CN104225797A - ATP light nasal cavity mucosa noninvasive therapeutic apparatus - Google Patents
ATP light nasal cavity mucosa noninvasive therapeutic apparatus Download PDFInfo
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- CN104225797A CN104225797A CN201410414932.0A CN201410414932A CN104225797A CN 104225797 A CN104225797 A CN 104225797A CN 201410414932 A CN201410414932 A CN 201410414932A CN 104225797 A CN104225797 A CN 104225797A
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Abstract
The invention provides an ATP light nasal cavity mucosa noninvasive therapeutic apparatus which comprises a host machine case, an ATP light emitter arranged in a case body, a microcomputer controller arranged in the host machine case and used for controlling the ATP light emitter, a hollow catheter, a probe connected and communicated with the hollow catheter and a hand-held connecting portion wrapping the connecting portion connected with the hollow catheter, of the probe. One end of the hollow catheter is communicated with the ATP light emitter and can extend from the inside of the host machine case to the outside of the host machine case.
Description
Technical field
The present invention relates to a kind of medical instruments field, particularly, relate to a kind of ATP light nasal membrane non-invasive therapy instrument.
Background technology
The mankind have a lot of disease to occur in the coating mucosal tissue of human viscera organ's cavity, modal is inflammation disease, as: the inflammation of mucosa, the inflammation of the inflammation of reproductive tract inner membrance, in addition urinary system inner membrance and otorhinolaryngology cavity lining mucosa inflammation etc. in digestive tract.The inflammation of mucosal tissue mainly with acute onset, due to treatment not in time or improper and transfer to chronic, then delay obstinate through for a long time, final a lot of disease development is that malignant tumor even loses one's life.Mucosa class inflammation is once delay obstinate becomes and may become persistent ailment, this is because do not have vascularity in mucosal tissue layer, Drug therapy is difficult to prove effective, and inflammation, once can not control its development in time, just may transform until bring out canceration to bad direction.Clinical experience is thought to the most expert of the treatment of mucosa, and local is disposed and is better than Formulations for systemic administration treatment.But be then difficult to accomplish that local is disposed to the lining mucosa of deep internal organs organ cavity in body, the concentration of medicine is also a difficult problem to the stimulation of mucosa in addition, Drug therapy failure even causes increasing the weight of the state of an illness being also FAQs, therefore clinical needs better method reply disease.
For this reason, scientific research personnel have studied some Medical luminous devices and treats or alleviate the pathological changes of these mucosas and skin organ, in these Medical luminous devices, is all utilize the temperature action of various light and infrared penetrance, disposes all kinds of sick cells in tissue.Such as, being generally 280 DEG C of-350 DEG C of high-temperature regions, solidify cell protein, then broken cell makes it to produce new cell again, processes pathological tissues with this.
Utilize in the luminous organ of various light at existing these, in order to produce high temperature and convenient focusing, the probe of luminous organ is not only thin but also long, (length of general probe is more than 15cm, be 19cm-20cm more), like this, time luminous, light loss is large, therapeutic effect is very undesirable, is also unfavorable for the control of doctor to probe simultaneously.
Such as, and in the prior art, being all improve the temperature of the light that luminous organ sends, is all utilize high temperature to carry out baking evaporation to the disposal of burn, very large to wound histiocyte secondary damage like this, makes pathological changes reverse slowly, convalescent period prolongation.And, owing to being process sick cell (high temperature illumination is easy to kill cell) by the temperature of light, therefore the mode of light output is the principle being similar to magnifier, light is focused on by probe, thus improve the temperature of the light sent of popping one's head in, but thus destroy the impaired cell (sick cell) that can also recover.
Therefore, need to propose a kind of lead light loss little, export light quantity large, can opereating specification large, do not have secondary damage, therapeutic effect is good, provide energy in time for cell protein and be convenient to the medical light therapy apparatus that controls.
Summary of the invention
For overcoming existing defect, reduce or avoid the destruction to protein, reduce the loss of the leaded light amount of luminous organ, improve light output amount, increase and can opereating specification and convenient operation and the local that can solve internal organs cavity lining mucosa inflammation dispose, accomplish that not damaged has no side effect fast treating, the present invention proposes a kind of ATP light nasal membrane non-invasive therapy instrument, comprising: mainframe box; ATP light luminous organ, described ATP light luminous organ is arranged in described casing; Microcomputer controller, described microcomputer controller is arranged on mainframe box inside, for controlling described ATP light luminous organ; Hollow conduit, one end of described hollow conduit is connected with described ATP light luminous organ, and can extend to described mainframe box from described mainframe box inside outside; Probe, the merging that connects of described probe and described hollow conduit is connected; With hand-held connecting portion, described hand-held connecting portion wraps up the junction surface that described probe engages with described hollow conduit.
Preferably, described hollow conduit and the described probe light irradiation tunnel that comprises the other end at the through junction surface away from described probe and described hollow conduit to described probe from one end be connected with described ATP light luminous organ of described hollow conduit and the shooting passage that extend side by side with described smooth irradiation tunnel.
Preferably, described smooth irradiation tunnel is connected with described ATP light luminous organ, for the optical transport that will send from described ATP light luminous organ to probe.
Preferably, described ATP light luminous organ comprises: luminous organ housing; Fixed cover, described fixed cover is contained in described luminous organ housing; Luminescence component, described luminescence component is arranged on one end of described fixed cover; Lamp holder, described luminescence component is plugged in described lamp holder, and described luminescence component is fixed between described lamp holder and described fixed cover, and by described lamp holder for described luminescence component provides energy; Wherein, described luminous organ housing is hollow, for described fixed cover, described luminescence component and described lamp holder being sequentially contained in described luminous organ housing.
Preferably, the bulb that described luminescence component comprises lamp bowl and inserts in described lamp bowl, the inside of described lamp bowl is coated with reflective medium.Preferably, the inside of described lamp bowl is gold-plated.
Preferably, the distance between described fixed cover and described luminescence component is fixed.
Preferably, the length of described probe is 10.0cm.
Preferably, the diameter of described probe is 0.6cm.
Preferably, the wavelength of light that sends of described probe is in the scope of 1.2 μm-4.9 μm.
Preferably, the light out-focus that described probe sends, and the wavelength of the light that described probe sends is in infrared wavelength intermediate zone and with light and shade district.
The ATP light nasal membrane non-invasive therapy instrument of the application of the invention; can instantaneous time or carry out ATP illumination at short notice and penetrate completed treatment; and directly repair on the basis of original injured mucosa; thus minimizing secondary damage; protection mucosa protein; diminish inflammation fast, cleaning extracellular environment, is more conducive to cytothesis simultaneously.
Accompanying drawing explanation
Fig. 1 is the axonometric chart of the ATP light nasal membrane non-invasive therapy instrument according to the embodiment of the present invention.
Fig. 2 is the sectional view extending the hollow conduit of mainframe box outside and the schematic diagram of probe and probe in Fig. 1.
Fig. 3 is the structural representation of the ATP light luminous organ according to the embodiment of the present invention.
Detailed description of the invention
Below in conjunction with the drawings and specific embodiments, ATP light nasal membrane non-invasive therapy instrument provided by the invention is described in detail.
Here, the concept of ATP light stems from Davydov theory.Particularly, be exactly according to ATP molecular distribution and the characteristic of hydrolysis and the feature of protein structure, the basis of Davydov theory proposes a kind of theory of new bio-energy transport, and in this being applied a theory to practice, utilize light and material to synthesize ATP bio-energy and bio-energy transport realizes treating the hurtless measure not damaged of mankind's cavity lining mucosa and skin organ wound inflammation and ulcer.
Particularly, be exactly that special optical wavelength is introduced in people's nasal cavity organ cavity, mainly solve people's nasal cavity inwall mucosa chronic inflammatory disease, carry out inflammation mucosa local and irradiate instantaneously and reach healing object.Research according to scientist: the light of this special wavelength occupy in spectral series, it can show equal with the energy that intracellular adenosine triphosphate discharges by quantity research, with this wavelength light direct irradiation inflammatory stimulus cell, can be utilized by intracellular protein transient absorption, and to intracellular protein activation point (amido link) and adenosine triphosphate activate a little act on identical, therefore by its called after ATP light.
Fig. 1 shows the axonometric chart of the ATP light nasal membrane non-invasive therapy instrument according to the embodiment of the present invention.As shown in Figure 1, ATP light nasal membrane non-invasive therapy instrument 100 comprises: mainframe box 10, be arranged on the ATP light luminous organ (not shown) of mainframe box 10 inside, microcomputer controller (not shown), microcomputer controller is arranged on mainframe box inside, for controlling described ATP light luminous organ, hollow conduit 20, one end of hollow conduit 20 is connected with ATP light luminous organ, and extend to mainframe box 10 from mainframe box 10 inside outside, probe 40, probe 40 and the merging that connects of described hollow conduit 20 are connected, with hand-held connecting portion 30, hand-held connecting portion 30 wraps up the junction surface engaged between probe 40 with hollow conduit 20, this hand-held connecting portion not only handled easily person grasps, the junction surface between probe 40 and hollow conduit 20 can also be protected.
This nasal membrane non-invasive therapy instrument can also comprise and stretches into the display of situation for the guidance panel of the operational order of input operation person and display probe, convenient operation person operates external control part (such as, foot-operated panel etc.), and be arranged on the roller being convenient to mainframe box movement bottom mainframe box.
Fig. 2 is the sectional view extending the hollow conduit of mainframe box outside and the schematic diagram of probe and hollow conduit and probe in Fig. 1.Specifically as shown in Figure 2, a part for hollow conduit 20 is made up of light-guide material, and at one end has multiple brasnch conduct.The brasnch conduct being wherein connected to ATP light luminous organ has the light irradiation tunnel 21 of the other end at the through junction surface engaged with hollow conduit 20 away from probe 40 to probe 40 from one end be connected with ATP light luminous organ of hollow conduit 20, for the ATP optical transport that will produce from ATP light luminous organ to the end of probe 40, finally send the ATP light be used for the treatment of from probe 40.Another brasnch conduct of the hollow conduit 20 be connected with microcomputer controller also has the shooting passage 22 extend side by side with light irradiation tunnel 21.Image information when shooting passage 22 is sent in cavity by the camera head Real-time Collection probe set within it, and by these image information display over the display, thus convenient operation person operates.
Here, the length of probe 40 is 10.0cm, and diameter is 0.6cm.The rigid endoscope that probe 40 is normally made up of quartz, medical aluminum or aluminum alloy.
Fig. 3 shows the structural representation of the ATP light luminous organ according to the embodiment of the present invention.As shown in Figure 3, the ATP light luminous organ in mainframe box comprises: luminous organ housing 9; Fixed cover 6, fixed cover 6 is contained in luminous organ housing 9; Luminescence component 7, luminescence component 7 is arranged on one end of fixed cover 6; Lamp holder 8, luminescence component 7 is plugged in lamp holder 8, and luminescence component 7 is fixed between lamp holder 8 and fixed cover 6, and by lamp holder 8 for luminescence component 7 provides energy; Wherein, described luminous organ housing is hollow, for described fixed cover, described luminescence component and described lamp holder being sequentially contained in described luminous organ housing.This luminous organ can also offer louvre or arrange radiating part 5 in end in outside, for heat radiation.
Luminescence component 7 is arranged on one end of fixed cover 6, and the bulb comprising lamp bowl 7 ' and insert in lamp bowl.Luminescence component 7 is integrally provided between fixed cover 6 and lamp holder 8, and its one end plugging bulb is inserted in lamp holder 8, thus provides energy by lamp holder 8 for luminescence component 7, makes bulb send infrared light.The infrared light wavelength that bulb sends is in the scope of 1.2 μm-4.9 μm, and the ATP light that the infrared light wavelength within the scope of these produces can provide activation to histiocyte, thus produces protein energy, makes the histiocyte of pathological changes obtain energy supplement.
The inside of lamp bowl 7 ' is coated with reflective medium.Here, the inside of lamp bowl 7 ' is gold-plated, and when gold-plated, the infrared light sent by the direction reflected to probe 40, thus makes light quantity increase, and then improves light efficiency, further improves medical effect.Also can at inner plating rhodium, but its effect is not as gold-plated ideal.
Lamp holder 8 combines with fixed cover 6 thus is fixed between which by luminescence component 7.
Luminous organ housing 9 is hollow, for fixed cover 6, luminescence component 7 and lamp holder 8 being contained in luminous organ housing 9.Its outside or inside can be provided with heat-barrier material, for when luminous organ works, heat insulation better for carrying out luminous organ main body.
Radiator 5 can be arranged on the tail end of luminous organ housing 9, for further for luminous organ provides good heat radiation.Generally, fan can be used as radiator, but the present invention is not limited to this, the cooling mechanism of other type any can be set as required.
In addition, the distance between fixed cover 6 and luminescence component 7 cannot regulate, and like this, reduce the error of the infrared light wavelength sent as much as possible, make luminous organ working stability of the present invention, therapeutic effect is very significantly improved.
Particularly, in ATP light nasal membrane non-invasive therapy instrument of the present invention, by specific probe length and diameter, reflective isolation technics is adopted to isolate the light with specific wavelength, these light with specific wavelength (1.2 μm-4.9 μm) are between to open and between concentrating (not optically focused), the length of probe and the size of diameter make light output amount improve (light quantity increase), and make the wavelength of the light sent from probe 40 be in infrared intermediate zone (visible ray fades, infrared light gradually grow) by ATP light luminous organ and with light and shade district.This with light and shade district and the not output light of optically focused can not increase the temperature (light be in room temperature under instead of high temperature) of light; can directly carry out repairing and not needing high temperature to kill injured albuminous cell on original basis like this; thus activation paraprotein matter is regrowed; protected protein matter; the growing environment of cleaning cell; diminish inflammation fast; be convenient to repair; and make to process the better effects if of cell protein and very little to the infringement of protein, even almost do not damage.When probe is after external opening is sent in body and arrived lining mucosa focus, carry out after ATP illumination penetrates some seconds (usually deciding irradiation time length according to the state of an illness time), the disposal to focus can being completed.
When operating this ATP light nasal mucosa non-invasive therapy instrument, first power-on, open ATP light source and then by conduit and probe, ATP light is inputted nasal cavity, after probe arrives focal area irradiation some seconds (according to the state of an illness), terminate treat and take out light output utensil (conduit, probe), completed treatment program also closes ATP light source, last cleaning and sterilizing light output utensil (or replacing).
Generally speaking, the hot spot that the output temperature of the effect of non-invasive therapy instrument of the present invention and the ATP light of this non-invasive therapy instrument and APT light produce has close relationship.The temperature too high meeting scalded tissue of light, damaging cells.Hot spot is excessive invalid, and too small focusing produces high temperature.The side effect such as the infrared light of Clinical practice was all adopt heat effect to be treatment means in the past, and its incrustation produced wound, decrustation, cicatrix, focus are remaining, the reaction of whole body sign, the course for the treatment of are long are difficult problems, almost unavoidably.Non-invasive therapy instrument of the present invention does not then have these side effect.
Finally it should be noted that, above embodiment is only in order to describe technical scheme of the present invention instead of to limit this technical method, the present invention can extend in application other amendment, change, application and embodiment, and therefore think that all such amendments, change, application, embodiment are all in spirit of the present invention and teachings.
Claims (10)
1. an ATP light nasal membrane non-invasive therapy instrument, comprising:
Mainframe box;
ATP light luminous organ, described ATP light luminous organ is arranged in described casing;
Microcomputer controller, described microcomputer controller is arranged on mainframe box inside, for controlling described ATP light luminous organ;
Hollow conduit, one end of described hollow conduit is connected with described ATP light luminous organ, and can extend to described mainframe box from described mainframe box inside outside;
Probe, the merging that connects of described probe and described hollow conduit is connected; With
Hand-held connecting portion, described hand-held connecting portion wraps up the junction surface that described probe engages with described hollow conduit.
2. ATP light nasal membrane non-invasive therapy instrument according to claim 1, wherein, described hollow conduit and the described probe light irradiation tunnel that comprises the other end at the through junction surface away from described probe and described hollow conduit to described probe from one end be connected with described ATP light luminous organ of described hollow conduit and the shooting passage that extend side by side with described smooth irradiation tunnel.
3. ATP light nasal membrane non-invasive therapy instrument according to claim 2, wherein, described smooth irradiation tunnel is connected with described ATP light luminous organ, for the optical transport that will send from described ATP light luminous organ to probe.
4. ATP light nasal membrane non-invasive therapy instrument according to claim 1, wherein, described ATP light luminous organ comprises:
Luminous organ housing;
Fixed cover, described fixed cover is contained in described luminous organ housing;
Luminescence component, described luminescence component is arranged on one end of described fixed cover;
Lamp holder, described luminescence component is plugged in described lamp holder, and described luminescence component is fixed between described lamp holder and described fixed cover, and by described lamp holder for described luminescence component provides energy;
Wherein, described luminous organ housing is hollow, for described fixed cover, described luminescence component and described lamp holder being sequentially contained in described luminous organ housing.
5. ATP light nasal membrane non-invasive therapy instrument according to claim 4, wherein, the bulb that described luminescence component comprises lamp bowl and inserts in described lamp bowl, the inside of described lamp bowl is coated with reflective medium, and preferably, the inside of described lamp bowl is gold-plated.
6. ATP light nasal membrane non-invasive therapy instrument according to claim 4, wherein, the distance between described fixed cover and described luminescence component is fixed.
7. ATP light nasal membrane non-invasive therapy instrument according to claim 1, wherein, the length of described probe is 10.0cm.
8. ATP light nasal membrane non-invasive therapy instrument according to claim 1, wherein, the diameter of described probe is 0.6cm.
9. ATP light nasal membrane non-invasive therapy instrument according to claim 1, wherein, the wavelength of the light that described probe sends is in the scope of 1.2 μm-4.9 μm.
10. ATP light nasal membrane non-invasive therapy instrument according to claim 1, wherein, the light out-focus that described probe sends, and the wavelength of the light that described probe sends is in infrared wavelength intermediate zone and with light and shade district.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410414932.0A CN104225797A (en) | 2014-08-21 | 2014-08-21 | ATP light nasal cavity mucosa noninvasive therapeutic apparatus |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410414932.0A CN104225797A (en) | 2014-08-21 | 2014-08-21 | ATP light nasal cavity mucosa noninvasive therapeutic apparatus |
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| CN104225797A true CN104225797A (en) | 2014-12-24 |
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| Application Number | Title | Priority Date | Filing Date |
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| CN201410414932.0A Pending CN104225797A (en) | 2014-08-21 | 2014-08-21 | ATP light nasal cavity mucosa noninvasive therapeutic apparatus |
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Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02174864A (en) * | 1989-10-20 | 1990-07-06 | Fuji Electric Co Ltd | Laser irradiation apparatus |
| JP2002336267A (en) * | 2001-05-18 | 2002-11-26 | Morita Mfg Co Ltd | Laser beam radiating device |
| CN102100524A (en) * | 2010-12-10 | 2011-06-22 | 广州宝胆医疗器械科技有限公司 | Electric bronchoscope system with thermal-infrared scanning function |
| CN201871134U (en) * | 2010-12-02 | 2011-06-22 | 哈尔滨亿尔诺医学科技有限公司 | Infrared nonthermal bioeffect gynecological therapeutic instrument |
-
2014
- 2014-08-21 CN CN201410414932.0A patent/CN104225797A/en active Pending
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02174864A (en) * | 1989-10-20 | 1990-07-06 | Fuji Electric Co Ltd | Laser irradiation apparatus |
| JP2002336267A (en) * | 2001-05-18 | 2002-11-26 | Morita Mfg Co Ltd | Laser beam radiating device |
| CN201871134U (en) * | 2010-12-02 | 2011-06-22 | 哈尔滨亿尔诺医学科技有限公司 | Infrared nonthermal bioeffect gynecological therapeutic instrument |
| CN102100524A (en) * | 2010-12-10 | 2011-06-22 | 广州宝胆医疗器械科技有限公司 | Electric bronchoscope system with thermal-infrared scanning function |
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Application publication date: 20141224 |