permeability may be commercially available with the outer side of the container 12 already covered with some exterior bag. If it is permeable, the present invention can be implemented. Therefore, in the “biologically applied liquid 11 contained in the container 12 having water vapor permeability” according to the present invention, even if the container 12 is doubled or multiplexed by an outer bag or the like, the outer bag is water vapor permeable. As long as it is a container 12 having the above, it is included in the concept of the “biologically applied liquid 11 contained in the container 12 having water vapor permeability” of the present invention.
- the hydrogen generating system 13 includes a hydrogen generating agent that reacts with moisture (water vapor) to generate hydrogen, and an appropriate hydrogen generating reaction accelerator that accelerates the hydrogen generating reaction, if necessary.
- the hydrogen generator include, but are not limited to, metals having a higher ionization tendency than hydrogen, hydrogenated compounds containing metal hydrides, and the like.
- metallic calcium, calcium hydride, metallic magnesium, magnesium hydride and the like are preferably used.
- metal magnesium, metal aluminum, metal zinc, metal nickel, metal cobalt and the like are also preferably used.
- Examples of the hydrogen generation reaction accelerator include a pH adjuster for adjusting to a pH suitable for promoting the reaction between moisture and the hydrogen generator.
- pH adjusters include substances that supply hydrogen ions (H +) such as citric acid, adipic acid, malic acid, acetic acid, succinic acid, gluconic acid, lactic acid, phosphoric acid, hydrochloric acid, sulfuric acid, and cation exchange resins.
- H + hydrogen ions
- an amphoteric metal such as aluminum or zinc
- an alkali agent such as calcium hydroxide, calcium oxide, or anion exchange resin can be used in addition to these acids.
- calcium hydroxide slaked lime
- quick lime quick lime
- calcium oxide calcined calcium
- magnesium oxide magnesium hydroxide
- anion exchange resin and the like are preferably used.
- the hygroscopic agent or the desiccant promotes the hydrogen generation reaction by absorbing moisture
- these hygroscopic agents or desiccants include, but are not limited to, the above-described ion exchange resins, deliquescent substances such as calcium chloride, and substances that adsorb moisture on a porous surface such as aluminum oxide. is not.
- the hydrogen generation system 13 containing the hydrogen generating agent is subjected to a heat treatment prevention by being covered with a nonwoven fabric or a gas permeable membrane.
- the packaging material 14 having a low hydrogen molecule permeability is that the container made of the packaging material 14 stably maintains a substantially saturated concentration (1.6 ppm under a water temperature of 20 ° C. and 1 atm). Even if the container containing the physiological saline solution is fully or almost fully immersed in the hydrogen-dissolved water having a volume 20 times the product, the dissolved hydrogen concentration in the physiological saline solution is 100 ppb or less, preferably 10 ppb or less. Particularly preferably, it can be said that the packaging material has a property of only 1 ppb or less.
- a packaging material 14 includes, but is not limited to, a packaging material having gas barrier properties including a packaging material using aluminum such as an aluminum foil packaging material or an aluminum foil laminated film.
- the reaction of the hydrogen generation system 13 can be started by the water vapor derived from the biological application liquid 11 that has permeated through the water vapor permeable container 12.
- the hydrogen generation system 13 since hydrogen gas only needs to be generated by a chemical reaction between water vapor derived from the biological application liquid 11 that has permeated the container 12 and the hydrogen generation system 13, the hydrogen generation system 13 is packaged in an auxiliary manner. Before coating with the material 14, water may be forcibly supplied by dropping water droplets on the hydrogen generation system 13.
- the temperature higher than room temperature is 20 ° C. or higher, which is the “standard temperature” of medicine storage temperature, more preferably 25 ° C. or higher, more preferably “room temperature upper limit temperature”, and more preferably “room temperature upper limit temperature”.
- the gas existing in the space between the container 12 and the packaging material 14 is air when the working environment for sealing the container 12 and the hydrogen generation system 13 in the packaging material 14 is an air environment.
- the following standards can be used as a guideline for the amount of hydrogen generating agent used in the hydrogen generating system. That is, the inventors of the present application applied the hydrogen-containing biological application liquid 11 obtained from the hydrogen molecule supply-type exterior body 1 to the hydrogen-containing biological application liquid 11 obtained by the present invention even though the concentration was the same at the time of manufacture. It was noticed that there was a sample in which the degree of decrease in dissolved hydrogen concentration after taking out the bag (container 12) was slower than other hydrogen-containing biological application liquids.
- the amount of the hydrogen generating agent used in the hydrogen generating system 13 is related to the above event, and the hydrogen generating agent has water vapor permeability. It is not always sufficient to use only the amount calculated to saturate the hydrogen molecules with respect to the amount (so-called capacity) of the biological application liquid 11 contained in the container 12, which is not necessarily sufficient. It has been discovered that it is desirable to use an amount that is sufficient to replace the upper space volume (so-called pre-dose) with hydrogen molecules.
- the hydrogen generating agent is used in an amount of 20.84056 mg or more.
- the substance amount (mmol) of the hydrogen generating agent used in the hydrogen generating system 13 of the present invention is (1.6 (mg / L) ⁇ total amount of the water vapor permeable container 12 containing the biological application liquid 11.
- Full capacity (L) / 2) ⁇ (coefficient of hydrogen generator on left side in reaction formula of hydrogen generator and water / coefficient of hydrogen molecule on right side in reaction formula of hydrogen generator and water) ⁇ 1
- a hydrogen molecule catalyst such as a noble metal colloid (platinum colloid, palladium colloid, etc.)
- the hydrogen molecule supply type outer package 1 is bundled.
- the hydrogen molecules generated from the hydrogen generation system 13 pass through the transparent or translucent second container 16 having hydrogen molecule permeability and react with the hydrogen molecule indicator, whereby the color of the redox indicator is changed. Since it changes, the generation of hydrogen molecules can be visually confirmed.
- the hydrogen molecule permeability of the second container 16 is equal to the hydrogen molecule permeability of the container 12 in which the biological application liquid 11 is stored, not only the generation of hydrogen molecules but also the biological application liquid of hydrogen molecules. The degree of penetration into 11 can also be verified.
- the oxidized methylene blue is reduced by activation of the hydrogen molecule with platinum colloid. Then, in order to make the blue solution transparent, by checking whether the hydrogen molecule indicator is transparent when the hydrogen molecule supply-type exterior body 1 is opened, the space 15 enclosed in the packaging material 14 having low hydrogen molecule permeability is provided. Thus, it can be determined nondestructively whether or not hydrogen molecules have been generated, and by extension, whether or not hydrogen molecules have permeated into the biological application liquid 11.
- the dissolved hydrogen concentration of the hydrogen-containing living body application liquid is 0.01 mg / L or more, preferably 0.05 mg / or more, at the time of use at a water temperature of 20 ° C. and 1 atm. More preferably 0.1 mg / L, more preferably 0.2 mg / L or more, more preferably 0.4 mg / L or more, more preferably 0.6 mg / L or more, more Preferably it is 0.8 mg / L or more, more preferably 1.0 mg / L or more.
- the dissolved hydrogen meter used to measure the dissolved hydrogen concentration of the biological application liquid 11 is a DH meter (main body model “DHDI-1”, the same electrode (probe) model, “HE-5321” manufactured by Toa DKK Corporation. ], Repeater model “DHM-F2”).
- Example 1 Polyethylene infusion bag containing 500 mL of physiological saline (Otsuka Pharmaceutical Co., Ltd .: “Japanese Pharmacopoeia Saline Otsuka Raw Food Injection”, which corresponds to the container 12 containing the biological application liquid 11 of the present invention,
- the hydrogen generation system 13 of the present invention obtained by wrapping 0.5 g of metallic calcium (made by Kanto Chemical Co., Ltd .: “Calcium”) with a nonwoven fabric and an aluminum bag (made by Hagios Co., Ltd .: “MZ-”).
- 05 which corresponds to the packaging material 14 of the present invention, and is coated with a degassing sealer (manufactured by Takato Technica:“ VP-300 ”) after being coated with an infusion bag at ⁇ 0.1 Mpa.
- the aluminum bag 14 was heat sealed while reducing the volume of the space 15 between the aluminum bag 12 and the aluminum bag 14.
- Each physiological saline solution (corresponding to the biologically applied solution 11 of the present invention is indicated by reference numeral 11 below). ) was measured with a DH meter.
- Example 2 Polyethylene infusion bag 12 containing 500 mL of physiological saline (Otsuka Pharmaceutical Co., Ltd .: “Japan Pharmacopoeia Saline Otsuka Raw Food Injection”) and metal calcium 0.5 g (Kanto Chemical Co., Ltd .: “Calcium”)
- the hydrogen generation system 13 of the present invention obtained by wrapping with a nonwoven fabric is covered with an aluminum bag 14 (manufactured by Hagios: “MZ-05”), and then degassed sealer (manufactured by Takato Technica: “VP-300”).
- Example 3 Polypropylene peritoneal dialysate bag 12 (Terumo's “Midpelic L135”) containing 2000 mL of peritoneal dialysate covered with a polypropylene outer bag and 3 g of calcium metal (manufactured by Kanto Chemical Co., Ltd .: “Calcium” )) Covered with a nonwoven fabric, the hydrogen generation system 13 of the present invention was covered with an aluminum bag 14 (Hagios: “MZ-05”), and then degassed sealer (Takato Technica: “VP”).
- the aluminum bag 14 is heat-sealed while reducing the volume of the space 15 between the infusion bag 12 and the aluminum bag 14 at -0.1 MPa, and a thermo-hygrostat (" LU-113 "manufactured by ESPEC CORP. ”, Room temperature: 60 ° C.), the aluminum bag 14 was held in a temperature environment higher than room temperature. After 5 days, the aluminum bag 14 was taken out from the thermo-hygrostat, and the dissolved hydrogen concentration of the peritoneal dialysis solution 11 was measured with a DH meter.
- Example 4 Polyethylene infusion bag 12 containing 500 mL of physiological saline (Otsuka Pharmaceutical Co., Ltd .: “Japan Pharmacopoeia Saline Otsuka Raw Food Injection”) and metal magnesium 0.4 g (Kanto Metals Co., Ltd .: “Magnesium Powder Mg100”) ) And 0.2 g of cation exchange resin (Mitsubishi Chemical Co., Ltd .: “Diaion FMK10”) wrapped in a non-woven fabric, the hydrogen generation system 13 of the present invention was converted into an aluminum bag 14 (Hagios Co., Ltd .: “MZ-”).
- Example 5 Polyethylene infusion bag 12 containing 500 mL of physiological saline (Otsuka Pharmaceutical Co., Ltd .: “Japan Pharmacopoeia Saline Otsuka Raw Food Injection”) and calcium hydride 0.5 g (Wako Pure Chemical Industries, Ltd .: “Hydrogen”
- the hydrogen generation system 13 of the present invention obtained by wrapping calcium fluoride ”) in a non-woven fabric is coated with an aluminum bag 14 (Hagios:“ MZ-05 ”), and then a degassing sealer (Takato Technica: Using “VP-300”), the aluminum bag 14 was heat-sealed while reducing the volume of the space 15 between the infusion bag 12 and the aluminum bag 14 at ⁇ 0.1 MPa.
- Example 6 Polyethylene infusion bag 12 containing 500 mL of physiological saline (Otsuka Pharmaceutical Co., Ltd .: “Japanese Pharmacopoeia Saline Otsuka Raw Food Injection”) and 0.4 g of metallic aluminum (Minalco: “Aluminum Powder”),
- the hydrogen generation system 13 of the present invention obtained by wrapping 0.2 g of cation exchange resin (same as above) and 0.1 g of calcium chloride (manufactured by Wako Pure Chemical Industries, Ltd .: “Calcium chloride”) in a non-woven fabric 14 (made by Hagios: “MZ-05”), and then between the infusion bag 12 and the aluminum bag 14 at ⁇ 0.1 MPa using a degassing sealer (Takato Technica: “VP-300”). The aluminum bag was heat sealed while reducing the volume of the space 15.
- Example 7 Polyethylene infusion bag 12 containing 500 mL of physiological saline (Otsuka Pharmaceutical Co., Ltd .: “Japan Pharmacopoeia physiological saline Otsuka raw food injection”), metal aluminum 0.4 g (same as above), calcium hydroxide 0.15 g ( Wako Pure Chemical Industries, Ltd .: “Calcium hydroxide”), and hydrogen generation system 13 of the present invention obtained by wrapping 0.1 g of calcium chloride (same as above) in a non-woven fabric, an aluminum bag 14 (Hagios Co., Ltd .: “ MZ-05 ”), and then the volume of the space 15 between the infusion bag 12 and the aluminum bag 14 is reduced by ⁇ 0.1 Mpa using a degassing sealer (manufactured by Takato Technica:“ VP-300 ”). The aluminum bag 14 was heat sealed.
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Abstract
Description
生理食塩液500mLが収容されたポリエチレン製の輸液バッグ(大塚製薬社製:『日本薬局方生理食塩液 大塚生食注』,本発明の生体適用液11が収納された容器12に相当するので、以下符号12で示す)と、金属カルシウム0.5g(関東化学社製:『カルシウム』)を不織布で包むことで得られた本発明の水素発生系13を、アルミバッグ(ハギオス社製:『MZ-05』,本発明の包装材14に相当するので、以下符号14で示す)で被覆した後、脱気シーラー(タカトテクニカ社製:『VP-300』)を用いて-0.1Mpaで輸液バッグ12とアルミバッグ14との間の空間15の体積を減じながらアルミバッグ14をヒートシールした。
生理食塩液500mLが収容されたポリエチレン製の輸液バッグ12(大塚製薬社製:『日本薬局方生理食塩液 大塚生食注』)と、金属カルシウム0.5g(関東化学社製:『カルシウム』)を不織布で包むことで得られた本発明の水素発生系13を、アルミバッグ14(ハギオス社製:『MZ-05』)で被覆した後、脱気シーラー(タカトテクニカ社製:『VP-300』)を用いて-0.1Mpaで輸液バッグ12とアルミバッグ14との間の空間15の体積を減じながらアルミバッグ14をヒートシールし、恒温恒湿器(エスペック社製『LU-113』、槽温:60℃)に放置することで室温より高い温度環境にアルミバッグ14を保持した。そして、48時間後にアルミバッグ14を恒温恒湿器から取り出し、生理食塩液11の溶存水素濃度をDHメーターで測定した。
外側をポリプロピレン製の外装袋で覆われた、腹膜透析液2000mLが収容されたポリプロピレン製の腹膜透析液バッグ12(テルモ社製『ミッドペリックL135』)と、金属カルシウム3g(関東化学社製:『カルシウム』)を不織布で包むことで得られた本発明の水素発生系13を、アルミバッグ14(ハギオス社製:『MZ-05』)で被覆した後、脱気シーラー(タカトテクニカ社製:『VP-300』)を用いて-0.1Mpaで輸液バッグ12とアルミバッグ14との間の空間15の体積を減じながらアルミバッグ14をヒートシールし、恒温恒湿器(エスペック社製『LU-113』、室温:60℃)に放置することで室温より高い温度環境にアルミバッグ14を保持した。そして、5日後にアルミバッグ14を恒温恒湿器から取り出し、腹膜透析液11の溶存水素濃度をDHメーターで測定した。
生理食塩液500mLが収容されたポリエチレン製の輸液バッグ12(大塚製薬社製:『日本薬局方生理食塩液 大塚生食注』)と、不織布に包まれた金属カルシウム0.5g(関東化学社製:『カルシウム』)13を、アルミバッグ14(ハギオス社製:『MZ-05』)で被覆した後、脱気することなくそのままヒートシールした。
生理食塩液500mLが収容されたポリエチレン製の輸液バッグ12(大塚製薬社製:『日本薬局方生理食塩液 大塚生食注』)をアルミバッグ14(ハギオス社製:『MZ-05』)で被覆した後、アルミバッグ14に、水素発生系13に代えて1.6mg/Lの飽和濃度の水素溶存水を満たしてヒートシールした。
生理食塩液500mLが収容されたポリエチレン製の輸液バッグ12(大塚製薬社製:『日本薬局方生理食塩液 大塚生食注』)と、金属マグネシウム0.4g(関東金属社製:『マグネシウム粉末 Mg100』)と陽イオン交換樹脂0.2g(三菱化学社製:『ダイヤイオン FMK10』)を不織布に包むことで得られた本発明の水素発生系13を、アルミバッグ14(ハギオス社製:『MZ-05』)で被覆した後、脱気シーラー(タカトテクニカ社製:『VP-300』)を用いて-0.1Mpaで輸液バッグ12とアルミバッグ14との間の空間15の体積を減じながらアルミバッグ14をヒートシールした。
生理食塩液500mLが収容されたポリエチレン製の輸液バッグ12(大塚製薬社製:『日本薬局方生理食塩液 大塚生食注』)と、水素化カルシウム0.5g(和光純薬工業社製:『水素化カルシウム』)を不織布に包むことで得られた本発明の水素発生系13を、アルミバッグ14(ハギオス社製:『MZ-05』)で被覆した後、脱気シーラー(タカトテクニカ社製:『VP-300』)を用いて-0.1Mpaで輸液バッグ12とアルミバッグ14との間の空間15の体積を減じながらアルミバッグ14をヒートシールした。
生理食塩液500mLが収容されたポリエチレン製の輸液バッグ12(大塚製薬社製:『日本薬局方生理食塩液 大塚生食注』)と、金属アルミニウム0.4g(ミナルコ社製:『アルミニウム粉末』)、陽イオン交換樹脂0.2g(同上)、及び塩化カルシウム0.1g(和光純薬工業社製:『塩化カルシウム』)を不織布に包むことで得られた本発明の水素発生系13を、アルミバッグ14(ハギオス社製:『MZ-05』)で被覆した後、脱気シーラー(タカトテクニカ社製:『VP-300』)を用いて-0.1Mpaで輸液バッグ12とアルミバッグ14との間の空間15の体積を減じながらアルミバッグをヒートシールした。
生理食塩液500mLが収容されたポリエチレン製の輸液バッグ12(大塚製薬社製:『日本薬局方生理食塩液 大塚生食注』)と、金属アルミニウム0.4g(同上)、水酸化カルシウム0.15g(和光純薬工業社製:『水酸化カルシウム』)、及び塩化カルシウム0.1g(同上)を不織布に包むことで得られた本発明の水素発生系13を、アルミバッグ14(ハギオス社製:『MZ-05』)で被覆した後、脱気シーラー(タカトテクニカ社製:『VP-300』)を用いて-0.1Mpaで輸液バッグ12とアルミバッグ14との間の空間15の体積を減じながらアルミバッグ14をヒートシールした。
実施例1~3と比較例1との結果から、実施例1~3のように容器12と包装材14との間の空間15を脱気することで、24時間後の溶存水素濃度DHが0.06mg/Lであったものが3週間後まで増加することが確認された。これに対して、容器12と包装材14との間の空間15を脱気しない比較例では、24時間後の溶存水素濃度DHが0.03mg/Lと低く、しかも3週間後の溶存水素濃度DHに至っては、実施例1の0.77mg/Lに対してDH=0.29mg/Lと明らかな増加の差が確認された。
11…生体適用液
12…容器
13…水素発生系
14…包装材
15…空間
16…第2容器
Claims (23)
- 水蒸気透過性を有する容器に収容された生体適用液に水素分子を供給して水素含有生体適用液を製造する方法であって、
前記容器と、前記容器の外側に位置する水素発生系とを、水素分子透過性の低い包装材で被覆する工程と、
前記容器と前記包装材との間の空間の湿度を高める工程と、
前記水素発生系より発生する水素分子を前記容器の外側から前記生体適用液中へ透過させる工程と、を含む水素含有生体適用液の製造方法。 - 前記湿度を高める工程が、前記容器と前記包装材との間の空間の体積を減らす工程を含む請求項1記載の水素含有生体適用液の製造方法。
- 前記容器と前記包装材との間の空間の体積を減らす工程が、前記容器と前記包装材との間の空間を占める気体を脱気する工程を含む請求項2記載の水素含有生体適用液の製造方法。
- 前記湿度を高める工程が、前記包装材に被覆された前記容器を、室温より高い温度環境に一定時間維持する工程を含む請求項1~3のいずれか一項に記載の水素含有生体適用液の製造方法。
- 前記室温より高い温度環境が、30℃以上である請求項4記載の水素含有生体適用液の製造方法。
- 前記水素発生系が、水素よりイオン化傾向の高い金属または水素化金属のうち少なくともいずれか一方を含む請求項1~5のいずれか一項に記載の水素含有生体適用液の製造方法。
- 前記水素よりイオン化傾向の高い金属が、金属カルシウムである請求項6記載の水素含有生体適用液の製造方法。
- 前記水素発生系が、さらに水素発生反応促進剤を含む請求項1~7のいずれか一項に記載の水素含有生体適用液の製造方法。
- 前記水素発生系が、さらに防熱処理されている請求項1~8のいずれか一項に記載の水素含有生体適用液の製造方法。
- 前記防熱処理が、不織布で覆うという防熱処理である請求項9記載の水素含有生体適用液の製造方法。
- 前記水素分子を前記生体適用液中へ透過させる工程は、前記生体適用液の溶存水素濃度が、1mg/L以上になるまで実施される請求項1~10のいずれか一項に記載の水素含有生体適用液の製造方法。
- 生体適用液が収納された水蒸気透過性を有する容器と、水分により水素を発生させる水素発生系と、前記容器と前記水素発生系とを被覆する水素分子透過性の低い包装材と、を備える水素含有生体適用液を製造するための水素分子供給型外装体であって、
前記包装材が、前記容器と前記容器の外側に位置する水素発生系を被覆し、かつ、前記容器と前記包装材との間の空間の湿度を高める処理が施されている水素分子供給型外装体。 - 前記湿度を高める処理が、前記容器と前記包装材との間の空間の体積を減らす処理を含む請求項12に記載の水素分子供給型外装体。
- 前記容器と前記包装材との間の空間の体積を減らす処理が、前記容器と前記包装材との間の空間を占める気体を脱気する処理を含む請求項13に記載の水素分子供給型外装体。
- 前記湿度を高める処理が、前記包装材に被覆された前記容器を、室温より高い温度環境に一定時間維持する処理を含む請求項12~14のいずれか一項に記載の水水素分子供給型外装体。
- 前記室温より高い温度環境が、30℃以上である請求項15に記載の水素分子供給型外装体。
- 前記水素発生系が、水素よりイオン化傾向の高い金属または水素化金属のうち少なくともいずれか一方を含む請求項12~16のいずれか一項に記載の水素分子供給型外装体。
- 前記水素よりイオン化傾向の高い金属が、金属カルシウムである請求項17に記載の水素分子供給型外装体。
- 前記水素発生系が、さらに水素発生反応促進剤を含む請求項12~18のいずれか一項に記載の水素分子供給型外装体。
- 前記水素発生系が、さらに防熱処理されている請求項12~19のいずれか一項に記載の水素分子供給型外装体。
- 前記防熱処理が、不織布で覆うという防熱処理である請求項20に記載の水素分子供給型外装体。
- 水素分子透過性を有する透明または半透明の容器に収納された酸化還元指示薬及び水素分子触媒を含む水素分子指示薬が、前記容器および前記水素発生系とともに前記包装材で被覆されている請求項12~21のいずれか一項に記載の水素分子供給型外装体。
- 前記酸化還元指示薬及び前記水素分子触媒が、メチレンブルー及び白金コロイドである請求項22記載の水素分子供給型外装体。
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| CN201580000856.1A CN105246492B (zh) | 2014-03-13 | 2015-03-13 | 含氢生物体应用液的制造方法、及用于该制造方法的外包装体 |
| JP2015543189A JP5935954B2 (ja) | 2014-03-13 | 2015-03-13 | 水素含有生体適用液の製造方法及びそのための外装体 |
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2015
- 2015-03-13 CN CN201580000856.1A patent/CN105246492B/zh not_active Expired - Fee Related
- 2015-03-13 KR KR1020157033926A patent/KR101653937B1/ko not_active Expired - Fee Related
- 2015-03-13 US US14/891,851 patent/US9636358B2/en not_active Expired - Fee Related
- 2015-03-13 JP JP2015543189A patent/JP5935954B2/ja active Active
- 2015-03-13 WO PCT/JP2015/057553 patent/WO2015137499A2/ja not_active Ceased
- 2015-03-13 EP EP15760863.9A patent/EP2985028B1/en active Active
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2016
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Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4486157B1 (ja) | 2009-03-13 | 2010-06-23 | ミズ株式会社 | 水素含有生体適用液の製造方法及び製造装置 |
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| See also references of EP2985028A4 |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20180297842A1 (en) * | 2016-10-27 | 2018-10-18 | Miz Company Limited | Method of generating hydrogen-containing liquid |
| JP2020164507A (ja) * | 2019-03-26 | 2020-10-08 | MiZ株式会社 | 分子状水素を含む腎臓疾患の腎機能改善のための組成物 |
| JP2021151980A (ja) * | 2020-03-24 | 2021-09-30 | MiZ株式会社 | 脳炎および/または髄膜炎と当該脳炎および/または髄膜炎に関連する症状を予防および/または改善するための分子状水素含有組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20150139632A (ko) | 2015-12-11 |
| US9636358B2 (en) | 2017-05-02 |
| WO2015137499A3 (ja) | 2015-11-05 |
| JP2016112562A (ja) | 2016-06-23 |
| CN105246492B (zh) | 2017-09-29 |
| JPWO2015137499A1 (ja) | 2017-04-06 |
| JP5935954B2 (ja) | 2016-06-15 |
| EP2985028B1 (en) | 2019-05-22 |
| CN105246492A (zh) | 2016-01-13 |
| EP2985028A2 (en) | 2016-02-17 |
| KR101653937B1 (ko) | 2016-09-02 |
| EP2985028A4 (en) | 2016-06-29 |
| US20160089394A1 (en) | 2016-03-31 |
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