JP2005272346A - New compound contained in hericium erinaceum and anti-methicillin-resistant staphylococcus aureus agent - Google Patents
New compound contained in hericium erinaceum and anti-methicillin-resistant staphylococcus aureus agent Download PDFInfo
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- JP2005272346A JP2005272346A JP2004087529A JP2004087529A JP2005272346A JP 2005272346 A JP2005272346 A JP 2005272346A JP 2004087529 A JP2004087529 A JP 2004087529A JP 2004087529 A JP2004087529 A JP 2004087529A JP 2005272346 A JP2005272346 A JP 2005272346A
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 29
- 229960003085 meticillin Drugs 0.000 title claims abstract description 9
- 241000191967 Staphylococcus aureus Species 0.000 title claims abstract description 8
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- 235000007328 Hericium erinaceus Nutrition 0.000 title abstract description 3
- 239000004480 active ingredient Substances 0.000 claims abstract description 8
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 33
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 33
- 239000003795 chemical substances by application Substances 0.000 claims description 33
- 239000002904 solvent Substances 0.000 claims description 23
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 18
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 235000013399 edible fruits Nutrition 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- 206010041925 Staphylococcal infections Diseases 0.000 abstract description 44
- 208000015688 methicillin-resistant staphylococcus aureus infectious disease Diseases 0.000 abstract description 44
- 230000000844 anti-bacterial effect Effects 0.000 abstract description 13
- RJQXTJLFIWVMTO-TYNCELHUSA-N Methicillin Chemical compound COC1=CC=CC(OC)=C1C(=O)N[C@@H]1C(=O)N2[C@@H](C(O)=O)C(C)(C)S[C@@H]21 RJQXTJLFIWVMTO-TYNCELHUSA-N 0.000 abstract description 2
- 238000000605 extraction Methods 0.000 description 22
- 239000000047 product Substances 0.000 description 22
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 20
- 235000013305 food Nutrition 0.000 description 19
- 238000011282 treatment Methods 0.000 description 13
- 239000003814 drug Substances 0.000 description 9
- 239000003242 anti bacterial agent Substances 0.000 description 7
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- 235000001674 Agaricus brunnescens Nutrition 0.000 description 2
- 208000035473 Communicable disease Diseases 0.000 description 2
- 206010011409 Cross infection Diseases 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
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- 241000123222 Hericium Species 0.000 description 1
- 241000959662 Hydnaceae Species 0.000 description 1
- 229930182555 Penicillin Natural products 0.000 description 1
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 1
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- WZPBZJONDBGPKJ-VEHQQRBSSA-N aztreonam Chemical compound O=C1N(S([O-])(=O)=O)[C@@H](C)[C@@H]1NC(=O)C(=N/OC(C)(C)C(O)=O)\C1=CSC([NH3+])=N1 WZPBZJONDBGPKJ-VEHQQRBSSA-N 0.000 description 1
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- YZBQHRLRFGPBSL-RXMQYKEDSA-N carbapenem Chemical compound C1C=CN2C(=O)C[C@H]21 YZBQHRLRFGPBSL-RXMQYKEDSA-N 0.000 description 1
- 150000001782 cephems Chemical class 0.000 description 1
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- 239000002132 β-lactam antibiotic Substances 0.000 description 1
- 229940124586 β-lactam antibiotics Drugs 0.000 description 1
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
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Abstract
Description
本発明は、ヤマブシタケの子実体に含まれる新規化合物、及び抗メチシリン耐性黄色ブドウ球菌剤に関する。 The present invention relates to a novel compound contained in the fruit body of Yamabushitake and an anti-methicillin-resistant Staphylococcus aureus agent.
従来、各種の抗生物質が開発され、火傷、切り傷、感染症等の治療目的、或いは手術時の感染予防の目的で、臨床上繁用されてきた。しかしながら、近年、抗生物質の過度の依存が、多種類の抗生物質に対して耐性を示す病原菌を出現させるに至り、これらの耐性菌が重篤な感染症を引き起こしている。とりわけ、メチシリン耐性黄色ブドウ球菌(methicillin resistant Stapylococcus aureus、以下MRSAという)は、ペニシリン系抗生物質、セフェム系抗生物質、モノバクタム系抗生物質、カルバペネム系抗生物質等のβラクタム系抗生物質に対して耐性を備え、しかも高い病原性を有しており、市中感染や院内感染により深刻な感染症を生じさせている。 Conventionally, various antibiotics have been developed and clinically used for the purpose of treating burns, cuts, infectious diseases, etc., or for the purpose of preventing infection during surgery. However, in recent years, excessive dependence of antibiotics has led to the emergence of pathogenic bacteria that are resistant to many types of antibiotics, and these resistant bacteria cause serious infections. In particular, methicillin resistant Stapylococcus aureus (hereinafter referred to as MRSA) is resistant to β-lactam antibiotics such as penicillin antibiotics, cephem antibiotics, monobactam antibiotics, carbapenem antibiotics, etc. Equipped with high pathogenicity, it causes serious infectious diseases due to community and hospital infections.
従来、MRSA感染症の治療剤としては、バイコマイシンが知られている。しかしながら、バイコマイシンには、聴覚や腎臓への副作用が知られており、安全性の点で問題があった。また、近年、バイコマイシンに対して耐性を備えるMRSAの出現が報告されており、バイコマイシンの投与では、MRSA感染症の治療効果が期待できなくなっている。 Conventionally, baicomycin is known as a therapeutic agent for MRSA infection. However, baicomycin is known to have side effects on hearing and kidney, and has a problem in terms of safety. In recent years, the emergence of MRSA having resistance to baicomycin has been reported, and the therapeutic effect of MRSA infection cannot be expected with the administration of baicomycin.
このような従来技術を背景として、安全性を有し、MRSAに対して有効な抗菌成分の開発が医療上の課題となっている。 Against the background of such conventional technology, the development of antibacterial components that are safe and effective against MRSA has become a medical problem.
ところで、近年、ハリタケ科のキノコであるヤマブシタケに含まれる化合物及びその薬効効果について、種々報告されている。例えば、ヤマブシタケには、クロマン誘導体が含まれており、これがプロスタグランジンＥ２の産生促進作用や神経成長因子の産生誘導作用を発揮することが報告されている（特許文献１参照）。しかしながら、ヤマブシタケにMRSAに対して抗菌作用を発揮する成分が含まれているか否かについては、一切知られていない。
そこで本発明の目的は、上記従来技術の課題を解決することである。より詳細には、本発明は、MRSAに対して有効な抗菌作用を発揮する成分を提供することを目的とするものである。 Accordingly, an object of the present invention is to solve the above-described problems of the prior art. More specifically, an object of the present invention is to provide a component that exhibits an effective antibacterial action against MRSA.
本発明者らは、上記課題を解決すべく鋭意検討したところ、ヤマブシタケには、下記構造式の化合物が含まれており、該化合物はMRSAに対して優れた抗菌作用を発揮することを見出した。本発明はかかる知見に基づいて、更に検討を重ねて開発されたものである。 As a result of intensive studies to solve the above problems, the present inventors have found that Yamabushitake contains a compound having the following structural formula, and that the compound exhibits an excellent antibacterial action against MRSA. . The present invention has been developed through further studies based on such findings.
即ち、本発明は、下記に掲げる発明を提供するものである：
項１． 下記一般式（１）で表される化合物。
That is, the present invention provides the following inventions:
Item 1. A compound represented by the following general formula (1).
項３． 酢酸エチル、エタノール、メタノール、アセトン及びこれらと水の混合物よりなる群から選択される少なくとも１種の溶媒を用いてヤマブシタケの子実体を抽出することにより得られる抽出物を有効成分とする、抗メチシリン耐性黄色ブドウ球菌剤。
Item 3. An anti-methicillin comprising, as an active ingredient, an extract obtained by extracting fruit bodies of Yamabushitake using at least one solvent selected from the group consisting of ethyl acetate, ethanol, methanol, acetone, and a mixture of these and water Resistant Staphylococcus aureus agent.
以下に、本発明を詳細に説明する。 The present invention is described in detail below.
本発明は、下記一般式（１）で表される化合物を提供する。 The present invention provides a compound represented by the following general formula (1).
一般式（１）で表される化合物を取得するための抽出溶媒の一例として、酢酸エチル、メタノール、エタノール、アセトン等の有機溶媒、及びこれらの有機溶媒と水の混合物が挙げられる。これらの溶媒は、１種単独で使用してもよく、また２種以上を任意に組み合わせて使用してもよい。上記抽出溶媒の中で、好ましくは、酢酸エチル、エタノール及びこれらと水の混合物であり、更に好ましくは酢酸エチル及びこれと水の混合物、特に好ましくは酢酸エチルである。上記有機溶媒と水の混合物を抽出溶媒として使用する場合、該混合物における有機溶媒と水の混合比率としては、例えば、該混合物中に水が１〜９９重量％、好ましくは５〜５０重量％、更に好ましくは５〜３０重量％となる割合が例示される。 Examples of the extraction solvent for obtaining the compound represented by the general formula (1) include organic solvents such as ethyl acetate, methanol, ethanol, and acetone, and a mixture of these organic solvents and water. These solvents may be used alone or in any combination of two or more. Among the above extraction solvents, ethyl acetate, ethanol and a mixture thereof with water are preferred, ethyl acetate and a mixture thereof with water are more preferred, and ethyl acetate is particularly preferred. When the mixture of the organic solvent and water is used as the extraction solvent, the mixing ratio of the organic solvent and water in the mixture is, for example, 1 to 99% by weight of water in the mixture, preferably 5 to 50% by weight, More preferably, the ratio which becomes 5 to 30 weight% is illustrated.
一般式（１）で表される化合物を得るには、まず、ヤマブシタケの子実体をそのまま、或いは必要に応じて乾燥、細切、破砕、圧搾又は煮沸処理したものを、上記抽出溶媒で抽出処理する。当該抽出処理は、抽出溶媒１００ｍｌに対して、ヤマブシタケの子実体が乾燥重量で通常５〜３０ｇ、好ましくは１５〜２５ｇ程度を加えて行うことができる。抽出処理は、通常室温で行われるが、３０〜９０℃に加熱して行ってもよい。また、抽出処理は、抽出溶媒中でヤマブシタケの子実体を攪拌又は静置させることにより行うことができるが、必要に応じて還流を行ってもよい。抽出時間は、通常２〜２４時間、好ましくは１０〜１５時間である。 In order to obtain the compound represented by the general formula (1), first, the fruit body of Yamabushitake is dried or shredded, crushed, pressed or boiled as it is, and extracted with the above extraction solvent. To do. The extraction treatment can be carried out by adding 5 to 30 g, preferably about 15 to 25 g, of dry weight of the fruit body of Yamabushitake to 100 ml of the extraction solvent. The extraction treatment is usually performed at room temperature, but may be performed by heating to 30 to 90 ° C. Moreover, although an extraction process can be performed by stirring or standing the fruit body of Yamabushitake in the extraction solvent, you may reflux as needed. The extraction time is usually 2 to 24 hours, preferably 10 to 15 hours.
上記抽出処理に先立って、ヤマブシタケの子実体をクロロホルムに浸漬（以下、単にクロロホルム処理という）して、クロロホルム可溶化画分を除去した後、得られた固形分を上記抽出処理に供してもよい。このように、前処理として、クロロホルム処理を行うことによって、より高い純度で一般式（１）で表される化合物を抽出溶媒に抽出させることが可能になる。当該クロロホルム処理における、クロロホルムに対するヤマブシタケの子実体の添加量、処理温度、処理時間、その他の条件等は、前記抽出処理の条件と同様である。 Prior to the extraction treatment, the fruit body of Yamabushitake is immersed in chloroform (hereinafter simply referred to as chloroform treatment) to remove the chloroform-solubilized fraction, and the resulting solid content may be subjected to the extraction treatment. . Thus, by performing chloroform treatment as pretreatment, it becomes possible to extract the compound represented by the general formula (1) with higher purity into the extraction solvent. In the chloroform treatment, the amount of Yamabushitake fruiting body added to chloroform, treatment temperature, treatment time, other conditions, and the like are the same as those for the extraction treatment.
また、生の状態のヤマブシタケの子実体を用いて抽出処理する場合、その抽出処理は、例えば、以下に示す態様の抽出方法によって行うこともできる：メタノール、エタノール、アセトン、又はこれらと水の混合物（例えば８０〜８５％エタノール水溶液、８０〜８５％メタノール水溶液、８５％アセトン水溶液等）を用いて、ヤマブシタケの子実体を室温〜９０℃で１〜７２時間抽出処理し、次いで固形分を除去して更に酢酸エチルを混合し、酢酸エチル中に抽出された成分を回収する。 In addition, in the case of performing an extraction process using the raw fruit body of Yamabushitake, the extraction process can also be performed by, for example, an extraction method of the following mode: methanol, ethanol, acetone, or a mixture of these and water (For example, 80-85% ethanol aqueous solution, 80-85% methanol aqueous solution, 85% acetone aqueous solution, etc.) are used to extract the fruit bodies of Yamabushitake at room temperature to 90 ° C. for 1 to 72 hours, and then the solid content is removed. Further, ethyl acetate is mixed, and the components extracted in ethyl acetate are recovered.
上記抽出処理後に、抽出溶媒から固形分（不溶化成分）を除去し、次いで減圧下で加熱して溶媒を蒸発させることにより、ヤマブシタケ溶媒抽出物を得ることができる。斯くして得られるヤマブシタケの溶媒抽出物には、一般式（１）で表される化合物が含まれている。当該ヤマブシタケの溶媒抽出物を、必要に応じて、シリカゲルカラムクロマトグラフィー、薄層クロマトグラフィー、高速液体クロマトグラフィー等の各種クロマト分画処理に供することによって、一般式（１）で表される化合物を単離することができる。 After the extraction treatment, a solid content (insolubilized component) is removed from the extraction solvent, and then the solvent is evaporated by heating under reduced pressure, whereby a Yamabushitake solvent extract can be obtained. The solvent extract of Yamabushitake thus obtained contains the compound represented by the general formula (1). By subjecting the Yamabushitake solvent extract to various chromatographic fractionation treatments such as silica gel column chromatography, thin layer chromatography, and high performance liquid chromatography as necessary, the compound represented by the general formula (1) is obtained. It can be isolated.
また、一般式（１）で表される化合物は、上記抽出処理後に、抽出溶媒をそのまま上記のクロマト分画処理に供することによっても得ることができる。 In addition, the compound represented by the general formula (1) can also be obtained by subjecting the extraction solvent to the chromatographic fractionation as it is after the extraction treatment.
斯くして得られる一般式（１）で表される化合物は、下記の物理化学的性質及び構造解析結果を示す。
(1)分子量：１９０．０８４１（Ｃ8Ｈ14Ｏ5）
(2)色及び形状：無色アモルファス
(3)溶媒に対する溶解性：（酢酸エチル、メタノール、エタノール、アセトン）に可溶；水にやや可溶
(4)塩基性、中性、酸性の別：（中性）
(5)核磁気共鳴スペクトル（1Ｈ−ＮＭＲ）：1.30 (d, J=6.4), 1.88 (d, J=14.3), 2.45 (dd, J=14.3, 9.8), 3.33 (b, s), 3.82 (q, J=6.4), 3.74 (d, J=8.1), 3.89 (J=9.8), 4.06 (d, J=8.1)
(6)核磁気共鳴スペクトル（13ＣＮＭＲ）：15.1, 39.7, 61.9, 66.5, 69.5, 70.5, 75.3, 97.6
当該一般式（１）で表される化合物は、MRSAに対して優れた抗菌作用を発揮できるので、抗MRSA剤の有効成分として用いることができる。また、前述するように、ヤマブシタケの上記溶媒抽出物には一般式（１）で表される化合物が含有されており、当該抽出物を抗MRSA剤の有効成分として用いることもできる。
The compound represented by the general formula (1) thus obtained exhibits the following physicochemical properties and structural analysis results.
(1) Molecular weight: 190.0841 (C 8 H 14 O 5 )
(2) Color and shape: colorless amorphous
(3) Solubility in solvents: soluble in (ethyl acetate, methanol, ethanol, acetone); slightly soluble in water
(4) Basic, neutral and acidic: (neutral)
(5) Nuclear magnetic resonance spectrum (1 H-NMR): 1.30 (d, J = 6.4), 1.88 (d, J = 14.3), 2.45 (dd, J = 14.3, 9.8), 3.33 (b, s), 3.82 (q, J = 6.4), 3.74 (d, J = 8.1), 3.89 ( J = 9.8), 4.06 (d, J = 8.1)
(6) Nuclear magnetic resonance spectrum ( 13 CNMR): 15.1, 39.7, 61.9, 66.5, 69.5, 70.5, 75.3, 97.6
Since the compound represented by the general formula (1) can exhibit an excellent antibacterial action against MRSA, it can be used as an active ingredient of an anti-MRSA agent. As described above, the above-mentioned solvent extract of Yamabushitake contains a compound represented by the general formula (1), and the extract can be used as an active ingredient of an anti-MRSA agent.
本発明の抗MRSA剤は、例えば、食品や医薬品の分野において使用され、これによって、MRSAに対して優れた抗菌作用を有する食品や医薬品が提供される。 The anti-MRSA agent of the present invention is used, for example, in the field of foods and pharmaceuticals, thereby providing foods and pharmaceuticals having an excellent antibacterial action against MRSA.
例えば、医薬分野では、本発明の抗MRSA剤は、薬学的に許容される基材や担体と共に製剤化されて、医薬製剤として使用される。当該医薬製剤には、必要に応じて、結合剤、崩壊剤、滑沢剤、湿潤化剤、緩衝剤、保存剤、香料等の薬学的に許容される添加剤を任意に配合してもよい。当該医薬製剤の形態としては、特に制限されるものではないが、一例として、フィルム剤、トローチ、散剤、錠剤、顆粒剤、カプセル剤、シロップ剤等を挙げることができる。 For example, in the pharmaceutical field, the anti-MRSA agent of the present invention is formulated with a pharmaceutically acceptable base or carrier and used as a pharmaceutical preparation. The pharmaceutical preparation may optionally contain pharmaceutically acceptable additives such as a binder, a disintegrant, a lubricant, a wetting agent, a buffer, a preservative, and a fragrance. . Although it does not restrict | limit especially as a form of the said pharmaceutical formulation, A film agent, a troche, a powder, a tablet, a granule, a capsule, a syrup agent etc. can be mentioned as an example.
本発明の抗MRSA剤を含む医薬製剤の投与量は、投与形態、投与目的、投与対象者の年齢や体重等によって異なるが、成人１日当たりの投与量として、一般式（１）で表される化合物が、例えば０．１〜５００ｍｇに相当する量を挙げることができる。また、本発明の抗MRSA剤を含む医薬製剤の一日当たりの投与回数は、投与対象者の年齢や体重、症状、該抗MRSA剤の１回当たりの投与量等に応じて適宜設定できる。 The dose of the pharmaceutical preparation containing the anti-MRSA agent of the present invention varies depending on the administration form, administration purpose, age and weight of the administration subject, etc., but is represented by the general formula (1) as the daily dose for an adult. An amount of the compound corresponding to, for example, 0.1 to 500 mg can be mentioned. In addition, the number of administrations per day of the pharmaceutical preparation containing the anti-MRSA agent of the present invention can be appropriately set according to the age, weight and symptoms of the administration subject, the dose per administration of the anti-MRSA agent, and the like.
また、例えば、食品分野では、本発明の抗MRSA剤は、食品素材として各種食品に配合されることによって使用される。本発明の抗MRSA剤が配合可能な食品は、一般の飲食品の他、特定保健用食品、栄養補助食品、機能性食品、病者用食品等を挙げることができる。 In addition, for example, in the food field, the anti-MRSA agent of the present invention is used by being blended in various foods as a food material. Examples of foods that can be formulated with the anti-MRSA agent of the present invention include foods for specified health use, nutritional supplements, functional foods, foods for the sick, and the like in addition to general foods and drinks.
本発明の抗MRSA剤を食品に配合する場合、食品中の該MRSA剤の配合割合については、該食品の種類、対象者の年齢、性別、期待される効果等に応じて、適宜設定することができる。一例として、上記食品の総重量に対して、一般式（１）で表される化合物が０．０１〜５重量％となる割合が挙げられる。 When blending the anti-MRSA agent of the present invention in food, the blending ratio of the MRSA agent in the food should be set appropriately according to the type of food, the age, sex, expected effect, etc. of the subject. Can do. As an example, the ratio by which the compound represented by General formula (1) will be 0.01 to 5 weight% with respect to the total weight of the said foodstuff is mentioned.
また、本発明の抗MRSA剤含む食品の１日当たりの摂取量や摂取回数は、前記抗MRSA剤を含む医薬製剤の場合と同様である。 In addition, the daily intake and the number of intakes of the food containing the anti-MRSA agent of the present invention are the same as in the case of the pharmaceutical preparation containing the anti-MRSA agent.
更に、本発明の抗MRSA剤は、上記食品や医薬品以外の分野の製品に対しても使用できる。例えば、本発明の抗MRSA剤を各種繊維製品、紙製品、化学製品等の製品に担持させることにより、これらの製品にMRSAに対する抗菌作用を備えさせることができる。これらの製品としては、例えば、寝具（布団、シーツ等）、カバー、カーペット、パジャマ、手術着、白衣、マスク、包帯、ガーゼ、紙タオル、紙製シーツ、紙製カバー、モップ、雑巾、便座カバー等が挙げられる。特に、医療用具（マスク、包帯、ガーゼ）、褥瘡患者等の寝具(布団・シーツ、パジャマ等)、MRSA感染患を媒介し得るもの等の製品に対しては、本発明の抗MRSA剤を好適に使用できる。 Furthermore, the anti-MRSA agent of the present invention can also be used for products in fields other than the above foods and pharmaceuticals. For example, by carrying the anti-MRSA agent of the present invention on products such as various fiber products, paper products, and chemical products, these products can be provided with an antibacterial action against MRSA. Examples of these products include bedding (futon, sheets, etc.), covers, carpets, pajamas, surgical clothes, lab coats, masks, bandages, gauze, paper towels, paper sheets, paper covers, mops, rags, toilet seat covers. Etc. In particular, the anti-MRSA agent of the present invention is suitable for products such as medical devices (masks, bandages, gauze), bedclothes such as pressure ulcer patients (futons / sheets, pajamas, etc.) and those that can mediate MRSA infections. Can be used for
本発明の抗MRSA剤を上記製品に担持させる方法としては、特に制限されず、当業界で一般的に使用されている方法を採用すればよい。例えば、本発明の抗MRSA剤を含有する水溶液を上記製品に直接噴霧する方法や、上記製品の構成材料に予め本発明の抗MRSA剤を練り込んでおき（又は付着させておき）、これを用いて上記製品を調製する方法等が挙げられる。 The method for supporting the anti-MRSA agent of the present invention on the product is not particularly limited, and a method generally used in the art may be employed. For example, a method in which an aqueous solution containing the anti-MRSA agent of the present invention is directly sprayed on the product, or the anti-MRSA agent of the present invention is kneaded (or adhered) in advance to the constituent material of the product, The method of preparing the said product using it etc. are mentioned.
上記製品に、本発明の抗MRSA剤を担持させる量としては、対象製品の種類、対象製品の使用環境等によって異なり一律に規定することはできないが、一例として対象製品の総重量に対して、一般式（１）で表される化合物が０．００１〜５重量％となる割合が挙げられる。 The amount of the anti-MRSA agent of the present invention supported on the product cannot be uniformly defined depending on the type of the target product, the usage environment of the target product, etc., but as an example, with respect to the total weight of the target product, The ratio by which the compound represented by General formula (1) will be 0.001 to 5 weight% is mentioned.
本発明の抗MRSA剤は、MRSAに対して顕著に優れた抗菌作用を発揮できる。そのため、本発明の抗MRSA剤を食品や医薬品に配合することにより、MRSA感染症治療用の食品又は医薬品を提供できる。また、本発明の抗MRSA剤を含有する食品又は医薬品は、MRSA感染予防用の食品又は医薬品としても有用である。 The anti-MRSA agent of the present invention can exhibit a remarkably excellent antibacterial action against MRSA. Therefore, the food or medicine for treating MRSA infection can be provided by blending the anti-MRSA agent of the present invention into food or medicine. Moreover, the food or medicine containing the anti-MRSA agent of the present invention is also useful as a food or medicine for preventing MRSA infection.
また、本発明の抗MRSA剤を、各種繊維製品、紙製品、化学製品等の各種製品に配合することにより、該製品に抗MRSA作用を備えさせることができる。このような抗MRSA作用を有する製品は、MRSAの感染症が起こりやすい病院、保育園、幼稚園、小学校、老人ホーム等の施設において有用である。また、特に、病院内で使用される上記各種製品（例えば、衛生用具、医療用具、入院患者の寝具等）に本発明の抗MRSA剤を担持させることによって、MRSAの院内感染の予防に有用である。 Further, the anti-MRSA agent of the present invention can be provided with various anti-MRSA effects by blending it with various products such as various fiber products, paper products, and chemical products. Such products having anti-MRSA activity are useful in facilities such as hospitals, nurseries, kindergartens, elementary schools, nursing homes where MRSA infections are likely to occur. In particular, the above-mentioned various products used in hospitals (for example, sanitary equipment, medical equipment, bedclothes for hospitalized patients, etc.) are useful for preventing MRSA nosocomial infections by carrying the anti-MRSA agent of the present invention. is there.
本発明の抗MRSA剤は、食用として使用されているヤマブシタケに含まれる化合物を有効成分とするものであるので、安全性の点でも問題なく使用することができる。 Since the anti-MRSA agent of the present invention comprises a compound contained in Yamabushitake, which is used for food, as an active ingredient, it can be used without any problem in terms of safety.
以下、実施例を挙げて本発明を説明するが、本発明はこれらの実施例に限定されるものではない。 EXAMPLES Hereinafter, although an Example is given and this invention is demonstrated, this invention is not limited to these Examples.
実施例１ 一般式（１）で表される化合物の調製
ヤマブシタケの乾燥子実体３．８ｋｇをクロロホルム２０Ｌに加えて、ホモジナイズ処理し２５℃で１２時間、静置した。次いで、固形分を回収し、該固形分（乾燥重量）３．７ｋｇを酢酸エチル２０Ｌに加えて、２５℃で１２時間、静置した。
Example 1 Preparation of Compound Represented by General Formula (1) 3.8 kg of dried fruit body of Yamabushitake was added to 20 L of chloroform, homogenized, and allowed to stand at 25 ° C. for 12 hours. Subsequently, solid content was collect | recovered, 3.7 kg of this solid content (dry weight) was added to 20 L of ethyl acetate, and it left still at 25 degreeC for 12 hours.
得られた酢酸エチル層４０ｇをシリカゲルカラム（silica gel 60N、関東化学社製）を用いたカラムクロマトグラフィーに供した。この際、展開溶媒として、順次極性が大きくなるように、クロロホルム／メタノール＝９：１、８：２、７：３、６：４、５：５、０：１０をそれぞれ１Ｌ用いて、４０ｍＬの画分を合計１５０画分得た。この内、クロロホルム／メタノール＝８：２溶出画分を、更に展開溶媒としてクロロホルム／メタノール＝８：２、６：４、０：１０を各１Ｌ用いて、シリカゲルカラムクロマトグラフィーを行い、４０ｍＬの画分を合計７５画分得た。次いで、得られた第２１〜２８画分について、クロロホルム／メタノール＝８：２を展開溶媒として用いて薄層クロマトグラフィー（ＴＬＣ）を行い、スポットが検出された画分をかき取った。更に、回収した画分をＨＰＬＣ（カラム；CAPCEL PAK C 18、流速；５ｍＬ／ｍｉｎ、溶媒１０％メタノール水溶液）に供し、一般式（１）で表される化合物４．１ｍｇを単離した。 40 g of the obtained ethyl acetate layer was subjected to column chromatography using a silica gel column (silica gel 60N, manufactured by Kanto Chemical Co., Inc.). At this time, chloroform / methanol = 9: 1, 8: 2, 7: 3, 6: 4, 5: 5, and 0:10 were each used as a developing solvent so that the polarity increased, and 40 mL A total of 150 fractions were obtained. Among these, chloroform / methanol = 8: 2 elution fraction was further subjected to silica gel column chromatography using chloroform / methanol = 8: 2, 6: 4, 0:10 1 L each as a developing solvent. A total of 75 fractions were obtained. Subsequently, the obtained 21st to 28th fractions were subjected to thin layer chromatography (TLC) using chloroform / methanol = 8: 2 as a developing solvent, and the fractions in which spots were detected were scraped off. Further, the collected fraction was subjected to HPLC (column; CAPCEL PAK C 18, flow rate: 5 mL / min, solvent 10% methanol aqueous solution), and 4.1 mg of the compound represented by the general formula (1) was isolated.
試験例１ 抗MRSA作用評価試験
MRSA2932株（臨床分離菌、名古屋大学医学部から入手）を５ｍＬの液体培地を用いて、３０℃で１６時間、２００ｒｐｍで振とう培養し、MRSA培養液を得た。このMRSA培養液を２０倍に希釈したもの１００μＬをトリプトソーヤ寒天培地プレート（表面積６０．８ｃｍ2、ＴＳＡ培地、Becton Dickinson社製）に塗抹し、これを検定用培地とした。該検定用培地に、実施例１で得られた一般式（１）で表される化合物を1ｍｇ／ｍＬの濃度で含有する水溶液を染み込ませて乾燥させたペーパーディスク（抗生物質検定用８ｍｍ、アドバンテック社製）を、静かにピンセットで乗せて、３０℃で２０時間培養を行った。培養後、検定用培地に生成した阻止円の直径を測定し、下記式に従って抗菌活性を求めた。
Test Example 1 Anti-MRSA activity evaluation test
MRSA2932 strain (clinical isolate, obtained from Nagoya University School of Medicine) was cultured with shaking at 200 rpm at 30 ° C. for 16 hours using 5 mL of liquid medium to obtain MRSA culture solution. 100 μL of this MRSA culture solution diluted 20-fold was smeared on a tryptosoya agar plate (surface area 60.8 cm 2 , TSA medium, Becton Dickinson) and used as a test medium. A paper disk (8 mm for antibiotic test, Advantech) in which the test medium was impregnated with an aqueous solution containing the compound represented by the general formula (1) obtained in Example 1 at a concentration of 1 mg / mL. Was gently put on with tweezers and cultured at 30 ° C. for 20 hours. After culturing, the diameter of the inhibition circle generated in the assay medium was measured, and antibacterial activity was determined according to the following formula.
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| JP2015071639A (en) * | 2011-07-15 | 2015-04-16 | 株式会社王樹製薬 | Antimicrobial agent and method for producing the same |
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