KR102672416B1 - Novel peptide with antibacterial and anticancer efficacy against multidrug-resistant pathogens - Google Patents
Novel peptide with antibacterial and anticancer efficacy against multidrug-resistant pathogens Download PDFInfo
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- KR102672416B1 KR102672416B1 KR1020230149140A KR20230149140A KR102672416B1 KR 102672416 B1 KR102672416 B1 KR 102672416B1 KR 1020230149140 A KR1020230149140 A KR 1020230149140A KR 20230149140 A KR20230149140 A KR 20230149140A KR 102672416 B1 KR102672416 B1 KR 102672416B1
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- peptide
- present
- antibacterial
- sapb
- acid
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- MECHNRXZTMCUDQ-RKHKHRCZSA-N vitamin D2 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)/C=C/[C@H](C)C(C)C)=C\C=C1\C[C@@H](O)CCC1=C MECHNRXZTMCUDQ-RKHKHRCZSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
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- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
- C07K14/36—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Actinomyces; from Streptomyces (G)
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/142—Amino acids; Derivatives thereof
- A23K20/147—Polymeric derivatives, e.g. peptides or proteins
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/17—Amino acids, peptides or proteins
- A23L33/18—Peptides; Protein hydrolysates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/005—Antimicrobial preparations
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2200/00—Function of food ingredients
- A23V2200/30—Foods, ingredients or supplements having a functional effect on health
- A23V2200/324—Foods, ingredients or supplements having a functional effect on health having an effect on the immune system
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A40/00—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
- Y02A40/70—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in livestock or poultry
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
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Abstract
본 발명의 발명자들은 직접 분리한 방선균 Micromonospora sp. 10종의 유전체에서 공통적으로 SapB peptide(lantipeptide)가 존재하는 것을 확인하였고, 서로 다른 지역과 생물에서 분리한 방선균에서 공통적인 유전자가 발견되어 연구를 시작하게 되었다. Lantipeptide는 항생 펩타이드로서 많이 알려져 있고 실제 상업적으로 이용되고 있는데(예 - 니신; nisin), SapB peptide는 연구가 미비한 현실이다. 이는 SapB peptide는 서로 응집하고 물에 잘 녹지 않는 성질이 있어 항생 효능을 평가하기 어려워 연구진행이 어렵기 때문이다. 따라서, 본 발명에서는 SapB peptide의 응집/비친수성 성질이 항생효능에 영향을 미친 것인지를 알아보기 위해 연구를 시작하게 되었고, 그 결과 신규의 SapB peptide를 개발하였고 이의 항생 및 암세포 생장억제 효능을 확인하여 본 발명을 완성하였다. 본 연구결과의 서열을 기반으로 더 증진된 생리활성 소재로 개발이 가능할 것이다.The inventors of the present invention directly isolated the actinomycete Micromonospora sp. The common presence of SapB peptide (lantipeptide) was confirmed in the genomes of 10 species, and a common gene was discovered in actinomycetes isolated from different regions and organisms, leading to research. Lantipeptide is widely known as an antibiotic peptide and is actually used commercially (e.g. nisin), but research on SapB peptide is insufficient. This is because SapB peptides tend to aggregate together and do not dissolve well in water, making it difficult to evaluate their antibiotic efficacy and conducting research. Therefore, in the present invention, we began research to determine whether the aggregation/non-hydrophilic nature of SapB peptide affected the antibiotic efficacy. As a result, we developed a new SapB peptide and confirmed its antibiotic and cancer cell growth inhibitory efficacy. The present invention has been completed. Based on the sequence of this research result, it will be possible to develop a more improved bioactive material.
Description
본 발명은 다제내성병원균에 대한 항균 및 항암 효능을 갖는 신규 펩타이드에 관한 것이다.The present invention relates to a novel peptide with antibacterial and anticancer efficacy against multidrug-resistant pathogens.
본 발명의 발명자들은 직접 분리한 방선균 Micromonospora sp. 10종의 유전체에서 공통적으로 SapB peptide(lantipeptide)가 존재하는 것을 확인하였고, 서로 다른 지역과 생물에서 분리한 방선균에서 공통적인 유전자가 발견되어 연구를 시작하게 되었다. Lantipeptide는 항생 펩타이드로서 많이 알려져 있고 실제 상업적으로 이용되고 있는데(예 - 니신; nisin), SapB peptide는 연구가 미비한 현실이다. 이는 SapB peptide는 서로 응집하고 물에 잘 녹지 않는 성질이 있어 항생 효능을 평가하기 어려워 연구진행이 어렵기 때문이다. 따라서, 본 발명에서는 SapB peptide의 응집/비친수성 성질이 항생효능에 영향을 미친 것인지를 알아보기 위해 연구를 시작하게 되었고, 그 결과 신규의 SapB peptide를 개발하였고 이의 항생 및 암세포 생장억제 효능을 확인하여 본 발명을 완성하였다. 본 연구결과의 서열을 기반으로 더 증진된 생리활성 소재로 개발이 가능할 것이다.The inventors of the present invention directly isolated the actinomycete Micromonospora sp. The common presence of SapB peptide (lantipeptide) was confirmed in the genomes of 10 species, and a common gene was discovered in actinomycetes isolated from different regions and organisms, leading to research. Lantipeptide is widely known as an antibiotic peptide and is actually used commercially (e.g. nisin), but research on SapB peptide is insufficient. This is because SapB peptides tend to aggregate together and do not dissolve well in water, making it difficult to evaluate their antibiotic efficacy and conducting research. Therefore, in the present invention, we began research to determine whether the aggregation/non-hydrophilic nature of SapB peptide affected the antibiotic efficacy. As a result, we developed a new SapB peptide and confirmed its antibiotic and cancer cell growth inhibitory efficacy. The present invention has been completed. Based on the sequence of this research result, it will be possible to develop a more improved bioactive material.
더욱 구체적으로는 본 발명의 신규 펩타이드 개발을 위해 SapB의 구조적 특성은 유지하되, 아미노산 서열을 변경하여 합성을 하였으며 다제내성균에 항균 효능이 있는 것을 확인하였다. 특히 항균 효능은 제어가 어려운 다제내성병원균(대장균, 녹농균, 바실루스 세레우스 및 황색포도상구균)을 대상으로 평가하였으며 그람양성 및 그람음성에 광범위한 항균 효능을 나타냄을 확인하였다. 이외에도 개량된 신규 펩타이드 들은 암세포(간암, 대장암, 폐암, 유방암 및 흑색종암)의 생장억제 효능을 나타내었다. 즉 기존 lantipeptide는 합성이 불가능하여 생합성으로 생산하지만, 본 연구의 개량된 신규 펩타이드는 합성이 매우 용이하고, 서열이 짧아 생산비용이 매우 경제적이다.More specifically, in order to develop a new peptide of the present invention, the structural characteristics of SapB were maintained, but the amino acid sequence was changed and synthesized, and it was confirmed that it has antibacterial effect against multidrug-resistant bacteria. In particular, the antibacterial efficacy was evaluated against multidrug-resistant pathogens that are difficult to control (E. coli, Pseudomonas aeruginosa, Bacillus cereus, and Staphylococcus aureus), and it was confirmed that it exhibits a wide range of antibacterial efficacy against Gram-positive and Gram-negative bacteria. In addition, the new improved peptides showed growth inhibitory effects on cancer cells (liver cancer, colon cancer, lung cancer, breast cancer, and melanoma cancer). In other words, existing lantipeptides cannot be synthesized and are produced through biosynthesis, but the improved new peptide in this study is very easy to synthesize and has a short sequence, making production costs very economical.
또한 Lantipeptide는 양쪽성으로 적혈구에 높은 용혈(hemolysis)를 나타낼 수 있지만, 개량된 본 발명의 신규 펩타이드 들은 높은 농도에서도 낮은(평균 5%미만) hemolysis를 나타내었다.In addition, lantipeptide is amphiphilic and can exhibit high hemolysis in red blood cells, but the improved new peptides of the present invention showed low hemolysis (less than 5% on average) even at high concentrations.
따라서, 본 발명의 신규 펩타이드 들은 다제내성병원균에 항균 효능을 나타내고, 암세포에 생장억제 효능을 나타내며, 합성이 훨씬 간단하여 생산이 쉽고, 기존 서열 대비 평균 50% 이상 짧아 합성 비용이 경제적이어서 산업에 이용하기 더 용이할 것으로 판단된다. 본 연구는 SapB peptide의 항생, 암세포 생장억제효능을 처음 확인한 사례이며, 본 연구결과의 서열을 기반으로 더 증진된 생리활성 소재로 개발이 가능할 것이다.Therefore, the new peptides of the present invention exhibit antibacterial efficacy against multi-drug-resistant pathogens and growth inhibitory efficacy against cancer cells, are much simpler to synthesize, are easy to produce, and are shorter than existing sequences by more than 50% on average, so the synthesis cost is economical, so they can be used in industry. It is thought to be easier to do. This study is the first to confirm the antibiotic and cancer cell growth inhibitory effects of SapB peptide, and it will be possible to develop an improved bioactive material based on the sequence of this study result.
상기 문제점을 해결하기 본 발명의 일 과제는 다제내성병원균에 대한 항균 또는 항암 효능을 갖는 신규 펩타이드를 제공하는 데 있다.To solve the above problems, one object of the present invention is to provide a novel peptide with antibacterial or anticancer efficacy against multidrug-resistant pathogens.
상기 문제점을 해결하기 본 발명의 일 과제는 상기 신규 펩타이드를 유효성분으로 포함하는 항균 또는 항암용 약학 조성물을 제공하는 데 있다.One object of the present invention to solve the above problems is to provide an antibacterial or anticancer pharmaceutical composition containing the novel peptide as an active ingredient.
상기 문제점을 해결하기 본 발명의 일 과제는 상기 신규 펩타이드를 유효성분으로 포함하는 항균용 의약외품 조성물, 화장료 조성물, 농축산 사료 조성물 또는 건강기능식품 조성물을 제공하는 데 있다.One object of the present invention to solve the above problems is to provide an antibacterial quasi-drug composition, cosmetic composition, agricultural and livestock feed composition, or health functional food composition containing the novel peptide as an active ingredient.
상기와 같은 목적을 달성하기 위해, 본 발명은 XCRAXLLC로 표시되는 아미노산 서열로 이루어진 항균 또는 항암 활성을 가지는 신규 펩타이드에서, 상기 아미노산 서열 중 X는 R, K 또는 H인 것을 특징으로 하는, 신규펩타이드를 제공한다.In order to achieve the above object, the present invention provides a novel peptide having antibacterial or anticancer activity consisting of an amino acid sequence represented by XCRAXLLC, wherein X in the amino acid sequence is R, K or H. to provide.
본 발명의 일 실시예에 있어서, 상기 "펩타이드"는 SapB 펩타이드의 응집문제를 개선시키고, 합성이 가능하도록 개량한 것을 특징으로 할 수 있으나 이에 한정되는 것은 아니다.In one embodiment of the present invention, the “peptide” may be improved to improve the aggregation problem of the SapB peptide and enable synthesis, but is not limited thereto.
본 발명의 일 실시예에 있어서, 상기 "펩타이드"는 서열번호 1, 서열번호 2 또는 서열번호 3의 아미노산 서열로 이루어진 각각의 펩타이드인 것을 특징으로 할 수 있으나 이에 한정되는 것은 아니다.In one embodiment of the present invention, the “peptide” may be characterized as each peptide consisting of the amino acid sequence of SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3, but is not limited thereto.
본 발명의 일 실시예에 있어서, 상기 "펩타이드"는 다제내성병원균에 대한 항균 효능을 가지는 것일 수 있다.In one embodiment of the present invention, the “peptide” may have antibacterial effect against multi-drug resistant pathogens.
본 발명의 일 실시예에 있어서, 상기 "다제내성병원균"은 대장균, 녹농균, 바실루스 세레우스 또는 황색포도상구균일 수 있다.In one embodiment of the present invention, the “multi-drug-resistant pathogen” may be Escherichia coli, Pseudomonas aeruginosa, Bacillus cereus, or Staphylococcus aureus.
본 발명의 일 실시예에 있어서, 상기 "펩타이드"는 항암 효능을 가지는 것일 수 있다.In one embodiment of the present invention, the “peptide” may have anti-cancer efficacy.
본 발명의 일 실시예에 있어서, 상기 "항암"은 간암, 대장암, 폐암, 유방암 또는 흑색종암에 항암 효능을 가지는 것일 수 있다.In one embodiment of the present invention, the “anticancer” may have anticancer efficacy against liver cancer, colon cancer, lung cancer, breast cancer, or melanoma cancer.
본 발명의 일 실시예에 있어서, 상기 "펩타이드"는 SapB 펩타이드의 응집문제를 개선시키고, 합성이 가능하도록 개량한 것이며, 낮은 용혈률을 나타내어 저독성인 것일 수 있다.In one embodiment of the present invention, the “peptide” is improved to improve the aggregation problem of the SapB peptide and enable synthesis, and may have a low hemolysis rate and thus be low toxic.
또한, 상기와 같은 목적을 달성하기 위해, 본 발명은 상기 신규 펩타이드를 유효성분으로 포함하는 항균 또는 항암용 약학 조성물을 제공한다.Additionally, in order to achieve the above object, the present invention provides an antibacterial or anticancer pharmaceutical composition containing the novel peptide as an active ingredient.
또한, 상기와 같은 목적을 달성하기 위해, 본 발명은 상기 신규 펩타이드를 유효성분으로 포함하는 항균용 의약외품 조성물을 제공한다.In addition, in order to achieve the above object, the present invention provides an antibacterial quasi-drug composition containing the novel peptide as an active ingredient.
또한, 상기와 같은 목적을 달성하기 위해, 본 발명은 상기 신규 펩타이드를 유효성분으로 포함하는 항균용 화장료 조성물을 제공한다.Additionally, in order to achieve the above object, the present invention provides an antibacterial cosmetic composition containing the novel peptide as an active ingredient.
또한, 상기와 같은 목적을 달성하기 위해, 본 발명은 상기 신규 펩타이드를 유효성분으로 포함하는 항균용 농축산 사료 조성물을 제공한다.In addition, in order to achieve the above object, the present invention provides an antibacterial concentrated acid feed composition containing the novel peptide as an active ingredient.
마지막으로, 상기와 같은 목적을 달성하기 위해, 본 발명은 상기 신규 펩타이드를 유효성분으로 포함하는 항균용 건강기능식품 조성물을 제공한다.Finally, in order to achieve the above object, the present invention provides an antibacterial health functional food composition containing the novel peptide as an active ingredient.
본 발명의 발명자들은 직접 분리한 방선균 Micromonospora sp. 10종의 유전체에서 공통적으로 SapB peptide(lantipeptide)가 존재하는 것을 확인하였고, 서로 다른 지역과 생물에서 분리한 방선균에서 공통적인 유전자가 발견되어 연구를 시작하게 되었다. Lantipeptide는 항생 펩타이드로서 많이 알려져 있고 실제 상업적으로 이용되고 있는데(예 - 니신; nisin), SapB peptide는 연구가 미비한 현실이다. 이는 SapB peptide는 서로 응집하고 물에 잘 녹지 않는 성질이 있어 항생 효능을 평가하기 어려워 연구진행이 어렵기 때문이다. 따라서, 본 발명에서는 SapB peptide의 응집/비친수성 성질이 항생효능에 영향을 미친 것인지를 알아보기 위해 연구를 시작하게 되었고, 그 결과 신규의 SapB peptide를 개발하였고 이의 항생 및 암세포 생장억제 효능을 확인하여 본 발명을 완성하였다. 본 연구결과의 서열을 기반으로 더 증진된 생리활성 소재로 개발이 가능할 것이다.The inventors of the present invention directly isolated the actinomycete Micromonospora sp. The common presence of SapB peptide (lantipeptide) was confirmed in the genomes of 10 species, and a common gene was discovered in actinomycetes isolated from different regions and organisms, leading to research. Lantipeptide is widely known as an antibiotic peptide and is actually used commercially (e.g. nisin), but research on SapB peptide is insufficient. This is because SapB peptides tend to aggregate together and do not dissolve well in water, making it difficult to evaluate their antibiotic efficacy and conducting research. Therefore, in the present invention, we began research to determine whether the aggregation/non-hydrophilic nature of SapB peptide affected the antibiotic efficacy. As a result, we developed a new SapB peptide and confirmed its antibiotic and cancer cell growth inhibitory efficacy. The present invention has been completed. Based on the sequence of this research result, it will be possible to develop a more improved bioactive material.
도 1은 본 발명의 일 실시예에 있어서, SapB 펩타이드 원서열을 나타낸 도이다.
도 2는 본 발명의 일 실시예에 있어서, 본 발명의 신규 펩타이드 서열번호 1의 화학식을 나타낸 도이다.
도 3은 본 발명의 일 실시예에 있어서, 본 발명의 신규 펩타이드 서열번호 2의 화학식을 나타낸 도이다.
도 4는 본 발명의 일 실시예에 있어서, 본 발명의 신규 펩타이드 서열번호 3의 화학식을 나타낸 도이다.
도 5는 본 발명의 일 실시예에 있어서, 본 발명의 신규 펩타이드 서열번호 1, 2 및 3의 용혈비율을 나타낸 도이다.Figure 1 is a diagram showing the original sequence of SapB peptide in one embodiment of the present invention.
Figure 2 is a diagram showing the chemical formula of the novel peptide SEQ ID NO: 1 of the present invention, in one embodiment of the present invention.
Figure 3 is a diagram showing the chemical formula of the novel peptide SEQ ID NO: 2 of the present invention in one embodiment of the present invention.
Figure 4 is a diagram showing the chemical formula of the novel peptide SEQ ID NO: 3 of the present invention in one embodiment of the present invention.
Figure 5 is a diagram showing the hemolysis rate of the novel peptide SEQ ID NOs: 1, 2, and 3 of the present invention in one embodiment of the present invention.
이하, 첨부된 도면을 참조하여 본 발명의 구현예로 본 발명을 상세히 설명하기로 한다. 다만, 하기 구현 예는 본 발명에 대한 예시로 제시되는 것으로, 당업자에게 주지 저명한 기술 또는 구성에 대한 구체적인 설명이 본 발명의 요지를 불필요하게 흐릴 수 있다고 판단되는 경우에는 그 상세한 설명을 생략할 수 있고, 이에 의해 본 발명이 제한되지는 않는다. 본 발명은 후술하는 특허 청구범위의 기재 및 그로부터 해석되는 균등 범주 내에서 다양한 변형 및 응용이 가능하다.Hereinafter, the present invention will be described in detail through embodiments of the present invention with reference to the attached drawings. However, the following implementation examples are provided as examples of the present invention, and if it is judged that a detailed description of a technology or configuration well known to those skilled in the art may unnecessarily obscure the gist of the present invention, the detailed description may be omitted. , the present invention is not limited thereby. The present invention is capable of various modifications and applications within the description of the patent claims described below and the scope of equivalents interpreted therefrom.
또한, 본 명세서에서 사용되는 용어(Terminology)들은 본 발명의 바람직한 실시 예를 적절히 표현하기 위해 사용된 용어들로서, 이는 사용자, 운용자의 의도 또는 본 발명이 속하는 분야의 관례 등에 따라 달라질 수 있다. 따라서 본 용어들에 대한 정의는 본 명세서 전반에 걸친 내용을 토대로 내려져야 할 것이다. 명세서 전체에서, 어떤 부분이 어떤 구성요소를 "포함"한다고 할 때, 이는 특별히 반대되는 기재가 없는 한 다른 구성요소를 제외하는 것이 아니라 다른 구성 요소를 더 포함할 수 있는 것을 의미한다.In addition, terminology used in this specification is a term used to appropriately express preferred embodiments of the present invention, and may vary depending on the intention of the user or operator or the customs of the field to which the present invention belongs. Therefore, definitions of these terms should be made based on the content throughout this specification. Throughout the specification, when a part "includes" a certain component, this means that it may further include other components rather than excluding other components, unless specifically stated to the contrary.
본 명세서 전체에 걸쳐, 특정 물질의 농도를 나타내기 위하여 사용되는 '%'는 별도의 언급이 없는 경우, 고체/고체는 (w/w) %, 고체/액체는 (w/v) %, 그리고 액체/액체는 (v/v) %이다.Throughout this specification, '%' used to indicate the concentration of a specific substance is (w/w) % for solid/solid, (w/v) % for solid/liquid, and Liquid/Liquid is (v/v) %.
일 측면에서, 본 발명은 SapB 펩타이드를 개량한 신규 펩타이드를 제공하는 것이다.In one aspect, the present invention provides a new peptide that is an improved version of the SapB peptide.
본 발명의 "신규 펩타이드"는 제어가 어려운 다양한 다제내성병원균(대장균, 녹농균, 바실루스 세레우스 및 황색포도상구균)에 뛰어난 항균 효능을 가지므로, 화장료 조성물, 의약외품 조성물, 약학 조성물, 농축산 사료 조성물 또는 건강기능식품 조성물 로 사용될 수 있다.The "novel peptide" of the present invention has excellent antibacterial efficacy against various multi-drug resistant pathogens (E. coli, Pseudomonas aeruginosa, Bacillus cereus and Staphylococcus aureus) that are difficult to control, and is therefore useful in cosmetic compositions, quasi-drug compositions, pharmaceutical compositions, agricultural and livestock feed compositions or health products. It can be used as a functional food composition.
본 발명의 "신규 펩타이드"는 다양한 암세포(간암, 대장암, 폐암, 유방암 및 흑색종암)에 뛰어난 생장억제 효능을 가지므로, 약학 조성물로 사용될 수 있다.The “novel peptide” of the present invention has excellent growth inhibitory effects on various cancer cells (liver cancer, colon cancer, lung cancer, breast cancer, and melanoma cancer), so it can be used as a pharmaceutical composition.
일 측면에서, 본 발명은 화장료 조성물로 이용될 수 있다.In one aspect, the present invention can be used as a cosmetic composition.
본 발명의 신규 펩타이드는 항균 효능을 나타내기 위한 제품으로 다양하게 이용될 수 있다. 본 조성물을 첨가할 수 있는 제품으로는, 예를 들어, 각종 크림, 로션, 스킨, 에센스 등과 같은 화장품류와 샴푸, 린스, 클렌징, 세안제, 비누, 트리트먼트, 팩, 미용액 등이 있다.The novel peptide of the present invention can be used in a variety of products to exhibit antibacterial efficacy. Products to which this composition can be added include, for example, cosmetics such as various creams, lotions, skins, and essences, as well as shampoos, rinses, cleansers, face washes, soaps, treatments, packs, and beauty essences.
본 발명의 화장료 조성물은 수용성 비타민, 유용성 비타민, 고분자 펩티드, 고분자 다당, 스핑고 지질 및 해초 추출물로 이루어진 군에서 선택된 조성물을 포함할 수 잇다.The cosmetic composition of the present invention may include a composition selected from the group consisting of water-soluble vitamins, oil-soluble vitamins, high molecular weight peptides, high molecular weight polysaccharides, sphingolipids, and seaweed extracts.
이때 수용성 비타민으로서는 화장품에 배합 가능한 것이라면 어떠한 것이라도 되지만, 바람직하게는 비타민 B1, 비타민 B2, 비타민 B6, 피리독신, 염산피리독신, 비타민 B12, 판토텐산, 니코틴산, 니코틴산아미드, 엽산, 비타민 C, 비타민 H 등을 들 수 있으며, 그들의 염 (티아민염산염, 아스코르빈산나트륨염 등)이나 유도체 (아스코르빈산-2-인산나트륨염, 아스코르빈산-2-인산마그네슘염 등)도 본 발명에서 사용할 수 있는 수용성 비타민에 포함된다. 수용성 비타민은 미생물 변환법, 미생물의 배양물로부터의 정제법, 효소법 또는 화학 합성법 등의 통상의 방법에 의해 수득할 수 있다.At this time, any water-soluble vitamin may be used as long as it can be mixed in cosmetics, but preferably vitamin B1, vitamin B2, vitamin B6, pyridoxine, pyridoxine hydrochloride, vitamin B12, pantothenic acid, nicotinic acid, nicotinic acid amide, folic acid, vitamin C, vitamin H, etc. and their salts (thiamine hydrochloride, sodium ascorbate, etc.) or derivatives (sodium ascorbic acid-2-phosphate, magnesium ascorbic acid-2-phosphate, etc.) are water-soluble vitamins that can be used in the present invention. included in Water-soluble vitamins can be obtained by conventional methods such as microbial transformation, purification from microbial cultures, enzymatic methods, or chemical synthesis.
유용성 비타민으로서는 화장품에 배합 가능한 것이라면 어떠한 것이라도 되지만, 바람직하게는 비타민 A, 카로틴, 비타민 D2, 비타민 D3, 비타민 E (d1-알파 토코페롤, d-알파 토코페롤, d-알파 토코페롤) 등을 들 수 있으며, 그들의 유도체(팔미틴산아스코르빈, 스테아르산아스코르빈, 디팔미틴산아스코르빈, 아세트산dl-알파 토코페롤, 니코틴산dl-알파 토코페롤비타민 E, DL-판토테닐알코올, D-판토테닐알코올, 판토테닐에틸에테르 등) 등도 본 발명에서 사용되는 유용성 비타민에 포함된다. 유용성 비타민은 미생물 변환법, 미생물의 배양물로부터의 정제법, 효소 또는 화학 합성법 등의 통상의 방법에 의해 취득할 수 있다.Oil-soluble vitamins may be any that can be mixed into cosmetics, but preferably include vitamin A, carotene, vitamin D2, vitamin D3, vitamin E (d1-alpha tocopherol, d-alpha tocopherol, d-alpha tocopherol), etc. , their derivatives (ascorbine palmitate, ascorbine stearate, ascorbine dipalmitate, dl-alpha tocopherol acetate, dl-alpha tocopherol nicotinate, vitamin E, DL-pantothenyl alcohol, D-pantothenyl alcohol, pantothenyl ethyl ether, etc.) are also included in the oil-soluble vitamins used in the present invention. Oil-soluble vitamins can be obtained by conventional methods such as microbial transformation, purification from microbial cultures, enzymatic or chemical synthesis.
고분자 펩티드로서는 화장품에 배합 가능한 것이라면 어떠한 것이라도 되지만, 바람직하게는 콜라겐, 가수 분해 콜라겐, 젤라틴, 엘라스틴, 가수 분해 엘라스틴, 케라틴 등을 들 수 있다. 고분자 펩티드는 미생물의 배양액으로부터의 정제법, 효소법 또는 화학 합성법 등의 통상의 방법에 의해 정제 취득할 수 있으며, 또는 통상 돼지나 소 등의 진피, 누에의 견섬유 등의 천연물로부터 정제하여 사용할 수 있다.The polymer peptide may be any peptide that can be blended into cosmetics, but preferably includes collagen, hydrolyzed collagen, gelatin, elastin, hydrolyzed elastin, and keratin. High molecular weight peptides can be purified and obtained by conventional methods such as purification from microbial culture media, enzymatic methods, or chemical synthesis, or they can usually be purified and used from natural products such as dermis of pigs or cows or silk fiber of silkworms.
고분자 다당으로서는 화장품에 배합 가능한 것이라면 어떠한 것이라도 되지만, 바람직하게는 히드록시에틸셀룰로오스, 크산탄검, 히알루론산나트륨, 콘드로이틴 황산 또는 그 염 (나트륨염 등) 등을 들 수 있다. 예를 들어, 콘드로이틴 황산 또는 그 염 등은 통상 포유 동물이나 어류로부터 정제하여 사용할 수 있다.The polymer polysaccharide may be any one that can be blended into cosmetics, but preferably includes hydroxyethyl cellulose, xanthan gum, sodium hyaluronate, chondroitin sulfate or its salts (sodium salt, etc.). For example, chondroitin sulfate or its salt can usually be purified and used from mammals or fish.
스핑고 지질로서는 화장품에 배합 가능한 것이라면 어떠한 것이라도 되지만, 바람직하게는 세라미드, 피토스핑고신, 스핑고당지질 등을 들 수 있다. 스핑고 지질은 통상 포유류, 어류, 패류, 효모 또는 식물 등으로부터 통상의 방법에 의해 정제하거나 화학 합성법에 의해 취득할 수 있다.The sphingolipid may be any one that can be blended into cosmetics, but preferred examples include ceramide, phytosphingosine, and sphingolipid. Sphingolipids can usually be purified by conventional methods from mammals, fish, shellfish, yeast, or plants, or obtained by chemical synthesis.
해초 추출물로는 화장품에 배합 가능한 것이라면 어떠한 것이라도 되지만, 바람직하게는 갈조 엑기스, 홍조 엑기스, 녹조 엑기스 등을 들 수 있으며, 또, 이들의 해초 엑기스로부터 정제된 칼라기난, 아르긴산, 아르긴산나트륨, 아르긴산칼륨 등도 본 발명에서 사용되는 해초 엑기스에 포함된다. 해초 엑기스는 해초로부터 통상의 방법에 의해 정제하여 취득할 수 있다.The seaweed extract can be any one that can be mixed into cosmetics, but preferably includes brown algae extract, red algae extract, green algae extract, etc. Also, calrageenan, arginic acid, sodium alginate, etc. purified from these seaweed extracts. Potassium arginate and the like are also included in the seaweed extract used in the present invention. Seaweed extract can be obtained by purifying seaweed by a conventional method.
본 발명의 화장료 조성물에는 상기 필수 성분과 더불어 필요에 따라 통상 화장료에 배합되는 다른 성분을 배합해도 된다. 이외에 첨가해도 되는 배합 성분으로서는 유지성분, 보습제, 에몰리엔트제, 계면 활성제, 유기 및무기안료, 유기 분체, 자외선 흡수제, 방부제, 살균제, 산화 방지제, 식물 추출물, pH 조정제, 알콜, 색소, 향료, 혈행 촉진제, 냉감제, 제한(制汗)제, 정제수 등을 들 수 있다. 유지 성분으로서는 에스테르계 유지, 탄화수소계 유지, 실리콘계 유지, 불소계 유지, 동물 유지, 식물 유지 등을 들 수 있다.In addition to the above-mentioned essential ingredients, the cosmetic composition of the present invention may contain other ingredients normally blended in cosmetics, if necessary. Other ingredients that may be added include oils and fats, moisturizers, emollients, surfactants, organic and inorganic pigments, organic powders, ultraviolet absorbers, preservatives, disinfectants, antioxidants, plant extracts, pH adjusters, alcohol, colorants, fragrances, Examples include blood circulation promoters, cooling agents, antiperspirants, and purified water. Examples of oil and fat components include ester-based fats and oils, hydrocarbon-based fats and oils, silicone-based fats and oils, fluorine-based fats and oils, animal fats and oils, and vegetable fats and oils.
에스테르계 유지로서는 트리2-에틸헥산산글리세릴, 2-에틸헥산산세틸, 미리스틴산이소프로필, 미리스틴산 부틸, 팔미틴산이소프로필, 스테아르산에틸, 팔미틴산옥틸, 이소스테아르산이소세틸, 스테아르산부틸, 리놀레산 에틸,리놀레산이소프로필, 올레인산에틸, 미리스틴산이소세틸, 미리스틴산이소스테아릴, 팔미틴산이소스테아릴, 미리스틴산옥틸도데실, 이소스테아르산이소세틸, 세바신산디에틸, 아디핀산디이소프로필, 네오펜탄산이소알킬, 트리(카프릴, 카프린산)글리세릴, 트리2-에틸헥산산트리메틸롤프로판, 트리이소스테아르산 트리메틸롤프로판, 테트라2-에틸헥산산펜타엘리슬리톨, 카프릴산세틸, 라우린산데실, 라우린산헥실, 미리스틴산데실, 미리스틴산미리스틸, 미리스틴산세틸, 스테아르산스테아릴, 올레인산데실, 리시노올레인산세틸, 라우린산이소스테아릴, 미리스틴산이소트리데실, 팔미틴산이소세틸, 스테아르산옥틸, 스테아르산 이소세틸, 올레인산이소데실, 올레인산옥틸도데실, 리놀레산옥틸도데실, 이소스테아르산이소프로필, 2-에틸헥산산세토스테아릴, 2-에틸헥산산스테아릴, 이소스테아르산헥실, 디옥탄산에틸렌글리콜, 디올레인산에틸렌글리콜, 디카프린산프로필렌글리콜, 디(카프릴, 카프린산)프로필렌글리콜, 디카프릴산프로필렌글리콜, 디카프린산네오펜 틸글리콜, 디옥탄산네오펜틸글리콜, 트리카프릴산글리세릴, 트리운데실산글리세릴, 트리이소팔미틴산글리세릴, 트리이소스테아르산글리세릴, 네오펜탄산옥틸도데실, 옥탄산이소스테아릴, 이소노난산옥틸, 네오데칸산헥실데실, 네오데칸산옥틸도데실, 이소스테아르산이소세틸, 이소스테아르산이소스테아릴, 이소스테아르산옥틸데실, 폴리글리세린올레인산에스테르, 폴리글리세린이소스테아르산에스테르, 시트르산트리이소세틸, 시트르산트리이소알킬, 시트르산트리이소옥틸, 락트산라우릴, 락트산미리스틸, 락트산세틸, 락트산옥틸데실, 시트르산트리에틸, 시트르산아세틸트리에틸, 시트르산아세틸트리부틸, 시트르산트리옥틸, 말산디이소스테아릴, 히드록시스테아르산 2-에틸헥실, 숙신산디2-에틸헥실, 아디핀산디이소부틸, 세바신산디이소프로필, 세바신산디옥틸, 스테아르산콜레스테릴, 이소스테아르산콜레스테릴, 히드록시스테아르산콜레스테릴, 올레인산콜레스테릴, 올레인 산디히드로콜레스테릴, 이소스테아르산피트스테릴, 올레인산피트스테릴, 12-스테알로일히드록시스테아르산이소세틸, 12-스테알로일히드록시스테아르산스테아릴, 12-스테알로일히드록시스테아르산이소스테아릴 등의 에스테르 계 등을 들 수 있다. Ester-based oils include glyceryl tri2-ethylhexanoate, cetyl 2-ethylhexanoate, isopropyl myristate, butyl myristate, isopropyl palmitate, ethyl stearate, octyl palmitate, isocetyl isostearate, and stearic acid. Butyl, ethyl linoleate, isopropyl linoleate, ethyl oleate, isocetyl myristate, isostearyl myristate, isostearyl palmitate, octyldodecyl myristate, isocetyl isostearate, diethyl sebacate, adipine. Diisopropyl acid, isoalkyl neopentanoate, tri(caprylic, capric acid)glyceryl, trimethylolpropane tri2-ethylhexanoate, trimethylolpropane triisostearate, pentaelislitol tetra2-ethylhexanoate , cetyl caprylate, decyl laurate, hexyl laurate, decyl myristate, myristyl myristate, cetyl myristate, stearyl stearate, decyl oleate, cetyl ricinooleate, isostear laurate. Reyl, isotridecyl myristate, isocetyl palmitate, octyl stearate, isocetyl stearate, isodecyl oleate, octyldodecyl oleate, octyldodecyl linoleate, isopropyl isostearate, cetoste 2-ethylhexanoate. Aryl, 2-ethylhexanoate stearyl, hexyl isostearate, ethylene glycol dioctanate, ethylene glycol dioleate, propylene glycol dicapric acid, di(capryl, capric acid) propylene glycol, propylene glycol dicaprylate, dicapric acid Neopentyl glycol prinate, neopentyl glycol dioctanate, glyceryl tricaprylate, glyceryl triundecylate, glyceryl triisopalmitate, glyceryl triisostearate, octyldodecyl neopentanoate, isostear octanoate. Reyl, octyl isononanoate, hexyldecyl neodecanoate, octyldodecyl neodecanoate, isocetyl isostearate, isostearyl isostearate, octyldecyl isostearate, polyglycerol oleic acid ester, polyglycerol isostearic acid ester. , triisocetyl citrate, triisoalkyl citrate, triisooctyl citrate, lauryl lactate, myristyl lactate, cetyl lactate, octyldecyl lactate, triethyl citrate, acetyltriethyl citrate, acetyltributyl citrate, trioctyl citrate, malic acid. Diisostearyl acid, 2-ethylhexyl hydroxystearate, di2-ethylhexyl succinate, diisobutyl adipate, diisopropyl sebacate, dioctyl sebacate, cholesteryl stearate, cholesteryl isostearate. , hydroxycholesteryl hydroxystearate, cholesteryl oleate, dihydrocholesteryl oleate, phytsteryl isostearate, phytsteryl oleate, 12-stealoyl hydroxystearate isocetyl, 12-steallo. Ester systems such as stearyl monohydroxystearate and isostearyl 12-stealoylhydroxystearate can be mentioned.
탄화 수소계 유지로서는 스쿠알렌, 유동 파라핀, 알파-올레핀올리고머, 이소파라핀, 세레신, 파라핀, 유동 이소파라핀, 폴리부덴, 마이크로크리스탈린왁스, 와셀린 등의 탄화수소계 유지 등을 들 수 있다.Examples of hydrocarbon oils include squalene, liquid paraffin, alpha-olefin oligomer, isoparaffin, ceresin, paraffin, liquid isoparaffin, polybudene, microcrystalline wax, and petroleum jelly.
실리콘계 유지로서는 폴리메틸실리콘, 메틸페닐실리콘, 메틸시클로폴리실록산, 옥타메틸폴리실록산, 데카메틸폴리실록산, 도데카메틸시클로실록산, 디메틸실록산 및 메틸세틸옥시실록산 공중합체, 디메틸실록산 및 메틸스테알록시실록산 공중합체, 알킬 변성 실리콘유, 아미노 변성 실리콘유 등을 들 수 있다.Silicone oils include polymethyl silicone, methylphenyl silicone, methylcyclopolysiloxane, octamethylpolysiloxane, decamethylpolysiloxane, dodecamethylcyclosiloxane, dimethylsiloxane and methylcetyloxysiloxane copolymer, dimethylsiloxane and methylstealoxysiloxane copolymer, and alkyl. Modified silicone oil, amino-modified silicone oil, etc. can be mentioned.
불소계 유지로서는 퍼플루오로폴리에테르 등을 들 수 있다.Examples of fluorine-based fats and oils include perfluoropolyether.
동물 또는 식물 유지로서는 아보카도유, 아르몬드유, 올리브유, 참깨유, 쌀겨유, 새플라워유, 대두유, 옥수수유, 유채유, 행인(杏仁)유, 팜핵유, 팜유, 피마자유, 해바라기유, 포도종자유, 면실유, 야자유, 쿠쿠이너트유, 소맥배아유, 쌀 배아유, 시아버터, 월견초유, 마커데이미아너트유, 메도홈유, 난황유, 우지(牛脂), 마유, 밍크유, 오렌지라피유, 호호바유, 캔데리러왁스, 카르나바왁스, 액상 라놀린, 경화피마자유 등의 동물 또는 식물 유지를 들 수 있다.Animal or plant oils include avocado oil, almond oil, olive oil, sesame oil, rice bran oil, birdflower oil, soybean oil, corn oil, rapeseed oil, apricot oil, palm kernel oil, palm oil, castor oil, sunflower oil, and grape seed oil. , cottonseed oil, palm oil, cucumber nut oil, wheat germ oil, rice germ oil, shea butter, walnut colostrum oil, marker damia nut oil, meadow oil, egg yolk oil, beef tallow, horse oil, mink oil, orange rape oil, jojoba oil. , animal or plant oils such as candelier wax, carnaba wax, liquid lanolin, and hydrogenated castor oil.
보습제로서는 수용성 저분자 보습제, 지용성 분자 보습제, 수용성 고분자, 지용성 고분자 등을 들 수 있다.Moisturizers include water-soluble low-molecular-weight moisturizers, oil-soluble molecular moisturizers, water-soluble polymers, and fat-soluble polymers.
수용성 저분자 보습제로서는 세린, 글루타민, 솔비톨, 만니톨, 피롤리돈-카르복실산나트륨, 글리세린, 프로필렌글리콜, 1,3-부틸렌글리콜, 에틸렌글리콜, 폴리에틸렌글리콜B(중합도 n = 2 이상), 폴리프로필렌글리콜 (중합도 n = 2 이상), 폴리글리세린B(중합도 n = 2 이상), 락트산, 락트산염 등을 들 수 있다.Water-soluble low-molecular-weight moisturizers include serine, glutamine, sorbitol, mannitol, sodium pyrrolidone-carboxylate, glycerin, propylene glycol, 1,3-butylene glycol, ethylene glycol, polyethylene glycol B (degree of polymerization n = 2 or more), and polypropylene. Examples include glycol (degree of polymerization n = 2 or more), polyglycerin B (degree of polymerization n = 2 or more), lactic acid, lactate, etc.
지용성 저분자 보습제로서는 콜레스테롤, 콜레스테롤에스테르 등을 들 수 있다.Examples of fat-soluble low-molecular-weight moisturizers include cholesterol and cholesterol esters.
수용성 고분자로서는 카르복시비닐폴리머, 폴리아스파라긴산염, 트라가칸트, 크산탄검, 메틸셀룰로오스, 히드록시메틸셀룰로오스, 히드록시에틸셀룰로오스, 히드록시프로필셀룰로오스, 카르복시메틸셀룰로오스, 수용성키틴, 키토산, 덱스트린 등을 들 수 있다.Water-soluble polymers include carboxyvinyl polymer, polyaspartate, tragacanth, xanthan gum, methyl cellulose, hydroxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, carboxymethyl cellulose, water-soluble chitin, chitosan, and dextrin. You can.
지용성 고분자로서는 폴리비닐피롤리돈 및 에이코센 공중합체, 폴리비닐피롤리돈 및 헥사데센 공중합체, 니트로셀룰로오스, 덱스트린지방산에스테르, 고분자 실리콘 등을 들수 있다. 에몰리엔트제로서는 장쇄아실글루타민산 콜레스테릴에스테르, 히드록시스테아르산콜레스테릴, 12-히드록시스테아르산, 스테아르산, 로진산, 라놀린지방산콜레스테릴에스테르 등을 들 수 있다.Examples of oil-soluble polymers include polyvinylpyrrolidone and eicosene copolymers, polyvinylpyrrolidone and hexadecene copolymers, nitrocellulose, dextrin fatty acid ester, and polymer silicone. Examples of emollients include long-chain acyl glutamic acid cholesteryl ester, hydroxystearic acid cholesteryl, 12-hydroxystearic acid, stearic acid, rosin acid, and lanolin fatty acid cholesteryl ester.
계면 활성제로서는 비이온성 계면 활성제, 음이온성 계면 활성제, 양이온성 계면 활성제, 양성 계면 활성제 등을 들 수 있다.Examples of surfactants include nonionic surfactants, anionic surfactants, cationic surfactants, and amphoteric surfactants.
비이온성 계면 활성제로서는 자기 유화형 모노스테아르산글리세린, 프로필렌글리콜지방산에스테르, 글리세린 지방산에스테르, 폴리글리세린지방산에스테르, 솔비탄지방산에스테르, POE(폴리옥시에틸렌)솔비탄지방산에스테르, POE 솔비트지방산에스테르, POE 글리세린지방산에스테르, POE 알킬에테르, POE 지방산에스테르, POE 경화피마자유, POE 피마자유, POE 및 POP (폴리옥시에틸렌 및 폴리옥시프로필렌) 공중합체, POE 및 POP 알킬에테르, 폴리에테르변성실리콘, 라우린산알카놀아미드, 알킬아민옥시드, 수소첨가대두인지질 등을 들 수 있다.Nonionic surfactants include self-emulsifying glycerin monostearate, propylene glycol fatty acid ester, glycerin fatty acid ester, polyglycerin fatty acid ester, sorbitan fatty acid ester, POE (polyoxyethylene) sorbitan fatty acid ester, POE sorbitan fatty acid ester, POE. Glycerin fatty acid ester, POE alkyl ether, POE fatty acid ester, POE hydrogenated castor oil, POE castor oil, POE and POP (polyoxyethylene and polyoxypropylene) copolymer, POE and POP alkyl ether, polyether modified silicone, lauric acid. Examples include alkanolamide, alkylamine oxide, and hydrogenated soybean phospholipid.
음이온성 계면 활성제로서는 지방산비누, 알파-아실술폰산염, 알킬술폰산염, 알킬알릴술폰산염, 알킬나프탈렌술폰산염, 알킬황산염, POE 알킬에테르황산염, 알킬아미드황산염, 알킬인산염, POE 알킬인산업, 알킬아미드 인산염, 알킬로일알킬타우린염, N-아실아미노산염, POE 알킬에테르카르복실산염, 알킬술포숙신산염, 알킬술포아세트산나트륨, 아실화 가수분해 콜라겐펩티드염, 퍼플루오로알킬인산에스테르 등을 들 수 있다.Anionic surfactants include fatty acid soap, alpha-acyl sulfonate, alkyl sulfonate, alkyl allyl sulfonate, alkyl naphthalene sulfonate, alkyl sulfate, POE alkyl ether sulfate, alkyl amide sulfate, alkyl phosphate, POE alkyl phosphate industry, alkyl amide. Phosphate, alkyloyl alkyl taurine salt, N-acylamino acid salt, POE alkyl ether carboxylate, alkyl sulfosuccinate, sodium alkyl sulfoacetate, acylated hydrolyzed collagen peptide salt, perfluoroalkyl phosphate ester, etc. there is.
양이온성 계면 활성제로서는 염화알킬트리메틸암모늄, 염화스테아릴트리메틸암모늄, 브롬화스테아릴트리메틸암모늄, 염화세토스테아릴트리메틸암모늄, 염화디스테아릴디메틸암모늄, 염화스테아릴디메틸벤질암모늄, 브롬화베헤닐트리메틸암모늄, 염화벤잘코늄, 스테아르산 디에틸아미노에틸아미드, 스테아르산디메틸아미노프로필아 미드, 라놀린 유도체 제 4급 암모늄염 등을 들 수 있다. 양성 계면 활성제로서는 카르복시베타인형, 아미드베타인형, 술포베타인형, 히드록시술포베타인형, 아미드 술포 베타인형, 포스포베타인형, 아미노카르복실산염형, 이미다졸린 유도체형, 아미드아민형 등의 양성 계면 활성제 등을 들 수 있다.Cationic surfactants include alkyltrimethylammonium chloride, stearyltrimethylammonium chloride, stearyltrimethylammonium bromide, cetostearyltrimethylammonium chloride, distearyldimethylammonium chloride, stearyldimethylbenzylammonium chloride, behenyltrimethylammonium bromide, and chloride. Examples include benzalkonium, diethylaminoethylamide stearate, dimethylaminopropyl stearate, and quaternary ammonium salts of lanolin derivatives. Amphoteric surfactants include carboxy beta type, amide beta type, sulfo beta type, hydroxy sulfo beta type, amide sulfo betaine type, phosphobetain type, aminocarboxylate type, imidazoline derivative type, and amidamine type. Amphoteric surfactants, etc. can be mentioned.
유기 및 무기 안료로서는 규산, 무수규산, 규산마그네슘, 탤크, 세리사이트, 마이카, 카올린, 벵갈라, 클레이, 벤토나이트, 티탄피막운모, 옥시염화비스무트, 산화지르코늄, 산화마그네슘, 산화아연, 산화티탄, 산화알루미늄, 황산칼슘, 황산바륨, 황산마그네슘, 탄산칼슘, 탄산마그네슘, 산화철, 군청, 산화크롬, 수산화크롬, 칼라민 및 이들의 복합체등의 무기 안료; 폴리아미드, 폴리에스테르, 폴리프로필렌, 폴리스티렌, 폴리우레탄, 비닐수지, 요소수지, 페놀수지, 불소수지, 규소수지, 아크릴수지, 멜라민수지, 에폭시수지, 폴리카보네이트 수지, 디비닐벤젠 및 스티렌 공중합체, 실크파우더, 셀룰로오스, CI 피그먼트옐로우, CI 피그먼트오렌지 등의 유기 안료 및 이들의 무기 안료와 유기 안료의 복합 안료 등을 들 수 있다.Organic and inorganic pigments include silicic acid, anhydrous silicic acid, magnesium silicate, talc, sericite, mica, kaolin, bengala, clay, bentonite, titanium-coated mica, bismuth oxychloride, zirconium oxide, magnesium oxide, zinc oxide, titanium oxide, and aluminum oxide. Inorganic pigments such as calcium sulfate, barium sulfate, magnesium sulfate, calcium carbonate, magnesium carbonate, iron oxide, ultramarine blue, chromium oxide, chromium hydroxide, calamine and complexes thereof; Polyamide, polyester, polypropylene, polystyrene, polyurethane, vinyl resin, urea resin, phenol resin, fluorine resin, silicon resin, acrylic resin, melamine resin, epoxy resin, polycarbonate resin, divinylbenzene and styrene copolymer, Examples include organic pigments such as silk powder, cellulose, CI pigment yellow, and CI pigment orange, and complex pigments of these inorganic pigments and organic pigments.
유기 분체로서는 스테아르산칼슘 등의 금속비누; 세틸린산아연나트륨, 라우릴린산아연, 라우릴린산칼슘 등의 알킬인산금속염; N-라우로일-베타-알라닌칼슘, N-라우로일-베타-알라닌아연, N-라우로일글리신칼슘 등의 아실아미노산 다가금속염; N-라우로일-타우린칼슘, N-팔미토일-타우린칼슘 등의 아미드술폰산 다가금속염; N-엡실론-라우로일-L-리진, N-엡실론-팔미토일리진, N-알파-파리토일올니틴, N-알파-라우로일아르기닌, N-알파-경화우지지방산아실아르기닌 등의 N-아실염기성아미노산; N-라우로일글리실글리신 등의 N-아실폴리펩티드; 알파-아미노카프릴산, 알파-아미노라우린산 등의 알파-아미노지방산; 폴리에틸렌, 폴리프로필렌, 나일론, 폴리메틸메타크릴레이트, 폴리스티렌, 디비닐벤젠 및 스티렌 공중합체, 사불화에틸렌 등을 들 수 있다.Examples of organic powder include metal soap such as calcium stearate; Alkyl phosphate metal salts such as sodium zinc cetilate, zinc laurylate, and calcium laurylate; Acyl amino acid polyvalent metal salts such as N-lauroyl-beta-alanine calcium, N-lauroyl-beta-alanine zinc, and N-lauroyl glycine calcium; Amidesulfonic acid polyvalent metal salts such as N-lauroyl-taurine calcium and N-palmitoyl-taurine calcium; N such as N-epsilon-lauroyl-L-lysine, N-epsilon-palmitoylizine, N-alpha-paritoylolnithine, N-alpha-lauroylarginine, N-alpha-hydrogenated beef tallow fatty acid acylarginine, etc. -Acyl basic amino acid; N-acyl polypeptides such as N-lauroylglycylglycine; Alpha-amino fatty acids such as alpha-aminocaprylic acid and alpha-aminolauric acid; Examples include polyethylene, polypropylene, nylon, polymethyl methacrylate, polystyrene, divinylbenzene and styrene copolymers, and ethylene tetrafluoride.
자외선 흡수제로서는 파라아미노벤조산, 파라아미노벤조산에틸, 파라아미노벤조산아밀, 파라아미노벤조산옥틸, 살리실산에틸렌글리콜, 살리신산페닐, 살리신산옥틸, 살리신산벤질, 살리신산부틸페닐,살리신산호모멘틸, 계피산벤질, 파라메톡시계피산-2-에톡시에틸, 파라메톡시계피산옥틸, 디파라메톡시계피산모노-2-에틸헥산글리세릴, 파라메톡시 계피산 이소프로필, 디이소프로필 및 디이소프로필계피산에스테르 혼합물, 우로카닌산, 우로카닌산에틸, 히드록시메톡시벤조페논, 히드록시메톡시벤조페논술폰산 및 그 염, 디히드록시메톡시벤조페논, 디히드록시메톡시벤조페논디술폰산나트륨, 디히드록시벤조페논, 테트라히드록시벤조페논, 4-tert-부틸-4'-메톡시디벤조일메탄, 2,4,6-트리아닐리노-p-(카르보-2'-에틸헥실-1'-옥시)-1,3,5-트리아진, 2-(2-히드록시-5-메틸페닐)벤조트리아졸 등을 들 수 있다.UV absorbers include para-aminobenzoic acid, ethyl para-aminobenzoate, amyl para-aminobenzoate, octyl para-aminobenzoate, ethylene glycol salicylate, phenyl salicylate, octyl salicylate, benzyl salicylate, butylphenyl salicylate, homomenthyl salicylate, and benzyl cinnamate. , paramethoxycinnamic acid-2-ethoxyethyl, octyl paramethoxycinnamic acid, mono-2-ethylhexane glyceryl diparamethoxycinnamic acid, isopropyl paramethoxycinnamic acid, diisopropyl and diisopropylcinnamic acid ester mixture, uro Kaninic acid, ethyl urocanate, hydroxymethoxybenzophenone, hydroxymethoxybenzophenone sulfonic acid and its salts, dihydroxymethoxybenzophenone, dihydroxymethoxybenzophenone disulfonate sodium, dihydroxybenzophenone , tetrahydroxybenzophenone, 4-tert-butyl-4'-methoxydibenzoylmethane, 2,4,6-trianilino-p-(carbo-2'-ethylhexyl-1'-oxy)-1 , 3,5-triazine, 2-(2-hydroxy-5-methylphenyl)benzotriazole, etc.
살균제로서는 히노키티올, 트리클로산, 트리클로로히드록시디페닐에테르, 크로르헥시딘글루콘산염, 페녹시에탄올, 레조르신, 이소프로필메틸페놀, 아줄렌, 살리칠산, 진크필리티온, 염화벤잘코늄, 감광소 301 호, 모노니트로과이어콜나트륨, 운데시렌산 등을 들 수 있다.Disinfectants include hinokitiol, triclosan, trichlorohydroxydiphenyl ether, chlorhexidine gluconate, phenoxyethanol, resorcin, isopropylmethylphenol, azulene, salicylic acid, zincphyllithione, benzalkonium chloride, and photosensitive. Sub-No. 301, sodium mononitroguaiacol, undecirenic acid, etc. can be mentioned.
산화 방지제로서는 부틸히드록시아니솔, 갈릭산프로필, 엘리소르빈산 등을 들 수 있다.Antioxidants include butylhydroxyanisole, propyl gallate, and elisorbic acid.
pH 조정제로서는 시트르산, 시트르산나트륨, 말산, 말산나트륨, 프말산, 프말산나트륨, 숙신산, 숙신산나트륨, 수산화나트륨, 인산일수소나트륨 등을 들 수 있다.Examples of pH adjusters include citric acid, sodium citrate, malic acid, sodium malate, fumal acid, sodium fumalate, succinic acid, sodium succinate, sodium hydroxide, and sodium monohydrogen phosphate.
알코올로서는 세틸알코올 등의 고급 알코올을 들 수 있다.Examples of alcohol include higher alcohols such as cetyl alcohol.
또한, 이외에 첨가해도 되는 배합 성분은 이에 한정되는 것은 아니며, 또, 상기 어느 성분도 본 발명의 목적 및 효과를 손상시키지 않는 범위 내에서 배합이 가능하다.Additionally, the ingredients that may be added are not limited to these, and any of the ingredients can be blended within the range that does not impair the purpose and effect of the present invention.
본 발명의 화장료 조성물은 용액, 유화물, 점성형 혼합물 등의 형상을 취할 수 있다.The cosmetic composition of the present invention may take the form of a solution, emulsion, viscous mixture, etc.
본 발명의 화장료 조성물에 포함되는 성분은 유효성분으로서 화장료 조성물에 통상적으로 이용되는 성분들을 포함할 수 있으며, 예를 들면, 안정화제, 용해화제, 비타민, 안료 및 향료와 같은 통상적인 보조제 및 담체를 포함한다.The ingredients included in the cosmetic composition of the present invention may include ingredients commonly used in cosmetic compositions as active ingredients, for example, conventional auxiliaries and carriers such as stabilizers, solubilizers, vitamins, pigments, and fragrances. Includes.
본 발명의 기능성 화장료 조성물은 당업계에서 통상적으로 제조되는 어떠한 제형으로도 제조될 수 있으며, 예를 들어 유액, 크림, 화장수, 팩, 파운데이션, 로션, 미용액, 모발화장료 등을 들 수 있다.The functional cosmetic composition of the present invention can be manufactured in any formulation commonly manufactured in the art, and examples include emulsions, creams, lotions, packs, foundations, lotions, beauty essences, hair cosmetics, etc.
구체적으로, 본 발명의 화장료 조성물은 스킨로션, 스킨소프너, 스킨토너, 밀크 로션, 아스트린젠트, 로션, 모이스쳐 로션, 영양로션, 맛사지크림, 영양크림, 모이스처크림, 핸드크림, 파운데이션, 에센스, 영양에센스, 팩, 비누, 클렌징폼, 클렌징로션, 클렌징크림, 헤어로션, 헤어토닉, 헤어에센스, 헤어샴푸, 헤어린스, 헤어트리트먼트, 바디로션 및 바디클린저의 제형을 포함한다.Specifically, the cosmetic composition of the present invention includes skin lotion, skin softener, skin toner, milk lotion, astringent, lotion, moisture lotion, nutritional lotion, massage cream, nutritional cream, moisture cream, hand cream, foundation, essence, nutritional essence, It includes formulations of packs, soaps, cleansing foams, cleansing lotions, cleansing creams, hair lotions, hair tonics, hair essences, hair shampoos, hair rinses, hair treatments, body lotions, and body cleansers.
본 발명의 제형이 페이스트, 크림 또는 겔인 경우에는 담체 성분으로서 동물섬유, 식물섬유, 왁스, 파라핀, 전분, 트라칸트, 셀룰로오스 유도체, 폴리에틸렌글리콜, 실리콘, 벤토나이트, 실리카, 탈크 또는 산화 아연 등이 이용될 수 있다.When the formulation of the present invention is a paste, cream or gel, animal fiber, plant fiber, wax, paraffin, starch, tracant, cellulose derivative, polyethylene glycol, silicone, bentonite, silica, talc or zinc oxide may be used as the carrier ingredient. You can.
본 발명의 제형이 파우더 또는 스프레이인 경우에는 담체 성분으로서 락토스, 탈크, 실리카, 알루미늄 히드록시드, 칼슘 실리케이트 또는 폴리아미드 파우더가 이용될 수 있고, 특히 스프레이인 경우에는 추가적으로 클로로플루오로히드로카본, 프로판/부탄 또는 디메틸 에테르와 같은 추진체를 포함할 수 있다.When the formulation of the present invention is a powder or spray, lactose, talc, silica, aluminum hydroxide, calcium silicate, or polyamide powder can be used as the carrier ingredient. In particular, when the formulation is a spray, chlorofluorohydrocarbon and propane may be used as carrier ingredients. /May contain propellants such as butane or dimethyl ether.
본 발명의 제형이 용액 또는 유탁액의 경우에는 담체 성분으로서 용매, 용매화제 또는 유탁화제가 이용되고, 예컨대 물, 에탄올, 이소프로판올, 에틸 카보네이트, 에틸 아세테이트, 벤질 알코올, 벤질 벤조에이트, 프로필렌글리콜, 1,3-부틸글리콜 오일, 글리세롤 지방족 에스테르, 폴리에틸렌 글리콜 또는 소르비탄의 지방산 에스테르가 있다.When the formulation of the present invention is a solution or emulsion, a solvent, solvating agent or emulsifying agent is used as a carrier component, such as water, ethanol, isopropanol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1 , 3-butyl glycol oil, glycerol aliphatic esters, polyethylene glycol or fatty acid esters of sorbitan.
본 발명의 제형이 현탁액인 경우에는 담체 성분으로서 물, 에탄올 또는 프로필렌 글리콜과 같은 액상 희석제, 에톡실화 이소스테아릴 알코올, 폴리옥시에틸렌 소르비톨 에스테르 및 폴리옥시에틸렌 소르비탄 에스테르와 같은 현탁제, 미소결정성 셀룰로오스, 알루미늄 메타히드록시드, 벤토나이트, 아가 또는 트라칸트 등이 이용될 수 있다.When the formulation of the present invention is a suspension, the carrier ingredients include water, a liquid diluent such as ethanol or propylene glycol, a suspending agent such as ethoxylated isostearyl alcohol, polyoxyethylene sorbitol ester, and polyoxyethylene sorbitan ester, and microcrystalline Cellulose, aluminum metahydroxide, bentonite, agar, or tracant may be used.
본 발명의 제형이 계면-활성제 함유 클린징인 경우에는 담체 성분으로서 지방족 알코올 설페이트, 지방족 알코올 에테르 설페이트, 설포숙신산 모노에스테르, 이세티오네이트, 이미다졸리늄 유도체, 메틸타우레이트, 사르코시네이트, 지방산 아미드 에테르 설페이트, 알킬아미도베타인, 지방족 알코올, 지방산 글리세리드, 지방산디에탄올아미드, 식물성 유, 리놀린 유도체 또는 에톡실화 글리세롤 지방산 에스테르 등이 이용될 수 있다.When the formulation of the present invention is a surfactant-containing cleansing agent, the carrier ingredients include aliphatic alcohol sulfate, aliphatic alcohol ether sulfate, sulfosuccinic acid monoester, isethionate, imidazolinium derivative, methyl taurate, sarcosinate, and fatty acid amide. Ether sulfate, alkylamidobetaine, fatty alcohol, fatty acid glyceride, fatty acid diethanolamide, vegetable oil, linoline derivative, or ethoxylated glycerol fatty acid ester can be used.
일 측면에서, 본 발명은 의약외품 조성물로 이용될 수 있다.In one aspect, the present invention can be used as a quasi-drug composition.
본 발명의 의약외품 조성물에 포함되는 성분은 유효성분으로서 상기 펩타이드 이외에 의약외품 조성물에 통상적으로 이용되는 성분들을 포함할 수 있으며, 예컨대 연마제, 습윤제, 결합제, 기포제, 감미제, 방부제, 약효성분, 향미제, 색소, 용제, 증백제, 가용화제 또는 pH 조정제를 포함할 수 있다.Ingredients included in the quasi-drug composition of the present invention may include ingredients commonly used in quasi-drug compositions in addition to the peptide as an active ingredient, such as abrasives, wetting agents, binders, foaming agents, sweeteners, preservatives, medicinal ingredients, flavoring agents, and colorants. , it may include a solvent, brightener, solubilizer, or pH adjuster.
일 측면에서, 본 발명은 약학 조성물로 이용될 수 있다.In one aspect, the present invention can be used as a pharmaceutical composition.
본 발명의 약학 조성물에는 유효성분인 펩타이드 이외에 보조제(adjuvant)를 추가로 포함할 수 있다. 상기 보조제는 당해 기술분야에 알려진 것이라면 어느 것이나 제한 없이 사용할 수 있으나, 예를 들어 프로인트(Freund)의 완전 보조제 또는 불완전 보조제를 더 포함하여 그 기능성을 증가시킬 수 있다. The pharmaceutical composition of the present invention may further include adjuvants in addition to the peptide, which is an active ingredient. The auxiliary agent may be any one known in the art without limitation, but its functionality may be increased by further including, for example, Freund's complete auxiliary agent or incomplete auxiliary agent.
본 발명에 따른 약학 조성물은 유효성분을 약학적으로 허용된 담체에 혼입시킨 형태로 제조될 수 있다. 여기서, 약학적으로 허용된 담체는 제약 분야에서 통상 사용되는 담체, 부형제 및 희석제를 포함한다. 본 발명의 약학 조성물에 이용할 수 있는 약학적으로 허용된 담체는 이들로 제한되는 것은 아니지만, 락토스, 덱스트로스, 수크로스, 솔비톨, 만니톨, 자일리톨, 에리스리톨, 말티톨, 전분, 아카시아 고무, 알지네이트, 젤라틴, 칼슘 포스페이트, 칼슘 실리케이트, 셀룰로스, 메틸 셀룰로스, 폴리비닐 피롤리돈, 물, 메틸히드록시벤조에이트, 프로필히드록시벤조에이트, 탈크, 마그네슘 스테아레이트 및 광물유를 들 수 있다.The pharmaceutical composition according to the present invention can be prepared by incorporating the active ingredient into a pharmaceutically acceptable carrier. Here, pharmaceutically acceptable carriers include carriers, excipients, and diluents commonly used in the pharmaceutical field. Pharmaceutically acceptable carriers that can be used in the pharmaceutical composition of the present invention include, but are not limited to, lactose, dextrose, sucrose, sorbitol, mannitol, xylitol, erythritol, maltitol, starch, gum acacia, alginate, gelatin, Examples include calcium phosphate, calcium silicate, cellulose, methyl cellulose, polyvinyl pyrrolidone, water, methylhydroxybenzoate, propylhydroxybenzoate, talc, magnesium stearate and mineral oil.
본 발명의 약학 조성물은 각각 통상의 방법에 따라 산제, 과립제, 정제, 캡슐제, 현탁액, 에멀전, 시럽, 에어로졸 등의 경구형 제형, 외용제, 좌제 또는 멸균 주사용액의 형태로 제형화하여 사용될 수 있다.The pharmaceutical composition of the present invention can be formulated and used in the form of oral dosage forms such as powders, granules, tablets, capsules, suspensions, emulsions, syrups, aerosols, external preparations, suppositories, or sterile injection solutions according to conventional methods. .
제제화할 경우에는 통상 사용하는 충진제, 증량제, 결합제, 습윤제, 붕해제, 계면활성제 등의 희석제 또는 부형제를 사용하여 조제될 수 있다. 경구투여를 위한 고형제제에는 정제, 환제, 산제, 과립제, 캡슐제 등이 포함되며, 그러한 고형 제제는 유효성분에 적어도 하나 이상의 부형제, 예를 들면 전분, 칼슘 카르보네이트, 수크로스, 락토오스, 젤라틴 등을 섞어 조제될 수 있다. 또한, 단순한 부형제 이외에 마그네슘 스테아레이트, 탈크 같은 윤활제들도 사용될 수 있다. 경구투여를 위한 액상 제제로는 현탁제, 내용액제, 유제, 시럽제 등이 해당되는데, 일반적으로 사용되는 희석제인 물, 리퀴드 파라핀 이외에 여러 가지 부형제, 예를 들면 습윤제, 감미제, 방향제, 보존제 등이 포함될 수 있다. 비경구 투여를 위한 제제에는 멸균된 수용액, 비수용성용제, 현탁제, 유제, 동결건조 제제 및 좌제가 포함된다. 비수용성용제, 현탁제로는 프로필렌 글리콜, 폴리에틸렌 글리콜, 올리브유와 같은 식물성 기름, 에틸올레이트와 같은 주사 가능한 에스테르 등이 사용될 수 있다. 좌제의 기제로는 위텝솔(witepsol), 트윈(tween) 61, 카카오지, 라우린지, 글리세로젤라틴 등이 사용될 수 있다.When formulated, it can be prepared using diluents or excipients such as commonly used fillers, extenders, binders, wetting agents, disintegrants, and surfactants. Solid preparations for oral administration include tablets, pills, powders, granules, capsules, etc., and such solid preparations contain the active ingredient plus at least one excipient, such as starch, calcium carbonate, sucrose, lactose, and gelatin. It can be prepared by mixing etc. Additionally, in addition to simple excipients, lubricants such as magnesium stearate and talc may also be used. Liquid preparations for oral administration include suspensions, oral solutions, emulsions, and syrups. In addition to the commonly used diluents such as water and liquid paraffin, they contain various excipients such as wetting agents, sweeteners, fragrances, and preservatives. You can. Preparations for parenteral administration include sterile aqueous solutions, non-aqueous solutions, suspensions, emulsions, lyophilized preparations, and suppositories. Non-aqueous solvents and suspensions include propylene glycol, polyethylene glycol, vegetable oil such as olive oil, and injectable ester such as ethyl oleate. As a base for suppositories, witepsol, tween 61, cacao, laurin, glycerogelatin, etc. can be used.
본 발명에 따른 약학 조성물은 개체에 다양한 경로로 투여될 수 있다. 투여의 모든 방식이 예상될 수 있는데, 예를 들면 경구, 정맥, 근육, 피하, 복강내 주사에 의해 투여될 수 있다.The pharmaceutical composition according to the present invention can be administered to an individual through various routes. All modes of administration are contemplated, for example, by oral, intravenous, intramuscular, subcutaneous, or intraperitoneal injection.
본 발명에 따른 약학 조성물의 투여량은 개체의 연령, 체중, 성별, 신체 상태 등을 고려하여 선택된다. 상기 약학 조성물 중 포함되는 유효성분의 농도는 대상에 따라 다양하게 선택할 수 있음은 자명하며, 바람직하게는 약학 조성물에 0.01 ~ 1,000 ㎍/ml의 농도로 포함되는 것이다. 그 농도가 0.01 ㎍/ml 미만일 경우에는 약학 활성이 나타나지 않을 수 있고, 1,000 ㎍/ml를 초과할 경우에는 인체에 독성을 나타낼 수 있다.The dosage of the pharmaceutical composition according to the present invention is selected taking into account the age, weight, gender, physical condition, etc. of the individual. It is obvious that the concentration of the active ingredient included in the pharmaceutical composition can be selected in various ways depending on the target, and is preferably included in the pharmaceutical composition at a concentration of 0.01 to 1,000 μg/ml. If the concentration is less than 0.01 ㎍/ml, pharmaceutical activity may not appear, and if it exceeds 1,000 ㎍/ml, it may be toxic to the human body.
상기 약학 조성물은 다양한 경구 또는 비경구 투여 형태로 제형화될 수 있다.The pharmaceutical composition may be formulated into various oral or parenteral dosage forms.
경구 투여용 제형으로는 예를 들면 정제, 환제, 경질, 연질 캅셀제, 액제, 현탁제, 유화제, 시럽제, 과립제 등이 있는데, 이들 제형은 유효성분 이외에 희석제(예: 락토즈, 덱스트로즈, 수크로즈, 만니톨, 솔비톨, 셀룰로즈 및/또는 글리신), 활택제(예: 실리카, 탈크, 스테아르산 및 그의 마그네슘 또는 칼슘염 및/또는 폴리에틸렌 글리콜)를 추가로 포함할 수 있다. 또한, 상기 정제는 마그네슘 알루미늄 실리케이트, 전분 페이스트, 젤라틴, 트라가칸스, 메틸셀룰로즈, 나트륨 카복시메틸셀룰로즈 및/또는 폴리비닐피롤리딘과 같은 결합제를 함유할 수 있으며, 경우에 따라 전분, 한천, 알긴산 또는 그의 나트륨 염과 같은 붕해제 또는 비등 혼합물 및/또는 흡수제, 착색제, 향미제 및 감미제를 함유할 수 있다. 상기 제형은 통상적인 혼합, 과립화 또는 코팅 방법에 의해 제조될 수 있다.Dosage forms for oral administration include, for example, tablets, pills, hard and soft capsules, solutions, suspensions, emulsifiers, syrups, granules, etc. These dosage forms contain diluents (e.g. lactose, dextrose, water) in addition to the active ingredient. crose, mannitol, sorbitol, cellulose and/or glycine), lubricants (e.g. silica, talc, stearic acid and magnesium or calcium salts thereof and/or polyethylene glycol). Additionally, the tablets may contain binders such as magnesium aluminum silicate, starch paste, gelatin, tragacanth, methylcellulose, sodium carboxymethylcellulose and/or polyvinylpyrrolidine, and in some cases starch, agar, alginic acid. or disintegrants such as sodium salts thereof or effervescent mixtures and/or absorbents, colorants, flavoring and sweetening agents. The formulation can be prepared by conventional mixing, granulating or coating methods.
또한, 비경구 투여용 제형의 대표적인 것은 주사용 제제이며, 주사용 제제의 용매로서 물, 링거액, 등장성 생리식염수 또는 현탁액을 들 수 있다. 상기 주사용 제제의 멸균 고정 오일은 용매 또는 현탁 매질로서 사용할 수있으며 모노-, 디-글리세라이드를 포함하여 어떠한 무자극성 고정오일도 이러한 목적으로 사용될 수 있다.In addition, representative formulations for parenteral administration are injectable formulations, and solvents for injectable formulations include water, Ringer's solution, isotonic saline solution, or suspension. The sterile fixed oil of the injectable preparation can be used as a solvent or suspending medium, and any non-irritating fixed oil, including mono- and di-glycerides, can be used for this purpose.
또한, 상기 주사용 제제는 올레산과 같은 지방산을 사용할 수 있다.Additionally, the injectable preparation may use fatty acids such as oleic acid.
일 측면에서, 본 발명은 식품/건강기능식품 조성물로 이용될 수 있다.In one aspect, the present invention can be used as a food/health functional food composition.
본 발명의 식품 조성물은 유효성분인 펩타이드를 함유하는 것 외에 통상의 식품 조성물과 같이 여러 가지 향미제 또는 천연 탄수화물 등을 추가 성분으로서 함유할 수 있다.In addition to containing peptide as an active ingredient, the food composition of the present invention may contain various flavoring agents or natural carbohydrates as additional ingredients like a typical food composition.
상술한 천연 탄수화물의 예는 모노사카라이드, 예를 들어, 포도당, 과당 등; 디사카라이드, 예를 들어 말토스, 슈크로스 등; 및 폴리사카라이드, 예를 들어 덱스트린, 시클로덱스트린 등과 같은 통상적인 당, 및 자일리톨,소르비톨, 에리트리톨 등의 당알콜이다. 상술한 향미제는 천연 향미제(타우마틴), 스테비아 추출물(예를 들어 레바우디오시드 A, 글리시르히진 등) 및 합성 향미제(사카린, 아스파르탐 등)를 유리하게 사용할 수 있다. 본 발명의 식품 조성물은 상기 약학적 조성물과 동일한 방식으로 제제화되어 기능성 식품으로 이용하거나, 각종 식품에 첨가할 수 있다. 본 발명의 조성물을 첨가할 수 있는 식품으로는 예를 들어, 음료류, 육류, 초코렛, 식품류, 과자류, 피자, 라면, 기타 면류, 껌류, 사탕류, 아이스크림류, 알코올 음료류, 비타민 복합제 및 건강보조식품류 등이 있다.Examples of the above-mentioned natural carbohydrates include monosaccharides such as glucose, fructose, etc.; Disaccharides such as maltose, sucrose, etc.; and polysaccharides, such as common sugars such as dextrin and cyclodextrin, and sugar alcohols such as xylitol, sorbitol, and erythritol. The above-described flavoring agents include natural flavoring agents (thaumatin), stevia extracts (e.g., rebaudioside A, glycyrrhizin, etc.), and synthetic flavoring agents (saccharin, aspartame, etc.). The food composition of the present invention can be formulated in the same way as the pharmaceutical composition and used as a functional food or added to various foods. Foods to which the composition of the present invention can be added include, for example, beverages, meat, chocolate, foods, confectionery, pizza, ramen, other noodles, gum, candy, ice cream, alcoholic beverages, vitamin complexes, health supplements, etc. There is.
또한 상기 식품 조성물은 유효성분인 펩타이드 외에 여러 가지 영양제, 비타민, 광물(전해질), 합성 풍미제 및 천연 풍미제 등의 풍미제, 착색제 및 충전제(치즈, 초콜릿 등), 펙트산 및 그의 염, 알긴산 및 그의 염, 유기산, 보호성 콜로이드 증점제, pH 조절제, 안정화제, 방부제, 글리세린, 알콜, 탄산음료에 사용되는 탄산화제 등을 함유할 수 있다. 그 밖에 본 발명의 식품 조성물은 천연 과일 쥬스 및 과일 쥬스 음료 및 야채 음료의 제조를 위한 과육을 함유할 수 있다.In addition, the food composition contains, in addition to the peptide as the active ingredient, various nutrients, vitamins, minerals (electrolytes), flavoring agents such as synthetic and natural flavors, colorants and fillers (cheese, chocolate, etc.), pectic acid and its salts, and alginic acid. and its salts, organic acids, protective colloidal thickeners, pH adjusters, stabilizers, preservatives, glycerin, alcohol, carbonating agents used in carbonated beverages, etc. In addition, the food composition of the present invention may contain pulp for the production of natural fruit juice, fruit juice beverages, and vegetable beverages.
본 발명의 건강기능식품 조성물은, 정제, 캅셀, 분말, 과립, 액상, 환 등의 형태로 제조 및 가공될 수 있다. 본 발명에서 '건강기능식품 조성물'이라 함은 건강기능식품에 관한 법률 제6727호에 따른 인체에 유용한 기능성을 가진 원료나 성분을 사용하여 제조 및 가공한 식품을 말하며, 인체의 구조 및 기능에 대하여 영양소를 조절하거나 생리학적 작용 등과 같은 보건용도에 유용한 효과를 얻을 목적으로 섭취하는 것을 의미한다. 본 발명의 건강기능식품은 통상의 식품 첨가물을 포함할 수 있으며, 식품 첨가물로서의 적합 여부는 다른 규정이 없는 한, 식품의약품안전청에 승인된 식품 첨가물 공전의 총칙 및 일반시험법 등에 따라 해당 품목에 관한 규격 및 기준에 의하여 판정한다. 상기 '식품 첨가물 공전'에 수재된 품목으로는 예를 들어, 케톤류, 글리신, 구연산칼슘, 니코틴산, 계피산 등의 화학적 합성물; 감색소, 감초추출물, 결정셀룰로오스, 고량색소, 구아검 등의 천연첨가물; L-글루타민산나트륨 제제, 면류첨가알칼리제, 보존료 제제, 타르색소제제 등의 혼합제제류 등을 들 수 있다. 예를 들어, 정제 형태의 건강기능식품은 본 발명의 유효성분을 부형제, 결합제, 붕해제 및 다른 첨가제와 혼합한 혼합물을 통상의 방법으로 과립화한 다음, 활택제 등을 넣어 압축성형하거나, 상기 혼합물을 직접 압축 성형할 수 있다. 또한 상기 정제 형태의 건강기능식품은 필요에 따라 교미제 등을 함유할 수도 있다. 캅셀 형태의 건강기능식품 중 경질 캅셀제는 통상의 경질 캅셀에 본 발명의 유효성분을 부형제 등의 첨가제와 혼합한 혼합물을 충전하여 제조할 수 있으며, 연질 캅셀제는 본 발명의 유효성분을 부형제 등의 첨가제와 혼합한 혼합물을 젤라틴과 같은 캅셀기제에 충전하여 제조할 수 있다. 상기 연질 캅셀제는 필요에 따라 글리세린 또는 소르비톨 등의 가소제, 착색제, 보존제 등을 함유할 수 있다. 환 형태의 건강기능식품은 본 발명의 유효성분과 부형제, 결합제, 붕해제 등을 혼합한 혼합물을 기존에 공지된 방법으로 성형하여 조제할 수 있으며, 필요에 따라 백당이나 다른 제피제로 제피할 수 있으며, 또는 전분, 탈크와 같은 물질로 표면을 코팅할 수도 있다. 과립 형태의 건강기능식품은 본 발명의 유효성분의 부형제, 결합제, 붕해제 등을 혼합한 혼합물을 기존에 공지된 방법으로 입상으로 제조할 수 있으며, 필요에 따라 착향제, 교미제 등을 함유할 수 있다.The health functional food composition of the present invention can be manufactured and processed in the form of tablets, capsules, powders, granules, liquids, pills, etc. In the present invention, 'health functional food composition' refers to a food manufactured and processed using raw materials or ingredients with functionality useful to the human body in accordance with Act No. 6727 on Health Functional Food, and has It means taking it for the purpose of controlling nutrients or obtaining useful health effects such as physiological effects. The health functional food of the present invention may contain common food additives, and its suitability as a food additive is determined in accordance with the general provisions of the food additive code and general test methods approved by the Food and Drug Administration, unless otherwise specified. Judgment is made according to specifications and standards. Items listed in the 'Food Additive Code' include, for example, chemical compounds such as ketones, glycine, calcium citrate, nicotinic acid, and cinnamic acid; Natural additives such as dark pigment, licorice extract, crystalline cellulose, kaoliang pigment, and guar gum; Examples include mixed preparations such as sodium L-glutamate preparations, noodle additive alkaline preparations, preservative preparations, and tar coloring preparations. For example, the health functional food in the form of a tablet is made by granulating a mixture of the active ingredient of the present invention with excipients, binders, disintegrants and other additives in a conventional manner, and then adding a lubricant and compression molding, or The mixture can be directly compression molded. Additionally, the health functional food in the form of tablets may contain flavoring agents, etc., if necessary. Among capsule-type health functional foods, hard capsules can be manufactured by filling a regular hard capsule with a mixture of the active ingredient of the present invention mixed with additives such as excipients, and soft capsules can be prepared by mixing the active ingredient of the present invention with additives such as excipients. It can be manufactured by filling the mixture with a capsule base such as gelatin. The soft capsule may contain plasticizers such as glycerin or sorbitol, colorants, preservatives, etc., if necessary. The health functional food in the form of a pill can be prepared by molding a mixture of the active ingredient of the present invention and excipients, binders, disintegrants, etc., using a known method. If necessary, it can be coated with white sugar or other coating agent. Alternatively, the surface can be coated with substances such as starch or talc. Health functional food in the form of granules can be manufactured into granules by mixing a mixture of excipients, binders, disintegrants, etc. of the active ingredients of the present invention by a known method, and may contain flavoring agents, flavoring agents, etc., if necessary. You can.
이하, 본 발명의 실시예를 첨부된 도면을 참고하여 보다 상세하게 설명하도록 한다. 그러나, 하기의 실시예는 본 발명의 내용을 구체화하기 위한 것일 뿐, 이에 의해 본 발명이 한정되는 것은 아닐 것이다.Hereinafter, embodiments of the present invention will be described in more detail with reference to the attached drawings. However, the following examples are only intended to embody the content of the present invention, and the present invention is not limited thereto.
<준비예> 펩타이드의 응집 문제 개선 및 합성<Preparation example> Improvement and synthesis of peptide aggregation problem
본 발명에서는 신규 펩타이드 개량 시 SapB의 구조적 특성은 유지하되, 아미노산 서열을 변경하여 합성이 가능하고, 응집의 문제가 개선된 펩타이드를 디자인하였다. 그후 상기 방법에 따라 디자인된 펩타이드 중에서 응집문제가 개선되어 합성이 가능해진 펩타이드만 선별하였다.In the present invention, when improving a new peptide, we designed a peptide that maintains the structural characteristics of SapB, can be synthesized by changing the amino acid sequence, and has improved aggregation problems. Afterwards, among the peptides designed according to the above method, only peptides that could be synthesized due to improved aggregation problems were selected.
펩타이드의 합성은 고체상 방법(solid phase method)으로 Peptron(Daejeon, Korea)에 의뢰하여 진행하였다. C-terminal로 왕 레진(wang resin)을 이용하였고 Fmoc-L-amino acids의 coupling은 O-Benzotriazole-N,N,N, HBTU(N'-tetramethyl-uronium-hexafluoro-phosphate)로 수행하였다. 아미노산 사이드 체인(Amino acid side chains)은 터트-부틸과 터트-부틸옥시카보닐(tert-butyloxycarbonyl)로 보호하였고 트리플루오로아세트산(trifluoroacetic acid), 물, 티오아니솔(thioanisole) 및 1,2-에탄디올(1,2-ethandithiol)(87.5, 5.0, 5.0, 2.5, v/v)의 혼합물을 이용하여deprotection과 절단을 수행하였다. 고리화는 서열 내의 시스테인 잔기의 이황화 결합으로 완성하였다. Crude 펩타이드는 디에틸에테르(diethylether)로 반복 수세 후 진공 건조 시 키고 RP-HPLC, Shimadzu 5-μm Shimpak ODS C18 칼럼(20Х250 mm)으로 정제하였다. 정제된 펩타이드는 분석용 RP-HPLC, Shimpak ODS C18 칼럼(4.6Х250 mm)으로 확인하였다. 합성한 펩타이드의 분자 질량(molecular masses)은 matrix-assisted laser desorption ionization MALDI-mass spectrometer(Shimadzu Axima Assurance)를 이용하여 확인하였다.The synthesis of the peptide was carried out by Peptron (Daejeon, Korea) using the solid phase method. Wang resin was used as the C-terminal, and coupling of Fmoc-L-amino acids was performed with O-Benzotriazole-N,N,N, HBTU (N'-tetramethyl-uronium-hexafluoro-phosphate). Amino acid side chains were protected with tert-butyl and tert-butyloxycarbonyl and protected with trifluoroacetic acid, water, thioanisole and 1,2- Deprotection and cleavage were performed using a mixture of 1,2-ethandithiol (87.5, 5.0, 5.0, 2.5, v/v). Cyclization was completed by disulfide bonding of cysteine residues in the sequence. Crude peptides were washed repeatedly with diethylether, dried under vacuum, and purified using RP-HPLC and Shimadzu 5-μm Shimpak ODS C18 column (20Х250 mm). The purified peptide was confirmed by analytical RP-HPLC and Shimpak ODS C18 column (4.6Х250 mm). The molecular masses of the synthesized peptide were confirmed using a matrix-assisted laser desorption ionization MALDI-mass spectrometer (Shimadzu Axima Assurance).
상기 방법에 따라 원서열 및 응집 문제 개선된 개량 펩타이드 서열 및 정보는 하기 표 1과 같다(도 1 내지 도 4 참조).The improved peptide sequences and information on which the original sequence and aggregation problems were improved according to the above method are shown in Table 1 below (see Figures 1 to 4).
<실험예 1> 신규 펩타이드의 다제내성균에 대한 항균 활성 측정<Experimental Example 1> Measurement of antibacterial activity of new peptide against multidrug-resistant bacteria
상기 표 1에 나타낸 신규 펩타이드 들의 다제내성균에 대한 항균 활성을 측정하기 위하여 다음과 같이 실험을 진행하였다.To measure the antibacterial activity of the new peptides shown in Table 1 against multidrug-resistant bacteria, an experiment was performed as follows.
균주는 항생제내성균주은행(Culture Collection of Antimicrobial Resistant Microbes)에서 구입하여 사용하였다. 실험에 사용된 균주는 대장균(Escherichia coli CCARM 1G440), 녹농균(Pseudomonas aeruginosa CCARM 0219), 바실루스 세레우스(Bacillus cereus CCARM 0120) 및 황색포도상구균(Staphylococcus aureus CCARM 3090)이다(표 2).Strains were purchased and used from the Culture Collection of Antimicrobial Resistant Microbes. The strains used in the experiment were Escherichia coli CCARM 1G440, Pseudomonas aeruginosa CCARM 0219), Bacillus cereus CCARM 0120, and Staphylococcus aureus CCARM 3090 (Table 2).
모든 균주를 LB 배지에서 배양한 다음, 106 세포/100 ㎕의 균체 농도로 희석하여 96-웰 플레이트에 접종하였다. 그런 다음, 상기 합성한 펩타이드를 각각 96-웰에 희석하여 50 ㎕씩 플레이트에 첨가한 후 최종농도를 0.1~1.8mM로 맞추었다. 플레이트를 37℃에서 16시간 동안 배양한 후, 분광광도계(spectrophotometer, Tecan, Mannedorf, Switzerland)를 이용하여 흡광도 600 nm에서 측정하여 각 균주에 대한 MIC 값을 결정하였다. 음성 대조군은 펩타이드와 동일한 양의 PBS 버퍼를 사용하였다.All strains were cultured in LB medium, then diluted to a cell concentration of 10 6 cells/100 ㎕ and inoculated into 96-well plates. Then, the synthesized peptides were diluted in each 96-well and added to the plate at 50 ㎕ each, and the final concentration was adjusted to 0.1~1.8mM. After culturing the plate at 37°C for 16 hours, the MIC value for each strain was determined by measuring absorbance at 600 nm using a spectrophotometer (Tecan, Mannedorf, Switzerland). As a negative control, the same amount of PBS buffer as the peptide was used.
실험결과는 하기 표 3에 나타내었다.The experimental results are shown in Table 3 below.
본 발명의 신규 펩타이드 서열번호 1, 2 및 3 중에서 1이 가장 뛰어난 항균 활성을 나타냄을 확인하였다. 기존 원서열 SapB이 Bacillus cereus에만 항균활성을 나타낸다는 보고와는 달리 변형된 펩타이드들은 그람양성과 그람음성균 모두에서 우수한 항균 활성을 나타내었다. 특히 글리코펩타이드 계열의 항생제인 반코마이신(Vancomycin) 저항능력이 있는 황생포도상구균에도 항균 활성을 나타냄을 확인하였다.It was confirmed that among the new peptides of the present invention, SEQ ID NOs: 1, 2, and 3, 1 exhibited the most excellent antibacterial activity. Contrary to reports that the original sequence SapB showed antibacterial activity only against Bacillus cereus , the modified peptides showed excellent antibacterial activity against both Gram-positive and Gram-negative bacteria. In particular, it was confirmed that it exhibits antibacterial activity against Staphylococcus aureus, which has resistance to vancomycin, a glycopeptide-based antibiotic.
<실험예 2> 신규 펩타이드의 항암 활성 측정<Experimental Example 2> Measurement of anticancer activity of new peptide
다음으로 상기 표 1에 나타낸 신규 펩타이드 들의 항암 활성을 측정하기 위하여 다음과 같이 실험을 진행하였다.Next, an experiment was conducted as follows to measure the anticancer activity of the new peptides shown in Table 1 above.
항암 활성 측정 대상은 간암세포 Hep G2(ATCC), 대장암세포 SW480(ATCC), 폐암세포 A549(ATCC), 유방암세포 MDA-MB-231(ATCC) 및 흑색종암세포 B16F10(ATCC) 세포주를 사용하였으며, 세포를 CO2(5%)를 포함한 습한 환경에서 37℃의 멸균 조건 하에 배양하였다. 배양 배지는 FBS(10%), 글루타민(4 mM) 및 페니실린/스트렙토마이신으로 보충된 RPMI 1640으로 구성되었다.The anticancer activity was measured using liver cancer cell Hep G2 (ATCC), colon cancer cell SW480 (ATCC), lung cancer cell A549 (ATCC), breast cancer cell MDA-MB-231 (ATCC), and melanoma cancer cell B16F10 (ATCC) cell lines. Cells were cultured under sterile conditions at 37°C in a humid environment containing CO 2 (5%). Culture medium consisted of RPMI 1640 supplemented with FBS (10%), glutamine (4 mM), and penicillin/streptomycin.
MTT assays를 위해 세포주들을 96-웰 플레이트에 1×105 cells(단세포 부유액(single-cell suspension)) 농도로 각 웰에 분주하고, 각 펩타이드들을 농도별(0.1 ~ 2mM)로 24시간 동안 처리하였다. CCK8 용액을 각 웰에 첨가하고, 배양 배지 제거 전에 반응이 일어나도록 플레이트를 37℃에서 1시간 동안 배양하였다. 세포 생존능을 분광광도계(spectrophotometer, Tecan, Mannedorf, Switzerland)를 이용하여 흡광도 450 nm에서 측정하였다. 각 그룹의 세포 생존능은 대조군에 대한 비율(%)로 계산하였다. 그 결과를 하기 표 4에 나타내었다.For MTT assays, cell lines were distributed to each well in a 96-well plate at a concentration of 1 × 10 5 cells (single-cell suspension), and each peptide was treated at different concentrations (0.1 ~ 2mM) for 24 hours. . CCK8 solution was added to each well, and the plate was incubated at 37°C for 1 hour to allow the reaction to occur before removing the culture medium. Cell viability was measured at absorbance at 450 nm using a spectrophotometer (Tecan, Mannedorf, Switzerland). Cell viability of each group was calculated as a ratio (%) to the control group. The results are shown in Table 4 below.
(Hep G2)(HepG2)
(SW480)(SW480)
(A549)(A549)
(MDA-MB-231)(MDA-MB-231)
(B16F10)(B16F10)
표 4에 나타낸 것처럼 본 발명의 신규 펩타이드는 암세포 생장억제 효능이 있었으며, 특히 서열번호 1은 Hep G2와 A549 세포주에 뛰어난 생장억제를 보였고, 서열번호 2는 SW480 세포주에, 서열번호 3은 MDA-MB-231 세포주에 뛰어난 생장억제를 보였다. 이는 각 암세포와 암세포 세포막의 특성이 다르기 때문에 가장 생장억제 효과가 뛰어난 펩타이드가 다른 것으로 예측된다.As shown in Table 4, the novel peptide of the present invention had cancer cell growth inhibition effect, and in particular, SEQ ID NO: 1 showed excellent growth inhibition in Hep G2 and A549 cell lines, SEQ ID NO: 2 showed excellent growth inhibition in SW480 cell line, and SEQ ID NO: 3 showed MDA-MB. It showed excellent growth inhibition in -231 cell line. This is because the characteristics of each cancer cell and the cancer cell membrane are different, so it is predicted that the peptide with the best growth inhibition effect will be different.
<실험예 3> 신규 펩타이드의 적혈구 용혈비율 측정<Experimental Example 3> Measurement of red blood cell hemolysis rate of new peptide
마지막으로 상기 표 1에 나타낸 신규 펩타이드 들의 적혈구 용혈비율을 측정하기 위하여 다음과 같이 실험을 진행하였다.Finally, the following experiment was conducted to measure the red blood cell hemolysis rates of the new peptides shown in Table 1 above.
펩타이드의 용혈비율을 측정하기 위해 Sheep Red Blood Cells(10% Suspension, MP Biomedicals)를 구입하여 사용하였다. PBS 버퍼로 수회 수세한 적혈구 세포를 20㎕씩 96-웰 플레이트에 분주하였다. 펩타이드를 PBS 버퍼에 충분히 녹인 뒤 20㎕씩 적혈구세포에 처리하고 최종 농도가 4, 2, 1, 0.5mM이 되도록 맞추었다. 37℃ 인큐베이터에서 3시간 동안 두고 500 xg로 원심분리 후 회수한 상층액을 405nm에서 흡광도를 측정하여 용혈비율을 계산하였다. 용혈비율의 계산은 양성대조군 처리 샘플을 100%로 하여 상대적인 비율로 계산하였다(하기 수학식 1). 양성대조군은 0.1% Triton X-100을 사용하였고, 음성대조군은 PBS 버퍼를 펩타이드와 동일한 양으로 사용하였다.To measure the hemolysis rate of the peptide, Sheep Red Blood Cells (10% Suspension, MP Biomedicals) were purchased and used. Red blood cells were washed several times with PBS buffer and dispensed into 20 ㎕ 96-well plates. After sufficiently dissolving the peptide in the PBS buffer, 20㎕ each was treated with red blood cells and the final concentrations were adjusted to 4, 2, 1, and 0.5mM. The supernatant was left in a 37°C incubator for 3 hours, centrifuged at 500 xg, and the absorbance of the recovered supernatant was measured at 405 nm to calculate the hemolysis rate. The hemolysis rate was calculated as a relative rate, taking the positive control treated sample as 100% (Equation 1 below). The positive control group used 0.1% Triton X-100, and the negative control group used PBS buffer in the same amount as the peptide.
[수학식 1][Equation 1]
결과는 하기 표 5 및 도 5에 나타내었다.The results are shown in Table 5 and Figure 5 below.
본 발명의 펩타이드들은 전반적으로 낮은 적혈구 용혈비율을 보였고, 항균 또는 항암의 효과를 나타내는 농도보다 더 높은 4mM의 고농도의 처리에도 낮은 용혈비율을 보임을 확인할 수 있었다. 도 5에서 확인할 수 있는 것처럼 0.5mM과 2mM까지 농도 의존적인 용혈비율을 보이지 않았다.The peptides of the present invention showed an overall low red blood cell hemolysis rate, and it was confirmed that they showed a low hemolysis rate even when treated at a high concentration of 4mM, which is higher than the concentration showing antibacterial or anticancer effects. As can be seen in Figure 5, there was no concentration-dependent hemolysis rate up to 0.5mM and 2mM.
이상에서 살펴본 바와 같이, 본 발명의 구체적인 실시예를 상세하게 설명되었으나, 본 발명의 사상을 이해하는 당업자는 동일한 사상의 범위 내에서 다른 구성요소를 추가, 변경, 삭제 등을 통하여, 퇴보적인 다른 발명이나 본 발명 사상의 범위 내에 포함되는 다른 실시예를 용이하게 제안할 수 있을 것이다. 그러므로 이상에서 기술한 실시예들은 모든 면에서 예시적인 것이며 한정적이 아닌 것으로 이해해야만 한다. 본 발명의 범위는 상술한 상세한 설명보다는 후술하는 특허청구의 범위에 의하여 나타내어지며, 특허청구의 범위의 의미 및 범위 그리고 그 균등 개념으로부터 도출되는 모든 변경 또는 변형된 형태가 본 발명의 범위에 포함되는 것으로 해석되어야 한다.As seen above, specific embodiments of the present invention have been described in detail, but those skilled in the art who understand the spirit of the present invention may add, change, delete, etc. other components within the scope of the same spirit, thereby creating other regressive inventions. However, other embodiments that are included within the scope of the present invention can be easily proposed. Therefore, the embodiments described above should be understood in all respects as illustrative and not restrictive. The scope of the present invention is indicated by the scope of the claims described below rather than the detailed description above, and all changes or modified forms derived from the meaning and scope of the claims and their equivalent concepts are included in the scope of the present invention. It should be interpreted as
Claims (8)
A novel peptide with antibacterial or anticancer activity consisting of the amino acid sequence represented by SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3.
상기 신규 펩타이드는 SapB 펩타이드의 응집문제를 개선시키고, 합성이 가능하도록 개량한 것을 특징으로 하는, 신규 펩타이드.
According to paragraph 1,
The new peptide is characterized by improving the aggregation problem of the SapB peptide and improving it to enable synthesis.
An antibacterial or anticancer pharmaceutical composition comprising the novel peptide of claim 1 or 2 as an active ingredient.
An antibacterial quasi-drug composition comprising the novel peptide of any one of claims 1 or 2 as an active ingredient.
An antibacterial cosmetic composition comprising the novel peptide of claim 1 or 2 as an active ingredient.
An antibacterial agricultural and livestock feed composition comprising the novel peptide of any one of claims 1 or 2 as an active ingredient.
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KR20220026803A (en) * | 2020-08-26 | 2022-03-07 | 주식회사 씨쥐케이바이오파마엘티디 | Antibiotic peptide with antibiotic effect on various microorganisms and antibiotics resistant bacteria |
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KR20200135601A (en) * | 2019-05-22 | 2020-12-03 | (주)셀인바이오 | Anti-inflammatory peptide and anti-inflammatory composition |
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