US2653611A - Closure - Google Patents

Description

Sept. 29, 1953 A. E. SMITH 2,653,611

CLOSURE Filed Nov. 24, 1950 INVENTOR. AETHUPE SM/TH,

ATTOf/VE) Patented Sept. 29, 1953 UNITED STATES PATENT OFFICE CLOSURE Arthur E. Smith, Los Angeles, Calif.

Application November 24, 1950, Serial No. 197,358

4 Claims. 1

This invention relates to a closure for a container whereby a fresh drug solution may be prepared easily, quickly, accurately and may be maintained in a sterile condition.

Heretofore, it has been the practice among physicians, surgeons and nurses to prepare a fresh drug solution such as penicillin, or the like, by injecting a measured quantity of a solvent such as water or normal saline solution through a resilient bottle cap and into a bottle wherein a quantity of the dry drug had been placed. This process of mixing necessary fresh solutions permits considerable error in that not always does the preparer know or remember the exact amount of solvent to be used, the correct type of solvent, or does he necessarily maintain the solvent in a sterile condition. These measurements must be rigidly complied with to maintain the fresh drug solutions in their correct concentrations, a factor vital in the administration of such drugs.

The problem of sterility of the solution is one that must be taken into consideration. Often a quantity of solvent is withdrawn at many difierent times from the same container. In so doing it is practically impossible to maintain the solvent in a sterile condition. This condition is also aggravated by the fact that often there is poor sterilization of the syringes and needles in the mixing.

Therefore, it is the main object of this invention to provide a novel closure for a container whereby a fresh drug solution may be prepared rapidly and accurately and may be maintained in a sterile condition.

Another object of the present invention is to provide a novel container closure including a novel removable portion.

A further object of the invention is to provide a novel closure including a drug holding cavity.

A still further object of the present invention is to provide a novel closure including a drug holding cavity and a novel opening member for removing a wall of the cavity.

Other and further objects of the present invention will be apparent from the following description taken in connection with the accompanying drawings, wherein:

Fig. 1 is a sectional view of a container with the closure of this invention thereon;

Fig. 2 is a, view similar to Fig. 1, showing the container as it appears after the fresh solution has been prepared;

Fig. 3 is a transverse sectional view taken as indicated by line 3-3, Fig. 1;

Fig. 4 is an enlarged, fragmentary, sectional View of the actuating rod, together with the diaphragm and its associated frangible portion;

Fig. 5 is a fragmentary, sectional view of a modification of the invention, and

Fig. 6 is a view similar to Fig. 5, showing a further modification of the invention.

Referring to the drawing by reference characters, wherein like characters indicate like parts, the invention is shown as embodied in a container which is indicated generally at H]. As shown the container includes a bottle ll having a body portion l2 and a reduced neck portion [3. The upper end of the neck portion I3 is provided with an outwardly directed flange M which forms the upper end of anannular groove 15. The opening [6 in the bottle neck receives a stopper ll which has an outwardly directed annular flange I 8, adapted to rest on the flange M.

The stopper H has an opening l9 which is closed at the lower end by adiaphragm 20 which has a pair of opposed, upper and lower annular V-shaped grooves 2| and 22, which define a frangible orbreakable portion 23. Theportion 23, as shown, has a centrally positioned indentation 24 which is adapted to receive the lower end of an actuating member orrod 25, the upper end of which is retained in a collar which depends from a resilient, inverted, cupshaped closure member 28.

Theclosure member 28 has a downwardly extending side wall orskirt 29 which surrounds the flanges I4 and I8 of the bottle and the stopper and at its lower end has an inwardly directedannular bead 30 which lies in the groove l5 of the bottle neck I3 to retain theclosure 28 in place. The central upper surface of theclosure member 28 is provided with a slight indentation 3|, the use of which will be later described.

In use, the container is delivered to the user in the condition shown in Fig. l, with a quantity of adrug 32 in the space surrounding therod 25 within theopening 19. The body I2 of the container is filled with the correct amount of the proper solvent orvehicle 33 for the drug being used.

To eifect mixing of the drug and the solvent, pressure is applied on the upper end of theclosure 28, thus forcing the actuatingmember 25 downwardly and, due to its engagement with the frangible orbreakable portion 23 of thediaphragm 20, causes theportion 23 to break away from thediaphragm 20 at theannular grooves 2| and 22. Therod 25,frangible portion 23 and thedrug 32 will then fall into thesolvent 33 to prepare a fresh solution. To obtain the required quantity of the prepared solution, a hypodermic needle connected to a syringe is inserted through the indentation 3! in theclosure 28 and the required amount of solution is withdrawn into the syringe.

Thus it may be seen that the container of the invention is of such a nature that a fresh drug solution may be quickly, easily and accurately prepared and that the solution will remain sterile 1n the container.

Referring now to Fig. 5, wherein a modification of the invention is shown and wherein like parts are indicated by single primed reference numer als, the opening IS in the stopper ll receives H. An annular, V-shaped groove 43 is provided in theinsert 40 adjacent the flange 4| to provide The flange 4| and a frangible area therefor.

groove 43 form a diaphragm. Theinsert 40 is;-

held in contact with theflange 42 by pressure on its upper end by theresilient closure 28. Theinsert 40 has an upwardly directed recess 44 wherein the drug 32' may be placed.

Pressure on the upper end of actuating member 4|! will cause the flange 4| to break from theinsert 40 at theannular groove 43, whereupon theinsert 40 together with the drug 32' will fall into thesolvent 33 to be dissolved therein.

Referring now to the further modification of Fig. 6, wherein like parts are indicated by double primed reference numerals, the stopper I1" is provided with annular V-shapedopposed grooves 50 and 50 adjacent its upper flange l8. The flange l8 and V-sh-aped grooves 50 and 50 provide a diaphragm. A recess is provided in the lower portion of the stopper IT" to receive thedrug 32".

Horizontal bores 52 connect the recess 5| with the outer periphery of the stopper. The recess 5| and thespace 53 formed between the stopper I1" and the neck [3" of the bottle are sealed by aresilient closure 54 adapted to engage the opening IS" in the bottle neck and aroove 55 in the lower outer edge of the stopper H.

The stopper I7" is also provided, at its upper end, with a raised actuatingmember portion 56 which may be engaged by aclosure 28". Pressure on theclosure 28" and theportion 56 will cause the stopper IT" to break away from its flange l8 at theannular grooves 50 and 50', thus causing the stopper,lower closure 54 and thedrug 32" to fall into thesolvent 33", whereupon the solvent will pass through thebores 52 to be mixed with thedrug 32".

Having thus described my invention, I claim:

1. In a container wherein a fresh drug solution may be prepared, a bottlehaving a body portion and a neck portion of reduced diameter, a stopper within said neck, portion and having an outwardly directed annular flange resting on the upper end of said neck portion, said stopper having an annular wall defining a recess adapted to hold a quantity of a drug, a removable diaphragm integral withsaid annular wall and closing said recess, an actuating rod in the stopper recess, said rod having a cross sectional area less than the area of the stopper recess, said actuating rod extending upwardly to a location above the upper end of said stopper flange, and an inverted cup shaped resilient closure member having a skirt portion engaging the stopper flange and engaging said bottle neck portion, said diaphragm and said closure having centering means thereon engaging the lower and, upper ends, respectively, of the rod.

2. In a container wherein a fresh drug solution may be prepared, a bottle having a body portion and a neck portion of reduced diameter, theupper end of said neck portion having an annular peripheral flange defining an annular groove about said neck portion adjacent to said body portion, a stopper within said neck portion and having an outwardly directed annular flange resting onthe upper. end of said neck portion, saidstopper having an. annularlwall defining a 4 recess adapted to hold a quantity of a drug, a diaphragm integral with said annular wall and extending across, and closing, said recess, there being a weakened portion on said diaphragm forming a removable section, an actuating rod in ,the stopper recess and having its lower end engaging said diaphragm, said rod having a cross sectional area less than the area of the stopper recess, means to center the lower end of said rod-on said diaphragm, said actuating rod extending upwardly to a location above the upper end of said stopper flange, and an inverted cup shaped resilient closure member having a skirt portion engaging the stopper flange, said skirt portion having an inwardly directed bead thereon engaging in said groove about said bottle neck portion, said closure having means thereon engaging the upper end of said rod to center the rod.

3. In a container wherein a fresh drug solution may be prepared, a bottle having a body portion and a neck portion of reduced diameter, the upper end of said neck portion having an annular peripheral flange defining an annular groove about said neck portion adjacent to said body portion, a stopper within said neck portion and having an outwardly directed annular flange resting on the upper end of said neck portion, said stopper having an annular wall defining a recess adapted to hold a quantity of a drug, a diaphragm integral with said annular wall and extending across and closing said recess, there being a pair of opposed annular V-shaped grooves on opposite sides of said diaphragm and forming a removable section, said removable section having a central indentation, an actuating rod in the stopper recess, said rod having a cross sectional area less than the area of the stopper recess and having its lower end arranged in said indentation, said actuating rod extending upwardly to a location above the upper end of said stopper flange, and an inverted cup shaped resilient closure member having a skirt portion extending over the stopper flange, said skirt portion having an inwardly directed bead thereon engaging in said groove about said bottle neck portion, said closure having a depending collar engaging the upper end of said rod.

4. In a container wherein a fresh solution may be prepared, a bottle having a body portion and a neck portion, a stopper within said neck portion and having an outwardly directed annular flange resting on the upper end of said neck portion, said stopper having an annular wall defining a recess adapted to hold a quantity of a drug, a removable diaphragm integral with said annular wall and closing said recess, an actuating rod in said stopper recess, said rod having a cross sectional area less than, the area of the stopper recess, said actuating rod extending upwardly to a location above the upper end of said stopper flange, and an inverted cup shaped resilient closure member having a skirt portion engaging the stopper flange and the bottle neck portion.

ARTHUR E. SMITH.

References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 2,251,527 Smith Aug. 5, 1941, 2,275,567 Smith Mar. 10,1942 2,524,366 Smith Oct. 3, 1950 2,524,607 Smith Oct. 3, 1950

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