Sterilization method and sterilization apparatus
11642548 · 2023-05-09
Assignee
Inventors
Cpc classification
A61P35/00
HUMAN NECESSITIES
A61Q17/04
HUMAN NECESSITIES
A61N2005/0643
HUMAN NECESSITIES
A61K8/44
HUMAN NECESSITIES
A61P17/02
HUMAN NECESSITIES
A61K31/198
HUMAN NECESSITIES
A61N5/0624
HUMAN NECESSITIES
International classification
Abstract
Provided a method of sterilization by ultraviolet irradiation whereby effects on the human body can be mitigated and an odor that arises after ultraviolet irradiation can be controlled. The sterilization method includes: a step (a) of irradiating a skin of a hand or arm with ultraviolet having a wavelength of 200 nm or more and 230 nm or less; and a step (b) of applying a topical skin preparation, cosmetic, or aqueous solution containing at least one amino acid or amino acid derivative selected from an amino acid group A to a region of the skin irradiated with the ultraviolet. The amino acid group A includes valine, leucine, isoleucine, glutamic acid, arginine, serine, aspartic acid, proline, and glycine.
Claims
1. A sterilization method comprising: a step (a) of irradiating a skin of a hand or arm with ultraviolet having a wavelength of 200 nm or more and 230 nm or less; and a step (b) of applying a topical skin preparation, cosmetic, or aqueous solution containing at least one amino acid or amino acid derivative selected from an amino acid group A to a region of the skin irradiated with the ultraviolet, the amino acid group A including valine, leucine, isoleucine, glutamic acid, arginine, serine, aspartic acid, proline, and glycine.
2. The sterilization method according to claim 1, wherein the topical skin preparation, cosmetic, or aqueous solution applied in the step (b) contains a moisturizing component or an adhesion/penetration component.
3. The sterilization method according to claim 1, wherein the step (a) is a step of irradiating the skin with radiation light from an excimer lamp containing a gas including KrCl or KrBr for light emission.
4. The sterilization method according to claim 1, wherein the steps (a) and (b) are performed in a non-clinical site.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1)
(2)
MODE FOR CARRYING OUT THE INVENTION
(3) The method according to the present invention is composed of the following two steps. The two steps are: step (a) irradiating a skin of a hand or arm with ultraviolet having a wavelength of 200 nm or more and 230 nm or less; and step (b) applying a topical skin preparation, cosmetic, or aqueous solution containing at least one amino acid or amino acid derivative selected from the following amino acid group A to a region of the skin irradiated with the ultraviolet. The “amino acid group A” in the step (b) is a group including valine, leucine, isoleucine, glutamic acid, arginine, serine, aspartic acid, proline, and glycine.
(4) <Step (a): Ultraviolet Irradiation Step>
(5) Ultraviolet irradiation of the skin of a hand or arm with a wavelength of 200 nm or more and 230 nm or less has little effect on the human body. This is because when the human body is irradiated with this wavelength band, the ultraviolet is absorbed in the stratum corneum of the skin and does not propagate deeper than that (toward the stratum basale). Corneocytes in the stratum corneum are cells without a nucleus, and do not contain DNA as with, for example, spinous cells. Therefore, there is hardly any risk of DNA being destroyed by ultraviolet absorbed by the cells, as with when irradiated with ultraviolet with a wavelength of about 250 nm. It is therefore possible to adjust the intensity or time of ultraviolet irradiation depending on the required sterilization performance.
(6) It is preferable to use a shorter wavelength of ultraviolet from the viewpoint of mitigating the effects on the cell nuclei (DNA) of the human body. However, the ultraviolet radiation in the wavelength band of less than 200 nm is absorbed by the air (oxygen in the air) so that the amount of light is largely reduced when the light reaches the skin of a hand or arm. Therefore, no sterilization effects can be guaranteed.
(7) As a light source of ultraviolet having a wavelength of 200 nm or more and 230 nm or less, an excimer lamp containing a gas including KrCl or KrBr for light emission can be used. This light source should preferably include a built-in filter for cutting light rays of wavelengths longer than 230 nm.
(8) For example, an ultraviolet irradiation apparatus 1 shown in
(9) When a hand or arm was irradiated with ultraviolet with a wavelength of 200 nm or more and 230 nm or less, a smell (odor) that resembled that of burning hair arose. This smell could not be removed by a wash with a soap. The details will be described later with reference to test examples.
(10) <Step (b): Amino Acid Application Step>
(11) A topical skin preparation, cosmetic, or aqueous solution containing at least one amino acid or amino acid derivative selected from the amino acid group A is applied to a region irradiated with the ultraviolet in the step (a), the amino acid group A including valine, leucine, isoleucine, glutamic acid, arginine, serine, aspartic acid, proline, and glycine. It was confirmed that the odor mentioned above was removed by this step. Hereinafter, the “topical skin preparation, cosmetic, or aqueous solution containing at least one amino acid or amino acid derivative selected from the amino acid group A” shall be referred to as “specified solvent B”.
(12) The inventor(s) of the present application speculated that the odor that arose after the step (a) was performed resulted from destruction of some of the amino acids contained in the keratin (epidermal keratin) in the corneocytes when irradiated with ultraviolet, and originated from a substance different from the amino acids. It is assumed that the destroyed amino acid was repaired by applying the specified solvent B in the region irradiated with ultraviolet so that aldehyde was reduced, as a result of which the odor was removed. The details will be described later with reference to test examples.
(13) As for irradiation of a hand or arm with ultraviolet at a wavelength of about 250 nm, the issue of whether or not there is an odor hardly becomes apparent because of the intrinsically large effects on the human body as described above. Moreover, if a hand or arm were irradiated with about 250 nm wavelength ultraviolet, the amount of light absorbed by the corneocytes would be lower than when irradiated with ultraviolet with a wavelength of 200 nm or more and 230 nm or less, since the light passes through the stratum corneum and reaches the stratum granulosum or stratum spinosum, and sometimes even the stratum basale. Therefore, it is assumed that, the issue of an odor originating from destruction of some of the amino acids contained in the epidermal keratin hardly becomes apparent with ultraviolet irradiation at a wavelength of 250 nm as compared with ultraviolet irradiation at a wavelength of 200 nm or more and 230 nm or less.
(14) The specified solvent B may take any form and may be formulated in the form of any of a liquid, emulsion, gel, spray, foam, and so on. The specified solvent B may be prepared in any way as long as it contains at least one amino acid or amino acid derivative selected from the amino acid group A, and may contain any of other components commonly mixed in pharmaceutical or quasi-pharmaceutical products, cosmetics and the like such as, for example, anionic surfactant, ampholytic surfactant, non-ionic surfactant, thickening agent, oil agent, preservative, perfume, moisturizer, bioactive component, antioxidant, sequestrant, pH adjuster, water, alcohol, colorant, fragrance component, and so on, as required.
(15) From the viewpoint of repair of amino acids contained in the epidermal keratin that were destroyed in the step (a), the specified solvent B should more preferably contain components that provide moisturizing and adhesion/penetration effects. As moisturizing components, for example, sodium hyaluronate, sodium pyrrolidonecarboxylic acid (PCA-Na) aqueous solution, butylene glycol, and glycerin can be applied. As components that provide adhesion/penetration effects, dimethicone and carbomer (carboxy vinyl polymer) can be applied.
(16) Hereinafter, the present invention will be described in detail with reference to test examples.
Test Example 1
(17) Using the ultraviolet irradiation apparatus 1 shown in
(18) Whether there is an odor or not was judged each time (1-1) immediately after the irradiation, (1-2) one minute after the irradiation, and (1-3) after the hand and arm were washed using alkaline soap after one minute after the irradiation. Table 1 shows the judgement results.
(19) TABLE-US-00001 TABLE 1 (1-1) Immediately (1-2) Several minutes (1-3) After a wash after irradiation after irradiation with soap M1 Odor detected Oder detected Oder detected M2 Odor detected Oder detected Oder detected M3 Odor detected Oder detected Oder detected M4 Odor detected Oder detected Oder detected M5 Odor detected Oder detected Oder detected M6 Odor detected Oder detected Oder detected
(20) As shown in Table 1, all six assessors determined that there was an odor each time (1-1) immediately after the irradiation, (1-2) one minute after the irradiation, and (1-3) after the hand and arm were washed using alkaline soap after one minute after the irradiation.
(21) Further, after sterilizing the hands and arms of the six assessor M1, M2, M3, M4, M5, and M6 with alcohol prior to the ultraviolet irradiation, their hands and arms near the wrists were irradiated with ultraviolet, similarly to Test Example 1. In this case, too, similarly to Test Example 1, all six assessors determined that there was an odor each time (1-1) immediately after the irradiation, (1-2) one minute after the irradiation, and (1-3) after the hand and arm were washed using alkaline soap after one minute after the irradiation.
Test Example 2
(22) Using the same light source as that of the ultraviolet irradiation apparatus 1, artificial skin produced by Japan Tissue Engineering Co., Ltd was irradiated with ultraviolet with a peak wavelength at 222 nm. The result was that an odor similar to that of Test Example 1 was generated.
(23) Since artificial skin is fabricated in aseptic conditions, it is assumed that the odor originates from a protein rather than a bacteria, based on the results of Test Example 1 and Test Example 2.
Test Example 3
(24) Looking at amino acids that form the proteins in the epidermis, then changes in the odor before and after irradiation of ultraviolet at a peak wavelength of 222 nm with respect to the following eighteen types of amino acids are examined More specifically, a 3 mL aqueous solution of each type of amino acid was put in a φ40 petri dish, and using the same light source as that of the ultraviolet irradiation apparatus 1, irradiated with ultraviolet with an irradiance of 3.8 mW/cm.sup.2 for an irradiation period of 30 seconds. The petri dish and the light source were spaced apart by 8 cm. The eighteen types of amino acids were: Cystine, glutamic acid, leucine, arginine, serine, threonine, aspartic acid, proline, glycine, valine, alanine, phenylalanine, isoleucine, tyrosine, lysine, histidine, methionine, and tryptophan. These eighteen amino acids are all known as the substances that form proteins contained in the epidermis.
(25) Table 2 shows the judgement results. Table 2 shows the odor before the ultraviolet irradiation, the odor after the ultraviolet irradiation, and comparison with the odor in Test Example 1 after the ultraviolet irradiation. The comparison with the odor in Test Example 1 was made by sensory evaluation performed by the six assessors M1, M2, M3, M4, M5, and M6.
(26) TABLE-US-00002 TABLE 2 Comparison Amino acid Before After with smells in name irradiation irradiation Test example 1 Cystine No smell No smell Different (no change) Glutamic acid Slight smell Slight smell Different (no change) Leucine Characteristic Smell of Almost smell burning hair identical Arginine Characteristic Characteristic Different smell smell (no change) Serine No smell No smell Different (no change) Threonine No smell No smell Different (no change) Aspartic acid No smell No smell Different (no change) Proline No smell Smell like lysine Different Glycine No smell No smell Different (no change) Valine Characteristic Smell of Almost smell burning hair identical Alanine Slight sour Slight sour Different smell smell (no change) Phenylalanine Slightly less Change in type of Different sweet smell sweetness Isoleucine Characteristic Smell of Almost smell burning hair identical Tyrosine No smell No smell Different (no change) Lysine Characteristic Characteristic Different smell smell (no change) Histidine No smell No smell Different (no change) Methionine Smell of Smell of Almost slightly burning hair identical rotting onions
(27) As shown in Table 2, with respect to leucine, valine, isoleucine, and methionine, it was confirmed that each of these amino acids produced an odor that was substantially the same as that detected after the ultraviolet irradiation of a human hand or arm after the irradiation of ultraviolet at a wavelength of 222 nm. It is considered, from these test results, that the odor that arose when the hand or arm was irradiated with 222 nm wavelength ultraviolet resulted from decomposition of one of the amino acids that form the skin, i.e., leucine, valine, isoleucine, and methionine.
Test Example 4
(28) Similarly to the method of Test Example 1, using the ultraviolet irradiation apparatus 1 shown in
(29) After that, each aqueous solution of the eighteen types of amino acids used in Test Example 3 (cystine, glutamic acid, leucine, arginine, serine, threonine, aspartic acid, proline, glycine, valine, alanine, phenylalanine, isoleucine, tyrosine, lysine, histidine, methionine, and tryptophan) was applied to the region irradiated with ultraviolet (molar concentration: 1 mM). More specifically, each aqueous solution was sprayed and rubbed in with the palm of the hand. This was followed by an assessment of any changes in the smell before and after application of each aqueous solution.
(30) Table 3 shows the judgement results. While Table 3 shows only the results given by Assessor M1, the other five assessors gave exactly the same results.
(31) TABLE-US-00003 TABLE 3 Before application of After application of Amino acid name amino acid solution amino acid solution Cystine Smell of Smell of burning hair burning hair (no change) Glutamic acid Smell disappeared Leucine Smell disappeared Arginine Smell disappeared Serine Smell disappeared Threonine Smell of burning hair (no change) Aspartic acid Smell disappeared Proline Smell disappeared Glycine Smell disappeared Valine Smell disappeared Alanine Smell of burning hair (no change) Phenylalanine Smell of burning hair (no change) Isoleucine Smell disappeared Tyrosine Smell of burning hair (no change) Lysine Smell of burning hair (no change) Histidine Smell of burning hair (no change) Methionine Smell disappeared Tryptophan Smell of burning hair (no change)
(32) The results in Table 3 show that no odor was detected when an aqueous solution of leucine, valine, isoleucine, or methionine was applied after ultraviolet irradiation, which were assumed to be the source of odor in Test Example 3. The results also show that, apart from leucine, valine, isoleucine, and methionine, no odor was detected when an aqueous solution of glutamic acid, arginine, serine, aspartic acid, proline, or glycine was applied after ultraviolet irradiation.
(33) It is concluded from the results of Test Example 3 and Test Example 4 that irradiation of the skin with ultraviolet at a wavelength of 222 nm destroys some amino acids and produces an odor, but applying a specific amino acid to the UV-irradiated skin thereafter repairs part or all of the destroyed amino acids, whereby the source of the odor is eliminated and the odor disappears.
(34) While the test examples described above were performed using ultraviolet of a wavelength of 222 nm, it is concluded that, with the light of wavelengths around 222 nm, and the light of wavelengths shorter than 222 nm, an odor arises in the step (a), and the odor that arose is reduced in the step (b), by the same principles.
(35) The results of Test Examples 3 and 4 described above confirmed that application of a specific amino acid after irradiation of ultraviolet at a wavelength of 222 nm stopped the odor. It follows that, for the same reasons, odor generation can be controlled by application of a material containing this specific amino acid, or a material containing a derivative of this specific amino acid.
Test Example 5
(36) Similarly to Test Example 4, using the ultraviolet irradiation apparatus 1 shown in
(37) After that, the following four commercial products were applied to the region irradiated with ultraviolet.
(38) (Commercial product A) Amino acid penetration gel produced by MATSUYAMA CO., LTD.
(39) Moisturizer contents: Sodium hyaluronic acid, sodium PCA, butylene glycol, and sodium lactate
(40) Amino acid contents: Proline, glycine, arginine, and betaine
(41) Adhesion/penetration contents: Carbomer (carboxy vinyl polymer)
(42) (Commercial product B) Atrix hand gel produced by Nivea-Kao Co., Ltd.
(43) Moisturizer contents: Sodium hyaluronic acid, sodium PCA, butylene glycol, and glycerin
(44) Amino acid contents: Proline, glycine, arginine, betaine, and lauroyl glutamate
(45) Adhesion/penetration contents: Dimethicone and carbomer (carboxy vinyl polymer)
(46) (Commercial product C) Men's deodorant spray produced by Shiseido Company, Limited
(47) Moisturizer contents: None
(48) Amino acid contents: None
(49) Adhesion/penetration contents: None
(50) Other ingredients: Disinfectant (IPMP: Isopropyl Methylphenol), zinc oxide, and deodorant (alum)
(51) (Commercial product D) Sunscreen cream produced by Taisho Pharmaceutical Co., Ltd.
(52) Moisturizer contents: Glycerin and butylene glycol
(53) Amino acid contents: None
(54) Adhesion/penetration contents: Dimethicone
(55) Other ingredients: UV absorber (ethylhexyl methoxycinnamate, diethylamino hydroxybenzoyl hexyl benzoate), oil and grease (for shine, skin protection, etc.)
(56) Table 4 shows the judgement results. While Table 4 shows only the results given by Assessor M1, the other five assessors gave exactly the same results.
(57) TABLE-US-00004 TABLE 4 Applied Amino Before application After application pharmaceutical acid of pharmaceutical of pharmaceutical formulation content formulation formulation Commercial Contained Smell of Smell disappeared product A burning hair Commercial Contained Smell disappeared product B Commercial Not Smell of burning hair product C contained (no change) Commercial Not Smell of burning hair product D contained (no change)
(58) The results in Table 4 ascertained that the odor after ultraviolet irradiation was not necessarily removed only by the application of a pharmaceutical formulation designed to provide a function such as adhesion, penetration, and removal of smell. The results in Table 4 also indicate that the speculation obtained based on the test results of Test Examples 1 to 4 is correct. Namely, it confirms that irradiation of the skin with ultraviolet at a wavelength of 222 nm destroys some amino acids and produces an odor, but applying a specific amino acid (proline, glycine, and arginine in Test Example 5) to the UV-irradiated skin thereafter repairs part or all of the destroyed amino acids, whereby the source of the odor is eliminated and the odor disappears.
Other Embodiments
(59) As shown in
DESCRIPTION OF REFERENCE SIGNS
(60) 1 Ultraviolet irradiation apparatus 2 Light source 3 Insertion hole 4 Platform 5 Spray port L1 Ultraviolet B Specified solvent