JP6869752B2 - Beauty equipment - Google Patents

Description

The present invention relates to a beauty device provided with a skin abnormality detecting unit that optically detects abnormalities on the skin surface such as age spots and dullness.

In connection with the present invention, for example, Patent Document 1 discloses a skin health sensor capable of detecting abnormalities on the skin surface such as age spots. There, a sensor is provided by a light source unit composed of a plurality of light sources, a probe connected to the light source unit via an irradiation light guide, a light amount measuring unit connected to the probe via a light receiving light guide, and the like. It is configured. When the probe is applied to the skin surface such as the face to emit light, the incident light from the light source is guided to the probe through the light guide for irradiation, and the reflected light reflected on the skin surface passes through the light guide for light reception. It is guided to the light amount measurement unit. The degree of skin health (presence or absence of abnormalities such as stains) can be calculated based on the ratio of the amount of incident light emitted from the light source to the amount of reflected light measured by the light amount measuring unit, that is, the reflected absorbance.

JP-A-11-253408 (Paragraph No. 0011, FIG. 1)

If the skin health sensor disclosed in Patent Document 1 and a beauty device that gives a beauty stimulus such as an electric current stimulus are used in combination, the abnormal part of the skin surface detected by the skin health sensor is intensively cared for by the beauty device. be able to. However, in the method of using the skin health sensor and the beauty device in order, when the skin abnormality is detected by the skin health sensor, it is necessary to mark or memorize the position and then care for the position with the beauty device. The overall time required, including detection and care of skin abnormalities, will be longer. In addition, if the position of the mark or memory of the abnormal part becomes ambiguous, it is necessary to care for a wide range including the periphery of the position, and it takes a long time to care for it.

An object of the present invention is to provide a cosmetological device capable of simultaneously detecting and caring for skin abnormalities, and therefore can significantly reduce these required times.

The beauty device according to the present invention includes a skin stimulating body 3 including a stimulating surface 3a that abuts on the skin surface and gives a stimulus, a skin stimulating source 116 that gives a physical beauty stimulus to the skin stimulating body 3, and a skin surface. It is provided with a skin abnormality detecting unit 88 that optically detects the abnormality of the above. The skin abnormality detection unit 88 has a lens 142 having a measurement unit 143 facing the measurement unit on the skin surface, a light emitting unit 138 that irradiates the test light toward the measurement unit on the skin surface, and reflection by the measurement unit. Includes a light receiving unit 139 that receives inspection light. In the front view facing the stimulation surface 3a, the measurement unit 143 is arranged inside the outer line of the stimulation surface 3a.

In the beauty device according to the present invention, an incoming light surface 185 orthogonal to the inspection light is formed on the inner surface of the lens 142 facing the light emitting unit 138. Here, orthogonality does not mean only a strict right angle (90 °), but is 90 ± 15 ° (75 ° or more and 105 ° or less), more preferably 90 ± 10 ° (80 ° or more and 100 ° or less). It is a concept that includes a range.

In the beauty device according to the present invention, an optical path forming body (140.141) having a hollow light guide path 187 through which inspection light passes is arranged between the light emitting unit 138 and the light receiving unit 139 and the lens 142. The light guide path 187 is formed in a V shape by a first light guide path 188 from the light emitting portion 138 to the lens 142 and a second light guide path 189 from the lens 142 to the light receiving portion 139. A recess 184 including an incoming light surface 185 is formed on the inner surface of the lens 142. The axis of the first light guide path 188 and the light entering surface 185 are orthogonal to each other. Again, orthogonality does not mean only a strict right angle (90 °), but 90 ± 15 ° (75 ° or more and 105 ° or less), more preferably 90 ± 10 ° (80 ° or more and 100 ° or less). It is a concept that includes a range.

In the beauty device according to the present invention, optical path forming bodies 140 and 141 having a hollow light guide path 187 through which inspection light passes are arranged between the light emitting unit 138 and the light receiving unit 139 and the lens 142. The light guide path 187 is formed in a V shape by a first light guide path 188 from the light emitting portion 138 to the lens 142 and a second light guide path 189 from the lens 142 to the light receiving portion 139. A recess 184 including an incoming light surface 185 is formed on the inner surface of the lens 142. At the contact surface between the lens 142 and the optical path forming bodies 140 and 141, the peripheral edge of the recess 184 is circumscribing the opening edges of the first light guide path 188 and the second light guide path 189.

In the beauty device according to the present invention, the measuring portion 143 of the lens 142 is projected from the stimulating surface 3a of the skin stimulating body 3.

In the beauty device according to the present invention, the lens 142 includes a protruding portion 142b and a measuring portion 143 provided at the front end of the protruding portion 142b and facing the measured portion on the skin surface. The curvature of the intersection C2 between the peripheral surface 142c of the protrusion 142b and the measurement unit 143 is smaller than the curvature of the intersection C1 between the hole surface 35a of the skin stimulator 3 and the stimulation surface 3a of the skin stimulator 3. Is set to.

The beauty device of the present invention includes a skin stimulator 3 including a stimulating surface 3a that abuts on the skin surface to give a stimulus, and a skin abnormality detecting unit 88 that optically detects an abnormality on the skin surface. If the measuring unit 143 provided on the lens 142 of the abnormality detecting unit 88 is arranged inside the outer line of the stimulating surface 3a, when the stimulating surface 3a is brought into contact with the skin surface, the measuring unit 143 simultaneously moves to the skin surface. Therefore, it is possible to care for the skin surface by the skin stimulator 3 while checking the condition of the skin surface with the skin abnormality detecting unit 88. Therefore, the time required for detecting and caring for skin abnormalities can be significantly shortened as compared with the conventional beauty method in which the skin health sensor and the beauty device are used separately. Moreover, the position of the abnormal part of the skin surface can be precisely identified in real time, and the identified abnormal part can be accurately and intensively cared for. Further, if the measuring unit 143 is arranged in the outer line of the stimulation surface 3a, the skin abnormality can be detected and the care can be performed in the same posture, so that it is possible to save the trouble of changing the posture of the beauty device and changing the holding. Contrary to the present invention, when the skin stimulator and the skin abnormality detection unit are arranged at different positions of the beauty device, it takes time and effort to change the posture of the beauty device and change the holding when shifting from the detection of the skin abnormality to the care. Occurs. In the above configuration, the physical cosmetological stimulus is a general term for current stimulus, vibration stimulus, thermal stimulus (thermal stimulus and cold stimulus) and the like. It is desirable that the measuring portion 143 facing the measured portion on the skin surface is formed by the surface of the lens 142 exposed from the stimulating surface 3a. This is because the lens 142 functions as a waterproof means and a dustproof means for beauty equipment, a protective means such as a sensor constituting the skin abnormality detection unit 88, a means for adjusting the amount of transmitted light, and the like.

When an incoming light surface 185 orthogonal to the inspection light is formed on the inner surface of the lens 142 facing the light emitting portion 138, the amount of reflection of the inspection light on the incoming light surface 185 can be reduced as much as possible, and the light of the lens 142 can be reduced. The transmittance can be increased. As a result, it is possible to constantly irradiate the measured portion of the skin surface with a sufficient amount of inspection light and supply a sufficient amount of reflected light to the light receiving portion 139. Therefore, the skin condition can always be accurately determined. can do. Further, if the light transmittance of the lens 142 is high, the light output of the light emitting unit 138 can be smaller when the same amount of inspection light is applied to the measured portion on the skin surface as compared with the case where the light transmittance is low. The cost and power consumption of the unit 138 can be suppressed.

By making the axis of the first light guide path 188 orthogonal to the light entry surface 185, the amount of reflection of the inspection light on the light entry surface 185 can be reduced as much as possible, and the light transmittance of the lens 142 can be increased. .. As a result, it is possible to constantly irradiate the measured portion of the skin surface with a sufficient amount of inspection light and supply a sufficient amount of reflected light to the light receiving portion 139. Therefore, the skin condition can always be accurately determined. can do. Further, if the light transmittance of the lens 142 is high, the light output of the light emitting unit 138 can be smaller when the same amount of inspection light is applied to the measured portion on the skin surface as compared with the case where the light transmittance is low. The cost and power consumption of the unit 138 can be suppressed.

At the contact surface between the lens 142 and the optical path forming bodies 140 and 141, the peripheral edge of the recess 184 on the inner surface of the lens 142 is externally attached to the opening edges of the first light guide path 188 and the second light guide path 189 of the optical path forming body 140 and 141. As a result, obstacles to the inspection light can be eliminated, the utilization efficiency of the inspection light can be improved, and the strength of the lens 142 can be further increased. Contrary to the present invention, when the periphery of the recess 184 in the lens 142 projects toward each of the light guide paths 188 and 189, a part of the inspection light may be blocked by this projecting portion. Further, when the recess 184 is enlarged so that the peripheral edge of the recess 184 is separated from the opening edges of both light guide paths 188 and 189, the strength of the lens 142 may be insufficient.

By projecting the measuring unit 143 of the lens 142 from the stimulating surface 3a of the skin stimulating body 3, it is difficult for foreign matter such as excess beauty liquid and dust to collect between the skin surface and the measuring unit 143, and the skin surface is measured. The test light can be applied to the part as set and reflected from the part to be measured on the skin surface as set. Therefore, the abnormality detection unit 88 can make an accurate determination.

Since the curvature of the intersecting portion C2 is set to be smaller than the curvature of the intersecting portion C1, the sliding movement of the skin surface in contact with the intersecting portion C2 is smoothly performed, and the skin contact is soft and smooth. Can be. Therefore, when the skin stimulator 3 is moved in the direction of the skin surface, the movement can be smoothly performed.

It is a cross-sectional plan view of the skin head of the beauty device which concerns on Example 1 of this invention. It is a front view of a beauty appliance. It is a side view of a beauty device. It is a longitudinal side view of the skin head. It is a cross-sectional plan view which shows the main part of FIG. 1 in an enlarged manner. FIG. 4 is a cross-sectional view taken along the line AA in FIG. It is an exploded view of a skin head. It is a block diagram of the control system of a beauty device. It is a schematic circuit diagram of the skin abnormality detection part. It is a flowchart which shows the control procedure of a reference voltage and a care level in a skin abnormality detection mode. It is a timing chart which shows the temporal change of the operation state of each part in a skin abnormality detection mode. It is explanatory drawing of the determination area which concerns on an output voltage. It is a timing chart which shows the temporal change of the operation state of each part when the skin abnormality detection mode is selected with the cotton mat attached to the outer surface of the skin stimulant body. It is a vertical cross-sectional view of the optical path forming body of the beauty apparatus which concerns on Example 2 of this invention. It is a cross-sectional plan view of the main part of the skin head of the beauty device which concerns on Example 3 of this invention. FIG. 15 is a cross-sectional view taken along the line BB in FIG.

(Example 1) FIGS. 1 to 13 show Example 1 of the beauty device according to the present invention. The front / rear, left / right, and up / down in this embodiment follow the crossing arrows shown in FIGS. 2 and 3 and the front / back, left / right, and up / down indications shown in the vicinity of each arrow. In both figures, the beauty device includes a main body case 1 that also serves as a vertically long grip, and a pair of front and rear skin heads 2 and 102 provided on the upper part of the main body case 1. The main body case 1 is formed in a hollow case shape by a front case 1a and a rear case 1b which are separately formed in the front and rear parts. The upper half of the main body case 1 constitutes the head support portion 100 that supports the pair of skin heads 2 and 102, and the lower half of the main body case 1 constitutes the grip portion 101.

Inside the main body case 1, a vertically long control board 7 facing the front wall of the front case 1a and a battery 8 electrically connected to the control board 7 are housed. A power switch 103 for turning on the power, a mode selection switch 104 for switching the drive mode, and a level changeover switch 105 for switching the drive strength are mounted on the lower part of the front surface of the control board 7. A switch panel 6 having three switch buttons 106 to 108 is provided on the front surface of the grip portion 101 of the main body case 1, and the user pushes each switch button 106 to 108 inward to correspond to the switch. 103 to 105 can be operated. Further, a mode display unit 109 that emits and displays the drive mode and a level display unit 110 that emits and displays the drive intensity are mounted on the upper part of the front surface of the control board 7. Both display units 109 and 110 are each composed of a plurality of LEDs, and a translucent window facing these LEDs is provided in the front case 1a and the switch panel 6. The user can visually recognize both the display units 109 and 110 through these translucent windows.

The skin head 102 on the rear side is housed in the head support portion 100 of the main body case 1 in a state where only the rear surface is exposed from the rear case 1b. A Peltier element 113 and a heat sink 114 are housed inside the skin head 102, the skin head 102 is bonded to the endothermic surface of the Peltier element 113, and the heat sink 114 is bonded to the heat generating surface. The Peltier element 113 is connected to the control board 7 via a lead wire (not shown). When a drive current is supplied from the control board 7 to the Peltier element 113, the skin head 102 is cooled through the heat absorbing surface thereof, and the heat generating surface of the Peltier element 113 is dissipated through the heat sink 114. The rear skin head 102 is used in a "cooling mode" for cooling the user's skin surface.

The beauty device according to this embodiment has an "ion derivation mode", an "ion introduction mode", and a "skin abnormality detection mode" in addition to the above-mentioned "cooling mode". The skin head 2 is used. Immediately after the user presses the power switch 103 to turn on the power, the "ion derivation mode" is selected, and the mode display unit 109 indicates that the mode is being selected. Each time the mode selection switch 104 is pressed from this state, the drive mode is switched in the order of "ion introduction mode", "skin abnormality detection mode", and "cooling mode", and at the same time, the display of the mode display unit 109 is switched. When the mode selection switch 104 is pressed in the "cooling mode", the mode returns to the "ion derivation mode" again. In FIG. 1, the skin head 2 on the front side is a head case 16 made of a round tubular plastic molded product, a skin stimulator 3 attached to the front end of the head case 16, and a head arranged on the outer peripheral surface of the head case 16. It is composed of a display unit (light emitting body) 117, a vibrator 118 housed in the head case 16, a skin abnormality detection unit 88, and the like. As will be described later, the "skin abnormality detection mode" is a drive mode in which ions are introduced while driving the skin abnormality detection unit 88.

A circular mounting seat 14 for mounting the head case 16 is provided on the upper front surface of the front case 1a, and a connecting cylinder wall 18 to be fitted into the mounting seat 14 is formed at the rear end of the head case 16. Has been done. The head case 16, the front case 1a, and the vibrator holder 120 that supports the vibrator 118 are integrated with two screws 22 screwed into the connecting cylinder wall 18 from the inner surface of the front case 1a. In this mounted state, the gap between the outer peripheral wall continuous with the mounting seat 14 and the connecting cylinder wall 18 is sealed with an O-ring 23.

A mounting cylinder wall 122 for mounting the skin stimulator 3 is formed at the front end of the head case 16. The skin stimulant 3 is made of metal, and more specifically, it is made of a round cap-shaped press-molded product made of a titanium plate material, and is integrated with the head case 16 by covering the mounting cylinder wall 122 from the front. The outer peripheral surface of the mounting cylinder wall 122 and the peripheral wall of the skin stimulator 3 facing the outer peripheral surface thereof are formed in a slightly constricted shape forward. An O-ring 123 is arranged on the outer peripheral surface of the mounting cylinder wall 122, and the O-ring 123 is sandwiched between the mounting cylinder wall 122 and the skin stimulator 3 and elastically deformed to form a gap between the two 122.3. Is sealed. A holding ring 124 is externally fitted to the rear end of the skin stimulating body 3, and the skin stimulating body 3 is fixed to the head case 16 by adhering the holding ring 124 to the cap mounting portion 17. Further, the head case 16 is provided with a cap mounting portion 17 that bulges in a circumferential shape on the rear side of the mounting cylinder wall 122, and the holding ring 124 is received by the front wall of the cap mounting portion 17. In FIG. 3, reference numeral 64 is a ring-shaped holding cap for holding the sheet-shaped cotton mat (sheet body / obstacle) M, and the holding cap 64 is pressure-fitted to the cap mounting portion 17 to stimulate the skin. The cotton mat M attached to the outer surface of the body 3 is fixedly held. Instead of the cotton mat M, another sheet body capable of absorbing a liquid, for example, a porous body such as a sponge or a sheet body made of paper can be used, and these are collectively referred to as a liquid absorbing sheet body M. be able to.

The head display portion 117 is arranged on the outer peripheral surface of the head case 16 between the cap mounting portion 17 and the connecting cylinder wall 18. In FIG. 4, the head display unit 117 includes an endless ring-shaped light guide ring 126 wound along the outer peripheral surface of the head case 16 and a pair of upper and lower light guide rings embedded in the wall surface of the head case 16 and facing the light guide ring 126. It is composed of LED 127. The light guide ring 126 is made of a polycarbonate resin, an acrylic resin, or the like having excellent light diffusivity, and the light incident from the LED 127 is repeatedly reflected in the light guide ring 126 so that the entire light guide ring 126 becomes substantially uniform. It emits light. The outer diameter of the light guide ring 126 is set sufficiently smaller than the outer diameter of the cap mounting portion 17. Therefore, when the user faces the stimulation surface 3a on the front surface of the skin stimulator 3, the light guide ring 126 itself is not blocked by the cap mounting portion 17 and is not visible to the user, and the light guide ring 126 emits light. Only light will be visible to the user. That is, the cap mounting portion 17 also serves as a light-shielding wall 128 for eliminating the irradiation of dazzling light to the user's eyes.

A vibrator 118 made of an eccentric motor and a vibrator holder 120 that supports the vibrator 118 are housed in the latter half of the head case 16. The vibrator holder 120 is composed of a pair of front and rear split holders 130 and 131 that jointly hold the vibrator 118. Three bosses 132 are provided on the rear surface of the front split holder 130, and the front and rear split holders 130 and 131 are integrated by screwing the screw 133 inserted into the rear split holder 131 into each boss 132. Has been done. As shown in FIG. 1, the rear split holder 131 integrally includes a pair of left and right flange-shaped base portions 134, and both base portions 134 together with the connecting cylinder wall 18 of the head case 16 described above It is fastened and fixed to the seat wall of the mounting seat 14 with screws 22. The vibrator holder 120 may be an integrally molded product that is not divided into a pair of divided holders 130 and 131.

A skin abnormality detection unit 88 is arranged between the skin stimulator 3 and the vibrator holder 120. In FIG. 5, the skin abnormality detection unit 88 has a light emitting element (light emitting unit) 138 and a light receiving element (light receiving unit) 139 mounted on the front surface of the substrate 137, and a V-shaped optical path from the light emitting element 138 to the light receiving element 139. It is composed of a pair of front and rear optical path forming bodies 140 and 141 to be formed, a lens 142 arranged in the center of the front surface of the first optical path forming body 140 located on the front side, and the like. A circular window opening 35 for exposing the lens 142 is formed in the center of the stimulating surface 3a of the skin stimulator 3, and the front surface of the lens 142 exposed from the window opening 35 is measured on the user's skin surface. A measuring unit 143 facing the unit is configured. In the driving state of the skin abnormality detection unit 88, the inspection light is irradiated from the light emitting element 138 toward the center of the measuring unit 143, reflected by the measured unit on the skin surface in contact with the measuring unit 143, and reaches the light receiving element 139. To reach. The lens 142 is made of polycarbonate having excellent translucency. The skin stimulator 3 has a circular shape when viewed from the side of the measured portion on the skin surface. That is, it has a circular shape in the front view facing the stimulating surface 3a of the skin stimulating body 3.

The second optical path forming body 141 located on the rear side includes a substantially disk-shaped base plate 145 facing the substrate 137 and a substantially conical cone-shaped portion 146 projecting from the center of the front surface of the base plate 145. It consists of a plastic molded product that is integrally provided. Accommodation holes (accommodation portions) 147 and 148 for accommodating the light emitting element 138 and the light receiving element 139 are formed on the left and right sides of the base plate 145, respectively. In order to prevent both elements 138 and 139 from coming into contact with the wall surface of the accommodating holes 147 and 148, the accommodating holes 147 and 148 are formed to be slightly larger than the accommodating elements 138 and 139. The conical surface of the conical portion 146 constitutes a joint surface 149 to be joined to the first optical path forming body 140, and the joint surface 149 has a pair of left and right optical path grooves 150 parallel to the generatrix and a pair of upper and lower optical path grooves. The engaging recess 151 is formed as a recess (see FIG. 6).

In FIG. 4, the first optical path forming body 140 has a substantially disk-shaped base plate 153 that is one size larger than the base plate 145 of the second optical path forming body 141, and a columnar portion projecting from the center of the rear surface of the base plate 153. It is composed of a plastic molded product integrally including a 154, a spring shaft 155 projecting from the peripheral portion of the rear surface of the base plate 153, and three bosses 156, so as to penetrate the central portion of the base plate 153 and the columnar portion 154. , A mortar-shaped cone-shaped hole 157 for accommodating the cone-shaped portion 146 is formed. The wall surface of the conical hole 157 constitutes a joint surface 158 to be joined to the joint surface 149 of the conical portion 146, and the joint surface 158 is formed on a pair of left and right joint surfaces facing the optical path groove 150 of the conical portion 146. The optical path groove 159 is formed as a recess, and a pair of upper and lower engaging convex portions 160 that engage with the engaging concave portion 151 of the conical portion 146 are projected (see FIG. 6). The spring shaft 155 is inserted into a coil spring 161 for energizing the skin stimulator 3 to support the spring 161.

When the conical portion 146 of the second optical path forming body 141 is formed in a substantially conical shape and the conical hole 157 of the first optical path forming body 140 is formed in a mortar shape, the conical portion 146 fits into the conical hole 157. Moreover, the pair of optical path forming bodies 140 and 141 are unlikely to be misaligned with each other. In a state where the joint surfaces 149 and 158 of the cone-shaped portion 146 and the cone-shaped hole 157 are joined to each other, the optical path grooves 150 and 159 formed on both joint surfaces 149 and 158 face each other, and a hollow shape through which inspection light passes. An optical path is formed. Further, by engaging the engaging convex portion 160 with the engaging concave portion 151, the relative rotation of the optical path forming bodies 140 and 141 around the central axis of the cone-shaped portion 146 is restricted. Further, the rear end surface of the columnar portion 154 is received by the front surface of the base plate 145 of the second optical path forming body 141. By screwing the screw 162 inserted into the front split holder 130 into each boss 156, the front split holder 130 and the first optical path forming body 140 are integrated, and both 130 and 140 are the substrate 137 and the first. The optical path forming body 141 of 2 is sandwiched from the front and back. The optical path grooves 150 and 159 may be formed on only one of both joint surfaces 149 and 158.

A lens hole 163 for accommodating the lens 142 is formed in a recess in the center of the front surface of the base plate 153 of the first optical path forming body 140, and a heater support portion 165 that supports the heater 164 so as to surround the lens hole 163. Is formed in a stepped shape. The heater 164 is composed of a flat film heater, and its rear surface is supported by a heater support portion 165. The front surface of the heater 164 is adhered to the inner surface of the skin stimulator 3 via an insulating double-sided tape 166. The skin stimulant 3 and the heater 164 are electrically shielded by the double-sided tape 166. A temperature sensor (thermistor) 167 for measuring the surface temperature of the heater 164 and a fuse 168 for cutting off the current supply to the heater 164 in the event of an abnormality are embedded in a part of the heater support portion 165 (FIG. 4). reference).

As shown enlarged in FIG. 5, front constricted and tapered guide surfaces 171 and 172 are formed in a circumferential shape on the rear surface of the lens 142 and the bottom surface of the lens hole 163 facing the lens 142, respectively. By bringing the lens 142 and the first optical path forming body 140 into close contact with each other in the front-rear direction and joining the guide surfaces 171, 172, the lens 142 can be positioned vertically and horizontally with respect to the optical path forming body 140. The front surface of the peripheral edge of the lens 142 is adhered to the inner surface of the skin stimulator 3 via an elastic double-sided tape 173. The double-sided tape 173 is pressed against the inner surface of the skin stimulator 3 by the lens 142 to watertightly seal the gap between the lens 142 and the skin stimulator 3. That is, the double-sided tape 173 also serves as a means for fixing the lens 142 to the skin stimulant body 3 and a sealing body for watertightness. Even if the lens 142 is adhered and fixed to the inner surface of the skin stimulator 3 with the double-sided tape 173, the displacement of the lens 142 with respect to the skin stimulator 3 is sufficiently prevented, and the watertightness between the two 3 and 142 is sufficient. However, in this embodiment, in order to further improve the prevention of misalignment and watertightness, the rear split holder 131, which is fastened and fixed to the head case 16 with the screw 22, is the front split holder 130 and a pair. The lens 142 is pressed against the inner surface of the skin stimulator 3 via the optical path forming bodies 140 and 141, and the two 3 and 142 are brought into close contact with each other more accurately.

An example of the procedure for assembling the skin head 2 to the front case 1a will be described with reference to FIG. 7. First, a pair of optical path forming bodies 140 and 141, a substrate 137, and a coil spring 161 are combined, a screw 162 is inserted into the front split holder 130, and the screw 162 is screwed into the boss 156 of the first optical path forming body 140 to screw the front split holder. By fixing the 130 to the first optical path forming body 140, a first assembly is obtained in which the second optical path forming body 141 and the substrate 137 are sandwiched between the two 130 and 140 from the front and back. Next, the vibrator 118 is assembled to the front split holder 130 from the rear, the screw 133 is inserted into the rear split holder 131, and the screw 133 is screwed into each boss 132 of the front split holder 130 to integrate the front and rear split holders 130 and 131. By doing so, a second assembly is obtained in which the vibrator 118 and the rear split holder 131 are added to the first assembly.

The obtained second assembly is inserted into the opening surrounded by the mounting seat 14 of the front case 1a from the rear, and the head case 16 to which the light guide ring 126, the LED 127, and the O-ring 23 are pre-mounted is inserted into the mounting seat 14. Insert from the front inside the continuous outer peripheral wall. In this state, the second assembly and the head case 16 are screwed into the connecting cylinder wall 18 of the head case 16 by inserting the screw 22 from the rear into the mounting seat 14 and the base portion 134 of the split holder 131 on the rear side. It is fixed to the front case 1a. Next, the temperature sensor 167, the fuse 168, the heater 164 and the lens 142 are assembled on the front surface of the first optical path forming body 140 exposed from the front surface of the head case 16, and the double-sided tapes 166 and 173 are attached to the front surfaces of the heater 164 and the lens 142. paste. Finally, the skin stimulator 3 is attached to the mounting tube wall 122 of the head case 16 in which the O-ring 123 is arranged in advance, and this is fixed by the holding ring 124. The above assembly procedure is only an example, and various other assembly procedures can be considered. In any case, the double-sided tape 166/173 is placed between the skin stimulator 3 and the rear split holder 131 in order from the front side. , The heater 164 and the lens 142, the first optical path forming body 140, the second optical path forming body 141, the substrate 137, and the front split holder 130 are sandwiched. The lens 142 and the first optical path forming body 140 may be integrally molded.

The skin stimulator 3 is connected to a current source 175 (see FIG. 8) mounted on the control board 7 via a coil spring 161 for energization and a lead wire (not shown). Further, a grip electrode 10 is fixed to the rear surface of the grip portion 101 of the main body case 1 (see FIG. 3), and the grip electrode 10 is also connected to the current source 175 via a lead wire (not shown). The current supply from the current source 175 to the skin stimulator 3 and the grip electrode 10 is controlled by the control unit 115 mounted on the control board 7. In the "ion derivation mode", a positive polarity pulse current is supplied to the skin stimulator 3 and a negative polarity pulse current is supplied to the grip electrode 10. In the "iontophoresis mode" and the "skin abnormality detection mode", a negative polarity pulse current is supplied to the skin stimulator 3 and a positive polarity pulse current is supplied to the grip electrode 10. In this embodiment, the current source 175, the vibrator 118, and the heater 164 constitute a skin stimulus source 116 that imparts physical cosmetic stimuli, that is, current stimuli, vibration stimuli, and thermal stimuli to the skin stimulator 3.

In the "ion derivation mode" and the "ion introduction mode", the stimulating surface 3a of the skin stimulating body 3 can be directly pressed against the skin surface for care, and the cotton mat M is held on the outer surface of the skin stimulating body 3. It can also be attached with a cap 64 and the cotton mat M can be pressed against the skin surface for care. When the cotton mat M is used, the cotton mat M may be impregnated with the beauty liquid, or the cotton mat M may be pressed against the skin surface to which the beauty liquid is directly applied. On the other hand, in the state where the cotton mat M is attached, since the cotton mat M is interposed between the skin surface and the measuring unit 143, the skin condition cannot be measured by the skin abnormality detecting unit 88. Therefore, if the cotton mat M is switched to the "skin abnormality detection mode" while the cotton mat M is attached, or if the cotton mat M is attached while the "skin abnormality detection mode" is selected, the normal "ion introduction mode" is used. The control to automatically shift to "" is performed, and the details will be described later.

In the "ion derivation mode", "ion introduction mode" and "skin abnormality detection mode", each time the user presses the level changeover switch 105, the pulse current supplied from the current source 175 to the skin stimulator 3 and the grip electrode 10 The strength switches in three stages of "weak", "medium", and "strong". Specifically, in the "ion derivation mode" and "ion introduction mode", a voltage of 6V at "weak", 8V at "medium", and 10V at "strong" is applied to the current source 175. Each is applied. In the "skin abnormality detection mode", the control unit 115 causes the current source 175 based on the drive intensity set by the user with the level changeover switch 105 and the care level determined based on the detection result of the skin abnormality detection unit 88. The voltage applied to is automatically controlled. In this embodiment, the applied voltage is 6 V when the drive intensity is "weak" and the care level is "1", the applied voltage is 8 V when the drive intensity is "medium" and the care level is "1", and the drive intensity is The applied voltage when the care level was "1" at "strong" was set to 10 V, and the applied voltage was set to increase by 1 V each time the care level increased by one at each drive intensity. The maximum value of the care level is "5", and the applied voltage at this time is 10V when the driving intensity is "weak", 12V when the driving intensity is "medium", and 14V when the driving intensity is "strong". ..

It should be noted that each of the above voltage values is only an example, and it is of course possible to adopt a value other than the above. The same applies to the voltage values and the like listed below. It is only an example that the drive intensity set by the level changeover switch 105 is set to 3 levels and the maximum value of the care level based on the detection result of the skin abnormality detection unit 88 is set to "5", which is different from this. The number of steps and the maximum value may be adopted. Further, in this embodiment, the intensity of the pulse current is changed by changing the voltage applied to the current source 175 to a large or small value and changing the peak value of the pulse current supplied from the current source 175 to a large or small value. Instead of the method, or in combination with this method, a method of changing the duty ratio of the pulse current to a large or small value may be adopted.

As shown in FIGS. 8 and 9, the control unit 115 supplies a pulse current from the current source 175 to the skin stimulator 3 and the grip electrode 10 based on the input signals from the switches 103 to 105 and the temperature sensor 167. It controls the drive current supplied to the heater 164 and the vibrator 118, and the display contents on the display units 109, 110, and 117. Further, the control unit 115 has a timer 176 capable of measuring the driving time of the beauty device, and a storage unit 177 that stores a reference voltage V0 (electrical reference value: an electrical output value corresponding to a predetermined reference light amount) described later. Be prepared. The light emitting element 138 is composed of a light emitting diode and is connected to the control unit 115 via a regulator 178, and a resistor (for example, 100Ω) is connected in series to the light emitting element 138. The inspection light emitted from the light emitting element 138 is purple visible light, and its peak wavelength is about 400 nm. The light receiving element 139 is composed of a photodiode and is connected to the control unit 115 via an operational amplifier 179. Specifically, the light receiving element 139 is connected to the inverting input terminal (−) of the operational amplifier 179, and the output terminal of the operational amplifier 179 is connected to the control unit 115.

When a voltage is applied from the control unit 115 to the light emitting element 138 via the regulator 178, the element 138 emits light and the inspection light is emitted toward the user's skin surface. The inspection light is reflected by the user's skin surface and reaches the light receiving element 139. The amount of reflected light at this time changes depending on the skin color of the user, that is, the amount of melanin. Specifically, in the case of a user with dark skin and a large amount of melanin, the amount of reflected light is reduced because the inspection light is absorbed in a relatively large amount on the skin surface. Conversely, for users with white skin and low melanin, the amount of reflected light is large because the amount of test light absorbed is relatively small. Further, even when used by the same user, more inspection light is absorbed and the amount of reflected light is smaller in an abnormal part such as a stain caused by melanin than in a normal part without a stain or the like. The skin abnormality detection unit 88 according to this embodiment detects skin abnormalities such as spots based on the difference in the amount of reflected light. Visible light of purple (380 to 430 nm) is more easily absorbed by melanin than visible light of other colors having a longer wavelength than that, and therefore the difference in the amount of reflected light when irradiating the normal part and the abnormal part is large. , Excellent in detecting skin abnormalities.

The more inspection light that is reflected by the user's skin and reaches the light receiving element 139, the larger current flows through the light receiving element 139, and a larger voltage is output from the operational amplifier 179 to the control unit 115. This output voltage V can be obtained by the product of the current I flowing through the light receiving element 139 and the resistor R (for example, 50 MΩ) arranged in the negative feedback circuit. The control unit 115 compares the output voltage V from the operational capacitor 179 with the reference voltage V0 stored in the storage unit 177, and if the output voltage V is the reference voltage V0 or more (V ≧ V0), the inspection portion is normal. On the contrary, if the output voltage V is less than the reference voltage V0 (V <V0), the inspection portion is determined to be abnormal. In this embodiment, the amplifier circuit is configured so that the output voltage V increases as the current I increases, but conversely, the amplifier circuit may be configured so that the output voltage V decreases as the current I increases. ..

The reference voltage V0 is a variable that changes according to the skin color of the user, and the whiter the color of the normal portion is, the higher the voltage is set, and the blacker the color is, the lower the voltage is set. As shown in the flowchart of FIG. 10, when the use of the beauty device in the "skin abnormality detection mode" is started, the control unit 115 sets the reference voltage V0 to, for example, 1.0 V (step S1), and sets the current source 175. The care level of the heater 164 and the vibrator 118 is set to "1" (step S2). Here, the voltage value of 1.0 V is slightly higher than the voltage value (about 0.8 V) output from the operational amplifier 179 when the inspection light is irradiated from the light emitting element 138 toward the mole. The care level "1" is a care level that generates an electric current stimulus or the like applied to a normal part of the skin surface.

In the next step S3, it is checked whether or not the cotton mat M is attached to the outer surface of the skin stimulator 3. Since a general cotton mat M is white and does not contain melanin at all, when the cotton mat M is irradiated with the inspection light, the amount of reflected light is larger than when the skin surface is irradiated with the inspection light. Using this mechanism, it is possible to determine whether or not the cotton mat M is attached. Specifically, the output voltage V output from the operational amplifier 179 to the control unit 115 is set to a predetermined maximum voltage VM (upper limit electrical reference value: electrical output value corresponding to a predetermined upper limit reference light amount) (for example, 2.8 V). ), If the output voltage V exceeds the maximum voltage VM (YES in step S3), it is determined that the cotton mat M is attached to the outer surface of the skin stimulator 3, and the "skin abnormality detection mode" is terminated. Then (step S4), the process shifts to the normal “ion introduction mode”. On the other hand, if the output voltage V is equal to or less than the maximum voltage VM (NO in step S3), it is determined that it is not the cotton mat M but the user's skin that faces the measuring unit 143, and the next step S5 Proceed to.

In the next step S5, the output voltage V is compared with the reference voltage V0. In the initial state where the reference voltage V0 is set to 1.0V, in most cases, the output voltage V exceeds the reference voltage V0 (V> V0), and the output voltage V is set as the new reference voltage V0 in the next step S6. Set. In the next step S7, if the care level is set to other than "1", the care level is set to "1" and the process returns to step S3. When the user moves the beauty device along the skin surface, the reference voltage V0 is repeatedly updated in step S6, and the reference voltage V0 corresponding to the user's skin color is set. That is, the output voltage V in the fairest part of the user's skin, that is, the normal part without stains, is set as the final reference voltage V0. The reference voltage V0 stored in the storage unit 177 is reset to an initial value (for example, 1.0 V) each time the power of the beauty device is turned off.

In step S5, if the output voltage V and the reference voltage V0 are equal (V = V0), the process proceeds to step S7 without going through step S6, and if the care level is set to other than "1", the care level is set to "1". Set to "1" and return to step S3. On the other hand, if the output voltage V is lower than the reference voltage V0 (V <V0) in step S5, the process proceeds to step S8, and the output voltage V is set to a predetermined minimum voltage Vm (lower limit electrical reference value: predetermined lower limit reference light amount). Compare with the corresponding electrical output value). The minimum voltage Vm is a constant set to 0.8 V, which is the same as the output voltage value when the mole is irradiated with the inspection light, and is stored in the storage unit 177 in advance. When the output voltage V is lower than the minimum voltage Vm (YES in step S8), it is determined that the skin stimulator 3 is facing a mole that does not need to be cared for, so as not to give unnecessary stimulation to the mole. The care level of each skin stimulus source 116 is set to "0" or more and "1" or less (step S9), the output of each skin stimulus source 116 is stopped or attenuated, and the process returns to step S3. The care level "0" is a care level at which the output of the skin stimulus source 116 is stopped and no irritation is generated from the skin stimulus source 116. The care levels of the current source 175, the heater 164, and the vibrator 118 here may be individually set between "0" and "1".

If the output voltage V is equal to or greater than the minimum voltage Vm in step S8 (NO in step S8), the process proceeds to step S10, and the difference between the reference voltage V0 and the output voltage V is compared with the predetermined constant C. The constant C is a positive number stored in advance in the storage unit 177 (C> 0). If the difference between the reference voltage V0 and the output voltage V is equal to or less than the constant C (YES in step S10), the care level is set to "2", which is stronger than "1" (step S11), and the process returns to step S3. On the contrary, when this difference exceeds the constant C (NO in step S10), the process proceeds to step S12.

In step S12, the difference between the reference voltage V0 and the output voltage V is compared with a value twice the constant C. If this difference is not more than twice the constant C (YES in step S12), the care level is set to "3", which is stronger than "2" (step S13), and the process returns to step S3. On the contrary, when this difference exceeds twice the constant C (NO in step S12), the process proceeds to step S14, and the difference between the reference voltage V0 and the output voltage V is compared with the value three times the constant C. If this difference is 3 times or less of the constant C (YES in step S14), the care level is set to "4", which is stronger than "3" (step S15), and the process returns to step S3. On the contrary, when this difference exceeds 3 times the constant C (NO in step S14), the care level is set to “5” which is stronger than “4” (step S16), and the process returns to step S3.

Summarizing steps S10 to S16, when the difference between the reference voltage V0 and the output voltage V is equal to or less than the constant C (0 <V0-V≤C), the care level is set to "2", and this difference exceeds the constant C. The care level is set to "3" when it does not exceed twice (C <V0-V ≦ 2C). When the difference between the reference voltage V0 and the output voltage V exceeds twice the constant C and not more than three times (2C <V0-V ≦ 3C), the care level is set to "4", and this difference is the constant C. The care level is set to "5" when it exceeds 3 times (3C <V0-V). Instead of the constant C used in this embodiment, for example, a variable that changes according to the reference voltage V0 can be used.

As described above, in step S9, when a mole is detected (YES in step S8), the output of each skin stimulus source 116 is stopped or attenuated. In the present invention, the attenuation of the output (care level) of the skin stimulus source 116 is a concept including not only reducing the output (care level) to the minimum output excluding the stopped state but also maintaining the output (care level) at the minimum output. That is, when step S9 sets the care level of the skin stimulus source 116 to "1", if the care level immediately before that is "2" or higher, the care level is lowered to "1" in step S9. On the other hand, if the care level immediately before that is already "1", the care level is maintained at "1" in step S9, but in the present invention, these are included and referred to as attenuation.

When the user grasps the grip portion 101 with his / her hand and touches the grip electrode 10 and brings the skin stimulator 3 into contact with the skin surface such as the face, the internal circuit of the beauty device connecting the skin stimulator 3 and the grip electrode 10 and the user. An electrically closed loop consisting of the human body is formed. The control unit 115 determines whether or not the stimulation surface 3a is in contact with the skin surface based on the presence or absence of the formation of the closed loop. That is, the skin stimulator 3 according to the present embodiment functions as a skin detection sensor that detects that the stimulating surface 3a is in contact with the skin surface. The control unit 115 supplies a pulse current for skin stimulation from the current source 175 to the skin stimulator 3 and the grip electrode 10 and supplies a drive current to the vibrator 118 only in the state of detecting this closed loop. Further, the control unit 115 supplies electric power to the light emitting element 138 to drive the skin abnormality detection unit 88 only in the state of detecting this closed loop, and also supplies electric power to the head display unit 117 to emit light. Let me. When the electrically closed loop is not formed, that is, when the stimulation surface 3a is separated from the skin surface, the pulse current for skin stimulation and the drive current of the vibrator 118 are supplied, and the skin abnormality detection unit 88 is driven. When the light emitting display of the head display unit 117 is stopped, the power consumption of the beauty device can be suppressed.

The skin detection sensor may be composed of an optical sensor or the like that is separate from the skin stimulator 3. When the optical sensor is arranged on the stimulating surface 3a of the skin stimulating body 3, the stimulating surface 3a comes into contact with the skin surface, so that the optical sensor cannot receive the room light. Taking this opportunity, a signal is transmitted from the optical sensor to the control unit 115, and the control unit 115 that receives this signal determines that the stimulation surface 3a has come into contact with the skin surface, and supplies a pulse current from the current source 175. , Start driving the skin abnormality detection unit 88 and the like.

Next, a case where the beauty device according to this embodiment is used in the "skin abnormality detection mode" will be described. As described above, the "skin abnormality detection mode" is a drive mode in which ions are introduced while driving the skin abnormality detection unit 88, and the control unit 115 not only drives the skin abnormality detection unit 88 but also the skin stimulator 3 A pulse current for skin stimulation is supplied to the grip electrode 10, and the heater 164 and the vibrator 118 are further driven. That is, while measuring the user's skin condition, current stimulation, thermal stimulation, and vibration stimulation are applied to the skin surface. When the skin abnormality detection unit 88 detects an abnormal part such as a spot, the current stimulation or the like is automatically enhanced in the abnormal part to strongly and intensively care for the abnormal part. That is, in the normal part of the skin surface, the care level of the skin stimulation source 116 (current source 175, heater 164, vibrator 118) is set to "1", and in the abnormal part, "2" to "2" depending on the degree of abnormality. Set to "5". In the mole portion, the care level of each skin stimulus source 116 is set to "0" to "1".

In the timing chart of FIG. 11, when the user turns on the power switch 103 and operates the mode selection switch 104 to select the “skin abnormality detection mode” (time point t0), the control unit 115 starts timing by the timer 176. At the same time, the current source 175 is controlled so as to start supplying a weak pulse current for skin detection to the skin stimulator 3 and the grip electrode 10. Further, about 5 seconds after the power is turned on, the heater 164 is energized to preheat the skin stimulator 3. The care level of the heater 164 at this time is "1". The control unit 115 controls the heater 164 on and off so as to maintain the surface temperature of the stimulating surface 3a of the skin stimulator 3 at about 40 ° C. based on the input signal from the temperature sensor 167.

In the beauty device according to this embodiment, the drive mode is reset to the "ion derivation mode" every time the power is turned off, so that the time when the "skin abnormality detection mode" is selected with the mode selection switch 104 after the power is turned on is , At the time point t0 in the timing chart of FIG. 11, in the beauty appliance in which the drive mode is memorized even when the power is turned off, if the power is turned off with the "skin abnormality detection mode" selected, the following Since the "skin abnormality detection mode" is selected from the beginning when the power is turned on, the time point when the power switch 103 is turned on is the time point t0 in FIG. Further, even in the beauty appliance having only the "skin abnormality detection mode" as the drive mode, the time point when the power switch 103 is turned on is the time point t0 in FIG.

When the user grips the grip portion 101 and brings the skin stimulator 3 into contact with the skin surface, the electrically closed loop described above is formed. The control unit 115 that detects this closed loop supplies a pulse current for skin stimulation from the current source 175 to the skin stimulator 3 and the grip electrode 10, supplies a drive current to the vibrator 118, and emits light from the head display unit 117. The display and the irradiation of the inspection light from the light emitting element 138 to the skin surface are started (time point t1). At this time, the care level of the current source 175 and the vibrator 118 is "1", and the care level of the heater 164 is also maintained at "1". The head display unit 117 indicates that the care level of the skin stimulus source 116 is "1", for example, with blue light.

When the care level is "1", the pulse current for skin stimulation supplied to the skin stimulator 3 is weak, so that the user cannot easily recognize that the current is being supplied. Therefore, in this embodiment, when the pulse current of the care level "1" is supplied, the vibrator 118 and the heater 164 are driven at the same time, and the head display unit 117 is made to emit light. Since it is easy for the user to recognize that the vibrator 118, the heater 164, and the head display unit 117 are energized regardless of the care level, the user can recognize that the energization is applied to the care level "1". It can be recognized that the pulse current of is supplied. That is, the vibrator 118, the heater 164, and the head display unit 117 function as an energizing display body that indicates that the pulse current for skin stimulation is supplied to the skin stimulating body 3.

Between the time point t1 and the time point t4, the reference voltage V0 is updated a plurality of times according to the procedure described with reference to FIG. At the time point t2, the output voltage V on the light receiving side falls below the reference voltage V0, so that the care level of the skin stimulus source 116 temporarily rises to "2", and at the next time point t3, the output voltage V becomes By exceeding the reference voltage V0, the reference voltage V0 is updated and the care level returns to "1". After the reference voltage V0 is set to 2.4V at the time point t4, the reference voltage V0 has not been updated. Therefore, at the time point t4, the skin abnormality detection unit 88 faces the fairest part of the user's skin. You can see that it was done. Of course, the voltage value of 2.4V is just an example, and if another user with a different skin color uses a beauty device, the reference voltage V0 will change. Further, even if one user continues to use the beauty device, the reference voltage V0 may change accordingly if the part to be cared for changes. Further, even if one user continues to use the beauty device for the care of one place, the reference voltage V0 may fluctuate due to the influence of the daily living environment and the like.

From the time point t5 to just before the time point t6, the output voltage V fluctuates between the reference voltage V0 (2.4V) and the minimum voltage Vm (0.8V), and the care level of the skin stimulus source 116 is "2" to " It fluctuates between "5". During this time, the head display unit 117 indicates that the care level is "2" to "5" with lights of different colors. For example, a green light can be displayed at a care level "2", a yellow light can be displayed at a care level "3", an orange light can be displayed at a care level "4", and a red light can be displayed at a care level "5". When light other than blue indicating the care level "1" is displayed on the head display unit 117, it is possible to notify the user that the skin abnormality detection unit 88 has detected the skin abnormality. That is, the head display unit 117 according to the present embodiment constitutes a notification body 89 that notifies the user that the skin abnormality detection unit 88 has detected the skin abnormality. The user can also recognize that the skin abnormality detection unit 88 has detected the skin abnormality by increasing the care level of the vibrator 118, that is, by increasing the vibration and sound caused by the vibrator 118. Further, the user can recognize that the skin abnormality detecting unit 88 has detected the skin abnormality by increasing the care level of the heater 164, that is, increasing the surface temperature of the stimulating surface 3a. That is, the vibrator 118 and the heater 164 not only form the skin stimulus source 116, but also form the notification body 89 together with the head display unit 117.

As described above, the vibrator 118, the heater 164, and the head display unit 117 function as an energization display body for the pulse current for skin stimulation. That is, the vibrator 118 and the heater 164 each have three roles of a skin stimulus source 116, a notification body 89, and an energization display body, and the head display unit 117 has two roles of the notification body 89 and the energization display body, respectively. I have. Contrary to this embodiment, the vibrator 118, the heater 164, and the head display unit 117 are stopped when the pulse current of the care level "1" is supplied, and the vibrator 118 and the like are supplied when the pulse current of the care level "2" or higher is supplied. Although the vibrator 118 and the like cannot be used as the energizing display body in the form of driving the vibrator, the role as the skin stimulating source 116 and the notification body 89 remains.

In this embodiment, the color of the head display unit 117 changes as the care level changes, but instead, the head display unit 117 is made a single color and its illuminance is gradually increased as the care level increases. It may be higher. In this case, the color of the head display unit 117 can be arbitrarily selected from blue, red, green, and the like. Further, a sounding means such as a buzzer or a synthetic voice can be adopted in place of or in combination with the light emitting means such as the head display unit 117. In this case, the user is informed that the care level has changed through hearing by changing the timbre of the sounding means as the care level changes or by gradually increasing the volume of the sounding means as the care level rises. I can inform you.

At time point t6, the output voltage V on the light receiving side shows 0.8 V, which is equal to the minimum voltage Vm. In this case, the control unit 115 determines that the skin abnormality detection unit 88 is facing the mole, sets the care level of the current source 175 and the vibrator 118 to "0" or more and "1" or less, and also sets the heater 164. Set the care level of to "1". Further, the control unit 115 blinks the head display unit 117 in an arbitrary color. The user can recognize that the skin abnormality detection unit 88 is facing the mole based on the fact that the head display unit 117 is switched to the blinking display and the vibration and sound of the vibrator 118 are weakened. The head display unit 117 at the time of mole determination can be displayed in a discolored state in which the color changes every few seconds, or can be turned off. Further, in this embodiment, each skin stimulus source 116 (current source 175, vibrator 118, heater 164) was driven during the mole determination, but instead, at least one of the skin stimulus sources 116 was driven during the mole determination. The care level may be set to "0" to stop the irritation applied to the skin surface from the skin irritation source 116.

At the time point t7, the electrically closed loop disappears when the user separates the skin stimulator 3 from the skin surface, and the control unit 115 that cannot detect this closed loop stops the irradiation of the inspection light from the light emitting element 138. At the same time, the pulse current supplied from the current source 175 to the skin stimulator 3 and the grip electrode 10 is switched from the one for skin stimulation to the weak one for skin detection. Further, the control unit 115 sets the care level of the vibrator 118 to "0" and sets the care level of the heater 164 to "1" to put it in a preheated state, and further turns off the head display unit 117. At the next time point t8, the control unit 115 re-detects the electrically closed loop, so that the irradiation of the inspection light from the light emitting element 138 is restarted. When 3 minutes have passed since the timer 176 started timing, the control unit 115 turns off the skin stimulus source 116, cuts off the power supply to the light emitting element 138 and the head display unit 117, and stops the beauty equipment. (Time point t9). That is, the power of the beauty equipment is turned off. If the power switch 103 is operated by the user before 3 minutes have passed from the start of timekeeping, the control unit 115 stops the beauty device at that time in the same manner as when 3 minutes have passed, and powers the beauty device. Cut off.

As shown in FIG. 12, regarding the output voltage V based on the light receiving amount of the light receiving element 139, three determination regions with the minimum voltage Vm (0.8V) and the maximum voltage VM (2.8V) as boundaries are assumed. Can be done. When the output voltage V is included in the "mole determination region" having a minimum voltage Vm or less, the control unit 115 determines that the skin stimulator 3 faces the mole. When the output voltage V is included in the "sheet body determination region" exceeding the maximum voltage VM, the control unit 115 determines that the cotton mat M is attached to the outer surface of the skin stimulator 3. The upper limit of 3.0 V in the "sheet body determination region" is substantially equal to the voltage value output from the operational amplifier 179 when 100% of the inspection light emitted from the light emitting element 138 is reflected. When the output voltage V is included in the "skin condition determination region" of the minimum voltage Vm or more and the maximum voltage VM or less, the control unit 115 compares the output voltage V with the reference voltage V0, and whether the skin condition is normal or abnormal. Is determined. The initial value of the reference voltage V0 is set to a low value within the range of the "skin condition determination region", preferably close to the minimum voltage Vm, and fluctuates (rises) according to the user's skin color within the range of the same region. To do. The reference voltage V0 does not fall below the minimum voltage Vm or exceed the maximum voltage VM.

On the other hand, the timing chart of FIG. 13 shows a case where the “skin abnormality detection mode” is selected with the white cotton mat M attached to the outer surface of the skin stimulator 3. From the time point t0 to immediately before the time point t1, the same as in FIG. 11 described above, but at the time point t1 when the irradiation of the inspection light is started, since the cotton mat M is attached, the output on the light receiving side is output. The voltage V shows 3.0 V, which exceeds the maximum voltage VM. At the next time point t10, the control unit 115 that has received the high output voltage V determines that the cotton mat M is attached, stops the irradiation of the inspection light, ends the "skin abnormality detection mode", and is normal. We are shifting to the "ion introduction mode". At the time of this transition, the head display unit 117 switches to the blinking red display. Based on this, the user can recognize that the skin abnormality detection unit 88 is not functioning because the cotton mat M is attached. After the time point t10, the output of each skin stimulus source 116 (current source 175, heater 164, vibrator 118) is maintained at a constant value corresponding to the care level "1" in the "skin abnormality detection mode". Since the time points t11 to t13 in FIG. 13 are the same as the time points t7 to t9 in FIG. 11, the description thereof will be omitted. Although the time interval between the time point t1 and the time point t10 is extremely short, in FIG. 13, this interval is set longer than the actual time for convenience of illustration.

In this embodiment, the head display unit 117 is switched to a red blinking display in order to notify the user that the function of the skin abnormality detection unit 88 has stopped at the time point t10. Instead, for example, the head display unit 117 is used. It may be lit or blinked in a color different from that when the skin abnormality detection unit 88 is driven, or it may be a discolored display in which the color changes at regular intervals. Further, instead of changing the display mode of the head display unit 117, or in conjunction with the change of the display mode, control may be performed to change the operating state of the voice means such as a buzzer. This voice control may switch the voice means from a stopped state to an operating state, or may change the volume or timbre of the voice means. It is also possible to use a synthetic voice that verbalizes the user to notify the user that the function of the skin abnormality detection unit 88 has stopped.

(Example 2) FIG. 14 shows Example 2 of the beauty device according to the present invention, which is different from the previous Example 1 in that a pair of upper and lower optical path forming bodies 140 and 141 are provided. Both optical path forming bodies 140 and 141 are fastened and fixed by a plurality of screws 181. The lower surface of the second optical path forming body 141 and the upper surface of the first optical path forming body 140, which are in close contact with each other, are bonded surfaces 149, respectively. -Consists of 158. A pair of left and right optical path grooves 150 and an engaging recess 151 located between the pair of left and right optical path grooves 150 are formed in the joint surface 149 of the second optical path forming body 141. A pair of left and right optical path grooves 159 facing the optical path groove 150 of the second optical path forming body 141 are recessed in the joint surface 158 of the first optical path forming body 140, and the second optical path forming body 141 is formed. An engaging convex portion 160 that engages with the engaging concave portion 151 of the above is projected. By engaging the engaging concave portion 151 and the engaging convex portion 160 to prevent the both optical path forming bodies 140 and 141 from shifting from each other along the joint surfaces 149 and 158, the both optical path forming bodies 140 by the screw 181 are used.・ 141 can be easily fastened and fixed. Since the other parts are the same as those in the first embodiment, the same members are designated by the same reference numerals and the description thereof will be omitted.

(Example 3) FIGS. 15 and 16 show Example 3 of the beauty device according to the present invention, and the structure of the lens 142 is mainly different from that of the previous Example 1. On the inner surface (rear surface) of the lens 142 of this embodiment, a recess 184 including a light entry surface 185 is formed in place of the guide surface 171 of the first embodiment. The light input surface 185 faces the light emitting element 138, and the angle θ1 formed by the inspection light directly emitted from the light emitting element 138 toward the center of the measuring unit 143 and the light input surface 185 is set to 94 °, which is close to a right angle. Has been done. Further, the angle θ2 formed by the axis of the first light guide path 188 and the light entering surface 185 is also set to 98 °, which is also close to a right angle. The slight difference between the angle θ1 and the angle θ2 is due to the mounting method of the light emitting element 138, and the angle θ1 and the angle θ2 can be the same depending on the mounting method of the light emitting element 138. For example, the inspection light from the light emitting element 138 can be irradiated along the axis of the first light guide path 188. In any case, the angle θ1 and the angle θ2 are set to a right angle or an angle close to a right angle. Since the inspection light passes along the first light guide path 188 and irradiates the center of the measuring unit 143, the meaning and directionality of the "inspection light" indicating the directionality in the present invention (claims) is shown. The meaning of "the axis of the first light guide path 188" can be regarded as having the same meaning from the viewpoint of directionality. In this way, when the lens 142 is formed with an incoming light surface 185 having an angle θ1 and an angle θ2 perpendicular to or close to the inspection light or the axis of the first light guide path 188, the amount of reflection of the inspection light on the incoming light surface 185 is reduced. It can be reduced as much as possible, and the light transmittance of the lens 142 can be increased. Orthogonality in the present invention (claims) does not mean only a strict right angle (90 °), but 90 ± 15 ° (75 ° or more and 105 ° or less), more preferably 90 ± 10 ° (90 ± 10 °). It is a concept including a range of 80 ° or more and 100 ° or less).

Also in this embodiment, by joining the first optical path forming body 140 and the second optical path forming body 141, the optical path grooves 159 and 150 provided in each face each other, and a hollow shape through which the inspection light passes. A light guide path 187 is formed. The light guide path 187 is formed in a V shape by a first light guide path 188 from the light emitting element 138 to the lens 142 and a second light guide path 189 from the lens 142 to the light receiving element 139. One end of each light guide path 188/189 opens toward the light emitting element 138 or the light receiving element 139, and the other end of each light guide path 188/189 opens toward the recess 184 of the lens 142.

In this embodiment, on the contact surface between the lens 142 and the first optical path forming body 140, the peripheral edge of the recess 184 is circumscribing the opening edges of the first light guide path 188 and the second light path 189. According to this, it is possible to eliminate obstacles to the inspection light, improve the utilization efficiency of the inspection light, and further increase the intensity of the lens 142. Contrary to this embodiment, when the periphery of the recess 184 in the lens 142 projects toward each of the light guide paths 188 and 189, a part of the inspection light may be blocked by this projecting portion. Further, when the recess 184 is enlarged so that the peripheral edge of the recess 184 is separated from the opening edges of the light guide paths 188 and 189, the strength of the lens 142 may be insufficient.

An O-ring 191 is attached between the front surface of the peripheral edge portion of the lens 142 (the base portion 142a below) and the inner surface of the skin stimulator 3 instead of the double-sided tape 173 of the first embodiment. The O-ring 191 is sandwiched between the skin stimulator 3 and the lens 142 and is elastically deformed, and the gap between the skin stimulator 3 and the lens 142 is hermetically sealed. Since the other parts are the same as those in the first embodiment, the same members are designated by the same reference numerals and the description thereof will be omitted.

In this embodiment, the front end of the lens 142 is slightly projected from the stimulating surface 3a of the skin stimulator 3 by the protruding dimension 142d, so that the measuring portion 143 at the front end of the lens 142 is brought into contact with the stimulating surface 3a on the skin surface. Since it can come into contact with the skin surface, the pressing force on the skin surface by the measuring unit 143 becomes stronger, and it is difficult for foreign substances such as excess beauty liquid and dust to collect between the skin surface and the measuring unit 143. It is possible to irradiate the skin with inspection light as set and reflect it from the part to be measured on the skin surface as set. In addition, the skin surface and the measuring unit 143 are easily in close contact with each other. Therefore, the abnormality detection unit 88 can make an accurate determination. On the contrary, if the front end of the lens 142 is set to be slightly recessed from the stimulating surface 3a of the skin stimulator 3, foreign substances such as cosmetic liquid and dust are likely to collect, and the inspection light is diffusely reflected by the cosmetic liquid and foreign matter. Therefore, there is a possibility that the inspection light cannot be reflected according to the intended setting and an accurate judgment cannot be made. Further, by slightly projecting the front end of the lens 142 from the stimulating surface 3a of the skin stimulating body 3, the peripheral edge of the window opening 35 of the skin stimulating body 3 is made difficult to come into contact with the skin surface, and the peripheral edge made of metal is made. Suppresses irritation of the skin surface. Although these points were not described in detail in Example 1, the same contents are given in Example 1.

The window opening 35 has a circular shape when viewed from the side of the measured portion on the skin surface. That is, it has a circular shape in the front view facing the stimulation surface 3a. The window opening 35 is formed by providing a through hole in the center of the stimulation surface 3a of the circular skin stimulator 3. The hole surface 35a of the through hole of the skin stimulator 3 faces the window opening 35. The lens 142 is provided on the front surface (front end) of the base portion 142a supported by the lens hole 163, the cylindrical protruding portion 142b continuously provided integrally with the base portion 142a, and the protruding portion 142b. It is configured to include a measuring portion 143 facing the measured portion on the skin surface. Further, the front surface (front end) of the protrusion 142b is a flat surface. The base portion 142a is fitted to the lens hole 163 of the base plate 153 of the first optical path forming body 140 in a concavo-convex relationship without a gap, and the movement of the measuring portion 143 of the lens 142 in the surface direction is restricted. .. As a result, even if an impact or the like is applied, the inspection light can be appropriately irradiated and reflected, so that accurate detection is always possible even if the test light is continuously used for a long period of time. Although not shown, the lens hole 163 is formed with a dent that is dented in the surface direction of the measuring unit 143, and the dent and the claw on the base portion 142 of the lens 142 that protrudes in the surface direction of the measuring unit 143. The lens 142 is fixed to the optical path forming bodies 140 and 141 by fitting the lens 142. As a result, the movement of the lens 142 in the direction orthogonal to the plane direction of the measuring unit 143 is restricted. The protruding portion 142b of the lens 142 is exposed to the outside of the skin stimulating body 3 in a protruding state with the through hole of the skin stimulating body 3 inserted. The peripheral surface 142c of the protruding portion 142b faces the hole surface 35a of the skin stimulator 3 through a slight gap or in contact with the hole surface 142c, so that the protruding portion 142b has a hole during use, drop impact, or the like. Since it is regulated by the surface 35a, the movement of the protrusion 142b in the direction orthogonal to the peripheral surface 142c is restricted. Preferably, it is easier to assemble at the time of production if the peripheral surface 142c and the hole surface 35a face each other with a slight gap between them. Therefore, in this embodiment, 0.15 mm between the peripheral surface 142c and the hole surface 35a. There is a gap between them.

The intersection C2 between the peripheral surface 142c of the protruding portion 142b and the measuring portion 143 has a rounded chamfered shape. That is, the curvature of the intersection C2 between the peripheral surface 142c of the protruding portion 142b and the measuring portion 143 is set to be small (radius of curvature R = 0.2 mm), resulting in a gentle curved outer protrusion curve (including a composite curve). ing. Further, the intersection C1 between the hole surface 35a of the skin stimulator 3 and the stimulating surface 3a of the skin stimulator 3 does not have a chamfered shape, or even if it has a chamfered shape, a large curvature is set (curvature radius R). = 0.1 mm) and there is almost no roundness. That is, the intersection C1 between the hole surface 35a of the skin stimulator 3 and the stimulating surface 3a of the skin stimulator 3 has a chamfered shape, which is a sharp curved outer protrusion curve (including a composite curve). .. That is, the curvature of the intersection C2 between the peripheral surface 142c of the protrusion 142b and the measurement unit 143 is larger than the curvature of the intersection C1 between the hole surface 35a of the skin stimulator 3 and the stimulation surface 3a of the skin stimulator 3. It is set to be smaller. As a result, the sliding movement of the skin surface in contact with the intersecting portion C2 can be smoothly performed, and the skin contact can be made soft and smooth. Therefore, when the skin stimulator 3 is moved in the direction of the skin surface, the movement can be smoothly performed. Further, as described above, the peripheral edge portion of the window opening 35 of the skin stimulator 3 (the intersection C1 between the hole surface 35a and the stimulating surface 3a) is made difficult to come into contact with the skin surface, and the metal peripheral edge portion is made of skin. It suppresses the irritation of the surface.

The protrusion dimension 142d that projects the front end (measurement unit 143) of the lens 142 from the stimulation surface 3a of the skin stimulator 3 is a dimension that is 3b or less in thickness of the skin stimulator 3 ) Is preferable. This is because if a dimension exceeding the thickness 3b of the skin stimulator 3 is projected, the irritation to the skin by the lens 142 becomes stronger and the skin feel becomes worse. Further, it is because the contact area of the stimulating surface 3a of the skin stimulating body 3 with the skin surface is reduced to prevent the stimulating range to the skin surface from being reduced.

With respect to the protruding dimension 142d in which the front end of the lens 142 is projected from the stimulating surface 3a of the skin stimulator 3, more preferably, it is ½ or more of the dimension of the thickness 3b of the skin stimulator 3 and not more than the thickness 3b of the skin stimulator 3. Protrude only the dimensions. As a result, it is possible to effectively prevent foreign substances such as excess cosmetic liquid and dust from accumulating on the surface of the measuring unit 143 while suppressing irritation to the skin. In this embodiment, the thickness 3b of the skin stimulator 3 is set to 0.3 mm. On the other hand, the protrusion dimension 142d for projecting the front end of the lens 142 from the stimulation surface 3a of the skin stimulator 3 is set to 0.21 mm. On the other hand, since the radius of curvature R of the intersecting portion C2 is 0.2 mm, the protruding dimension 142d from the stimulating surface 3a of the skin stimulator 3 to the front end of the lens 142 and the end of the curved portion of the intersecting portion C2 on the measuring portion 143 side. The difference from the dimension in the protruding direction of the lens 142 from the portion to the end portion on the peripheral surface 142c side is set so that the latter does not become larger. In other words, the curved portion of the intersecting portion C2 is located within the range of the protruding dimension 142d from the stimulating surface 3a of the skin stimulating body 3 to the front end of the lens 142. That is, the end portion of the curved portion of the intersecting portion C2 on the peripheral surface 142c side is set so as not to enter within the range of the thickness 3b of the skin stimulator 3. As a result, it is possible to prevent the skin from dripping between the lens 142 and the skin stimulant 3 while making the skin feel soft and smooth. Further, since the sagging of the skin can be prevented as much as possible, the irritation to the skin surface by the intersecting portion C1 can be suppressed. The effect that the skin does not sag is also due to the fact that the curvature of the intersecting portion C1 is larger than the curvature of the intersecting portion C2. The skin stimulator 3 and the window opening 35 do not have to have a circular shape when viewed from the side of the measured portion on the skin surface, and may have a triangular shape, a quadrangular shape, or the like. Further, the protruding portion 142b of the lens 142 may have a triangular columnar shape, a square columnar shape, or the like according to the shape of the window opening 35.

As described above, the beauty equipment according to each of the above embodiments includes a skin stimulator 3 that abuts on the skin surface to apply current stimulation and the like, and a skin abnormality detecting unit 88 that optically detects an abnormality on the skin surface. In the stimulating surface 3a of the skin stimulating body 3, a measuring unit 143 composed of the front surface of the lens 142 of the skin abnormality detecting unit 88 is arranged. According to this beauty device, when the stimulating surface 3a is brought into contact with the skin surface, the measuring unit 143 faces the skin surface at the same time, so that the skin stimulus is performed while checking the condition of the skin surface with the skin abnormality detecting unit 88. It is possible to take care of the skin surface by the body 3. Therefore, the time required for detecting and caring for skin abnormalities can be significantly shortened as compared with the conventional beauty method in which the skin health sensor and the beauty device are used separately. Moreover, the position of the abnormal part of the skin surface can be precisely identified in real time, and the identified abnormal part can be accurately and intensively cared for. Further, when the skin abnormality detection unit 88 detects an abnormality on the skin surface, the output of the skin stimulation source 116 is automatically increased, and when the notification body 89 including the head display unit 117 is activated, the skin abnormality detection unit is activated. The detection result of 88 is immediately reflected in the output of the skin stimulus source 116, and the abnormal part is strongly and intensively cared for without giving the user the trouble of switching the output, and the skin stimulator 3 is faced. It is possible to notify the user that there is a skin abnormality in the part of the skin and promote intensive care of the part.

In the above embodiment, the amount of light received by the light receiving unit 139 is converted into a voltage value and output to the control unit 115, but the electrical output value may be a current value or a power value. As the inspection light emitted from the light emitting unit 138, for example, ultraviolet rays in the UVA region (315-380 nm) or UVB region (280 to 315 nm) can be used in addition to the purple visible light. When ultraviolet rays are used as the inspection light, skin abnormalities such as blemishes can be detected with high accuracy equal to or higher than that when purple visible light is used. Since the output of the inspection light is very weak, the skin surface will not be damaged even if the inspection light consisting of ultraviolet rays is used, but it is necessary to increase the output of the inspection light due to structural factors. If there is, it is effective to irradiate the inspection light intermittently.

When the lens 142 is arranged in the window opening 35 of the skin stimulator 3, it is possible to prevent liquids and dust from entering the inside of the skin head 2 through the window opening 35, and the light emitting element 138 is caused by foreign matter invading through the window opening 35. It is possible to prevent the light receiving element 139 and the like from being damaged. Further, the amount of transmitted light of the inspection light can be adjusted by the lens 142. However, since it is possible to irradiate the inspection light of the light emitting element 138 and receive the reflected light by the light receiving element 139 without the lens 142, the lens 142 may be omitted if necessary. When the lens 142 is omitted, the space inside the window opening 35 constitutes the measuring unit 143. The light emitting element 138 and the light receiving element 139 do not need to be arranged on the skin head 2, and may be arranged inside the main body case 1. In this case, the optical path between both elements 138 and 139 and the lens 142 may be formed by an optical fiber or the like. Further, the skin abnormality detection unit 88 may include, for example, a camera instead of the light emitting unit 138 and the light receiving unit 139. In this case, the image of the skin surface captured by the camera is sent to the determination unit provided on the control board 7, where the presence or absence of skin abnormalities such as spots is determined in real time.

The light emitting body 117 as the notification body 89 is not limited to the endless ring shape as in the above embodiment, and may be formed in an intermittent ring shape, or may be formed in a U shape, a semicircular shape, or the like. Good. The ring in the present invention is a concept including a U-shape and a semicircular shape. Further, the light emitting body 117 can be provided in the main body case 1 in addition to the skin head 2. In this case, the light emitting body 117 is preferably provided on the head support portion 100 that is not covered by the hand, rather than the grip portion 101 that is covered by the user's hand when using the beauty device. It may straddle both the head support portion 100 and the grip portion 101. Further, the notification body 89 may be composed of, for example, a buzzer that emits a sound, in addition to the light emitting body 117, the vibrator 118, and the heater 164. Further, the notification body 89 can be composed of a display panel such as a liquid crystal panel or an organic EL panel, and in this case, characters such as "stain detection", "mole detection", and "seat body mounting" are displayed on the display panel. It can be displayed. The skin stimulant 3 can be formed of a conductive resin or a conductive rubber in addition to the metal. In the case of a beauty device that does not supply a pulse current to the skin stimulator 3, the skin stimulator 3 may be formed of an insulating resin or an insulating rubber.

The beauty equipment according to each of the above embodiments can be carried out in the following forms.

A skin stimulating body 3 including a stimulating surface 3a that abuts on the skin surface to give a stimulus, a skin stimulating source 116 that gives a physical beauty stimulus to the skin stimulating body 3, and a control unit 115 that controls the skin stimulating source 116. And a skin abnormality detection unit 88 that optically detects abnormalities on the skin surface.
The skin abnormality detecting unit 88 includes a measuring unit 143 facing the measured unit on the skin surface, and includes a measuring unit 143.
A cosmetological instrument characterized in that the measuring unit 143 is arranged inside the outer line of the stimulating surface 3a in a front view facing the stimulating surface 3a.
In the above configuration, the physical cosmetological stimulus is a general term for current stimulus, vibration stimulus, thermal stimulus (thermal stimulus and cold stimulus) and the like. It is desirable that the measurement unit 143 facing the measurement unit on the skin surface is formed by the surface of the lens (detection head) exposed from the stimulation surface 3a. This is because the lens functions as a waterproof means and a dustproof means for beauty equipment, a protective means such as a sensor constituting the skin abnormality detection unit 88, a means for adjusting the amount of transmitted light, and the like. However, since it is possible to measure the skin condition without a lens, the measuring unit 143 may be configured in a space without a lens.

The above-mentioned beauty device according to the present invention includes a skin stimulator 3 including a stimulating surface 3a that abuts on the skin surface to give a stimulus, and a skin abnormality detecting unit 88 that optically detects an abnormality on the skin surface. The measurement unit 143 of the skin abnormality detection unit 88 is arranged inside the outer line of the stimulation surface 3a. According to this beauty device, when the stimulating surface 3a is brought into contact with the skin surface, the measuring unit 143 faces the skin surface at the same time, so that the skin stimulus is performed while checking the condition of the skin surface with the skin abnormality detecting unit 88. It is possible to take care of the skin surface by the body 3. Therefore, the time required for detecting and caring for skin abnormalities can be significantly shortened as compared with the conventional beauty method in which the skin health sensor and the beauty device are used separately. Moreover, the position of the abnormal part of the skin surface can be precisely identified in real time, and the identified abnormal part can be accurately and intensively cared for. Further, if the measuring unit 143 is arranged in the outer line of the stimulation surface 3a, the skin abnormality can be detected and the care can be performed in the same posture, so that it is possible to save the trouble of changing the posture of the beauty device and changing the holding. Contrary to the present invention, when the skin stimulator and the skin abnormality detection unit are arranged at different positions of the beauty device, it takes time and effort to change the posture of the beauty device and change the holding when shifting from the detection of the skin abnormality to the care. Occurs.

A beauty device in which the control unit enhances the output of the skin stimulus source when the skin abnormality detection unit 88 detects an abnormality on the skin surface.

According to a beauty device in which the control unit 115 enhances the output of the skin stimulus source 116 when the skin abnormality detection unit 88 detects an abnormality on the skin surface, the detection result of the skin abnormality detection unit 88 immediately determines the intensity of skin irritation. It is possible to strongly and intensively care for the detected abnormal part by reflecting it on. Further, since the skin irritation is automatically enhanced when the skin abnormality is detected, the user can save the trouble of switching and operating the output of the skin irritation source 116.

It is equipped with a notification body 89 that generates at least one of sound, light, and vibration.
A beauty device in which the control unit 115 activates the notification body 89 when the skin abnormality detection unit 88 detects an abnormality on the skin surface.

When the skin abnormality detection unit 88 detects an abnormality on the skin surface, the control unit 115 immediately notifies the user of the abnormal part of the skin surface by sound or the like according to the beauty device that activates the notification body 89. Intensive care of the part can be promoted.

A cosmetological device in which a measuring unit 143 is arranged at the center of a stimulating surface 3a of a skin stimulating body 3.

When the measuring unit 143 is arranged at the center of the stimulating surface 3a of the skin stimulating body 3, the user can accurately identify the abnormal portion of the skin surface as compared with the case where the measuring unit 143 is provided at the peripheral portion of the stimulating surface 3a. The user who has identified that there is a skin abnormality in the portion of the stimulating surface 3a that abuts on the central portion can evenly care for the abnormal portion and its surroundings by keeping the beauty device at that position.

The skin stimulator 3 is formed of a conductor, and constitutes a skin detection sensor that detects that the stimulating surface 3a is in contact with the skin surface.
A beauty device in which the control unit 115 controls the driving state of the skin abnormality detection unit 88 based on the detection signal of the skin detection sensor.

When the skin stimulator 3 is formed of a conductor and constitutes a skin detection sensor that detects that the stimulating surface 3a abuts on the skin surface, the skin detection sensor is separated from the skin stimulator 3. Compared with the case, it is possible to easily and accurately detect that the stimulating surface 3a is in contact with the skin surface. When the control unit 115 controls the driving state of the skin abnormality detection unit 88 based on the detection signal of the skin detection sensor, the skin abnormality detection unit 88 is not unnecessarily driven while the stimulation surface 3a is away from the skin surface. The power consumption of beauty equipment can be suppressed.

It is equipped with a skin head 2 including a skin stimulant body 3 and a main body case 1.
The main body case 1 includes a head support portion 100 that supports the skin head 2 and a grip portion 101 that can be used as a grip.
A beauty device in which at least a part of the light emitting body 117 constituting the notification body 89 is provided on the head support portion 100 or the skin head 2.

When the user holds the grip portion 101 of the main body case 1, the head support portion 100 and the skin head 2 are easier to see in the user's field of view than the grip portion 101, and can be hidden by the user's hand like the grip portion 101. Absent. Therefore, if at least a part of the light emitting body 117 constituting the notification body 89 is provided on the head support portion 100 or the skin head 2, the user can easily see the light emitting body 117, so that the skin abnormality detecting unit 88 can perform the skin abnormality detection unit 88. It is possible to reliably notify the user that a surface abnormality has been detected.

A cosmetological device in which a light emitting body 117 is formed in an intermittent or continuous ring shape.

When the light emitting body 117 is formed in an intermittent or continuous ring shape, the appearance and silhouette of the beauty device can be highlighted in a state of illuminating a wider area as compared with the case where the point-shaped light emitting body 117 is locally arranged. it can. Therefore, the design of the beauty device can be improved and the commercial value thereof can be increased.

A light emitting body 117 is arranged on the outer peripheral surface of the skin head 2 between the skin stimulator 3 and the head support portion 100.
A light-shielding wall 128 is formed between the stimulating surface 3a of the skin stimulating body 3 and the light emitting body 117.
A beauty device in which the light emitting surface of the light emitting body 117 is located inside the outer line of the light-shielding wall 128 and the light emitting body 117 emits light to the outside of the outer line in the front view facing the stimulation surface 3a. ..

According to a beauty device in which the light emitting body 117 is located inside the outer line of the light-shielding wall 128 and emits light to the outside of the outer line, when the user looks at the stimulating surface 3a of the skin stimulating body 3 from the front. In addition, the light emitting surface of the light emitting body 117 can be blocked by the light shielding wall 128 to hide it from the user's eyes, and only the light emitted by the light emitting body 117 can be projected to the user's eyes. Therefore, it is possible to eliminate the irradiation of dazzling light to the user's eyes and to create a fantastic atmosphere surrounding the skin stimulator 3 with a vague soft light to further enhance the design of the beauty device.

A beauty device in which the notification body 89 includes a vibrator 118.

When the notifying body 89 is configured to include the vibrator 118, it is possible to notify the user via the tactile sensation by the vibration of the vibrator 118 that the skin abnormality detecting unit 88 has detected the abnormality on the skin surface. Therefore, the presence of skin abnormalities can be reliably notified to visually impaired users and users with their eyes closed.

The skin abnormality detection unit 88 includes a light emitting unit 138 that irradiates the test light toward the measurement unit on the skin surface facing the measurement unit 143, and a light receiving unit 139 that receives the inspection light reflected by the measurement unit.
The control unit 115 determines that the measured unit is in a normal state when the light receiving amount of the light receiving unit 139 is equal to or more than a predetermined reference light amount, while the measured unit 115 determines that the light receiving amount is less than the reference light amount. A cosmetological device that determines that it is in an abnormal state and performs at least one of a control for increasing the output of the skin stimulus source 116 and a control for activating the notification body 89.

When the light emitting unit 138 irradiates the measured portion on the skin surface with inspection light, and the reflected light amount at that time, that is, the received light amount of the light receiving portion 139 is equal to or more than a predetermined reference light amount, it is determined that the measured portion is in a normal state. On the contrary, if the amount of received light is less than the reference amount of light, the measured portion is determined to be in an abnormal state. According to this determination method, the skin condition can be determined based on a simple and quantitative standard of the amount of light, so that the configuration of the skin abnormality detection unit 88 can be simplified and the skin condition can always be accurately determined. By increasing the output of the skin stimulus source 116 in the abnormal part of the skin surface, it is possible to take care of the part strongly and intensively and to save the user the trouble of switching and operating the output of the skin stimulus source 116. Further, when the notification body 89 is activated on the abnormal portion of the skin surface, the portion can be immediately notified to the user to promote intensive care of the portion.

The skin abnormality detection unit 88 receives the light emitting unit 138 that irradiates the inspection light toward the measurement unit on the skin surface facing the measurement unit 143 and the inspection light reflected by the measurement unit, and receives electricity according to the amount of light received. Includes a light receiving unit 139 that outputs a target output value
The control unit 115 determines the state of the unit to be measured by comparing the electrical output value of the light receiving unit 139 with a predetermined electrical reference value, and if it is determined to be in an abnormal state, it is a skin stimulus source. A cosmetological device that performs at least one of a control for increasing the output of the 116 and a control for operating the alarm body 89.

The light emitting unit 138 irradiates the skin surface with inspection light, and the light receiving unit 139 that receives the reflected light at that time outputs an electrical output value such as a current or voltage according to the amount of received light. Then, the state of the skin surface is determined by comparing the electrical output value of the light receiving unit 139 with a predetermined electrical reference value. According to this determination method, the skin condition can be determined based on a simple and quantitative standard called an electrical output value, so that the configuration of the skin abnormality detection unit 88 can be simplified and the skin condition can always be accurately determined. .. By increasing the output of the skin stimulus source 116 in the abnormal part of the skin surface, it is possible to take care of the part strongly and intensively and to save the user the trouble of switching and operating the output of the skin stimulus source 116. Further, when the notification body 89 is activated on the abnormal portion of the skin surface, the portion can be immediately notified to the user to promote intensive care of the portion.

The control unit 115 includes a storage unit 177 that stores an electrical reference value.
When the light receiving amount corresponding to the electric output value of the light receiving unit 139 is larger than the reference light amount indicated by the electric reference value stored in the storage unit 177, the electric output value is used as a new electric reference value. A beauty device that is stored in the storage unit 177.

The amount of inspection light reflected on the user's skin surface increases as the skin becomes whiter and decreases as the skin becomes darker. Therefore, if the amount of reflected light in the average skin color is set as the reference amount, when a user who is fairer than the average uses a beauty device, the amount of reflected light exceeds the reference amount even in an abnormal part such as a stain, and the abnormality is concerned. There is a risk that the part will be mistakenly determined to be normal. On the contrary, when a user who is darker than the average uses a beauty device, the amount of reflected light may be less than the reference light amount even in the normal part, and the normal part may be erroneously determined as abnormal. Therefore, in the present invention, when the light receiving amount corresponding to the electric output value of the light receiving unit 139 is larger than the reference light amount indicated by the electric reference value stored in the storage unit 177, the output value is set to a new electrical. It was made to be stored in the storage unit 177 as a reference value. According to this, every time the user moves the beauty device along the skin surface and the measuring unit 143 faces the fairer part, the electrical reference value is updated, so that the user's most fair part is selected. An electrical reference value can be set based on this. As described above, according to the present invention, it is possible to set an appropriate electrical reference value according to the skin color of the user and accurately detect skin abnormalities such as spots regardless of the skin color.

The skin stimulator 3 including the stimulating surface 3a that abuts on the skin surface to give stimulus, the skin stimulating source 116 that gives physical beauty stimulus to the skin stimulator 3, and the abnormality of the skin surface are optically detected. Equipped with a skin abnormality detection unit 88,
The skin abnormality detection unit 88 has a measuring unit 143 facing the measured portion on the skin surface, a light emitting unit 138 that irradiates the test light toward the measured portion, and a light receiving unit 139 that receives the inspection light reflected by the measured portion. Including and
Regarding the light receiving amount of the light receiving unit 139, a predetermined reference light amount and a predetermined upper limit reference light amount larger than the reference light amount are set.
When the light receiving amount of the light receiving unit 139 is equal to or more than the reference light amount and equal to or less than the upper limit reference light amount, it is determined that the measured part is in a normal state, and when the received light amount is less than the reference light amount, the measured part is in an abnormal state. If the amount of received light exceeds the upper limit reference amount of light, the measuring unit 143 has an obstacle that hinders the detection of the skin (for example, it is covered with a white sheet body M). A beauty device characterized by judging.

When the light emitting unit 138 irradiates the area to be measured on the skin surface with inspection light, and the amount of reflected light at that time, that is, the amount of light received by the light receiving unit 139 is equal to or more than a predetermined reference amount and equal to or less than the upper limit reference amount, the measured portion is If it is determined that the state is normal, and conversely, if the amount of received light is less than the reference amount of light, the measured portion is determined to be in an abnormal state. According to this determination method, the skin condition can be determined based on a simple and quantitative standard of the amount of light, so that the configuration of the skin abnormality detection unit 88 can be simplified and the skin condition can always be accurately determined. Further, when the light receiving amount of the light receiving unit 139 exceeds the upper limit reference light amount, it is determined that the measuring unit 143 has an obstacle that hinders the detection of the skin (for example, it is covered with the white sheet body M). Then, an obstacle such as the sheet body M is misidentified as a fair skin surface, and the output of the skin stimulus source 116 is controlled based on this misidentification, so that it is possible to avoid the inconvenience of not being able to properly care for the skin surface.

The skin stimulator 3 including the stimulating surface 3a that abuts on the skin surface to give stimulus, the skin stimulating source 116 that gives physical beauty stimulus to the skin stimulator 3, and the abnormality of the skin surface are optically detected. Equipped with a skin abnormality detection unit 88,
The skin abnormality detection unit 88 receives the measurement unit 143 facing the measurement unit on the skin surface, the light emitting unit 138 that irradiates the measurement light toward the measurement unit, and the inspection light reflected by the measurement unit, and receives light. Includes a light receiving unit 139 that outputs an electrical output value according to the amount.
Regarding the electrical output value of the light receiving unit 139, a predetermined electrical reference value and a predetermined upper limit electrical reference value larger than the electrical reference value are set.
When the electrical output value of the light receiving unit 139 is equal to or greater than the electrical reference value and equal to or less than the upper limit electrical reference value, it is determined that the device under test is in a normal state, and the electrical output value determines the electrical reference value. If it falls below this, it is determined that the part to be measured is in an abnormal state, and if the electrical output value exceeds the upper limit electrical reference value, the measuring part 143 has an obstacle that hinders the detection of skin ( (For example, it is covered with a white sheet body M)).

The light emitting unit 138 irradiates the area to be measured on the skin surface with inspection light, and the light receiving unit 139 that receives the reflected light at that time outputs an electrical output value such as a current or voltage according to the amount of received light. If the electrical output value of the light receiving unit 139 is equal to or higher than a predetermined electrical reference value and equal to or lower than the upper limit electrical reference value, it is determined that the measured unit is in a normal state, and conversely, the electrical output value is electric. If it falls below the target reference value, the measured portion is determined to be in an abnormal state. According to this determination method, the skin condition can be determined based on a simple and quantitative standard called an electrical output value, so that the configuration of the skin abnormality detection unit 88 can be simplified and the skin condition can always be accurately determined. .. Further, when the electrical output value of the light receiving unit 139 exceeds the upper limit electrical reference value, the measuring unit 143 has an obstacle in detecting the skin (for example, covered with a white sheet body M). It is possible to avoid the inconvenience of not being able to properly care for the skin surface by misidentifying an obstacle such as the sheet body M as a fair skin surface and controlling the output of the skin stimulation source 116 based on this misidentification. it can.

At least one of a control for increasing the output of the skin stimulus source 116 and a control for activating the notification body 89 for notifying the abnormal state of the skin surface when it is determined that the measured portion of the skin surface is in an abnormal state. Beauty equipment to do.

By increasing the output of the skin stimulus source 116 in the abnormal part of the skin surface, it is possible to take care of the part strongly and intensively and to save the user the trouble of switching and operating the output of the skin stimulus source 116. Further, when the notification body 89 is activated on the abnormal portion of the skin surface, the portion can be immediately notified to the user to promote intensive care of the portion.

When it is determined that the measuring unit 143 has an obstacle that hinders the detection of the skin (for example, it is covered with the white sheet body M), the control for stopping the driving of the skin abnormality detecting unit 88 and the control. A beauty device that performs at least one of the controls for operating the notification body 89.

When the measuring unit 143 is covered with an obstacle such as the sheet body M, the skin condition cannot be measured by the skin abnormality detecting unit 88. In this case, if the driving of the skin abnormality detecting unit 88 is stopped, the driving of the skin abnormality detecting unit 88 is stopped. It is possible to reliably prevent the skin abnormality detection unit 88 from being unnecessarily driven and increasing the power consumption. Further, when the notification body 89 is activated in this case, the measurement unit 143 is covered with an obstacle such as the seat body M to notify the user that the skin abnormality detection unit 88 is not functioning, and the seat body M or the like is notified. It is possible to encourage the user to take appropriate measures such as removing obstacles.

The skin stimulator 3 including the stimulating surface 3a that abuts on the skin surface to give stimulus, the skin stimulating source 116 that gives physical beauty stimulus to the skin stimulator 3, and the abnormality of the skin surface are optically detected. Equipped with a skin abnormality detection unit 88,
The skin abnormality detection unit 88 includes a light emitting unit 138 that irradiates the inspection light toward the measurement unit on the skin surface and a light receiving unit 139 that receives the inspection light reflected by the measurement unit.
Regarding the light receiving amount of the light receiving unit 139, a predetermined reference light amount and a predetermined lower limit reference light amount smaller than the reference light amount are set.
When the light receiving amount of the light receiving unit 139 is equal to or more than the reference light amount, it is determined that the measured part is in a normal state, and when the received light amount is less than the reference light amount and equal to or more than the lower limit reference light amount, the measured part is abnormal. A beauty device characterized in that it is determined to be in a state, and when the amount of received light is less than the lower limit reference amount of light, it is determined that the part to be measured is not an abnormal state but a mole.

When the light emitting unit 138 irradiates the measured portion on the skin surface with inspection light, and the reflected light amount at that time, that is, the received light amount of the light receiving portion 139 is equal to or more than a predetermined reference light amount, it is determined that the measured portion is in a normal state. On the contrary, if the amount of received light is less than the reference amount of light and equal to or more than the lower limit reference amount of light, the measured portion is determined to be in an abnormal state. According to this determination method, the skin condition can be determined based on a simple and quantitative standard of the amount of light, so that the configuration of the skin abnormality detection unit 88 can be simplified and the skin condition can always be accurately determined. Further, when the light receiving amount of the light receiving unit 139 is less than the lower limit reference light amount, if it is determined that the measured part is not an abnormal state but a mole, the mole that does not need to be cared for is accurately detected and the part is wasted. You can prevent it from being taken care of.

The skin stimulator 3 including the stimulating surface 3a that abuts on the skin surface to give stimulus, the skin stimulating source 116 that gives physical beauty stimulus to the skin stimulator 3, and the abnormality of the skin surface are optically detected. Equipped with a skin abnormality detection unit 88,
The skin abnormality detection unit 88 receives the light emitting unit 138 that irradiates the test light toward the measured part on the skin surface and the test light reflected by the measured part, and outputs an electrical output value according to the amount of received light. Including the light receiving unit 139
Regarding the electrical output value of the light receiving unit 139, a predetermined electrical reference value and a predetermined lower limit electrical reference value smaller than the electrical reference value are set.
When the electrical output value of the light receiving unit 139 is equal to or higher than the electrical reference value, it is determined that the device under test is in a normal state, and the electrical output value is lower than the electrical reference value and equal to or higher than the lower limit electrical reference value. If, it is determined that the measured part is in an abnormal state, and if the electrical output value is lower than the lower limit electrical reference value, it is determined that the measured part is not in an abnormal state but a hollow. Beauty equipment.

The light emitting unit 138 irradiates the area to be measured on the skin surface with inspection light, and the light receiving unit 139 that receives the reflected light at that time outputs an electrical output value such as a current or voltage according to the amount of received light. If the electrical output value of the light receiving unit 139 is equal to or higher than the predetermined electrical reference value, it is determined that the device under test is in a normal state, and conversely, the electrical output value is lower than the electrical reference value and the lower limit electricity. If it is equal to or higher than the target reference value, the device under test is determined to be in an abnormal state. According to this determination method, the skin condition can be determined based on a simple and quantitative standard called an electrical output value, so that the configuration of the skin abnormality detection unit 88 can be simplified and the skin condition can always be accurately determined. .. Further, when the electrical output value of the light receiving unit 139 is lower than the lower limit electrical reference value, if it is determined that the measured unit is not in an abnormal state and is a mole, the mole that does not need to be cared for is accurately detected and the mole is detected. It is possible to prevent unnecessary care.

At least one of a control for increasing the output of the skin stimulus source 116 and a control for activating the notification body 89 for notifying the abnormal state of the skin surface when it is determined that the measured portion of the skin surface is in an abnormal state. Beauty equipment to do.

By increasing the output of the skin stimulus source 116 in the abnormal part of the skin surface, it is possible to take care of the part strongly and intensively and to save the user the trouble of switching and operating the output of the skin stimulus source 116. Further, when the notification body 89 is activated on the abnormal portion of the skin surface, the portion can be immediately notified to the user to promote intensive care of the portion.

It was determined that the light receiving amount of the light receiving unit 139 was lower than the lower limit reference light amount, or the electrical output value of the light receiving unit 139 was lower than the lower limit electrical reference value, and the measured part on the skin surface was not in an abnormal state but was a mole. A cosmetological device that performs at least one of a control for attenuating or stopping the output of the skin stimulus source 116 and a control for activating the alarm body 89.

When it is determined that the part to be measured on the skin surface is a mole rather than an abnormal state, if the output of the skin stimulus source 116 is attenuated or stopped, it is possible to more reliably prevent the mole from being unnecessarily cared for. Further, when the notification body 89 is activated in this case, it is possible to immediately notify the user that the part to be measured is a mole and call attention not to give unnecessary stimulation to the mole.

The light emitting body 117 and / or the vibrator 118 is operating in a state where the skin stimulating body 3 gives a beauty stimulus to the skin surface.
A beauty device in which the control unit 115 changes the operating state of the light emitting body 117 and / or the vibrator 118 when the skin abnormality detecting unit 88 detects a skin abnormality.

When the light emitting body 117 and / or the vibrator 118 is activated while the skin stimulator 3 gives a beauty stimulus to the skin surface, the user is more certain that the skin stimulus is output from the skin stimulator 3. Can be recognized. Further, according to the configuration in which the operating state of the light emitting body 117 and / or the vibrator 118 is changed when a skin abnormality is detected, not only as a display body indicating that the skin stimulus is output from the skin stimulating body 3, but also the skin. Since the light emitting body 117 and / or the vibrator 118 can be used as the notification body 89 for notifying that an abnormality has been detected, the number of parts constituting the beauty device is higher than that in the case where the display body and the notification body 89 are separately provided. Can be reduced and the cost can be reduced accordingly.

A beauty device that controls to increase the illuminance of the light emitting body 117 and / or to increase the vibration level of the vibrator 118 when a skin abnormality is detected.

When the skin abnormality is detected, if the control to increase the illuminance of the light emitting body 117 and / or the control to increase the vibration level of the vibrator 118 is performed, the user can intuitively recognize that the skin abnormality has been detected. it can.

A beauty device in which the inspection light emitted from the light emitting unit 138 is visible light having a peak in the purple wavelength region.

The inspection light emitted from the light emitting unit 138 is preferably an electromagnetic wave having a significantly different reflectance between a normal portion and an abnormal portion of the skin surface, that is, an electromagnetic wave that is easily absorbed by melanin that causes spots and the like. As such an electromagnetic wave, purple visible light can be mentioned. When visible light having a peak in the purple wavelength region is used as inspection light, skin abnormalities such as spots can be detected with higher accuracy than when visible light having a longer wavelength is used. Further, when the inspection light is visible light, the user can clearly recognize that the inspection light is emitted from the light emitting unit 138 without damaging the skin surface.

A beauty device in which the inspection light emitted from the light emitting unit 138 is ultraviolet rays in the UVA region or the UVB region.

When ultraviolet rays in the UVA region or UVB region are used as inspection light, skin abnormalities such as spots can be detected with high accuracy equal to or higher than that when visible light having a peak in the purple wavelength region is used.

A beauty device in which the light emitting unit 138 intermittently irradiates the inspection light.

By intermittently irradiating the inspection light composed of ultraviolet rays, the damage to the skin surface can be reduced as compared with the case of continuously irradiating the inspection light. In general, a very weak output of the inspection light is sufficient, so even if the inspection light consisting of ultraviolet rays is used, the skin surface will not be damaged, but the output of the inspection light can be increased due to structural factors. When necessary, it is effective to irradiate the test light intermittently.

The skin stimulus source 116 is configured to include a current source 175.
A beauty device in which a current for skin stimulation is supplied from a current source 175 to a skin stimulator 3 formed of a conductor.

When a skin stimulating current is supplied from the current source 175 to the skin stimulating body 3, the skin surface including the abnormal portion detected by the skin abnormality detecting unit 88 has an effect such as iontophoresis that allows the beauty liquid to permeate the skin surface. Beauty treatment can be performed.

A grip electrode 10 is provided on the grip portion 101 of the main body case 1, and the grip electrode 10 is provided.
When the grip electrode 10 comes into contact with the surface of the hand and the stimulating surface 3a of the skin stimulating body 3 comes into contact with the skin surface, a closed loop that can be detected by the control unit 115 is formed between the beauty device and the human body. And
The control unit 115 is a beauty device that controls the current source 175 so as to supply a current for skin stimulation to the skin stimulator 3 in a state of detecting the closed loop.

When the grip electrode 10 comes into contact with the surface of the hand and the stimulating surface 3a of the skin stimulating body 3 comes into contact with the skin surface, a closed loop that can be detected by the control unit 115 is formed between the beauty device and the human body. The skin stimulator 3 can function as a skin detection sensor that detects that the stimulating surface 3a is in contact with the skin surface. According to this, it is possible to easily and accurately detect that the stimulating surface 3a is in contact with the skin surface, as compared with the case where the skin detecting sensor is provided at a place different from the skin stimulating body 3. When a current for skin stimulation is supplied to the skin stimulator 3 in a state where the control unit 115 detects a closed loop, the skin stimulation is performed in a state where the closed loop is not formed, that is, in a state where the stimulation surface 3a is separated from the skin surface. The power supply of the beauty device can be suppressed by stopping the supply of electric current.

The skin abnormality detection unit 88 irradiates the inspection light toward the measurement unit on the skin surface facing the measurement unit 143, the light emitting unit 138, the light receiving unit 139 that receives the inspection light reflected by the measurement unit, and the first and first. Including the second optical path forming bodies 140 and 141,
The first optical path forming body 140 and the second optical path forming body 141 are joined via the joining surfaces 149 and 158.
A beauty instrument in which optical path grooves 150 and 159 that partition an optical path for inspection light are recessed along the joint surfaces 149 and 158 of the pair of optical path forming bodies 140 and 141.

When the optical path grooves 150 and 159 that partition the optical path of the inspection light are formed by denting along the joint surfaces 149 and 158 of the pair of optical path forming bodies 140 and 141, the optical path forming bodies 140 and 141 are joined to each other when assembling the beauty equipment. Only by itself, the optical path of the inspection light can be easily and accurately formed.

The first optical path forming body 140 faces the inner surface of the stimulating surface 3a of the skin stimulating body 3,
A beauty device in which the second optical path forming body 141 includes a light emitting unit 138 and a housing unit 147.148 of a light receiving unit 139.

When the second optical path forming body 141 includes the light emitting unit 138 and the accommodating units 147 and 148 of the light receiving unit 139, the skin abnormality detecting unit 88 is compared with the case where a holder such as the light emitting unit 138 is separately prepared. The number of parts that make up the above can be reduced, and the cost can be reduced accordingly.

The skin stimulating source 116 is configured to include a heater 164 that heats the skin stimulating body 3.
A beauty device in which a heater support portion 165 for supporting the heater 164 is formed on a surface of the first optical path forming body 140 facing the skin stimulating body 3.

When the skin stimulator 3 is heated by the heater 164, an effective cosmetological treatment that gives a thermal stimulus to the skin surface including the abnormal portion detected by the skin abnormality detecting unit 88 can be performed. When the heater support portion 165 that supports the heater 164 is formed on the first optical path forming body 140, the number of parts constituting the skin abnormality detection unit 88 is reduced as compared with the case where a holder for the heater 164 is separately prepared. , The cost can be reduced accordingly.

A beauty device in which the skin stimulating source 116 includes a current source 175 and a heater 164 for heating the skin stimulating body 3.

When the skin stimulus source 116 includes the current source 175 and the heater 164, it is possible to apply a thermal stimulus in addition to the current stimulus to the skin surface including the abnormal portion detected by the skin abnormality detection unit 88. it can. Therefore, it is possible to apply a plurality of stimuli to the skin surface to perform more effective cosmetological treatment.

The skin stimulating source 116 is configured to include a vibrator 118 that vibrates the skin stimulating body 3.
The vibrator 118 is supported by the vibrator holder 120 and is housed inside the skin stimulator 3.
A beauty device in which a skin abnormality detection unit 88 is sandwiched and fixed by a skin stimulator 3 and a vibrator holder 120.

When the skin stimulator 3 is vibrated by the vibrator 118, an effective beauty treatment that gives a vibration stimulus to the skin surface including the abnormal portion detected by the skin abnormality detecting unit 88 can be performed. When the skin abnormality detection unit 88 is sandwiched and fixed between the skin stimulator 3 and the vibrator holder 120, the posture of the skin abnormality detection unit 88 can be stabilized and the reliability of detection by the skin abnormality detection unit 88 can be improved.

The skin abnormality detection unit 88 includes a light emitting unit 138 that irradiates the test light toward the measurement unit on the skin surface facing the measurement unit 143, and a light receiving unit 139 that receives the inspection light reflected by the measurement unit.
A beauty device in which a substrate 137 that supports a light emitting unit 138 and a light receiving unit 139 is sandwiched and fixed by a skin stimulator 3 and a vibrator holder 120 together with a skin abnormality detecting unit 88.

When the substrate 137 supporting the light emitting unit 138 and the light receiving unit 139 is sandwiched and fixed by the skin stimulator 3 and the vibrator holder 120 together with the skin abnormality detecting unit 88, the substrate 137 is fixed by a means different from the fixing means of the skin abnormality detecting unit 88. Compared with the case of fixing, the procedure for assembling the beauty device can be simplified and the cost can be reduced accordingly.

The skin stimulator 3 including the stimulating surface 3a that abuts on the skin surface to give stimulus, the skin stimulating source 116 that gives physical beauty stimulus to the skin stimulator 3, and the abnormality of the skin surface are optically detected. Equipped with a skin abnormality detection unit 88,
The skin abnormality detection unit 88 reflects the lens 142 having the measurement unit 143 facing the measurement unit on the skin surface, the light emitting unit 138 that irradiates the test light toward the measurement unit on the skin surface, and the measurement unit. Including the light receiving unit 139 that receives the inspection light,
A cosmetological device in which the measuring unit 143 is arranged inside the outer line of the stimulating surface 3a in a front view facing the stimulating surface 3a.

A skin stimulator 3 including a stimulating surface 3a that abuts on the skin surface to give a stimulus, and a skin abnormality detecting unit 88 that optically detects an abnormality on the skin surface are provided, and a lens 142 of the skin abnormality detecting unit 88. If the measuring unit 143 provided on the skin surface is arranged inside the outer line of the stimulating surface 3a, the measuring unit 143 faces the skin surface at the same time when the stimulating surface 3a is brought into contact with the skin surface. It is possible to take care of the skin surface by the skin stimulator 3 while confirming the state of the skin abnormality detection unit 88. Therefore, the time required for detecting and caring for skin abnormalities can be significantly shortened as compared with the conventional beauty method in which the skin health sensor and the beauty device are used separately. Moreover, the position of the abnormal part of the skin surface can be precisely identified in real time, and the identified abnormal part can be accurately and intensively cared for. Further, if the measuring unit 143 is arranged in the outer line of the stimulation surface 3a, the skin abnormality can be detected and the care can be performed in the same posture, so that it is possible to save the trouble of changing the posture of the beauty device and changing the holding. Contrary to the present invention, when the skin stimulator and the skin abnormality detection unit are arranged at different positions of the beauty device, it takes time and effort to change the posture of the beauty device and change the holding when shifting from the detection of the skin abnormality to the care. Occurs. In the above configuration, the physical cosmetological stimulus is a general term for current stimulus, vibration stimulus, thermal stimulus (thermal stimulus and cold stimulus) and the like. It is desirable that the measuring portion 143 facing the measured portion on the skin surface is formed by the surface of the lens 142 exposed from the stimulating surface 3a. This is because the lens 142 functions as a waterproof means and a dustproof means for beauty equipment, a protective means such as a sensor constituting the skin abnormality detection unit 88, a means for adjusting the amount of transmitted light, and the like.

A beauty instrument in which an incoming light surface 185 orthogonal to the inspection light is formed on the inner surface of the lens 142 facing the light emitting unit 138.

When an incoming light surface 185 orthogonal to the inspection light is formed on the inner surface of the lens 142 facing the light emitting portion 138, the amount of reflection of the inspection light on the incoming light surface 185 can be reduced as much as possible, and the light of the lens 142 can be reduced. The transmittance can be increased. As a result, it is possible to constantly irradiate the measured portion of the skin surface with a sufficient amount of inspection light and supply a sufficient amount of reflected light to the light receiving portion 139. Therefore, the skin condition can always be accurately determined. can do. Further, if the light transmittance of the lens 142 is high, the light output of the light emitting unit 138 can be smaller when the same amount of inspection light is applied to the measured portion on the skin surface as compared with the case where the light transmittance is low. The cost and power consumption of the unit 138 can be suppressed.

Between the light emitting unit 138 and the light receiving unit 139 and the lens 142, optical path forming bodies 140 and 141 having a hollow light guide path 187 through which the inspection light passes are arranged.
The light guide path 187 is formed in a V shape by a first light guide path 188 from the light emitting portion 138 to the lens 142 and a second light guide path 189 from the lens 142 to the light receiving portion 139.
A recess 184 including an incoming light surface 185 is formed on the inner surface of the lens 142.
A beauty device in which the axis of the first light guide path 188 and the light entering surface 185 are orthogonal to each other.

By making the axis of the first light guide path 188 orthogonal to the light entry surface 185, the amount of reflection of the inspection light on the light entry surface 185 can be reduced as much as possible, and the light transmittance of the lens 142 can be increased. .. As a result, it is possible to constantly irradiate the measured portion of the skin surface with a sufficient amount of inspection light and supply a sufficient amount of reflected light to the light receiving portion 139. Therefore, the skin condition can always be accurately determined. can do. Further, if the light transmittance of the lens 142 is high, the light output of the light emitting unit 138 can be smaller when the same amount of inspection light is applied to the measured portion on the skin surface as compared with the case where the light transmittance is low. The cost and power consumption of the unit 138 can be suppressed.

Between the light emitting unit 138 and the light receiving unit 139 and the lens 142, optical path forming bodies 140 and 141 having a hollow light guide path 187 through which the inspection light passes are arranged.
The light guide path 187 is formed in a V shape by a first light guide path 188 from the light emitting portion 138 to the lens 142 and a second light guide path 189 from the lens 142 to the light receiving portion 139.
A recess 184 including an incoming light surface 185 is formed on the inner surface of the lens 142.
A beauty instrument in which the peripheral edge of the recess 184 is circumscribing the opening edges of the first light guide path 188 and the second light guide path 189 on the contact surface between the lens 142 and the optical path forming bodies 140 and 141.

At the contact surface between the lens 142 and the optical path forming bodies 140 and 141, the peripheral edge of the recess 184 on the inner surface of the lens 142 is externally attached to the opening edges of the first light guide path 188 and the second light guide path 189 of the optical path forming body 140 and 141. As a result, obstacles to the inspection light can be eliminated, the utilization efficiency of the inspection light can be improved, and the strength of the lens 142 can be further increased. Contrary to the present invention, when the periphery of the recess 184 in the lens 142 projects toward each of the light guide paths 188 and 189, a part of the inspection light may be blocked by this projecting portion. Further, when the recess 184 is enlarged so that the peripheral edge of the recess 184 is separated from the opening edges of both light guide paths 188 and 189, the strength of the lens 142 may be insufficient.

A beauty device in which a through hole is formed in the skin stimulator 3 and the measuring portion 143 (front end) of the lens 142 is projected from the stimulating surface 3a of the skin stimulator 3 through the through hole.

By slightly projecting the measuring unit 143 of the lens 142 from the stimulating surface 3a of the skin stimulating body 3, it is difficult for foreign substances such as excess beauty liquid and dust to collect between the skin surface and the measuring unit 143, and the skin surface The test light can be applied to the part to be measured as set and reflected from the part to be measured on the skin surface as set. Therefore, the abnormality detection unit 88 can make an accurate determination.

A cosmetological device having a protrusion dimension 142d for projecting the measurement unit 143 (front end) of the lens 142 from the stimulation surface 3a of the skin stimulator 3 to have a thickness of 3b or less of the skin stimulator 3.

Since the protruding dimension 142d of the measuring unit 143 of the lens 142 is set to the thickness 3b or less of the skin stimulator 3, it is possible to prevent the lens 142 from intensifying the skin irritation.

The protrusion dimension 142d for projecting the measurement unit 143 (front end) of the lens 142 from the stimulation surface 3a of the skin stimulator 3 is ½ or more of the dimension of the thickness 3b of the skin stimulator 3 and the thickness of the skin stimulator 3. Beauty equipment that is 3b or less.

When the protruding dimension 142d of the measuring unit 143 of the lens 142 is ½ or more of the dimension of the thickness 3b of the skin stimulating body 3 and the thickness of the skin stimulating body 3 is 3b or less, the irritation to the skin is suppressed. , It is possible to effectively prevent foreign substances such as excess cosmetic liquid and dust from accumulating on the surface of the measuring unit 143.

The lens 142 includes a protruding portion 142b and a measuring portion 143 provided at the front end of the protruding portion 142b and facing the measured portion on the skin surface.
A through hole is formed in the stimulating surface 3a of the skin stimulating body 3, and the hole surface 35a is provided.
The measuring portion 143 of the lens 142 protrudes from the stimulating surface 3a of the skin stimulating body 3 through the through hole.
The curvature of the intersection C2 between the peripheral surface 142c of the protrusion 142b and the measurement unit 143 is smaller than the curvature of the intersection C1 between the hole surface 35a of the skin stimulator 3 and the stimulation surface 3a of the skin stimulator 3. Beauty equipment set to.

Since the curvature of the intersecting portion C2 is set to be smaller than the curvature of the intersecting portion C1, the sliding movement of the skin surface in contact with the intersecting portion C2 is smoothly performed, and the skin contact is soft and smooth. Can be. Therefore, when the skin stimulator 3 is moved in the direction of the skin surface, the movement can be smoothly performed.

The lens 142 includes a protruding portion 142b and a measuring portion 143 provided at the front end of the protruding portion 142b and facing the measured portion on the skin surface.
The intersecting portion C2 between the peripheral surface 142c of the protruding portion 142b and the measuring portion 143 has an outer protrusion curved shape.
A cosmetological device in which the curved portion of the intersecting portion C2 is located within the range of the protruding dimension 142d from the stimulating surface 3a of the skin stimulating body 3 to the front end of the lens 142.

When the curved portion of the intersecting portion C2 is located within the range of the protruding dimension 142d from the stimulating surface 3a of the skin stimulating body 3 to the front end of the lens 142, the lens 42 and the skin while making the skin contact soft and smooth. It is possible to prevent the skin from dripping between the stimulator 3 and the stimulator 3.

In the above configuration, the mode in which "greater than or equal to" and "greater than" are replaced with each other and the mode in which "less than or equal to" and "below" are replaced with each other have substantially the same meaning.

2 Skin head 3 Skin stimulator 3a Stimulation surface 10 Grip electrode 88 Skin abnormality detection unit 89 Notification body 100 Head support 101 Grip 115 Control 116 Skin stimulus source 117 Light emitter (head display)
118 Vibrator 120 Vibrator holder 137 Board 138 Light emitting part (light emitting element)
139 Light receiving part (light receiving element)
140 First optical path forming body 141 Second optical path forming body 142 Lens 143 Measuring part 147 Accommodating part (accommodating hole)
148 Containment section (accommodation hole)
149 Joint surface 150 Optical path groove 158 Joint surface 159 Optical path groove 164 Heater 165 Heater support 175 Current source 177 Storage unit 184 Recessed 185 Ingress surface 187 Light guide path 188 First light guide path 189 Second light guide path

Claims (1)

A skin stimulant body (3) including a stimulating surface (3a) that abuts on the skin surface to give stimulation, a skin stimulating source (116) that gives physical beauty stimulation to the skin stimulating body (3), and a skin surface. It is equipped with a skin abnormality detection unit (88) that optically detects abnormalities in the skin.
The skin abnormality detection unit (88) has a lens (142) having a measurement unit (143) facing the measurement unit on the skin surface, and a light emitting unit (138) that irradiates the test light toward the measurement unit on the skin surface. And a light receiving part (139) that receives the inspection light reflected by the part to be measured.
In the front view facing the stimulation surface (3a), the measurement unit (143) is arranged inside the outer line of the stimulation surface (3a) .
A recess (184) including an incoming light surface (185) is formed on the inner surface of the lens (142) facing the light emitting portion (138).
The light entry surface (185) is formed so as to be orthogonal to the inspection light.
An optical path forming body (140/141) having a hollow light guide path (187) through which inspection light passes is arranged between the light emitting unit (138) and the light receiving unit (139) and the lens (142).
The light guide path (187) includes a first light guide path (188) from the light emitting unit (138) to the lens (142) and a second light guide path (189) from the lens (142) to the light receiving unit (139). It is formed in a shape and
At the contact surface between the lens (142) and the optical path forming body (140/141), the peripheral edge of the recess (184) is circumscribed with the opening edges of the first light guide path (188) and the second light guide path (189).
A beauty instrument characterized in that a lens hole (163) is formed at the opening edge of the optical path forming body (140/141), and the lens hole (163) and the lens (142) are fitted in a concavo-convex relationship. ..

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