JP2003213548A - Auxiliary therapeutic tool - Google Patents
Auxiliary therapeutic toolInfo
- Publication number
- JP2003213548A JP2003213548A JP2002009968A JP2002009968A JP2003213548A JP 2003213548 A JP2003213548 A JP 2003213548A JP 2002009968 A JP2002009968 A JP 2002009968A JP 2002009968 A JP2002009968 A JP 2002009968A JP 2003213548 A JP2003213548 A JP 2003213548A
- Authority
- JP
- Japan
- Prior art keywords
- metal phthalocyanine
- phthalocyanine derivative
- derivative
- yarn
- iron
- 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.)
- Pending
Links
- 230000001225 therapeutic effect Effects 0.000 title claims abstract description 18
- 229910052751 metal Inorganic materials 0.000 claims abstract description 41
- 239000002184 metal Substances 0.000 claims abstract description 41
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical class N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 claims abstract description 38
- 239000002253 acid Substances 0.000 claims abstract description 19
- KMHSUNDEGHRBNV-UHFFFAOYSA-N 2,4-dichloropyrimidine-5-carbonitrile Chemical compound ClC1=NC=C(C#N)C(Cl)=N1 KMHSUNDEGHRBNV-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229920000742 Cotton Polymers 0.000 claims abstract description 9
- MPMSMUBQXQALQI-UHFFFAOYSA-N cobalt phthalocyanine Chemical compound [Co+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 MPMSMUBQXQALQI-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 8
- 229920000297 Rayon Polymers 0.000 claims abstract description 6
- 239000002964 rayon Substances 0.000 claims abstract description 6
- 210000002268 wool Anatomy 0.000 claims abstract description 6
- 239000004952 Polyamide Substances 0.000 claims abstract description 5
- 229920002647 polyamide Polymers 0.000 claims abstract description 5
- 150000003839 salts Chemical class 0.000 claims abstract description 4
- 208000003251 Pruritus Diseases 0.000 claims description 37
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 8
- 239000010949 copper Substances 0.000 claims description 7
- 239000011572 manganese Substances 0.000 claims description 6
- 239000010936 titanium Substances 0.000 claims description 6
- 244000025254 Cannabis sativa Species 0.000 claims description 4
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 claims description 4
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 claims description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 4
- 235000009120 camo Nutrition 0.000 claims description 4
- 235000005607 chanvre indien Nutrition 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 239000011487 hemp Substances 0.000 claims description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 3
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 239000010941 cobalt Chemical group 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical group [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- 229910052748 manganese Inorganic materials 0.000 claims description 3
- 229910052750 molybdenum Inorganic materials 0.000 claims description 3
- 239000011733 molybdenum Substances 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 3
- 229910052721 tungsten Inorganic materials 0.000 claims description 3
- 239000010937 tungsten Substances 0.000 claims description 3
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- 239000011701 zinc Substances 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- 206010061218 Inflammation Diseases 0.000 abstract description 12
- 230000004054 inflammatory process Effects 0.000 abstract description 12
- 206010012438 Dermatitis atopic Diseases 0.000 abstract description 10
- 201000008937 atopic dermatitis Diseases 0.000 abstract description 10
- 238000009940 knitting Methods 0.000 abstract description 4
- 230000001914 calming effect Effects 0.000 abstract description 2
- 230000002708 enhancing effect Effects 0.000 abstract description 2
- 241000208202 Linaceae Species 0.000 abstract 1
- 235000004431 Linum usitatissimum Nutrition 0.000 abstract 1
- 230000005722 itchiness Effects 0.000 abstract 1
- 239000002994 raw material Substances 0.000 abstract 1
- 230000007803 itching Effects 0.000 description 21
- 239000000835 fiber Substances 0.000 description 14
- -1 iron phthalocyanine tetracarboxylic acid Chemical class 0.000 description 8
- 206010013786 Dry skin Diseases 0.000 description 6
- 230000037336 dry skin Effects 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 230000001139 anti-pruritic effect Effects 0.000 description 5
- 201000004624 Dermatitis Diseases 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 210000003414 extremity Anatomy 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- 150000003431 steroids Chemical class 0.000 description 4
- 239000004909 Moisturizer Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003908 antipruritic agent Substances 0.000 description 3
- 208000010668 atopic eczema Diseases 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000001333 moisturizer Effects 0.000 description 3
- 208000006820 Arthralgia Diseases 0.000 description 2
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 description 2
- 208000000112 Myalgia Diseases 0.000 description 2
- 206010052428 Wound Diseases 0.000 description 2
- 208000027418 Wounds and injury Diseases 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- 229940125715 antihistaminic agent Drugs 0.000 description 2
- 239000000739 antihistaminic agent Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 229920006306 polyurethane fiber Polymers 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- JBQYATWDVHIOAR-UHFFFAOYSA-N tellanylidenegermanium Chemical compound [Te]=[Ge] JBQYATWDVHIOAR-UHFFFAOYSA-N 0.000 description 2
- 230000000699 topical effect Effects 0.000 description 2
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- CSPHGSFZFWKVDL-UHFFFAOYSA-M (3-chloro-2-hydroxypropyl)-trimethylazanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC(O)CCl CSPHGSFZFWKVDL-UHFFFAOYSA-M 0.000 description 1
- 206010015150 Erythema Diseases 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 206010024438 Lichenification Diseases 0.000 description 1
- 206010030113 Oedema Diseases 0.000 description 1
- 208000002193 Pain Diseases 0.000 description 1
- 241000282320 Panthera leo Species 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000013566 allergen Substances 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- APUPEJJSWDHEBO-UHFFFAOYSA-P ammonium molybdate Chemical compound [NH4+].[NH4+].[O-][Mo]([O-])(=O)=O APUPEJJSWDHEBO-UHFFFAOYSA-P 0.000 description 1
- 239000011609 ammonium molybdate Substances 0.000 description 1
- 229940010552 ammonium molybdate Drugs 0.000 description 1
- 235000018660 ammonium molybdate Nutrition 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000012636 effector Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 231100000321 erythema Toxicity 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229960001340 histamine Drugs 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 210000002414 leg Anatomy 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000013008 moisture curing Methods 0.000 description 1
- 210000004400 mucous membrane Anatomy 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 208000013465 muscle pain Diseases 0.000 description 1
- 210000002569 neuron Anatomy 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000001823 pruritic effect Effects 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- PUVAFTRIIUSGLK-UHFFFAOYSA-M trimethyl(oxiran-2-ylmethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC1CO1 PUVAFTRIIUSGLK-UHFFFAOYSA-M 0.000 description 1
- 210000001364 upper extremity Anatomy 0.000 description 1
- LTVDFSLWFKLJDQ-UHFFFAOYSA-N α-tocopherolquinone Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(C)(O)CCC1=C(C)C(=O)C(C)=C(C)C1=O LTVDFSLWFKLJDQ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Knitting Of Fabric (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、アトピー性皮膚炎
など皮膚の炎症に伴う痒みを鎮静させ、炎症の治療を助
ける治療補助具に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a therapeutic aid for soothing itching associated with inflammation of the skin such as atopic dermatitis and assisting the treatment of inflammation.
【0002】[0002]
【従来の技術】近年アトピー性皮膚炎を始め、乾燥肌、
ギブス着用患者など痒みを伴う炎症がある患者が増加し
ており、アトピー性皮膚炎の患者だけでも900万人に
達しているといわれている。特にアトピー性皮膚炎は完
治するのに長期間要し、その間不快感を我慢しなくては
ならず、患者にとっては大きな苦痛となっている。痒み
を伴う炎症をもつ患者は、痒みに耐えられずにあるいは
就寝中などに無意識に引っ掻くことがあって、引っ掻き
傷が完治を遅らせる原因ともなっている。従って、痒み
を取除くあるいは鎮めることは、患者の不快感を和らげ
るのみならず、治療効果を大いに助けることになる。2. Description of the Related Art Recently, atopic dermatitis has begun to occur, dry skin,
The number of patients with inflammation accompanied by itching, such as those wearing casts, is increasing, and it is said that the number of patients with atopic dermatitis alone reaches 9 million. In particular, atopic dermatitis requires a long period of time to be completely cured, and during that time, it is necessary to endure discomfort, which is a great pain for patients. Patients with inflammation accompanied by itching sometimes scratch the patient's eyes without being able to tolerate itching or while sleeping, and the scratches also cause a delay in healing. Therefore, removing or soothing the itch not only alleviates the discomfort of the patient, but also greatly assists the therapeutic effect.
【0003】一般に疾患において痒みが起きる主なメカ
ニズムは、ヒスタミン、アレルゲンなど痒みを引き起こ
す物質、物理的刺激などが皮膚や一部の粘膜に在る痒み
受容体に作用し、これが神経細胞を通じて脳に伝達され
ることによっていると考えられている。すなわち、体の
一部に痒みを感ずるとその痒みは、他の箇所にも痒みを
感じるようになったり、痒いという感覚が加速度的に激
しくなったりして不快感が一層増していくことになる。Generally, the main mechanism of itching in diseases is that substances such as histamine and allergens that cause itching and physical irritation act on itching receptors present on the skin and some mucous membranes, and these act on the brain through nerve cells. It is believed to be due to being transmitted. In other words, when itching is felt on a part of the body, the itching also causes itching on other parts, and the sensation of itching becomes more intense at an accelerating rate, which further increases the discomfort. .
【0004】痒みを抑える方法は、抗ヒスタミン剤、ス
テロイド剤、保湿剤などが主に使われているが、抗ヒス
タミン剤やステロイド剤には副作用の心配があって、過
度の使用は控える必要があり、また保湿剤はその効果に
限界があった。この他、銀、銅、亜鉛などの化合物を担
持するゼオライトを含ませたギプス下巻き用不織布包帯
〔特開平5−154174号公報〕、ポリエーテルポリ
オールとポリイソシアネートとを反応して得られる末端
にイソシアネート基を含有するプレポリマーに、蛋白質
粉末、抗菌性ゼオライトを水不溶性の多孔質無機化合物
によって内包した抗菌多孔質無機カプセルを配合した樹
脂組成物を含ませた湿気硬化型固定用包帯〔特開平6−
039027号公報〕など痒み止め効果のある化合物を
繊維に担持させ、これを痒みのある箇所に密着させると
いう提案もあるが、その効果に限界がある上、長時間続
けると皮膚に二次的な炎症を起こす可能性もあり、さら
にこれらの繊維は洗濯すると薬効成分が流れてしまい繰
り返し使用が出来ない問題もあった。Antihistamines, steroids, moisturizers, etc. are mainly used as a method for suppressing itch, but antihistamines and steroids may cause side effects, so it is necessary to refrain from excessive use, and moisturizers should be used. The agent had a limited effect. In addition to this, a non-woven fabric bandage for undercast casting containing a zeolite carrying a compound such as silver, copper or zinc [JP-A-5-154174], at the end obtained by reacting a polyether polyol and a polyisocyanate A moisture-curing fixing bandage containing a resin composition containing an antibacterial porous inorganic capsule containing a protein powder and an antibacterial zeolite encapsulated by a water-insoluble porous inorganic compound in a prepolymer containing an isocyanate group (Patent Document 1 6-
There is also a proposal that a compound having an antipruritic effect is carried on the fiber and adhered to the itchy spot, but there is a limit to the effect, and when it is continued for a long time, it is secondary to the skin. There is also a problem that it may cause inflammation, and further, when these fibers are washed, the medicinal component flows and cannot be used repeatedly.
【0005】[0005]
【発明が解決しようとする課題】上記問題点に鑑み、本
発明の目的は、アトピー性皮膚炎などの炎症に伴う痒み
を鎮静化して、患者の不快感を和らげ、炎症の治療効果
を高める治療補助具を提供することにある。SUMMARY OF THE INVENTION In view of the above problems, an object of the present invention is a treatment for soothing the itch associated with inflammation such as atopic dermatitis, soothing the discomfort of the patient and enhancing the therapeutic effect of inflammation. To provide auxiliary equipment.
【0006】[0006]
【課題を解決するための手段】上記課題を解決すべく請
求項1に係る発明は、痒みを伴う炎症のある肌に密着さ
せて痒みを鎮静化させる治療補助具であり、肌に接する
内面は式(I)〔式中、Rはカルボキシル基、スルホン
酸基、あるいはこれらの水溶性塩基から選ばれる基であ
り、nはRの数で1あるいは2、Mは、鉄(Fe)、コ
バルト(Co)、マンガン(Mn)、チタン(Ti)、
バナジウム(V)、ニッケル(Ni)、銅(Cu)、亜
鉛(Zn)、モリブデン(Mo)、タングステン(W)
から選ばれる金属である〕で示される金属フタロシアニ
ン誘導体を担持した糸を含み、外面は該金属フタロシア
ニン誘導体を担持しない糸からなる二重構造に編んで構
成されていることを特徴としている。In order to solve the above-mentioned problems, the invention according to claim 1 is a therapeutic aid for calming itch by adhering it to the irritated skin with itching, and the inner surface in contact with the skin is Formula (I) [In the formula, R is a carboxyl group, a sulfonic acid group, or a group selected from these water-soluble bases, n is 1 or 2 in the number of R, M is iron (Fe), cobalt ( Co), manganese (Mn), titanium (Ti),
Vanadium (V), nickel (Ni), copper (Cu), zinc (Zn), molybdenum (Mo), tungsten (W)
It is characterized in that it includes a thread carrying a metal phthalocyanine derivative represented by the formula [1], and the outer surface is knitted into a double structure consisting of threads not carrying the metal phthalocyanine derivative.
【化2】 [Chemical 2]
【0007】請求項2に係る発明は、請求項1記載の治
療補助具であり、金属フタロシアニン誘導体は、鉄フタ
ロシアニンポリカルボン酸、鉄フタロシアニンポリスル
ホン酸、コバルトフタロシアニンポリカルボン酸、コバ
ルトフタロシアニンポリスルホン酸、およびこれらの水
溶性塩から選ばれる一種以上であることを特徴としてい
る。The invention according to claim 2 is the therapeutic aid according to claim 1, wherein the metal phthalocyanine derivative is iron phthalocyanine polycarboxylic acid, iron phthalocyanine polysulfonic acid, cobalt phthalocyanine polycarboxylic acid, cobalt phthalocyanine polysulfonic acid, and It is characterized in that it is at least one selected from these water-soluble salts.
【0008】請求項3に係る発明は、請求項1記載の治
療補助具であり、金属フタロシアニン誘導体を担持した
糸は、木綿、レーヨン、麻、羊毛、絹、ポリアミドから
選ばれる一種以上の素材をカチオン化剤で処理し、次い
で金属フタロシアニン誘導体を作用させて担持させたこ
とを特徴としている。The invention according to claim 3 is the therapeutic aid according to claim 1, wherein the thread carrying the metal phthalocyanine derivative is one or more materials selected from cotton, rayon, hemp, wool, silk and polyamide. It is characterized in that it is treated with a cationizing agent, and then a metal phthalocyanine derivative is allowed to act thereon for supporting.
【0009】[0009]
【発明の実施の形態】本発明の治療補助具は、痒みのあ
る部分、炎症のある部分の皮膚に直接接するように装着
して、痒みを鎮静化させ、炎症の治療効果を高めるもの
である。治療補助具の形体は、シャツ、パンツ、ストッ
キングのような通常の肌着の形であってもよく、あるい
は手、肘、肩、腰、膝、脚、足に装着して関節や筋肉の
痛みを和らげる筒型や巻き付け型のサポーターのように
部分的に覆うものであってもよい。しかし、本発明の治
療補助具は、関節や筋肉の痛みの緩和を目的としたサポ
ーターと違って体にきつく締めて装着する必要はなく、
対象とする皮膚の部分に常に接し、かつ自由に動かせる
程度で充分であり、この観点から糸を編んで縦横方向に
伸縮性に富んだニット生地とするのが都合がよい。BEST MODE FOR CARRYING OUT THE INVENTION The therapeutic aid of the present invention is attached so as to directly contact the skin of an itchy part or an inflamed part, soothes the itching and enhances the therapeutic effect on inflammation. . The shape of the treatment aid may be in the form of normal undergarments such as shirts, pants or stockings, or it may be worn on the hands, elbows, shoulders, hips, knees, legs and feet to reduce joint and muscle pain. It may be partially covered, such as a softening tubular or wound supporter. However, the treatment aid of the present invention does not need to be tightly attached to the body unlike a supporter for the purpose of relieving pain in joints and muscles,
It suffices that it is always in contact with the target skin portion and that it can be moved freely. From this viewpoint, it is convenient to knit a yarn to form a knit fabric that is highly stretchable in the longitudinal and transverse directions.
【0010】治療補助具におけるニット生地は、主とし
て肌に接する面に使う糸と、主に肌に直接接しない外側
面に使う糸を別にした二重構造に編んでおり、その編み
方は平織り、ゴム編み、パール編みなど任意に選ばれ
る。肌に接する面は、本発明の目的とする痒みを鎮静化
させる作用を付与し、外側面は治療補助具を肌に密着す
るように適度に締め付け、さらに保温性、色彩などの機
能を付与する。The knitted fabric in the treatment aid is knitted in a double structure in which the yarn mainly used for the surface contacting the skin and the yarn mainly used for the outer surface not directly contacting the skin are separated, and the knitting method is plain weave, Rubber knitting or pearl knitting can be selected arbitrarily. The surface in contact with the skin imparts an effect of soothing itching, which is the object of the present invention, and the outer surface moderately tightens the therapeutic aid so that it closely adheres to the skin, and further imparts functions such as heat retention and color. .
【0011】肌に接する面は、痒みを鎮静化させる作用
のある金属フタロシアニン誘導体を担持した糸を一部あ
るいは全てに用いる。その素材は、木綿、レーヨン、
麻、毛、絹、ポリアミドなどであり、使用する場所が痒
みのある個所であることを考えれば木綿、レーヨン、
麻、毛、絹などの天然繊維とするのが特に好ましい。For the surface in contact with the skin, a thread carrying a metal phthalocyanine derivative having an action of soothing itching is used as a part or all of the thread. The material is cotton, rayon,
It is linen, wool, silk, polyamide, etc. Considering that the place to use is an itchy place, cotton, rayon,
It is particularly preferable to use natural fibers such as hemp, wool and silk.
【0012】金属フタロシアニン誘導体は、止痒・鎮痒
作用があり〔特開平5−58897号公報〕、これを繊
維に担持させた止痒・鎮痒性繊維〔2001−3034
37号公報〕は知られている。しかし、金属フタロシア
ニン誘導体は青く着色しており、これを担持した糸も着
色しているのでその外観は万人が満足できるでものでは
ない。そこで本発明では、少なくとも肌に接する面は金
属フタロシアニン誘導体を担持した糸を含むようにし、
外側面は別の糸を用いて二重構造に編んだところにその
特徴がある。もちろん、外側も金属フタロシアニン誘導
体を担持した糸となっても本発明の痒みを鎮静化させる
という趣旨は生かされる。The metal phthalocyanine derivative has an antipruritic / antipruritic effect [JP-A-5-58897], and an antipruritic / antipruritic fiber [2001-3034] carrying this on a fiber.
No. 37] is known. However, the metal phthalocyanine derivative is colored blue, and the yarn carrying the metal phthalocyanine derivative is also colored, so that its appearance cannot be satisfied by everyone. Therefore, in the present invention, at least the surface in contact with the skin includes a thread carrying a metal phthalocyanine derivative,
The outer surface is characterized by being knitted in a double structure using another thread. Needless to say, the effect of soothing the itch of the present invention can be utilized even when the thread carrying the metal phthalocyanine derivative on the outer side is also used.
【0013】本発明に使用する金属フタロシアニン誘導
体は、前記式(I)に示した化合物である。式中の、R
はカルボキシル基、スルホン酸基、あるいはこれらの水
溶性塩基から選ばれ、nはRの数で1あるいは2であ
る。式中のMは、鉄(Fe)、コバルト(Co)、マン
ガン(Mn)、チタン(Ti)、バナジウム(V)、ニ
ッケル(Ni)、銅(Cu)、亜鉛(Zn)、モリブデ
ン(Mo)、タングステン(W)から選ばれる金属であ
る。好ましい金属フタロシアニン誘導体の具体例を挙げ
ると、鉄フタロシアニンテトラカルボン酸、鉄フタロシ
アニンオクタカルボン酸などの鉄フタロシアニンポリカ
ルボン酸、コバルトフタロシアニンテトラカルボン酸、
コバルトフタロシアニンオクタカルボン酸などのコバル
トフタロシアニンポリカルボン酸、鉄フタロシアニンテ
トラスルホン酸、コバルトフタロシアニンテトラスルホ
ン酸、あるいはこれらの水溶性塩である。The metal phthalocyanine derivative used in the present invention is the compound represented by the above formula (I). R in the formula
Is a carboxyl group, a sulfonic acid group, or a water-soluble base thereof, and n is 1 or 2 in the number of R. M in the formula is iron (Fe), cobalt (Co), manganese (Mn), titanium (Ti), vanadium (V), nickel (Ni), copper (Cu), zinc (Zn), molybdenum (Mo). , A metal selected from tungsten (W). Specific examples of preferred metal phthalocyanine derivatives include iron phthalocyanine tetracarboxylic acid, iron phthalocyanine polycarboxylic acid such as iron phthalocyanine octacarboxylic acid, cobalt phthalocyanine tetracarboxylic acid,
A cobalt phthalocyanine polycarboxylic acid such as cobalt phthalocyanine octacarboxylic acid, iron phthalocyanine tetrasulfonic acid, cobalt phthalocyanine tetrasulfonic acid, or a water-soluble salt thereof.
【0014】金属フタロシアニン誘導体の製造方法は、
この分野において既に知られているので詳細な説明は省
略するが、鉄フタロシアニンテトラカルボン酸を例にと
って説明すると、トリメリット酸無水物、尿素、モリブ
デン酸アンモニウム、塩化第二鉄無水物とを有機溶媒中
で加熱して反応させ、次いで加水分解して鉄フタロシア
ニンテトラカルボン酸とする〔特開平5―58897号
公報等参照〕。同様にしてトリメリット酸無水物の代わ
りにピロメリット酸無水物無水物を用いることにより鉄
フタロシアニンオクタカルボン酸を得ることができる。The method for producing the metal phthalocyanine derivative is as follows:
Detailed description will be omitted because it is already known in this field, but when iron phthalocyanine tetracarboxylic acid is taken as an example, trimellitic acid anhydride, urea, ammonium molybdate, and ferric chloride anhydride are used as organic solvents. The reaction is carried out by heating in a medium and then hydrolyzed to give an iron phthalocyanine tetracarboxylic acid [see JP-A-5-58897]. Similarly, iron phthalocyanine octacarboxylic acid can be obtained by using pyromellitic anhydride anhydride instead of trimellitic anhydride.
【0015】繊維素材に金属フタロシアニン誘導体を担
持する方法は、代表的には該素材をカチオン化剤で処理
し、次いで金属フタロシアニン誘導体を作用させる。カ
チオン化剤は、分子中にヒドロキシル基、あるいはアミ
ノ基を反応する基と四級アンモニウム塩のカチオン基を
持った化合物であり、素材中のヒドロキシル基やアミノ
基を反応して素材中にカチオン座席を作るものである。
例えば、2,3−エポキシプロピルトリメチルアンモニ
ウムクロライド、3−クロロ−2−ヒドロキシプロピル
トリメチルアンモニウムクロライドなどがあり、阪本薬
品工業(株)「SY−GTA80」、一方社油脂(株)
「カチオノン−UK」、ナガセケムテックス(株)「」
ワイステックスN−50]「ワイステックスE−10
0」、ライオン(株)「カチオマスターC」、大日精化
(株)「KSエフェクター」などが市販されている。繊
維中にカチオン化剤を取り込むには、水酸化ナトリウム
などのアルカリ性水溶液中に、繊維とカチオン化剤を加
え、80〜100℃で30〜60分処理することで達せ
られる。In the method of supporting a metal phthalocyanine derivative on a fiber material, typically, the material is treated with a cationizing agent, and then the metal phthalocyanine derivative is allowed to act. A cationizing agent is a compound that has a hydroxyl group or an amino group-reactive group in the molecule and a quaternary ammonium salt cation group, and reacts with the hydroxyl group or amino group in the material to form a cationic seat in the material. Is what makes
For example, there are 2,3-epoxypropyltrimethylammonium chloride, 3-chloro-2-hydroxypropyltrimethylammonium chloride and the like, “SY-GTA80” of Sakamoto Yakuhin Kogyo Co., Ltd.
"Cationon-UK", Nagase Chemtex Co., Ltd. ""
Weistex N-50] "Weistex E-10
0 ”, Lion Corporation“ Catiomaster C ”, Dainichiseika Ltd.“ KS Effector ”and the like are commercially available. The incorporation of the cationizing agent into the fiber can be achieved by adding the fiber and the cationizing agent to an alkaline aqueous solution such as sodium hydroxide and treating at 80 to 100 ° C. for 30 to 60 minutes.
【0016】次いで、カチオン座席が付与された繊維
を、金属フタロシアニン誘導体を含む水溶液に浸漬して
80〜100℃で30〜60分処理することで繊維中に
金属フタロシアニン誘導体を担持させることができる。
治療補助具に用いる糸は、糸の形状で金属フタロシアニ
ン誘導体を担持させるのが便利であるが、糸にする前の
綿の状態で行っても差し支えない。繊維中の金属フタロ
シアニン誘導体の担持量は、特に限定するものではない
が、通常繊維に対して0.2〜1.0重量%程度であ
る。Next, the fiber having the cation seats is immersed in an aqueous solution containing a metal phthalocyanine derivative and treated at 80 to 100 ° C. for 30 to 60 minutes, so that the metal phthalocyanine derivative can be supported in the fiber.
It is convenient to carry the metal phthalocyanine derivative in the shape of a thread on the thread used for the treatment aid, but it is also possible to use the cotton state before forming the thread. The amount of the metal phthalocyanine derivative supported in the fiber is not particularly limited, but is usually about 0.2 to 1.0% by weight based on the fiber.
【0017】本発明の治療補助具では、少なくとも肌に
接する面は、上記金属フタロシアニン誘導体を担持した
糸を編んだ生地を用いる。このとき金属フタロシアニン
誘導体を担持した糸のみで編んでもよく、金属フタロシ
アニン誘導体を担持した繊維と金属フタロシアニン誘導
体を担持してない繊維を混紡した糸を編んでもよく、あ
るいは金属フタロシアニン誘導体を担持した糸と金属フ
タロシアニン誘導体を担持してない糸を混ぜて編んだ生
地としてもよい。いずれの場合においても金属フタロシ
アニン誘導体の濃度は生地中0.2重量%以上にするこ
とが痒みを鎮静化させるためには好ましい。In the treatment aid of the present invention, at least the surface that comes into contact with the skin is made of a cloth knitted with a thread carrying the metal phthalocyanine derivative. At this time, it may be knitted only with a thread carrying a metal phthalocyanine derivative, or may be knitted with a thread obtained by mixing fibers carrying a metal phthalocyanine derivative and fibers not carrying a metal phthalocyanine derivative, or with a thread carrying a metal phthalocyanine derivative. It is also possible to make a knitted fabric by mixing yarns that do not carry a metal phthalocyanine derivative. In any case, it is preferable that the concentration of the metal phthalocyanine derivative is 0.2% by weight or more in the dough in order to sooth the itch.
【0018】一方、本発明の治療補助具における外側面
は肌に直接接しない面であり、金属フタロシアニン誘導
体を含まなくてよい。外側面は、治療補助具を肌に密着
するように適度に締め付ける力を与え、さらに保温性、
色彩などの機能を付与するもので、その素材は、ポリエ
ステル、ポリアミド、ポリアクリロニトリル、ポリウレ
タンなどの合成繊維、木綿、レーヨン、麻、羊毛、絹な
どの天然繊維など幅広い素材から任意に選ばれる。On the other hand, the outer surface of the treatment aid of the present invention is a surface that does not come into direct contact with the skin and does not need to contain a metal phthalocyanine derivative. The outer surface provides the power to properly tighten the treatment aid so that it is in close contact with the skin, and also retains heat,
It imparts functions such as color, and its material is arbitrarily selected from a wide range of materials such as synthetic fibers such as polyester, polyamide, polyacrylonitrile and polyurethane, and natural fibers such as cotton, rayon, hemp, wool and silk.
【0019】[0019]
【実施例】〔実施例−1〕日本皮膚科学会診断基準に合
致する小児・成人のアトピー性皮膚炎患者19人を対象
にし、痒みの激しい個所に筒状サポーター形状の本発明
治療補助具を装着した。治療補助具は、金属フタロシア
ニンテトラカルボン酸0.5重量%担持する木綿糸を内
側に、ポリウレタン繊維を外側に配した二重構造に編ん
だニット製品である。各患者に対する薬による治療は試
験開始前と同じにして継続し、試験中は新たな治療を控
えた。4週間経過した後、そのうち12人について改善
がみられ、内訳は表1の通りであった。ここで痒みの改
善は患者自身の判断であり、その他掻破傷、乾燥肌、紅
斑/浮腫、丘診/小水疱、苔癬化/痒疹結節は医師の診
断によった。[Example] [Example-1] The treatment aid of the present invention in the form of a tubular supporter was applied to 19 severely itchy areas, targeting 19 children / adults with atopic dermatitis who meet the diagnostic criteria of the Japanese Dermatological Association. I put it on. The treatment aid is a knit product knitted in a double structure with a cotton thread carrying 0.5% by weight of metal phthalocyanine tetracarboxylic acid on the inside and a polyurethane fiber on the outside. Treatment with the drug for each patient continued the same as before the start of the study, and new treatment was withheld during the study. After 4 weeks, 12 of them improved, and the details are shown in Table 1. Here, the improvement of the itch was judged by the patient himself, and other factors such as scratches, dry skin, erythema / edema, swelling / small blisters, and lichenification / pruritic nodules were determined by the doctor.
【0020】[0020]
【表1】 [Table 1]
【0021】上記試験を行った19例の痒み、掻破傷、
乾燥肌、湿疹について、その程度が激しいものを
「4」、軽度のものを「1」として採点し、装着前、2
週間後、4週間後のスコアを集計した。結果を図1に示
す。図1では、各スコアの数を統計的に処理し、その有
意差をF分布検定法で検討した。この結果から、痒み、
掻破傷、湿疹、乾燥肌について装着前と装着2週間後で
有意差があり、改善が認められた。19 cases of itching, scratches,
For dry skin and eczema, those with a severe degree were scored as "4", those with a mild degree as "1", and before wearing, 2
The scores after four weeks were totaled. The results are shown in Fig. 1. In FIG. 1, the number of each score was statistically processed, and the significant difference was examined by the F distribution test method. From this result, itching,
Regarding scratches, eczema, and dry skin, there was a significant difference before and 2 weeks after wearing, and improvement was observed.
【0022】〔実施例−2〕アトピー性皮膚炎と診断さ
れて20年経過し、現在ステロイド剤外用薬で治療を受
けている28歳の男性に本発明治療補助具を装着した。
治療補助具は上記と同じ金属フタロシアニンテトラカル
ボン酸0.5重量%担持する木綿糸を内側に、ポリウレ
タン繊維を外側に配した二重構造に編んだニット製品か
らなり、痒みの多い上肢部に装着した。二週間装着し続
けたところ痒みは減り、掻くことが少なくなって掻破傷
が治ってきた。[Example-2] A 20-year-old man who had been diagnosed with atopic dermatitis and is currently being treated with a topical steroid drug was equipped with the therapeutic aid of the present invention.
The treatment aid consists of a knit product with a double structure in which a cotton thread carrying 0.5% by weight of the same metal phthalocyanine tetracarboxylic acid as the above is knitted inside and a polyurethane fiber is arranged outside, and it is attached to the itchy upper limbs. did. After continuing to wear it for two weeks, itching decreased, scratches decreased, and scratches healed.
【0023】〔実施例−3〕アトピー性皮膚炎と診断さ
れて23年経過し、現在ステロイド剤外用薬と保湿剤で
治療を受けている37歳の女性に本発明治療補助具を装
着した。上記と同じ治療補助具を、炎症のある左上肢部
に二週間装着したところ痒みは減り、掻破傷、乾燥肌が
改善され、同様炎症がある右上肢部とあきらかな有意差
が生じた。次いで右上肢部にも本発明治療補助具を装着
し二週間経過したところ右上肢部にも改善がみられ、左
右の有意差がなくなった。[Example-3] [0023] A 37-year-old woman who had been diagnosed with atopic dermatitis for 23 years and is currently treated with a topical steroid drug and a moisturizer was equipped with the therapeutic aid of the present invention. When the same treatment aid as the above was applied to the inflamed upper left limb for two weeks, itching was reduced, scratches and dry skin were improved, and there was a significant difference from the similarly inflamed upper right limb. Next, when the treatment aid of the present invention was attached to the upper right limb and two weeks passed, improvement was also observed in the upper right limb and the significant difference between the left and right disappeared.
【0024】[0024]
【発明の効果】本発明の治療補助具により痒みが鎮静化
し、これにより患者が引っ掻くことが少なくなって、
傷、腫れなどの炎症も緩和することができる。これは痒
みの不快感を少なくするばかりでなく、炎症の治療効果
を上げることになり、アトピー性皮膚炎など痒みのある
炎症をもつ患者にとって福音となるものである。EFFECTS OF THE INVENTION The treatment aid of the present invention subsides pruritus, which reduces patient scratching,
Inflammation such as wounds and swelling can also be relieved. This not only reduces the discomfort of itching but also enhances the therapeutic effect on inflammation, which is a good news for patients with itchy inflammation such as atopic dermatitis.
【図1】試験を行った19例の痒み、掻破傷、乾燥肌、
湿疹について、装着前、2週間後、4週間後のスコアを
集計したものである。BRIEF DESCRIPTION OF THE FIGURES Figure 1: 19 cases of itching, scratches, dry skin tested
With regard to eczema, the scores before, 2 weeks, and 4 weeks after the attachment are tabulated.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) D04B 21/00 D04B 21/00 B D06M 13/352 D06M 13/352 13/463 13/463 (71)出願人 591188217 神村 昌孝 長野県小県郡丸子町大字中丸子994 (72)発明者 小 宮 山 淳 長野県松本市大字原31−11 (72)発明者 白 井 汪 芳 長野県小県郡丸子町長瀬2496 (72)発明者 横 関 徳 二 長野県上田市中央西1−15−25 (72)発明者 神 村 昌 孝 長野県小県郡丸子町大字中丸子994 Fターム(参考) 4C076 AA71 BB31 CC04 CC18 EE13 EE31 EE41 4C086 AA01 DA38 MA02 MA05 MA63 NA10 ZA89 4L002 AA00 AA01 AA02 AA03 AA05 AA06 AC00 BB01 EA00 FA00 FA06 4L033 AA02 AA03 AA08 AB06 AC10 BA56 BA86 DA07 ─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 7 Identification code FI theme code (reference) D04B 21/00 D04B 21/00 B D06M 13/352 D06M 13/352 13/463 13/463 (71) Application People 591188217 Masataka Kamimura Nakamaruko, Marugo-cho, Oka-gun, Nagano 994 (72) Inventor Atsushi Komiyayama 31-11, Ojira, Matsumoto-shi, Nagano (72) Inventor Shirai, Nagase Nagase Prefecture (72) Inventor Tokuji Yokozeki 1-15-25 Chuonishi, Ueda City, Nagano Prefecture (72) Inventor Masataka Kamimura 994 F term, Nakamaruko, Maruko-machi, Ogo-gun, Nagano Prefecture (reference) 4C076 AA71 BB31 CC04 CC18 EE13 EE31 EE41 4C086 AA01 DA38 MA02 MA05 MA63 NA10 ZA89 4L002 AA00 AA01 AA02 AA03 AA05 AA06 AC00 BB01 EA00 FA00 FA06 4L033 AA02 AA03 AA08 AB06 AC10 BA56 BA86 DA07
Claims (3)
みを鎮静化させる治療補助具であり、肌に接する内面は
式(I)〔式中、Rはカルボキシル基、スルホン酸基、
あるいはこれらの水溶性塩基から選ばれる基であり、n
はRの数で1あるいは2、Mは、鉄(Fe)、コバルト
(Co)、マンガン(Mn)、チタン(Ti)、バナジ
ウム(V)、ニッケル(Ni)、銅(Cu)、亜鉛(Z
n)、モリブデン(Mo)、タングステン(W)から選
ばれる金属である〕で示される金属フタロシアニン誘導
体を担持した糸を含み、外面は該金属フタロシアニン誘
導体を担持しない糸からなる二重構造に編んで構成され
ていることを特徴とする治療補助具。 【化1】 1. A therapeutic aid for soothing itch by adhering to itchy and inflamed skin, wherein the inner surface in contact with the skin is of formula (I) [wherein R is a carboxyl group, a sulfonic acid group,
Alternatively, it is a group selected from these water-soluble bases, and n
Is the number of R, 1 or 2, M is iron (Fe), cobalt (Co), manganese (Mn), titanium (Ti), vanadium (V), nickel (Ni), copper (Cu), zinc (Z).
n), molybdenum (Mo), or tungsten (W)], the outer surface of which is knitted into a double structure including a thread supporting a metal phthalocyanine derivative and an outer surface of which is a thread not supporting the metal phthalocyanine derivative. A therapeutic aid characterized by being configured. [Chemical 1]
シアニンポリカルボン酸、鉄フタロシアニンポリスルホ
ン酸、コバルトフタロシアニンポリカルボン酸、コバル
トフタロシアニンポリスルホン酸、およびこれらの水溶
性塩から選ばれる一種以上であることを特徴とする請求
項1記載の治療補助具。2. The metal phthalocyanine derivative is one or more selected from iron phthalocyanine polycarboxylic acid, iron phthalocyanine polysulfonic acid, cobalt phthalocyanine polycarboxylic acid, cobalt phthalocyanine polysulfonic acid, and water-soluble salts thereof. The treatment aid according to claim 1.
は、木綿、レーヨン、麻、羊毛、絹、ポリアミドから選
ばれる一種以上の素材をカチオン化剤で処理し、次いで
金属フタロシアニン誘導体を作用させて担持させたこと
を特徴とする請求項1記載の治療補助具。3. A thread carrying a metal phthalocyanine derivative is prepared by treating one or more materials selected from cotton, rayon, hemp, wool, silk and polyamide with a cationizing agent, and then allowing the metal phthalocyanine derivative to act and carry it. The treatment aid according to claim 1, wherein
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JPWO2005021860A1 (en) * | 2003-09-01 | 2006-10-26 | 株式会社信州Tlo | Fiber material for allergen decomposition and fiber product using the same |
KR100722794B1 (en) * | 2003-10-30 | 2007-05-31 | 유겐가이샤 판메디카 | Glove for relieving itch and inflammation, and method for producing the same |
JP2009106597A (en) * | 2007-10-31 | 2009-05-21 | Teiken:Kk | Tubular bandage for atopic dermatitis |
US20090291934A1 (en) * | 2003-11-12 | 2009-11-26 | Shinshu Tlo Co., Ltd. | Method for decomposing an allergen |
CN105220335A (en) * | 2015-08-28 | 2016-01-06 | 太仓市鑫泰针织有限公司 | A kind of variable color viscose knit fabric |
CN105247124A (en) * | 2013-05-29 | 2016-01-13 | 东丽株式会社 | Fibrous structure |
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2002
- 2002-01-18 JP JP2002009968A patent/JP2003213548A/en active Pending
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPWO2005021860A1 (en) * | 2003-09-01 | 2006-10-26 | 株式会社信州Tlo | Fiber material for allergen decomposition and fiber product using the same |
KR100722794B1 (en) * | 2003-10-30 | 2007-05-31 | 유겐가이샤 판메디카 | Glove for relieving itch and inflammation, and method for producing the same |
US7341962B2 (en) * | 2003-10-30 | 2008-03-11 | Keikichi Kitamura | Less irritant or inflammatory glove and method for producing the same |
US7749572B2 (en) * | 2003-10-30 | 2010-07-06 | Keikichi Kitamura | Less irritant or inflammatory glove and method for producing the same |
US20090291934A1 (en) * | 2003-11-12 | 2009-11-26 | Shinshu Tlo Co., Ltd. | Method for decomposing an allergen |
JP2009106597A (en) * | 2007-10-31 | 2009-05-21 | Teiken:Kk | Tubular bandage for atopic dermatitis |
CN105247124A (en) * | 2013-05-29 | 2016-01-13 | 东丽株式会社 | Fibrous structure |
CN105220335A (en) * | 2015-08-28 | 2016-01-06 | 太仓市鑫泰针织有限公司 | A kind of variable color viscose knit fabric |
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