JPH1160480A - Peptic ulcer treatment - Google Patents

Peptic ulcer treatment

Info

Publication number
JPH1160480A
JPH1160480A JP22261997A JP22261997A JPH1160480A JP H1160480 A JPH1160480 A JP H1160480A JP 22261997 A JP22261997 A JP 22261997A JP 22261997 A JP22261997 A JP 22261997A JP H1160480 A JPH1160480 A JP H1160480A
Authority
JP
Japan
Prior art keywords
weight
peptic ulcer
vitamin
squalane
therapeutic 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
JP22261997A
Other languages
Japanese (ja)
Inventor
Koji Inagaki
孝司 稲垣
Mitsuaki Watabe
光朗 渡部
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.)
Sekisui Chemical Co Ltd
Original Assignee
Sekisui Chemical Co Ltd
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 Sekisui Chemical Co Ltd filed Critical Sekisui Chemical Co Ltd
Priority to JP22261997A priority Critical patent/JPH1160480A/en
Publication of JPH1160480A publication Critical patent/JPH1160480A/en
Pending legal-status Critical Current

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

(57)【要約】 【課題】 より安全で有用性の高い消化性潰瘍治療剤を
提供する。 【解決手段】 ビタミンE及びスクワランを含有する消
化性潰瘍治療剤。更に、ビタミンEの含有量が0.1重
量%を超え99重量%未満、スクワランの含有量が0.
1重量%を超え、99重量%未満である上記の消化性潰
瘍治療剤。剤型例:ビタミンE、スクワラン及びアラビ
アゴム水溶液からなる液剤。
(57) [Problem] To provide a therapeutic agent for peptic ulcer which is safer and highly useful. SOLUTION: The therapeutic agent for peptic ulcer containing vitamin E and squalane. Furthermore, the content of vitamin E is more than 0.1% by weight and less than 99% by weight, and the content of squalane is 0.1% by weight.
The above-mentioned therapeutic agent for peptic ulcer, which is more than 1% by weight and less than 99% by weight. Formulation example: a liquid formulation comprising vitamin E, squalane and an aqueous solution of gum arabic.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、消化性潰瘍治療剤
に関する。
The present invention relates to a therapeutic agent for peptic ulcer.

【0002】[0002]

【従来の技術】消化性潰瘍は、胃潰瘍、十二指腸潰瘍及
び吻合部潰瘍などの総称であり、胃又は十二指腸などの
粘膜下層以下に及ぶ部分的な粘膜欠損と定義される。消
化性潰瘍の発症機序としては、一般にバランス説が受け
入れられている。すなわち、消化管内部では、酸やペプ
シンなどの攻撃因子と、粘膜、重炭酸、粘膜血流などの
防御因子のバランスが維持されているが、何らかの原因
によってこのバランスが崩れ、攻撃因子の作用が防御因
子の作用を上回ったときに潰瘍が生じると考えられてい
る(鈴木ら、検査と技術、23巻、7号、466〜47
2頁、1995年)。本疾患は、一般的に持続性の痛み
を伴い、患者に多大な苦痛をもたらす上、一度発症する
と、治癒後も再発を繰り返して慢性化することが多い。
2. Description of the Related Art Peptic ulcer is a general term for gastric ulcer, duodenal ulcer, anastomotic ulcer and the like, and is defined as a partial mucosal defect extending below the submucosa such as the stomach or duodenum. As a pathogenesis mechanism of peptic ulcer, the balance theory is generally accepted. In other words, inside the digestive tract, the balance between aggressive factors such as acid and pepsin and protective factors such as mucous membrane, bicarbonate, and mucosal blood flow is maintained. It is believed that ulcers form when the action of protective factors is exceeded (Suzuki et al., Inspection and Technology, Vol. 23, No. 7, 466-47).
2, p. 1995). This disease is generally accompanied by persistent pain, causing a great deal of pain to the patient, and once onset, it often becomes recurrent and chronic after healing.

【0003】消化性潰瘍の治療薬としては、制酸薬(重
曹、炭酸カルシウム、水酸化アルミニウム、水酸化マグ
ネシウムなど)、H2レセプターアンタゴニスト(シメ
チジン、ラニチジン、ファモチジンなど)、プロトンポ
ンプインヒビター(オメプラゾール等)及びスクラルフ
ァートなどが用いられる。これらの薬剤は、上記バラン
ス説における、ある攻撃因子を減弱又はある防御因子を
増強し、その結果、生体の自然治癒力が発揮され効果を
現す。
[0003] Drugs for treating peptic ulcer include antacids (such as sodium bicarbonate, calcium carbonate, aluminum hydroxide and magnesium hydroxide), H2 receptor antagonists (such as cimetidine, ranitidine and famotidine), and proton pump inhibitors (such as omeprazole). And sucralfate. These drugs attenuate certain aggressive factors or enhance certain protective factors in the above-mentioned balance theory, and as a result, the natural healing power of the living body is exerted to exert its effect.

【0004】[0004]

【発明が解決しようとする課題】しかしながら、上記薬
剤が無効な難治性の症例が存在すること、各薬剤に固有
の副作用を有することから、新しい薬剤の開発が望まれ
ている。本発明の目的は、上記の点に鑑み、より安全で
有用性の高い消化性潰瘍治療剤を提供することにある。
However, since there are intractable cases where the above drugs are ineffective and each drug has its own side effects, development of new drugs is desired. An object of the present invention is to provide a safer and more useful therapeutic agent for peptic ulcer in view of the above points.

【0005】[0005]

【課題を解決するための手段】請求項1記載の消化性潰
瘍治療剤は、ビタミンE及びスクワランを含有すること
を特徴とする。
The remedy for peptic ulcer according to claim 1 is characterized by containing vitamin E and squalane.

【0006】請求項2記載の消化性潰瘍治療剤は、ビタ
ミンEの含有量が0.1重量%を超え99重量%未満、
スクワランの含有量が0.1重量%を超え99重量%未
満であることを特徴とする請求項1記載の消化性潰瘍治
療剤である。
[0006] The therapeutic agent for peptic ulcer according to claim 2 has a vitamin E content of more than 0.1% by weight and less than 99% by weight;
2. The therapeutic agent for peptic ulcer according to claim 1, wherein the content of squalane is more than 0.1% by weight and less than 99% by weight.

【0007】上記ビタミンEとは、トコフェロール(ビ
タミンE)及びその誘導体をいい、日本薬局方に収載さ
れているものとしては、例えば、酢酸トコフェロール
(ビタミンE酢酸エステル)、コハク酸トコフェロール
(ビタミンEコハク酸エステル)等が挙げられる。上記
以外のものとしては、例えば、α−トコフェロール、β
−トコフェロール、γ−トコフェロール、δ−トコフェ
ロール、ニコチン酸トコフェロール(ビタミンEニコチ
ン酸エステル)、リン酸トコフェロール(ビタミンEリ
ン酸エステル)、天然型ビタミンE等が挙げられるが、
これらに限定されるものではなく、トコフェロールの単
糖、オリゴ糖又は多糖との結合物や水溶性のビタミンE
も含まれる。なお、ビタミンEは、過剰摂取しても副作
用がなく、局所に対する刺激性も殆どなく、安全である
ことが一般に知られている。
[0007] The above-mentioned vitamin E refers to tocopherol (vitamin E) and its derivatives. Examples of those listed in the Japanese Pharmacopoeia include tocopherol acetate (vitamin E acetate) and tocopherol succinate (vitamin E succinate). Acid ester). Other than the above, for example, α-tocopherol, β
-Tocopherol, γ-tocopherol, δ-tocopherol, tocopherol nicotinate (vitamin E nicotinate), tocopherol phosphate (vitamin E phosphate), natural vitamin E, and the like.
However, the present invention is not limited thereto.
Is also included. It is generally known that vitamin E has no side effects even if it is excessively taken, has little local irritation, and is safe.

【0008】上記スクワランとは、深海産の魚類、特
に、サメ類の肝油中、又は植物油、例えばオリーブ油、
コメヌカ油、小麦胚芽油、ゴマ油、綿実油などに存在す
る不飽和炭化水素であるスクワレンを還元してなる飽和
炭化水素である。また、ゲラニルアセトン及びアセチレ
ン化合物を原料として合成して得られる合成スクワラン
も含まれる。なお、スクワランは、上記のように食品中
にも多く含まれているとともに、化粧品の添加物として
実績があり、局所に対して安全であることが一般に知ら
れている。
[0008] The above-mentioned squalane is fish in the deep sea, especially in shark liver oil or vegetable oil such as olive oil.
It is a saturated hydrocarbon obtained by reducing squalene which is an unsaturated hydrocarbon present in rice bran oil, wheat germ oil, sesame oil, cottonseed oil and the like. Further, a synthetic squalane obtained by using geranylacetone and an acetylene compound as raw materials is also included. In addition, as described above, squalane is contained in a large amount in foods, has a track record as an additive for cosmetics, and is generally known to be locally safe.

【0009】本発明の消化性潰瘍治療剤中のビタミンE
の含有量は、少なくなると潰瘍治癒促進効果が十分でな
くなり、多くなっても潰瘍治癒促進効果が含有量に応じ
て著しく高くなることはないので、0.1重量%を超え
99重量%未満が好ましく、、10〜95重量%がより
好ましく、20〜50重量%が特に好ましい。
Vitamin E in the therapeutic agent for peptic ulcer of the present invention
When the content of ulcer decreases, the effect of promoting ulcer healing becomes insufficient, and even when it increases, the effect of promoting ulcer healing does not increase significantly depending on the content. Preferably, it is more preferably from 10 to 95% by weight, particularly preferably from 20 to 50% by weight.

【0010】本発明の消化性潰瘍治療剤中のスクワラン
の含有量は、少なくなると潰瘍治癒促進効果が十分でな
くなり、多くなっても潰瘍治癒促進効果が含有量に応じ
て著しく高くなることはないので、0.1重量%を超え
99重量%未満が好ましく、5〜90重量%がより好ま
しく、10〜50重量%が特に好ましい。
When the content of squalane in the therapeutic agent for peptic ulcer of the present invention decreases, the effect of promoting ulcer healing becomes insufficient, and even if it increases, the effect of promoting ulcer healing does not increase significantly depending on the content. Therefore, it is preferably more than 0.1% by weight and less than 99% by weight, more preferably 5 to 90% by weight, and particularly preferably 10 to 50% by weight.

【0011】本発明の消化性潰瘍治療剤中のビタミンE
及びスクワランの含有量の組み合わせとしては、ビタミ
ンEの含有量が0.1重量%を超え99重量%未満、ス
クワランの含有量が0.1重量%を超え99重量%未満
が好ましく、ビタミンEの含有量が10〜95重量%、
スクワランの含有量が5〜90重量%がより好ましく、
ビタミンEの含有量が20〜50重量%、スクワランの
含有量が10〜50重量%が特に好ましい。
Vitamin E in the therapeutic agent for peptic ulcer of the present invention
And the squalane content is preferably a combination of a vitamin E content of more than 0.1% by weight and less than 99% by weight, and a squalane content of more than 0.1% by weight and less than 99% by weight. Content of 10 to 95% by weight,
The content of squalane is more preferably 5 to 90% by weight,
Particularly preferably, the content of vitamin E is 20 to 50% by weight, and the content of squalane is 10 to 50% by weight.

【0012】本発明の請求項1及び2の消化性潰瘍治療
剤には、種々の製剤用担体が含まれてもよい。担体とし
ては、剤型に応じた薬剤を調製するために、通常、使用
される充填剤、崩壊剤、増量剤、結合剤、着色剤、矯味
矯臭剤、pH調整剤、可溶化剤、懸濁化剤(例、アラビ
アゴム水溶液)、緩衝剤、安定化剤、保存剤、付質剤、
表面活性剤、滑沢剤、賦形剤などが例示される。また、
そのまま、又は適当な溶剤を選定することにより、液剤
として使用することもできる。
[0012] The therapeutic agent for peptic ulcer of claims 1 and 2 of the present invention may contain various pharmaceutical carriers. As the carrier, a filler, disintegrant, bulking agent, binder, coloring agent, flavoring agent, pH adjusting agent, solubilizing agent, suspending agent, which is usually used for preparing a drug according to the dosage form, Agents (eg, gum arabic solution), buffers, stabilizers, preservatives, qualifiers,
Examples include surfactants, lubricants, excipients, and the like. Also,
It can be used as a liquid as it is or by selecting an appropriate solvent.

【0013】本発明の消化性潰瘍治療剤の剤型として
は、上記のような液剤のほか、錠剤、丸剤、散剤、懸濁
剤、乳剤、顆粒剤、シロップ剤、トローチ剤、カプセル
剤などが挙げられる。
[0013] The dosage form of the therapeutic agent for peptic ulcer of the present invention includes tablets, pills, powders, suspensions, emulsions, granules, syrups, troches, capsules, etc., in addition to the above-mentioned liquid preparations. Is mentioned.

【0014】本発明の消化性潰瘍治療剤の投与量は、使
用目的、症状などにより適宜選択されるが、1日当たり
好ましくは500mg〜20gであり、1〜4回/日に
分けて投与することも差し支えない。
The dose of the therapeutic agent for peptic ulcer of the present invention is appropriately selected depending on the purpose of use, symptoms, etc., but is preferably 500 mg to 20 g per day, and is administered in 1 to 4 doses / day. No problem.

【0015】[0015]

【発明の実施の形態】本発明の実施例及び比較例を説明
する。 (実施例1及び比較例1)表1に示した所定量(重量
%)の酢酸トコフェロール(BASF社製)、スクワラ
ン(マルハ社製)及び5重量%アラビアゴム水溶液を均
一に混和して液剤を得た。
DESCRIPTION OF THE PREFERRED EMBODIMENTS Examples of the present invention and comparative examples will be described. Example 1 and Comparative Example 1 A predetermined amount (% by weight) of tocopherol acetate (manufactured by BASF), squalane (manufactured by Maruha), and a 5% by weight aqueous solution of gum arabic shown in Table 1 were uniformly mixed to prepare a liquid agent. Obtained.

【0016】試験例 高木らの方法(Jpn.J.Pharmacol.1
9,418〜426,1969年)に従って、ラット酢
酸潰瘍モデルを作成した。すなわち、体重200〜25
0gのSD系雄性ラットをエーテル麻酔下で開腹し、胃
漿膜下に20重量%酢酸水溶液20μlを注入した後、
腹部を縫合し、酢酸潰瘍を誘発した。潰瘍誘発の48時
間後に、上記実施例1の液剤を5ml/kg経口投与し
た。以後薬剤の投与は1日2回行い、14日間連続して
行った。コントロール群のラットには、比較例1の液剤
を同様に投与した。なお、本試験は各群20匹のラット
を用いた。
Test Example The method of Takagi et al. (Jpn. J. Pharmacol. 1)
9, 418-426, 1969) to create a rat acetate ulcer model. That is, a weight of 200 to 25
A 0 g SD male rat was laparotomized under ether anesthesia, and 20 μl of a 20% by weight acetic acid aqueous solution was injected under the gastric serosa.
The abdomen was sutured and an acetate ulcer was induced. 48 hours after ulcer induction, 5 ml / kg of the solution of Example 1 was orally administered. Thereafter, administration of the drug was performed twice a day for 14 consecutive days. To the rats of the control group, the liquid preparation of Comparative Example 1 was similarly administered. This test used 20 rats in each group.

【0017】最後の投与から24時間後に、ラットを剖
検し、胃を摘出して潰瘍の有無を調べて、潰瘍のない個
体の割合(治癒率)を算出し、潰瘍のあるものについて
は潰瘍の面積を測定した。この結果を表1に示す。
Twenty-four hours after the last administration, the rats are necropsied, the stomach is excised and the presence or absence of ulcers is examined to calculate the percentage of individuals without ulcers (healing rate). The area was measured. Table 1 shows the results.

【0018】[0018]

【表1】 [Table 1]

【0019】本発明の消化性潰瘍治療剤を投与した群で
は、コントロール群に比べて、潰瘍の治癒した個体数が
明らかに多く、また潰瘍面積も明らかに小さかった。す
なわち、本発明の消化性潰瘍治療剤は、消化性潰瘍治癒
促進作用を有する。
In the group to which the therapeutic agent for peptic ulcer of the present invention was administered, the number of ulcers healed was clearly higher and the area of the ulcer was clearly smaller than the control group. That is, the therapeutic agent for peptic ulcer of the present invention has a peptic ulcer healing promoting effect.

【0020】[0020]

【発明の効果】請求項1記載の消化性潰瘍治療剤の構成
は、上述のとおりであり、ビタミンEとスクワランが奏
効することにより、消化性潰瘍治癒促進作用を奏する。
The composition of the therapeutic agent for peptic ulcer according to claim 1 is as described above, and the effect of vitamin E and squalane exerts a peptic ulcer healing promoting effect.

【0021】請求項2記載の消化性潰瘍治療剤の構成
は、上述のとおりであり、特定範囲でビタミンE及びス
クワランが含有されているので、消化性潰瘍治癒促進作
用をより強く奏する。
[0021] The composition of the therapeutic agent for peptic ulcer according to claim 2 is as described above, and contains vitamin E and squalane in a specific range, so that the peptic ulcer healing promoting effect is further enhanced.

【0022】従って、本発明はより安全で有用性の高い
消化性潰瘍治療剤を提供する。
Accordingly, the present invention provides a safer and more useful agent for treating peptic ulcer.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 ビタミンE及びスクワランを含有するこ
とを特徴とする消化性潰瘍治療剤。
1. A therapeutic agent for peptic ulcer, comprising vitamin E and squalane.
【請求項2】 ビタミンEの含有量が0.1重量%を超
え99重量%未満、スクワランの含有量が0.1重量%
を超え99重量%未満であることを特徴とする請求項1
記載の消化性潰瘍治療剤。
2. A vitamin E content of more than 0.1% by weight and less than 99% by weight, and a squalane content of 0.1% by weight.
2. The amount is more than 99% by weight.
The therapeutic agent for peptic ulcer according to the above.
JP22261997A 1997-08-19 1997-08-19 Peptic ulcer treatment Pending JPH1160480A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22261997A JPH1160480A (en) 1997-08-19 1997-08-19 Peptic ulcer treatment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22261997A JPH1160480A (en) 1997-08-19 1997-08-19 Peptic ulcer treatment

Publications (1)

Publication Number Publication Date
JPH1160480A true JPH1160480A (en) 1999-03-02

Family

ID=16785299

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22261997A Pending JPH1160480A (en) 1997-08-19 1997-08-19 Peptic ulcer treatment

Country Status (1)

Country Link
JP (1) JPH1160480A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004269460A (en) * 2003-03-11 2004-09-30 Cci Corp Prophylactic and therapeutic agent for peptic ulcer
US7645816B2 (en) 1999-04-02 2010-01-12 National Research Council Of Canada Water-soluble compositions of bioactive lipophilic compounds
US8524696B2 (en) 1999-04-02 2013-09-03 National Research Council Of Canada Water-soluble compositions of bioactive lipophilic compounds

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7645816B2 (en) 1999-04-02 2010-01-12 National Research Council Of Canada Water-soluble compositions of bioactive lipophilic compounds
US8524696B2 (en) 1999-04-02 2013-09-03 National Research Council Of Canada Water-soluble compositions of bioactive lipophilic compounds
JP2004269460A (en) * 2003-03-11 2004-09-30 Cci Corp Prophylactic and therapeutic agent for peptic ulcer

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