JPS6127906A - Sintered article having antimicrobial action - Google Patents

Sintered article having antimicrobial action

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Publication number
JPS6127906A
JPS6127906A JP59147358A JP14735884A JPS6127906A JP S6127906 A JPS6127906 A JP S6127906A JP 59147358 A JP59147358 A JP 59147358A JP 14735884 A JP14735884 A JP 14735884A JP S6127906 A JPS6127906 A JP S6127906A
Authority
JP
Japan
Prior art keywords
sintered article
heavy metal
sintered body
group
fine powder
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.)
Granted
Application number
JP59147358A
Other languages
Japanese (ja)
Other versions
JPH0475884B2 (en
Inventor
Akira Tsuzuki
章 都築
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.)
Menicon Co Ltd
Original Assignee
Toyo Contact Lens 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 Toyo Contact Lens Co Ltd filed Critical Toyo Contact Lens Co Ltd
Priority to JP59147358A priority Critical patent/JPS6127906A/en
Publication of JPS6127906A publication Critical patent/JPS6127906A/en
Publication of JPH0475884B2 publication Critical patent/JPH0475884B2/ja
Granted legal-status Critical Current

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  • Compositions Of Oxide Ceramics (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:A sintered article containing heavy metal elements mentioned below, having an antimicrobial action with an improved stability of antibacterial action against heat, light, etc., obtained by sintering heavy metal elements having antibacterial action selected from silver, copper and zinc. CONSTITUTION:A sintered article obtained by sintering (a) about 5-80wt%, preferably about 10-40wt%, fine powder of a compound containing a heavy metal element selected from silver, copper and zinc using both (b) about 20- 95wt%, preferably about 50-90wt%, fine powder of inorganic substances usable as the sintered article and (c) about 0-20wt%, preferably about 0-10wt%, fine powder of inorganic glasses or alkali metal compounds used to make the sintering easy, to obtain the sintered article having the antimicrobial action containing the above-mentioned heavy metal components. Said sintered article has superior heat resistance and light resistance, is durable in strength and exhibits a long-period stable antimicrobial action.

Description

【発明の詳細な説明】 〔発明の技術分野〕 本発明は抗菌作用を冑する焼結体に関するものである。[Detailed description of the invention] [Technical field of invention] The present invention relates to a sintered body that has antibacterial properties.

〔従来技W−およびその問題点〕[Conventional technology W- and its problems]

従来より、重金属を用いて抗菌効果を発揮さ曽ようとす
る試みは存在している。
Conventionally, there have been attempts to exert antibacterial effects using heavy metals.

たとえば、米国特許1g 8691Sj19号公報に開
示されたごとく、金属銀で満たされた陽イオン交換渭脂
を波体上接触させ、その液体内に次出される銀イオンを
用iて抗菌効果を発揮さ曽ることを特徴としたヒドロゲ
ル体の保存装置とか、特開@8?−96608号公報に
開示されたCとく、コンタクトレンズの保管のための装
置において、抗菌作用を有する重金属(銀、アンチモン
)をコンタクトレンズの保管用溶液と接触さぜ、その中
に保管されたコンタクトレンズに抗菌作用を与える装置
などがある。
For example, as disclosed in U.S. Pat. Is there a storage device for hydrogel bodies that is characterized by immersion? Part C disclosed in Publication No. 96608 is a contact lens storage device in which heavy metals (silver, antimony) having an antibacterial effect are brought into contact with a contact lens storage solution, and the contact lenses stored therein are brought into contact with a contact lens storage solution. There are devices that provide antibacterial effects to lenses.

前者は、重金属である金属銀を、多孔質のピード状や膜
シート状の陽イオン交換覆脂体の内部に含有する形で使
用しており、後者は、装置の一部に重金属を保存する場
所を設け、そこに重金属を入れたり、装置の内部のコン
タクトレンズ保存場所表面を重金属で被覆したりして使
用している。
The former uses metallic silver, which is a heavy metal, contained inside a cation-exchange coating in the form of porous peas or membrane sheets, and the latter stores the heavy metal in a part of the device. A space is set up and heavy metals are placed there, or the surface of the contact lens storage area inside the device is coated with heavy metals.

これらの従来技術において、重金属イオンが抗菌作用を
発揮することは可能であるが、後述するとおり、たとえ
ば銀化合物は熱、光などに対して不安定なものであり、
こうした抗菌システムを利用した場合、安定した抗菌作
用を持続させることに問題点が残っていた。
In these conventional techniques, it is possible for heavy metal ions to exert antibacterial effects, but as will be explained later, for example, silver compounds are unstable to heat, light, etc.
When such antibacterial systems are used, problems remain in maintaining stable antibacterial effects.

そこで本発明者は、前記従来技術に開示されている重金
属化合物イオンの抗菌作用を利用して、その作用をより
安定的に持続できるシステムを開発すべく、銚意研究を
続けた結果、本発明を完成した。
Therefore, the present inventor continued intensive research in order to utilize the antibacterial effect of heavy metal compound ions disclosed in the prior art and to develop a system that can sustain the effect more stably, and as a result, the present invention was developed. completed.

〔発明の8威〕 すなわち本発明は、銀、飼および亜鉛よりなる群から選
ばれた重金属元素を含有する抗菌作用を有する焼結体に
関するものである。
[Eighth Advantages of the Invention] That is, the present invention relates to a sintered body having an antibacterial effect and containing a heavy metal element selected from the group consisting of silver, silver, and zinc.

す)ユとにして 本発明の焼結体は焼結       、とくにイ仁り(
2 熱、光などに対して安定勢たものであり、FL菌作用を
持続的に与えうるものである。
The sintered body of the present invention is suitable for sintering, especially for
2. It is stable against heat, light, etc., and can provide continuous FL bacterial action.

次に、本発明の焼結体を製造するための方法を説明する
Next, a method for manufacturing the sintered body of the present invention will be explained.

本発明の焼結体の製造原料は以下に示す1群、1群、1
群よりなる。
The raw materials for producing the sintered body of the present invention are as follows:
Consists of groups.

1群:焼結体として使用可能な58iI物の微粉末Xm
:銀、鋸および亜鉛から選ばれた重金属元素を含有する
化合物の微粉オ ■群二焼結を容易にするための無機ガラスまたはアルカ
リ金属化合物の微粉末 1群に属する化合物としては、たとえば、カオリン、シ
リカ、アルミナ、ジルコニアなどの各種酸化物なとがあ
蚤ブられる。
Group 1: 58iI fine powder Xm that can be used as a sintered body
: Fine powder of a compound containing a heavy metal element selected from silver, sawdust and zinc.Group 2.Fine powder of an inorganic glass or alkali metal compound for facilitating sintering.For example, kaolin. Various oxides such as silica, alumina, and zirconia are used.

1群に属する化合物としては、各重金属の酸化物、塩化
物、炭酸塩、硝酸塩、硫酸塩などがあげられる。
Examples of compounds belonging to the first group include oxides, chlorides, carbonates, nitrates, and sulfates of various heavy metals.

■群に属する化合物としては、水溶性化合物として、ナ
トリウム、カリウムなどのアルカリ金属のケイ酸塩、炭
酸塩、塩化物、硝酸塩、硫酸塩、水酸化物などの各種化
合物があげられ、非水溶性化合物として、パイレックス
ガラスをはじめとする無機ガラスがあげられる。
Compounds belonging to this group include water-soluble compounds such as silicates, carbonates, chlorides, nitrates, sulfates, and hydroxides of alkali metals such as sodium and potassium; Examples of compounds include inorganic glasses such as Pyrex glass.

前記発明の焼結体を製造するための各原料の使用量は、
1群が約20〜95%(重量%、以下同様)、1群が約
5〜80%、1群が約0〜20%、好ましくは、1群が
約50〜905X、11群が約10〜40%、■群が約
0〜10%である。1群は、焼結体とするための必須原
料であり、少なくとも20%以上は使用しないと焼結体
形成が困難となり、1群は本発明の抗菌作用の源となる
原料であり、少なくとも596以上は使用しないと十分
な坑菌効果が発揮されにくくなり、好ましくは約10%
以上である。1群は焼結を容易にするために補助的に使
用するものであり、その使用限度は20%程度であり、
これ以上使用すると本発明の焼結体の多孔性が損われ、
十分な抗菌効果が期待できなくなる。
The amount of each raw material used to manufacture the sintered body of the invention is:
Group 1 is about 20-95% (wt%, the same applies hereinafter), Group 1 is about 5-80%, Group 1 is about 0-20%, preferably Group 1 is about 50-905X, Group 11 is about 10 -40%, and group ■ about 0-10%. Group 1 is an essential raw material for making a sintered body, and if it is not used at least 20%, it will be difficult to form a sintered body. Group 1 is a raw material that is the source of the antibacterial action of the present invention, and contains at least 596 If the above amount is not used, sufficient antibacterial effect will not be exhibited, preferably about 10%
That's all. Group 1 is used auxiliary to facilitate sintering, and its usage limit is about 20%.
If it is used more than this, the porosity of the sintered body of the present invention will be impaired.
A sufficient antibacterial effect cannot be expected.

前記製造原料中、■群として水溶性化合物を用いた場合
には、まず1群の化合物と1群の化合物とを適量の水を
用いて混合ペースト状になるよう混疎し、さらに濃縮乾
固させ、再度微粉末化したものと、1群の化合物とを適
量のアルコール類の溶媒を用いて十分に練合し、所望の
鋳型内に圧入して成形したものを数百〜千数百0Cにて
数〜数十時間焼いて焼結体とすればよい。
When a water-soluble compound is used as Group (1) among the raw materials for production, first, the compound of Group 1 and the compound of Group 1 are mixed with an appropriate amount of water to form a paste, and then concentrated to dryness. The mixture was thoroughly kneaded with the first group of compounds using an appropriate amount of alcoholic solvent, and the mixture was press-fitted into a desired mold and molded at several hundred to several hundred degrees centigrade. The sintered body may be obtained by baking it for several to several tens of hours.

一方、■群として非水溶性化合物を用いた場合には、適
量の水を用いて1群、1群および■群の化合物を混合ベ
ース1−化したものを所望の鋳型内へ圧入して成形する
以外は′fm記水溶水溶性化合物いた場合と同様である
On the other hand, when a water-insoluble compound is used as Group ①, the compounds of Group 1, Group 1 and Group ① are mixed into a 1- base using an appropriate amount of water, and the mixture is press-fitted into the desired mold and molded. The process is the same as in the case of using the water-soluble compound 'fm' except that.

前記溶媒として用いるアルコール類は、たとえばメタノ
ール、エタノール、プロパツール、イソプロパツール、
ブタノールなどの通常のアルコール類が使用される。ま
た用いる鋳型は、SS、板状、円筒状、ブロック状、球
状などのいかなる形状のものでもよく、たとえば本発明
の焼結体をそのままボトル、容器などの底ぶたとして用
いようとする場合には、そういった用途に適合するよう
な形状、大きさのmmを用いて製造すればよいし、また
溶液中に保存する医療用具、たとえば、コンタクトレン
ズ、カテーテルなどの収納容器に本発明の焼結体を適用
する場合はその一部、あるいは全部を形成できるような
鋳型を用いて作ればよい。
The alcohols used as the solvent include, for example, methanol, ethanol, propatool, isopropateol,
Common alcohols such as butanol are used. The mold to be used may be of any shape such as SS, plate, cylinder, block, or spherical. For example, if the sintered body of the present invention is to be used as it is as a bottom lid of a bottle or container, The sintered body of the present invention may be manufactured using a shape and size (mm) suitable for such uses, and the sintered body of the present invention may be used in containers for storing medical devices such as contact lenses and catheters that are stored in solutions. When applied, it may be made using a mold that can form part or all of it.

〔発明の効果〕 本発明の抗菌性を有する焼結体は、単なる重金属化合物
と無機化合物との混合物ではなく、焼結することにより
、該重金属化合物と該無機化合物とが化学反応を起こす
ことによって耐勲牲および耐光性に優れ、かつ強度的に
も耐久性のあるものとなり、故に、長時間の安定した抗
菌作用の供給を可能とするものである。また、成形する
際に用いる鋳型を自由に選択することにより、本発明の
焼結体を任意の形状、大きさに成彩できる点からも工業
的に利用可能性の高いものである。
[Effects of the Invention] The sintered body having antibacterial properties of the present invention is not simply a mixture of a heavy metal compound and an inorganic compound. It has excellent durability and light resistance, and is also durable in terms of strength, thus making it possible to provide stable antibacterial action over a long period of time. Furthermore, the sintered body of the present invention can be made into any shape and size by freely selecting the mold used for molding, and therefore has high industrial applicability.

〔発明の産業上の利用可能性〕[Industrial applicability of the invention]

本発明の筑菌性を有する焼結体は、その有効性から踵々
の分野、用途に利用できる。たとえば、微生物汚染の防
止が可能であることから、ふる水、金魚ばちの水、花び
んの水などの微生物汚染の防止に利用することも可能で
ある。また、本発明の焼結体を浸漬した水溶液の安全性
の面から、水溶液中で保存、保管する物品の中でも特に
無菌状態を維持する必要のあるもの、たとえば、コンタ
クトレンズ、カテーテルなどの医療用具類の汚染防止に
好ましく応用できるものである。
Due to its effectiveness, the sintered body of the present invention having sintered properties can be used in the field and applications of heels. For example, since it is possible to prevent microbial contamination, it can also be used to prevent microbial contamination of hometown water, goldfish bee water, flower vase water, etc. In addition, from the viewpoint of the safety of the aqueous solution in which the sintered body of the present invention is immersed, among the articles that must be kept in an aqueous solution, it is particularly important to maintain sterile conditions, such as medical devices such as contact lenses and catheters. It can be preferably applied to the prevention of contamination of types.

〔実施例〕〔Example〕

実施例1 微粉末状のカオリン100gと炭酸ナトリウム3Iiと
を混合するのに適量の水を用いてペースト状とした後、
45℃、20〜3011JIHg減圧下、エバポレータ
ーにて濃縮乾固したものを硝子製乳鉢を用いて微粉末化
した。
Example 1 After mixing 100 g of finely powdered kaolin and sodium carbonate 3Ii using an appropriate amount of water to form a paste,
The mixture was concentrated to dryness in an evaporator at 45° C. under a reduced pressure of 20 to 3011 JIHg, and then pulverized using a glass mortar.

次いで、前記カオリン−炭酸す)・リウム混合微粉末体
101iと酸化銀2gを微粉末化したものとを適量のイ
ソプロピルアルコールを用いて十分に練合し、鋳型(1
7X17X3m)に圧入し、乾燥させ、取り出した成形
物をi 100 ”Cにて6時間節いて焼結体を得た。
Next, the kaolin-lium carbonate mixed fine powder 101i and 2 g of silver oxide were thoroughly kneaded using an appropriate amount of isopropyl alcohol.
7 x 17 x 3 m), dried, and the molded product taken out was kneaded at i 100 ''C for 6 hours to obtain a sintered body.

実施例2 実施例1で得たカオリン−炭酸ナトリウム−酸化銀混合
体を、ソフトコンタクトレンズ用ケースの収納部分を形
成するのに適した鋳型に圧入して型どり、乾燥後、取り
出し、1100℃にて10時時間−てソフトコンタクト
レンズ用ケースの収納部分を得た。
Example 2 The kaolin-sodium carbonate-silver oxide mixture obtained in Example 1 was press-fitted into a mold suitable for forming the housing part of a soft contact lens case, and after drying, it was taken out and heated to 1100°C. At 10 o'clock, I got the storage part for the soft contact lens case.

実施例3〜4 実施例1で用いた酸化銀21を酸化@2gへ変えたほか
は実施例1と同様にm製したものを実施例3として、酸
化亜鉛2gへ変えたほかは実施例1と同様にW製したも
のを実施例4として各々鋳ffi (17X17X3M
)を用いて実施例1と同様の方法で焼結体を得た。
Examples 3 to 4 Example 3 was made in the same manner as in Example 1, except that the silver oxide 21 used in Example 1 was changed to oxide@2g, and Example 1 was used, except that zinc oxide was changed to 2g. As Example 4, cast ffi (17X17X3M
) was used to obtain a sintered body in the same manner as in Example 1.

実施例5〜7 択 微粉末のカオリン1001iと微粉末化したパイへ レックスガラス0.311及び微粉末化した表1に示す
金属酸化物2gとを適量の水を用いてペースト状となる
よう十分に練合させた後、各々円柱状の鋳型(径10朋
、厚さ5順)中に圧入させ乾固させたものを1100℃
にて6時間節いて円柱状の焼結体を得た。
Examples 5 to 7 Selectively finely powdered kaolin 1001i, finely powdered Pyhex glass 0.311, and 2g of finely powdered metal oxide shown in Table 1 were mixed with an appropriate amount of water to make a paste. After kneading them, they were press-fitted into cylindrical molds (diameter 10, thickness 5 in order) and dried at 1100℃.
A cylindrical sintered body was obtained by kneading for 6 hours.

表1 実施例8 一トクレーブ処理を施し、無菌化した状態で、大腸菌浮
遊液(10@/fig)をエッペンドルフのマイクロピ
ペッタ−で100μlずつ添加し、10・/1とした。
Table 1 Example 8 After being toclaved and sterilized, E. coli suspension (10@/fig) was added in 100 μl portions using an Eppendorf micropipettor to give a concentration of 10·/1.

そののち、サンプル1霞!を採取してメンブランフィル
タ−法(注1)にて1日(24時間)後の生菌数を調べ
たところ表2のとおりであった。
After that, Sample 1 Kasumi! The number of viable bacteria after one day (24 hours) was determined using the membrane filter method (Note 1), and the results were as shown in Table 2.

表2 (注1)メンブランフィルタ−法 試料液1ntをツベルクリン用注射器(テルモシリンジ
1 frLl )にて採取し、孔径o、45μmのメン
ブランフィルタ−(直径13頭)でろ過した後、滅菌ペ
プトン水1omtで上記フィルターを洗浄し、を測定し
た。
Table 2 (Note 1) Membrane filter method Collect 1 nt of sample solution with a tuberculin syringe (Terumo syringe 1 frLl), filter it with a membrane filter (13 heads in diameter) with a pore size o of 45 μm, and then remove 1 nt of sterile peptone water. The above filter was washed and measured.

実施例9〜16 焼結体組成を表3のとおりにした焼結体の粉末102K
Fを試験管(φ=25順)に入れ、オートクo、snt
入れ、20℃で振りながら、接触1時間後、6時間後、
24時間後の生菌数をカンテン平板混釈法(注2)にて
測定した。その結果を表3に示す。
Examples 9 to 16 Sintered body powder 102K with sintered body composition as shown in Table 3
Put F into a test tube (φ = 25 order), autoquark o, snt
After 1 hour and 6 hours of contact, while shaking at 20℃,
The number of viable bacteria after 24 hours was measured by the agar plate pouring method (Note 2). The results are shown in Table 3.

(注2)カンテン平板混釈法 試料液1rrL7!をシャーレに採取し、あらかじめ加
温溶解し、45〜50℃に保持した5CDLP寒天培地
30Mを無菌的に注ぎ、静かに回転あるい日間培養し、
出現したコロニー数を測定した。
(Note 2) Agar plate pouring method sample solution 1rrL7! Collected in a petri dish, preheated and dissolved, poured 30M of 5CDLP agar medium kept at 45 to 50°C aseptically, and gently rotated or cultured for a day.
The number of colonies that appeared was measured.

Claims (1)

【特許請求の範囲】[Claims] 銀、銅および亜鉛よりなる群から選ばれた重金属元素を
含有する抗菌作用を有する焼結体。
A sintered body having an antibacterial effect and containing a heavy metal element selected from the group consisting of silver, copper and zinc.
JP59147358A 1984-07-16 1984-07-16 Sintered article having antimicrobial action Granted JPS6127906A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59147358A JPS6127906A (en) 1984-07-16 1984-07-16 Sintered article having antimicrobial action

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59147358A JPS6127906A (en) 1984-07-16 1984-07-16 Sintered article having antimicrobial action

Publications (2)

Publication Number Publication Date
JPS6127906A true JPS6127906A (en) 1986-02-07
JPH0475884B2 JPH0475884B2 (en) 1992-12-02

Family

ID=15428388

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59147358A Granted JPS6127906A (en) 1984-07-16 1984-07-16 Sintered article having antimicrobial action

Country Status (1)

Country Link
JP (1) JPS6127906A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01258792A (en) * 1988-04-09 1989-10-16 Kenji Ichikawa Antibacterial agent, antibacterial base material and antibacterial water tank
JPH02101003A (en) * 1988-10-11 1990-04-12 Nippon Foil Mfg Co Ltd Antibacterial film
JPH037201A (en) * 1989-06-02 1991-01-14 Ishizuka Glass Co Ltd Antifungal and deodorant agent
GB2247421A (en) * 1990-07-19 1992-03-04 Sangi Kk Contact lens material
JPH0558829A (en) * 1991-05-27 1993-03-09 Sakuramoto Plast Kogyo Kk Germicidal deodorant
JPH06154030A (en) * 1993-07-06 1994-06-03 Dentaru Kagaku Kk Antimicrobial apatite and antimicrobial resin containing the same
US6030627A (en) * 1994-01-29 2000-02-29 Lucky Ltd. Antimicrobial cosmetic pigment, its production process, and a cosmetic containing it
JP2001199822A (en) * 2000-01-14 2001-07-24 Shiseido Co Ltd Antibacterial mildewproofing agent and antibacterial mildewproofing composition

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01258792A (en) * 1988-04-09 1989-10-16 Kenji Ichikawa Antibacterial agent, antibacterial base material and antibacterial water tank
JPH02101003A (en) * 1988-10-11 1990-04-12 Nippon Foil Mfg Co Ltd Antibacterial film
JPH037201A (en) * 1989-06-02 1991-01-14 Ishizuka Glass Co Ltd Antifungal and deodorant agent
GB2247421A (en) * 1990-07-19 1992-03-04 Sangi Kk Contact lens material
US5213801A (en) * 1990-07-19 1993-05-25 Kabushiki Kaisha Sangi Contact lens material
GB2247421B (en) * 1990-07-19 1994-08-24 Sangi Kk Contact lens material
JPH0558829A (en) * 1991-05-27 1993-03-09 Sakuramoto Plast Kogyo Kk Germicidal deodorant
JPH06154030A (en) * 1993-07-06 1994-06-03 Dentaru Kagaku Kk Antimicrobial apatite and antimicrobial resin containing the same
US6030627A (en) * 1994-01-29 2000-02-29 Lucky Ltd. Antimicrobial cosmetic pigment, its production process, and a cosmetic containing it
JP2001199822A (en) * 2000-01-14 2001-07-24 Shiseido Co Ltd Antibacterial mildewproofing agent and antibacterial mildewproofing composition

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