This disclosure generally relates to the delivery of oxygen to a user and, in particular, to an improved system, method and apparatus for a dynamic oxygen conserver with an inhalation sensor.
Research shows that most people have uneven nasal airflow. In particular, many people have a dominant naris and nasal blockage, either structural or from viruses, colds, allergies, etc. According to one study, 80% of the population has a nasal cycle. The nasal cycle is a phenomenon where the nasal passages alternate congestion and decongestion in cycles. It typically occurs all of the time, day and night. A pattern of blockage can occur in a range from about 30 minutes to four hours.
Conventional oxygen devices and nasal cannulas, however, split oxygen delivery approximately 50% to each nostril, which is a cannula style unchanged since the year 1948. That means they can be delivering oxygen to blocked nasal passages, which wastes the dose. To compensate, the oxygen amount may have to be doubled, which is not only wasteful, it's expensive. With nasal blockage occurring most of the time, users are challenged to get their entire dose. Thus, improvement in oxygen devices continue to be of interest.
Embodiments of system, method and apparatus for a dynamic oxygen conserver with an inhalation sensor are disclosed. For example, the dynamic oxygen conserver can include a housing and an inhalation sensor coupled to the housing. The sensor can have a printed circuit board (PCB) assembly. The PCB assembly can include a first PCB configured to be a breathing side for a user of the dynamic oxygen conserver. A second PCB can be coupled to the first PCB. The second PCB can be configured to be an atmosphere side opposite the breathing side. In addition, a spacer assembly can be coupled between the first PCB and the second PCB. The spacer assembly can include a metallized diaphragm configured to be dynamically responsive to breathing by the user of the dynamic oxygen conserver.
An alternate embodiment of a dynamic oxygen conserver can include a housing and an inhalation sensor coupled to the housing having a PCB assembly. The PCB assembly can include a base PCB configured to be a breathing side for the user of the dynamic oxygen conserver. First and second PCBs can be coupled opposite the base PCB and configured to be an atmosphere side opposite the breathing side. In addition, a spacer assembly can be coupled between the base PCB and the first and second PCBs. The spacer assembly can include a metallized diaphragm configured to be dynamically responsive to breathing by the user. The base, first and second PCBs can have holes extending therethrough and aligned with portions of the diaphragm. The holes for the base PCB can be configured to be fluidically coupled to respective nostrils and a mouth of the user.
For a detailed description of example embodiments, reference will now be made to the accompanying drawings in which:
Various terms are used to refer to particular system components. Different companies may refer to a component by different names—this document does not intend to distinguish between components that differ in name but not function. In the following discussion and in the claims, the terms “including” and “comprising” are used in an open-ended fashion, and thus should be interpreted to mean “including, but not limited to . . . .” Also, the term “couple” or “couples” is intended to mean either an indirect or direct connection. Thus, if a first device couples to a second device, that connection may be through a direct connection or through an indirect connection via other devices and connections.
The following discussion is directed to various embodiments of the invention. Although one or more of these embodiments may be preferred, the embodiments disclosed should not be interpreted, or otherwise used, as limiting the scope of the disclosure, including the claims. In addition, one skilled in the art will understand that the following description has broad application, and the discussion of any embodiment is meant only to be exemplary of that embodiment, and not intended to intimate that the scope of the disclosure, including the claims, is limited to that embodiment.
Each of the following patent assets is incorporated herein by reference in its entirety.
Embodiments of the first PCB 111 can be configured to be proximal to the user. In some examples, the first PCB 111 comprises holes 113 extending therethrough and aligned with portions of the metallized diaphragm 151. A version of the holes 113 can include a pair of holes 113 configured to be fluidically coupled to respective nostrils of the user.
Embodiments of the second PCB 121 can be configured to be distal to the user. The second PCB 121 can include holes 123 extending therethrough and aligned with portions of the metallized diaphragm 151. The holes 123 can include sets of holes 123 configured to communicate with an atmosphere in which the user is located.
In some versions of the inhalation sensor 101 (
Embodiments of the spacer assembly 131 can comprise a laminate having a plurality of layers. For example, the plurality of layers can include spacers 133, 135 and adhesive sheets 137. In some versions, each spacer 133, 135 and adhesive sheet 137 can have holes 139 configured to be aligned with portions of the diaphragm 151. Embodiments of the spacers 133, 135 can have identical or different thicknesses. For example, the spacer 133 (e.g., on the atmosphere side) can have a thickness of about 0.03 mm, or a thickness in a range of about 0.01 mm to about 0.2 mm. Versions of the spacer 135 (e.g., on the breathing side) can have a thickness of about 0.25 mm, or a thickness in a range of about 0.05 mm to about 0.6 mm. The spacers 133 can comprise a film, such as a non-metallic film. In one example, the spacers 133 comprise a polyester film, such as Mylar.
Versions of each of the adhesive sheets 137 can comprise a thickness of about 0.05 mm, or a thickness in a range of about 0.03 mm to about 0.07 mm. In some embodiments, each of the adhesive sheets 137 can comprise adhesive on proximal and/or distal surfaces thereof. Each of the adhesive sheets 137 can include comprises a base layer comprising a film, such as a non-metallic film like polyester film. The adhesive sheets 137 an adhesive, such as a medical grade adhesive (e.g., acrylic). The adhesive sheets 137 can be identical to or different from each other.
The inhalation sensor 101 can have a selected construction. For example, from a proximal side (i.e., the user side, or breathing side) to a distal side (i.e., the atmosphere side, opposite the user), the spacer assembly 131 (
Some embodiments of the dynamic oxygen conserver 200 can include an inhalation sensor 201 (
Embodiments of the inhalation sensor 201 can include a printed circuit board (PCB) assembly 203 (
Embodiments of the first PCB 211 (
Embodiments of the second PCB 221 (
Some versions of the inhalation sensor 201 can be identical to or differ from the inhalation sensor 101, including parts, materials and construction. The diaphragm 251 can be configured like diaphragm 151, including a base layer having a metallic coating. Examples of the diaphragm 251 can be identical to or different from diaphragm 151 as described herein. Similarly, embodiments of the spacer assembly 231 can be identical to or differ from spacer assembly 131 as described herein.
Other embodiments can include one or more of the following items.
1. A dynamic oxygen conserver, comprising:
2. The inhalation sensor of any of these items, wherein the first PCB is configured to be proximal to the user, the first PCB comprises one or more holes extending therethrough and aligned with portions of the metallized diaphragm, and the one or more holes are configured to be fluidically coupled to respective nostrils and a mouth of the user.
3. The inhalation sensor of any of these items, wherein the second PCB is configured to be distal to the user, the second PCB comprises one or more holes extending therethrough and aligned with portions of the metallized diaphragm, and the one or more holes are configured to communicate with an atmosphere in which the user is located.
4. The inhalation sensor of any of these items, wherein the metallized diaphragm comprises a base layer having a metallic coating.
5. The inhalation sensor of any of these items, wherein the metallic coating is located only on one side of the base layer and is configured to be located opposite of the user.
6. The inhalation sensor of any of these items, wherein the base layer comprises a non-metallic film and has a thickness in a range of about 0.01 mm to about 0.05 mm, and the metallic coating has a metallic coating thickness in a range of about 0.0003 mm to about 0.01 mm.
7. The inhalation sensor of any of these items, wherein the metallic coating comprises at least one of aluminum or silver.
8. The inhalation sensor of any of these items, wherein the spacer assembly comprises a laminate having a plurality of layers.
9. The inhalation sensor of any of these items, wherein the plurality of layers comprises spacers and adhesive sheets.
10. The inhalation sensor of any of these items, wherein each spacer and adhesive sheet comprises holes configured to be aligned with portions of the metal diaphragm.
11. The inhalation sensor of any of these items, wherein the spacers have different thicknesses.
12. The inhalation sensor of any of these items, wherein a first spacer has a first thickness in a range of about 0.01 mm to about 0.2 mm, and a second spacer has a second thickness of about 0.05 mm to about 0.6 mm.
13. The inhalation sensor of any of these items, wherein the spacers comprise non-metallic film.
14. The inhalation sensor of any of these items, wherein each of the adhesive sheets comprises a same thickness in a range of about 0.03 mm to about 0.07 mm.
15. The inhalation sensor of any of these items, wherein each of the adhesive sheets comprises adhesive on proximal and distal surfaces thereof.
16. The inhalation sensor of any of these items, wherein each of the adhesive sheets comprises a base layer comprising non-metallic film and medical grade adhesive.
17. The inhalation sensor of any of these items, wherein from a proximal side to a distal side, the spacer assembly comprises:
18. The inhalation sensor of any of these items, wherein the PCB assembly is configured to sense electrical capacitance based on dynamic movement of the metallized diaphragm.
19. A dynamic oxygen conserver, comprising:
Many of the electrical connections in the drawings are shown as direct couplings having no intervening devices, but not expressly stated as such in the description above. Nevertheless, this paragraph shall serve as antecedent basis in the claims for referencing any electrical connection as “directly coupled” for electrical connections shown in the drawing with no intervening device(s).
The above discussion is meant to be illustrative of the principles and various embodiments of the present invention. Benefits, other advantages, and solutions to problems have been described above with regard to specific embodiments. However, the benefits, advantages, solutions to problems, and any feature(s) that can cause any benefit, advantage, or solution to occur or become more pronounced are not to be construed as a critical, required, sacrosanct or an essential feature of any or all the claims. Numerous variations and modifications will become apparent to those skilled in the art once the above disclosure is fully appreciated. It is intended that the following claims be interpreted to embrace all such variations and modifications.
This application claims priority to and the benefit of U.S. Prov. Pat. App. No. 62/832,695, filed Apr. 11, 2019, which is incorporated herein by reference in its entirety.
Filing Document | Filing Date | Country | Kind |
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PCT/US20/27733 | 4/10/2020 | WO | 00 |
Number | Date | Country | |
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62832695 | Apr 2019 | US |