The present invention is directed to a method and apparatus for accurate dosing of liquids. While the device relates more particularly to oral dosing of tinctures, the invention is designed to replace a standard dropper or Pasteur pipette and may be used to dispense specific quantities of any liquid.
Eye droppers or Pasteur pipettes are devices commonly used to withdraw liquid from a vial or container while minimizing exposure of that liquid to the external environment. The dropper device is generally comprised of a glass or plastic tube or barrel that tapers to a narrowed opening on one end while the opposing end is fitted with a malleable bulb. This bulb is squeezed to create a vacuum within the pipette prior to its insertion into the liquid. When the bulb is released, the pressure differential between the interior of the pipette and the liquid within the container creates suction thereby drawing liquid into the pipette. The user may add or remove material from the pipette by squeezing the malleable bulb.
The problem with these devices is that they do not provide accurate dosing of the desired liquid. A standard dropper or Pasteur pipette often includes graduations on the barrel to estimate the volume of liquid withdrawn; however, these graduations are not particularly precise and visualization of the fluid meniscus complicates the measurement. Furthermore, one must withdraw a quantity of fluid and remove the pipette from the vial to visualize the graduations. If an excess of liquid has been withdrawn, the bulb must be compressed to return the additional material to the vial. This practice may introduce contaminants if the user has touched the tip or exterior surface of the pipette to another surface while inspecting the volume within the barrel.
If an insufficient amount of liquid has been withdrawn into the dropper, the likelihood of contamination is even greater as the user repeatedly inserts and withdraws the barrel from the liquid in an attempt to extract the appropriate dose. These subsequent squeezes may additionally introduce air bubbles within the tube, making it difficult to properly gauge the quantity of fluid within the pipette.
Inaccurate dosing can pose a serious health danger when an exact quantity of medication is required. Patients who are self-administering prescriptions may find it challenging to accurately measure their medications using standard droppers based on the reasoning described above. Tinctures often come in varying potencies and the strength of the drug may vary greatly depending on the mode of manufacture or other variables. Improper dosing becomes even more of a concern if that individual is operating with compromised motor skills or vision.
Those suffering from illnesses such as Parkinson's disease, multiple sclerosis, glaucoma, fibromyalgia, as well as chronic inflammation and pain disorders frequently have weakened eyesight, diminished hand strength, and poor motor control. Consequently, self-administration of medications through a dropper is often difficult and dangerous when one considers the possibility of accidental overdose.
There is therefore a need in the art for an apparatus that provides a safe, simple, and effective means for administering accurate quantities of medications or other liquids through a dropper.
Tinctures and other liquid medications are typically administered through standard eye droppers or Pasteur pipettes inserted into a liquid containment vessel (hereinafter a “vial”). The user relies on graduations printed or molded on the surface of the pipette barrel or alternatively, the user counts the number of drops exiting the tip of the pipette. The graduations are not designed for accuracy and offer only very basic volumetric reference points. Drop sizes may vary in volume depending on the force exerted on the dropper bulb and the user may lose track of the number of drops administered. Consequently, neither the graduations nor the drop counting method offer an accurate means of dosing. The present invention seeks to provide a device and method for the accurate administration of material within a vial using a modified dropper.
The modified dropper described herein, allows the user to focus on proper volumetric dosing and improves safety by offering audio, visual, and tactile cues as each dose is dispensed. This is of particular importance when one possessing diminished sensory or motor skills is administering liquid doses from a dropper. While inventors anticipate the use of this method and device for dispensing medications, one will appreciate that it may also be used for delivering epoxies, adhesives, and other liquids that require the application of a specific volume.
The present invention replaces a standard dropper with a modified dropper assembly having a plunger inserted into a hollow tube. This modified dropper assembly may work as a standalone device or it may be affixed to a vial containing the desired material. The plunger incorporates specific features on its geometric profile that engage with corresponding geometric features on an engagement mechanism within the dropper assembly. The profile contours on the plunger correspond to a desired dose of material, hereinafter referred to as a “unit dose”.
To extract liquid from the vial, the plunger is depressed fully into the hollow tube. The hollow tube of modified dropper assembly is submerged in a desired liquid which may be held by any container. For the purpose of this application the desired liquid shall be held within an optional vial. The cap of the modified dropper assembly may be placed loosely on the vial or it may be screwed or press fit onto the vial for a more secure and watertight fit.
Once the modified dropper assembly is within the container, the tip of the tube must be fully immersed in the liquid. To extract the liquid, the user retracts the plunger partially withdrawing it from the tube. The user may disengage the engagement mechanism from the plunger using an optional disengagement mechanism to allow free movement of the plunger within the tube or the plunger geometry may be configured to allow retraction of the plunger within the engagement mechanism without having to disengage these mating profiles. As the user withdraws the plunger, the resulting vacuum within the tube draws liquid into the hollow tube.
To dispense the liquid, the user positions the dispensing end of the tube in, on, or near the desired administration site. The plunger is depressed and liquid exits the end of the tube. As the plunger is depressed, the profile features on the plunger mate with the engagement mechanism within the dropper cap. A distinct noise and vibration is generated with each administered unit dose as the features of the plunger and engagement mechanism engage with one another. The dropper cap shall also be referred to as a stabilizing unit as this component need not necessarily function as a cap.
The plunger and engagement mechanism work in concert to control the motion and rate of advancement of the plunger, thereby providing more uniform and controlled dispensing of the material exiting the tip of the tube. Regulation of the plunger motion and its advancement can be achieved through the use of threads on both the engagement mechanism and plunger, by corresponding positive and negative contours on these two components, or through a combination of these elements. The threads and contours within the plunger profile and engagement mechanism are designed to create audible and tactile feedback to the user as each unit dose is dispensed from the tip of the tube.
Contours on the plunger may take the form of cavities, channels, or protrusions to create “interlocking elements”. The engagement mechanism is comprised of a complimentary geometric profile or feature (hereinafter “receiving element”) that facilitates recurrent engagement with the interlocking element as the plunger advances within the dropper cap and tube. The receiving element may take the form of a deformable component such as an elastic tab, spring loaded element, or similar mechanical device as described more fully below.
As the plunger advances within the engagement mechanism, the receiving element yields in a manner that allows it to store mechanical energy. An audible clicking sound and accompanying vibration emanates from the modified dropper assembly as the receiving element engages with the interlocking element. Sound and tactile cues are generated as the potential energy is rapidly converted into noise and vibration when the receiving element snaps into the interlocking element. The geometry, material properties, or spring-loaded nature of the receiving element allow the engagement mechanism to disengage from the interlocking element as the plunger end is depressed or rotated (depending on the type of profile used), causing the plunger to advance the next unit dose. The audio, visual, and tactile feedback provided with the advancement of the plunger allows the user to see, hear, and feel the number of unit doses or drops that they have administered.
In one embodiment, the auditory and tactile cues are provided through a toothed plunger having a series of peaks and flat segments or valleys. The distance between the flat sections or valleys on the plunger defines the unit dose and can therefore be designed to suit the potency of the medication being administered. As the user applies pressure to the end of the plunger, the peaks on the plunger profile force the receiving element within the engagement mechanism to deform and store potential energy. As previously noted, this energy is released as a noise and vibration when the receiving element reaches an interlocking element on the plunger profile. An optional dosing key may be affixed to the interlocking elements within the plunger profile to limit the plunger's travel distance within the tube. Labeled or color coded keys may also be used to track dosing schedules and minimize the potential for inadvertent overdose.
In another embodiment, a threaded plunger having one or more channels mates with a spring loaded pin within the engagement mechanism. The plunger emits a noise and vibration as the energy stored within the spring propels the pin into the channel as the plunger rotates into place with each administered unit dose. The channel or channels are positioned along the longitudinal axis of the plunger. This embodiment is ideally suited for those requiring micro doses of a liquid within the vial. As previously noted, one or more channels may be positioned along the longitudinal axis of the plunger depending on the desired dose.
5 Modified Dropper Assembly
10 Hollow Tube
15 Plunger
18 Liquid
20 Interlocking Element
22 Through-hole
25 Engagement Mechanism
30 Receiving Element
35 Dropper Cap/Stabilizing Unit
38 Dropper Cap Threads
40 Vial
42 Vial Threads
45 Dosing Key
50 Plunger Profile Geometry
55 Tip of Tube
60 Vial Base
65 Funnel Cavity
70 Disengagement mechanism
75 Spring
80 Tip of Plunger
85 O-Ring
88 Rubber Tip
90 Projecting Element/Pin/Collar
95 Knob
100 Spring Guide
105 Dropper Cap Cover
110 Gasket
L-L Longitudinal Axis of Plunger
Specific terms are used for the sake of clarity in describing the embodiments below. The invention is not intended to be limited to the selected terminology and it should be understood that each specific element includes all technical equivalents operating in a similar manner to accomplish a similar function.
In this patent application, materials dispensed by the modified dropper device, including those with extremely high viscosities such as oils, syrups, polymers, adhesives, and similar substances, shall be referred to as a “liquid,” “fluid,” or “material.” For the purposes of this application a “unit dose” shall be defined as the amount of a medication administered to a patient in a single dose or drop. The “dropper cap” may be referred to alternatively as a “stabilizing unit” if this component is used solely to steady the user's hand rather than function as a cap.
The device and method described herein seek to provide uniform drops of liquid as well as a multi-sensory experience with each administered unit dose. These additional features improve safety by offering multiple cues to the user as each drop is dispensed. This is accomplished through a set of components that intermittently mate within the device as described more fully below.
The present invention 5 is comprised of a tube 10, a plunger 15 sized to fit within the tube 10 and having a plunger profile geometry 50, an appropriately sized dropper cap (stabilizing unit) 35 that may be suited to fit an optional vial 40 of the desired liquid, an engagement mechanism 25 integral to or fitted within the dropper cap 35 and designed to engage with the plunger profile geometry 50, an optional disengagement mechanism 70, and one or more optional dose limiting keys 45. Please see
The dropper cap 35 has a through-hole 22 which penetrates the thickness of the dropper cap 35. The engagement mechanism 25 abuts the perimeter of, sits within, or surrounds said through-hole 22. The engagement mechanism 25 may be placed within or, alternatively, may form an integral part of said dropper cap 35. Please see
The hollow tube 10 may form an integral part of the dropper cap 35 as shown in
The tip of the plunger 80 is inserted into the through-hole 22 of the dropper cap 35 and into the tube 10 such that the plunger profile geometry 50 makes contact with the engagement mechanism 25 as shown in
In instances where the complimentary geometry between the plunger profile 50 and the engagement mechanism 25 allows only for forward motion (or advancement) of the plunger 15 into the tube 10, an optional disengagement mechanism 70 may be introduced. One example of such disengagement mechanism 70 is depicted in
Referring now to
To use the modified dropper device 5, liquid must be present within the tube 10. The user must advance the plunger 15 within the tube and submerge the tube tip 55 into a desired liquid either within a container of liquid or in an optional vial. The user may advance the plunger 15 by stepping through the entire series of intermittent engagements with the interlocking elements 20 or by depressing an optional disengagement mechanism 70. Please refer to
To extract material, the plunger 15 is withdrawn from the hollow tube 10 as the tube tip 55 remains submerged in the liquid. The optional disengagement mechanism 70, described above, may be included within a modified dropper assembly 5 if the specific plunger profile geometry 50 being implement does not permit retraction of the plunger 15. The tight seal between the plunger tip 80 and interior of the tube 10 results in a pressure differential and resulting vacuum within the interior of the tube 10. Liquid is subsequently drawn into the hollow tube 10 as the pressure equalizes. When a sufficient amount of liquid has been extracted from the liquid containment vessel or vial 40, the user places the dispensing end of the tube 10 near the tube tip 55 into the desired administration location and depresses the end of the plunger or knob 95. The application of force to the plunger end advances the interlocking elements 20 on the plunger profile geometry 50 through the receiving element 30 of the engagement mechanism 25. The receiving element 30 recurrently engages with the interlocking elements 20 on the plunger 15 such that a distinct sound and vibration is generated with each unit dose dispensed.
In the embodiments depicted in
The pin or collar 90 within the receiving element 30 moves over the contours of the plunger profile geometry 50 as it advances within the engagement mechanism 25. Force from the advancing plunger 15 causes the spring 75 to compress and store potential energy. When the pin or collar 90 is propelled into an interlocking element 20 on the plunger profile geometry 50, the stored potential energy within the spring 75 transforms into kinetic energy in the form of noise and vibration. These audible and tactile cues signal the administration of a unit dose. As the user continues to apply force to the plunger 15, this force is transferred to the pin or collar 90. The spring-loaded nature of the receiving element 30 allows the pin or collar 90 to advance and retract to follow the contours of the plunger profile geometry 50. The engagement mechanism 25 thereby periodically “clicks” as the receiving element 30 engages with each interlocking element 20. See
Each “unit dose” is determined by the distance between the interlocking elements 20 in the profile. Plunger profile geometries 50 will vary and may be customized depending on the potency of the material being administered. The distance between the interlocking elements 20 will be shorter for more potent medications and longer for medications having reduced potency.
It should be appreciated that any number of plunger profile geometries 50 may be used to achieve the communication of each unit dose provided that the profile 50 provides peaks to store potential energy and flat segments or discrete valleys in which a noise and vibration is emitted. These profiles may be used with or without threads.
It should also be understood that the receiving element 30 may be elastic in nature and may take the form of a deformable spring or tab, eliminating the need for a separate spring 75. It should be further appreciated that the plunger 15 may include an elastic element or protrusion that recurrently snaps into corresponding complimentary geometries within the engagement mechanism 25.
Ideally, the interaction between the engagement mechanism 25 and plunger profile geometry allows for stepped motion of the plunger 15 both as it is withdrawn and extended; however, there may be some instances where it is preferable to lock the plunger 15 in place to prevent inadvertent retraction. In such a case, the connection between the engagement mechanism 25 and interlocking elements 20 may be designed to facilitate advancement of the plunger 15 only. In such a case, the disengagement mechanism 70, as described above, may be included to disengage the plunger 15 from the receiving element 30.
Referring now to
If desired, a watertight seal between the dropper cap 35 and optional vial 40 may be achieved through use of a gasket 110 or similar sealing device. Alternatively, tightly fitting and complimentary vial threads 42 and dropper cap threads 38 as shown in
Inventors anticipate that the components described herein will be manufactured from durable autoclavable plastics such as polypropylene and polyethylene; however it should be recognized that any suitable material may be used.
While the above description contains many specifics, these should be considered exemplifications of one or more embodiments rather than limitations on the scope of the invention. As previously discussed, many variations are possible and the scope of the invention should not be restricted by the examples illustrated herein.
This application claims benefit of priority from U.S. Provisional Patent Application No. 63/209,278 of Sereyviseth Pheng and Sophornarak Horn filed Jul. 12, 2021, entitled MODIFIED DROPPER DEVICE AND METHOD FOR ACCURATE DOSING the entirety of which is incorporated herein by reference. Not Applicable Not Applicable Not Applicable
Number | Date | Country | |
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63209978 | Jun 2021 | US |