KR101573738B1 - Perfume composition for awakening effect or enhancing ability to concentration comprising essential oil of Zizyphus jujuba Miller as an effective component - Google Patents

Abstract

The perfume composition comprising the acidophilic essential oil of the present invention as an active ingredient activates the brain to reach a state of arousal and reaches a highly concentrated state, so that the perfume composition for enhancing the awakening effect or the concentration ability or the cosmetic composition containing the same, the soap or the bathing agent Can be used as a composition for external application for skin.

Description

[0001] The present invention relates to a fragrance composition for enhancing an arousal effect or concentration using an acid essential oil as an active ingredient,

The present invention relates to a perfume composition for enhancing an awakening effect or concentration ability containing natural essential oils as an active ingredient or a composition for external application for skin such as a cosmetic, a soap or a bathing agent containing the above-mentioned antioxidant composition.

Human brain waves are classified into three groups according to the frequency range: delta (0.5-3 Hz), theta (4-7 Hz), alpha (8-13 Hz), beta (14-30 Hz) (gamma; 30 Hz or more).

The delta wave is an irregular wave corresponding to a frequency of 0.5 to 3 Hz. It is predominantly at deep sleep and appears awake when abnormalities such as epilepsy, brain tumor, and mental retardation are present.

Cetaphas are regular waves of frequencies between 4 and 8 Hz, usually recorded in the occipital lobe and temporal lobe. It involves deeply internalized, silent physical, emotional and thought activities. It usually occurs when you are sleepy, not in a deep sleep state, and it is great when you are hurt, artistic, and enjoyable and joyful at work or play.

Alpha waves are the basis of brain waves and correspond to frequencies between 8 and 13 Hz. (7 ~ 8Hz), mid - alpapa (9 ~ 11Hz), fast alfapar (12 ~ 12Hz), and normal alfalfa (12 ~ 13Hz).

The slow alpha wave is a state of the brain that is relaxed, sleeps, or rests, and the mid-alpha wave is characterized by the fact that it is not normally accompanied by stress, and it is mediated, creative activity, And fast alpha is present when you have to cope with a stressful concentration in an urgent or dangerous state and are extremely concentrated in one job so you can not afford to think of the rest and do not respond to other signals or stimuli.

Beta waves are 13 to 30 Hz of frequency, and they appear when doing normal work or conscious actions and are activated when there is mental activity such as information processing. It is also divided into low-beta waves (12 to 15 Hz), mid-beta waves (15 to 20 Hz) and high-beta waves (20 to 30 Hz).

The low-beta is sensory motor rhythm (SMR) parasympathetic, and the motion sensation without body movements. When minimizing the activity of the cortex, it becomes preponderant when performing a relatively simple task, and the mid- High-beta waves become dominant when performing relatively complex reasoning or complex information processing activities, or emotional tension, anxious excitability.

Gamma waves correspond to 30 to 50 Hz, and are the fastest of the brain activity waves, emotionally more irritable, or active at higher cognitive functions such as reasoning and judgment. In addition, the relative gamma power spectrum value increases in the parietal lobe when attention is drawn by visual stimulation or cognitive activity.

On the other hand, Sanjin ( Zizyphus jujuba Miller) is a kind of jujube, a broad-leaved arboreous tree belonging to the Fhamnaceae family. It is widely grown from Europe to Asia. In one room, there are three kinds of plants, such as control (大 夏), dried (夏 夏), swan (白 棗), grape (桂 夏), brew (棗), 조 (棗) It is also called hydration, and it can be used as a sedative, hypnotic action, heart failure, stomach cramps, circulatory diseases, hepatitis, cirrhosis, diuretic, tonic, emollient, anemia, anorexia, nervous breakdown and hysterical treatment, , Bronchitis, tuberculosis, hemorrhagic disease, and expectorant drugs.

It is described in Korean Patent No. 10-0931880 that a herbal medicine containing a sanjoin, an oriental soya, a soya sauce and a raw paper has a depression relieving effect and a heart attack prevention effect by solving insomnia Korean Patent No. 10-0763620 discloses that a sanjoin extract is used as a composition for promoting growth hormone secretion and Korean Patent No. 10-1071154 discloses an anti-stress composition using a sedative effect of a sanjoin have.

In addition, the sanjoin is used as an effective ingredient of the external preparation for skin, Korean Patent Laid-Open No. 10-2005-0026806 discloses that the acidophilus exhibits an effect of prolonging the sleeping time and suppressing the secretion of cortisol by the stress hormone, thereby being used as a cosmetic composition .

However, Korean Patent Nos. 10-0931880, 10-0763620 and 10-1071154 exhibit functional or medical efficacy through oral ingestion, and it is an invention using a crude acid extract rather than a sanjoin essential oil, 10-2005-0026806 has been used as an external preparation for skin, but it is only referring to the prolongation of sleeping time or soothing effect, which is opposite to the effect of stimulation or concentration, by using a sanjoin extract rather than a sanjoin essential oil.

It is an object of the present invention to provide a fragrance composition for enhancing an arousal or concentration of concentration, which leads to a highly concentrated state by activating the brain from an essential oil of a natural plant to reach an arousal state.

It is also an object of the present invention to provide an external preparation for skin comprising the above-mentioned perfume composition.

In order to achieve the above object, the present invention provides a perfume composition for enhancing an arousal or concentration of health by using essential oil of Zizyphus jujuba Miller as an active ingredient.

In the present invention, essential oil refers to volatile organic compounds extracted from leaves, stems, fruits, roots and flowers of plants by various methods.

The acidophilus essential oil according to one embodiment of the present invention may be one extracted from a sanofi-aventis dry sample.

The acidophilus essential oil according to one embodiment of the present invention can be extracted by various known extraction methods such as steam distillation method, cold precipitation method, organic solvent method and supercritical extraction method, and supercritical extraction method is preferably used. The recovery rate of the essential oil is less than 0.01% when the crude oil is extracted by the steam distillation method. However, when the supercritical extraction method is used, the recovery rate of the essential oil increases by at least 10 to 100 times as compared with the steam distillation method.

In the case of supercritical extraction, extraction with CO ₂ as the extraction solvent at 45 to 65 ° C, preferably 50 to 60 ° C and 300 to 500 bar, preferably 350 to 450 bar, can increase the extraction yield .

The acidophilus essential oil according to one embodiment of the present invention is not particularly limited but can be expressed as a combination of balsamic, oily, spicy and woody fragrance, It is strong in flavor.

When the acidophilus essential oil of the present invention is inhaled through the nose, the absolute theta power spectrum (AT) index decreases and the relative gamma power spectrum (RG), the relative fast alpha power spectrum (RFA) ) By increasing the index, the brain is activated to reach a state of awakening, leading to a highly concentrated state.

The fragrance composition according to an embodiment of the present invention contains the acidic essential oil as an active ingredient, and may be a perfume or a fragrance.

In the perfume composition according to an embodiment of the present invention, the acidophilus essential oil may be contained in an amount of 0.01 to 100% by weight, preferably 0.1 to 99% by weight, more preferably 1 to 90% by weight.

The present invention provides an external preparation for skin comprising the above-mentioned perfume composition.

The composition for external application for skin is not particularly limited, but may be a cosmetic, a soap or a bathing agent.

The perfume composition or composition for external application for skin of the present invention may further comprise an appropriate carrier, excipient or diluent commonly used in the production of perfume, fragrance or cosmetic, soap, bathing agent and the like.

Examples of the carrier, excipient or diluent include purified water, oil, wax, fatty acid, fatty acid alcohol, fatty acid ester, surfactant, humectant, thickening agent, antioxidant, viscosity stabilizer, , Buffers, lower alcohols, and the like, but are not limited thereto. If necessary, whitening agents, moisturizing agents, vitamins, ultraviolet screening agents, perfumes, dyes, and antimicrobial agents may be included.

Examples of the wax include beeswax, wax, carnauba, candelilla, montan, ceresin, liquid paraffin, lanolin, and the like. Examples of the oil include hydrogenated vegetable oil, pharmacopoeia, cottonseed oil, olive oil, palm oil, jojoba oil and avocado oil. Can be used.

As the fatty acid, stearic acid, linoleic acid, linolenic acid and oleic acid may be used. As the fatty acid alcohol, cetyl alcohol, octyldodecanol, oleyl alcohol, panthenol, lanolin alcohol, stearyl alcohol and hexadecanol may be used As fatty acid esters, isopropyl myristate, isopropyl palmitate, and butyl stearate may be used.

Examples of the surfactant include anionic surfactants such as sodium stearate, sodium cetyl sulfate, polyoxyethylene lauryl ether phosphate and sodium N-acyl glutamate; Cationic surfactants such as stearyldimethylbenzylammonium chloride and stearyltrimethylammonium chloride; Amphoteric surfactants such as alkylaminoethylglycine hydrochloride and lecithin; Glycerin monostearate, sorbitan monostearate, sucrose fatty acid ester, propylene glycol monostearate, polyoxyethylene oleyl ether, polyethylene glycol monostearate, polyoxyethylene sorbitan monopalmitate, polyoxyethylene coconut fatty acid monoethanol Nonionic surfactants such as monoethanol arnide, polyoxypropylene glycol, polyoxyethylene castor oil, polyoxyethylene lanolin, and the like.

As the moisture absorbent, glycerin, 1,3-butylene glycol, propylene glycol may be used, and as the lower alcohol, ethanol and isopropanol may be used. Examples of thickeners include sodium alginate, sodium caseinate, gelatin agar, xanthan gum, starch, cellulose ethers (e.g., hydroxyethylcellulose, methylcellulose, carboxymethylcellulose, hydroxypropylmethylcellulose), polyvinylpyrrolidone, Polyvinyl alcohol, polyethylene glycol, sodium carboxymethyl cellulose, and the like.

Examples of the antioxidant include butylated hydroxytoluene, butylated hydroxyanisole, propyl gallate, citric acid, and ethoxyquin; chelating agents include disodium edetate, ethanedioxy diphosphate Is available.

As the buffer, citric acid, sodium citrate, boric acid, borax, and disodium hydrogen phosphate can be used.

However, it is not limited to the above-mentioned carrier, excipient or diluent.

Formulations of a perfume composition or a composition for external application for skin according to an embodiment of the present invention may be formulated as a solution, a suspension, an emulsion, a lotion, a cream, an emulsion, a soap, a surfactant-containing cleansing oil, But are not limited to, an image, a suspension, an emulsion, a cream, a gel, a spray, a papermaking, an alarm, a patch,

The amount of the perfume composition of the present invention contained in the composition for external application for skin may be appropriately selected and blended according to the conventional techniques in the art and in order to achieve the desired effects.

In the composition for external application for skin of the present invention, the perfume composition may be contained in an amount of 0.001 to 20% by weight, preferably 0.01 to 10% by weight, based on the total weight of the cosmetic composition. If the content is below the lower limit, the desired effect can not be obtained. If the content is above the upper limit, there is a problem that the palatability to the fragrance is poor.

However, the content of the perfume composition in the composition for external application for skin corresponds to one embodiment, and can be appropriately adjusted according to the characteristics of the formulation to be applied or the desired effect.

Since the acidophilus essential oil of the present invention is inhaled through the nose, it activates the brain to reach a state of arousal and reaches a highly concentrated state, so that the perfume composition for enhancing the awakening effect or the concentration ability such as perfume or fragrance or the cosmetic, And can be used as a skin external composition composition such as a bathing agent.

Figure 1 shows the electrode attachment site of the International 10-20 EEG system.
2 is a photograph of a testee wearing a test cap for EEG test.
Fig. 3 is a brain map showing changes in AT index before and after inhalation of fragrance of Sanjoin essential oil.
Fig. 4 is a brain map showing the change of the RG index before and after the incense suction of the acidophilus essential oil.
FIG. 5 is a brain map showing changes in RFA indices before and after inhalation of fragrance of Sanjoin essential oil.
Fig. 6 is a brain map showing the change of the SEF50 index before and after the incense-sucking of the sanjoin essential oil.

The present invention will be described in more detail with reference to the following examples. However, the scope of the present invention is not limited to the embodiments.

Production Example 1: Production of acidophilus essential oil by steam distillation

Zizyphus jujuba Miller was used at room temperature while drying samples from Bien Hub (Pyeongchang, Korea) were stored.

5 L of distilled water was added to the steam generation site of the steam distillation apparatus (Hanil LabTech., Korea), 1500 g of the sample was placed in the refinery area, and cooling water of -4 ° C. was continuously flown in the cooling tube. The vapors were extracted from the vapors while the steam was kept at 100 ° C for 1 hour. The vapors were extracted from the vapors and the extracted vapors were condensed in a cooling tube and classified as distilled water and essential oil . The oil layer was passed through a triangular funnel containing anhydrous sodium sulfate to remove water and stored in a refrigerator at 4 ° C until analysis.

The essential oil extracted from 1500 g of the dried acid was 0.1 g, and the oil recovery was 0.007%.

Production Example 2: Preparation of acidophilus essential oil by supercritical extraction

200 g of the acidogenic sample used in Preparation Example 1 was pulverized using a grinding machine (Hanil, Korea), placed in a sample container of a supercritical extractor (ILSHIN, Korea), and a supercritical CO _2, and the crude oil was extracted for 1 hour.

Table 1 below shows the flow rate, recovery rate, and properties of the acidophilus essential oil when the pressure was fixed at 400 bar and the temperature was changed from 40 to 70 ° C.

Temperature (℃) Pressure (bar) Constant flow rate (g) Refinery recovery rate (%) Appearance 40 400 0.23 0.115 oil 50 400 1.01 0.505 oil 60 400 1.19 0.595 oil 70 400 0.38 0.190 oil

When the temperature was too low or too high at 40 ° C and 70 ° C at the pressure of 400 bar, the recovery rate of the essential oil decreased sharply. Therefore, the recovery of the essential oil was high when extracted at 45 to 65 ° C.

Table 2 below shows the flow rate, recovery rate and properties of the acidophilus essential oil extracted at a fixed temperature of 60 ° C and a pressure of 200 to 400 bar.

Temperature (℃) Pressure (bar) Constant flow rate (g) Refinery recovery rate (%) Appearance 60 200 0.09 0.045 oil 60 300 0.59 0.295 oil 60 400 1.19 0.595 oil

It was found that the recovery of the essential oil was drastically reduced at a temperature of 60 ° C. and below the pressure of 300 bar. Therefore, it was found that the recovery of the essential oil was high when the extraction was performed at 300 bar or more, preferably 400 bar or more.

The recovery of the essential oil when extracted under the optimum temperature and pressure conditions, that is, at 60 ° C and 400 bar, was 85 times the recovery rate of the oil of Production Example 1.

Experimental Example 1: Evaluation of flavor of Sanjoin essential oil

The crude oil of supercritical extraction at 60 ° C and 400 bar of Preparation Example 2 was subjected to a rosso-sharon specialist group (7 persons) of Kangwon University Perfume Development Club, .

The crude oil of the sanjoin refined oil was wetted with a sprayer on a shade paper (0.5 cm ㅧ 13 cm), perfumed at a position 5 cm from the nose, described using fragrance evaluation terms, and then collected in common fragrances. Respectively. The scent type used in Rose of Sharon is aldehyde, animalic, balsamic, citrus, coniferous, earthy, floral, fruity, green, herbal, medicinal, minty, marine, mossy, musky, oily, oriental, powdery, smoky, spicy, sweet, and woody, and the fragrance intensity was generally from 0 to 10.

Drape type Intensity of fragrance Drape type Intensity of fragrance Aldehyde 0 Minty 0 Animalic 0 Marine 0 Balsamic 3 Wet 0 Citrus 0 Musky 0 Coniferous 0 Oily 4 Earthy 0 Oriental 0 Floral 0 Powdery 0 Fruity 0 Smoky 0 Green 0 Spicy 3 Herbal 0 Sweet (sweet) 0 Medicinal 0 Woody One

The acidophilus essential oil of the present invention had balsamic, oily, spicy and woody flavors and characteristic oily flavor.

Experimental Example 2: EEG analysis of Sanjoin essential oil

The effect of supernatant-extracted essential oil extracted at 60 ° C and 400 bar of Preparation Example 2 on human brain waves was analyzed by electroencephalography. The instrument used for EEG was a QEEG-8 system (LXE3208, Laxa, Korea). EEG signals were measured using a data collection device and an analysis program (Telescan).

EEG measurements were performed in a stable room with a maximum noise level of 32.5 m ² , maintaining a constant temperature (23 ^° C) and humidity (50%). The subjects were 20 men and 20 women in their 20s The mean age of the patients was 25.9 ± 1.9 years. EEG analysis was carried out using 10 standard international standard electrode systems, and 8 pre-echocardiographic (Fp1, Fp2), frontal (F3, F4), temporal (T3 , T4), parietal lobes (P3, P4), and one electrode was attached to the left and right ear lobes. The odd numbers are assigned to the left side and the even numbers are assigned to the right side at the attachment sites. The 10-20 international standard electrode attachment site for EEG is shown in FIG. A photograph of the subject having the analytical cap for EEG is shown in FIG.

The sanjoin essential oil contained in the vial was poured into the shijiji paper and kept at a distance of 5 cm from the nose of the subject. In the state where the subject closed the eyes, the pre-incense (unstimulated) and the inhaled state (incense stimulus) were measured for 1 minute each. Only EEG signals were measured for 30 seconds during 1 minute measurement of EEG. Data were processed by batch processing and corresponding sample T test was performed using statistical processing program of SPSS version 18.0.

Table 4 shows the meanings of the EEG analysis, the analysis waveband or the calculation formula and the analysis index used in the EEG analysis used to confirm the awakening effect or the concentration improvement.

division Analysis index Full name of EEG indicator Waveband (Hz) Meaning of the analysis index One AT Absolute Theta Power Spectrum 4 to 8 Meditation, sleepy 2 RG Relative Gamma Power Spectrum (30 to 50) / (4 to 50) A high degree of cognitive function 3 RFA Relative Fast Alpha Power Spectrum (11 to 13) / (4 to 50) Comfortable, immersive, creativity 4 SEF50 Spectral Edge Frequency 50% 4 to 50 EEG arousal

One) AT ( absolute theta power spectrum ) Indicator Analysis

The AT index is the absolute power spectral value of a 4 to 8 Hz setter region in the EEG spectrum, and a seta wave usually occurs during sleepy or deep meditation.

The measurement results of the AT indicator before and after inhalation of the sanjoin essential oil fractions are shown in Table 5 and Fig.

Attachment site Suction Average Standard Deviation t-test Fp1 Before inhalation 13.871 8.711 .880 After inhalation 13.067 Fp2 Before inhalation 12.944 9.226 .329 After inhalation 12.514 F3 Before inhalation 19.036 13.857 1.334 After inhalation 17.125 F4 Before inhalation 18.403 13.923 .338 After inhalation 17.705 T3 Before inhalation 11.422 8.837 1.232 After inhalation 10.413 T4 Before inhalation 6.358 4.294 .261 After inhalation 6.159 P3 Before inhalation 17.277 12.371 2.750 After inhalation 13.854 P4 Before inhalation 15.324 11.355 2.729 After inhalation 13.020

Table 5 shows that the mean values of AT indexes decreased at all electrode attachment sites. Especially, P3 (left parietal lobe) and P4 (right parietal lobe) showed statistically significant decrease in AT mean value ). Such a change in the AT index is expressed in a brain map and is shown in FIG.

Therefore, it was confirmed that the cerebellum was activated by the reduction of the cetaphase after the inhalation of the sanjoin oil, leading to a highly concentrated state.

2) Relative gamma power spectrum (RG)

The RG index is the absolute power ratio of the gamma wave band to the absolute power of the entire frequency domain in the EEG spectrum, which is the spectral value divided by the gamma wave region (30 to 50 Hz) into the entire frequency region (4 to 50 Hz) It belongs to the fastest wave in the wave, and it is activated when it is in an emotionally irritated state, or in a high cognitive function such as reasoning or judgment.

Table 6 and FIG. 4 show the measurement results of RG indicators before inhalation and during inhalation of Sanjoin essential oils.

Attachment site Suction Average Standard Deviation t-test Fp1 Before inhalation .085 .072 -1.053 After inhalation .091 Fp2 Before inhalation .091 .097 -.425 After inhalation .093 F3 Before inhalation .040 .024 -2.569 After inhalation .049 F4 Before inhalation .036 .023 -1.703 After inhalation .041 T3 Before inhalation .122 .094 -.632 After inhalation .130 T4 Before inhalation .128 .086 -.399 After inhalation .134 P3 Before inhalation .044 .030 -1.002 After inhalation .049 P4 Before inhalation .041 .029 -.198 After inhalation .041

According to Table 6, the average value of RG index increased at all electrode attachment sites, and especially in F3 (left frontal lobe), RG mean value of gamma-wave EEG was statistically significant (p <0.05). This RG indicator change is schematized as a brain map and is shown in FIG.

Therefore, it was confirmed that the gamma wave was increased after inhaling the Sanjoin essential oil to become awake.

3) Relative fast alpha power spectrum (RFA)

The RFA index is a spectrum value obtained by dividing the fast ALPHA region (11 to 13 Hz) by the entire frequency region (4 to 50 Hz) as the absolute power ratio of the fast ALPHA band to the absolute power of the entire frequency region in the EEG spectrum, The wave is known to occur when it is necessary to cope with a situation of intense concentration in an urgent or dangerous state

Table 7 and FIG. 5 show the measurement results of RFA indices before and after inhalation of Sanjoin essential oils.

Attachment site Suction Average Standard Deviation t-test Fp1 Before inhalation .063 .072 -2.167 After inhalation .085 Fp2 Before inhalation .064 .081 -2.133 After inhalation .085 F3 Before inhalation .073 .080 -2.151 After inhalation .100 F4 Before inhalation .071 .083 -1.949 After inhalation .095 T3 Before inhalation .072 .053 -2.398 After inhalation .088 T4 Before inhalation .070 .057 -1.165 After inhalation .080 P3 Before inhalation .115 .104 -.761 After inhalation .125 P4 Before inhalation .109 .099 -.872 After inhalation .120

According to Table 7, the mean value of RFA index increased at all electrode attachment sites. Especially, Fp1 (left prefrontal), Fp2 (right prefrontal), F3 (left frontal), P3 (left parietal) The mean value of RFA was found to be statistically significant (p <0.05). Such an RFA indicator change is schematized as a brain map and is shown in FIG.

Therefore, it was confirmed that the fast ALPHA increased after inhaling the Sanjoin essential oils, resulting in increased attention or concentration.

4) Analysis of SEF50 (Spectral edge frequency 50%)

The spectral edge frequency (SEF) index is a method of quantifying how much the power spectrum distribution of the EEG is deflected toward the high frequency as compared with the low frequency, and is used as the area ratio to the entire frequency domain. The value of the area up to the value represents 50% of the total frequency. It is used to evaluate EEG by brain activity.

The measurement results of the SEF50 indicator before and after inhalation of the sanjoin essential oil fractions are shown in Table 8 and Fig.

Attachment site Suction Average Standard Deviation t-test Fp1 Before inhalation .063 .072 -2.167 After inhalation .085 Fp2 Before inhalation .064 .081 -2.133 After inhalation .085 F3 Before inhalation .073 .080 -2.151 After inhalation .100 F4 Before inhalation .071 .083 -1.949 After inhalation .095 T3 Before inhalation .072 .053 -2.398 After inhalation .088 T4 Before inhalation .070 .057 -1.165 After inhalation .080 P3 Before inhalation .115 .104 -.761 After inhalation .125 P4 Before inhalation .109 .099 -.872 After inhalation .120

Table 8 shows that the mean value of the SEF50 index was increased at all electrode attachment sites, especially in the F3 (left frontal lobe), the SEF50 average value was statistically significantly increased (p <0.05). Such an SEF 50 indicator change is schematically shown in FIG. 6 as a brain map.

Therefore, it was confirmed that EEG increased after inhalation of Sanjoin essential oil.

The formulation of the present invention will be described in more detail through the following formulation examples. However, the scope of the present invention is not limited to the formulation example.

Formulation Example 1: Spray formulation perfume composition

95% Ethanol 25.0%

10.0 wt% of a crude acid extracted with supernatant from 400 bar at 60 DEG C in Production Example 2,

Ion-exchanged water 40.0 wt%

25.0 wt% of liquefied petroleum gas (4 kg / cm 2 20 ° C)

Components other than the liquefied petroleum gas were mixed and stirred to be uniform, and a predetermined amount was put in an aerosol container to mount a valve, and then a liquefied petroleum gas was injected to prepare a spray composition perfume composition.

Formulation Example 2: Gel form fragrance composition

Carrageenan 3.0 wt%

Propylene glycol 2.0 wt%

Propyl paraben 0.3 wt%

5.0% by weight of a crude oil extracted with supercritical carbon at 400 DEG C at 60 DEG C in Production Example 2,

Ion-exchanged water 89.7 wt%

Carrageenan, propylene glycol and propylparaben are mixed, and ion-exchanged water is added while stirring, and this is heated to about 80 캜 while being stirred slowly. Thereafter, the mixture was adjusted to about 65 ° C, and the mixture was stirred at 3000 rpm using a homogenizer. The composition for psychoacoustic perfuming was added to the mixture to form a homogeneous phase. The mixture was poured into a predetermined container and cooled naturally to prepare a gel-type perfume composition.

Formulation Example 3: Liquid Formulation Flavoring composition

95% Ethanol 25.0%

5.0% by weight of a surfactant (polyoxyethylene nonylphenyl ether)

3.0% by weight of crude saponin extracted with supercritical carbon at 400 DEG C at 60 DEG C in Production Example 2,

Ion-exchanged water 67.0 wt%

The components other than the ion-exchanged water were mixed, ion-exchanged water was added while stirring slowly, and the mixture was homogenized to prepare a liquid formulation-type perfume composition.

Formulation Example 4: Bath salts

Sodium hydrogencarbonate 70.0 wt%

Anhydrous sodium sulfate 29.0 wt%

1.0% by weight of a crude acid extracted with supernatant at 60 DEG C and 400 bar in Production Example 2,

The components except for the acidophilus essential oil were stirred until they became homogeneous with a V-type mixer, and then the acidophilus essential oil was added and sufficiently stirred until uniformity was obtained.

Formulation Example 5: Skin (lotion)

3.0% by weight of crude saponin extracted with supercritical carbon at 400 DEG C at 60 DEG C in Production Example 2,

12.0% by weight of hydroxyethylene cellulose (2% aqueous solution)

Xanthan gum (2% aqueous solution) 2.0 wt%

Butylene glycol 6.0 wt%

Glycerin 4.0 wt%

5.0% by weight sodium hyaluronate (1% aqueous solution)

Ion-exchanged water 73.0 wt%

Lotion was prepared by a conventional method of producing the lotion.

Claims (6)

Zizyphus jujuba Miller A fragrance composition for enhancing an arousal effect or concentration, comprising an essential oil as an active ingredient.
The perfume composition according to claim 1, wherein the acidophilus essential oil is a supercritical extract.
3. The perfume composition according to claim 2, wherein the supercritical extract is an extract extracted at 45 to 65 DEG C and 300 to 500 bar.
The perfume composition according to claim 1, wherein the perfume composition is perfume or a perfume.
A composition for external application for skin for enhancing an arousal effect or concentration comprising the perfume composition according to any one of claims 1 to 4.
6. The composition for external application for skin according to claim 5, wherein the composition for external application for skin is cosmetic, soap or bathing agent.

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