JPH06107550A - Anti-inflammatory agent for oral administration - Google Patents

Anti-inflammatory agent for oral administration

Info

Publication number
JPH06107550A
JPH06107550A JP29906292A JP29906292A JPH06107550A JP H06107550 A JPH06107550 A JP H06107550A JP 29906292 A JP29906292 A JP 29906292A JP 29906292 A JP29906292 A JP 29906292A JP H06107550 A JPH06107550 A JP H06107550A
Authority
JP
Japan
Prior art keywords
hyaluronic acid
mucous membrane
inflammation
inflammatory
inflammatory agent
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
Application number
JP29906292A
Other languages
Japanese (ja)
Inventor
Kiyoshi Kita
喜代司 喜多
Yutaka Kurachi
裕 倉知
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to JP29906292A priority Critical patent/JPH06107550A/en
Publication of JPH06107550A publication Critical patent/JPH06107550A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To provide a peroral anti-inflammatory agent containing hyaluronic acid as an active component, having little side effect and high safety and useful for the treatment of inflammation of mucous membrane in amygdalitis, pharyngitis and larynxitis. CONSTITUTION:Hyaluronic acid is used as an active component. The agent can be prepared in various forms such as jelly, a drop-like aqueous agent or a saliva-soluble capsule. Hyaluronic acid is a kind of acidic mucopolysaccharides and widely present between the tissues and in the body fluid of vertebrate animal. Hyaluronic acid can be bonded to the inflammation part of the mucous membrane from the oral cavity to the upper respiratory tract and cure the inflammation by oral administration of hyaluronic acid. In a connective tissue component in a wound healing stage, hyaluronic acid is developed first and, according to the elimination of the acid, chondroitin sulfate is developed to synthesize a collagen, form cicatrices and heal the wound. Early recovery is possible because of the adhesion of hyaluronic acid to the inflammatory mucous membrane, the promotion of exudation of healing substance and the protection of the inflammatory mucous membrane.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明の経口抗炎症剤は口内粘膜
や咽・喉頭粘膜治療の為の医療に関する。
BACKGROUND OF THE INVENTION The oral anti-inflammatory agent of the present invention relates to medical treatment for treating oral mucosa and pharyngeal / larynx mucosa.

【0002】[0002]

【従来技術の説明】ヒアルロン酸は脊椎動物の組織間や
体液中等に広く存在している。特に人では、臍帯、関節
液、硝子体中に高濃度に見られる。現在、ヒアルロン酸
を局所に応用したものとしては、眼科手術補助剤、点眼
剤、変形性関節治療剤がある。
Description of the Prior Art Hyaluronic acid is widely present between tissues of vertebrates and in body fluids. Especially in humans, it is found in high concentrations in the umbilical cord, synovial fluid and vitreous. Currently, topical applications of hyaluronic acid include ophthalmic surgery auxiliary agents, eye drops, and therapeutic agents for degenerative joints.

【0003】ヒアルロン酸には薬理作用として、多形核
白血球の機能の抑制、リンパ球と標的細胞の接触抑制、
マクロファージの遊走及び貧食抑制、低分子ヒアルロン
酸の血管新生活性、ラジカルスカベンジャー作用、細胞
増殖に対する作用があると言われている。しかしなが
ら、ヒアルロン酸自体には生理活性は無く、物理的性質
がこれら生理活性の誘因物質になっているとも考えられ
る。つまり、例えば、ヒアルロン酸が生理活性物質であ
る創傷治癒物質や炎症性物質の運搬体となり、創傷治癒
過程や炎症の過程に深く関与していると考えられるから
である。
Hyaluronic acid has the pharmacological effects of suppressing the function of polymorphonuclear leukocytes, suppressing contact between lymphocytes and target cells,
It is said to have migration of macrophages and suppression of phagocytosis, angiogenic activity of low molecular weight hyaluronic acid, radical scavenger action, and cell proliferation action. However, hyaluronic acid itself has no physiological activity, and its physical properties are considered to be an inducer of these physiological activities. That is, for example, it is considered that hyaluronic acid serves as a carrier for a wound healing substance or an inflammatory substance that is a physiologically active substance and is deeply involved in the wound healing process and the inflammation process.

【0004】日本では水性注射剤である事より薬効の無
い薬剤として、また米国では医療器具として分類されて
いる。 従来より使われている1%ヒアルロン酸水溶液
の物理的性質は粘性や弾性に優れており、一般的に粘弾
性物質と言われている。
In Japan, it is classified as a drug having no medicinal effect rather than being an aqueous injection, and in the US as a medical device. The conventionally used 1% aqueous solution of hyaluronic acid has excellent physical properties in viscosity and elasticity, and is generally called a viscoelastic substance.

【0005】[0005]

【発明が解決しようとする課題】扁桃、咽頭、喉頭炎及
び気道疾患時の気道上部や食道上部より口内までの粘膜 はヒアルロン酸が存在する。
[Problems to be Solved by the Invention] Mucosa from the upper respiratory tract or upper esophagus to the oral cavity during tonsils, pharynx, laryngitis and respiratory tract diseases Is present in hyaluronic acid.

【0006】 ヒアルロン酸の滲出が阻害される場合がある。例えば、
塩酸ブロムヘキシンやメ て処方されるが、これら塩酸ブロムヘキシンやメチルシ
ステイン等は痰が切れやすくなるような分泌物を増加さ
せ、痰の成分の一つである酸性ムコ多糖類を低分子化す
ることにより痰の切れを良くするといわれている。
[0006] Exudation of hyaluronic acid may be inhibited. For example,
Bromhexine hydrochloride and However, bromhexine hydrochloride, methyl cysteine, etc. increase secretions that make sputum easier to cut, and reduce the molecular weight of acidic mucopolysaccharide, which is one of the components of sputum, to cut sputum. It is said to improve.

【0007】[0007]

【課題を解決する為の手段】そこで、この酸性ムコ多糖
類の一つであるヒアルロン酸を経口より投与し、口内よ
り気道上部までの粘膜の炎症部位にヒアルロン酸を接着
させその部位を治癒させようとするものである。特にヒ
アルロン酸は炎症性蛋白質と接着性があることより投与
したヒアルロン酸は炎症部位に特異的に接着する。接着
しなかったヒアルロン酸は食道、胃、腸を通り、分解吸
収される。
[Means for solving the problem] Therefore, hyaluronic acid, which is one of the acidic mucopolysaccharides, is orally administered, and hyaluronic acid is adhered to the inflammatory site of the mucous membrane from the mouth to the upper respiratory tract to cure the site. It is something to try. In particular, since hyaluronic acid has adhesiveness with inflammatory proteins, the administered hyaluronic acid specifically adheres to the site of inflammation. Hyaluronic acid that has not adhered is decomposed and absorbed through the esophagus, stomach, and intestines.

【0008】ヒアルロン酸は塩基とすると水によく溶け
る。そのヒアルロン酸は水性剤、ゼリー、飴玉、或いは
唾液溶解性カプセル剤とすると服用しやすい。
Hyaluronic acid as a base is well soluble in water. The hyaluronic acid is easy to take when it is used as an aqueous agent, jelly, candy, or saliva-soluble capsule.

【0009】ヒアルロン酸は創傷治癒物質と知られてい
るが、本発明はヒアルロン酸を経口投与し、扁桃、咽
頭、喉頭炎における粘膜の炎症の治療を行うことを特徴
としている。
Although hyaluronic acid is known to be a wound healing substance, the present invention is characterized by oral administration of hyaluronic acid to treat mucosal inflammation in tonsils, pharynx and laryngitis.

【0010】[0010]

【作用】創傷治癒過程における結合組織成分ではヒアル
ロン酸が最初に出現し、それが消失すると共にコンドロ
イチン硫酸が出現し、そしてコラーゲンが合成され瘢痕
化し、傷が治癒することが知られている。つまり何等か
の原因で、例えば炎症による、組織障害後の組織の修復
過程では創傷治癒物質を運ぶヒアルロン酸が存在するこ
とが必要であると考えられている。精製されたヒアルロ
ン酸は蛋白質と共有結合する性質を持っているので炎症
性蛋白質の存在する炎症下の粘膜上に特異的に接着す
る。ヒアルロン酸ナトリウムは保水力が強く、乾燥物容
積の約1,000倍の水和容積となる事が知られてい
る。保水時は非ニュートン流動の粘弾性特性を持ってお
り、組織保護や潤滑剤の役目を持っている。本発明では
これら全ての作用が応用され、口内粘膜や喉頭粘膜の治
療に服用される。
It is known that hyaluronic acid first appears in connective tissue components in the process of wound healing, and then disappears, chondroitin sulfate appears, and collagen is synthesized to scar and heal the wound. In other words, it is considered necessary that hyaluronic acid, which carries a wound healing substance, is present in the process of repairing the tissue after tissue damage due to some cause, for example, inflammation. Since purified hyaluronic acid has a property of covalently binding to a protein, it specifically adheres to mucous membranes under inflammation in which inflammatory proteins are present. It is known that sodium hyaluronate has a strong water retention capacity and has a hydration volume about 1,000 times the dry matter volume. It has a non-Newtonian viscoelastic property during water retention, and has the role of tissue protection and lubricant. In the present invention, all of these effects are applied, and the present invention is used for treating oral mucosa and larynx mucosa.

【0011】[0011]

【実施例1】ヒアルロン酸ナトリウム10mgを塩化ナ
トリウム90mgと共に蒸留水1mlに溶解し、ヒアル
ロン酸ナトリウム水溶液を作成した。ヒアルロン酸ナト
リウムは平均分子量約90万ダルトンで鶏冠より抽出精
製したものを使用した。本発明者自ら喉頭炎における粘
膜の炎症の治療に飲用したところ、飲用直後より炎症粘
膜にべとつき感があり、翌日には咳が止まり、軽快し
た。
Example 1 10 mg of sodium hyaluronate was dissolved in 1 ml of distilled water together with 90 mg of sodium chloride to prepare an aqueous solution of sodium hyaluronate. The sodium hyaluronate used had an average molecular weight of about 900,000 daltons and was extracted and purified from chicken caps. When the present inventor himself took the medicine to treat inflammation of the mucous membrane in laryngitis, he felt a sticky feeling on the inflamed mucous membrane immediately after drinking, and stopped coughing on the next day, and was relieved.

【0012】[0012]

【実施例2】平均分子量約120万ダルトンで鶏冠より
抽出精製した3%ヒアルロン酸ナトリウム水溶液を作成
し、ゼリー状とした。無水アルコールに24時間浸し、
ゼリー状の周囲をより脱水し固くした。このヒアルロン
酸のゼリーを口に含んだところ殆ど無味ではあったが、
緩徐に膨潤含水し溶解した。
Example 2 A 3% sodium hyaluronate aqueous solution having an average molecular weight of about 1.2 million daltons and extracted and purified from a chicken cob was prepared into a jelly form. Soak in absolute alcohol for 24 hours,
The jelly-like surroundings were dehydrated and hardened. When I put this hyaluronic acid jelly in my mouth, it was almost tasteless,
It swelled slowly and contained water.

【0013】[0013]

【実施例3】平均分子量約120万ダルトンで鶏冠より
抽出精製した3%ヒアルロン酸ナトリウム水溶液を作成
し、ゼリー状で板状にした。無水アルコールに24時間
浸し、ゼリー状の周囲をより脱水し固くした。固化した
ヒアルロン酸ナトリウムを水飴と共に丸め、乾燥させ、
飴玉状とした。このヒアルロン酸の飴玉を口に含んだと
ころ、甘く、また、緩徐に膨潤含水し溶解した。
[Example 3] A 3% sodium hyaluronate aqueous solution having an average molecular weight of approximately 1.2 million daltons was extracted and purified from a chicken cob and formed into a jelly plate. It was soaked in anhydrous alcohol for 24 hours to further dehydrate and harden the jelly-like surroundings. Roll the solidified sodium hyaluronate with starch syrup, dry,
Made candy-shaped. When this hard candy of hyaluronic acid was put in the mouth, it was sweet and swollen slowly, hydrated and dissolved.

【0014】[0014]

【実施例4】平均分子量約120万ダルトンで鶏冠より
抽出精製した2%ヒアルロン酸ナトリウム水溶液を作成
し、ゼリー状とした。これを口内で溶解するカプセル剤
とした。
[Example 4] A 2% aqueous solution of sodium hyaluronate extracted and purified from chicken combs having an average molecular weight of about 1.2 million daltons was prepared into a jelly form. This was made into a capsule that dissolves in the mouth.

【0015】[0015]

【発明の効果】以上説明したように本発明のヒアルロン
酸を主成分とする経口抗炎症剤で扁桃、咽頭、喉頭炎に
おける粘膜の炎症の治療が行える。本薬剤自体は薬理活
性が無いと考えられるので副作用は殆ど無く、安全であ
る。特に、ゼリーや飴玉状等にして服用すれば、老人や
子供でも簡単に服用される。ヒアルロン酸は多糖類であ
り、喉飴として転用可能な物質である。本発明のヒアル
ロン酸を主成分とする経口抗炎症剤は炎症粘膜に接着
し、治癒物質の滲出を促し、その炎症粘膜を保護するの
で患者の早期回復が期待できる。
As described above, the oral anti-inflammatory drug containing hyaluronic acid as a main component of the present invention can treat mucosal inflammation in tonsils, pharynx and laryngitis. Since the drug itself is considered to have no pharmacological activity, it has few side effects and is safe. In particular, if it is taken in the form of jelly or candy, it can be easily taken by old people and children. Hyaluronic acid is a polysaccharide and a substance that can be used as a soothing candy. The oral anti-inflammatory agent of the present invention containing hyaluronic acid as a main component adheres to inflamed mucosa, promotes exudation of a healing substance, and protects the inflamed mucosa, so that early recovery of the patient can be expected.

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 ヒアルロン酸を有効成分とする経口抗炎
症剤。
1. An oral anti-inflammatory agent containing hyaluronic acid as an active ingredient.
【請求項2】 ヒアルロン酸を有効成分とし、ゼリー状
の剤型とした経口抗炎症剤。
2. An oral anti-inflammatory agent containing hyaluronic acid as an active ingredient in the form of a jelly.
【請求項3】 ヒアルロン酸を有効成分とし、飴玉状の
剤型とした経口抗炎症剤。
3. An oral anti-inflammatory agent which comprises hyaluronic acid as an active ingredient and has a candy-like dosage form.
【請求項4】 ヒアルロン酸を有効成分とし、水性剤型
とした経口抗炎症剤。
4. An oral anti-inflammatory agent containing hyaluronic acid as an active ingredient in the form of an aqueous formulation.
【請求項5】 ヒアルロン酸を有効成分とし、カプセル
に封入したカプセル剤とした経口抗炎症剤。
5. An oral anti-inflammatory agent comprising hyaluronic acid as an active ingredient and encapsulated in capsules.
JP29906292A 1992-09-29 1992-09-29 Anti-inflammatory agent for oral administration Pending JPH06107550A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP29906292A JPH06107550A (en) 1992-09-29 1992-09-29 Anti-inflammatory agent for oral administration

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP29906292A JPH06107550A (en) 1992-09-29 1992-09-29 Anti-inflammatory agent for oral administration

Publications (1)

Publication Number Publication Date
JPH06107550A true JPH06107550A (en) 1994-04-19

Family

ID=17867714

Family Applications (1)

Application Number Title Priority Date Filing Date
JP29906292A Pending JPH06107550A (en) 1992-09-29 1992-09-29 Anti-inflammatory agent for oral administration

Country Status (1)

Country Link
JP (1) JPH06107550A (en)

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996024362A1 (en) * 1995-02-07 1996-08-15 Shiseido Company, Ltd. Antiinflammatory agents
WO2000056344A1 (en) * 1999-03-24 2000-09-28 Seikagaku Corporation Artificial saliva
JP2001270829A (en) * 2000-03-24 2001-10-02 Seikagaku Kogyo Co Ltd Smooth muscle cell growth promoter
WO2002024223A3 (en) * 2000-09-21 2002-06-06 Brigham & Womens Hospital Prevention and treatment of streptococcal and staphylococcal infection
US6607745B2 (en) * 2001-05-18 2003-08-19 Harry Leneau Ingestion of hyaluronic acid for improved joint function and health
WO2003096877A2 (en) * 2001-12-05 2003-11-27 The Brigham And Women's Hospital, Inc. Prevention and treatment of streptococcal and staphylococcal infection
US6911436B2 (en) * 1994-05-12 2005-06-28 Dermal Reserach Laboratories, Inc. Pharmaceutical composition of complex carbohydrates and essential oils and methods of using the same
JP2007269806A (en) * 1999-03-24 2007-10-18 Seikagaku Kogyo Co Ltd Artificial saliva
JP2007291117A (en) * 1999-03-24 2007-11-08 Seikagaku Kogyo Co Ltd Artificial saliva
US7338943B2 (en) * 2001-12-21 2008-03-04 Soft Gel Technologies, Inc. Hyaluronic acid in soft gel form
US7879824B2 (en) 2001-07-31 2011-02-01 Dermal Research Laboratories, Inc. Methods of preventing or treating diseases and conditions using complex carbohydrates
US8003782B1 (en) 1999-02-01 2011-08-23 Dermal Research Laboratories, Inc. Pharmaceutical composition of complex carbohydrates and essential oils and methods of using the same
WO2013129577A1 (en) * 2012-03-01 2013-09-06 キユーピー株式会社 ORAL PREPARATION FOR PROMOTING EXPRESSION OF TGF-β, ORAL PREPARATION FOR INHIBITING PRODUCTION OF PAIN-MEDIATING SUBSTANCE, AND ORAL PREPARATION FOR PREVENTING EDEMA
JP2014501733A (en) * 2010-11-30 2014-01-23 リチェルファルマ ソシエタ レスポンサビリタ リミタータ Topical composition for preserving or restoring the intact state of the mucosa
US8865692B2 (en) 2007-11-13 2014-10-21 Meritage Pharma, Inc Compositions for the treatment of gastrointestinal inflammation
US10293052B2 (en) 2007-11-13 2019-05-21 Meritage Pharma, Inc. Compositions for the treatment of gastrointestinal inflammation
JP2020054262A (en) * 2018-10-01 2020-04-09 ユーハ味覚糖株式会社 Mucus membrane protection-related gene expression enhancer and use of the same
US11413296B2 (en) 2005-11-12 2022-08-16 The Regents Of The University Of California Viscous budesonide for the treatment of inflammatory diseases of the gastrointestinal tract

Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6911436B2 (en) * 1994-05-12 2005-06-28 Dermal Reserach Laboratories, Inc. Pharmaceutical composition of complex carbohydrates and essential oils and methods of using the same
WO1996024362A1 (en) * 1995-02-07 1996-08-15 Shiseido Company, Ltd. Antiinflammatory agents
US5872109A (en) * 1995-02-07 1999-02-16 Shiseido Company, Ltd. Anti-inflammatory agent
US8003782B1 (en) 1999-02-01 2011-08-23 Dermal Research Laboratories, Inc. Pharmaceutical composition of complex carbohydrates and essential oils and methods of using the same
US9220290B2 (en) 1999-02-01 2015-12-29 Dermal Research Laboratories, Inc. Pharmaceutical composition of complex carbohydrates and essential oils and methods of using the same
JP2007269806A (en) * 1999-03-24 2007-10-18 Seikagaku Kogyo Co Ltd Artificial saliva
WO2000056344A1 (en) * 1999-03-24 2000-09-28 Seikagaku Corporation Artificial saliva
JP2007291117A (en) * 1999-03-24 2007-11-08 Seikagaku Kogyo Co Ltd Artificial saliva
JP2001270829A (en) * 2000-03-24 2001-10-02 Seikagaku Kogyo Co Ltd Smooth muscle cell growth promoter
JP4587148B2 (en) * 2000-03-24 2010-11-24 生化学工業株式会社 Smooth muscle cell proliferation promoter
US8367642B2 (en) 2000-07-31 2013-02-05 Dermal Research Laboratories, Inc. Methods of preventing or treating diseases and conditions using complex carbohydrates
WO2002024223A3 (en) * 2000-09-21 2002-06-06 Brigham & Womens Hospital Prevention and treatment of streptococcal and staphylococcal infection
US6607745B2 (en) * 2001-05-18 2003-08-19 Harry Leneau Ingestion of hyaluronic acid for improved joint function and health
US7879824B2 (en) 2001-07-31 2011-02-01 Dermal Research Laboratories, Inc. Methods of preventing or treating diseases and conditions using complex carbohydrates
WO2003096877A2 (en) * 2001-12-05 2003-11-27 The Brigham And Women's Hospital, Inc. Prevention and treatment of streptococcal and staphylococcal infection
WO2003096877A3 (en) * 2001-12-05 2005-03-31 Brigham & Womens Hospital Prevention and treatment of streptococcal and staphylococcal infection
US7338943B2 (en) * 2001-12-21 2008-03-04 Soft Gel Technologies, Inc. Hyaluronic acid in soft gel form
US8551975B1 (en) 2001-12-21 2013-10-08 Soft Gel Technologies, Inc. Hyaluronic acid in soft gel form
US11413296B2 (en) 2005-11-12 2022-08-16 The Regents Of The University Of California Viscous budesonide for the treatment of inflammatory diseases of the gastrointestinal tract
US8865692B2 (en) 2007-11-13 2014-10-21 Meritage Pharma, Inc Compositions for the treatment of gastrointestinal inflammation
US9050368B2 (en) 2007-11-13 2015-06-09 Meritage Pharma, Inc. Corticosteroid compositions
US10293052B2 (en) 2007-11-13 2019-05-21 Meritage Pharma, Inc. Compositions for the treatment of gastrointestinal inflammation
US11357859B2 (en) 2007-11-13 2022-06-14 Viropharma Biologics Llc Compositions for the treatment of gastrointestinal inflammation
JP2014501733A (en) * 2010-11-30 2014-01-23 リチェルファルマ ソシエタ レスポンサビリタ リミタータ Topical composition for preserving or restoring the intact state of the mucosa
WO2013129577A1 (en) * 2012-03-01 2013-09-06 キユーピー株式会社 ORAL PREPARATION FOR PROMOTING EXPRESSION OF TGF-β, ORAL PREPARATION FOR INHIBITING PRODUCTION OF PAIN-MEDIATING SUBSTANCE, AND ORAL PREPARATION FOR PREVENTING EDEMA
JP2020054262A (en) * 2018-10-01 2020-04-09 ユーハ味覚糖株式会社 Mucus membrane protection-related gene expression enhancer and use of the same

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