Manufacturing method of an ascorbic acid dispersion material

Abstract

A manufacturing method of an ascorbic acid dispersion material includes a heating step of adding an ascorbic acid into a solvent including one or more selected from the group consisting of glycerin, diglycerin, polyglycerin represented by a following formula, and propylene glycol, and heating the ascorbic acid to a predetermined temperature to dissolve the ascorbic acid; a cooling step of cooling a solution with the ascorbic acid dissolved therein at a cooling rate of 5 to 20° C./min until a temperature of the solution reaches 35 to 50° C. to remove heat from the solution; and a growth step of storing the solution after completion of the cooling step at 27 to 38° C. for a predetermined period to promote crystal growth so that the ascorbic acid crystal has a flat plate shape, a thickness of 0.05 to 3 μm, and an average particle diameter of 50 to 100 μm. ##STR00001##

Claims

1. A manufacturing method of an ascorbic acid dispersion material, comprising: a heating step of adding an ascorbic acid into a solvent consisting of one or more selected from the group consisting of glycerin, diglycerin, polyglycerin represented by a following formula (1), and propylene glycol, and heating a mixture of the ascorbic acid and the solvent to a temperature of 100 to 125° C. to dissolve the ascorbic acid in the solvent; a cooling step of cooling the mixture with the ascorbic acid dissolved therein at a cooling rate of 5 to 20° C./min until a temperature of the solution reaches 35 to 50° C. to remove heat from the solution; and a growth step of storing the solution after completion of the cooling step at 27 to 38° C. for a period of 5 hours or longer to promote crystal growth so that the ascorbic acid crystal has a flat plate shape, a thickness of 0.05 to 3 μm, and an average particle diameter of 50 to 100 μm, wherein n is an integer from 3 to 10, ##STR00003## wherein a particle size distribution of the ascorbic acid crystal has a distribution such that a particle diameter of 30 to 120 μm is 40 to 80% of overall particles.

2. The manufacturing method of ascorbic acid dispersion material according to claim 1, wherein the ascorbic acid concentration is 20 to 40 wt %.

3. The manufacturing method of ascorbic acid dispersion material according to claim 1, wherein an average density in an ascorbic acid dispersion material is 1.3 to 1.4 g/cm.sup.3.

4. The manufacturing method of ascorbic acid dispersion material according to claim 1, wherein the viscosity in an ascorbic acid dispersion material is 5000 to 300,000 mPa.Math.s.

5. The manufacturing method of ascorbic acid dispersion material according to claim 1, wherein a particle size distribution of the ascorbic acid crystal has a distribution such that a particle diameter of 1.151 to 29.907 μm is 11.398-28.133%, a particle diameter of greater than 29.907 to 133.103 μm is 61.874-77.458%, and a particle diameter of greater than 133.103 μm is 9.171-22.185%, with respect to the overall particles in a total of 100%.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a scanning electron micrograph image (drawing substitute photograph) of an ascorbic acid crystal in Example 1.

(2) FIG. 2 is a scanning electron micrograph image (drawing substitute photograph) of an ascorbic acid crystal in Example 2.

(3) FIG. 3 is a scanning electron micrograph image (drawing substitute photograph) of an ascorbic acid crystal in Example 3.

(4) FIG. 4 is a scanning electron micrograph image (drawing substitute photograph) of a commercially available ascorbic acid crystal powder.

(5) FIG. 5 is a chart illustrating the results of the particle size distribution analysis of an ascorbic acid dispersion material in Example 1.

(6) FIG. 6 is a chart illustrating the results of the particle size distribution analysis of an ascorbic acid dispersion material in Example 2.

(7) FIG. 7 is a chart illustrating the results of the particle size distribution analysis of an ascorbic acid dispersion material in Example 3.

(8) FIG. 8 is a chart illustrating the results of the X-ray diffraction analysis of the ascorbic acid crystal in Example 1.

(9) FIG. 9 is a chart illustrating the results of the X-ray diffraction analysis of the ascorbic acid crystal in Example 2.

(10) FIG. 10 is a chart illustrating the results of the X-ray diffraction analysis of the ascorbic acid crystal in Example 3.

MODE FOR CARRYING OUT THE INVENTION

(11) While not limited to the following, the ascorbic acid dispersion material of the present invention will now be described.

(12) (Overall Configuration of the Ascorbic Acid Dispersion Material)

(13) The ascorbic acid dispersion material of the present invention is obtained by dispersing an ascorbic acid crystal in a solvent, wherein the abovementioned ascorbic acid crystal has a specific shape and particle diameter.

(14) The shape and particle diameter of the abovementioned ascorbic acid crystal will be described in detail later.

(15) (Solvent)

(16) While the abovementioned solvent used in the present invention is not particularly limited, for example, glycerin, diglycerin, polyglycerin represented by the following formula, propylene glycol, etc., can be used, and any one of these may be used, or two or more of these may be mixed and used.

(17) ##STR00002##

(18) In the formula, n is an integer from 3 to 10.

(19) Among other possibilities, the solvent is preferably glycerin and diglycerin, from the perspective that ascorbic acid tends to have the crystal shape described below, and from the perspectives of safety to the human body including skin, and usage characteristics upon application onto skin. Moreover, in obtaining a mixed solvent of glycerin and diglycerin, the blending ratio of diglycerin is preferably 0.1 to 5 wt % in the solvent.

(20) (Ascorbic Acid Crystal)

(21) The abovementioned ascorbic acid crystal in the ascorbic acid dispersion material of the present invention has a flat plate shape. Moreover, the abovementioned ascorbic acid crystal has gentle angles in the corners, with few sharp angles (see FIGS. 1 to 3)

(22) As a result, the ascorbic acid dispersion material of the present invention has a smoothness upon application onto skin, with superior usage characteristics. Moreover, it is not known why the crystals tend to not be aggregated, as a result of which the chemical stability of the ascorbic acid is increased.

(23) Note that while crystals having shapes other than a flat plate shape, such as a sphere, may be present among the ascorbic acid crystals, the ratio of such crystals is generally 10 wt % or lower.

(24) While the thickness of the abovementioned ascorbic acid crystal is not particularly limited, it is preferably 0.05 to 3 μm. Within this range, the abovementioned usage characteristics are superior.

(25) Note that the thickness of the abovementioned ascorbic acid crystal used herein is obtained by randomly selecting 100 crystals from a scanning electron microscope image, obtaining the thickness of each of the selected crystals by image analysis, and obtaining the average value thereof. Moreover, the particle shape, etc. is obtained using a scanning electron microscope, and measured using the particulate powder obtained in the measurement of the particle diameter described below.

(26) (Particle Diameter)

(27) The average particle diameter of the abovementioned ascorbic acid crystal is 50 to 100 μm, preferably 60 to 95 μm. Within this range, the abovementioned usage characteristics are superior.

(28) Note that the abovementioned average particle diameter and shape of particles are measured using the following method.

(29) Method:

(30) 1. Commercially available ascorbic acid crystals are infused into acetone, and dissolved to obtain a saturated state.

(31) 2. Fine particulate crystals of the ascorbic acid present in the ascorbic acid saturated acetone solution of 1 are subjected to ultracentrifugation using a generally known ultracentrifuge via a generally known method, to precipitate and remove particles of the ascorbic acid, thus preparing an ascorbic acid saturated acetone solution (hereinafter, referred to as a dispersion medium) not containing fine particulate crystals of the ascorbic acid.

(32) 3. A small amount (5 mL) of the ascorbic acid dispersion material of the present invention, as an analyte, is infused into 20 mL of the dispersion medium prepared in 2, lightly shaken, and mixed.

(33) 4. The suspension liquid of 3 is subjected to ultracentrifugation using an ultracentrifuge under generally known conditions, to precipitate particles of the ascorbic acid, and remove the supernatant.

(34) 5. 20 mL of the dispersion medium prepared in 2 is added to the obtained precipitate, lightly shaken, and dispersed.

(35) 6. The operations of 4 and 5 are further carried out to remove the solvent component of the ascorbic acid dispersion material of the present invention, following which the operation of 4 is further carried out to precipitate particles of the ascorbic acid, and remove the supernatant, and the particles are then dried at a low temperature to obtain particulate powder.

(36) 7. An appropriate amount of hexane for measuring the particle size distribution is added to the particulate powder obtained in 6, to slightly disperse the precipitate, and obtain a sample for particle size analysis.

(37) 8. The sample of 7 for particle size analysis is subjected to measurement of its laser diffraction/scattering particle diameter distribution.

(38) Note that it was found (not illustrated) that the particle diameter and particle shape that are measured after grinding commercially available ascorbic acid crystals and dispersing them in hexane are not significantly different from the particle diameter and particle shape which are measured using the abovementioned method after grinding commercially available ascorbic acid crystals. As a result, the particles extracted via the abovementioned method are able to faithfully reproduce the shape and particle diameter of the particles in the dispersion material.

(39) (Particle Size Distribution)

(40) While the particle size distribution of the abovementioned ascorbic acid crystal is not particularly limited, particles having a particle diameter of 30 to 120 μm account for preferably 40 to 80%, more preferably 50 to 75%, of the overall particles. Within this range, the abovementioned usage characteristics are superior.

(41) Note that the abovementioned particle size distribution refers to the value that is obtained by a laser diffraction/scattering particle diameter distribution measurement using the sample for particle size analysis obtained in the abovementioned particle diameter measurement method.

(42) (Ascorbic Acid Concentration)

(43) While the concentration of the ascorbic acid in the ascorbic acid dispersion material of the present invention is not particularly limited, the ascorbic acid in the overall ascorbic acid dispersion material is preferably 10 to 45 wt %, and more preferably 20 to 40 wt %. Within this range, the ascorbic acid can be effectively used at a high concentration; and in case where it is used for cosmetics, skin care preparations, etc., the effects on skin are superior.

(44) Note that while the state of the ascorbic acid in the abovementioned concentration is not particularly limited, examples thereof may include crystal and noncrystal states, as well as the state of being dissolved in a solvent, etc.

(45) (Density)

(46) While the density of the ascorbic acid dispersion material of the present invention is not particularly limited, the average density is preferably 1.30 to 1.40 g/cm.sup.3, and more preferably 1.31 to 1.39 g/cm.sup.3. Within this range, the ascorbic acid can be effectively used at a high concentration; and in cases where it is used for cosmetics, skin care preparations, etc., the abovementioned effects and usage characteristics are superior.

(47) Note that the abovementioned density refers to a value measured using a dry densimeter.

(48) (Viscosity)

(49) While the viscosity of the ascorbic acid dispersion material of the present invention is not particularly limited, the average viscosity is preferably 5000 to 300000 mPa.Math.s, and more preferably 8000 to 240000 mPa.Math.s, from the perspectives of storage stability and usage characteristics. Within this range, the ascorbic acid can be effectively used at a high concentration; and in cases where it is used for cosmetics and skin care preparations, etc., the abovementioned usage characteristics are superior.

(50) The abovementioned average viscosity used herein refers to a value measured using a Brookfield rotation viscometer under temperature conditions of 20° C.

(51) (Manufacturing Method)

(52) While the manufacturing method for the ascorbic acid dispersion material of the present invention is not particularly limited, it is preferably manufactured via the manufacturing method of the present invention, described below.

(53) The manufacturing method of the present invention includes: a heating step involving infusing an ascorbic acid into a solvent, and heating the ascorbic acid to a predetermined temperature to dissolve the ascorbic acid; a cooling step involving cooling the solution with the ascorbic acid dissolved therein to remove the heat of the solution; and a growth step involving storing the solution after the completion of the abovementioned cooling step for a predetermined period to promote crystal growth.

(54) As a result, the ascorbic acid dispersion material of the present invention can be more efficiently manufactured.

(55) Below, each step will be described.

(56) [Heating Step]

(57) The abovementioned heating step refers to a step involving infusing an ascorbic acid into a solvent, and heating the ascorbic acid to a predetermined temperature to dissolve the ascorbic acid.

(58) While the raw material of the abovementioned ascorbic acid is not particularly limited, for example, crystal powder of a commercially available ascorbic acid, etc. can be used, and may be subjected to treatment such as grinding, etc.

(59) The abovementioned solvent is as mentioned above, and for example, glycerin, etc., can be used.

(60) While the method for infusing an ascorbic acid into the abovementioned solvent is not particularly limited, it can be carried out via methods such as a method for directly infusing the raw material powder of the abovementioned ascorbic acid into the abovementioned solvent.

(61) After infusing the raw material powder of the ascorbic acid into the abovementioned solvent, and subsequently heating it to a predetermined temperature, the raw material powder of the ascorbic acid is dissolved.

(62) While the temperature of the abovementioned heating varies based on the shape/concentration of the ascorbic acid of the raw material, the kind of solvent, etc., the temperature of the solvent is preferably 100 to 125° C.

(63) Moreover, the method of the abovementioned dissolution is preferably carried out by stirring, from the perspectives of the dissolution speed and homogeneous dispersion. Note that stirring under the abovementioned heating temperature conditions can be carried out via known methods. For example, it can be carried out by heating using known heating devices, and using known stirring machines.

(64) Moreover, while heating in the abovementioned dissolution varies based on the shape/concentration of the ascorbic acid of the raw material, the kind of solvent, etc., this heating is preferably rapidly finished after the completion of the dissolution, from the perspectives of preventing the modification and decomposition of the ascorbic acid due to excessive heating.

(65) For example, in cases where the abovementioned solvent is glycerin, the completion of the abovementioned dissolution is determined when the color of the mixed liquid changes, becoming transparent.

(66) Moreover, the container for carrying out the abovementioned dissolution is not particularly limited as long as the container is tolerant to the solvent, the ascorbic acid, etc., and also tolerant to the temperatures in this heating step and the cooling step described below; for example, containers made of glass or plastic can be used. While the shape of the abovementioned container is also not particularly limited, general beakers and flask shapes can be used. Moreover, the abovementioned container is preferably a container having sealing and shading properties because storage after manufacturing the ascorbic acid dispersion liquid of the present invention can be carried out in the same container.

(67) Note that, as required, the abovementioned dissolution can be carried out in an inert gas stream such as a nitrogen gas.

(68) [Cooling Step]

(69) The abovementioned cooling step refers to a step involving cooling the solution with the ascorbic acid dissolved therein, as obtained after the abovementioned heating step, to remove heat from the solution.

(70) While the method of the abovementioned cooling is not particularly limited, the cooling speed is preferably 5 to 20° C./min. Such cooling can be carried out by a method involving, after the completion of the abovementioned heating step, immersing the container used in the abovementioned heating step into water with the solution contained in the container. While water used in this case is not particularly limited, tap water can be used as is. Moreover, a sufficient amount of water is preferably used for cooling to the temperatures described below, with the temperature generally being preferably approximately 4 to 20° C.

(71) The removal of heat in this step is intended to set the temperature in the internal solution to 35 to 50° C., preferably approximately 40° C.; once it reaches a temperature within this range, the removal of heat is completed.

(72) [Growth Step]

(73) The abovementioned growth step refers to a step involving storing the solution after the abovementioned cooling step for a predetermined period to promote crystal growth.

(74) The abovementioned growth step can be carried out by keeping the abovementioned solution after the abovementioned cooling step at preferably 27 to 38° C., more preferably approximately 30° C.

(75) The abovementioned growth step is carried out for a period of 5 hours or longer, until the abovementioned crystal grows to be the desired size (particle diameter, thickness).

(76) While the abovementioned specific period varies depending on the kind of solvent, the concentration of the ascorbic acid, etc., for example, in cases where the abovementioned solvent is glycerin, and the ascorbic acid is 10 to 45 parts by weight in 100 parts by weight of the total amount of the ascorbic acid and glycerin, the abovementioned period is 3 hours or longer, and preferably half a day or longer.

(77) After carrying out the abovementioned growth step, the ascorbic acid dispersion material of the present invention can be obtained.

(78) When the ascorbic acid dispersion material of the present invention is manufactured as mentioned above, it is possible to obtain the abovementioned ascorbic acid crystals in the dispersion material of the present invention, which are not conventionally obtained.

(79) For example, there is a method involving heating to dissolve, then quenching using dry ice, thereby rapidly generating a large number of crystal cores. Because a large number of crystal cores develop, the number of molecules available for crystal growth decreases, and the cores grow to be crystal particles having a small crystal particle diameter. Moreover, rapid cooling also allows the viscosity of glycerin, which is a solvent, to rapidly increase giving rise to a small value for the degrees of freedom in the solution. For this reason, crystal growth tends to not occur, and this presumably gives rise to crystals having a small particle diameter (crystals having a smaller particle diameter than the abovementioned ascorbic acid crystal).

(80) In contrast, in the present invention, heat is simply removed instead of cooling, and therefore crystal cores gradually develop. For this reason, crystal growth can be sufficiently promoted, and well-formed crystals can be obtained. Moreover, because the growth step can be carried out with a high value for the degrees of freedom in glycerin, this also allows the growth of crystal to be sufficiently carried out, and allows a dispersion material, in which ascorbic acid crystals having the abovementioned characteristic crystal shape is dispersed, to be obtained.

(81) Below, applications and usage methods for the ascorbic acid dispersion material of the present invention are described.

(82) (Applications)

(83) Because the dispersion material of the ascorbic acid according to the present invention has the abovementioned properties, it can be used in various applications such in cosmetics, skin care preparations, quasi drugs, drugs, storage liquids for ascorbic acid, and food additives. Among others, because the ascorbic acid has effects such as antioxidative action, the generation and maintenance of collagen, and skin whitening, it can be suitably used in cosmetics and skin care preparations.

(84) (Usage Methods)

(85) In cases where the ascorbic acid dispersion material of the present invention is used in cosmetics and skin care preparations, the ascorbic acid dispersion material of the present invention can be used by application onto skin.

(86) Note that in cases where the ascorbic acid dispersion material of the present invention is used in cosmetics and skin care preparations, the abovementioned solvent is preferably a solvent containing glycerin, from the perspective of safety to human body, including skin, as well as usage characteristics upon application onto skin (stimulation aspect), etc. Moreover, in cases where it is used in cosmetics and skin care preparations, the preferable aspect regarding crystals of the abovementioned ascorbic acid is as mentioned above.

(87) (Storage)

(88) Because redissolution starts when the ascorbic acid dispersion material of the present invention is 25° C. or higher, it is preferably stored at 25° C. or lower. Moreover, shaded storage is preferable from the perspective of preventing the decomposition caused by light. Moreover, nitrogen gas, etc. is preferably enclosed, substituted, etc., and followed by sealing and storing, in order to prevent the decomposition and modification of the ascorbic acid due to dissolved oxygen. Such storage enables the decomposition/modification of the ascorbic acid to be suppressed, allowing storage for further extended periods of time.

(89) While the present invention is not limited to the abovementioned embodiments, various modifications can be made without departing from the spirit of the present invention.

(90) For example, the ascorbic acid dispersion material of the present invention can contain other components without departing from the spirit of the present invention. Examples of such other components may include useful components used for formulations such as drugs, quasi drugs, and cosmetics, for example, ultraviolet inhibitors, whitening agents, perfumes, etc. Moreover, the abovementioned other components can be blended during the abovementioned heating step to cooling step, after the completion of the cooling step, etc., with the timing of such blending not being particularly limited.

Examples

(91) While not limited thereto, the present invention will be described below in further detail using examples and comparative examples.

Example 1

(92) (Manufacture of the Ascorbic Acid Dispersion Material)

(93) [Heating Step]

(94) 38 g of an ascorbic acid raw material fine powder (pharmacopeia, produced by DSM Nutrition) and 62 g of glycerin as a solvent were each weighed, and infused into a conical flask made of glass. After infusing, the mixture was heated such that the temperature thereof reached 115° C., and stirred using a blade type stirring device Immediately after the temperature of the mixture reached 115° C., the color of the mixed liquid changed from yellow to transparent. As a result, the fact that the ascorbic acid was completely dissolved was confirmed, and the heating step was thus completed.

(95) [Cooling Step]

(96) The temperature in the conical flask after the completion of the abovementioned heating step was monitored with 5 L of tap water at a temperature of 20° C., using a temperature meter, and it was cooled until the temperature of the mixture reached 40° C.

(97) Note that the cooling period was 5 minutes.

(98) [Growth Step]

(99) The conical flask after the completion of the abovementioned cooling step was sealed with a rubber plug, placed into an incubator having a temperature of 30° C., and left for 3 days to obtain the ascorbic acid dispersion material of the present invention (hereinafter, also referred to as GAG38) having an ascorbic acid concentration of 38 wt %.

Example 2

(100) An ascorbic acid dispersion material of the present invention (hereinafter, also referred to as GAG30) having an ascorbic acid concentration of 30 wt % was obtained as in Example 1, except that 30 g of ascorbic acid raw material fine powder and 70 g of glycerin as a solvent were used in the heating step, and the temperature retention time in the growth step was 2 days.

Example 3

(101) An ascorbic acid dispersion material of the present invention (hereinafter, also referred to as GAG22) having an ascorbic acid concentration of 22 wt % was obtained as in Example 1, except that 22 g of ascorbic acid raw material fine powder and 78 g of glycerin as a solvent were used in the heating step, and the temperature retention time in the growth step was 1 day.

Test Example 1 Observation of the Crystals Using a Scanning Electron Microscope

(102) The ascorbic acid crystals contained in the ascorbic acid dispersion material of the present invention obtained in Examples 1 to 3 were observed using a scanning electron microscope.

(103) Note that as a control sample, crystals of commercially available ascorbic acid were ground using a mortar, and observed alongside.

(104) (Preparation of Samples for the Scanning Electron Microscope)

(105) Samples for the scanning electron microscope were prepared via the following method.

(106) Method:

(107) 1. Ascorbic acid crystals were infused into acetone, and dissolved to obtain a saturated state.

(108) 2. Fine particulate crystals of the ascorbic acid present in the ascorbic acid saturated acetone solution of 1 were subjected to ultracentrifugation using an ultracentrifuge under generally known conditions, to precipitate and remove particles of the ascorbic acid, thus preparing an ascorbic acid saturated acetone solution (hereinafter, referred to as the dispersion medium) not containing fine particulate crystals of the ascorbic acid.

(109) 3. 5 mL of the ascorbic acid dispersion material of the present invention obtained in Examples 1 to 3 as an analyte and 0.5 g of commercially available ascorbic acid crystal powder were both infused into 20 mL of the dispersion medium prepared in 2, lightly shaken, and mixed.

(110) 4. The suspension liquid of 3 was subjected to ultracentrifugation using an ultracentrifuge under generally known conditions, to precipitate particles of the ascorbic acid, and remove the supernatant.

(111) 5. 20 mL of the dispersion medium prepared in 2 was added to the obtained precipitate, lightly shaken, and dispersed.

(112) 6. The operations of 4 and 5 were further carried out to remove the solvent component of the ascorbic acid dispersion material of the present invention, following which the operation of 4 was further carried out to precipitate particles of the ascorbic acid, and remove the supernatant, and the particles were dried at a low temperature to obtain particulate powder.

(113) 7. The obtained particulate powder was used as a sample for the scanning electron microscope.

(114) (Observation Using a Scanning Electron Microscope)

(115) Regarding the obtained sample for a scanning electron microscope, an electron microscope image was acquired using a scanning electron microscope under the following conditions, and the acquired image was observed.

(116) Conditions:

(117) acceleration voltage: 10 kV

(118) magnification: 1000 times (5000 times for the ascorbic acid powder of the control sample)

(119) The obtained results are shown in FIG. 1 (Example 1: GAG38), FIG. 2 (Example 2: GAG30), FIG. 3 (Example 3: GAG22), and FIG. 4 (control testing: commercially available ascorbic acid crystal powder).

(120) (Measurement of the Crystal Thickness)

(121) Further, 100 crystals were randomly selected from the obtained scanning electron microscope image, and an image analysis of the obtained scanning electron microscope image was carried out to obtain the average value of the thickness of the selected crystals.

(122) The results thereof are shown below.

(123) Average value of the crystal thickness:

(124) Example 1 (GAG38): 1.194 μm

(125) Example 2 (GAG30): 1.040 μm

(126) Example 3 (GAG22): 0.924 μm

(127) (Results and Remarks)

(128) The results show that most of the ascorbic acid crystals contained in the ascorbic acid dispersion material of the present invention obtained in Examples 1 to 3 have a flat plate shape, have gentle angles at the corners with few sharp angles, and have a low thickness with small variations in thickness.

(129) In contrast, the results show that the ascorbic acid crystal powder, which is an object sample, has an indeterminate crystal shape, which is totally different from the crystal shape of the ascorbic acid contained in the ascorbic acid dispersion material of the present invention.

(130) Due to properties of the crystal structure, the ascorbic acid dispersion material of the present invention is presumed to have superior usage characteristics upon application onto skin.

Test Example 2Particle Size Analysis

(131) A particle size analysis of the ascorbic acid crystals contained in the ascorbic acid dispersion material of the present invention obtained in Examples 1 to 3 was carried out.

(132) (Preparation of Samples for Particle Size Analysis)

(133) Samples for particle size analysis were prepared from the ascorbic acid dispersion material of the present invention obtained in Examples 1 to 3, as in Steps 1 to 6 of the method used to obtain particulate powder in preparing samples for the scanning electron microscope of Test Example 1, an appropriate amount of hexane for measuring the particle size distribution was added to the particulate powder, and the precipitate was slightly dispersed to obtain samples for particle size analysis.

(134) (Particle Size Analysis)

(135) The particle size analysis of the obtained samples for particle size analysis was carried out using a laser diffraction/scattering particle diameter distribution measurement device (type name: LA-950V2, manufactured by Horiba, Ltd.). The obtained results (histogram) are shown in FIG. 5 (Example 1: GAG38), FIG. 6 (Example 2: GAG30), and FIG. 7 (Example 3: GAG22).

(136) The results (particle diameter and frequency) are shown in Table 1 (Example 1: GAG38), Table 2 (Example 2: GAG30), and Table 3 (Example 3: GAG22).

(137) Moreover, the average particle diameter, the median diameter, the mode diameter, and the ratio of particles having a particle diameter of 30 to 120 μm are shown in Table 4.

(138) TABLE-US-00001 TABLE 1 Passing portion Particle diameter Frequency cumulative No. (μm) (%) (%) 35 1.151 0.000 0.000 36 1.318 0.000 0.000 37 1.510 0.000 0.000 38 1.729 0.000 0.000 39 1.981 0.000 0.000 40 2.269 0.000 0.000 41 2.599 0.000 0.000 42 2.976 0.000 0.000 43 3.409 0.000 0.000 44 3.905 0.000 0.000 45 4.472 0.000 0.000 46 5.122 0.000 0.000 47 5.867 0.000 0.000 48 6.720 0.108 0.108 49 7.097 0.215 0.324 50 8.816 0.397 0.721 51 10.097 0.687 1.407 52 11.565 1.138 2.546 53 13.246 1.728 4.274 54 15.172 2.402 6.076 55 17.377 3.085 9.761 56 19.904 3.729 13.490 57 22.797 4.328 17.818 58 26.111 4.892 22.709 59 29.907 5.424 28.133 60 34.255 5.925 34.058 61 39.234 6.394 40.452 62 44.938 6.797 47.250 63 51.471 7.025 54.275 64 58.953 7.006 61.281 65 67.523 6.710 67.991 66 77.339 6.162 74.153 67 88.583 5.381 79.534 68 101.400 4.506 84.040 69 116.210 3.675 87.715 70 133.103 3.114 90.829 71 152.453 2.657 93.487 72 174.616 2.185 95.672 73 200.000 1.701 97.372 74 229.075 1.252 98.624 75 262.376 0.884 99.509 76 300.518 0.491 100.000 77 344.206 0.000 100.000 78 394.244 0.000 100.000 79 451.556 0.000 100.000 80 517.200 0.000 100.000 81 592.387 0.000 100.000 82 678.504 0.000 100.000 83 777.141 0.000 100.000 84 890.116 0.000 100.000 85 1019.515 0.000 100.000

(139) TABLE-US-00002 TABLE 2 Passing portion Particle diameter Frequency cumulative No. (μm) (%) (%) 35 1.151 0.000 0.000 36 1.318 0.000 0.000 37 1.510 0.000 0.000 38 1.729 0.000 0.000 39 1.981 0.000 0.000 40 2.269 0.000 0.000 41 2.599 0.000 0.000 42 2.976 0.000 0.000 43 3.409 0.000 0.000 44 3.905 0.000 0.000 45 4.472 0.000 0.000 46 5.122 0.000 0.000 47 5.867 0.102 0.102 48 6.720 0.180 0.282 49 7.597 0.294 0.576 50 8.816 0.442 1.019 51 10.097 0.624 1.642 52 11.565 0.839 2.481 53 13.246 1.032 3.513 54 15.172 1.168 4.681 55 17.377 1.233 5.914 56 19.904 1.256 7.171 57 22.797 1.285 8.455 58 26.111 1.370 9.825 59 29.907 1.573 11.398 60 34.255 1.986 13.384 61 39.234 2.772 15.156 62 44.938 4.109 20.265 63 31.471 5.953 26.218 64 58.953 8.048 34.266 65 67.523 9.821 44.088 66 77.339 11.253 55.341 67 88.583 11.250 66.591 68 101.460 9.604 76.195 69 116.210 7.243 83.438 70 133.103 5.418 88.856 71 152.453 4.015 92.871 72 174.616 2.863 95.734 73 200.000 1.936 97.670 74 229.073 1.219 98.889 75 262.376 0.714 99.603 76 300.518 0.397 100.000 77 344.206 0.000 100.000 78 394.244 0.000 100.000 79 451.558 0.000 100.000 80 517.200 0.000 100.000 81 592.387 0.000 100.000 82 678.504 0.000 100.000 83 777.141 0.000 100.000 84 890.116 0.000 100.000 85 1019.515 0.000 100.000

(140) TABLE-US-00003 TABLE 3 Passing portion Particle diameter Frequency cumulative No. (μm) (%) (%) 35 1.151 0.000 0.000 36 1.318 0.000 0.000 37 1.510 0.000 0.000 38 1.729 0.000 0.000 39 1.981 0.000 0.000 40 2.269 0.000 0.000 41 2.599 0.000 0.000 42 2.976 0.000 0.000 43 3.409 0.000 0.000 44 3.905 0.000 0.000 45 4.472 0.000 0.000 46 5.122 0.000 0.000 47 5.867 0.000 0.000 48 6.720 0.119 0.119 49 7.697 0.210 0.335 50 8.816 0.363 0.698 51 10.097 0.575 1.273 52 11.565 0.874 2.147 53 13.246 1.222 3.369 54 15.172 1.559 4.938 55 17.377 1.660 6.798 56 19.904 2.073 8.871 57 22.797 2.223 11.094 58 20.111 2.347 13.441 59 29.907 2.500 15.941 60 34.255 2.747 18.688 61 39.234 3.184 21.872 62 44.938 3.900 25.772 63 51.471 4.810 30.582 64 58.953 5.815 36.397 65 67.523 6.732 43.129 66 77.339 7.514 50.643 67 88.583 7.822 58.465 68 101.400 7.408 65.873 69 116.210 6.386 72.259 70 133.103 5.556 77.815 71 152.453 4.889 82.704 72 174.616 4.203 86.967 73 200.000 3.666 90.633 74 229.075 3.057 93.690 75 262.376 2.453 96.143 76 300.518 1.895 98.038 77 344.206 1.053 99.090 78 394.244 0.585 99.675 79 451.556 0.325 100.000 80 517.200 0.000 100.000 81 592.387 0.000 100.000 82 678.504 0.000 100.000 83 777.141 0.000 100.000 84 890.116 0.000 100.000 85 1019.515 0.000 100.000

(141) TABLE-US-00004 TABLE 4 Average Ratio of particles having particle Median Mode a particle diameter of 30 Analyte diameter diameter diameter to 120 μm Example 1 61.99 μm 47.39 μm 48.19 μm 53.66% (GAG38) Example 2 79.50 μm 72.51 μm 72.51 μm 70.05% (GAG30) Example 3 94.79 μm 76.45 μm 82.70 μm 53.40% (GAG22)

(142) (Results and Remarks)

(143) The results show that particles of the ascorbic acid contained in the ascorbic acid dispersion material of the present invention obtained in Examples 1 to 3 have little deviation in the particle diameter. As a result, usage characteristics upon application onto skin are presumed to be superior.

Test Example 3 X-Ray Diffraction Analysis

(144) The X-ray diffraction analysis of the ascorbic acid crystals contained in the ascorbic acid dispersion material of the present invention obtained in Examples 1 to 3 was carried out. Note that as a control sample, commercially available ascorbic acid was ground using a mortar, and tested alongside.

(145) (Samples for X-Ray Diffraction Analysis)

(146) As a sample for X-ray diffraction analysis, the samples for the scanning electron microscope (particulate powder) manufactured in Test Example 1 were used.

(147) (X-Ray Diffraction Analysis)

(148) The X-ray diffraction analysis of the obtained sample for the X-ray diffraction analysis was carried out using an X-ray diffraction analysis device (device name: XPERT-PRO MPD, produced by PANalytical) under the following conditions.

(149) Conditions:

(150) scanning range: (° 20): 10.000 to 30.00

(151) target: Cu

(152) X-ray output setting: 40 mA, 45 kV

(153) step size (° 20): 0.017

(154) type of scanning: continuous

(155) sample width (mm): 10.00

(156) The obtained results are shown in FIG. 9 (Example 1: GAG38), FIG. 10 (Example 2: GAG30), and FIG. 11 (Example 3: GAG22).

(157) (Results and Remarks)

(158) The results show that in the X-ray diffraction analysis, the ascorbic acid crystals contained in the ascorbic acid dispersion material of the present invention obtained in Examples 1 to 3 includes peaks of 2θ angles at 10.6, 15.9, 16.2, 17.6, 20.0, 25.4, 27.0, 27.3 and 28.2 degrees (±0.2 degrees). As a result, these crystals have a specific crystal structure.

Test Example 4Viscosity Analysis

(159) A viscosity analysis of the ascorbic acid dispersion material of the present invention obtained in Examples 1 to 3 was carried out.

(160) The viscosity analysis regarding the ascorbic acid dispersion material of the present invention obtained in Examples 1 to 2 was carried out using a Brookfield viscometer (trade name: RVDV-I+, manufactured by BROOKFIELD) under the following conditions.

(161) Conditions:

(162) temperature: 20 degrees

(163) rotation speed: 6 r/min, after 1 minute

(164) rotor No: No. 7

(165) The ascorbic acid dispersion material of the present invention obtained in Example 3 was measured using a Brookfield viscometer (trade name: LVDV-I+, produced by BROOKFIELD) under the following conditions.

(166) Conditions:

(167) temperature: 20 degrees

(168) rotation speed: 6 r/min, after 1 minute

(169) rotor No: No. 64

(170) The obtained results are shown in Table 5.

(171) TABLE-US-00005 TABLE 5 Analyte Test results Example 1 (GAG38) 210000 mPa .Math. s Example 2 (GAG30) 130000 mPa .Math. s Example 3 (GAG22)  9700 mPa .Math. s

(172) (Results and Remarks)

(173) The obtained results show that the ascorbic acid dispersion material of the present invention has a higher viscosity as the ascorbic acid concentration increases.

(174) The results also show that the viscosity of the ascorbic acid dispersion material of the present invention obtained in Examples 1 to 3 is a suitable viscosity as an application agent onto skin, etc. As a result, usage characteristics upon application onto skin are presumed to be superior.

Test Example 5Density Analysis

(175) A density analysis of the ascorbic acid dispersion material of the present invention obtained in Examples 1 to 3 was carried out.

(176) Density was measured using a dry automatic densimeter (trade name: AccuPycII, produced by Shimadzu Corporation).

(177) The results thereof are shown in Table 6.

(178) TABLE-US-00006 TABLE 6 Analyte Average density Example 1 (GAG38) 1.3876 g/cm.sup.3 Example 2 (GAG30) 1.3548 g/cm.sup.3 Example 3 (GAG22) 1.3260 g/cm.sup.3

(179) (Results and Remarks)

(180) The results show that the ascorbic acid dispersion material of the present invention has a higher density as the ascorbic acid concentration increases, and it is an appropriate density.

(181) Moreover, the ascorbic acid dispersion material of the present invention obtained in Examples 1 to 3 has superior usage characteristics upon application onto skin, and has properties of the density obtained by this testing, in addition to the abovementioned properties.

(182) The above results show that the ascorbic acid dispersion material of the present invention has higher chemical stability, and has superior usage characteristics, such as spreadability and smoothness, upon application onto skin.