JPH05246863A - Pesticide adsorbent - Google Patents

Pesticide adsorbent

Info

Publication number
JPH05246863A
JPH05246863A JP4827392A JP4827392A JPH05246863A JP H05246863 A JPH05246863 A JP H05246863A JP 4827392 A JP4827392 A JP 4827392A JP 4827392 A JP4827392 A JP 4827392A JP H05246863 A JPH05246863 A JP H05246863A
Authority
JP
Japan
Prior art keywords
adsorbent
pesticides
polyamino acid
pesticide
antidote
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
JP4827392A
Other languages
Japanese (ja)
Inventor
Masanao Oya
正尚 大屋
Akira Miwa
明 三輪
Yasuko Iizuka
靖子 飯塚
Makoto Iwatsuki
誠 岩月
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.)
Ajinomoto Co Inc
Original Assignee
Ajinomoto Co Inc
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 Ajinomoto Co Inc filed Critical Ajinomoto Co Inc
Priority to JP4827392A priority Critical patent/JPH05246863A/en
Publication of JPH05246863A publication Critical patent/JPH05246863A/en
Pending legal-status Critical Current

Links

Landscapes

  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Polyamides (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

PURPOSE:To provide the subject adsorbent great in adsorbing power, eliminating no pesticide adsorbed even under coexistence of other adsorbent(s), causing no vomiting even if taken, also excellent in molding processability. CONSTITUTION:The objective adsorbent or antidote for pesticides, containing, as active ingredient, a hydrophobic polyamino acid (pref. polyleucine). Use of this hydrophobic polyamino acid as antidote finds application to detoxication of a wide range of pesticides; thus being advantageous for first aid even in case the type of pesticides in question cannot be identified. Also, the hydrophobic amino acid is a material inert to the human body; therefore, having such advantages that, even after orally administered, this compound does not irritate the mucous membrane of the esophagus and stomach, resulting in being seldom vomitted. Besides, the adsorbent of the present invention is easy in molding processing, and can be used in the suction protective masks or clothing in pesticide application.

Description

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

【0001】[0001]

【産業上の利用分野】農薬の吸着剤、解毒剤に関するも
のである。
[Industrial application] The present invention relates to agricultural chemical adsorbents and antidotes.

【0002】[0002]

【従来の技術】[Prior Art]

【0003】リン酸系農薬は、1936年西ドイツの S
chrader 等によって合成されて以来、同類のものが開発
され現在に至っているが、毒性が強いことが知られてい
る。農薬として散布する際に誤って吸引したり、皮膚か
ら浸透したりして体内に吸収する例は少なくない。誤飲
等で体内に吸引した場合の、初期治療法として胃洗浄、
腸洗浄を行い同時に吸着剤を投与している。体内に吸着
された場合は透析や吸着により血液の浄化を行なうが、
現在用いられている吸着剤としては粉末の活性炭やアド
ソルビン(日本薬局方、天然ケイ酸アルミニウム)があ
るが、充分なものではない。
Phosphoric acid-based pesticides were introduced in 1936 by West Germany S.
Since it was synthesized by chrader et al., the same kind has been developed and has reached the present time, but it is known to be highly toxic. When sprayed as a pesticide, there are many cases where it is inhaled accidentally or penetrated through the skin and absorbed into the body. Gastric lavage as an initial treatment when inhaled into the body due to accidental ingestion,
Intestinal lavage is performed and adsorbent is administered at the same time. When it is adsorbed in the body, blood is purified by dialysis or adsorption,
The currently used adsorbents include powdered activated carbon and adsorbin (Japanese Pharmacopoeia, natural aluminum silicate), but they are not sufficient.

【0004】活性炭は吸着力は優れているが、脱着量も
多く(吉田直弘他、第5回 日本中毒研究会東日本支部
予稿集、8、1991)、品質にばらつきが多く、服用
の際飛散する、服用しても嘔吐する等の問題がある。パ
ラコ−トの吸着剤として開発されたケイキサレ−トは有
機リン系の農薬を吸着しない。一方、無機系のアドソル
ビンは、投与量が多くなると会合を起こし、また脱着量
も多い。また、活性炭は共存する他の薬剤、例えば血液
凝結防止剤のヘパリン、フサン、ケイキサレ−トが共存
すると一旦吸着した農薬がヘパリン、フサンにより置換
され脱着してしまう欠点があり、血液浄化系に使用され
ているが効率が悪い。また、これらは繊維に加工するこ
とが困難か、繊維となっても極めて高価であり、例えば
農薬散布時の防護用マスクや衣料として用いられない。
[0004] Activated carbon has an excellent adsorptive power, but also has a large desorption amount (Naohiro Yoshida et al., The 5th Japan Poisoning Research Society East Japan Chapter Preliminary Proceedings, 8, 1991). , There is a problem such as vomiting even when taken. Developed as a paracoat adsorbent, the keixarate does not adsorb organophosphorus pesticides. On the other hand, inorganic adsorbin is associated with a large dose and also has a large desorption amount. In addition, activated carbon has a drawback that once adsorbed pesticide is replaced by heparin or fusan and desorbed when other coexisting drugs such as heparin, fusan, and caixarate, which are blood coagulation inhibitors, coexist and are used in blood purification systems. However, it is inefficient. Further, these are difficult to process into fibers or are extremely expensive even when they become fibers, and are not used, for example, as protective masks or clothing when spraying pesticides.

【0005】[0005]

【発明が解決しようとする課題】本発明の課題は、吸着
力が大きく、他の吸着剤の共存下でも脱着せず、服用し
ても嘔吐しない、と同時に成型加工性にも優れる農薬の
吸着剤、解毒剤を提供することである。
The object of the present invention is to adsorb an agricultural chemical which has a large adsorption power, does not desorb even in the coexistence of other adsorbents, does not vomit even when taken, and is also excellent in molding processability. To provide a drug and an antidote.

【0006】[0006]

【課題を解決するための手段】発明者らは、疎水性ポリ
アミノ酸がリン酸系農薬、ジニトロアニリン系、アニリ
ン系農薬等の農薬に対し大きい吸着力を有し、かつ他の
吸着剤の共存下でも脱着しないことを見いだし本発明を
完成した。すなわち、本発明は、ポリアミノ酸を有効成
分とする農薬の吸着剤、解毒剤に関するものである。
[Means for Solving the Problems] The inventors have found that a hydrophobic polyamino acid has a large adsorptive power for pesticides such as phosphate-based pesticides, dinitroaniline-based pesticides, aniline-based pesticides, and the coexistence of other adsorbents. The present invention has been completed by discovering that they cannot be detached even underneath. That is, the present invention relates to a pesticide adsorbent and antidote containing polyamino acid as an active ingredient.

【0007】本発明にいう農薬とはリン酸系農薬、アニ
リン系除草剤等をいう。リン酸系農薬とは、4−ニトロ
−m−トリルジメチルチオエ−ト(フェニトロチオン、
商品名スミチオン)、カルホス(商品名)等があり、ア
ニリン系除草剤としては、クサノン(商品名)、ジニト
ロアニリン系除草剤としてトレファノサイト(商品名)
等がある。
The pesticides referred to in the present invention are phosphoric acid type pesticides, aniline type herbicides and the like. Phosphoric acid-based pesticides include 4-nitro-m-tolyldimethylthioate (fenitrothion,
Trade name: Sumithion), Carphos (trade name), etc., Aniline herbicide is xanone (trade name), dinitroaniline herbicide is trefanosite (trade name)
Etc.

【0008】本発明にいう疎水性ポリアミノ酸とは、ア
ミノ酸であるアラニン、ロイシン、イソロイシン、フェ
ニルアラニン、バリンの重合体をいう。アミノ酸はL
体、D体、ラセミ体のいずれを用いてもよい。
The term "hydrophobic polyamino acid" as used in the present invention means a polymer of amino acids alanine, leucine, isoleucine, phenylalanine and valine. Amino acid is L
Any of the body, the D body, and the racemic body may be used.

【0009】本発明の疎水性ポリアミノ酸は、単独重合
体、または他のアミノ酸との共重合体でも良く、他のア
ミノ酸としてはグルタミン酸エステル、アスパラギン酸
エステル、メチオニン、カルボベンゾキシリジン等ほと
んどのアミノ酸が用いられ、他のアミノ酸はL体、D
体、ラセミ体のいずれを用いてもよい。他のアミノ酸の
含有量は全体の70モル%以下が好ましい。
The hydrophobic polyamino acid of the present invention may be a homopolymer or a copolymer with other amino acids. As other amino acids, most amino acids such as glutamic acid ester, aspartic acid ester, methionine and carbobenzoxylidine are included. Is used, other amino acids are L-form, D-form
Either the body or the racemate may be used. The content of other amino acids is preferably 70 mol% or less of the total.

【0010】疎水性ポリアミノ酸の製造法は、一般的な
アミノ酸重合体の製造法が用いられ、例えば、N−カル
ボキシアミノ酸無水物法、アミノ酸塩化物法、アミノ酸
活性エステル化法が用いられる。日本化学会編、大屋正
尚ら、「新実験化学講座」−ポリペプチド−244頁
(丸善) 遠藤剛編、「アミノ酸ポリマ−」−ポリアミノ酸の合成
−36頁(シ−エムシ−)
As the method for producing the hydrophobic polyamino acid, a general method for producing an amino acid polymer is used, and for example, the N-carboxyamino acid anhydride method, the amino acid chloride method and the amino acid active esterification method are used. Edited by The Chemical Society of Japan, Masahisa Ohya et al., "New Experimental Chemistry Lecture" -Polypeptide-244 (Maruzen) Takeshi Endo, "Amino Acid Polymer" -Synthesis of Polyamino Acids-Page 36 (Chemiec)

【0011】本発明に用いられる疎水性ポリアミノ酸の
分子量は、1000〜500、000であり、通常1
0、000以上が好ましい。
The molecular weight of the hydrophobic polyamino acid used in the present invention is 1,000 to 500,000, and usually 1
It is preferably at least 2,000.

【0012】本発明の吸着剤に用いられる疎水性ポリア
ミノ酸の形状は粉末、繊維、フィルム等使用形態に合わ
せ適宜選択される。成型加工方法は常法により行われ
る。
The shape of the hydrophobic polyamino acid used in the adsorbent of the present invention is appropriately selected according to the usage form such as powder, fiber and film. The molding and processing method is performed by a conventional method.

【0013】本発明の吸着剤を、人に経口で投与するこ
とにより、農薬の解毒剤として用いることができる。投
与は通常粉末で行われ、好ましい粉末の粒径は0.01
mmから0.1mmであり、好ましい投与量は0.5〜
5g程度であるがこれらに限定されるものではない。本
発明の疎水性ポリアミノ酸を解毒剤として用いる場合、
他の薬剤、例えばアドソルビンを併用しても何等差し支
えなく、むしろ効果的である。つまり、本発明の疎水性
ポリアミノ酸を解毒剤として用いることにより、広範囲
の農薬の解毒に適用できるめ、農薬中毒患者のように農
薬の種類を特定できない救急処置に有利である。疎水性
ポリアミノ酸は生体にたいして不活性な材料であり(ポ
リロイシンは創傷被覆材として実用化されている)、経
口投与した場合にも食道や胃の粘膜を刺激することがな
く嘔吐されがたい長所がある。
By orally administering the adsorbent of the present invention to humans, it can be used as an antidote for agricultural chemicals. Administration is usually by powder, with a preferred powder particle size of 0.01
mm to 0.1 mm, with a preferred dose of 0.5-
It is about 5 g, but is not limited to these. When using the hydrophobic polyamino acid of the present invention as an antidote,
Other drugs, such as adsorbin, can be used together without any problem, and are rather effective. That is, by using the hydrophobic polyamino acid of the present invention as an antidote, it can be applied to the detoxification of a wide range of pesticides, which is advantageous for emergency treatment such as pesticide poisoning patients in which the type of pesticide cannot be specified. Hydrophobic polyamino acid is a material that is inactive to the living body (polyleucine has been put into practical use as a wound dressing material), and it has the advantage that even if it is taken orally, it will not vomit without irritating the esophagus or stomach mucosa. There is.

【0014】本発明の疎水性ポリアミノ酸を有効成分と
する吸着剤は、農薬散布時等の吸引防護用のマスクや、
衣料にも用いることができ、粉末状で用いても良く、必
要により繊維状やフィルム状に成型加工して用いてもよ
い。土壌中の農薬流出防止用シ−トやフェンス等にも使
用可能である。用途に応じて他の吸着剤や、添加物、高
分子化合物等を混合して用いてもよい。例えば、活性炭
やエチルセルロ−ス系の繊維素誘導体、ナイロン等の合
成高分子化合物、活性アルミナ系の無機吸着剤が例とし
て挙げられる。
The adsorbent containing the hydrophobic polyamino acid of the present invention as an active ingredient is a mask for suction protection when spraying agricultural chemicals,
It can also be used for clothing, and may be used in the form of powder, and if necessary, it may be used after being molded into a fiber or film. It can also be used as a sheet or fence for preventing pesticide runoff in soil. Other adsorbents, additives, polymer compounds and the like may be mixed and used depending on the application. Examples include activated carbon, ethylcellulose-based fibrin derivatives, synthetic polymer compounds such as nylon, and activated alumina-based inorganic adsorbents.

【0015】[0015]

【実施例】【Example】

実施例1 疎水性ポリアミノ酸の合成 ポリロイシン、ポリフェニルアラニンはいずれも、N−
カルボキシ酸無水物法により合成した。日本化学会編、
大屋正尚ら、「新実験化学講座」−ポリペプチド−24
4頁(丸善) 遠藤剛編、「アミノ酸ポリマ−」−ポリアミノ酸の合成
−36頁(シ−エムシ−)
Example 1 Synthesis of hydrophobic polyamino acid Both polyleucine and polyphenylalanine were N-
It was synthesized by the carboxylic acid anhydride method. Edited by The Chemical Society of Japan,
Masahisa Ohya et al., "New Experimental Chemistry Course" -Polypeptide-24
Page 4 (Maruzen), edited by Takeshi Endo, "Amino Acid Polymers" -Synthesis of Polyamino Acids-Page 36 (CMS)

【0016】実施例2 農薬の吸、脱着実験 1.試料 フェニトロチオン標準品(純度98%)は和光純薬株式
会社、スミチオンは八州化学株式会社の製品を、トレフ
ァノサイトはシオノギ製薬の製品を、カルフォスは三共
(株)の製品を、クサノンは武田薬品工業(株)の製品
を、アドソルビン、95%エチルアルコ−ルは日本薬局
方のものを、他の試薬はいずれも試薬特級を用いた。ヘ
パリン、フサン、ケイキサレ−トは市販品をそれぞれ用
いた。人工胃液、人工腸液は日本薬局法崩壊試験法第一
液、第二液を調製使用した。
Example 2 Absorption and desorption experiments of pesticides 1. Sample Fenitrothion standard product (purity 98%) is a product of Wako Pure Chemical Industries, Sumithion is a product of Yashu Chemical Co., Ltd. Trefanosite is a product of Shionogi Pharmaceutical, Calfos is a product of Sankyo Co., Ltd., and Xanon is Takeda. The products of Yakuhin Kogyo Co., Ltd., Adsorbin and 95% ethyl alcohol were those of the Japanese Pharmacopoeia, and all other reagents were of special grade. Commercially available heparin, fusan and keixarate were used. As the artificial gastric juice and the artificial intestinal fluid, the Japanese Pharmacopoeia disintegration test method first liquid and second liquid were prepared and used.

【0017】2.吸着率の測定 薬剤標準品を人工胃液または生理食塩水に溶解し、それ
ぞれの紫外吸収帯の吸光度により検量線を作製した。そ
れを基準として薬剤を95%エチルアルコ−ル、人工胃
液、人工腸液,生理食塩水等の溶液で希釈し0.5〜1
mmol/10mlに調製し標準液とした。この標準液
10mlに吸着剤をそれぞれ1g、50mg、10mg
加え37℃で振とうさせ一定時間後上清を濾過して吸着
剤を除去し吸光度を測定、吸着率を求めた。
2. Measurement of Adsorption Rate A drug standard was dissolved in artificial gastric juice or physiological saline, and a calibration curve was prepared from the absorbance of each ultraviolet absorption band. Based on this, the drug is diluted with a solution of 95% ethyl alcohol, artificial gastric juice, artificial intestinal fluid, physiological saline, etc. to 0.5-1.
It was adjusted to mmol / 10 ml and used as a standard solution. 1 g, 50 mg, and 10 mg of the adsorbent were added to 10 ml of this standard solution, respectively.
The mixture was shaken at 37 ° C., and after a certain period of time, the supernatant was filtered to remove the adsorbent and the absorbance was measured to determine the adsorption rate.

【0018】3.脱離率の測定 ポリロイシン、ポリフェニルアラニン、アドソルビン、
活性炭約120mgを10mmol/10ml中で飽和
吸着させ、乾燥後100mgを正確に計りとり、人工胃
液または95%エタノ−ル溶液または生理食塩水とうの
溶媒10mlを加え37℃で60分振とう後、吸着剤を
濾別し、濾液の吸光度を測定して脱離量とした。
3. Measurement of desorption rate Polyleucine, polyphenylalanine, adsorbin,
About 120 mg of activated carbon was saturated and adsorbed in 10 mmol / 10 ml, 100 mg was accurately weighed after drying, 10 ml of artificial gastric juice or 95% ethanol solution or physiological saline solution was added, and the mixture was shaken at 37 ° C. for 60 minutes, The adsorbent was filtered off, and the absorbance of the filtrate was measured as the desorption amount.

【0019】[0019]

【表1】 [Table 1]

【0020】[0020]

【表2】 [Table 2]

【0021】[0021]

【発明の効果】本発明の疎水性ポリアミノ酸を有効成分
とする農薬の吸着剤は、アドソルビンと同等の吸着力を
持ち、かつ、他の吸着剤の共存下でも脱着しない優れた
性能を有するものである。
The adsorbent for agricultural chemicals containing the hydrophobic polyamino acid of the present invention as an active ingredient has an adsorbing power equivalent to that of adsorbin, and has excellent performance not desorbing even in the presence of other adsorbents. Is.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】疎水性ポリアミノ酸を有効成分とする農薬
の吸着剤。
1. A pesticide adsorbent containing a hydrophobic polyamino acid as an active ingredient.
【請求項2】疎水性ポリアミノ酸がポリロイシンである
請求項1記載の吸着剤。
2. The adsorbent according to claim 1, wherein the hydrophobic polyamino acid is polyleucine.
【請求項3】疎水性ポリアミノ酸を有効成分とする農薬
の解毒剤。
3. A pesticide antidote containing a hydrophobic polyamino acid as an active ingredient.
【請求項4】疎水性ポリアミノ酸がポリロイシンである
請求項3記載の解毒剤。
4. The antidote according to claim 3, wherein the hydrophobic polyamino acid is polyleucine.
JP4827392A 1992-03-05 1992-03-05 Pesticide adsorbent Pending JPH05246863A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4827392A JPH05246863A (en) 1992-03-05 1992-03-05 Pesticide adsorbent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4827392A JPH05246863A (en) 1992-03-05 1992-03-05 Pesticide adsorbent

Publications (1)

Publication Number Publication Date
JPH05246863A true JPH05246863A (en) 1993-09-24

Family

ID=12798839

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4827392A Pending JPH05246863A (en) 1992-03-05 1992-03-05 Pesticide adsorbent

Country Status (1)

Country Link
JP (1) JPH05246863A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5635447A (en) * 1996-03-22 1997-06-03 Donlar Corporation Polyorganic acids and their analogues to enhance herbicide effectiveness
US5646133A (en) * 1996-03-14 1997-07-08 Donlar Corporation Polyaspartic acid and its analogues in combination with insecticides

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5646133A (en) * 1996-03-14 1997-07-08 Donlar Corporation Polyaspartic acid and its analogues in combination with insecticides
US5709890A (en) * 1996-03-14 1998-01-20 Donlar Corporation Polyaspartic acid and its analogues in combination with insecticides
US5635447A (en) * 1996-03-22 1997-06-03 Donlar Corporation Polyorganic acids and their analogues to enhance herbicide effectiveness

Similar Documents

Publication Publication Date Title
US5519020A (en) Polymeric wound healing accelerators
RU2219906C2 (en) New aqueous ready medicinal forms for preparing propellant-free aerosols
TW580392B (en) Process for preparing synthetic soil-extract materials and medicaments based thereon
RU2005116680A (en) AN ADSORBENT FOR ORAL ADMINISTRATION AND MEANS FOR TREATING OR PREVENTING A KIDNEY OR LIVER DISEASE
CA1232839A (en) Ddavp antidiuretic and method therefor
FR2651677B1 (en) PHARMACEUTICAL COMPOSITION BASED ON SALMETEROL AND FLUTICASONE PROPIONATE.
PT1079806E (en) PREPARATIONS FOR THE APPLICATION OF ANTI-INFLAMMATORY, ESPECIALLY, ANTI-SEPTIC AGENTS AND / OR WOUND HEALING PROMOTION AGENTS, IN THE SUPERIOR AND / OR HEARING RESPIRATORY TRACT
EP0922461A1 (en) Remedies for hyperphosphatemia
JPS5978116A (en) Pharmaceutical preparation of sucralfate
WO1993003708A1 (en) Pharmaceutical aerosol preparation and its use for treatment and prophylaxis of viral diseases
ATE25690T1 (en) PLASMA PROTEIN SOLUTION WITH ACTIVE COAGAGATION, PROCESS FOR ITS PREPARATION AND ITS USE IN THE TREATMENT OF DISORDERS OF THE HEMOSTASIS SYSTEM.
JP2600653B2 (en) Oral preparation
RU2005116683A (en) ADSORBENT FOR ORAL ADMINISTRATION
WO2003059326A1 (en) Pharmaceutical composition having thrombolytic, anti-inflammatory and cytoprotective properties
JPH05246863A (en) Pesticide adsorbent
CA1181006A (en) Therapeutic agent for treating respiratory diseases
CA1182049A (en) Apap antacid composition
Kazantzis Chronic mercury poisoning—clinical aspects
ATE104146T1 (en) DELAYED-RELEASE PREPARATION OF A HYDROCHLORIDE OF A BASIC DRUG.
RU2240784C1 (en) Arbidol-base medicinal agent
CN101756949A (en) Composition of ambroxol hydrochloride and cysteine and preparation method thereof
AU722095B2 (en) N-(4-acetyl-1-piperazinyl)-4-fluorobenzamide hydrate
RU2192248C2 (en) Preparation "antiagrippin"
RU2203062C2 (en) Broncholithic preparation and method for its obtaining
DE60202299D1 (en) PHARMACEUTICAL COMPOSITION CONTAINING SALMETEROL AND BUDESONIDE FOR THE TREATMENT OF RESPIRATORY DISEASES