Inhalation Device
20230173200 · 2023-06-08
Assignee
Inventors
Cpc classification
A61M15/02
HUMAN NECESSITIES
A61M11/02
HUMAN NECESSITIES
International classification
Abstract
This invention relates to a device (1) for producing an aerosol for inhalation by a person, comprising a fluid reservoir (2) for a fluid, a nebulizing element (3) provided in order to convert the fluid from the fluid reservoir (2) into an aerosol, and a dispensing tube (4) with a discharge opening (5) along which the aerosol produced is dispensable so that it can be inhaled by a person, wherein the device (1) further comprises a laser (6) provided in order to generate a light beam suitable for irradiating the aerosol during its trajectory through the dispensing tube (4).
Claims
1. Device (1) for producing an aerosol for inhalation by a person, comprising a fluid reservoir (2) for a fluid, a nebulizing element (3) provided in order to convert the fluid from the fluid reservoir (2) into an aerosol, and a dispensing tube (4) with a discharge opening (5) along which the aerosol produced is dispensable so that it can be inhaled by a person, characterized in that the device (1) further comprises a laser (6) provided in order to generate a light beam suitable for irradiating the aerosol during its trajectory through the dispensing tube (4).
2. Device (1) according to claim 1, characterized in that the laser (6) is provided in order to generate a light beam with a wavelength of between 500 nm and 1000 nm.
3. Device (1) according to claim 1, characterized in that the laser (6) is provided in order to generate a light beam with a wavelength of between 550 nm and 850 nm.
4. Device (1) according to claim 1, characterized in that the laser (6) is provided in order to generate a light beam with a wavelength of between 400 nm and 500 nm.
5. Device (1) according to claim 1, characterized in that the laser (6) is a diode laser.
6. Device (1) according to claim 1, characterized in that the dispensing tube (4) has a length of between 100 mm and 200 mm.
7. Device (1) according to claim 1, characterized in that the dispensing tube (4) comprises a tapered part (8), wherein the discharge opening (5) is provided in the tapered part (8).
8. Device (1) according to claim 1, characterized in that the dispensing tube (4) comprises a supply channel (9) for aerosol and an uptake channel (10) suitable for holding the laser (6).
9. Device (1) according to claim 1, characterized in that the device (1) comprises a compressed air source (11), a compressed air line (12) for transporting compressed air from the compressed air source (10) to the fluid reservoir (2), and a suction line (16) for aspirating ambient air.
10. Device (1) according to claim 9, characterized in that the device (1) comprises a housing (15) containing a filter chamber (17) for filtering the aspirated ambient air.
11. Method for obtaining an aerosol suitable for the treatment of acute and chronic lung disorders, characterized in that the method comprises the following steps: conversion of a fluid into an aerosol; and irradiation of the aerosol formed with laser light having a wavelength of between 500 nm and 1000 nm.
12. Method according to claim 11, characterized in that the above-mentioned fluid is physiological saline.
13. Method according to claim 11, characterized in that the aerosol formed is irradiated with laser light having a wavelength of between 550 nm and 850 nm.
Description
[0023] In this detailed description, the attached drawings are referred to by means of reference numbers, wherein:
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[0034] This invention relates to a device (1) for producing an aerosol for inhalation by a person, wherein so-called aerosol laser therapy is used. In this therapy, one is to inhale nebulized physiological saline irradiated with laser light, preferably red laser light. We know from quantum physics that laser light from the red and infrared regions (and thus also the energy associated therewith) is absorbed by water vapour. Water vapour is used as a vehicle for inhaling laser energy, not as an inhalation medication. The inhaled ‘enriched’ water vapor condenses on the mucosa of the respiratory tract, and the absorbed laser energy thus also comes into contact with the mucous membrane.
[0035] From this point on, the effect is analogous to the effect after direct irradiation with an infrared laser: at the molecular level, atoms and molecules are brought into an excited state by energetic stimulation. When they return to a stable state, the stored energy is released again, bringing an adjacent atom or molecule into an excited state. This gives rise to a chain reaction wherein the energy released can be used in each case to reduce inflammation and repair tissue. In addition to the supply of directly usable energy, capillary dilation is produced that promotes both the immune reaction and tissue repair.
[0036] The device (1) in accordance with the invention is shown in
[0037] The device (1) is further equipped with a dispensing tube (4) that is connected to the nebulizing unit (13). The dispensing tube (4) has a discharge opening (5) along which the aerosol produced leaves the device (1) so that it can be inhaled by a person. In the dispensing tube (4), the aerosol is irradiated with laser light from a laser (6). The laser is a diode laser and comprises in a preferred embodiment two laser diodes (7), each having a capacity of 5 mW, and in practice, a laser beam is generated with a wavelength of 650 nm. Of course, the wavelength of the laser beam may vary. Preference is given to a wavelength of between 500 nm and 1000 nm.
[0038] The fluid reservoir (2) is produced from high-quality PVC and has a capacity of 10 (± 0.5) ml. The nebulizing element (3) nebulizes the fluid provided in the fluid reservoir (2) in the known manner by means of compressed air. The nebulized fluid (aerosol) leaves the fluid reservoir via an outlet (20). In order to be able to nebulize the fluid, as shown in
[0039] The dispensing tube (4) is placed on the outlet (20) of the fluid reservoir (2) so that the aerosol formed flows directly into the dispensing tube (4). The dispensing tube has a length of between 100 mm and 200 mm and should converge slightly in the direction of the discharge opening. In practice, the dispensing tube (4) has a diameter of approximately 45 mm at its beginning and a diameter of approximately 38 mm at its end (at the level of the discharge opening). The dispensing tube (4) may be configured as a single piece or may be composed of multiple parts (21; 22). In the device shown, the dispensing tube (4) is composed of two parts, particularly a first part (21) along which the aerosol formed comes in and a second part (22) wherein the discharge opening (5) is provided. In order to connect the first part (21) to the second part (22), the end of the first part (21), as shown in
[0040] The aerosol comes into the dispensing tube (4) via the first part (21). For this purpose, the first part (21) comprises a supply channel (9) (cf.
[0041] The second part (22) of the dispensing tube (4) has a longer configuration, with the length of the second part (22) being approximately 14 cm to 17 cm. It is primarily in the second part (22) of the dispensing tube (4) that the aerosol is irradiated with laser light. The second part (22) also comprises a tapered part (8). In the tapered part (8), the discharge opening (5) of the dispensing tube (4) is provided. By means of a tapered configuration of the end, e.g. the last 3 cm, of the second part (22), it becomes possible to create a turbulent flow of the aerosol inside the tube, particularly at the level of the transition to the tapered part (8), which allows the aerosol mist to be held in place for a longer period and thus to be irradiated for a longer period. After the aerosol irradiated with laser light leaves the dispensing tube (4), it can be inhaled by a user.
[0042] Moreover, the device in accordance with the invention, particularly the housing (15), further comprises a control unit (27) for controlling the compressed air source (11) (compressor), a touch control panel (23), a power supply for the laser module, a plug connector (24), a USB port (28) and an on/off switch (25). The device (1) may also be equipped with an RFID module (26) that can be used to prevent unauthorised parties from using the device. Instead of an RFID module (26), one may also use a key lock.
[0043] The device (1) in accordance with the invention offers a broad range of possibilities for application, particularly in the treatment of: [0044] 1. Bronchial asthma; [0045] 2. Post-infectious cough; [0046] 3. Small airways disease; [0047] 4. Allergic asthma; [0048] 5. COPD due to smoking; [0049] 6. Bronchiectasis; [0050] 7. Emphysema; [0051] 8. Viral tracheobronchitis; [0052] 9. Bacterial bronchitis; [0053] 10. Eradication of multiresistant bacteria from sputum; [0054] 11. Pulmonary sarcoidosis; [0055] 12. Mucoviscidosis; and [0056] 13. Repair of damaged lung tissue following pneumonia (e.g. COVID-19)
[0057] This list is not exhaustive. It is illustrative of the diversity of the spectrum of lung disorders in which the technology and device are applicable. Theoretically, one may expect a positive effect in any lung disease accompanied by inflammation and/or sputum production.
1. BRONCHIAL ASTHMA
[0058] The effect on bronchial asthma can be understood as that of detaching sputum from the airway walls, with the inflammation then being gradually suppressed until the amount of sputum produced is finally reduced to a normal level. Whether or not in combination with a long-acting β2 agonist, while discontinuing inhaled corticosteroids, this initially leads to a reduction in shortness of breath and coughing fits. The reduction in inflammation leads to less sputum production, which in turn results in less reflux and therefore also fewer superinfections. Spirometry shows an increase in FVC, FEV1 and Tiffeneau values.
[0059] In a patient dependent on inhaled corticosteroids in whom administration of inhaled corticosteroids is medically contraindicated, for example, following discontinuation of inhaled corticosteroids, the patient is free of attacks with 60 treatments per year, and has continued to be so for 26 months at present.
2. POST-INFECTIOUS COUGH
[0060] Similarly to the effect on bronchial asthma, sputum is detached from the airway walls, while the inflammation is gradually suppressed until the amount of sputum produced is finally reduced to a normal level.
3. SMALL AIRWAYS DISEASE
[0061] Similarly to the effect on bronchial asthma, sputum is detached from the airway walls, while the inflammation is gradually suppressed until the amount of sputum produced is finally reduced to a normal level.
4. ALLERGIC ASTHMA
[0062] Aerosol laser therapy has also been shown to be useful in treatment of allergic asthma. On spirometry, this therapy shows better results than a combination of inhaled corticosteroids and a β2 agonist.
[0063] Because of the anti-inflammatory effect, the inflammatory reaction inherent in asthma is minimized, and wheezing, coughing and dyspnoea are suppressed.
5. COPD DUE TO SMOKING
[0064] COPD patients suffer from hyperproduction of sputum. Aerosol laser therapy has a ‘washing’ effect on the sputum present, after which sputum production decreases.
[0065] Spirometry shows an increase in FVC, FEV1 and Tiffeneau values.
[0066] This also limits the number of exacerbations.
6. BRONCHIECTASIS
[0067] Patients with bronchiectasis (known to be irreversible), in which parts of the lungs are constantly dilated and irritated, are susceptible to recurrent infections. They benefit from this treatment primarily due to a bronchial lavage effect. The reduced amount of residual sputum then leads to fewer exacerbations and thus less need for antibiotics. Not only the inflammation-reducing effect is important; in addition, the effect of repairing and healing tissue also appears to lead to noteworthy results.
[0068] For example, in a patient known to have already suffered from bronchiectasis for more than 12 years, after 30 30-minute sessions of aerosol laser therapy, the radiologist reported that on high-resolution thoracic CT, bronchiectasis was no longer present, compared to high-resolution CT results from 2.5 years earlier, while the professor of pulmonology described it as limited.
[0069] In a patient who had shown clear bronchiectasis on a high-resolution CT scan conducted almost 12 years earlier, after 30 30-minute sessions of aerosol laser therapy, bronchiectasis was described in a report on recently-conducted HRCT as minimal.
[0070] It appears that in this case, one cannot rule out that the tissue-repairing effect of the laser energy applied to the mucosa may have played a role.
7. PULMONARY EMPHYSEMA
[0071] Long-term treatment due to pronounced persistent densification in a pulmonary lobe following pneumonia caused supposedly irreversible emphysematous bullae to disappear. After 80 1-hour treatments, the emphysema was reported on HRCT to be only minimal.
8. VIRAL TRACHEOBRONCHITIS
[0072] A test was conducted in order to determine whether aerosol laser therapy should be continued or interrupted if a viral respiratory tract infection occurs during treatment. A case of viral bronchitis was completely supressed after 2 days (without any type of medication).
9 BACTERIAL BRONCHITIS
[0073] A test was also conducted in order to determine whether aerosol laser therapy should be continued or interrupted if a bacterial respiratory tract infection occurs during treatment. A case of bacterial bronchitis was completely cured after 8 days (without any type of medication).
10. ERADICATION OF MULTIRESISTANT/NOSOCOMIAL BACTERIAL FROM SPUTUM
[0074] Patients experience great benefit from this treatment due to the effect of bronchial lavage. This allows the patient to gradually cough up infected material that is a breeding ground for bacteria, after which the inflammation is further suppressed. In combination with a long-acting β2 agonist, without any inhaled corticosteroids or antibiotics, this leads to a reduction in shortness of breath. Coughing fits decrease in intensity, duration and frequency. Lumps of sputum become ever smaller and less viscous until the production of sputum is finally reduced to a normal level. O.sub.2 saturation again increases. The tissue-repairing effect of the laser energy deposited on the mucosa allows the inflammatory processes to be reduced to a minimum.
11. PULMONARY SARCOIDOSIS
[0075] A patient with pulmonary sarcoidosis, who despite the use of a β2 agonist and an inhaled corticosteroid continued to complain of dyspnoea and showed O.sub.2 saturation of 90-93%, progressed to a status in which the dyspnoea was barely present and O.sub.2 saturation was about 97-98% without administration of any β2 agonists or inhaled corticosteroids.
12. MUCOVISCIDOSIS
[0076] Although the efficacy of this treatment in mucoviscidosis patients has not yet been proven, it can safely be expected from prior experience that the effects will be the same in mucoviscidosis patients. Congenital production of viscous sputum will of course remain unchanged, but it is possible that the sputum produced will be less viscous. However, the question of whether viscous sputum is the result of mucoviscidosis or is due to another cause cannot affect the patient’s capacity to cough up and evacuate this sputum. There is no reason to assume that capillary dilation will not occur after aerosol laser treatment, and this will therefore not only have a healing effect on the mucosa, but will also possibly make the mucus more fluid and thus less viscous.
13. REPAIR OF DAMAGED LUNG TISSUE FOLLOWING PNEUMONIA (E.G. COVID-19)
[0077] In this specific case, efficacy in the acute phase of COVID-19 pneumonia has now also been established. The effect can without doubt be described as quite clear and lead after only the first 30-minute treatment to a noticeable difference, which was experienced both by the patient (easier breathing, less feeling of constriction, significant improvement in coughing, spontaneous reports of good night-time sleep) (subjectively) and by the treating physician on auscultation (objectively).
[0078] It is also known that severe residual scarring after pneumonia, which was predicted by the pneumonologist to be permanent, was completely resorbed following intensive treatment, resulting in normalisation of the lung parenchyma on HRCT. In this specific case, spirometry showed a volume increase in forced vital capacity of 33 times the level considered the current pharmaceutical gold standard. There is no reason why the results in the case of lung damage following COVID-19 pneumonia should be any different.
CONCLUSION
[0079] Despite the already broad range of lung disorders in which the aerosol laser technique is applicable, one may expect, as mentioned above, a positive effect in any lung disease accompanied by inflammation and/or sputum production.
[0080] As it is known that aerosol laser therapy without the use of antibiotics is capable of healing bacterial infections and that the number of exacerbations is drastically reduced in chronic use, it is highly likely that the number of hospitalisations due to exacerbations will also be decreased.
[0081] Not only in the case of the chronic pulmonary patient (greater well-being, fewer exacerbations, less medication, fewer complications), but also from a health economic standpoint (fewer antibiotics, fewer hospitalisation days, the possibility of combatting chronic infections with multiresistant nosocomial microbes, less intensive care, reduction in the number or postponement of lung transplants, etc.), aerosol laser therapy, which is also inexpensive, appears to be capable of having a significant impact on the health care budget.
[0082] Treatment by ALT (red light, 650 nm) has not been capable of preventing Candida species (not C. albicans) from being grown from sputum cultures. Scientific studies have established that irradiation of the skin with blue light (400-500 nm) results in both antimicrobial and fungicidal effects.
[0083] For example, irradiation with blue light has a fungicidal effect on Candida and results in an antimicrobial effect on species such as Pseudomonas aeruginosa, which is a significant finding in view of the increasing resistance to current antibiotics.
[0084] In an initial qualitative test conducted in a dark room of a laser physics laboratory, the laser light appears to partially “travel along” with the aerosol. The following test is to be conducted with a sensitive performance meter.
[0085] If the blue light also travels along with the aerosol, this may be of significant further importance in the treatment of both bacterial and fungal infections.
[0086] The device is therefore equipped with a supplementary laser module, preferably a 470 nm laser module.