Solid Medication Insertion Device

Abstract

A solid medication insertion device includes a barrel having an insertion end portion and a proximal end portion opposite the insertion end portion and having a continuous side wall extending therebetween that defines an interior area. A medicament is initially positioned in the interior area of the barrel. The medication insertion device includes a plunger slidably coupled to the barrel that has a first end engaging a proximal end of the medicament, the plunger having a cylindrical configuration selectively slidable from a starter configuration extending away from the proximal end portion of the barrel to a deployed configuration positioned downstream inside the interior area of the barrel. Pressure applied to the plunger causes the plunger to urge the medicament downstream within the interior area of the barrel. The medication insertion device, i.e., the suppository applicator, is constructed using a material consisting essentially of hemp plastic.

Claims

1. A medication insertion device for insertion of a medicament into a body cavity, comprising: a barrel having an insertion end portion and a proximal end portion opposite said insertion end portion and having a continuous side wall extending therebetween that defines an interior area for initially receiving the medicament; and wherein the insertion end portion defines an outlet; wherein said barrel consists of a hemp-fiber reinforced biopolymer.

2. The medication insertion device as in claim 1, wherein said barrel is biodegradable.

3. The medication insertion device as in claim 1, further comprising: a plunger operably coupled to said barrel and having a first end engaging a proximal end of said medicament, said plunger having a cylindrical configuration proximal end portion of the barrel to a deployed configuration positioned inside the barrel; and wherein pressure applied to said plunger causes said plunger to urge said medicament downstream within said interior area of said barrel.

4. The medication insertion device as in claim 3, wherein said barrel and said plunger constitute a suppository applicator.

5. The medication insertion device as in claim 3, wherein said plunger consists of a hemp-fiber reinforced biopolymer.

6. The medication insertion device as in claim 5, wherein said biopolymer of said plunger is the same as said biopolymer of said barrel.

7. The medication insertion device as in claim 3, wherein said outlet is an open end that allows the medicament to pass downstream of the interior area of said barrel.

8. A medication insertion device for insertion of a medicament, comprising: a barrel having an insertion end portion and a proximal end portion opposite said insertion end portion and having a continuous side wall extending therebetween that defines an interior area configured to initially hold the medicament; a plunger operably coupled to said barrel and having a first end engaging a proximal end of said medicament, said plunger having a cylindrical configuration selectively slidable from a starter configuration extending away from the proximal end portion of the barrel to a deployed configuration positioned inside the barrel; wherein said barrel and said plunger are comprised of about 1-100 wt % of a hemp-fiber reinforced biopolymer; wherein pressure applied to said plunger causes said plunger to urge said medicament downstream within said interior area of said barrel.

9. The medication insertion device as in claim 8, wherein said barrel is biodegradable.

10. The medication insertion device as in claim 8, wherein said barrel further comprises about 1-99 wt % of said biopolymer and about 1-99 wt % of said hemp fibers.

11. The medication insertion device as in claim 10, wherein said plunger is completely biodegradable.

12. The medication insertion device as in claim 10, wherein said plunger comprises about 1-99 wt % of said biopolymer and about 1-99 wt % of said hemp fibers.

13. The medication insertion device as in claim 10, wherein said insertion end portion defines an opening configured to release the medicament when the plunger is actuated.

14. A medication insertion device for insertion of a medicament into a body cavity, comprising: a barrel constructed of hemp plastic material comprising at least one biodegradable polymer and a plurality of hemp fibers, said barrel having an insertion end portion and a proximal end portion opposite said insertion end portion and having a continuous side wall extending therebetween that defines an interior area for initially holding the medicament; and a plunger consisting of hemp plastic material comprising at least one biodegradable polymer and a plurality of hemp fibers, said plunger being operably coupled to said barrel and having a first end engaging a proximal end of said medicament, said plunger having a cylindrical configuration selectively slidable from a starter configuration extending away from the proximal end portion of the barrel to a deployed configuration positioned inside the barrel; wherein pressure applied to said plunger causes said plunger to urge said medicament downstream toward said insertion end portion.

15. The medication insertion device as in claim 14, wherein said at least one biodegradable polymer of said barrel is the same as said at least one biodegradable polymer of said plunger.

16. The medication insertion device as in claim 16, wherein said insertion end portion defines an opening configured to release the medicament when the plunger is moved toward said deployed configuration.

17. The medication insertion device as in claim 14, wherein said barrel and said plunger constitute a suppository applicator.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0015] FIG. 1a is a perspective view of a tampon insertion device according to a preferred embodiment of the present invention, illustrated in ready to use or retracted configuration;

[0016] FIG. 1b is another perspective view of the tampon insertion device as in FIG. 1a, illustrated in a deployed or extended configuration;

[0017] FIG. 2 is an exploded view of the tampon insertion device as in FIG. 1a;

[0018] FIG. 3a is a top view of the tampon insertion device as in FIG. 1a;

[0019] FIG. 3b is a sectional view taken along line 3b-3b of FIG. 3a;

[0020] FIG. 4a; is a top view of the tampon insertion device in a partially deployed configuration;

[0021] FIG. 4b is a sectional view taken along line 4b-4b of FIG. 4a;

[0022] FIG. 5a is a perspective view of a solid medication insertion device according to a preferred embodiment of the present invention, illustrated in ready to use or retracted configuration;

[0023] FIG. 5b is another perspective view of the solid medication insertion device as in FIG. 1a, illustrated in a deployed or extended configuration;

[0024] FIG. 6a is a side view of the solid medication insertion device as in FIG. 5a;

[0025] FIG. 6b is a sectional view taken along line 6b-6b of FIG. 6a;

[0026] FIG. 7a is a side view of the solid medication insertion device as in FIG. 5a;

[0027] FIG. 7b is a sectional view taken along line 7b-7b of FIG. 7a; and

[0028] FIG. 8 is an exploded view of the tampon insertion device as in FIG. 5a.

DESCRIPTION OF THE PREFERRED EMBODIMENT

[0029] A medication insertion device according to a preferred embodiment of the present invention will now be described in detail with reference to FIGS. 1a to 8 of the accompanying drawings. As will be first described, a tampon insertion device 10, also referred to as a tampon applicator (also referred to by reference numeral 10), includes a barrel 20, a tampon 50 initially positioned in the barrel 20, a plunger 40 for pushing the tampon 50 out of the barrel. Specific reference will be made to a process of making the barrel 20 and plunger 40 using a process that includes hemp plastic.

[0030] The barrel 20 has an insertion end portion 22 and a proximal end portion 24 opposite the insertion end portion 22, i.e., opposed ends. While the proximal end portion 24 defines an open end, the insertion end portion 22 is initially closed but then opens up as a tampon 50 is pushed out as will be described later. More particularly, a continuous side wall 26 extends between the proximal end portion 24 and the insertion end portion 22, the continuous side wall 26 having a cylindrical configuration that defines an interior area into which other components are situated and some of which move slidably as will be described.

[0031] The insertion end portion 22 includes two or more (also referred to as a plurality) lines of separation 28 that divides the insertion portion into a plurality of flaps 30 or panels. Initially, the plurality of flaps may have a curved end or domed configuration that limit access to the interior area (FIG. 1) but that separate to form or define an open end when the tampon 50 is pushed downstream and out of the interior area of the barrel 20 (FIG. 1b), as will be described in more detail below.

[0032] Further, the tampon 50 is initially positioned within the interior area of the barrel 20 and is configured to move slidably when pushed or urged downstream by operation of the plunger 40 as explained below. The tampon 50 may be constructed of cotton or a blend of materials suitable to absorb blood and other fluids common to a woman's menstrual period. More particularly, the tampon 50 may have a cylindrical configuration with a flat or truncated distal end 52 (i.e. the upper end). Further, the tampon 50 may include a proximal end 54 opposite the distal end 52 from which a string 56 extends. The string enables a user to extract the tampon 50 more efficiently. In one embodiment, a wax plug (not shown) may be included on the string 56 to absorb blood and to enhance grip.

[0033] The tampon insertion device 10 includes a plunger 40 configured to move slidably in the barrel 20. More particularly, the plunger 40 may have a tubular or cylindrical configuration that enters the barrel 20 via the proximal end portion 24 and has a first end 42 (i.e. the upper end as illustrated) that engages and bears against a lower end of the tampon 50. The plunger 40 is configured to move downstream toward the insertion end portion 22 when pressure is applied thereto by the hand of a user, downstream movement of the tampon 50. In an embodiment, the plunger 40 may be pushed downstream in the barrel 20 and moves slidably. Continued pressure on the plunger 40 causes the tampon to be pushed out of the insertion end portion 22 (FIG. 4). In some embodiments, the plunger 40 may be threadably linked to the barrel 20 such that a twisting of the plunger 40 results in movement between a starter configuration extending outwardly away from the barrel 20 and a deployed configuration substantially or completely inside the interior area of the barrel 20.

[0034] As is described in greater detail herein, in various embodiments of the invention, the tampon applicator 10 may be made exclusively, or at least partially, of hemp plastic. No material other than hemp plastic may be necessary or preferred; however, in some embodiments, the addition of biodegradable polymer(s) may be added to the hemp plastic for construction of the barrel and plunger. Hemp plastic refers to hemp plant fibers that may be extracted and combined with polymers in a manufacturing process. More particularly, Hemp, or industrial hemp, is a strain of the Cannabis sativa plant species that is grown specifically for the industrial uses of its derived products. A cannabis fibrous tampon applicator 10 is novel and non-obvious.

[0035] Hemp plastic can be entirely biodegradable when made or combined with biodegradable polymers. A biodegradable polymer is a polymer that can be decomposed by bacteria. Examples of biodegradable polymers which can broken down by micro-organisms within a suitable amount of time include polyglycolic acid (PGA), polyhydroxy butyrate (PHB), polyhydroxy butyrates-co-beta hydroxyl valerate (PHBV), polycaprolactone (pcl), nylon-2-nylon-6. If made properly and in the right environment, hemp plastic can decompose in 3 to 6 months which is unexpected in view of petroleum-based plastic which are toxic and degrade very little even after decades.

[0036] Now with further reference to the tampon applicator 10 and, specifically, to the barrel 20 and plunger 40, in embodiments, the barrel 20 and plunger 40 consist essentially of hemp plastic rather than petrochemical plastics. In the embodiments, the basic and novel characteristic of the invention is that the barrel 20 and the plunger 40 are constructed of hemp plastic such that the applicator is entirely biodegradable and is at least two times stronger than conventional applicators while maintaining the flexibility necessary to operate the applicator according to standard operation.

[0037] In some embodiments, the material forming the tampon applicator 10, and more specifically the barrel 20 and the plunger 40, consists essentially of a combination of a hemp plastic and a biodegradable polymer or polymers. Here, the basic and novel characteristics of the invention are that the applicator is formed essentially of a combination of hemp plastic and a biodegradable polymer such that the applicator is biodegradable and maintains a strength of at least two times the strength of conventional plastics. The hemp plant is fibrous, i.e., includes a plurality of fibers. In a preferred embodiment of the present invention, the tampon applicator, including the barrel and plunger, but in the line may include a hemp-fiber reinforced biopolymer. Stated another way, the biopolymer is reinforced with a plurality of hemp-fibers.

[0038] More particularly, hemp plants may be harvested, broken down into essential components for production of the barrel 20 and plunger 40 of the tampon insertion device 10. The tampon 50 may be inserted into the barrel 20 prior to packaging. Constructed of hemp plastic, the barrel and, in an embodiment where both the barrel and plunger are constructed of hemp plastic, the overall tampon applicator exhibits a firmness and certain lack of flexibility that is both unexpected and highly desirable, while maintaining the necessary flexibility such that operation of the applicator may proceed according to conventional wisdom. Specifically, a tampon applicator constructed of hemp-plastic overcomes a problem typical with tampons constructed of traditional or petroleum-based plastic—namely to bend and become difficult to locate when lodged in a woman's vagina. The advantages of hemp plastic are only experienced when the tampon applicator recited in the present claims is constructed essentially of hemp plastic, or a combination of hemp plastic and biodegradable polymer(s).

[0039] According to further embodiments, the tampon applicator 10 may be constructed only of hemp plastic, with only slight amounts of naturally occurring impurities or impurities that are introduced by virtue of the processing process. In such embodiments, the applicator may exhibit strength properties that are superior to conventional applicators.

[0040] In still other embodiments, the tampon applicator 10 is constructed only of hemp plastic together with a biodegradable polymer, such as the biodegradable polymers described herein. In such embodiments, the applicator may further include slight amounts of naturally occurring impurities, or impurities that are introduced into the material during the manufacturing process. According to some aspects, the applicator is constructed of about 1-100 wt % hemp plastic and about 0-99 wt % biodegradable polymer or polymers. In further aspects, the applicator is constructed of about 10-100 wt %, about 20-100 wt %, about 30-100 wt %, or about 40-100 wt % hemp plastic, and the remainder biodegradable polymer or polymers. According to still further aspects, the applicator consists of at least about 50 wt % hemp plastic and the remainder biodegradable polymer or polymers. In some embodiments it may be preferable for the amount of hemp plastic to be greater than about 50 wt %, greater than about 60 wt %, greater than about 70 wt %, greater than about 80 wt %, or greater than about 90 wt %, with the remainder, if any, being biodegradable polymer or polymers. In use, a user inserts the barrel 20 of the tampon insertion device 10 into her vagina. Specifically, then, the user may push or rotate the plunger 40 upwardly into the barrel 20 so as to urge the tampon 50 upwardly, i.e., downstream. The tampon 50 is, thus, deployed into the vagina.

[0041] The tampon applicator 10 described above is configured for insertion into a vaginal body cavity for delivery of the tampon, the tampon being representative of a medicament. In a substantially related embodiment, the present invention may include a suppository applicator 10′ (also referred to as a solid medicine insertion device) having a construction that is substantially similar to the tampon applicator 10 described above except as specifically referenced below and will be described using primed reference numerals representing structures that are the same as those described previously. In other words, the suppository applicator 10′ also includes a barrel 20′ and a plunger 30; and a medicament 50′ (previously, the medicament was referred to as a tampon 50 whereas, now, the medicament 50′ may be a pill or other pharmaceutical). Accordingly, the same numerals used to describe the physical structures associated with the tampon applicator 10 are used to label the suppository applicator 10′ shown in FIGS. 5a to 8. Although structures that are substantially the same will not be re-described herein, they are shown in the attached figures. Conversely, structures having a different configuration will be described below.

[0042] More particularly, the medicament 50′ (which may be a pill or other pharmaceutical), may be initially positioned partially in the interior area defined by the outer wall yet extending partially outside the upper end of the outer wall 26′ (FIG. 5a). In other words, the insertion end portion 22′ may be open, i.e., a defined and open end or opening. (FIG. 5b).

[0043] The plunger 40′ associated with the suppository applicator 10′ is configured to move downstream toward the insertion end portion 22′ when pressure is applied thereto by the hand of a user until contact is made with a rear end of the medicament 50. Continued pressure on the plunger 40′ causes the medicament to be pushed out of the insertion end portion 22′ and into the body cavity (FIG. 4). It is understood that the body cavity may be either the that vagina or rectum and the medicament 50 may be a pill which may dissolve or otherwise be absorbed into a patient's tissue or bloodstream.

[0044] According to the present invention, the suppository applicator 10′ may be constructed of a hemp-reinforced biopolymer in a manner substantially as described above. Namely, the material forming the suppository applicator 10′, and, more specifically, the barrel 20′ and the plunger 40′, consist essentially of a combination of a hemp plastic and a biodegradable polymer or polymers. Here, the basic and novel characteristics of this embodiment are that the suppository applicator is formed essentially of a combination of hemp plastic and a biodegradable polymer such that the applicator is biodegradable and maintains a strength of at least two times the strength of conventional plastics. The hemp plant is fibrous, i.e., includes a plurality of fibers. Accordingly, the suppository applicator 10′, including the barrel and plunger, may include a hemp-fiber reinforced biopolymer. Stated another way, the biopolymer is reinforced with a plurality of hemp-fibers. Other details regarding the hemp-plastic material are substantially similar or identical to those first described above and are not repeated here for the sake of brevity.

[0045] It is understood that other embodiments of the present invention are contemplated and have a structural construction that is substantially similar to the tampon applicator 10 and suppository applicator 10′ described above. In an embodiment, a liquid medicament applicator may be a syringe that may be constructed of a hemp-reinforced biopolymer in a manner substantially as described above, the liquid medicament applicator also having a barrel configured to hold a liquid medicament and having a plunger configured for incrementally pushing the liquid medicament through an insertion in of the barrel. In still another embodiment, an applicator having a barrel and plunger construction incrementally disposes a lip balm medicament.

[0046] It is understood that while certain forms of this invention have been illustrated and described, it is not limited thereto except insofar as such limitations are included in the following claims and allowable functional equivalents thereof.