JPH0569092B2 - - Google Patents
Info
- Publication number
- JPH0569092B2 JPH0569092B2 JP28304785A JP28304785A JPH0569092B2 JP H0569092 B2 JPH0569092 B2 JP H0569092B2 JP 28304785 A JP28304785 A JP 28304785A JP 28304785 A JP28304785 A JP 28304785A JP H0569092 B2 JPH0569092 B2 JP H0569092B2
- Authority
- JP
- Japan
- Prior art keywords
- rotavirus
- sodium polyacrylate
- present
- mammals
- 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.)
- Expired - Lifetime
Links
- 230000002953 anti-rotaviral effect Effects 0.000 claims description 10
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 claims description 9
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 241000124008 Mammalia Species 0.000 claims description 6
- 241000702670 Rotavirus Species 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 229920002261 Corn starch Polymers 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- 241000700605 Viruses Species 0.000 description 3
- 239000008120 corn starch Substances 0.000 description 3
- 229940099112 cornstarch Drugs 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 241000283690 Bos taurus Species 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 2
- 241001494479 Pecora Species 0.000 description 2
- 241000282887 Suidae Species 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 239000008101 lactose Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 239000006188 syrup Substances 0.000 description 2
- 235000020357 syrup Nutrition 0.000 description 2
- 206010004016 Bacterial diarrhoea Diseases 0.000 description 1
- 241000282693 Cercopithecidae Species 0.000 description 1
- 208000005156 Dehydration Diseases 0.000 description 1
- 206010012735 Diarrhoea Diseases 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 241000617996 Human rotavirus Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 235000019764 Soybean Meal Nutrition 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229960003563 calcium carbonate Drugs 0.000 description 1
- MKJXYGKVIBWPFZ-UHFFFAOYSA-L calcium lactate Chemical compound [Ca+2].CC(O)C([O-])=O.CC(O)C([O-])=O MKJXYGKVIBWPFZ-UHFFFAOYSA-L 0.000 description 1
- 239000001527 calcium lactate Substances 0.000 description 1
- 229960002401 calcium lactate Drugs 0.000 description 1
- 235000011086 calcium lactate Nutrition 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 210000004748 cultured cell Anatomy 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000001605 fetal effect Effects 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 210000004347 intestinal mucosa Anatomy 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 229960001375 lactose Drugs 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000004455 soybean meal Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 238000002636 symptomatic treatment Methods 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 229960005486 vaccine Drugs 0.000 description 1
- 230000005727 virus proliferation Effects 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
〔産業上の利用分野〕
本発明はポリアクリル酸ナトリウムを含有する
哺乳動物用抗ロタウイルス剤に関する。
〔従来の技術〕
ロタウイルスは人間の乳幼児や牛、豚、羊等の
家畜の幼動物の腸管上皮で増殖し、しばしば重篤
な非細菌性下痢を引き起こすものでその治療及び
予防法としてワクチンによる方法やロタウイルス
を免疫した採乳用動物からの乳成分を投与する方
法(特開昭58−154513号)などが知られている。
〔発明が解決しようとする問題点〕
しかし、これらの治療及び予防法は未だ実用化
されておらず、対策としては、下痢による脱水症
状の対症療法として経口的又は非経口的な輸液を
実施する他の手段は無く、根本的な治療法が確立
されていない。
〔問題点を解決するための手段〕
そこで本発明者らは哺乳動物用抗ロタウイルス
剤について種々研究した結果、ポリアクリル酸ナ
トリウムが抗ロタウイルス作用を有することを見
い出した。
本発明は上記知見に基づき完成されたものであ
る。
本発明で使用されるポリアクリル酸ナトリウム
は平均分子量1万以上好ましくは10万〜1000万の
ものがよい。
本発明の抗ロタウイルス剤を投与する対象とし
ては、人及び牛、豚、羊などの家畜があげられ
る。その投与量は、体重1Kg当り0.02〜0.2gが
好ましく、経口的に投与するのが良い。
投与期間は通常ロタウイルス疾患の罹患期間で
あるが、その予防をかねてロタウイルス疾患に罹
患しやすい期間、例えば乳児期又は幼令期間を通
じて投与してもよい。
本発明の哺乳動物用抗ロタウイルス剤はポリア
クリル酸ナトリウムをそのままあるいは製剤中に
ポリアクリル酸ナトリウムが1%以上、好ましく
は10%以上となるように生理的に無害な固体又は
液体担体と混合して製造した製剤で、例えば錠
剤、カプセル剤、顆粒剤、散剤、シロツプ剤など
の固体状製剤又は液体状製剤の形で、そのまま投
与しても良く、又水、牛乳、人工乳などの食物又
は飼料に添加して投与しても良い。ここで用いら
れる固体担体としては、例えば乳糖、コーンスタ
ーチ、炭酸カルシウム、乳酸カルシウム、セルロ
ース、脱脂米ヌカ、大豆粕、フスマ、とうもろこ
し粉、とうもろこしでんぷん等があげられ、液体
担体としては例えば水、生理食塩水、シロツプ等
があげられる。この他必要に応じて乳化剤、分散
剤、懸濁剤、湿潤剤、安定剤、甘味剤等の補助剤
又は添加剤を使用しても良い。
なお、本発明の恒温動物用抗ロタウイルス剤に
他の薬剤を添加することは何ら差支えない。
実施例 1
散剤の製造例を以下の通り説明する。
ポリアクリル酸ナトリウム1重量部に、とうも
ろこしでんぷん4重量部をV型混合器に入れ充分
撹拌混合して粉末状の散剤を得た。
実施例 2
ポリアクリル散ナトリウム1重量部と乳糖7重
量部を均一に混合し、水を加えて練合混和し次い
で押し出し造粒機で造粒し顆粒剤を得た。
〔効果〕
以下本発明の哺乳動物用抗ロタウイルス剤が優
れた効果を有するものであることを実験例により
説明する。
実験例
(1) 実験方法
ロタウイルスに対する抗ロタウイルス作用を
培養細胞系を用いて検討した。
使用したウイルスはヒトのロタウイルス
(MO株)でこのウイルスをサル胎児腎由来の
MA104細胞にm.o.i0.5で感染後、ポリアクリル
酸ナトリウム添加無血清MEM培地で5時間ご
とに培地を交換しながら20時間培養した。
次いで培地中に放出されたウイルスの量をフ
ルオレセンスフオーカスアツセイ
(fluorescencefocus assay)法を用いて調べ
た。
(2) 実験結果
結果を表1に示す。
[Industrial Application Field] The present invention relates to an anti-rotavirus agent for mammals containing sodium polyacrylate. [Prior Art] Rotavirus proliferates in the intestinal epithelium of human infants and young domestic animals such as cows, pigs, and sheep, and often causes severe non-bacterial diarrhea.Vaccines are used as a treatment and prevention method for this. A method of administering milk components from a dairy animal immunized with rotavirus (Japanese Unexamined Patent Publication No. 154513/1983) is known. [Problems to be solved by the invention] However, these treatment and prevention methods have not yet been put into practical use, and as a countermeasure, oral or parenteral infusions are implemented as symptomatic treatment for dehydration symptoms caused by diarrhea. There are no other options, and no fundamental treatment has been established. [Means for Solving the Problems] The present inventors conducted various studies on anti-rotavirus agents for mammals and found that sodium polyacrylate has an anti-rotavirus effect. The present invention has been completed based on the above findings. The sodium polyacrylate used in the present invention preferably has an average molecular weight of 10,000 or more, preferably 100,000 to 10,000,000. Subjects to which the anti-rotavirus agent of the present invention is administered include humans and livestock such as cows, pigs, and sheep. The dosage is preferably 0.02 to 0.2 g per 1 kg of body weight, and preferably administered orally. The administration period is usually the period of rotavirus disease, but it may also be administered throughout the period when rotavirus disease is likely to occur, for example, during infancy or early childhood. The anti-rotavirus agent for mammals of the present invention contains sodium polyacrylate as it is or mixed with a physiologically harmless solid or liquid carrier such that the sodium polyacrylate content is 1% or more, preferably 10% or more in the preparation. These preparations can be administered as they are in the form of solid preparations such as tablets, capsules, granules, powders, and syrups, or in the form of liquid preparations. Alternatively, it may be administered by adding it to feed. Examples of solid carriers used here include lactose, cornstarch, calcium carbonate, calcium lactate, cellulose, defatted rice bran, soybean meal, bran, corn flour, and corn starch, and examples of liquid carriers include water and physiological saline. Examples include water and syrup. In addition, auxiliary agents or additives such as emulsifiers, dispersants, suspending agents, wetting agents, stabilizers, and sweeteners may be used as necessary. Note that there is no problem in adding other drugs to the anti-rotavirus agent for homeothermic animals of the present invention. Example 1 An example of manufacturing a powder will be explained as follows. 1 part by weight of sodium polyacrylate and 4 parts by weight of corn starch were placed in a V-type mixer and mixed with sufficient stirring to obtain a powder. Example 2 1 part by weight of sodium polyacrylic powder and 7 parts by weight of lactose were uniformly mixed, water was added and the mixture was kneaded and then granulated using an extrusion granulator to obtain granules. [Effect] The excellent effects of the anti-rotavirus agent for mammals of the present invention will be explained below using experimental examples. Experimental example (1) Experimental method The anti-rotavirus effect against rotavirus was investigated using a cultured cell system. The virus used was human rotavirus (MO strain), and this virus was derived from monkey fetal kidney.
After infecting MA104 cells at an moi of 0.5, they were cultured in serum-free MEM medium supplemented with sodium polyacrylate for 20 hours while changing the medium every 5 hours. The amount of virus released into the medium was then determined using a fluorescence focus assay method. (2) Experimental results The results are shown in Table 1.
【表】
この表からポリアクリル酸ナトリウムは
200ppm以上の濃度でウイルスの増殖を顕著に抑
制することがわかる。
従つて、本発明の製剤は哺乳動物用の抗ロタウ
イルス剤として期待される。[Table] From this table, sodium polyacrylate is
It can be seen that virus proliferation is significantly inhibited at concentrations of 200 ppm or higher. Therefore, the preparation of the present invention is expected to be used as an anti-rotavirus agent for mammals.
Claims (1)
物用抗ロタウイルス剤。1. Anti-rotavirus agent for mammals containing sodium polyacrylate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP28304785A JPS62145021A (en) | 1985-12-18 | 1985-12-18 | Anti-rotavirus agent for mammal |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP28304785A JPS62145021A (en) | 1985-12-18 | 1985-12-18 | Anti-rotavirus agent for mammal |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62145021A JPS62145021A (en) | 1987-06-29 |
| JPH0569092B2 true JPH0569092B2 (en) | 1993-09-30 |
Family
ID=17660523
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP28304785A Granted JPS62145021A (en) | 1985-12-18 | 1985-12-18 | Anti-rotavirus agent for mammal |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62145021A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7765249B2 (en) * | 2021-11-01 | 2025-11-06 | 積水化学工業株式会社 | Virus infection inhibitors and virus infection inhibitor products |
| JP2023142828A (en) * | 2022-03-25 | 2023-10-05 | 積水化学工業株式会社 | Virus infection inhibitors, virus infection prevention particles and virus infection prevention paints |
-
1985
- 1985-12-18 JP JP28304785A patent/JPS62145021A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62145021A (en) | 1987-06-29 |
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