JP2003339826A - Member and means for inactivating pathogenic microbe in one minute and sterilizing and washing method for medical device - Google Patents

Member and means for inactivating pathogenic microbe in one minute and sterilizing and washing method for medical device

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Publication number
JP2003339826A
JP2003339826A JP2002149926A JP2002149926A JP2003339826A JP 2003339826 A JP2003339826 A JP 2003339826A JP 2002149926 A JP2002149926 A JP 2002149926A JP 2002149926 A JP2002149926 A JP 2002149926A JP 2003339826 A JP2003339826 A JP 2003339826A
Authority
JP
Japan
Prior art keywords
medical device
pathogenic microorganisms
composite solution
titanium oxide
minute
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
JP2002149926A
Other languages
Japanese (ja)
Inventor
Masamichi Kinomoto
雅通 木ノ本
Yoichi Ito
洋一 伊藤
Hideyo Yamaguchi
英世 山口
Junichi Kobayashi
純一 小林
Motofumi Tokita
基文 時田
Satoshi Shinogaya
聰 篠ケ谷
Tazuru Izumi
田鶴 泉
Hiroshi Akaishi
啓 赤石
Akio Maeda
明男 前田
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.)
Sougo Giken Co Ltd
Original Assignee
Sougo Giken 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 Sougo Giken Co Ltd filed Critical Sougo Giken Co Ltd
Priority to JP2002149926A priority Critical patent/JP2003339826A/en
Publication of JP2003339826A publication Critical patent/JP2003339826A/en
Pending legal-status Critical Current

Links

Abstract

<P>PROBLEM TO BE SOLVED: To solve the problem of nosocomial infection due to insufficient sterilization and washing caused by saving labor and time because it takes much time and cost to increase in the number of devices, staff and cost caused by implementation of washing, disinfect and sterilization according to a guide line (GL washing method) of the Japan Digestive Endoscope Society because of long processing work time and harmful effect of disinfectant in spite of an effort to wash, disinfect and sterilize along the GL washing method. <P>SOLUTION: A medical device with pathogenic microbe adhering thereto is immersed in a compound solution composed of a mixture containing a photocatalyst titanium oxide, nitrate and alcohol and irradiated with UV while being shaked. <P>COPYRIGHT: (C)2004,JPO

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、病原微生物に汚染
されている医療機器を、安全に、確実に、素早く不活化
して、滅菌洗浄する方法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for sterilizing and safely inactivating medical devices contaminated with pathogenic microorganisms safely, reliably, and quickly.

【0002】[0002]

【従来の技術】従来技術の方法としては、用手消毒、自
動洗浄機消毒、ガス滅菌および電解酸性水、低温プラズ
マ、過酢酸などの消毒滅菌方法が採用されている。
2. Description of the Related Art As prior art methods, manual disinfection, automatic cleaning machine disinfection, gas sterilization and disinfection and sterilization methods such as electrolytic acid water, low temperature plasma, peracetic acid, etc. are adopted.

【0003】[0003]

【発明が解決しようとする課題】用手消毒方法にあって
は、血液、組織片等をブラシで擦り取る滅菌洗浄方法で
あるが、血液(脂肪、タンパク質)は水に溶けない粘着
性の汚れであり、ブラッシングすることは汚れを塗りつ
ぶし、汚染面を拡大させ付着強度を高める結果となって
いる。また、ブラッシング作業をすることによって汚染
飛沫を招き、肝炎ウィルス等の交差感染を生ずる危険性
の課題がある。
The manual disinfection method is a sterilization cleaning method in which blood, tissue pieces, etc. are rubbed off with a brush, but blood (fat, protein) is an adhesive stain that does not dissolve in water. Therefore, brushing results in filling dirt, expanding the contaminated surface, and increasing the adhesion strength. In addition, there is a risk that the brushing operation may cause contamination and a risk of cross infection such as hepatitis virus.

【0004】自動洗浄機消毒方法の場合でも、内視鏡を
用いた検査後には必ず用手洗浄が必要となる。特に、チ
ャンネル内のブラッシングが不十分な場合には確実な消
毒効果を得ることが出来ない等の課題がある。
Even in the case of the automatic washing machine disinfection method, manual washing is always required after the examination using the endoscope. In particular, when brushing in the channel is insufficient, there is a problem that a reliable disinfection effect cannot be obtained.

【0005】ガス滅菌の場合にあっては、長時間を要す
るため消毒・滅菌方法としては一般的ではないが滅菌効
果は高い。ガス滅菌を実施する場合は、チャンネル内に
水分が残っていると十分な滅菌効果が得られない課題が
ある。
In the case of gas sterilization, it takes a long time and is not a general disinfection / sterilization method, but the sterilization effect is high. When performing gas sterilization, there is a problem that a sufficient sterilization effect cannot be obtained if water remains in the channel.

【0006】電解酸性水は微量な塩化ナトリウムを添加
した水道水を電気分解して得られる水であり、人体に対
する副作用はほとんど無く、低価格であり近年多くの現
場で採用されている。しかし、その作用が十分解明され
ていないことから消毒剤としての医療品認可が取れてい
ない課題がある。
Electrolyzed acidic water is water obtained by electrolyzing tap water to which a trace amount of sodium chloride is added, has almost no side effects on the human body, is inexpensive, and has been adopted in many fields in recent years. However, there is a problem that the approval of medical products as a disinfectant has not been obtained because its action is not fully understood.

【0007】低温プラズマにあっては、固体、液体、気
体とは異なり、イオンや電子等を多量に含む活性の高い
状態の物質であり、プラズマ中にはフリ−ラジカルが多
く含有されており、この作用により微生物を殺滅できる
と考えられている。しかしながら、セルロ−ス製品およ
び液体には使用できない課題がある。
Unlike low-temperature solids, liquids, and gases, low-temperature plasma is a highly active substance containing a large amount of ions and electrons, and plasma contains a large amount of free radicals. It is believed that this action can kill microorganisms. However, there are problems that cannot be applied to cellulosic products and liquids.

【0008】過酢酸の殺菌力は公知であるが安全性に問
題があり余り採用されなかった。近年は技術の進歩によ
り新しい消毒剤として見直されてきた。過酢酸の強い酸
化力により細胞膜や細胞の酵素仕組みを破壊し、細菌を
殺滅できると考えられているが、腐食性を有するため殺
菌する対象物の耐久性を確認しなければならない課題が
存在する。
Although the bactericidal activity of peracetic acid is known, it has not been adopted because it has a safety problem. In recent years, it has been reviewed as a new disinfectant due to technological progress. It is thought that the strong oxidative power of peracetic acid can destroy the cell membrane and the enzymatic mechanism of the cell to kill bacteria, but since it is corrosive, there is a problem that the durability of the object to be sterilized must be confirmed. To do.

【0009】上記のごとく様々な方法が試みられている
が、現時点では解決しなければならない課題も多く、い
まだ完全な消毒・滅菌方法は確立されていない。医療施
設側も例えば、日本消化器内視鏡学会のガイドライン
(GL洗浄法)に添って洗浄・消毒・滅菌を実施するな
ど努力はしているが、処理作業時間が長いことや消毒剤
の有害性、GL洗浄法の実施に伴う機器の増設、人員の
増員、経費増等々の課題が生じている。
Although various methods have been tried as described above, there are still many problems to be solved at the present time, and a complete disinfection / sterilization method has not been established yet. Medical facilities are also making efforts such as implementing cleaning, disinfection, and sterilization in accordance with the Japanese Society of Gastroenterological Endoscopy (GL cleaning method), but the processing time is long and the disinfectant is harmful. , The increase in equipment, the increase in personnel, the increase in costs, etc. have occurred due to the implementation of the GL cleaning method.

【0010】本発明は、手間と経費が掛かりすぎて、滅
菌、洗浄が不十分な原因による、院内感染が心配されて
いる。安全に確実に素早く医療機器に付着している病原
微生物を不活化し、医療従事者および患者の院内感染予
防に貢献する手段を提供することが目的である。
The present invention requires too much labor and cost, and there is a concern about nosocomial infection due to insufficient sterilization and cleaning. It is an object of the present invention to provide a means for safely and quickly inactivating pathogenic microorganisms adhering to medical devices and contributing to prevent nosocomial infections of medical staff and patients.

【0011】[0011]

【課題を解決するための手段】上記目的を達成するため
に本発明は、医療機器に付着している病原微生物と共に
光触媒性酸化チタンと硝酸とアルコ−ルを含む混合物で
構成された複合溶液に浸漬し、加振しながらUV照射す
る。
In order to achieve the above object, the present invention provides a composite solution composed of a mixture containing photocatalytic titanium oxide, nitric acid and alcohol together with pathogenic microorganisms attached to a medical device. Dip and irradiate with UV while shaking.

【0012】[0012]

【作用】一般的に、光触媒性酸化チタンにUV照射し
活性化させる殺菌法。硝酸など強酸性による殺菌法。
アルコ−ルによる殺菌法。UV照射による殺菌法。
等々による殺菌方法は公知である。しかし、本発明によ
る実施例が示すが如く、当該手段の発明により、本来不
可能であった病原微生物も短時間に不活化出来るように
なった。なお、より短時間に滅菌洗浄する効果的な手段
は、アルコ−ル溶液又は洗浄剤を用いて、医療機器に付
着している、汚物、血液、粘膜組織をブラッシングによ
り、十分に洗い落としたのち、本発明手段を採用する方
法が好まれる。
Function: Generally, a sterilization method in which photocatalytic titanium oxide is irradiated with UV to be activated. Sterilization method using strong acid such as nitric acid.
Sterilization method by alcohol. Sterilization method by UV irradiation.
Sterilization methods by etc. are known. However, as shown by the examples according to the present invention, the invention of the means makes it possible to inactivate pathogenic microorganisms which were originally impossible in a short time. Incidentally, an effective means of sterilizing and cleaning in a shorter time is to use an alcohol solution or a cleaning agent, and after thoroughly washing off dirt, blood, and mucous membrane tissue adhered to the medical device by brushing, A method employing the means of the present invention is preferred.

【0013】光触媒性酸化チタンに光の波長が380n
m以下の近紫外線(一部では可視光も可)を照射すると
電子と正孔の二つのキャリアができる。光触媒性酸化チ
タンの特徴でもある励起電子のもつ還元力よりも正孔の
もつ酸化力が強力である点を利用し、触媒表面のH2
に正孔が作用し、ヒドロキシラジカルが生じる。このヒ
ドロキシラジカルは水道の消毒などに広く使われている
塩素やオゾンに比べて非常に強い酸化力をもっており、
有機物を構成する分子中の炭素−炭素結合(83kcal/mo
l)、炭素−水素結合(99kcal/mol)、炭素−窒素結合
(73kcal/mol)、炭素−酸素結合(84kcal/mol)、酸素
−水素結合( 111kcal/mol)、窒素−水素結合(93kcal
/mol)、の結合エネルギ−であるのに対して、ヒドロキ
シラジカルのエネルギ−は 120kcal/molとはるかに大き
いため、これらの結合を簡単に切断して分解することが
できる。この作用により細菌感染症などで産出されるエ
ンドトキシンなどの毒素も分解できることが確認されて
いる。さらに、Pt、Ag、Cuなどの遷移金属を添加
することにより酸化還元機能を向上させ滅菌力を高める
ことが可能である。
The photocatalytic titanium oxide has a light wavelength of 380 n.
Irradiation with near-ultraviolet rays of m or less (some of which may be visible light) creates two carriers, electrons and holes. Utilizing the fact that the oxidizing power of holes is stronger than the reducing power of excited electrons, which is also characteristic of photocatalytic titanium oxide, and H 2 O on the catalyst surface is utilized.
The holes act on the base to generate hydroxy radicals. This hydroxy radical has a very strong oxidizing power compared to chlorine and ozone, which are widely used for disinfecting water,
Carbon-carbon bonds in molecules that make up organic matter (83 kcal / mo
l), carbon-hydrogen bond (99kcal / mol), carbon-nitrogen bond (73kcal / mol), carbon-oxygen bond (84kcal / mol), oxygen-hydrogen bond (111kcal / mol), nitrogen-hydrogen bond (93kcal)
/ mol), and the energy of hydroxy radicals is much larger at 120 kcal / mol, so these bonds can be easily cleaved and decomposed. It has been confirmed that this action can also decompose toxins such as endotoxin produced in bacterial infections. Furthermore, by adding a transition metal such as Pt, Ag or Cu, it is possible to improve the redox function and enhance the sterilization power.

【0014】病原微生物が付着している医療機器を、光
触媒性酸化チタンと、硝酸とアルコ−ルを含む混合物で
構成された複合溶液に浸漬させる手段が好ましく、ここ
で推奨するアルコ−ルは、好ましくは、エタノ−ル50
〜95v/v%、より好ましくは、65〜85v/v%含有水溶
液である。しかしながら、イソプロパノ−ル、フェノル
を用いても良い。
Means for immersing a medical device to which pathogenic microorganisms are attached in a composite solution composed of a photocatalytic titanium oxide and a mixture containing nitric acid and alcohol is preferable. The alcohol recommended here is Preferably, ethanol 50
It is an aqueous solution containing ˜95 v / v%, more preferably 65-85 v / v%. However, isopropanol and phenol may be used.

【0015】病原微生物が付着している医療機器を、光
触媒性酸化チタンと、硝酸とアルコ−ルを含む混合物で
構成された複合溶液に浸漬し、加振する方法が好まれる
が、加振する手段としては、超音波加振方法、マグネチ
ックスタ−ラ−加振方法、コンプレッサ−を用いてのエ
ア−レ−ション加振方法、などが考慮される。
A method of immersing a medical device to which pathogenic microorganisms are adhered in a composite solution composed of a mixture containing photocatalytic titanium oxide and nitric acid and alcohol, and vibrating is preferred. As means, an ultrasonic vibration method, a magnetic stirrer vibration method, an air-lation vibration method using a compressor, and the like are considered.

【0016】病原微生物が付着している医療機器を、光
触媒性酸化チタンと、硝酸とアルコ−ルを含む混合物で
構成された複合溶液に浸漬し、前記手段等の方法により
加振しながらUV照射するのが好ましい。最近では必ず
しも紫外線を含まない光でも有効な光触媒性酸化チタン
が開発されている。
A medical device to which pathogenic microorganisms are attached is dipped in a composite solution composed of a photocatalytic titanium oxide and a mixture containing nitric acid and alcohol, and is irradiated with UV while being vibrated by the method described above. Preferably. Recently, a photocatalytic titanium oxide that is effective even with light that does not necessarily contain ultraviolet rays has been developed.

【0017】病原微生物が付着している医療機器を、光
触媒性酸化チタンと硝酸とアルコ−ルを含む混合物で構
成された複合溶液に浸漬する工程、当該医療機器を前記
複合溶液に浸漬し加振する工程、当該医療機器を前記複
合溶液に浸漬し加振しながらUV照射する工程、を含ん
でなる方法が望ましい。
The step of immersing the medical device to which the pathogenic microorganism is attached in a composite solution composed of a mixture containing photocatalytic titanium oxide, nitric acid and alcohol, and immersing the medical device in the composite solution and shaking. And a step of irradiating the medical device with the composite solution and irradiating with UV while vibrating.

【0018】医療機器滅菌洗浄装置の工程としては、病
原微生物が付着している医療機器を、光触媒性酸化チタ
ンと硝酸とアルコ−ルを含む混合物で構成された複合溶
液に浸漬する工程、当該医療機器を前記複合溶液に浸漬
し加振する工程、当該医療機器を前記複合溶液に浸漬し
加振しながらUV照射する工程、が完了したら、次に、
当該医療機器の前記複合溶液を含む残存付着物を濯ぎ洗
浄する工程、当該医療機器の前記複合溶液を含む残存付
着物を濯ぎ洗浄で濡れた部分を乾燥する工程、当該医療
機器の前記複合溶液を含む残存付着物を濯ぎ洗浄で濡れ
た部分を乾燥させた後衛生的に保管する工程、を組み込
む方法が望まれる。濯ぎ洗浄に用いる液体としては、清
浄水、無菌水、滅菌精製水であって良い。
As a step of the medical equipment sterilization cleaning device, a step of immersing the medical equipment to which pathogenic microorganisms are attached in a composite solution composed of a mixture containing photocatalytic titanium oxide, nitric acid and alcohol, When the step of immersing the device in the composite solution and shaking, the step of irradiating the medical device in the composite solution and irradiating with UV while vibrating, next
The step of rinsing and washing the remaining deposit containing the composite solution of the medical device, the step of rinsing and washing the residual deposit containing the composite solution of the medical device to dry the complex solution of the medical device. A method of incorporating a step of drying the wet portion of the remaining adhered substance containing it by rinsing and washing and then storing it hygienically is desired. The liquid used for rinsing and washing may be clean water, sterile water, or sterile purified water.

【0019】医療機器滅菌洗浄装置には、病原微生物を
光触媒性酸化チタンと硝酸とアルコ−ルを含む混合物で
構成された複合溶液には、収納部を完備し、常にUV照
射している状態を保持する仕組みにする事が好ましく、
更には、当該複合溶液の流液回路には、フィルタ−等の
浄化装置を配設し循環使用する手段が望まれる。
In the medical device sterilizing and washing apparatus, the pathological microorganism is a composite solution composed of a mixture containing photocatalytic titanium oxide, nitric acid, and alcohol, and is provided with a storage section and is constantly irradiated with UV. It is preferable to keep it
Further, a means for circulating and using a purifying device such as a filter is desired in the flow circuit of the composite solution.

【0020】病原微生物が付着している医療機器の、光
触媒性酸化チタンと、硝酸とアルコ−ルを含む混合物で
構成された複合溶液への浸漬時間は、1秒以上1時間以
内であってよい。
The immersion time of the medical device to which the pathogenic microorganisms are attached in the composite solution composed of the mixture containing photocatalytic titanium oxide and nitric acid and alcohol may be 1 second or more and 1 hour or less. .

【0021】病原性微生物は大旨1μm程度から、芽胞
菌である結核菌は1〜4μmと比較的大きく、病原性微
生物やウイルス類にあっては、例えば、内視鏡スコ−プ
チュ−ブのクラック部分やチャンネル作動部分又は、そ
の他の被滅菌洗浄物の凹部等に侵入し潜んでいても、本
発明に採用している光触媒性酸化チタンの粒子径は7n
mと究めて微細で分散性の優れたものを使用しているた
め、芽胞を含む全ての病原微生物やウイルス等が如何な
る場所に侵入し、潜んでいても接触滅菌洗浄できる。
Pathogenic microorganisms are roughly 1 μm, and tubercle bacilli, which are spore-forming bacteria, are relatively large at 1 to 4 μm. For pathogenic microorganisms and viruses, for example, endoscope scope tubes are used. Even if the photocatalytic titanium oxide used in the present invention has a particle size of 7 n even if it penetrates and lurks in cracks, channel operating parts, or other recesses of the article to be sterilized.
m, which is extremely fine and has excellent dispersibility, allows all pathogenic microorganisms and viruses, including spores, to invade any place, and even if they are hidden, they can be contact sterilized and washed.

【0022】[0022]

【発明の実施の形態】本発明は、従来から多く採用され
ている光触媒性酸化チタンをコ−テイング(薄膜塗布形
成)する方法とは異なり、目的とする医療機器に光触媒
性酸化チタンを固着させることなく活用する手段に特徴
を見いだしたことである。一般的な方法としては、基材
(内視鏡や付属器具)の表面に光触媒性酸化チタンを塗
布(コ−ティング)して、その表面に光励起することに
より、表面の光触媒性酸化チタンに接触する病原菌を含
む有機物を分解除去できることは公知であり多方面で実
用化されている。しかしながら、そのすべて(?)の方
法は、基材の表面に光触媒性酸化チタンを固定(接着)
して出来るかぎり長期に渡り、その有効性を維持する手
段が用いられている。さらに、従来の方法では、医療機
器の全部または一部に光触媒性酸化チタンを塗布(コ−
ティング)することにより、その部分に光励起して接触
する有害物を分解する手段による特許出願も見受けられ
る。それに対して、光触媒性酸化チタンと硝酸とアルコ
−ルを含む複合溶液に光励起して活性化させた、当該複
合溶液に病原微生物が付着している医療機器を浸漬する
ことで、いかなる場所に潜んでいる病原微生物であって
も光励起された光触媒性酸化チタンの光触媒反応によ
り、接触する該病原微生物を不活化させるする手段は前
例が無く、全く新しい独創的な考え方である。
BEST MODE FOR CARRYING OUT THE INVENTION The present invention is different from the method of coating (forming thin film coating) of photocatalytic titanium oxide, which has been widely adopted in the past, to fix the photocatalytic titanium oxide to a target medical device. That is, I found a feature in the means to utilize it without any problems. As a general method, the photocatalytic titanium oxide is applied to the surface of the base material (endoscope or accessory) (coating), and the surface is photoexcited to contact the photocatalytic titanium oxide on the surface. It is known that organic substances containing pathogenic bacteria can be decomposed and removed, and has been put to practical use in various fields. However, all (?) Methods fix (bond) photocatalytic titanium oxide to the surface of the substrate.
Then, as long as possible, a means to maintain its effectiveness is used. Furthermore, in the conventional method, a photocatalytic titanium oxide is applied (co-coated) to all or part of the medical device.
There is also a patent application by means of decomposing harmful substances that are brought into contact with the portion by photoexcitation. On the other hand, the photocatalytic titanium oxide, nitric acid and alcohol are photoexcited and activated in a composite solution, and the medical solution in which pathogenic microorganisms are adhered is immersed in the composite solution so that it can be hidden anywhere. There is no precedent for any means for inactivating the pathogenic microorganisms that come into contact with it by photocatalytic reaction of photocatalytic titanium oxide that is photoexcited, and it is a completely new and original idea.

【0023】医療機器の完全滅菌に着目した理由は、使
用された医療機器による「医原性感染」が社会問題化し
ている中、被検者に使用された医療機器を次の被検者に
使用するには二次感染を防ぐために完全に滅菌された清
潔なものを提供する義務と権利と責任感を痛感したから
である。院内感染の感染経路や感染源は究めて多岐にわ
たり、多様化しているが少なくとも医療機器による感染
源の予防に大きく貢献でき、交差感染の危険性が減少す
ることにより看護婦等の安全業務の遂行および二次感染
防止を通じて社会に貢献できることである。
The reason for paying attention to the complete sterilization of medical devices is that the medical device used by a subject is given to the next subject while the "iatrogenic infection" caused by the used medical device is becoming a social problem. This is because I was keenly aware of the duty, right, and responsibility to provide clean, completely sterilized products to prevent secondary infection before use. The infection routes and sources of nosocomial infections have been diversified and diversified, but at least they can make a significant contribution to the prevention of infection sources by medical devices, and the risk of cross-infection is reduced, thereby performing safety work for nurses, etc. And to contribute to society by preventing secondary infections.

【0024】最近、エイズ(HIV)の問題など医療方
面では、細菌やウイルスによる感染症の流行が問題視さ
れています。少し前までは、結核が激減しWHOは天然
痘の撲滅を宣言するなど感染症はすでに時代遅れとさえ
言われた。しかし、エボラ出血熱ウィルス、腸管出血性
大腸菌O157は大きな社会問題となっている。また、MR
SAのように健常者にはほとんど影響がなくとも、ひと
たび抵抗力の落ちた病人やお年寄りには感染症を引き起
こし、抗生物質も効かず最悪の場合には死に至らしめる
という院内感染の問題もいまだに解決されていない。そ
のため、医学の方面では、どうすれば細菌やウィルスを
退治できるかということに非常に関心が集まっている。
細菌やウィルスの性質として、初めから大量にそこにい
るのではなく、よそから何かの方法で移ってきて、その
場所が増殖するのに適した環境とわかるやネズミ算的に
増殖する。光触媒は一度に大量の物質を分解することに
は不向きであるが、このように最初は少しのものが徐々
に増えてくるようなものに対しては大変大きな効果があ
ることが判明している。抗菌剤、消毒剤、滅菌剤という
ことならこれまでにもいくつもの種類が活躍している
が、大きな違いはどこかと言うと、一つにAgなどの抗
菌剤の場合、細菌を殺すことができてもその死骸は残っ
てしまうのに対し、光触媒性酸化チタンの場合は単に細
菌を殺滅すだけではなく、その死骸も分解してしまう性
質を持っていることである。
Recently, in the medical field such as the AIDS (HIV) problem, epidemics of infectious diseases caused by bacteria and viruses have been regarded as problems. Not long ago, it was said that infectious diseases were already obsolete, as tuberculosis had fallen sharply and WHO had declared the eradication of smallpox. However, Ebola virus and enterohemorrhagic Escherichia coli O157 have become major social problems. Also, MR
There is also the problem of nosocomial infection, such as SA, which causes almost no effect on healthy people but causes infections in sick people and elderly people who have once become less resistant, and that antibiotics do not work and in the worst case cause death. Still not resolved. Therefore, in the medical field, there is great interest in how to get rid of bacteria and viruses.
Due to the nature of bacteria and viruses, they are not there in large numbers from the beginning, but they are transferred from somewhere in some way, and when they are found to be in a suitable environment in which to multiply, they multiply in a rat. The photocatalyst is not suitable for decomposing a large amount of substances at once, but it has been found to be very effective for such a small amount that gradually increases at first. . There are many types of antibacterial agents, disinfectants, and sterilizers that have been used so far, but the main difference is that antibacterial agents such as Ag can kill bacteria. However, while the carcass remains, the photocatalytic titanium oxide not only kills bacteria, but also has the property of decomposing the carcass.

【0025】[0025]

【実施例】以下、実施例によって本発明を更に詳しく説
明するが、本発明はこれら実施例によってなんら制限さ
れるものではない。 実施例1. 試験目的:大腸菌の不活化効果試験 試薬・光触媒性酸化チタンと硝酸とアルコ−ルを含む
混合物で構成された複合溶液(クリアックス#001・
総合技研)を試薬とした。 供試菌・大腸菌(Escherichia coli ATCC 8739) 菌液調整・供試菌をSCDブイヨン培地で35℃、2
4時間培養し、滅菌リン酸緩衝液に懸濁したものを菌液
とした。(菌液:約106cfu/ml) 操作・ガラス管(直径8mm, 高サ10mm)に0.1%アスパラ
ギン酸塩を被膜した後菌液に15分間浸漬し、滅菌ろ紙
上で30分間乾燥させキャリアとした。汚染したキャリ
アをあらかじめブラックライトで活性化させた試薬(100
ml) の中にいれ、撹拌しながらブラックライトを照射
し、1分、5分間作動させた。作動させた後、キャリア
を取り出し10mlの滅菌精製水で7回水洗し、10mlの普通
ブイヨン培地にいれ、35℃、48時間培養し、菌の発
育の有無を観察した。対照は汚染したキャリアを10mlの
滅菌精製水で7回水洗したものを普通ブイヨン培地にい
れ培養した。ただし、試験は繰り返し10回行った。 試験結果 10本中菌の発育した本数 作用時間
(分) 1分→0本 5分→0本 対照→10本
The present invention will be described in more detail with reference to the following examples, but the present invention is not limited to these examples. Example 1. Test purpose: Escherichia coli inactivation effect test reagent-Composite solution composed of a mixture containing photocatalytic titanium oxide, nitric acid, and alcohol (CLEARX # 001.
General Research Institute) was used as a reagent. Escherichia coli ATCC 8739: Preparation of Escherichia coli ATCC 8739: SCD broth medium at 35 ℃, 2
The cells were cultured for 4 hours and suspended in sterilized phosphate buffer to give a bacterial solution. (Bacterial solution: about 10 6 cfu / ml) Operation ・ Coating a glass tube (diameter 8 mm, height 10 mm) with 0.1% aspartate, immersing in bacterial solution for 15 minutes, and drying on sterile filter paper for 30 minutes and carrier And Reagents (100
ml) and irradiated with black light with stirring, and operated for 1 minute and 5 minutes. After the operation, the carrier was taken out, washed with 10 ml of sterilized purified water seven times, placed in 10 ml of a normal broth medium and cultured at 35 ° C. for 48 hours, and the presence or absence of bacterial growth was observed. As a control, a contaminated carrier was washed with 10 ml of sterilized purified water seven times and put in a normal broth medium and cultured. However, the test was repeated 10 times. Test result Number of 10 bacteria developed Number of times Action time (min) 1 minute → 0 5 minutes → 0 Control → 10

【0026】実施例2. 試験目的:MRSAの不活化効果試験 試薬・光触媒性酸化チタンと硝酸とアルコ−ルを含む
混合物で構成された複合溶液(クリアックス#001・
総合技研)を試薬とした。 供試菌・MRSA(Staphyiococcus aureus MRSA ヒト
分離株) 菌液調整・供試菌をSCDブイヨン培地で35℃、2
4時間培養し、滅菌リン酸緩衝液に懸濁したものを菌液
とした。(菌液:約106cfu/ml) 操作・ガラス管(直径8mm, 高サ10mm)に0.1%アスパラ
ギン酸塩を被膜した後菌液に15分間浸漬し、滅菌ろ紙
上で30分間乾燥させキャリアとした。汚染したキャリ
アをあらかじめブラックライトで活性化させた試薬(100
ml) の中にいれ、撹拌しながらブラックライトを照射
し、1分、5分間作動させた。作動させた後、キャリア
を取り出し10mlの滅菌精製水で7回水洗し、10mlの普通
ブイヨン培地にいれ、35℃、48時間培養し、菌の発
育の有無を観察した。対照は汚染したキャリアを10mlの
滅菌精製水で7回水洗したものを普通ブイヨン培地にい
れ培養した。ただし、試験は繰り返し10回行った。 試験結果 10本中菌の発育した本数 作用時間
(分) 1分→0本 5分→0本 対照→10本
Example 2. Test purpose: MRSA inactivation effect test reagent ・ Composite solution composed of a mixture containing photocatalytic titanium oxide, nitric acid and alcohol (Clriax # 001.
General Research Institute) was used as a reagent. Test bacterium / MRSA (Staphyiococcus aureus MRSA human isolate) Preparation of bacterium solution / Test bacterium in SCD broth medium at 35 ℃, 2
The cells were cultured for 4 hours and suspended in sterilized phosphate buffer to give a bacterial solution. (Bacterial solution: about 10 6 cfu / ml) Operation ・ Coating a glass tube (diameter 8 mm, height 10 mm) with 0.1% aspartate, immersing in bacterial solution for 15 minutes, and drying on sterile filter paper for 30 minutes and carrier And Reagents (100
ml) and irradiated with black light with stirring, and operated for 1 minute and 5 minutes. After the operation, the carrier was taken out, washed with 10 ml of sterilized purified water seven times, placed in 10 ml of a normal broth medium and cultured at 35 ° C. for 48 hours, and the presence or absence of bacterial growth was observed. As a control, a contaminated carrier was washed with 10 ml of sterilized purified water seven times and put in a normal broth medium and cultured. However, the test was repeated 10 times. Test result Number of 10 bacteria developed Number of times Action time (min) 1 minute → 0 5 minutes → 0 Control → 10

【0027】実施例3. 試験目的:緑膿菌の不活化効果試験 試薬・光触媒性酸化チタンと硝酸とアルコ−ルを含む
混合物で構成された複合溶液(クリアックス#001・
総合技研)を試薬とした。 供試菌・緑膿菌(Pseudomonas aeruginosa ATCC 902
7) 菌液調整・供試菌をSCDブイヨン培地で35℃、2
4時間培養し、滅菌リン酸緩衝液に懸濁したものを菌液
とした。(菌液:約106cfu/ml) 操作・ガラス管(直径8mm, 高サ10mm)に0.1%アスパラ
ギン酸塩を被膜した後菌液に15分間浸漬し、滅菌ろ紙
上で30分間乾燥させキャリアとした。汚染したキャリ
アをあらかじめブラックライトで活性化させた試薬(100
ml) の中にいれ、撹拌しながらブラックライトを照射
し、1分、5分間作動させた。作動させた後、キャリア
を取り出し10mlの滅菌精製水で7回水洗し、10mlの普通
ブイヨン培地にいれ、35℃、48時間培養し、菌の発
育の有無を観察した。対照は汚染したキャリアを10mlの
滅菌精製水で7回水洗したものを普通ブイヨン培地にい
れ培養した。ただし、試験は繰り返し10回行った。 試験結果 10本中菌の発育した本数 作用時間
(分) 1分→0本 5分→0本 対照→10本
Example 3. Test purpose: Pseudomonas aeruginosa inactivating effect test reagent ・ Composite solution composed of a mixture containing photocatalytic titanium oxide, nitric acid and alcohol (Clriax # 001.
General Research Institute) was used as a reagent. Pseudomonas aeruginosa ATCC 902
7) Prepare the bacterial solution and test bacteria in SCD broth medium at 35 ℃ for 2
The cells were cultured for 4 hours and suspended in sterilized phosphate buffer to give a bacterial solution. (Bacterial solution: about 10 6 cfu / ml) Operation ・ Coating a glass tube (diameter 8 mm, height 10 mm) with 0.1% aspartate, immersing in bacterial solution for 15 minutes, and drying on sterile filter paper for 30 minutes and carrier And Reagents (100
ml) and irradiated with black light with stirring, and operated for 1 minute and 5 minutes. After the operation, the carrier was taken out, washed with 10 ml of sterilized purified water seven times, placed in 10 ml of a normal broth medium and cultured at 35 ° C. for 48 hours, and the presence or absence of bacterial growth was observed. As a control, a contaminated carrier was washed with 10 ml of sterilized purified water seven times and put in a normal broth medium and cultured. However, the test was repeated 10 times. Test result Number of 10 bacteria developed Number of times Action time (min) 1 minute → 0 5 minutes → 0 Control → 10

【0028】実施例4. 試験目的:カンジダ菌の不活化効果試験 試薬・光触媒性酸化チタンと硝酸とアルコ−ルを含む
混合物で構成された複合溶液(クリアックス#001・
総合技研)を試薬とした。 供試菌・Candida aibicans ATCC 10231 菌液調整・供試菌をSCDブイヨン培地で35℃、2
4時間培養し、滅菌リン酸緩衝液に懸濁したものを菌液
とした。(菌液:約106cfu/ml) 操作・ガラス管(直径8mm, 高サ10mm)に0.1%アスパラ
ギン酸塩を被膜した後菌液に15分間浸漬し、滅菌ろ紙
上で30分間乾燥させキャリアとした。汚染したキャリ
アをあらかじめブラックライトで活性化させた試薬(100
ml) の中にいれ、撹拌しながらブラックライトを照射
し、1分、5分間作動させた。作動させた後、キャリア
を取り出し10mlの滅菌精製水で7回水洗し、10mlの普通
ブイヨン培地にいれ、35℃、48時間培養し、菌の発
育の有無を観察した。対照は汚染したキャリアを10mlの
滅菌精製水で7回水洗したものを普通ブイヨン培地にい
れ培養した。ただし、試験は繰り返し10回行った。 試験結果 10本中菌の発育した本数 作用時間
(分) 1分→0本 5分→0本 対照→10本
Example 4. Test purpose: Inactivation effect test reagent for Candida bacteria-Composite solution composed of a mixture containing photocatalytic titanium oxide and nitric acid and alcohol (Clriax # 001.
General Research Institute) was used as a reagent. Sample bacteria ・ Candida aibicans ATCC 10231 Preparation of bacterial solution ・ Sample bacteria in SCD broth medium at 35 ℃, 2
The cells were cultured for 4 hours and suspended in sterilized phosphate buffer to give a bacterial solution. (Bacterial solution: about 10 6 cfu / ml) Operation ・ Coating a glass tube (diameter 8 mm, height 10 mm) with 0.1% aspartate, immersing in bacterial solution for 15 minutes, and drying on sterile filter paper for 30 minutes and carrier And Reagents (100
ml) and irradiated with black light with stirring, and operated for 1 minute and 5 minutes. After the operation, the carrier was taken out, washed with 10 ml of sterilized purified water seven times, placed in 10 ml of a normal broth medium and cultured at 35 ° C. for 48 hours, and the presence or absence of bacterial growth was observed. As a control, a contaminated carrier was washed with 10 ml of sterilized purified water seven times and put in a normal broth medium and cultured. However, the test was repeated 10 times. Test result Number of 10 bacteria developed Number of times Action time (min) 1 minute → 0 5 minutes → 0 Control → 10

【0029】[0029]

【発明の効果】本発明は、以上説明したように構成され
ているので、以下に記載されているような効果を奏す
る。
Since the present invention is constructed as described above, it has the following effects.

【0030】日本で多く使用されているグルタルアルデ
ヒド製剤は、蛋白変性作用が強く皮膚に付着すると着色
や皮膚炎等を起こし、更に、蒸気は眼や鼻などに粘膜刺
激を与えるため十分注意しなければならないが、本手段
の主剤に採用している酸化チタンは、歯磨剤、化粧品、
白色顔料など広く使われている人畜無害の食品添加物に
認定されている安全な物質であり、医療従事者は安心し
て作業できる効果がある。
Glutaraldehyde preparations, which are widely used in Japan, have a strong protein denaturing effect and cause coloring and dermatitis when attached to the skin. Further, steam causes mucous membrane irritation to the eyes and nose. Titanium oxide, which is the main ingredient of this method, must be used for toothpaste, cosmetics,
It is a safe substance that has been certified as a food additive that is harmless to humans and animals, such as white pigment, and has the effect that medical personnel can work with peace of mind.

【0031】芽胞菌を含むすべての病原微生物に光触媒
は有効であり、感染源の遮断方法としては、グルタルア
ルデヒド製剤、電解酸性水、二酸化塩素水、過酢酸など
と比較すると、消毒滅菌時間が非常に短く品質が安定し
ており低価格で安心して採用できる効果がある。
The photocatalyst is effective for all pathogenic microorganisms including spore bacteria, and as a method of blocking the infection source, the disinfection and sterilization time is much shorter than that of glutaraldehyde preparation, electrolytic acid water, chlorine dioxide water, peracetic acid, etc. It is very short and stable in quality, so it can be adopted at a low price and with peace of mind.

【0032】本発明で採用している光触媒性酸化チタン
の粒子径は、ナノメ−トルサイズで細菌と比べて究めて
微細であり細菌が内視鏡スコ−プのチュ−ブのクラック
部分やチャンネル作動部に侵入し潜んでいても、その全
ての部分に浸漬して接触することで完全滅菌できる効果
がある。
The particle size of the photocatalytic titanium oxide used in the present invention is nanometer size, which is extremely fine as compared with bacteria, and bacteria act as cracks or channels in the tube of an endoscope scope. Even if it invades and lurks in a part, it is possible to completely sterilize it by immersing it in all parts and contacting it.

【0033】従来の消毒剤・滅菌剤では、細菌が殺滅さ
れるとその死骸が残ってしまうが、本発明に採用してい
る光触媒性酸化チタンは死骸も分解する効果がある。
In the conventional disinfectant / sterilizer, when the bacteria are killed, the carcass remains, but the photocatalytic titanium oxide used in the present invention has an effect of decomposing the carcass.

【0034】洗浄液および複合溶液は、使用→回収→浄
化→再利用の循環サイクルシステムによりコストや資源
の節約に効果がある。
The cleaning liquid and the composite solution are effective in saving cost and resources by the circulation cycle system of use → recovery → purification → reuse.

【図面の簡単な説明】[Brief description of drawings]

【図1】医療機器に付着している病原微生物を不活化し
ている一例を示す図である。
FIG. 1 is a diagram showing an example in which pathogenic microorganisms attached to a medical device are inactivated.

【符号の説明】[Explanation of symbols]

1 医療機器 2 病原微生物 3 光触媒性酸化チタン 4 UV照射 5 UVランプ 6 UVランプ用光源 1 medical equipment 2 pathogenic microorganisms 3 Photocatalytic titanium oxide 4 UV irradiation 5 UV lamp 6 UV lamp light source

───────────────────────────────────────────────────── フロントページの続き (72)発明者 山口 英世 東京都八王子市大塚359 帝京大学医真菌 研究センタ− (72)発明者 小林 純一 静岡県袋井市豊沢2200番地2 静岡理工科 大学総合技術研究所 (72)発明者 時田 基文 静岡県静岡市本通七丁目9番地の9 有限 会社総合技研 (72)発明者 篠ケ谷 聰 静岡県静岡市本通七丁目9番地の9 有限 会社総合技研 (72)発明者 泉 田鶴 静岡県静岡市本通七丁目9番地の9 有限 会社総合技研 (72)発明者 赤石 啓 静岡県静岡市井宮町6番地の1 アカイシ ア−ルディ株式会社 (72)発明者 前田 明男 東京都新宿区西新宿3丁目9番5号 株式 会社エス・エス・ジェイ Fターム(参考) 4C058 AA12 AA13 AA14 AA15 AA16 AA17 BB02 BB06 BB07 BB09 CC02 CC06 CC07 JJ06 JJ07 JJ08 KK02    ─────────────────────────────────────────────────── ─── Continued front page    (72) Inventor Hideyo Yamaguchi             359 Otsuka, Hachioji-shi, Tokyo Teikyo University Medical Fungus             Research Center (72) Inventor Junichi Kobayashi             2200 Toyozawa, Fukuroi City, Shizuoka Prefecture 2 Shizuoka Science and Technology             University Institute of Technology (72) Inventor Motofumi Tokita             9 finite, 7-9 Hondori, Shizuoka City, Shizuoka Prefecture             Corporate Research Institute (72) Inventor Satoshi Shinogaya             9 finite, 7-9 Hondori, Shizuoka City, Shizuoka Prefecture             Corporate Research Institute (72) Inventor Izumi Tazuru             9 finite, 7-9 Hondori, Shizuoka City, Shizuoka Prefecture             Corporate Research Institute (72) Inventor Kei Akaishi             1 Akashi, 6-6 Imiya-cho, Shizuoka City, Shizuoka Prefecture             Ardy Co., Ltd. (72) Inventor Akio Maeda             3-9-5 Nishi-Shinjuku, Shinjuku-ku, Tokyo Stocks             Company SJ F-term (reference) 4C058 AA12 AA13 AA14 AA15 AA16                       AA17 BB02 BB06 BB07 BB09                       CC02 CC06 CC07 JJ06 JJ07                       JJ08 KK02

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 病原微生物が付着している医療機器を、
光触媒性酸化チタンと、硝酸とアルコ−ルを含む混合物
で構成された複合溶液に、浸漬させてなることを特徴と
する病原微生物を1分で不活化する部材と手段。
1. A medical device to which pathogenic microorganisms are attached,
A member and means for inactivating pathogenic microorganisms in 1 minute, which is characterized by being immersed in a composite solution composed of a photocatalytic titanium oxide, and a mixture containing nitric acid and alcohol.
【請求項2】 病原微生物が付着している医療機器を、
前記複合溶液に浸漬し、加振してなることを特徴とす
る、特許請求項1記載の病原微生物を1分で不活化する
部材と手段。
2. A medical device to which pathogenic microorganisms are attached,
The member and means for inactivating the pathogenic microorganisms according to claim 1, wherein the member and means are soaked in the composite solution and shaken.
【請求項3】 病原微生物が付着している医療機器を、
前記複合溶液に浸漬し、加振しながらUV照射してなる
ことを特徴とする、特許請求項1、2記載の病原微生物
を1分で不活化する部材と手段。
3. A medical device to which pathogenic microorganisms are attached,
The member and means for inactivating pathogenic microorganisms according to claim 1 or 2, wherein the member and means are soaked in the composite solution and irradiated with UV while vibrating.
【請求項4】 病原微生物が付着している医療機器を光
触媒性酸化チタンと硝酸とアルコ−ルを含む混合物で構
成された複合溶液に浸漬する工程、病原微生物が付着し
ている医療機器を前記複合溶液に浸漬し加振する工程、
病原微生物が付着している医療機器を前記複合溶液に浸
漬し加振しながらUV照射する工程、を含んでなること
を特徴とする病原微生物を1分で不活化する部材と手
段、及び医療機器の滅菌洗浄方法。
4. A step of immersing a medical device to which pathogenic microorganisms are attached in a composite solution composed of a mixture containing photocatalytic titanium oxide, nitric acid and alcohol, wherein the medical device to which pathogenic microorganisms are attached is said. A step of immersing in a composite solution and shaking,
A member and means for inactivating pathogenic microorganisms in 1 minute, and a step of immersing a medical device to which pathogenic microorganisms adhere in the composite solution and irradiating with UV while vibrating. Sterile cleaning method.
【請求項5】 特許請求項4記載の工程完了後、医療機
器の前記複合溶液を含む残存付着物を濯ぎ洗浄する工
程、医療機器の前記複合溶液を含む残存付着物を濯ぎ洗
浄で濡れた部分を乾燥する工程、医療機器の前記複合溶
液を含む残存付着物を濯ぎ洗浄で濡れた部分を乾燥させ
た後衛生的に保管する工程、を含んでなることを特徴と
する病原微生物を1分で不活化する部材と手段、及び医
療機器の滅菌洗浄方法。
5. A step of rinsing and washing residual deposits containing the composite solution of a medical device after completion of the step according to claim 4, a portion of the residual deposits of the medical device containing the complex solution being rinsed and washed. In a minute, and a step of storing residual deposits containing the composite solution of the medical device by rinsing and washing to dry the wet part and then storing the pathogenic microorganisms in 1 minute. Inactive member and means, and method for sterilizing and cleaning medical equipment.
JP2002149926A 2002-03-20 2002-05-24 Member and means for inactivating pathogenic microbe in one minute and sterilizing and washing method for medical device Pending JP2003339826A (en)

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JP2002077741 2002-03-20
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010214040A (en) * 2009-03-19 2010-09-30 Panasonic Corp Antibacterial treatment method

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010214040A (en) * 2009-03-19 2010-09-30 Panasonic Corp Antibacterial treatment method

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