US2622598A - Drain-clear container for aqueous liquid pharmaceutical preparations - Google Patents
Drain-clear container for aqueous liquid pharmaceutical preparations Download PDFInfo
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- US2622598A US2622598A US214561A US21456151A US2622598A US 2622598 A US2622598 A US 2622598A US 214561 A US214561 A US 214561A US 21456151 A US21456151 A US 21456151A US 2622598 A US2622598 A US 2622598A
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- 239000007788 liquid Substances 0.000 title description 16
- 239000000825 pharmaceutical preparation Substances 0.000 title description 13
- 229920001296 polysiloxane Polymers 0.000 description 49
- 239000003795 chemical substances by application Substances 0.000 description 24
- 239000002518 antifoaming agent Substances 0.000 description 23
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- 239000005871 repellent Substances 0.000 description 6
- 239000007900 aqueous suspension Substances 0.000 description 5
- 239000008135 aqueous vehicle Substances 0.000 description 5
- 239000006260 foam Substances 0.000 description 5
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 4
- KZDCMKVLEYCGQX-UDPGNSCCSA-N 2-(diethylamino)ethyl 4-aminobenzoate;(2s,5r,6r)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid;hydrate Chemical group O.CCN(CC)CCOC(=O)C1=CC=C(N)C=C1.N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 KZDCMKVLEYCGQX-UDPGNSCCSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical class O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 230000008602 contraction Effects 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000012780 transparent material Substances 0.000 description 2
- 239000003981 vehicle Substances 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 229930182555 Penicillin Natural products 0.000 description 1
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 1
- 229920002323 Silicone foam Polymers 0.000 description 1
- NWGKJDSIEKMTRX-AAZCQSIUSA-N Sorbitan monooleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-AAZCQSIUSA-N 0.000 description 1
- IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 description 1
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
- PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 1
- 239000004147 Sorbitan trioleate Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- FBZANXDWQAVSTQ-UHFFFAOYSA-N dodecamethylpentasiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C FBZANXDWQAVSTQ-UHFFFAOYSA-N 0.000 description 1
- 229940087203 dodecamethylpentasiloxane Drugs 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000003028 elevating effect Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 1
- 229940073561 hexamethyldisiloxane Drugs 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229940049954 penicillin Drugs 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 239000006069 physical mixture Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- -1 polysiloxane Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229920006268 silicone film Polymers 0.000 description 1
- 239000013514 silicone foam Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 229950004959 sorbitan oleate Drugs 0.000 description 1
- 229950003429 sorbitan palmitate Drugs 0.000 description 1
- 229950011392 sorbitan stearate Drugs 0.000 description 1
- 229960000391 sorbitan trioleate Drugs 0.000 description 1
- 235000019337 sorbitan trioleate Nutrition 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 125000005425 toluyl group Chemical group 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D23/00—Details of bottles or jars not otherwise provided for
- B65D23/02—Linings or internal coatings
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S215/00—Bottles and jars
- Y10S215/06—Resin-coated bottles
Definitions
- My invention relates to drain-clear containers for aqueous liquid pharmaceutical preparations (hereinafter referred to as aqueous pharmaceuticals)
- aqueous pharmaceuticals aqueous liquid pharmaceutical preparations
- the present invention is an improvement of the drain-clear container shown, described and claimed in U. S. Letters Patent No. 2,504,482 issued April 18, 1950 to the assignee of the instant application.
- aqueous base pharmaceuticals a container whose interior surface has a film which not only will permit the container to drain clear, but to drain clear very rapidly, for example, in as little as five seconds.
- my invention is achieved by providing a pharmaceutical container with an internal surface which has been rendered waterrepellent by silicone treatment and which also has been treated, preferably at the same time, with a silicone antifoam agent.
- pharmaceutical container I refer to any type of vessel which can receive and hold an aqueous-vehicle pharmaceutical preparation. Typical of such containers are vials, bottles, ampoules, hypodermic syringes, pipettes and burettes.
- silicones I refer to organo-polysiloxanes, i. e. organo-silicon oxide polymers.
- antifoam agen I refer to a composition which has the ability to prevent or rapidly dispel foam when incorporated in the liquid wherein the foam is to be suppressed.
- a silicone and a silicone antifoam agent carried in a vaporizable liquid vehicle are applied to the internal surfaces to be treated, as, for example, by rinsing the inside of a container with a liquid containing a silicone and a silicone antifoam agent dissolved or dispersed in such liquid. Thereafter, the liquid is evaporated, thus leaving a very thin, transparent solid film of the silicone and silicone antifoam agent.
- Said film is water-repellent so that when a container thus treated, and containing an aqueous-vehicle pharmaceutical preparation is emptied, the film which normally would remain on its internal surfaces contracts into globules which fall toward the bottom of the container and leave the walls clean.
- my invention is achieved by I have observed that. such dissolving a silicone and a silicone antifoam agent in an organic solvent, such as chloroform or ether.
- the composite fluid, solvent and solutes is introduced into a container. Thereafter, the composite fluid is drained out, leaving a film thereof on the inner wall of the container.
- the solvent in this film is permitted to evaporate.
- evaporation may proceed at room temperatures, and satisfactory results are secured in such fashion. Even better results are obtained where the solvent not only is evaporated, but the residual film of the silicone and the silicone antifoam agent is heat-treated to bake the same.
- Such heat treatment consists in elevating the temperature of the container to any point above room temperature and below a temperature at which the silicone or the silicone antifoam agent vaporizes from the container surface.
- the actual temperature used is not critical. It is believed that the layer of silicone and silicone antifoam agent is molecularly fused to the walls of the container, particularly when the container is glass.
- Organo-polysiloxanes which function satisfactorily in the practice of my invention are of the formula where n is any integral number and R is any single alkyl or aryl group or combination thereof, that is to say different R groups may be combined in a single organo-polysiloxane to add up to. the total number of R groups required by the formula.
- the alkyl groups may be saturated or unsaturated and examples thereof are methyl, ethyl, propyl, butyl, amyl, hexyl, heptyl, octyl, decyl, dodecyl, vinyl and allyl.
- Examples of the aryl groups are phenyl, toluyl and naphthyl. Satisfactory silicones are:
- Silicone antifoam agents which function satisfactorily in the practice of my invention are mixtures of alkyl silicones such as described above and unsubstituted silica, an example of the same being a physical mixture of methyl polysiloxane and finely divided silica.
- a silicone antifoam agent such as described is characterized by its ability, when added to a liquid, to prevent or suppress foam, it being noted that as already mentioned said antifoam agent in accordance with my invention is not added to the liquid pharmaceutical preparation, but, as a solid,
- a suitable baking time is one-half hour at 300 0., or nine hours at 180 C.
- silicones or silicone antifoam agents the same percentages by weight can be used as well as the same baking temperature and time provided that the temperature does not exceed that at which the silicone or silicone antifoam agent will vaporize from the container surface.
- the film of water repellent silicone and silicone antifoam agent is transparent, the best visual results are obtained when the container likewise is made of transparent material such as glass, for example.
- a film applied in the manner described is so thin that its thickness is measured in hundreds of molecules.
- a typical aqueous pharmaceutical preparation which the container is adapted to dispense is a procaine penicillin in aqueous suspension, said pharmaceutical containing a slight amount, e. g. 0.1% by weight of a surface-active agent to maintain the stability of the suspension after the same has been agitated.
- Suitable surfaceactive agents that may be employed are: sorbitan polyoxyalkylene monolaurate, sorbitan polyoxyalkylene palniitate, sorbitan polyoxyalkylene stearate, sorbitan polyoxyalkylene oleate, sorbitan monolaurate, sorbitan palmitate, sorbitan stearate, sorbitan oleate, and sorbitan trioleate.
- the same may be washed either with water, or soap and water, without affecting the applied film.
- a pharmaceutical container constituting a transparent glass bottle l0 whose internal surface has been coated, as aforesaid, with a thin transparent film I2 of a silicone and a silicone antifoam agent.
- the interior surface thereby is rendered water-repellent and is characterized by its ability to prevent or suppress foam in a liquid aqueouspharmaceutical preparation held by the container.
- the film is extremely thin. However, its thickness has beenv increased, as illustrated in the drawing, so that the same can be seen and a reference numeral applied thereto.
- the bottle is filled with an opaque aqueous-vehicle liquid pharmaceutical preparation l4, such for example, as procaine penicillin in aqueous suspension, the same containing a slight amount of a surface-active agent.
- the silicone and the silicone antifoam agent maybe applied separately to the internal surfaces to be treated.
- Either the silicone or the silicone antifoam agent can be appliedv first and the manner of individual application can be the same as the manner of joint application outlined hereinabove.
- a clear-draining dispensing container of transparent material filled with an aqueousvehicle liquid pharmaceutical preparation said container having on its internal surface a thin transparent film of a silicone and a silicone antifoam agent whereby when said pharmaceutical preparation is dispensed, the container will drain clear rapidly.
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- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Medical Preparation Storing Or Oral Administration Devices (AREA)
Description
Dec. 23, 1952 H. ROSENBLUM 2,622,598
DRAIN-CLEAR CONTAINER FOR AQUEOUS LIQUID PHARMACEUTICAL PREPARATIONS Filed March 8 1951 I TRANSPARENT BOTTLE OPAQUE AQUEOUS- Z VEHICLE LIQUID PHARMACEUTICAL, mg. penicillin in aqueous suspension THIN TRANSPARENT FILM 0F SILICONE AND SILICONE ANTI- FOAM AGENT ATTORNEY Patented Dec. 23, 1952 DRAIN-CLEAR CONTAINER FOR AQUEOUS LIQUID PHARMACEUTICAL PREPARATIONS Harold Rosenblum, Hackensack, N. J assignor to Premo Pharmaceutical Laboratories, Inc.,
South Hackensack, N. J a corporation of New York Application March 8, 1951, Serial No. 214,561
2 Claims.
My invention relates to drain-clear containers for aqueous liquid pharmaceutical preparations (hereinafter referred to as aqueous pharmaceuticals) The present invention is an improvement of the drain-clear container shown, described and claimed in U. S. Letters Patent No. 2,504,482 issued April 18, 1950 to the assignee of the instant application.
As pointed out in said patent, coating the internal surface of a dispensing container with a thin, transparent water-repellent silicone film will cause the container to drain clear when an aqueous-vehicle liquid pharmaceutical preparation is dispensed therefrom. A typical preparation of such character is procaine penicillin in aqueous suspension. It has been observed, that although such a container has the ability to drain clear, there is a tendency for a film to cling to the inside of the container for a short time, thereby somewhat delaying the time in which it drains clear. A container treated in accordance with said patent and filled with an aqueous suspension of procaine penicillin takes about thirty seconds to drain clear. In the event that all the pharmaceutical preparation is withdrawn rapidly from the container, although the film temporarily clinging to the walls of the container is extremely thin and therefore constitutes but a very small percentage of the containers original contents, the presence of the film does represent some wastage and may leave the doctor unsure that he has secured a correct dose from a container which is not supposed to have any film left on its walls.
Accordingly, it is an object of the present in vention to provide for aqueous base pharmaceuticals a container whose interior surface has a film which not only will permit the container to drain clear, but to drain clear very rapidly, for example, in as little as five seconds.
Other objects of my invention will in part be" obvious and in part will be pointed out hereinafter.;
In the accompanying drawing in which is shown one of the various possible embodiments of my invention, the single figure is an elevation view, partially broken away, of a bottle having a film such as described hereinabove.
I believe that the tendency to leave on the walls of the container for a short period of time, in the order of a half a minute, a residual film of the containers contents is due to the presence of bubbles in the preparation after the same has been shaken prior to aspirating the pharmaceutical into a hypodermic syringe. Upon occasion, these bubbles are visible, particularly when the-- In general, I carry out my invention by incorporating in the water-repellent film which is provided on the internal surfaces of the container, a foam inhibitor, and more particularly a silicone foam inhibitor.
More specifically, my invention is achieved by providing a pharmaceutical container with an internal surface which has been rendered waterrepellent by silicone treatment and which also has been treated, preferably at the same time, with a silicone antifoam agent. By pharmaceutical container, I refer to any type of vessel which can receive and hold an aqueous-vehicle pharmaceutical preparation. Typical of such containers are vials, bottles, ampoules, hypodermic syringes, pipettes and burettes. By silicones," I refer to organo-polysiloxanes, i. e. organo-silicon oxide polymers. By antifoam agen I refer to a composition which has the ability to prevent or rapidly dispel foam when incorporated in the liquid wherein the foam is to be suppressed.
In practicing the invention, a silicone and a silicone antifoam agent carried in a vaporizable liquid vehicle are applied to the internal surfaces to be treated, as, for example, by rinsing the inside of a container with a liquid containing a silicone and a silicone antifoam agent dissolved or dispersed in such liquid. Thereafter, the liquid is evaporated, thus leaving a very thin, transparent solid film of the silicone and silicone antifoam agent. Said film is water-repellent so that when a container thus treated, and containing an aqueous-vehicle pharmaceutical preparation is emptied, the film which normally would remain on its internal surfaces contracts into globules which fall toward the bottom of the container and leave the walls clean. Moreover, I have discovered that such film has the property of very substantially speeding up the contraction of the film into globules. a marked speed up of the contraction of the film actually takes place where the coating on the inside of the container includes an antifoam agent in addition to a water-repellent agent. Thi increased speed of clear-draining occurs whether a surface active agent is present in the pharmaceutical composition or not, but is more marked where such an agent has been added.
More specifically, my invention is achieved by I have observed that. such dissolving a silicone and a silicone antifoam agent in an organic solvent, such as chloroform or ether. The composite fluid, solvent and solutes, is introduced into a container. Thereafter, the composite fluid is drained out, leaving a film thereof on the inner wall of the container. The solvent in this film is permitted to evaporate. Optionally, evaporation may proceed at room temperatures, and satisfactory results are secured in such fashion. Even better results are obtained where the solvent not only is evaporated, but the residual film of the silicone and the silicone antifoam agent is heat-treated to bake the same. Such heat treatment consists in elevating the temperature of the container to any point above room temperature and below a temperature at which the silicone or the silicone antifoam agent vaporizes from the container surface. In general, the higher the temperature employed, the less time is required for baking. The actual temperature used is not critical. It is believed that the layer of silicone and silicone antifoam agent is molecularly fused to the walls of the container, particularly when the container is glass.
Organo-polysiloxanes which function satisfactorily in the practice of my invention are of the formula where n is any integral number and R is any single alkyl or aryl group or combination thereof, that is to say different R groups may be combined in a single organo-polysiloxane to add up to. the total number of R groups required by the formula. The alkyl groups may be saturated or unsaturated and examples thereof are methyl, ethyl, propyl, butyl, amyl, hexyl, heptyl, octyl, decyl, dodecyl, vinyl and allyl. Examples of the aryl groups are phenyl, toluyl and naphthyl. Satisfactory silicones are:
Hexamethyl disiloxane (CH3) sSizO Dodecamethyl pentasiloxane (CH3)12S1504 Methylphenylpolysiloxane where a: is any integral number less than 2n+2.
Other satisfactory silicones have the same formulae except that for the methyl groups in the first two silicones and for the methyl and phenyl groups in the last silicone any other aryl or alkyl groups can be substituted.
It may be mentioned that in commercial silicones 11. reaches very high values and the chain is so long that the values of n are not used to denote the compounds, but rather physical properties are employed for this purpose. The physical property commonly employed is viscosity. I have found silicones of all viscosities to be operable in the practice of my invention-even as high as 100,000 centistokes.
Silicone antifoam agents which function satisfactorily in the practice of my invention are mixtures of alkyl silicones such as described above and unsubstituted silica, an example of the same being a physical mixture of methyl polysiloxane and finely divided silica. A silicone antifoam agent such as described is characterized by its ability, when added to a liquid, to prevent or suppress foam, it being noted that as already mentioned said antifoam agent in accordance with my invention is not added to the liquid pharmaceutical preparation, but, as a solid,
forms part of a coating for the internal surface 7 of, a pharmaceutical container.
4 By way of example and without limiting my invention thereto, the following constitutes a specific embodiment of a composite fluid with which I have secured very good results:
1 part by weight of methyl silicone fluid viscosity 50 centistokes 0.1 part by weight of silicone antifoam agent Enough chloroform to make up parts by weight.
Satisfactory results have been obtained with the silicone antifoam agent varying from as little as 0.0005 to 0.2 part by weight in the foregoing formulation. A suitable baking time is one-half hour at 300 0., or nine hours at 180 C.
Where other silicones or silicone antifoam agents are employed, the same percentages by weight can be used as well as the same baking temperature and time provided that the temperature does not exceed that at which the silicone or silicone antifoam agent will vaporize from the container surface.
Inasmuch as the film of water repellent silicone and silicone antifoam agent is transparent, the best visual results are obtained when the container likewise is made of transparent material such as glass, for example. A film applied in the manner described is so thin that its thickness is measured in hundreds of molecules.
A typical aqueous pharmaceutical preparation which the container is adapted to dispense is a procaine penicillin in aqueous suspension, said pharmaceutical containing a slight amount, e. g. 0.1% by weight of a surface-active agent to maintain the stability of the suspension after the same has been agitated. Suitable surfaceactive agents that may be employed are: sorbitan polyoxyalkylene monolaurate, sorbitan polyoxyalkylene palniitate, sorbitan polyoxyalkylene stearate, sorbitan polyoxyalkylene oleate, sorbitan monolaurate, sorbitan palmitate, sorbitan stearate, sorbitan oleate, and sorbitan trioleate.
If it is desired to reuse a container whose internal surface has been treated in accordance with the foregoing process, the same may be washed either with water, or soap and water, without affecting the applied film.
In the drawing I have shown a pharmaceutical container constituting a transparent glass bottle l0 whose internal surface has been coated, as aforesaid, with a thin transparent film I2 of a silicone and a silicone antifoam agent. The interior surface thereby is rendered water-repellent and is characterized by its ability to prevent or suppress foam in a liquid aqueouspharmaceutical preparation held by the container. As noted heretofore, the film is extremely thin. However, its thickness has beenv increased, as illustrated in the drawing, so that the same can be seen and a reference numeral applied thereto. The bottle is filled with an opaque aqueous-vehicle liquid pharmaceutical preparation l4, such for example, as procaine penicillin in aqueous suspension, the same containing a slight amount of a surface-active agent.
If desired, the silicone and the silicone antifoam agent maybe applied separately to the internal surfaces to be treated. Either the silicone or the silicone antifoam agent can be appliedv first and the manner of individual application can be the same as the manner of joint application outlined hereinabove.
It thus will be seen that I have provided a container which achieves the several objects of my invention and is well adapted to meet the conditions of practical use.
As various possible embodiments might be made of the above invention, and as various changes might be made in the embodiment above set forth, it is to be understood that all matter herein described and. shown in the accompanying drawings is to be interpreted as illustrative and not in a limiting sense.
Having thus described my invention, I claim as new and desire to secure by Letters Patent:
1. A clear-draining dispensing container of transparent material filled with an aqueousvehicle liquid pharmaceutical preparation, said container having on its internal surface a thin transparent film of a silicone and a silicone antifoam agent whereby when said pharmaceutical preparation is dispensed, the container will drain clear rapidly.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,504,482 Goldman Apr. 18, 1950 2,523,281 Currie Sept. 26, 1950 2,573,637 Bender Oct. 30, 1951
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US214561A US2622598A (en) | 1951-03-08 | 1951-03-08 | Drain-clear container for aqueous liquid pharmaceutical preparations |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US214561A US2622598A (en) | 1951-03-08 | 1951-03-08 | Drain-clear container for aqueous liquid pharmaceutical preparations |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2622598A true US2622598A (en) | 1952-12-23 |
Family
ID=22799558
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US214561A Expired - Lifetime US2622598A (en) | 1951-03-08 | 1951-03-08 | Drain-clear container for aqueous liquid pharmaceutical preparations |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2622598A (en) |
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2785985A (en) * | 1954-03-09 | 1957-03-19 | Paul L Magill | Glass containers for alcoholic beverages |
| US2830721A (en) * | 1956-03-28 | 1958-04-15 | Plax Corp | Plastic coated articles |
| US2872923A (en) * | 1957-03-20 | 1959-02-10 | Birch And Gattone Inc | Means for administering pressurized medicaments, gases, combinations thereof and liquids into body cavities |
| US2926094A (en) * | 1957-07-16 | 1960-02-23 | Robert J Herbold | A method of processing and sterilizing milk |
| US3182839A (en) * | 1963-03-29 | 1965-05-11 | American Can Co | Glass container |
| US3424218A (en) * | 1966-12-07 | 1969-01-28 | Garrett Corp | Medical material container |
| US3939834A (en) * | 1974-09-24 | 1976-02-24 | Mcmahon Patrick J | Metal coated articles |
| US5226538A (en) * | 1992-07-29 | 1993-07-13 | The Procter & Gamble Company | Filled package exhibiting a substantially colorless transparent appearance |
| US5858016A (en) * | 1992-07-14 | 1999-01-12 | Baxter International Inc. | Sterile/aseptic connector |
| WO1998043886A3 (en) * | 1997-03-31 | 2002-09-26 | Procter & Gamble | Package providing good drainage to viscous contents |
| US20070090010A1 (en) * | 2005-10-20 | 2007-04-26 | The Procter & Gamble Company | Transparent or translucent filled package exhibiting a colored appearance |
| EP2324845A1 (en) * | 2003-05-13 | 2011-05-25 | Ares Trading S.A. | Liquid stabilized protein formulations in coated pharmaceutical containers |
| US20140311940A1 (en) * | 2013-04-17 | 2014-10-23 | Jonathan Braveman | Closeable silicon container |
| US10391506B2 (en) | 2014-10-28 | 2019-08-27 | 3M Innovative Properties Company | Spray application system components comprising a repellent surface and methods |
| US10584249B2 (en) | 2015-10-28 | 2020-03-10 | 3M Innovative Properties Company | Articles subject to ice formation comprising a repellent surface |
| US10907070B2 (en) | 2016-04-26 | 2021-02-02 | 3M Innovative Properties Company | Articles subject to ice formation comprising a repellent surface comprising a siloxane material |
| US10946399B2 (en) | 2016-04-26 | 2021-03-16 | 3M Innovative Properties Company | Liquid reservoirs and articles comprising a repellent surface comprising a siloxane material |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2504482A (en) * | 1949-06-17 | 1950-04-18 | Premo Pharmaceutical Lab Inc | Drain-clear container for aqueous-vehicle liquid pharmaceutical preparations |
| US2523281A (en) * | 1950-09-26 | automobile polish | ||
| US2573637A (en) * | 1950-05-22 | 1951-10-30 | Lilly Co Eli | Treated stopper for and method of introducing antifoam agent into a liquid medicament or the like |
-
1951
- 1951-03-08 US US214561A patent/US2622598A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2523281A (en) * | 1950-09-26 | automobile polish | ||
| US2504482A (en) * | 1949-06-17 | 1950-04-18 | Premo Pharmaceutical Lab Inc | Drain-clear container for aqueous-vehicle liquid pharmaceutical preparations |
| US2573637A (en) * | 1950-05-22 | 1951-10-30 | Lilly Co Eli | Treated stopper for and method of introducing antifoam agent into a liquid medicament or the like |
Cited By (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2785985A (en) * | 1954-03-09 | 1957-03-19 | Paul L Magill | Glass containers for alcoholic beverages |
| US2830721A (en) * | 1956-03-28 | 1958-04-15 | Plax Corp | Plastic coated articles |
| US2872923A (en) * | 1957-03-20 | 1959-02-10 | Birch And Gattone Inc | Means for administering pressurized medicaments, gases, combinations thereof and liquids into body cavities |
| US2926094A (en) * | 1957-07-16 | 1960-02-23 | Robert J Herbold | A method of processing and sterilizing milk |
| US3182839A (en) * | 1963-03-29 | 1965-05-11 | American Can Co | Glass container |
| US3424218A (en) * | 1966-12-07 | 1969-01-28 | Garrett Corp | Medical material container |
| US3939834A (en) * | 1974-09-24 | 1976-02-24 | Mcmahon Patrick J | Metal coated articles |
| US5858016A (en) * | 1992-07-14 | 1999-01-12 | Baxter International Inc. | Sterile/aseptic connector |
| US5226538A (en) * | 1992-07-29 | 1993-07-13 | The Procter & Gamble Company | Filled package exhibiting a substantially colorless transparent appearance |
| WO1998043886A3 (en) * | 1997-03-31 | 2002-09-26 | Procter & Gamble | Package providing good drainage to viscous contents |
| EP1633388B1 (en) * | 2003-05-13 | 2014-03-19 | Ares Trading S.A. | Liquid stabilized interferon-beta formulations in coated pharmaceutical containers |
| EP2324845A1 (en) * | 2003-05-13 | 2011-05-25 | Ares Trading S.A. | Liquid stabilized protein formulations in coated pharmaceutical containers |
| USRE43331E1 (en) | 2003-05-13 | 2012-05-01 | Ares Trading S.A. | Stabilized liquid protein formulations in pharmaceutical containers |
| US20070090010A1 (en) * | 2005-10-20 | 2007-04-26 | The Procter & Gamble Company | Transparent or translucent filled package exhibiting a colored appearance |
| US20140311940A1 (en) * | 2013-04-17 | 2014-10-23 | Jonathan Braveman | Closeable silicon container |
| US10391506B2 (en) | 2014-10-28 | 2019-08-27 | 3M Innovative Properties Company | Spray application system components comprising a repellent surface and methods |
| US10987686B2 (en) | 2014-10-28 | 2021-04-27 | 3M Innovative Properties Company | Spray application system components comprising a repellent surface and methods |
| US10987685B2 (en) | 2014-10-28 | 2021-04-27 | 3M Innovative Properties Company | Spray application system components comprising a repellent surface and methods |
| US10584249B2 (en) | 2015-10-28 | 2020-03-10 | 3M Innovative Properties Company | Articles subject to ice formation comprising a repellent surface |
| US11136464B2 (en) | 2015-10-28 | 2021-10-05 | 3M Innovative Properties Company | Articles subject to ice formation comprising a repellent surface |
| US10907070B2 (en) | 2016-04-26 | 2021-02-02 | 3M Innovative Properties Company | Articles subject to ice formation comprising a repellent surface comprising a siloxane material |
| US10946399B2 (en) | 2016-04-26 | 2021-03-16 | 3M Innovative Properties Company | Liquid reservoirs and articles comprising a repellent surface comprising a siloxane material |
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