KR20170110977A - Composition for protecting and treating acne comprising Siegesbeckia pubescens - Google Patents

Abstract

The present invention relates to a composition for inhibiting acne, which comprises an extract of Comvita and a comedium extract containing compounds of Chemical Formulas 1 to 7 as an active ingredient. The present invention relates to an antimicrobial effect against P. acnes, Is an invention which can provide a pharmaceutical composition and a cosmetic composition by utilizing an extract which is visible and has no toxicity to skin cells.

Description

TECHNICAL FIELD [0001] The present invention relates to a composition for improving, preventing and treating acne,

The present invention relates to a composition for preventing or treating acne and an improvement cosmetic composition, and more particularly, to a cosmetic composition for prevention or treatment of acne, which contains, as an active ingredient, an extract of a natural product, or a diterpene compound isolated from the extract. A therapeutic pharmaceutical composition or a cosmetic composition for improving acne.

Acne is caused by inflammatory diseases of the fur branch, and it is a very common skin disease that causes inflammation in the facial skin of adolescents and young people. In puberty, both men and women become vigorous in male hormone secretion, stimulating the sebaceous glands attached to the hair follicles. As a result, sebaceous glands are enlarged and many sebum are secreted. At the same time, the stratum corneum at the entrance of the pore becomes thicker and the adhesive strength becomes higher. As a result, the pores become narrowed or clogged, sebum accumulates in the hair follicle, and the bacteria living in the hair follicle grows and inflammation develops. The root cause of acne is the male hormone, which stimulates the sebaceous glands, and the hormone action of progesterone during the menstruation period, which is the male hormone of the sebaceous glands. Or it breaks down the sebaceous glands in the fur branch and produces the free fatty acid. The bacteria called Propionbacterium acnes act there, There are two factors that cause inflammation in the pores and block the pores.

Drugs can be applied by topical application or oral administration for acne treatment. Light acne can be cured by topical application, but if symptoms are severe, oral therapy is effective in combination. The main drugs used for external composition include bezoyl peroxide, azelaic acid, retinoic acid, salicylic acid, and sulfur. However, these substances are not satisfactory because of their inadequate antimicrobial effect against acne bacteria and the risk of side effects .

On the other hand, the present inventors have separated various diterpene derivatives from "comedium", which is a prelude to a hair fitter or a companion plant of the Asteraceae family (Chemical Constituents of Sigesbeckia pubescens Herb, Thesis, Master's Degree, Seoul National University, Feb. 2009). It is an annual plant growing at a height of 40-100cm. It is common in mountains and fields. It has dense short hairs on the whole. It has a pointed end and sawtooth on the edge. It grows in August-September, but at the end of the stem, a yellow flower runs in a flower bed, and the fur on the outer surface of the five spatula-shaped scabbins surrounding the fruit sticks to other objects with sticky liquid. It has been used for the treatment of limb paralysis, hypertension, rheumatism and the like because it has the effect of eliminating (removing) customs from the herb, strengthening the muscles and bones, and lowering the blood pressure.

However, it has been known that the extract is effective for improving skin damage, promoting wrinkles, promoting hair growth, etc., and it has not been studied to be effective for the improvement or treatment of acne.

The present inventors have searched for a substance having antibacterial activity against various compounds derived from natural products. As a result, it was surprisingly found that the extract of Flavonaceae showed a remarkably high activity against Propionibacterium acnes, which is the main causative agent of acne, and that the extract had a kauran skeleton of various diterpene derivatives It was confirmed that diterpene derivatives were contained. Therefore, it has been found that the comed extract containing the specific diterpene derivative can be used as an active ingredient for improving, preventing or treating acne.

Accordingly, it is an object of the present invention to provide a pharmaceutical composition for preventing or treating acne, which comprises the above-mentioned tryna extract or diterpene derivative as an active ingredient.

It is still another object of the present invention to provide a cosmetic composition for improving acne comprising the above-mentioned comedium extract or diterpene derivative as an active ingredient.

The present invention provides a pharmaceutical composition for preventing or treating acne and a cosmetic composition for improving acne, which comprises a comedium extract as an active ingredient.

In addition, the present invention provides a pharmaceutical composition for preventing or treating acne and a cosmetic composition for acne improvement, which comprises any one of diterpene compounds represented by the following formulas (1) to (7).

&Lt; Formula 1 > < EMI ID =

&Lt; Formula 3 > < Formula 4 >

&Lt; Formula 5 > < EMI ID =

In addition, the present invention provides a pharmaceutical composition for preventing or treating acne and a cosmetic composition for improving acne, wherein the comedium extract is extracted with water, C1-C6 alcohol, or a mixed solvent thereof.

The acne is characterized by being caused by Propionibacterium acnes or Staphylococcus epidermidis.

According to the present invention, a specific diterpene derivative having a kauran skeleton isolated from a comedium extract and the extract, that is, the compound of the formula (1) is excellent in antibacterial activity against bacteria causing acne and has excellent anti-inflammatory activity, Can be used in a cosmetic composition for improvement and prevention of acne, and is also useful for the production of pharmaceuticals for the treatment of acne.

Figure 1 shows the antimicrobial effect against P.Acnes versus the concentration of the comedium extract.
Fig. 2 shows the inhibitory activity of an animal dermal fibroblast (NIH3T3) against P. acnes.
Fig. 3 shows cytotoxicity according to the concentration of the comedium extract.

Hereinafter, preferred embodiments of the present invention will be described in detail. It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory and are intended to provide further explanation of the invention as claimed. It will be obvious to those who have knowledge of. In the following description of the present invention, a detailed description of known functions and configurations incorporated herein will be omitted when it may make the subject matter of the present invention rather unclear.

The term "prevention" in the present invention means to inhibit or delay the onset of acne from the cause of acne.

As used herein, the term "treatment" means to inhibit the progression and / or worsening of symptoms without completely healing, thereby stopping the progress of the damage, or improving some or all of the symptoms to induce healing.

It has been found by the present inventors that the diterpene compounds of the coran series isolated from the comed extract and the above extracts, that is, the compounds of the formulas (1) to (7), markedly lower the occurrence of acne. The flavor extract may be obtained by extracting the flavor with water, a C1 to C6 alcohol, or a mixed solvent of water and C1 to C6 alcohol, preferably a mixed solvent of water and methanol. As the mixed solvent of water and methanol, for example, 70 to 90% by volume, preferably about 80% by volume of methanol may be used. The extraction method may be carried out by a conventional method, for example, extraction with stirring at room temperature for 2 to 5 hours, or extraction using a high frequency extractor for 2 to 5 hours. If necessary, the extraction may be carried out at a temperature (for example, about 40 to 60 DEG C), and the extraction may be performed once or plural times (for example, about 3 times). The obtained extract can be dried by a conventional drying method, for example, vacuum drying, hot air drying and the like.

The compounds of the formulas (1) to (7) are known substances and can be isolated from the compound according to a known method. In other words, the method reported by the present inventors (Chemical Constituents of Sigesbeckia pubescens Herb, Master Thesis, Seoul National University, Feb. 2009) or Jiang X, Yunbao M and Yunlong X 1992) Diterpenoids from Siegesbeckia pubescens. Phytochemistry 3 917-921, or a method disclosed in Published Public Publication No. 10-1026070 and the like.

The compositions of the present invention may be formulated in the form of pharmaceutical compositions. The pharmaceutical composition may include a comedium extract or a comedium extract containing the compounds of formulas (1) to (7) as an active ingredient, and may include a pharmaceutically acceptable carrier and may be formulated into a solution, suspension, emulsion, Shampoo, shampoo, ointment, lyophilization, and the like. Preferably, it can be formulated into a transdermal dosage form such as a solution for external use, an emulsion, and an ointment. The pharmaceutically acceptable carrier includes an aqueous diluent or solvent such as phosphate buffered saline, purified water, sterilized water, etc., and may be a non-aqueous diluent such as propylene glycol, polyethylene glycol, olive oil, . Further, if necessary, it may contain a wetting agent, a fragrance, a preservative, and the like.

The dosage of the enteral extract containing the above-mentioned tryptic extract or the compound of Chemical Formulas 1 to 7 contained in the pharmaceutical composition of the present invention varies depending on the condition and the weight of the patient, the degree of the disease, the drug form, the administration route and the period, And the like. For example, the compound of formula 1 may be administered at a dose of 1 to 1000 mg / kg daily, preferably 5 to 500 mg / kg, more preferably about 10 to 50 mg / kg The above administration may be administered once a day or divided into several times. In addition, when formulated into a liquid unit formulation such as a solution for external use or an emulsion, the concentration of the compound of Formula 1 may be in the range of 100 nM to 1 mM, preferably in the range of 1 to 1000 μM And more preferably in the range of 1 to 200 [mu] M.

The composition of the present invention can be formulated in the form of a cosmetic composition. The cosmetic composition of the present invention is not limited to the cosmetic composition of the present invention. The cosmetic composition of the present invention is a cosmetic composition for improving skin damage caused by ultraviolet rays, comprising the above-mentioned comed extract or a comedium extract containing the compound of Chemical Formulas 1 to 7 as an active ingredient. May be in the form of a conventional cosmetic composition such as a cream, a pack, a lotion, an essence, a lotion, a foundation and a makeup base, and the cosmetic composition may be formulated according to a conventional method together with a carrier conventionally used in cosmetics have. The content (or, for example, the extract or the compound corresponding to the dose of the above-mentioned pharmaceutical composition) of the above-mentioned coma extract or the comedium extract containing the compound of the formulas (1) to (7) contained in the unit cosmetic composition depends on the form of the extract / And may range, for example, from 100 nM to 1 mM, preferably from 1 to 1000 μM, and preferably from 1 to 200 μM, per unit cosmetic composition. Of course, the above content may vary depending on the degree of occurrence of acne.

Hereinafter, the present invention will be described in more detail with reference to examples. However, these examples are for illustrating the present invention, and the scope of the present invention is not limited to these examples.

< Example  1> Celebration  Preparation of extract

5 Kg of the dried mixture was added to 10 L of 70% methanol (water: ethanol = 30: 70, v / v) and extracted using a high frequency extractor at room temperature for 3 hours. The extract was filtered to obtain a filtrate, and the remaining residue was further extracted twice by repeating the same procedure with addition of 70% ethanol. The filtrates were combined and dried under reduced pressure at 40 DEG C to obtain 433 g of an extract.

< Example  2> Analysis of Antimicrobial Activity of Extracts

The following experiment was conducted to confirm whether the extract of the present invention prepared in Example 1 had antibacterial activity. The antimicrobial activity was measured by a broth dilution method using a 96-well plate. Heat-sterilized Brain Heart Infusion broth (BHI broth) was added to each well of a 96-well plate, Respectively. Subsequently, the test organism suspension was injected into all wells and incubated at 37 ° C in an anaerobic state. After incubation for 3 days, alamar blue solution was added to each well and cultured for 1 hour. The color development state was observed and the concentration at which no color change from blue to pink was observed was determined as the MIC value.

As a test material to investigate the antimicrobial activity against acne causing bacteria and the antimicrobial effect of each fraction solvent of plant extract, Also, hexane, ethyl acetate, butanol and distilled water were used as a fractionating solvent for the plant extract. Examples of the acne causative agents include Staphylococcus. epidermidis (KCTC 1917, KSC 3709) and Propionibacterium. acnes (KCTC 3314, KSC 9009, 9010) was used.

The results of extracting the pomace and pomegranate with ethanol are shown in Table 1 below. Extraction yields were 13.5 ~ 17.3% in the beef broth and 5.5 ~ 5.6% in the pomegranate broth.

Botanical name Yield (%) Primary Secondary Celebration 17.3 13.5 Chinese yam 5.6 5.5

Botanical name Extract concentration (%) The number of bacteria (cfu / 10 ⁶ bacteria) S. epidernidis P. acnes KCTC 1917 KSC 3709 KCTC 3314 KSC 9009 KSC 9010 Celebration 0.125 2.6 2.3 0 2.8 0.7 0.25 1.1 0.4 2.6 One 1.4 0.5 2.4 1.7 0 2 0 One 0.7 3 0 0 0 Chinese yam 0.125 0 0 0.7 0.6 0.3 0.25 0 0.3 0 1.4 0 0.5 0.6 2.3 0.3 0.3 0.4 One 6.6 3.9 2 0 0.7 Sterilized water 0 26.7 15.9 12.4 14.5 16.5

As shown in Table 2, the antimicrobial activity of the epidermidis and pomegranate extracts was significantly lower than that of sterilized water in all strains of S. epidermidis and P. acnes, The extracts showed almost the same antimicrobial effect. The antimicrobial effect of the compounds contained in the extract was also shown in Table 3 below.

compound P.acnes
IC ₅₀ (μg / ml) One 0.9 2 1.8 3 0.8 4 1.9 5 2.5 6 5.5 7 7.9

< Example  3> Anti-inflammatory cytotoxicity assay

Extract concentration cell 0.5% E 1.0% E 2% E 4% E Cytotoxicity (%) 0 -70 -48 89 68

Anti-inflammatory cytotoxicity assays were performed on skin fivroblast (HDF), which is a skin cell, using comedones, pomegranate, and antibiotics. MTT assay was used for cytotoxicity assays, and the absorbance at 570 mm to 690 mm was measured. The cytotoxicity against human skin cells according to the concentration of the extract was not cytotoxic up to 1% of the extract.

< Example  4> Inhibitory activity of fibroblast adhesion to skin pathogens

As a result of measuring the inhibitory activity of the extract of the comedium against the adherence of an animal skin fibroblast (NIH3T3) of a skin pathogen, the inhibitory activity against acne bacterium (P. acnes) was shown according to the concentration (0.01-1.0 mg / ml). Fig. 2 shows the inhibitory activity of the extract of Flaviviridae against adherence of animal skin fibroblasts to skin pathogens.

concentration (mg / ml) 0 0.25 0.5 0.1 Attached P. acnes 100 77 66 44

The foregoing description is merely illustrative of the present invention, and various modifications may be made without departing from the essential characteristics of the present invention. Accordingly, the embodiments disclosed herein are for the purpose of limiting the present invention and are not to be construed as limiting the spirit and scope of the present invention. The scope of protection of the present invention should be construed according to the claims, and all the techniques within the scope of the same should be construed as being included in the scope of the present invention.

Claims (8)

A pharmaceutical composition for prevention or treatment of acne, comprising an extract of Comvitae as an active ingredient
The pharmaceutical composition for preventing or treating acne according to claim 1, wherein the formula extract comprises any one of diterpene compounds represented by the following formulas (1) to (7)
&Lt; Formula 1 >< EMI ID =

&Lt; Formula 3 &gt;&lt; Formula 4 &gt;

&Lt; Formula 5 &gt;&lt; EMI ID =

The pharmaceutical composition for preventing or treating acne according to claim 1, wherein the flavor extract is extracted with water, a C1-C6 alcohol, or a mixed solvent thereof
The acne-preventing or treating composition according to claim 1, wherein the acne is caused by Propionibacterium acnes or Staphylococcus epidermidis.
A cosmetic composition for improving acne, comprising as an active ingredient a flavor extract
The cosmetic composition for improving acne according to claim 5, wherein the formula extract comprises any one of diterpene compounds represented by the following formulas (1) to (7)
&Lt; Formula 1 >< EMI ID =

&Lt; Formula 3 &gt;&lt; Formula 4 &gt;

&Lt; Formula 5 &gt;&lt; EMI ID =

[Claim 6] The cosmetic composition for improving acne according to claim 5, wherein the formula extract is extracted with water, C1-C6 alcohol or a mixed solvent thereof
The acne-improving cosmetic composition according to claim 5, wherein the acne is caused by Propionibacterium acnes or Staphylococcus epidermidis.

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