JPH0116806B2 - - Google Patents

Info

Publication number
JPH0116806B2
JPH0116806B2 JP56085067A JP8506781A JPH0116806B2 JP H0116806 B2 JPH0116806 B2 JP H0116806B2 JP 56085067 A JP56085067 A JP 56085067A JP 8506781 A JP8506781 A JP 8506781A JP H0116806 B2 JPH0116806 B2 JP H0116806B2
Authority
JP
Japan
Prior art keywords
antidote
mixture
hours
pesticide
extract
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.)
Expired
Application number
JP56085067A
Other languages
Japanese (ja)
Other versions
JPS57200313A (en
Inventor
Shosei Kin
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 JP56085067A priority Critical patent/JPS57200313A/en
Publication of JPS57200313A publication Critical patent/JPS57200313A/en
Publication of JPH0116806B2 publication Critical patent/JPH0116806B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Medicines Containing Plant Substances (AREA)
  • Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は動物用薬物解毒剤の製造方法に関し、
更に詳しく言えば、生薬剤を主材とする、動物の
農薬ダイメクロンによる中毒を解毒するための薬
剤を製造する方法に関するものである。 〔従来の技術〕 近年、種々の農薬中毒事故による家畜などの動
物の被害が増加している。 そのため、生態が少なからず破壊されており、
我々の周辺に棲息している動物資源が影響を受け
ているのが実状であるにも掛かわらず、今までこ
れを予防乃至治癒するための根本的な対策が見つ
からず、そのまゝ放置されてきた。 〔発明が解決しようとする課題〕 本発明が解決しようとする課題は、このような
薬害、特に動物の農薬ダイメクロンによる中毒を
短時間に解毒できる薬剤の製造方法を提供するこ
とにある。 〔課題を解決するための手段およびその作用〕 本発明による農薬ダイメクロン中毒用解毒剤の
製造方法は、くぬぎの葉または皮の粉砕乾燥物70
重量%と、ねずの木の葉または杜松の根の粉砕乾
燥物20重量%と、みかんの皮5重量%と、くずの
木の根2.5重量%と、かんぞう(甘草)2.5重量%
とからなる混合物を水と1:3の容積比で均一に
混合し、これを40〜60℃で5〜6時間蒸湯し、そ
の結果生成した蒸湯液を減圧抽出して得られた抽
出物を、混合物と3:1の容積比でまた混合し、
これを更に110℃で0.5〜1.0時間真空沸騰し、こ
れを抽出したのち、この抽出物を110℃で5〜6
時間真空のまゝ沸騰させてから得られる抽出物に
グリセリン0.5重量%を添加して高速分散するこ
とにより行われる。 漢方医薬において、くぬぎの葉や皮は収斂剤ま
たは媒染剤などに使用され、ねずの木の葉または
杜松の根は利尿剤または鎮痙剤などに使用され、
みかんの皮はリモネンおよび配糖体のヘスペリデ
イン(hesperidion)などを含有するもので、芳
香族健胃剤、消化剤、鎮嘔鎭咳疾薬等として使
用されており、くずの木の根はダイドジン
(daidzin)およびその分解物であるダイドジエン
(daidzein)とイソフラボン(isoflavone)誘導
体であるプエラリアン(puerarian)などを含有
しているため、鎮痙作用、駆風解毒作用を有して
おり、発汗解熱薬として、熱性病風邪、鎮痛、扁
桃腺炎、結膜炎などに使用され、そして、かんぞ
うは一種のサポニンであつて甘味成分であるグリ
キルヒチン(glycyrrhizin)を主成分として、鎮
咳、疾、矯味薬、解毒薬、甘味剤などに使用さ
れている。グリセリンは一般用剤、軟化剤、灌腸
剤、座剤などのキヤリアとして使用される。本発
明において、グリセリン分子は、800〜1000r.p.
m.で高速分散される。 本発明の方法によつて製造された解毒剤を、薬
物、例えばBPM油剤、DDVP油剤などの農薬
(特にダイメクロン)に中毒した動物に経口また
は鼻腔より投与すれば呼吸によつて体内に吸収さ
れ、その中毒程度に応じて直ちにあるいは緩やか
に面腹し、残存する毒性が除去される。 この解毒の薬理学的乃至生理学的メカニズムは
今だ明確には解明されていないが、本発明の方法
による解毒剤が酸素伝達反応促進剤として強力に
作用し、体内の毒性物質を中和させる基本的な生
体反応を増進するものであろうと考えられる。 本発明の方法による解毒剤は、製薬業界におい
て通常考えられる色々な剤形で製造することも出
来るが、経口および鼻腔投与が最も効果的であ
り、それ故、液のまゝ解毒剤として利用すること
もまた可能である。1回の投与量は、中毒の程度
によつて適切に増減される。 〔実施例およびその効果〕 (a) 解毒剤の製造 十分に乾燥したくぬぎの葉KLの粉末70g、ね
ずの木の葉JLの粉末20g、みかんの皮GLの粉末
5g、くずの木の根CHの粉末2.5gおよびかんぞ
うKAの粉末2.5gを均一に混合した混合物Aに水
300mlを加え、撹拌しながら50℃で約5時間加温
して蒸湯したのち、その結果生成した蒸湯液を減
圧抽出する。 これにより得られた抽出物300mlに混合物Aと
同一組成の混合物100gを加え、110℃で0.5時間
真空沸騰させて抽出する。これにより得られた抽
出物を110℃で4時間さらに真空沸騰し、その抽
出物を継続して110℃で4時間また真空沸騰した
のち、これを冷却機で冷やし、グリセリン0.5重
量%を800〜1000r.p.m.で高速分散して混合し、
解毒剤1を製造する。 (b) 解毒剤の製造 上述した混合物Aのうち、くぬぎの葉KLの代
わりにくぬぎの皮KLの乾燥粉末70g、ねずの木
の葉JLの代わりに杜松の根JPの乾燥粉末20gと
それぞれ使用し、その他の成分に変更を加えずに
混合物Bを用意し、上記解毒剤の製造と同様に
して解毒剤2を製造する。 (c) 試験例 本発明の方法による解毒剤の効果を確認するた
めに、食用淡水魚のサンプルとして、どじようを
使用して次のような試験を行つた。 水で100倍に稀釈した農薬ダイメクロン溶液
(0.001%水溶液)を使用して体調8〜12cmのどじ
ようを中毒させたのち、)混合物Aおよび各成
分を解毒剤の製造またはの方法に準じて製造
したものをそれぞれ単独で添加した場合、)混
合物AおよびBの各成分のうちの2つ成分を解毒
剤の製造またはの方法に準じて製造したもの
をそれぞれ単独で添加した場合、)水を加えて
稀釈した場合、そして、)解毒剤1および2を
それぞれ添加した場合の解毒作用についてそれぞ
れ試験した。 この試験時における環境条件は、風速0.5〜
1m/sec.、室内温度25〜26℃であつた。 その結果、表1に示すような解毒作用を示すこ
とが判明した。
[Industrial Application Field] The present invention relates to a method for producing a drug antidote for animals,
More specifically, the present invention relates to a method for producing a drug for detoxifying animals from poisoning caused by the pesticide Dimecuron, which is based on crude drugs. [Prior Art] In recent years, damage to livestock and other animals due to various pesticide poisoning accidents has been increasing. As a result, the ecology has been destroyed to a large extent.
Despite the fact that the animal resources that live around us are being affected, no fundamental measures have been found to prevent or cure this problem, and the problem has been left as it is. It's here. [Problems to be Solved by the Invention] The problem to be solved by the present invention is to provide a method for producing a drug that can quickly detoxify such drug-induced poisoning, particularly poisoning caused by the pesticide Dimeclone in animals. [Means for Solving the Problems and Their Effects] The method for producing an antidote for poisoning with the pesticide Dimecuron according to the present invention is to produce a pulverized dried product of oak leaves or bark, 70 g.
20% by weight of crushed dried juniper leaves or juniper roots, 5% by weight of tangerine peel, 2.5% by weight of kudzu roots, and 2.5% by weight of licorice.
An extraction obtained by uniformly mixing a mixture of and water at a volume ratio of 1:3, steaming this at 40 to 60°C for 5 to 6 hours, and extracting the resulting steamed liquid under reduced pressure. are also mixed with the mixture in a volume ratio of 3:1;
This was further vacuum boiled at 110℃ for 0.5 to 1.0 hours, extracted, and the extract was boiled at 110℃ for 5 to 6 hours.
This is done by boiling under vacuum for an hour, then adding 0.5% by weight of glycerin to the resulting extract and dispersing it at high speed. In Chinese medicine, oak leaves and bark are used as astringents and mordants, and juniper leaves and juniper roots are used as diuretics and antispasmodics.
Mandarin orange peel contains limonene and the glycoside hesperidion, and is used as an aromatic stomachic, digestive agent, anti-nausea and cough medicine, etc., and the root of the kuzu tree contains daidzin and It contains daidzein, a decomposition product, and puerarian, an isoflavone derivative, which has antispasmodic and carminative detoxifying effects, and is used as a sweating and antipyretic drug for febrile diseases. It is used for colds, pain relief, tonsillitis, conjunctivitis, etc. Kanzo is a type of saponin and contains glycyrrhizin, which is a sweetening ingredient, as its main ingredient, and is used as an antitussive, for diseases, as a flavor corrective, as an antidote, and as a sweetener. etc. is used. Glycerin is used as a carrier for over-the-counter preparations, emollients, enemas, suppositories, etc. In the present invention, the glycerin molecule is 800-1000 r.p.
Dispersed at high speed by m. When the antidote produced by the method of the present invention is administered orally or nasally to an animal poisoned by a drug, such as a pesticide such as BPM oil or DDVP oil (especially Dimeclone), it will be absorbed into the body through respiration. Depending on the degree of poisoning, the poison will be killed immediately or slowly, and the remaining toxicity will be removed. The pharmacological and physiological mechanisms of this detoxification have not yet been clearly elucidated, but the basic principle is that the detoxification agent produced by the method of the present invention acts strongly as an oxygen transfer reaction promoter and neutralizes toxic substances in the body. It is thought that it promotes biological reactions. Although the antidote according to the method of the present invention can be prepared in various dosage forms commonly considered in the pharmaceutical industry, it is most effective for oral and nasal administration and is therefore used as an antidote in liquid form. It is also possible. A single dose is appropriately increased or decreased depending on the degree of intoxication. [Examples and their effects] (a) Production of antidote 70g powder of sufficiently dried sawtooth leaf KL, 20g powder of juniper leaf JL, 5g powder of mandarin peel GL, 2.5g powder of Kuzu tree root CH Add water to mixture A, which is a uniform mixture of 2.5 g of powder
After adding 300 ml and heating at 50°C for about 5 hours with stirring, the resulting steamed liquid is extracted under reduced pressure. 100 g of a mixture having the same composition as Mixture A is added to 300 ml of the resulting extract, and the mixture is boiled under vacuum at 110° C. for 0.5 hour for extraction. The extract thus obtained was further vacuum boiled at 110°C for 4 hours, and the extract was continued to be vacuum boiled at 110°C for 4 hours, cooled in a cooler, and 0.5% by weight of glycerin was added to Disperse and mix at high speed at 1000rpm,
Manufacture antidote 1. (b) Manufacture of antidote Of the mixture A mentioned above, 70 g of dry powder of sawtooth bark KL was used in place of sawtooth leaf KL, and 20 g of dry powder of juniper root JP was used in place of juniper leaf JL. Mixture B is then prepared without changing the other components, and Antidote 2 is produced in the same manner as in the production of the above-mentioned Antidote. (c) Test Example In order to confirm the effectiveness of the antidote according to the method of the present invention, the following test was conducted using locust as a sample of edible freshwater fish. After poisoning a loach with a body size of 8 to 12 cm using a pesticide dimeclone solution (0.001% aqueous solution) diluted 100 times with water, mixture A and each component are manufactured according to the method of manufacturing an antidote. (1) When two of the components of mixtures A and B are added separately, (2) When two of the components of mixtures A and B are manufactured according to the method of (1) or (2) are added separately, (2) Water is added. The detoxification effects were tested when diluted with a) antidotes 1 and 2, respectively. The environmental conditions during this test were wind speeds of 0.5~
1m/sec., and the room temperature was 25-26℃. As a result, it was found that it exhibited detoxifying effects as shown in Table 1.

【表】【table】

【表】 この結果から、本発明の混合物の構成成分を単
独乃至2種を混合して使用しても、その解毒効果
は最大60%(単独の場合)または65%(2種混合
の場合)しかなく、十分な解毒を遂行できないも
のであることが解かつた。 これに対し、本発明の方法による解毒剤1およ
び2は、共に、95%の解毒効果を発揮でき、その
解毒作用が始まるまでの時間は2秒という極めて
短い時間であり、その使用量についても、少量で
もつて分に解毒作用を発揮できることが解つた。 (d) 試験例 本発明の方法による解毒剤の哺乳動物に対する
解毒効果を確認するために、兎を使用して次のよ
うな試験を行つた。、 100倍に稀釈した農薬ダイメクロン溶液(0.001
%水溶液)25ml、体重約3.5Kgの兎に経口投与し
たところ、投与後、約5分間経過時に発作を始
め、農薬ダイメクロンの毒性が体内に十分吸収さ
れるように約20分間経過した後に、解毒剤1およ
び2をそれぞれの投与量を変更して経口投与し、
その後の解毒作用による発作の鎮静状態を肉眼観
察した。 その結果、表2に示すような解毒作用を示すこ
とが判明した。
[Table] From this result, even if the constituent components of the mixture of the present invention are used alone or in combination, the detoxification effect is up to 60% (in the case of a single component) or 65% (in the case of a mixture of the two components). However, it was found that sufficient detoxification could not be achieved. On the other hand, both antidotes 1 and 2 produced by the method of the present invention can exhibit a detoxification effect of 95%, and the time required for the detoxification action to begin is extremely short, 2 seconds. It was found that even a small amount can have a detoxifying effect. (d) Test Example In order to confirm the detoxifying effect of the antidote according to the method of the present invention on mammals, the following test was conducted using rabbits. , 100 times diluted pesticide Dimecuron solution (0.001
% aqueous solution) was orally administered to a rabbit weighing approximately 3.5 kg, the seizure began approximately 5 minutes after administration, and detoxification occurred after approximately 20 minutes to allow the toxicity of the pesticide Dimecuron to be fully absorbed into the body. Agents 1 and 2 were orally administered at different doses,
The state of sedation of the attack due to the subsequent detoxification was visually observed. As a result, it was found that it exhibited detoxifying effects as shown in Table 2.

【表】 過後に恢復した。
この結果から、解毒剤1および2の兎に対する
投与量は、約30〜35ml以上であれば十分な解毒作
用を発揮でき、好ましくは、約50〜55ml以上であ
ることが解つた。また、投与量が約60〜65ml以上
となつた場合、その解毒作用に大差がないことが
解つた。 ここにおいて、本発明による解毒剤を使用した
とき、解毒作用による兎の最初の兆候は、発作の
減衰であり、解毒作用により発作が完成に鎮静さ
れると睡眠状態に入ることが解つた。また、睡眠
状態から抜けた後の兎の状態は、農薬ダイメクロ
ン投与前と変化ないことが確認された。 本発明による解毒剤の投与量は、農薬ダイメク
ロンの吸収量や投与からの経過時間等の中毒の程
度、体重や体質等の個体差等によつて、適宜に変
更されるべきであるが、概略、農薬ダイメクロン
の吸収量の約2倍以上の量で解毒剤を投与すれば
完全に解毒することができる。 しかしながら、実際の投与に当たつて農薬ダイ
メクロンの吸収量を特定することは一般的に不可
能であり、そのような場合、30分〜1時間毎に発
作の鎮静状態に応じた量を追加して投与していく
のが効果的である。 本発明の方法による解毒剤は、製薬業界におい
て通常考えられる色々な剤形で製造することは出
来るが、経口および鼻腔投与が物も効果的であ
り、その故、抽出液をそのまゝ解毒剤として利用
することもまた可能である。
[Table] The patient recovered after some time.
From this result, it was found that the amount of antidote 1 and 2 administered to rabbits should be about 30 to 35 ml or more to exhibit sufficient detoxifying effect, and preferably about 50 to 55 ml or more. It was also found that there was no significant difference in the detoxification effect when the dose was about 60 to 65 ml or more. Here, when using the antidote according to the present invention, the rabbit's first sign of detoxification was attenuation of the seizures, and when the seizures were completely subdued by the detoxification, the rabbits entered a sleep state. It was also confirmed that the condition of the rabbits after coming out of the sleeping state was unchanged from before the administration of the pesticide Dimeclon. The dose of the antidote according to the present invention should be changed as appropriate depending on the degree of intoxication such as the amount of pesticide Dimecuron absorbed, the time elapsed from administration, and individual differences such as body weight and constitution, but approximately Complete detoxification can be achieved by administering an antidote in an amount more than twice the absorbed amount of the pesticide Dimecuron. However, it is generally impossible to determine the absorption amount of the pesticide Dimecuron during actual administration, and in such cases, the amount should be added every 30 minutes to 1 hour depending on the state of sedation of the attack. It is effective to administer the drug. Although the antidote according to the method of the present invention can be prepared in various dosage forms commonly considered in the pharmaceutical industry, oral and nasal administration are also effective, and therefore, the extract can be used directly as an antidote. It is also possible to use it as

Claims (1)

【特許請求の範囲】[Claims] 1 くぬぎの葉または皮の粉砕乾燥物70重量%、
ねずの木の葉または杜松の根の粉砕乾燥物20重量
%、みかんの皮5重量%、くずの木の根2.5重量
%およびかんぞう2.5重量%からなる混合物(A,
B)を水と1:3の容積比で均一に混合し、これ
を40〜60℃で5〜6時間蒸湯し、その結果生成し
た蒸湯液を減圧抽出して得られた抽出物を、混合
物(A,B)と3:1の容積比で混合し、これを
110℃で0.5〜1.0時間真空沸騰し、これを抽出し
たのち、この抽出物を110℃で5〜6時間真空の
まゝ沸騰させてから得られる抽出物にグリセリン
0.5重量%を添加して高速分散することを特徴と
する農薬ダイメクロン中毒用解毒剤の製造方法。
1 70% by weight of crushed dried oak leaves or bark,
A mixture (A,
Mix B) uniformly with water at a volume ratio of 1:3, steam this at 40 to 60°C for 5 to 6 hours, and extract the resulting steamed liquid under reduced pressure. , mixed with mixture (A, B) in a volume ratio of 3:1, and
After boiling under vacuum at 110°C for 0.5 to 1.0 hours and extracting it, boil the extract under vacuum at 110°C for 5 to 6 hours, and add glycerin to the extract obtained.
A method for producing an antidote for poisoning with the pesticide Dimecuron, which is characterized by adding 0.5% by weight and dispersing at high speed.
JP56085067A 1981-06-03 1981-06-03 Manufacture of drug detoxifying agent Granted JPS57200313A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56085067A JPS57200313A (en) 1981-06-03 1981-06-03 Manufacture of drug detoxifying agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56085067A JPS57200313A (en) 1981-06-03 1981-06-03 Manufacture of drug detoxifying agent

Publications (2)

Publication Number Publication Date
JPS57200313A JPS57200313A (en) 1982-12-08
JPH0116806B2 true JPH0116806B2 (en) 1989-03-27

Family

ID=13848278

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56085067A Granted JPS57200313A (en) 1981-06-03 1981-06-03 Manufacture of drug detoxifying agent

Country Status (1)

Country Link
JP (1) JPS57200313A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6090563A (en) * 1983-10-24 1985-05-21 長谷川香料株式会社 Deodorant
US4683140A (en) * 1985-08-14 1987-07-28 Kang Kwon J Process for manufacturing an herb tea from the leaves of Ginko, Persimmon and Pine

Also Published As

Publication number Publication date
JPS57200313A (en) 1982-12-08

Similar Documents

Publication Publication Date Title
Aderibigbe et al. Antihyperglycaemic effect of Mangifera indica in rat
TW550079B (en) A novel pharmaceutical composition for the control and treatment of anorectal and colonic diseases and a process for the manufacture thereof
Cushny A textbook of pharmacology and therapeutics
DE3328262A1 (en) PREPARATION OF MEDICINES FOR IMPROVING CANCER SYMPTOMS
JPH07110811B2 (en) Beef yellow heart fluid and method for producing the same
US5603935A (en) Composition for the treatment of snoring and methods of use thereof
CN101579423B (en) Medicament composition for treating beriberi and preparation method thereof
Cushny A Textbook of pharmacology and therapeutics, or, the Action of drugs in health and disease
JPH0473413B2 (en)
JPH0116806B2 (en)
Cushny A Textbook of pharmacology and therapeutics, or, the Action of drugs in health and disease
CN102698204B (en) Zhuang nationality transdermal patch for treating hyperplasia of mammary glands and preparation method of Zhuang nationality transdermal patch
US4528192A (en) Process for preparing an antitoxic composition
CN110538280A (en) antidepressant confirmed by pharmacological activity and preparation method thereof
KR810000614B1 (en) Process for preparing antidote
JPS6137731A (en) Remedy for diabetes for oral administration containing guava leaf extract as active component
RU2032419C1 (en) Hepatoprotective preparation and process for producing same
CN111840448B (en) Preparation method and application of anti-chapping compound traditional Chinese medicine liposome
Agrahari et al. Biological Evaluation (Antidabetics Activity) of Methanolic Extract of Achyranthes Aspera Leaves
CN111467423B (en) Honeysuckle flower and lotus root heat-clearing spray and preparation method thereof
CN109381596A (en) A kind of drug and its preparation method and application for preventing cold
Sehajpal et al. A Review on Gymnema sylvestre Pharmacognostical Profile and its Anti-hyperglycemic Activity.
Xu et al. Clematis chinensis extract protects against diabetic nephropathy in rats
CN111419920B (en) Medicine composition with hypoglycemic effect and preparation method and application thereof
RU2157226C2 (en) Anticoughing preparation and method of its preparing