US701438A - Compressed tablet. - Google Patents
Compressed tablet. Download PDFInfo
- Publication number
- US701438A US701438A US9329602A US1902093296A US701438A US 701438 A US701438 A US 701438A US 9329602 A US9329602 A US 9329602A US 1902093296 A US1902093296 A US 1902093296A US 701438 A US701438 A US 701438A
- Authority
- US
- United States
- Prior art keywords
- tablet
- pill
- chemicals
- compressed tablet
- dry
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000007891 compressed tablet Substances 0.000 title description 4
- 239000000126 substance Substances 0.000 description 17
- 239000003826 tablet Substances 0.000 description 17
- 239000006187 pill Substances 0.000 description 13
- 239000003153 chemical reaction reagent Substances 0.000 description 7
- 239000003814 drug Substances 0.000 description 7
- 229940079593 drug Drugs 0.000 description 7
- 239000002131 composite material Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000011790 ferrous sulphate Substances 0.000 description 2
- 235000003891 ferrous sulphate Nutrition 0.000 description 2
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 2
- YPJCVYYCWSFGRM-UHFFFAOYSA-H iron(3+);tricarbonate Chemical compound [Fe+3].[Fe+3].[O-]C([O-])=O.[O-]C([O-])=O.[O-]C([O-])=O YPJCVYYCWSFGRM-UHFFFAOYSA-H 0.000 description 2
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 239000004277 Ferrous carbonate Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 235000019268 ferrous carbonate Nutrition 0.000 description 1
- RAQDACVRFCEPDA-UHFFFAOYSA-L ferrous carbonate Chemical compound [Fe+2].[O-]C([O-])=O RAQDACVRFCEPDA-UHFFFAOYSA-L 0.000 description 1
- 229960004652 ferrous carbonate Drugs 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910000015 iron(II) carbonate Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 229940093956 potassium carbonate Drugs 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000036647 reaction Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2072—Pills, tablets, discs, rods characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms
- A61K9/2086—Layered tablets, e.g. bilayer tablets; Tablets of the type inert core-active coat
Definitions
- My invention has relation to a novel form of compressed tablet, pill, or the like, and has for its object the provision of means whereby may be given appropriate doses in proper proportions of two drugs having the property of reacting when wet and producing in a nascent r5 or fresh condition acompound having therapeutic properties.
- My present 5 invention provides a novel and improved means to this end and includes anovel-process for producing such means with a considerably-diminished expense.
- myinvention is not limited to use of the specific reagents or drugs herein named nor to pills or tablets for the final production of any one chemical substance.
- the tablet is shown as produced in two layers in contact through the middle.
- the relative thickness of these layers may be whatever proves desirable in prac- 5 5 tice, and the size of the tablet usually depends upon the quantity appropriate for a single dose of the drug in question.
- a layer of one of the reagents such, for instance, as carbonate of potash (K OO,)while the layer 2 represents the layer of the second reagentas, for instance, ferrous sulfate, (FeSO Upon solution either in water, before taking, or in the stomach these reagents produce a 6 5 greenish ferrous carbonate, which is the beneficial agent in Blauds pills. In a short time, however, this substance if exposed to the air absorbs oxygen, changes color, and becomes ferric carbonate, Fe (CO which is valueless as a drug.
- my improved tablet or pill may be produced by any desired process. Any Well-known tablet-mold being used, it is first filled to a proper depth with one of the reagents in a 0 dry powdered form. Upon this I place the .proper quantity of the second reagent in the same form and apply the necessary degree of pressure. There is thus required only a single compression-stroke and the resultant composite tablet willprove permanent and fit for sale and shipment.
- What I claim is 1.
- the method of making composite dry tablets or pills which consists in forming a layer of a dry powdered chemical, then forming a second layer in contact with the first of a dry powdered chemical capable of reaction with the first chemical and compressing the entire mass.
- a composite pill or tablet consisting of two parts or sections of dry chemicals compressed together in contact the one section with the other, said chemicals being adapted when wet to react and produce a desired drn g.
- a composite pill or tablet consisting of two layers of different chemicals compressed together in contact, said chemicals being adapted when wet to react and produce a desired drug.
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- Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Preparation (AREA)
Description
UNITED STATES,
PATENT OFFICE.
ROBERT M. \VIIYTE, OF JERSEY CITY, NEW JERSEY, ASSIGNOR TO SCHIEF- FELIN AND COMPANY, OF NEW YORK, N. Y., A COPARTNERSHIP.
COM PRESSED TABLET.
SPECIFICATION forming part of Letters Patent No. 701,438, dated June 3, 1902.
Application filed February 10, 1902- Serial No. 93,296- (No specimens.)
To all whom it may concern.-
Be it known that I, ROBERT M. WHYTE, a
citizen of the United States, residingin J ersey City, in the county of Hudson and State of New Jersey, have invented a certain new and useful Improvement in Compressed Tablets or Pills, of which the following is a specification.
My invention has relation to a novel form of compressed tablet, pill, or the like, and has for its object the provision of means whereby may be given appropriate doses in proper proportions of two drugs having the property of reacting when wet and producing in a nascent r5 or fresh condition acompound having therapeutic properties.
Many pharmaceutical preparations are of such a nature as to lose their value in time by more or less rapid oxidation or other chemical change. Such substances are necessarily administered immediately after preparation, and in order to render them conveniently available to ordinary purchasers means must be adopted for separating the constituent parts until the dose is to be given.
It has been found that many substances useful in producing a desired drug react more or less rapidly even when mixed dry, and are thus subject to deterioration. To prevent this, expensive and complicated devices have been resorted to in producing doses of such drugs for universal consumption in a form insuring the separation of the two reagents until the dose is administered. My present 5 invention provides a novel and improved means to this end and includes anovel-process for producing such means with a considerably-diminished expense.
My invention is illustrated in the accompanying drawing, which illustrates in central section a preferred form of my improved tablet or pill.
For greater clearness I shall describe myinvention as applied to the production of nascentferrous carbonate by the reagents used in what are known as Blauds pills. It is to be understood, however, that my invention is not limited to use of the specific reagents or drugs herein named nor to pills or tablets for the final production of any one chemical substance.
In the drawing the tablet is shown as produced in two layers in contact through the middle. The relative thickness of these layers may be whatever proves desirable in prac- 5 5 tice, and the size of the tablet usually depends upon the quantity appropriate for a single dose of the drug in question.
In the drawing is shown at l a layer of one of the reagentssuch, for instance, as carbonate of potash (K OO,)while the layer 2 represents the layer of the second reagentas, for instance, ferrous sulfate, (FeSO Upon solution either in water, before taking, or in the stomach these reagents produce a 6 5 greenish ferrous carbonate, which is the beneficial agent in Blauds pills. In a short time, however, this substance if exposed to the air absorbs oxygen, changes color, and becomes ferric carbonate, Fe (CO which is valueless as a drug.
I have found that if the dry potassium car bonate and ferrous sulfate be intimately mixed and compressed into a tablet there will be a react-ion soon resulting in the production of ferric carbonate and consequent deterioration of the tablet. On the other hand, by compressing these reagents together in layers, as shown at 1 and 2, the reaction can only take place along the surface of contact, and I have found that here the extent of the reaction is so small as not to materially impair the value of the tablet.
In making my pill or tablet I prefer the following cheap and simple method, although it 8 5 is to be understood that in its broadest aspect .my improved tablet or pill may be produced by any desired process. Any Well-known tablet-mold being used, it is first filled to a proper depth with one of the reagents in a 0 dry powdered form. Upon this I place the .proper quantity of the second reagent in the same form and apply the necessary degree of pressure. There is thus required only a single compression-stroke and the resultant composite tablet willprove permanent and fit for sale and shipment.
While my invention is not limited in its broadest aspect to the use of any given substance, there are certain chemicals which are known to react and produce a gaseous product in material proportions. Such chemicals are not appropriate for use where the tablets are to be kept long before using, as there is apt to be such a disengagement of gas along the surface of contact as to split the tablet in two. It is further obvious that while in the drawing 1 have shown the two parts of my tablet or pill set one beneath the other the same end is attained where the two parts or layers are set side by side in contact, although the form shown is preferable, as it facilitates the operation of compression in the mold.
What I claim is 1. The method of making composite dry tablets or pills which consists in forming a layer of a dry powdered chemical, then forming a second layer in contact with the first of a dry powdered chemical capable of reaction with the first chemical and compressing the entire mass.
2. A composite pill or tablet consisting of two parts or sections of dry chemicals compressed together in contact the one section with the other, said chemicals being adapted when wet to react and produce a desired drn g.
3. A composite pill or tablet consisting of two layers of different chemicals compressed together in contact, said chemicals being adapted when wet to react and produce a desired drug.
4. In a composite pill or tablet consisting of dry chemicals which tend when mixed and compressed together to suffer deterioration, a section of each of such chemicals unmixed with the other, said two sections being com- ROBERT M. \VIIYTE.
W'itnesses:
C. W'Ml MONTGOMERY, XVM. JAY SCHIEFFELIN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9329602A US701438A (en) | 1902-02-10 | 1902-02-10 | Compressed tablet. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9329602A US701438A (en) | 1902-02-10 | 1902-02-10 | Compressed tablet. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US701438A true US701438A (en) | 1902-06-03 |
Family
ID=2769969
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US9329602A Expired - Lifetime US701438A (en) | 1902-02-10 | 1902-02-10 | Compressed tablet. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US701438A (en) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2757124A (en) * | 1952-03-08 | 1956-07-31 | Merck & Co Inc | Tablets and method of producing same |
| US2798443A (en) * | 1954-07-21 | 1957-07-09 | Smith Kline French Lab | Multilayer tablet compressing machine |
| US2809917A (en) * | 1955-10-17 | 1957-10-15 | Victor M Hermelin | Sustained release pharmaceutical tablets |
| US2944493A (en) * | 1956-11-23 | 1960-07-12 | Stokes F J Corp | Multi-layer tablet manufacture |
| US2951792A (en) * | 1959-11-18 | 1960-09-06 | Smith Kline French Lab | Sustained release pharmaceutical tablets |
| US3048526A (en) * | 1958-08-04 | 1962-08-07 | Wander Company | Medicinal tablet |
| US3269905A (en) * | 1955-03-02 | 1966-08-30 | Charles W Damaskus | Dry stratiform products and methods of producing same |
| US3873685A (en) * | 1973-09-10 | 1975-03-25 | Fmc Corp | Contiguous shaped chlorine releasing structure |
| US5431918A (en) * | 1992-10-30 | 1995-07-11 | Soremartec S.A. | Breath mint configuration |
| US6663892B1 (en) | 2002-08-19 | 2003-12-16 | L. Perrigo Company | Multiple portion tablet |
| US20040180089A1 (en) * | 2002-12-26 | 2004-09-16 | Pozen Inc. | Multilayer dosage forms containing NSAIDs and triptans |
| US8022095B2 (en) | 1996-08-16 | 2011-09-20 | Pozen, Inc. | Methods of treating headaches using 5-HT agonists in combination with long-acting NSAIDs |
-
1902
- 1902-02-10 US US9329602A patent/US701438A/en not_active Expired - Lifetime
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2757124A (en) * | 1952-03-08 | 1956-07-31 | Merck & Co Inc | Tablets and method of producing same |
| US2798443A (en) * | 1954-07-21 | 1957-07-09 | Smith Kline French Lab | Multilayer tablet compressing machine |
| US3269905A (en) * | 1955-03-02 | 1966-08-30 | Charles W Damaskus | Dry stratiform products and methods of producing same |
| US2809917A (en) * | 1955-10-17 | 1957-10-15 | Victor M Hermelin | Sustained release pharmaceutical tablets |
| US2944493A (en) * | 1956-11-23 | 1960-07-12 | Stokes F J Corp | Multi-layer tablet manufacture |
| US3048526A (en) * | 1958-08-04 | 1962-08-07 | Wander Company | Medicinal tablet |
| US2951792A (en) * | 1959-11-18 | 1960-09-06 | Smith Kline French Lab | Sustained release pharmaceutical tablets |
| US3873685A (en) * | 1973-09-10 | 1975-03-25 | Fmc Corp | Contiguous shaped chlorine releasing structure |
| US5431918A (en) * | 1992-10-30 | 1995-07-11 | Soremartec S.A. | Breath mint configuration |
| US8022095B2 (en) | 1996-08-16 | 2011-09-20 | Pozen, Inc. | Methods of treating headaches using 5-HT agonists in combination with long-acting NSAIDs |
| US6663892B1 (en) | 2002-08-19 | 2003-12-16 | L. Perrigo Company | Multiple portion tablet |
| US20040180089A1 (en) * | 2002-12-26 | 2004-09-16 | Pozen Inc. | Multilayer dosage forms containing NSAIDs and triptans |
| US7332183B2 (en) * | 2002-12-26 | 2008-02-19 | Pozen Inc. | Multilayer dosage forms containing NSAIDs and triptans |
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