ULTRAVIOLET IRRADIATION DEVICE, ATTACHMENT AND ELASTIC MEMBER FOR USE IN ULTRAVIOLET IRRADIATION DEVICE, AND ULTRAVIOLET IRRADIATION METHOD
20200324137 ยท 2020-10-15
Assignee
- Public University Corporation Nagoya City University (Aichi, JP)
- Ushio Denki Kabushiki Kaisha (Tokyo, JP)
- ISHIZUKA GLASS CO., LTD. (Aichi, JP)
Inventors
- Akimichi MORITA (Aichi, JP)
- Hideyuki MASUDA (Tokyo, JP)
- Makoto KIMURA (Tokyo, JP)
- Yuji OGAWA (Iwakura-shi, JP)
- Miki YOSHIDA (Iwakura-shi, JP)
Cpc classification
A61N2005/063
HUMAN NECESSITIES
International classification
Abstract
Provided is an ultraviolet irradiation device capable of increasing the irradiance at an affected site (target cells) even when ultraviolet light having the same intensity is emitted. This ultraviolet irradiation device is provided with: a device body configured to be capable of emitting ultraviolet light from a light emission unit; an ultraviolet-transparent substrate disposed on the light emission unit; and an elastic member which is disposed on the surface of the substrate facing away from the device body and made of an ultraviolet-transparent material.
Claims
1. An ultraviolet irradiation device comprising: a device body configured to emit ultraviolet light from a light emitting portion; a substrate disposed at the light emitting portion, exhibiting transparency to the ultraviolet light, and including a first surface and a second surface facing the first surface; and an elastic member placed on the second surface of the substrate opposite to the first surface located on the device body side and formed of a material having transparency to the ultraviolet light.
2. The ultraviolet irradiation device according to claim 1, further comprising an attachment formed of a frame-shaped member including an opening region and detachably attached to the device body, wherein the elastic member is fitted into the opening region, and an outer peripheral portion of the elastic member is fixed to the device body via the attachment.
3. The ultraviolet irradiation device according to claim 2, wherein the elastic member has a first surface located on a side closer to the substrate and a second surface opposite to the first surface, and the second surface is disposed projecting opposite to the device body relative to the attachment.
4. The ultraviolet irradiation device according to claim 3, wherein the elastic member has a step portion formed at a position between the first surface and the second surface, and when the frame-shaped member of the attachment comes into contact with the step portion, the elastic member is fitted into the opening region.
5. The ultraviolet irradiation device according to claim 1, wherein the elastic member has a thickness of 3 mm to 10 mm.
6. The ultraviolet irradiation device according to claim 1, wherein the device body includes an ultraviolet light source.
7. The ultraviolet irradiation device according to claim 1, wherein the elastic member comprises an organic-inorganic hybrid composition (X), and the organic-inorganic hybrid composition (X) has no phenyl group in its molecule, has only a methyl group in its side chain, and has a skeleton composed of dimethylpolysiloxane having a hydroxy terminal.
8. The ultraviolet irradiation device according to claim 7, wherein the organic-inorganic hybrid composition (X) is a product formed by dehydration-condensation of dimethylpolysiloxane (A), aluminum alkoxide (B), and silicon alkoxide (C).
9. An ultraviolet irradiation method comprising: placing an elastic member, formed of a material having transparency to ultraviolet light, on a surface of an irradiation target region; and in a state where in a surface of the elastic member, which is opposite to the irradiation target region, in a substrate exhibiting transparency to ultraviolet light and including a first surface and a second surface facing the first surface, the second surface is in contact with the elastic member, applying the ultraviolet light to the first surface and the second surface of the substrate and the irradiation target region via the elastic member.
10. An attachment for use in the ultraviolet irradiation device according to claim 2.
11. An elastic member for use in the ultraviolet irradiation device according to claim 7.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0032]
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[0035]
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[0044]
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[0050]
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[0052]
MODE FOR CARRYING OUT THE INVENTION
[0053] An embodiment of an ultraviolet irradiation device according to the present invention will be described with reference to the drawings. The following drawings are schematically illustrated, and the dimensional ratio in the drawings does not necessarily coincide with the actual dimension ratio. Also, the dimensional ratios in the drawings do not necessarily coincide with the explanation.
[Device Structure]
[0054]
[0055]
[0056] The ultraviolet irradiation device 1 includes a device body 3, an elastic member 11, an attachment 13, and a substrate 15 (see
[0057]
[0058]
[0059] As shown in
[0060] In the present embodiment, the elastic member 11 is placed on a surface of the substrate 15 in a +Z direction. The surface of the substrate 15 in the +Z direction refers to a surface of the substrate 15 in a light emitting direction (a surface opposite to the device body 3). The elastic member 11 is continuous so as not to drop off from the device body 3 by the attachment 13. By fixing by the attachment 13, a surface of the elastic member 11 comes into contact with a surface of the substrate 15.
[0061] As shown in
[0062] As shown in
[0063] The length of each side of the elastic member 11 on the XY plane in the second portion 11b1 is shorter than the length of each side on the XY plane that forms the outer peripheral portion of the opening region 13a of the attachment 13. On the other hand, the length of each side of the elastic member 11 on the XY plane in the first portion 11a1 is longer than the length of each side on the XY plane that forms the outer peripheral portion of the opening region 13a of the attachment 13. A thickness of the elastic member 11 (length in a Z direction) is larger than a thickness of a portion of the attachment 13 that constitutes the frame-shaped member 13b.
[0064] When configured in this manner, the second portion 11b1 of the elastic member 11 can pass through the opening region 13a of the attachment 13, and on the other hand, the first portion 11a1 of the elastic member 11 cannot pass through the opening region 13a of the attachment 13. That is, when the elastic member 11 is fitted into the opening region 13a of the attachment 13, the elastic member 11 is fixed at the step portion 11c located at a boundary between the first portion 11a1 and the second portion 11b1 in a state of being in contact with the outer peripheral portion of the opening region 13a of the attachment 13. At this time, on both sides (Z direction) of the opening region 13a, a portion of the elastic member 11, that is, the first surface 11a and the second surface 11b project outside the opening region 13a.
[0065] When the elastic member 11 is attached to the device body 3 in a stale of being fitted into the opening region 13a of the attachment 13, as shown in
[0066]
[0067] As will be described later, the elastic member 11 is formed of a material having high transparency to ultraviolet light and elasticity. Thus, the shape of the elastic member 11 changes along a curved surface of the skin outer surface 51, and the elastic member 11 comes into surface contact with the skin outer surface 51. The skin in the region is compressed inward by applying the load f1 to the skin outer surface 51.
[0068] As shown in
[0069] In such a state, the ultraviolet irradiation device 1 irradiates the irradiation subject (patient) 50 with the ultraviolet light L1. At this time, since the load f1 is applied to the region S1, inflow of blood is temporarily blocked or reduced. As a result, the number of hemoglobins in the region S1 temporarily decreases. Since hemoglobin is one of factors absorbed by the ultraviolet light L1, irradiance of the ultraviolet light L1 reaching an affected region existing inside the skin is increased by reducing the number of hemoglobins.
[0070] In particular, since the elastic member 11 comes into surface contact with the skin outer surface 51 in the region S1, the load f1 is applied to the irradiation subject 50 through the skin outer surface 51 via the device body 3, so that the effect of temporarily blocking the inflow of blood in the region S1 is exhibited.
[Elastic Member 11]
[0071] As a member that transmits ultraviolet light (for example, UVB light), hard materials such as quartz glass and fluorite (calcium fluoride) have been known. However, a material that exhibits a transmittance of 90% or more to ultraviolet light and is easily bent (has elasticity) by hand at a thickness of 1 mm or more has been scarcely known. When the elastic member 11 is formed of a material described below, although this material is very soft to be deformed along a curved surface having a diameter of 200 mm with a force of 1 kgf, the material has a low stickiness, and the transmittance for UVB light is 90% or more in a 1 mm thick member.
(Material)
[0072] The elastic member 11 included in the ultraviolet irradiation device 1 of the present embodiment is formed of an organic-inorganic hybrid composition (X). The organic-inorganic hybrid composition (X) can be realized by having no phenyl group in its molecule, having only a methyl group in its side chain, and having a skeleton composed of dimethylpolysiloxane having a hydroxy terminal. As an example, the organic-inorganic hybrid composition is preferably a product containing dimethylpolysiloxane (A), aluminum alkoxide (B), and silicon alkoxide (C) and produced by crosslinking with a dehydration condensation reaction of these materials.
[0073] The organic-inorganic hybrid composition (X) has a structure in which a polysiloxane having a siloxane bond is three-dimensionally and complexly crosslinked. Thus, the organic-inorganic hybrid composition (X) has a structure similar to that of a so-called inorganic glass, and suitable properties such as heat resistance and ultraviolet resistance can be obtained.
[0074] The dimethylpolysiloxane (A) having a hydroxy terminal is a material that forms a skeleton structure of the organic-inorganic hybrid composition (X) and is a silicon compound having no phenyl group in its molecule and having only a methyl group in its side chain. Although the transmittance of the organic-inorganic hybrid composition (X) of the type containing a phenyl group is 75% or more in a wavelength region of 300 nm or more, the phenyl group absorbs ultraviolet light in the 260 nm region, so that ultraviolet light is hardly transmitted. On the other hand, the absorption of ultraviolet light can be prevented by using as a raw material the hydroxy-terminated dimethylpolysiloxane (A) having no phenyl group.
[0075] According to the organic-inorganic hybrid composition (X) having a skeleton formed of the dimethylpolysiloxane (A) having no phenyl group in its molecule, having only a methyl group in its side chain, and having a hydroxy terminal, the organic-inorganic hybrid composition (X) is resistant to bending and is less likely to be damaged when curved, so that high elasticity is ensured.
[0076] In order to increase crosslinking reactivity between the dimethylpolysiloxanes (A) or between the dimethylpolysiloxane (A) and the alkoxide molecule (B) or (C), the terminal portion of the dimethylpolysiloxane (A) is substituted with a hydroxy group. The hydroxy-terminated dimethylpolysiloxane (A) is a molecule serving as the structural skeleton of the organic-inorganic hybrid composition (X), and is generally selected from a molecular weight (weight average molecular weight) of from 500 to 30,000.
[0077] The aluminum alkoxide (B) has a role of forming a network structure of molecules by a condensation reaction with a hydroxy group which is a terminal portion of the hydroxy-terminated dimethylpolysiloxane (A). Examples of the aluminum alkoxide (B) include various types of aluminum alkoxides including aluminum sec-butoxide, aluminum tert-butoxide, monosec-butoxyaluminum diisopropylate (also known as aluminum (2-butanolate) di (2-propanolate)) and the like. From the viewpoint of securing a high transmittance for ultraviolet light, aluminum sec-butoxide is particularly preferable.
[0078] The aluminum alkoxide (B) has higher reactivity such as hydrolysis and condensation than the silicon alkoxide (C). As a result, the aluminum alkoxide (B) causes hydrolysis without using a catalyst such as an acid or a base. Specifically, the aluminum alkoxide (B) undergoes a condensation reaction with a hydroxy group of the hydroxy-terminated dimethylpolysiloxane (A) without using a tin-based reaction accelerator such as dibutyltin diacetate, dibutyltin dilaurate, dioctyltin dilaurate, bis(acetoxydibutyltin) oxide, and bis(lauroxydibutyltin) oxide, and a crosslink can be formed.
[0079] From the viewpoint of ensuring high transparency to ultraviolet light, a high energy band gap is required for a metal oxide derived from a reaction product of a highly reactive metal alkoxide contained in the organic-inorganic hybrid composition (X). The energy band gap of Al.sub.2O.sub.3 is 6.9 eV, and an absorption edge is 179.7 nm. Therefore, the aluminum alkoxide (B) achieves high transparency to ultraviolet light.
[0080] The silicon alkoxide (C) also has a role of forming a network structure of molecules by a condensation reaction with a hydroxy group which is a terminal portion of the hydroxy-terminated dimethylpolysiloxane (A). Examples of the silicon alkoxide (C) include various types of silicon alkoxides including, such as tetraethoxysilane, tetramethoxysilane, tetrabutoxysilane, tetraisopropoxysilane, tetrapropoxysilane, methyltriethoxysilane, ethyltriethoxysilane, n-propyltriethoxysilane, isobutyltriethoxysilane, n-hexyltriethoxysilane, n-octyltriethoxysilane, n-dodecyltriethoxysilane, methyltrimethoxysilane, ethyltrimethoxysilane, n-propyltrimethoxysilane, n-butyltrimethoxysilane, isobutyltrimethoxysilane, n-hexyltrimethoxysilane and n-dodecyltrimethoxysilane, and condensates thereof. As a silicon alkoxide oligomer as the condensate. KC-89S commercially manufactured by Shin-Etsu Chemical Co., Ltd. can also be used.
[0081] The hydroxy-terminated dimethylpolysiloxane (A), the aluminum alkoxide (B), and the silicon alkoxide (C) are mixed, for example:, in an alcohol solvent. Alcohol dissolves alkoxide and is mixed with the dimethylpolysiloxane (A). After mixing each material, the alcohol solvent used is removed by evaporation by drying.
[0082] To a precursor crosslinked by dehydration condensation between the aluminum alkoxide (B) and the terminal hydroxy group of the dimethylpolysiloxane (A), the silicon alkoxide (C) is further crosslinked by dehydration condensation. Thereafter, moisture in the air is absorbed from a crosslinked product of the above three compounds, that is, the surface of the organic-inorganic hybrid composition (X). Hydrolysis of the aluminum alkoxide (B) and the silicon alkoxide (C) proceeds by the moisture absorbed from the surface of the composition. In addition, dehydration condensation with the hydroxy-terminated dimethylpolysiloxane (A) is promoted. Hydrolysis of the aluminum alkoxide (B) and the silicon alkoxide (C) is further induced due to water generated by the condensation.
[0083] As described above, the hydrolysis of the alkoxide and the dehydration condensation of the polysiloxane occur sequentially, and cross-linking and curing reactions from the surface of the organic-inorganic hybrid composition (X) proceed gradually throughout the entire interior of the organic-inorganic hybrid composition (X). Finally, the organic-inorganic hybrid composition (X) which has been a fluid is crosslinked, cured, and then molded into a predetermined shape (for example, the shape described with reference to
[0084] As the hydroxy-terminated dimethylpolysiloxane (A) used for the organic-inorganic hybrid composition (X), two or more types of hydroxy-terminated dimethylpolysiloxanes having different weight average molecular weights may be used.
(Example Regarding Constituent Material of Elastic Member 11)
Dimethylpolysiloxane (A): Examples 1 to 6, Comparative Examples 1 and 2
[0085] As the hydroxy-terminated dimethylpolysiloxane (A), two types having different molecular weights (average degree of polymerization) were used. As low molecular weight dimethylpolysiloxane (A1), YF3800 (weight average molecular weight: 3,500) manufactured by Momentive Performance Materials Japan Kk was used, and as high molecular weight dimethylpolysiloxane (A2), XF3905 (weight average molecular weight: 20,000) manufactured by Momentive Performance Materials Japan Kk was used.
Aluminum Alkoxide (B): Examples 1 to 6
[0086] As the aluminum alkoxide (B), aluminum sec-butoxide (aluminum sec-butyrate), manufactured by Kawaken Fine Chemicals Co., Ltd., trade name: ASBD was used.
Titanium Alkoxide (B1): Comparative Example 1
[0087] In Comparative Example 1, titanium alkoxide (B1) was used instead of aluminum alkoxide (B). As the titanium alkoxide (B1), trade name: Orgatics TA-25 manufactured by Matsumoto Fine Chemical Co., Ltd. was used.
Zirconium Alkoxide (B2): Comparative Example 2
[0088] In Comparative Example 2, zirconium alkoxide (B2) was used instead of aluminum alkoxide (B). As the zirconium alkoxide (B2), trade name: Orgatics ZA-65 manufactured by Matsumoto Fine Chemical Co., Ltd. was used.
Silicon Alkoxide (C): Examples 1 to 6, Comparative Examples 1 and 2
[0089] As the silicon alkoxide (C), KC-89S (manufactured by Shin-Etsu Chemical Co., Ltd.) as silicon alkoxide oligomer was used.
<Evaluation Method>
(Curability)
[0090] Each of the above materials was prepared by a blending amount shown in Table 1, and a predetermined amount was put into a mold made of a fluororesin, and then, after heating at 70 C. for 24 hours, at 105 C. for 24 hours, and 48 hours at 150 C., respectively, a 50 mm50 mm5 mm elastic member was prototyped. Each prototype elastic member was tested by tactual sense, and the presence or absence of stickiness was evaluated. If the stickiness is large, as shown in
(Ultraviolet Light Transmittance)
[0091] A 1 mm thick cured product obtained by curing each of the above materials, prepared by the blending amount shown in Table 1, in a Teflon (registered trademark) Petri dish was used as a measurement target. The curing method is the same as described above. Then, ultraviolet light having a wavelength of 280 nm to 315 nm was applied while being changed in steps of 1 nm, and whether or not the transmittance at all wavelengths was 90% or more was evaluated. At all wavelengths, the cured products having a transmittance of 90% or more are indicated by A, and the others are indicated by B.
(Elasticity)
[0092] A 50 mm50 mm5 mm elastic member was prototyped in the same manner as in the evaluation of the curability, and this elastic member was placed on a side surface of a cylindrical vinyl chloride pipe having a diameter of 200 mm. Then, when a 1 kg iron plate was placed on the elastic member, it was evaluated whether or not the entire 50 mm50 mm surface of the elastic member was in contact with the side surface (curved surface) of the cylinder. The elastic members whose entire surface is in contact are indicated by A, and the others are indicated by B.
(Bending Strength)
[0093] A 1 mm thick cured product obtained by being cured in a Teflon (registered trademark) petri dish was used as a measurement target in the same manner as in the evaluation of the ultraviolet light transmittance, When the cured product was bent by hand, it was evaluated whether the cured product was broken. The cured products that were not broken when bent are indicated by A, and the broken cured products are indicated by B.
(Comprehensive Evaluation)
[0094] In all items including curability, ultraviolet light transmittance, elasticity, and bending strength, the case where the evaluation of A was obtained was judged as A, and the case where the evaluation of B was obtained even in some items was judged as B. Comparative Examples 1 and 2 were not evaluated in the elasticity and bending strength tests because transmittance for ultraviolet light was low. Table 1 below shows that when the elastic member 11 is formed of each of the compositions of Examples 1 to 6, both high transmittance of 90% or more for ultraviolet light and bending characteristics (elasticity) are realized simultaneously.
TABLE-US-00001 TABLE 1 Comparative Comparative Example 1 Example 2 Example 3 Example 4 Example 5 Example 6 Example 1 Example 2 Material Dimethyl- Low molecular 5.0 5.0 0.0 0.0 50.0 50.0 5.0 5.0 polysiloxane (A) weight (A1) High molecular 45 45 50 50 0 0 45 45 weight (A2) Aluminum alkoxide (B) 0.02 0.045 0.02 0.15 0.02 0.15 0 0 Titanium alkoxide (B1) 0 0 0 0 0 0 0.15 0 Zirconium alkoxide (B2) 0 0 0 0 0 0 0 0.15 Silicon alkoxide (C) 1.0 1.0 1.0 1.0 1.0 1.0 1.0 1.0 Evaluation Curability A A A A A A A A Ultraviolet light transmittance A A A A A A B B Elasticity A A A A A A Bending strength A A A A A A Comprehensive evaluation A A A A A A B B
[Verification]
[0095] The fact that the irradiance of ultraviolet light to an affected area is improved by the ultraviolet irradiation device 1 will be verified below,
<Thickness of Elastic Member 11>
[0096] Hemoglobin has heme, which is a red pigment, and is reddish.
[0097] The numerical value of 12 kPa is, for example, a value calculated based on each value, assuming that an area of a region of the elastic member 11 in contact with the skin outer surface 51 is 855 mm.sup.2, the weight of the device body 3 is 670 g, and the load f1 is 1 kgf (10 N) in order to apply a slight load to the irradiation subject 50 in a state where the device body 3 is gripped.
[0098] In each drawing, the horizontal axis indicates the thickness of the elastic member 11. A thickness of 0 mm on the horizontal axis corresponds to a state without the elastic member 11 (initial state). In each drawing, the vertical axis represents values of L, a, and b, and is shown as a relative value when a value at a thickness of 0 mm is 1.
[0099] Among the values measured by the SCI method, the a value is a value indicating a degree of redness, and it is considered that hemoglobin is retracted as the a value decreases. The L value is a value indicating lightness, and as the L value decreases, the color approaches black and absorbs light. Thus, by reducing the a value within a range that does not cause the decrease in the L value, absorption by the hemoglobin or the like until incident ultraviolet light reaches an affected area is suppressed.
[0100]
[0101]
[0102]
<Measurement of Minimal Erythema Dose (MED)>
[0103] A comparison was made between the case where a subject D (irradiation subject 50) was irradiated with the ultraviolet light L1 via the elastic member 11 and the case where the subject D was irradiated with the ultraviolet light L1 without the elastic member 11. The elastic member 11 had a size of 50 mm50 mm5 mm, and an irradiation area was 10 mm square. At the time of irradiation, an aluminum foil was wound three times around an upper surface of the skin outer surface 51, and a hole was made in a portion corresponding to the irradiation region to form a mask.
[0104] A peak wavelength of the light source 31 was 308 nm, and while an irradiation amount was changed to 150, 300, and 600 mK/cm.sup.2, the irradiation amount at which the irradiation region of the skin outer surface 51 became red for the first time was specified to measure the minimal erythema dose (MED). The results are shown in the photograph of
[0105] According to the results shown in
[Another Embodiment]
[0106] Hereinafter, another embodiment of the ultraviolet irradiation device 1 will be described.
[0107] <1> In the embodiment described above, the case where the device body 3 incorporates the light source 31 has been described, but the light source 31 may be disposed outside the device body 3. For example, as shown in
[0108] <2> In the example illustrated in
[0109] <3> The shapes of the device body 3, the elastic member 11, and the attachment 13 described above are merely examples, and various modifications are possible within the scope of achieving the object of the present invention.
DESCRIPTION OF REFERENCE SIGNS
[0110] 1 Ultraviolet irradiation device
[0111] 3 Device body
[0112] 11 Elastic member
[0113] 11a First surface of elastic member
[0114] 11b Second surface of elastic member
[0115] 11c Step portion of elastic member
[0116] 13 Attachment
[0117] 13a Opening region
[0118] 13b Frame-shaped member
[0119] 13c Claw portion
[0120] 15 Substrate
[0121] 31 Light source
[0122] 32 Gripping portion
[0123] 33 Light emitting portion
[0124] 41 Operator
[0125] 50 Irradiation subject
[0126] 51 Skin outer surface
[0127] 61 Light source device
[0128] 62 Light guide member
[0129] L1 Ultraviolet light