KR102253875B1 - Antibacterial deodorant composition - Google Patents

Antibacterial deodorant composition Download PDF

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KR102253875B1
KR102253875B1 KR1020200173670A KR20200173670A KR102253875B1 KR 102253875 B1 KR102253875 B1 KR 102253875B1 KR 1020200173670 A KR1020200173670 A KR 1020200173670A KR 20200173670 A KR20200173670 A KR 20200173670A KR 102253875 B1 KR102253875 B1 KR 102253875B1
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antibacterial
weight
odors
complex
present
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Korean (ko)
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장래영
최창호
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(주)모테크바이오
최창호
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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N59/00Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/06Aluminium; Calcium; Magnesium; Compounds thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/44Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
    • A01N37/46N-acyl derivatives
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N59/00Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/16Heavy metals; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L9/00Disinfection, sterilisation or deodorisation of air
    • A61L9/01Deodorant compositions

Abstract

The present invention relates to an antibacterial deodorant composition that can provide immediate and continuous antibacterial and deodorizing functions by using a complex metal salt in which zinc chloride, manganese chloride and calcium chloride are combined, and a complex amino acid, and has excellent antibacterial effects against gram-positive bacteria and gram-negative bacteria as well as deodorizing power against basic odors, neutral odors and acid odors. The present invention includes 0.1 to 10% by weight of a complex metal salt, 0.05 to 1.5% by weight of a reducing agent compound, 0.01 to 10% by weight of a complex amino acid, 0.01 to 1.0 parts by weight of a pH adjuster, and the remainder of water.

Description

항균 탈취제 조성물{Antibacterial deodorant composition}Antibacterial deodorant composition}

본 발명은 염화아연, 염화망간 및 염화칼슘을 조합한 복합금속염과, 복합 아미노산을 함께 사용함으로써, 인체에 안전하며 즉각적이고 지속적인 항균 및 탈취 기능을 제공할 수 있으며, 그람양성균, 그람 음성균에 대한 항균효과는 물론 염기성 취기, 중성 취기 및 산성 취기에 대한 탈취력이 우수한 항균 탈취제 조성물에 관한 것이다.The present invention uses a combination of zinc chloride, manganese chloride, and calcium chloride together with a complex metal salt and a complex amino acid to provide safe, immediate and continuous antibacterial and deodorizing functions for the human body, and has antibacterial effects against gram-positive bacteria and gram-negative bacteria. Of course, it relates to an antibacterial deodorant composition having excellent deodorizing power for basic odor, neutral odor and acidic odor.

미생물 유기체들 중 일부는 사람이나 다른 포유동물에 식중독과 연쇄상구균 감염 등과 같은 여러가지 질병 및 질환을 일으킨다.Some of the microbial organisms cause a number of diseases and disorders in humans and other mammals, such as food poisoning and streptococcal infection.

일반적으로, 항균제로는 유기 항균제를 많이 사용하고 있는데, 이러한 유기 항균제들은 대부분 양이온을 함유하고 있어서 음이온성인 세균의 세포막을 교란 또는 파괴하거나, 세포 안으로 확산되어 대사장애를 일으키는 작용으로 세균들을 사멸시키는 효능을 발휘한다.In general, organic antibacterial agents are widely used as antimicrobial agents, but these organic antibacterial agents mostly contain cations, so they have the effect of destroying bacteria by disturbing or destroying the cell membrane of anionic bacteria or by spreading into cells to cause metabolic disorders. Exert.

이러한 유기 항균제로는 탄화수소, 페놀, 카본산류, 아민류, 제4급 암모늄화합물, 에폭시화합물, 아미드화합물 등의 물질이 사용되고 있다. 그러나 이러한 유기 항균제들은 그 내성 및 유해성 등으로 문제가 되어 부적합한 것으로 건강상에도 좋지 않은 영향을 미치는 것으로 의학상으로 보고되고 있다.As such organic antimicrobial agents, substances such as hydrocarbons, phenols, carbon acids, amines, quaternary ammonium compounds, epoxy compounds, and amide compounds are used. However, these organic antimicrobial agents are medically reported as being unsuitable because of their tolerance and harmfulness, and adversely affecting health.

살균 특성을 갖는 다수의 제재가 매우 오랫동안 공지되어 왔고 다양한 용도로 사용되고 있다. 현재 알려진 항박테리아 및 항 진균제는 아래 표와 같이 종류가 많으며, 제한적으로 사용되고 있다.A number of preparations having bactericidal properties have been known for a very long time and are used for various purposes. Currently known antibacterial and antifungal agents have many types as shown in the table below, and are used in a limited manner.

Figure 112020134924661-pat00001
Figure 112020134924661-pat00001

상기 표에서 알 수 있듯이 항 박테리아 및 항 진균 처리제는 대부분 양이온을 함유하고 있는 바, 이는 음이온성인 세균의 세포막을 교란 또는 파괴하거나 세포 안으로 확산해 들어가 대사 장애를 일으킴으로써 세균을 사멸시키게 된다.As can be seen from the above table, antibacterial and antifungal treatment agents mostly contain cations, which perturb or destroy cell membranes of anionic bacteria or diffuse into cells to cause metabolic disorders, thereby killing bacteria.

또한, 여러가지의 항균제가 제공되어 있는 바, 일반적으로 항균 작용이 강한 것일수록, 당연히 인축(人畜)에 대한 독성이 높고, 그로 인해 사용의 목적, 대상물, 범위 등이 한정되며, 사용자에게는 전문 지식이 요구되고, 강력한 항균 작용을 나타내는 것에 대해서는 누구나 편하게 사용할 수 있는 것이 아니었다. 따라서 안전하게 사용할 수 있는 항균제의 개발이 필요한 실정이다.In addition, various antibacterial agents are provided. In general, the stronger the antibacterial action is, the higher the toxicity to humans is, of course, the purpose, object, and scope of use are limited. What was required and showed strong antibacterial activity was not something that anyone could use comfortably. Therefore, it is necessary to develop an antimicrobial agent that can be used safely.

한편, 일상생활에서 냄새가 나는 요소는 다양한데, 대표적으로 음식물에서 발생하는 냄새, 의류, 신발 등에서 발생하는 냄새, 흡연으로 발생하는 담배 냄새, 다습한 환경에서 발생하는 곰팡이 냄새를 포함하는 복합적인 냄새 등이 있을 수 있는데, 이러한 악취의 주요 원인 물질로는 황화수소류, 암모니아, 유기산류, 메틸메르캅탄, 포름알데하이드, 아민류 등이 있다.On the other hand, there are various factors that cause odors in everyday life, including odors from food, odors from clothing, shoes, etc., tobacco odors from smoking, and complex odors including mold odors from humid environments. There may be, but the main causes of such odor include hydrogen sulfide, ammonia, organic acids, methyl mercaptan, formaldehyde, amines, and the like.

이러한 냄새 내지 악취를 제거하기 위해서 탈취제 내지 소취제가 다양하게 제공되고 있는데, 예를 들면, 취기(臭氣) 성분(악취물질)을 약품이나, 미생물, 광촉매 등을 이용하여 화학적으로 분해하거나, 또는 활성탄, 제오라이트(zeolite), 실리카겔(silica gel) 등을 이용하여 물리적으로 흡착하거나, 혹은 향료를 이용하여 마스킹하거나, 또는 화학 약품들을 사용하는 등 다종다양(多種多樣)한 방법을 이용한 것을 볼 수 있다.In order to remove such odors or odors, various deodorants and deodorants are provided. For example, chemically decomposing odor components (malodorous substances) using drugs, microorganisms, photocatalysts, etc., or activated carbon , Zeolite, silica gel, etc., physical adsorption, masking using fragrance, or using chemicals.

그러나 시판되는 대부분의 탈취제 내지 소취제는 화학 약품들을 사용하여 제조된 것이므로 인체에 유해성을 가진다.However, most of the commercially available deodorants or deodorants are manufactured using chemicals, so they are harmful to the human body.

또한, 탈취를 목적으로 하는 시판 제품들을 보면 유기성을 가진 액상의 스프레이 또는 방향성 제품이 대부분이며, 이들은 2차적으로 환경의 오염과 독성, 인체에의 유해성으로 논란이 되고 있다. 따라서 안전하게 사용할 수 있는 탈취제 내지 소취제의 개발이 필요한 실정이다.In addition, when looking at commercial products for the purpose of deodorization, liquid sprays or fragrance products with organic properties are mostly, and these are secondarily controversial for environmental pollution, toxicity, and harmfulness to the human body. Therefore, there is a need to develop deodorants or deodorants that can be used safely.

한편, 대한민국 등록특허 제10-1180117호에서는 아연금속염과 황 화합물과 환원제 및 안정제를 포함하는 항 박테리아 및 항 진균특성이 있는 티올 보호면을 갖는 황화아연 나노미립자, 유기 항균제, 니트로이미다졸, 킬레이트제로서 금속 포착성 관능기를 갖는 이미다졸-실란 반응생성물, 물 및 물 혼화성 용매를 포함하여 이루어짐을 특징으로 하는 항균,탈취제 조성물이 개시하고 있다.On the other hand, Korean Patent Registration No. 10-1180117 discloses zinc sulfide nanoparticles, organic antibacterial agents, nitroimidazoles, and chelating agents, which have antibacterial and antifungal properties, including zinc metal salts, sulfur compounds, reducing agents, and stabilizers. As an antibacterial and deodorant composition comprising an imidazole-silane reaction product having a metal trapping functional group, water and a water miscible solvent is disclosed.

상기 등록특허는 본 출원의 발명자가 개발한 것으로서 항균 성능 및 탈취 성능을 발휘하는 데 상당한 시간이 많이 걸린다는 점을 확인하였기에, 즉각적이고, 지속적인 항균 및 탈취 성능을 제공할 수 있고 인체에 안전한 항균 탈취제를 개발하게 되었다.The above registered patent was developed by the inventor of the present application, and it was confirmed that it takes a considerable amount of time to exhibit antibacterial and deodorant performance, so it is possible to provide immediate and continuous antibacterial and deodorant performance, and is an antibacterial deodorant that is safe for the human body. Was developed.

대한민국 등록특허 제10-1727864호Korean Patent Registration No. 10-1727864 대한민국 등록특허 제10-1180117호Korean Patent Registration No. 10-1180117 대한민국 등록특허 제10-1039043호Korean Patent Registration No. 10-1039043

이에 본 발명은 상기와 같은 문제점을 해결하기 위해 안출된 것으로서, 본 발명의 목적은 염화아연, 염화망간 및 염화칼슘을 조합한 복합금속염과, 복합 아미노산을 함께 사용함으로써, 인체에 안전하며 즉각적이고 지속적인 항균 및 탈취 기능을 제공할 수 있으며, 그람양성균, 그람 음성균에 대한 항균효과는 물론 염기성 취기, 중성 취기 및 산성 취기에 대한 탈취력이 우수한 항균 탈취제 조성물을 제공하는 것이다.Accordingly, the present invention was conceived to solve the above problems, and an object of the present invention is to use a combination of zinc chloride, manganese chloride and calcium chloride with a complex metal salt, and by using a complex amino acid, it is safe for the human body, and is immediately and persistently antibacterial. And it can provide a deodorizing function, as well as antibacterial effect against gram-positive bacteria and gram-negative bacteria, as well as to provide an antibacterial deodorant composition having excellent deodorizing power for basic, neutral and acidic odors.

본 발명의 해결하고자 하는 과제는 이상에서 언급된 것들에 한정되지 않으며, 언급되지 아니한 다른 해결과제들은 아래의 기재로부터 당업자에게 명확하게 이해되어 질 수 있을 것이다.The problem to be solved of the present invention is not limited to those mentioned above, and other problems that are not mentioned will be clearly understood by those skilled in the art from the following description.

상기한 목적을 달성하기 위하여 본 발명에 따른 항균 탈취제 조성물은 증류수 100g, 염화아연(ZnCl2) 2.41g, 염화망간4수화물(MnCl2·4H2O) 1.23g 및 염화칼슘2수화물(CaCl2·2H2O) 0.54g, 티오황산나트륨5수화물(Na2S2O3·5H2O) 0.5g, 테트라메틸렌디아민 0.12g, 인산디나트륨(Na2HPO4) 0.25g 및 시트르산 0.25g을 혼합한 혼합용액을 제조하는 제1단계;
상기 혼합용액을 65℃로 승온하여 60분 동안 환원반응을 진행하는 제2단계; 및
환원반응이 끝난 혼합용액을 17℃로 냉각시킨 다음, 환원반응이 끝난 혼합용액에 히스티딘(Histidine) 0.5g, 리신(L-Lysine) 0.5g, 글리신(Glycine) 0.5g, 디글리신(Diglycine) 0.5g을 첨가하는 제3단계;
를 포함하는 것을 특징으로 한다.
In order to achieve the above object, the antibacterial deodorant composition according to the present invention includes 100 g of distilled water, 2.41 g of zinc chloride (ZnCl 2 ), 1.23 g of manganese chloride tetrahydrate (MnCl 2 ·4H 2 O) and calcium chloride dihydrate (CaCl 2 ·2H). 2 O) 0.54 g, sodium thiosulfate pentahydrate (Na 2 S 2 O 3 ·5H 2 O) 0.5 g, tetramethylenediamine 0.12 g, disodium phosphate (Na 2 HPO 4 ) 0.25 g and citric acid 0.25 g mixed A first step of preparing a solution;
A second step of heating the mixed solution to 65° C. to perform a reduction reaction for 60 minutes; And
After cooling the mixed solution after the reduction reaction to 17℃, Histidine 0.5g, L-Lysine 0.5g, Glycine 0.5g, Diglycine 0.5g in the mixed solution after the reduction reaction a third step of adding g;
It characterized in that it comprises a.

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이상과 같은 구성의 본 발명에 따른 항균 탈취제 조성물은 염화아연, 염화망간 및 염화칼슘을 조합한 복합금속염과, 복합 아미노산을 함께 사용함으로써, 인체에 안전하며 즉각적이고 지속적인 항균 및 탈취 기능을 제공할 수 있으며, 그람양성균, 그람 음성균에 대한 항균효과는 물론 염기성 취기, 중성 취기 및 산성 취기에 대한 탈취력이 우수하다.The antibacterial deodorant composition according to the present invention having the above configuration can provide a safe, immediate and continuous antibacterial and deodorant function for the human body by using a combination metal salt of zinc chloride, manganese chloride and calcium chloride and a complex amino acid together. It has excellent antibacterial effect against gram-positive and gram-negative bacteria, as well as deodorizing power against basic, neutral and acidic odors.

본 발명의 항균 탈취 조성물은 섬유제품, 스프레이제품, 공조용필터, 에어컨필터, 방호복, 일회용 흡수용품, 부직포시트 등에 항균, 탈취 처리를 실시하기 위해서는, 더욱 안전한 배려를 필요로 하고, 또한 항균과 동시에 탈취 성능도 요구되는데, 이러한 경우라 하더라도 누구라도 인체에 안전하고 항균과 탈취의 양(兩) 작용을 함께 높은 차원으로 겸비한 항균, 탈취제 조성물을 적용할 수 있다.The antibacterial and deodorizing composition of the present invention requires more safe consideration in order to perform antibacterial and deodorant treatment on textile products, spray products, air conditioning filters, air conditioner filters, protective clothing, disposable absorbent articles, nonwoven sheets, etc., and at the same time as antibacterial. Deodorant performance is also required, and even in this case, anyone can apply an antibacterial and deodorant composition that is safe for the human body and has both antibacterial and deodorant positive effects at a high level.

본 발명의 효과는 이상에서 언급된 것들에 한정되지 않으며, 언급되지 아니한 다른 효과들은 아래의 기재로부터 당업자에게 명확하게 이해되어 질 수 있을 것이다.The effects of the present invention are not limited to those mentioned above, and other effects not mentioned will be clearly understood by those skilled in the art from the following description.

도 1 내지 도 3은 본 발명에 따른 항균 탈취제 조성물에 대한 세포독성시험, 항균 시험 및 탈취 시험 결과를 나타낸 시험성적서이다.1 to 3 are test reports showing the results of a cytotoxicity test, an antibacterial test, and a deodorant test for the antibacterial deodorant composition according to the present invention.

이하, 첨부 도면을 참조하여 본 발명의 실시 예를 상세히 설명하면 다음과 같다.Hereinafter, exemplary embodiments of the present invention will be described in detail with reference to the accompanying drawings.

본 발명을 설명함에 있어서, 관련된 공지기능 혹은 구성에 대한 구체적인 설명이 본 발명의 요지를 불필요하게 흐릴 수 있다고 판단되는 경우 그 상세한 설명은 생략한다. 또한, 후술되는 용어들은 본 발명에서의 기능을 고려하여 정의된 용어들로서 이는 사용자, 운용자의 의도 또는 판례 등에 따라 달라질 수 있다. 그러므로 그 정의는 본 명세서 전반에 걸친 내용을 토대로 내려져야 할 것이다.In describing the present invention, when it is determined that a detailed description of a related known function or configuration may unnecessarily obscure the subject matter of the present invention, a detailed description thereof will be omitted. In addition, terms to be described later are terms defined in consideration of functions in the present invention, which may vary according to the intentions or precedents of users or operators. Therefore, the definition should be made based on the contents throughout the present specification.

본 발명에 따른 항균 탈취제 조성물은 복합금속염 0.1~10중량%와, 환원제화합물 0.05~1.5중량%와, 복합 아미노산 0.01~10중량%와, pH조정제 0.01~1.0중량부와, 잔량으로서 물로 이루어지는 것을 예시할 수 있다.The antibacterial deodorant composition according to the present invention is composed of 0.1 to 10% by weight of a complex metal salt, 0.05 to 1.5% by weight of a reducing agent compound, 0.01 to 10% by weight of a complex amino acid, 0.01 to 1.0 parts by weight of a pH adjuster, and water as the balance. can do.

상기 복합금속염은 Mn, Zn, Ca, Na, Mg, K, Al의 염화물 중 적어도 2종이 선택되는 것을 예시할 수 있다. The composite metal salt may exemplify that at least two of chlorides of Mn, Zn, Ca, Na, Mg, K, and Al are selected.

예를 들어, 염화아연(ZnCl2), 염화망간(MnCl2) 및 염화칼슘(CaCl2)의 조합으로 이루어지는 것을 예시할 수 있다.For example, a combination of zinc chloride (ZnCl 2 ), manganese chloride (MnCl 2 ) and calcium chloride (CaCl 2 ) may be exemplified.

상기 염화아연(ZnCl2), 염화망간(MnCl2) 및 염화칼슘(CaCl2)의 조성비는 1 : 0.1~1 : 0.1~1이며, 보다 바람직하게는 1 : 0.4~0.6 : 0.1~0.3인 것을 예시할 수 있다.The composition ratio of the zinc chloride (ZnCl 2 ), manganese chloride (MnCl 2 ) and calcium chloride (CaCl 2 ) is 1: 0.1 to 1: 0.1 to 1, more preferably 1: 0.4 to 0.6: 0.1 to 0.3 can do.

상기 환원제화합물은 티오황산나트륨, 아황산나트륨, 메르캅토아세트산, EDTA염, 테트라메틸렌디아민 중 적어도 1종이 선택되는 것을 예시할 수 있다.The reducing agent compound may exemplify that at least one of sodium thiosulfate, sodium sulfite, mercaptoacetic acid, EDTA salt, and tetramethylenediamine is selected.

상기 복합아미노산은 복합금속나노미립자의 독성을 저독성으로 완화시키고 동시에 항균 및 탈취 기능을 갖는 것으로서, 리신(Lysine), 히스티딘(Histidine), 시스테인(Cystein), 디글리신(Diglycine), 아르기닌(Arginine), 알라닌(Alanine) 중 적어도 2종이 선택되는 것을 예시할 수 있다.The complex amino acids alleviate the toxicity of complex metal nanoparticles with low toxicity and at the same time have antibacterial and deodorizing functions, such as lysine, histidine, cysteine, diglycine, arginine, It may be exemplified that at least two types of alanine are selected.

상기 pH조정제는 인산디나트륨, 아세트산염, 시트르산 중 적어도 1종이 선택되는 것을 예시할 수 있다.The pH adjuster may exemplify that at least one of disodium phosphate, acetate, and citric acid is selected.

이하에서는 본 발명에 따른 항균 탈취제 조성물의 바람직한 실시예를 통해 보다 자세하게 설명한다.Hereinafter, it will be described in more detail through a preferred embodiment of the antibacterial deodorant composition according to the present invention.

비이커에 증류수 100g에 복합금속염으로서 염화아연(ZnCl2) 2.41g, 염화망간4수화물(MnCl2·4H2O) 1.23g 및 염화칼슘2수화물(CaCl2·2H2O) 0.54g과, 환원제 화합물로 티오황산나트륨5수화물(Na2S2O3·5H2O) 0.5g과, 테트라메틸렌디아민 0.12g과, pH조정제로 인산디나트륨(Na2HPO4) 0.25g과, 시트르산 0.25g을 투입한 후 마그네틱 교반기로 교반하여 1% 농도의 복합금속나노미립자 조성물을 제조하였다. Zinc chloride (ZnCl 2 ) 2.41 g, manganese chloride tetrahydrate (MnCl 2 ·4H 2 O) 1.23 g and calcium chloride dihydrate (CaCl 2 ·2H 2 O) 0.54 g as a complex metal salt in 100 g of distilled water in a beaker, and a reducing agent compound. After adding 0.5 g of sodium thiosulfate pentahydrate (Na 2 S 2 O 3 ·5H 2 O), 0.12 g of tetramethylenediamine , 0.25 g of disodium phosphate (Na 2 HPO 4 ) and 0.25 g of citric acid as a pH adjuster. Agitated with a magnetic stirrer to prepare a composite metal nanoparticle composition having a concentration of 1%.

그리고 상기 혼합용액을 65℃로 승온하여 60분 동안 환원반응을 진행시켰고, 환원반응이 끝난 혼합용액을 17℃로 냉각시킨 다음, 히스티딘(Histidine) 0.5g, 리신(L-Lysine) 0.5g, 글리신(Glycine) 0.5g, 디글리신(Diglycine) 0.5g을 투입하고 마그네틱 교반기로 교반하여 복합아미노산 함유 복합금속 나노미립자 혼합용액의 제조를 완료하였다.Then, the mixed solution was heated to 65°C to proceed with the reduction reaction for 60 minutes, and the mixed solution after the reduction reaction was cooled to 17°C, and then histidine 0.5g, L-Lysine 0.5g, and glycine. 0.5 g of (Glycine) and 0.5 g of diglycine were added and stirred with a magnetic stirrer to complete the preparation of a mixed solution of complex metal nanoparticles containing complex amino acids.

[시험예 1]세포독성시험[Test Example 1] Cytotoxicity test

실시예 1의 복합금속 나노미립자 조성물의 세포독성시험을 하였으며, 그 결과는 도 1에 나타난 바와 같이 독성이 없는 것으로 확인되었다.The cytotoxicity test of the composite metal nanoparticle composition of Example 1 was performed, and the results were confirmed to be non-toxic as shown in FIG. 1.

[시험예 2]항균 활성 실험[Test Example 2] Antibacterial activity test

1. 시편 제조1. Specimen preparation

(1) 상술한 실시예 1의 항균 성능 및 소취 성능을 확인하기 위해 실시예에서 제조한 복합금속 나노미립자 조성물 99.5g과 글리시독시프로필트리메톡시실란바인더 0.5g을 투입한 후 상온에서 교반하여 항균탈취 코팅액을 얻었다.(1) In order to confirm the antibacterial and deodorizing performance of Example 1, 99.5 g of the composite metal nanoparticle composition prepared in Example and 0.5 g of glycidoxypropyltrimethoxysilane binder were added, and then stirred at room temperature. An antibacterial and deodorizing coating solution was obtained.

(2) 폴리에스터 원단(120g/㎡) 10㎝×10㎝ 시편을 상기 코팅액에 침지한 후 원단 무게중량 70%의 pickup율로 탈수하고 80℃에서 5분간 열풍 건조한 시편을 제조하였다.(2) Polyester fabric (120g/m2) A 10cm×10cm specimen was immersed in the coating solution, dehydrated at a pickup rate of 70% by weight of the fabric, and dried with hot air at 80°C for 5 minutes to prepare a specimen.

2. 항균 활성 실험2. Antibacterial activity test

상기 시편에 대한 항균 활성 시험은 JIS L 1902:2015E에 의거하여 수행하였으며, 그 결과는 도 2에 나타난 바와 같이 대장균(Escherichia coli), 황색포도상구균(Staphylococcus aureus) 및 폐렴막대균(Klebsiella pneumoniae)의 감소율이 정균력과 살균력 항목에서 모두 99.9% 이상이라는 것을 확인할 수 있었다.The antimicrobial activity test for the specimen was performed according to JIS L 1902:2015E, and the results were as shown in FIG. 2 of Escherichia coli, Staphylococcus aureus, and Klebsiella pneumoniae. It was confirmed that the reduction rate was 99.9% or more in both the bacteriostatic and sterilizing power items.

실시예 1에서 복합금속염으로서 염화아연(ZnCl2) 1.82g, 염화망간4수화물(MnCl2·4H2O) 1.95g 및 염화칼슘2수화물(CaCl2·2H2O) 1.33g을 사용한 것을 제외하고 실시예 1과 동일한 방법으로 복합금속 나노미립자 조성물을 제조하였다.Except for using 1.82 g of zinc chloride (ZnCl 2 ), 1.95 g of manganese chloride tetrahydrate (MnCl 2 ·4H 2 O) and 1.33 g of calcium chloride dihydrate (CaCl 2 ·2H 2 O) as the composite metal salt in Example 1 A composite metal nanoparticle composition was prepared in the same manner as in Example 1.

실시예 1에서 복합금속염으로서 염화아연(ZnCl2) 1.25g, 염화망간4수화물(MnCl2·4H2O) 1.38g 및 염화칼슘2수화물(CaCl2·2H2O) 1.36g을 사용한 것을 제외하고 실시예 1과 동일한 방법으로 복합금속 나노미립자 조성물을 제조하였다.Except for the use of 1.25 g of zinc chloride (ZnCl 2 ), 1.38 g of manganese chloride tetrahydrate (MnCl 2 ·4H 2 O) and 1.36 g of calcium chloride dihydrate (CaCl 2 ·2H 2 O) as the composite metal salt in Example 1 A composite metal nanoparticle composition was prepared in the same manner as in Example 1.

[시험예 3]소취성 시험 1[Test Example 3] Deodorant test 1

1. 시편 제조1. Specimen preparation

(1) 상술한 실시예 1 내지 3의 항균 성능 및 소취 성능을 확인하기 위해 실시예 1 내지 3의 복합금속 나노미립자 조성물 99.5g과 글리시독시프로필트리메톡시실란바인더 0.5g을 투입한 후 상온에서 교반하여 항균탈취 코팅액을 얻었다. (1) In order to check the antibacterial and deodorant performance of Examples 1 to 3 described above, 99.5 g of the composite metal nanoparticle composition of Examples 1 to 3 and 0.5 g of glycidoxypropyltrimethoxysilane binder were added, and then at room temperature. Stirred at to obtain an antibacterial and deodorizing coating solution.

(2) 폴리에스터 원단(120g/㎡) 10㎝×10㎝ 시편을 상기 코팅액에 침지한 후 원단 무게중량 70%의 pickup율로 탈수하고 80℃에서 5분간 열풍 건조한 시편 1, 2, 3을 제조하였다.(2) Polyester fabric (120g/m²) 10cm×10cm specimens were immersed in the coating solution, dehydrated at a pickup rate of 70% by weight of the fabric, and dried with hot air at 80°C for 5 minutes to prepare specimens 1, 2, and 3 .

소취성 시험은 시편 1, 2, 3을 각각 5L의 테트라백에 넣고 초기 농도를 조정한 암모니아 가스 3L를 주입한 뒤 10분과 2시간 후의 암모니아 가스 농도를 검지관으로 측정하였으며, 그 결과는 아래 표 1에 기재하였다.For the deodorization test, specimens 1, 2, and 3 were placed in a 5L tetrabag, and 3L of ammonia gas adjusted to the initial concentration was injected, and the concentration of ammonia gas after 10 minutes and 2 hours was measured with a detection tube.The results are shown in the table below. It is described in 1.

구분division 시험결과(암모니아 가스)Test result (ammonia gas) 초기 농도(mg/kg)Initial concentration (mg/kg) 10분 후(mg/kg)After 10 minutes (mg/kg) 2시간 후(mg/kg)After 2 hours (mg/kg) 실시예 1Example 1 시료 1Sample 1 100100 1.81.8 00 감소율(%)Reduction rate (%) -- 98.298.2 99.999.9 실시예 2Example 2 시료 2Sample 2 100100 16.516.5 4.64.6 감소율(%)Reduction rate (%) -- 83.583.5 95.495.4 실시예 3Example 3 시료 sample 100100 18.118.1 8.88.8 감소율(%)Reduction rate (%) -- 81.981.9 91.291.2

소취성 시험은 시편 1, 2, 3을 각각 5L의 테트라백에 넣고 초기 농도를 조정한 황화수소 가스 3L를 주입한 뒤 10분과 2시간 후의 황화수소 가스 농도를 검지관으로 측정하였으며, 그 결과는 아래 표 2에 기재하였다.For the deodorization test, specimens 1, 2, and 3 were placed in a 5L tetrabag, and 3L of hydrogen sulfide gas adjusted to the initial concentration was injected, and the concentration of hydrogen sulfide gas after 10 minutes and 2 hours was measured with a detection tube.The results are shown in the table below. It is described in 2.

구분division 시험결과(황화수소 가스)Test result (hydrogen sulfide gas) 초기 농도(mg/kg)Initial concentration (mg/kg) 10분 후(mg/kg)After 10 minutes (mg/kg) 2시간 후(mg/kg)After 2 hours (mg/kg) 실시예 1Example 1 시료 1Sample 1 4.04.0 0.080.08 00 감소율(%)Reduction rate (%) -- 97.997.9 99.999.9 실시예 2Example 2 시료 2Sample 2 4.04.0 0.620.62 0.340.34 감소율(%)Reduction rate (%) -- 84.584.5 91.591.5 실시예 3Example 3 시료 sample 4.04.0 0.790.79 0.410.41 감소율(%)Reduction rate (%) -- 80.280.2 89.789.7

위 표 1 및 표 2에서 확인할 수 있는 바와 같이, 실시예 1은 2시간이 지난 후 암모니아 및 황화수소 가스의 감소율이 99.9%를 나타냈으며, 10분 후 암모니아 및 황화수소 가스의 감소율은 실시예 1이 실시예 2, 3에 비해 높았다.As can be seen in Tables 1 and 2 above, Example 1 showed a reduction rate of 99.9% of ammonia and hydrogen sulfide gas after 2 hours, and Example 1 showed a reduction rate of ammonia and hydrogen sulfide gas after 10 minutes. It was higher than in Examples 2 and 3.

[비교예 1] [ Comparative Example 1 ]

실시예 1에서 복합금속염으로서, 황산망간(MnSO4) 1.25g, 황산아연(ZnSO4) 1.38g, 황산칼슘(CaSO4) 1.36g을 사용한 것을 제외하고 실시예 1과 동일한 방법으로 복합금속 나노미립자 조성물을 제조하였다.Composite metal nanoparticles in the same manner as in Example 1 except that manganese sulfate (MnSO 4 ) 1.25 g, zinc sulfate (ZnSO 4 ) 1.38 g, and calcium sulfate (CaSO 4 ) 1.36 g were used as the composite metal salt in Example 1 The composition was prepared.

[비교예 2] [ Comparative Example 2 ]

실시예 1에서 복합금속염 대신 염화아연(ZnCl2) 3.9g을 단독 사용한 것을 제외하고 실시예 1과 동일한 방법으로 복합금속 나노미립자 조성물을 제조하였다.In Example 1, a composite metal nanoparticle composition was prepared in the same manner as in Example 1, except that 3.9 g of zinc chloride (ZnCl 2) was used alone instead of the composite metal salt.

[비교예 3] [ Comparative Example 3 ]

실시예 1에서 복합금속염 대신 염화망간4수화물(MnCl2·4H2O) 4.1g을 단독 사용한 것을 제외하고 실시예 1과 동일한 방법으로 복합금속 나노미립자 조성물을 제조하였다.In Example 1, a composite metal nanoparticle composition was prepared in the same manner as in Example 1, except that 4.1 g of manganese chloride tetrahydrate (MnCl 2 ·4H 2 O) was used alone instead of the composite metal salt.

[비교예 4] [ Comparative Example 4 ]

실시예 1에서 복합금속염 대신 염화칼슘2수화물(CaCl2·2H2O) 4.0g을 단독 사용한 것을 제외하고 실시예 1과 동일한 방법으로 복합금속 나노미립자 조성물을 제조하였다.In Example 1, a composite metal nanoparticle composition was prepared in the same manner as in Example 1, except that 4.0 g of calcium chloride dihydrate (CaCl 2 ·2H 2 O) was used alone instead of the composite metal salt.

[비교예 5] [ Comparative Example 5 ]

비교예 1에서 복합아미노산 대신 글리신(Glycine) 2g을 단독으로 사용한 것을 제외하고 실시예 1과 동일한 방법으로 복합금속 나노미립자 조성물을 제조하였다.In Comparative Example 1, a composite metal nanoparticle composition was prepared in the same manner as in Example 1, except that 2 g of glycine was used alone instead of the composite amino acid.

[비교예 6] [ Comparative Example 6 ]

비교예 1에서 복합아미노산인 히스티딘(Histidine), 리신(L-Lysine), 글리신(Glycine), 디글리신(Diglycine)을 모두 투입하지 않은 것을 제외하고 실시예 1과 동일한 방법으로 복합금속 나노미립자 조성물을 제조하였다.In Comparative Example 1, a composite metal nanoparticle composition was prepared in the same manner as in Example 1, except that all of the complex amino acids Histidine, L-Lysine, Glycine, and Diglycine were not added. Was prepared.

[시험예 3]소취성 시험 2[Test Example 3] Deodorant test 2

(1) 상술한 비교예 1 내지 6의 항균 성능 및 소취 성능을 확인하기 위해 비교예 1 내지 6의 복합금속 나노미립자 조성물 99.5g과 글리시독시프로필트리메톡시실란바인더 0.5g을 투입한 후 상온에서 교반하여 항균탈취 코팅액을 얻었다. (1) In order to confirm the antibacterial and deodorizing performance of Comparative Examples 1 to 6, 99.5 g of the composite metal nanoparticle composition of Comparative Examples 1 to 6 and 0.5 g of glycidoxypropyltrimethoxysilane binder were added, and then at room temperature. Stirred at to obtain an antibacterial and deodorizing coating solution.

(2) 폴리에스터 원단(120g/㎡) 10㎝×10㎝ 시편을 상기 코팅액에 침지한 후 원단 무게중량 70%의 pickup율로 탈수하고 80℃에서 5분간 열풍 건조한 시편 4 내지 9를 제조하였다.(2) Polyester fabric (120g/m2) 10cm×10cm specimens were immersed in the coating solution, then dehydrated at a pickup rate of 70% by weight of the fabric, and hot air dried specimens 4 to 9 were prepared at 80°C for 5 minutes.

소취성 시험은 시편 4 내지 9를 각각 5L의 테트라백에 넣고 초기 농도를 조정한 암모니아 가스 3L를 주입한 뒤 10분과 2시간 후의 암모니아 가스 농도를 검지관으로 측정하였으며, 그 결과는 아래 표 3에 기재하였다.In the deodorization test, specimens 4 to 9 were placed in a tetrabag of 5 L each, and 3 L of ammonia gas adjusted to the initial concentration was injected, and the concentration of ammonia gas after 10 minutes and 2 hours was measured with a detection tube, and the results are shown in Table 3 below. Written.

구분division 시험결과(암모니아 가스)Test result (ammonia gas) 초기 농도(mg/kg)Initial concentration (mg/kg) 10분 후(mg/kg)After 10 minutes (mg/kg) 2시간 후(mg/kg)After 2 hours (mg/kg) 비교예 1Comparative Example 1 시료 4Sample 4 100100 18.618.6 5.55.5 감소율(%)Reduction rate (%) -- 81.481.4 94.594.5 비교예 2Comparative Example 2 시료 5Sample 5 100100 38.738.7 24.924.9 감소율(%)Reduction rate (%) -- 61.361.3 75.175.1 비교예 3Comparative Example 3 시료 6Sample 6 100100 37.037.0 25.325.3 감소율(%)Reduction rate (%) -- 63.063.0 74.774.7 비교예 4Comparative Example 4 시료 7Sample 7 100100 40.140.1 28.828.8 감소율(%)Reduction rate (%) -- 59.959.9 71.271.2 비교예 5Comparative Example 5 시료 8Sample 8 100100 26.226.2 14.514.5 감소율(%)Reduction rate (%) -- 73.873.8 85.585.5 비교예 6Comparative Example 6 시료 9Sample 9 100100 71.871.8 57.457.4 감소율(%)Reduction rate (%) -- 28.228.2 42.642.6

위 표 2 및 표 3에서 확인할 수 있는 바와 같이, 비교예 1의 시료는 복합금속염으로 황산염을 사용한 경우 실시예 1 내지 3과 대비할 때 10분, 2시간 후 암모니아 농도 감소율이 줄어든다는 것을 확인할 수 있었다.As can be seen in Tables 2 and 3 above, it was confirmed that the ammonia concentration reduction rate decreased after 10 minutes and 2 hours when the sample of Comparative Example 1 used sulfate as the complex metal salt compared to Examples 1 to 3 .

그리고 비교예 2 내지 4의 시료는 복합금속염 대신 단독 염화염을 사용한 경우 실시예 1 내지 3 또는 비교예 1과 대비할 때 10분, 2시간 후 암모니아 농도 감소율이 크게 줄어든다는 것을 확인할 수 있었다.In addition, when the samples of Comparative Examples 2 to 4 used a single chloride salt instead of a complex metal salt, it was confirmed that the ammonia concentration reduction rate significantly decreased after 10 minutes and 2 hours as compared to Examples 1 to 3 or Comparative Example 1.

그리고 비교예 5의 시료는 비교예 1에서 복합아미노산 대신 단독 아미노산을 사용한 것인데, 비교예 1과 대비할 때 암모니가 가스가 줄어들었고, 비교예 6의 시료는 비교예 1에서 복합아미노산을 전혀 사용하지 않은 경우에는 비교예 중에서 암모니아 감소율이 가장 낮았다는 것을 확인할 수 있었다.In addition, the sample of Comparative Example 5 used a single amino acid instead of the complex amino acid in Comparative Example 1. When compared to Comparative Example 1, the ammonia gas was reduced, and the sample of Comparative Example 6 did not use the complex amino acid at all in Comparative Example 1. In the case, it was confirmed that the ammonia reduction rate was the lowest among the comparative examples.

이상에서 설명된 본 발명은 예시적인 것에 불과하며, 본 발명이 속한 기술분야의 통상의 지식을 가진 자라면 이로부터 다양한 변형 및 균등한 타 실시예가 가능하다는 점을 잘 알 수 있을 것이다. 그러므로 본 발명은 상기의 상세한 설명에서 언급되는 형태로만 한정되는 것은 아님을 잘 이해할 수 있을 것이다. 따라서 본 발명의 진정한 기술적 보호 범위는 첨부된 특허청구범위의 기술적 사상에 의해 정해져야 할 것이다. 또한, 본 발명은 첨부된 청구범위에 의해 정의되는 본 발명의 정신과 그 범위 내에 있는 모든 변형물과 균등물 및 대체물을 포함하는 것으로 이해되어야 한다.The present invention described above is merely exemplary, and those of ordinary skill in the art will appreciate that various modifications and other equivalent embodiments are possible therefrom. Therefore, it will be appreciated that the present invention is not limited to the form mentioned in the detailed description above. Therefore, the true technical protection scope of the present invention should be determined by the technical spirit of the appended claims. In addition, the present invention is to be understood as including the spirit of the present invention as defined by the appended claims and all modifications, equivalents and substitutes within the scope thereof.

Claims (6)

증류수 100g, 염화아연(ZnCl2) 2.41g, 염화망간4수화물(MnCl2·4H2O) 1.23g 및 염화칼슘2수화물(CaCl2·2H2O) 0.54g, 티오황산나트륨5수화물(Na2S2O3·5H2O) 0.5g, 테트라메틸렌디아민 0.12g, 인산디나트륨(Na2HPO4) 0.25g 및 시트르산 0.25g을 혼합한 혼합용액을 제조하는 제1단계;
상기 혼합용액을 65℃로 승온하여 60분 동안 환원반응을 진행하는 제2단계; 및
환원반응이 끝난 혼합용액을 17℃로 냉각시킨 다음, 환원반응이 끝난 혼합용액에 히스티딘(Histidine) 0.5g, 리신(L-Lysine) 0.5g, 글리신(Glycine) 0.5g, 디글리신(Diglycine) 0.5g을 첨가하는 제3단계;
를 포함하는 것을 특징으로 하는 항균 탈취제 조성물 제조방법.
Distilled water 100 g, zinc chloride (ZnCl 2 ) 2.41 g, manganese chloride tetrahydrate (MnCl 2 ·4H 2 O) 1.23 g and calcium chloride dihydrate (CaCl 2 ·2H 2 O) 0.54 g, sodium thiosulfate pentahydrate (Na 2 S 2 O 3 · 5H 2 O) 0.5g, tetramethylenediamine 0.12g, disodium phosphate (Na 2 HPO 4 ) 0.25g and a first step of preparing a mixed solution of the citric acid 0.25g;
A second step of heating the mixed solution to 65° C. to perform a reduction reaction for 60 minutes; And
After cooling the mixed solution after the reduction reaction to 17℃, Histidine 0.5g, L-Lysine 0.5g, Glycine 0.5g, Diglycine 0.5g in the mixed solution after the reduction reaction a third step of adding g;
Antibacterial deodorant composition manufacturing method comprising a.
청구항 1의 방법으로 제조된 것을 특징으로 하는 항균 탈취제 조성물.Antibacterial deodorant composition, characterized in that prepared by the method of claim 1. 삭제delete 삭제delete 삭제delete 삭제delete
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