USRE28011E - Pharmaceutical preparation - Google Patents
Pharmaceutical preparation Download PDFInfo
- Publication number
- USRE28011E USRE28011E US28011DE USRE28011E US RE28011 E USRE28011 E US RE28011E US 28011D E US28011D E US 28011DE US RE28011 E USRE28011 E US RE28011E
- Authority
- US
- United States
- Prior art keywords
- formulation
- oxidase
- milligrams
- polyethylene glycol
- sigma
- 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
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/43—Enzymes; Proenzymes; Derivatives thereof
- A61K38/44—Oxidoreductases (1)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y104/00—Oxidoreductases acting on the CH-NH2 group of donors (1.4)
- C12Y104/03—Oxidoreductases acting on the CH-NH2 group of donors (1.4) with oxygen as acceptor (1.4.3)
- C12Y104/03004—Monoamine oxidase (1.4.3.4)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y104/00—Oxidoreductases acting on the CH-NH2 group of donors (1.4)
- C12Y104/03—Oxidoreductases acting on the CH-NH2 group of donors (1.4) with oxygen as acceptor (1.4.3)
- C12Y104/03022—Diamine oxidase (1.4.3.22)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y111/00—Oxidoreductases acting on a peroxide as acceptor (1.11)
- C12Y111/01—Peroxidases (1.11.1)
- C12Y111/01006—Catalase (1.11.1.6)
Definitions
- these amines are destroyed by the application of suitable oxidase enzymes and by the presence of a catalase enzyme which will provide the necessary oxygen.
- the catalase enzyme may in some instances be present in the tissue, or it may be supplied as an ingredient of the preparation.
- FORMULATION B (a) An ointment base and enzyme stabilizing action was compounded by melting 50 grams of polyethylene glycol (Carbowax) 6000 with 30 grams of polyethylene glycol (Carbowax) 1540, and by then cooling the mixture to 50 C.
- Formulation C was found to be very effective in the treatment of hemorrhoids. Moreover, tests were made on all the preceding formulations, and they were found to maintain their activity indefinitely. For example, Formulation B was tested at two month intervals for almost a year and was found to lose none of its activity.
- FORMULATION D (a) An ointment and enzyme stabilizing agent was compounded by melting 25 grams of polyethylene glycol (Carbowax) 6000 with 15 grams of polyethylene glycol (Carbowax) 1540, and by then cooling the mixture to 50 C.
- FORMULATION E (a) An ointment and enzyme stabilizing agent was compounded by melting 25 grams of polyethylene glycol (Carbowax) 6000 with 15 grams of polyethylene glycol (Carbowax) 1540, and by then cooling the mixture to 50 C.
- FORMULATION F (a) An ointment and enzyme stabilizing agent was compounded by melting 25 grams of polyethylene glycol (Carbowax) 6000 with 15 grams of polyethylene glycol (Carbowax) 1540, and by then cooling the mixture to 50 C.
- FORMULATION G (a) An ointment and enzyme stabilizing agent was compound by melting 25 grams polyethylene glycol (Carbowax) 4000 with 20 grams polyethylene glycol (Carbowax) 400 and by cooling the mixture to 50 C.
- FORMULATION H (a) An ointment and enzyme stabilizing agent was compounded by melting 25 grams polyethylene glycol (Carbowax) 4000 with 20 grams polyethylene glycol (Carbowax) 400 and by cooling the mixture to 50 C.
- FORMULATION I (a) An ointment and enzyme stabilizing agent was compounded by melting 25 grams polyethylene glycol (Carbowax) 4000 with 20 grams polyethylene glycol (Carbowax) 400 and by cooling the mixture to 50 C.
- the invention provides, therefore, a formulation which is relatively simple and inexpensive to prepare, and which uses readily available and relatively inexpensive ingredients.
- the formulation is also easy to apply, and it has been found most effective in accomplishing its desired purpose.
- a pharmaceutical formulation for the treatment of hemorrhoids and which includes ingredients in approximately the following proportions: 0.l50 milligrams monoamine oxidase, and 10-20 cubic centimeters of a stabilizing buffer in which said oxidase is dissolved to prevent the formulation from assuming the pH of the area being treated.
- a pharmaceutical formulation for the treatment of hemorrhoids and which includes ingredients in approximately the following proportions: 0.1-50 milligrams monoamine oxidase derived from crude beef plasma and dissolved in 10-20 cubic centimeters of a phosphate buffer of a pH 7.2 and 0.1 molar, said phosphate buffer being selected to hold the pH of the formulation in a predetermined range and to prevent the formulation from assuming the pH of the area being treated.
- a pharmaceutical preparation for the treatment of hemorrhoids and which includes ingredients in approximately the following proportions: 0.1-50 milligrams diamine oxidase; 0.1-50 milligrams catalase; and 10-20 cubic centimeters of a stabilizing bufler in which said oxidase is dissolved to prevent the formulation from assuming the pH of the area being treated.
Abstract
A PHARMACEUTICAL PREPARATION IS PROVIDED FOR THE TREATMENT OF HEMORRHOIDS, AND WHICH CONTAINS OXIDASE ENZYMES, SUCH AS MONOAMINE OXIDASE, OR DIAMINE OXIDASE, OR BOTH. THE OBJECT OF THE INVENTION IS TO DESTROY THE AMINES FROMED IN THE COLON BY BACTERIA. THE AMINES ARE DESTROYED BY THE OXIDIZING ACTION OF THE OXIDASES ON THE TISSUE AND BY THE PRODUCTION OF OXYGEN. THE OXYGEN IS PRODUCED, IN SOME INSTANCES, BY THE ACTION OF THE TISSUE ITSELF, OR A CATALASE ENZYME MAY BE ADDED TO THE PREPARATION WHICH DECOMPOSE THE HYDROGEN PEROXIDE WHICH IS PRESENT INTO WATER OXYGEN.
Description
United States Patent Oflice Re. 28,011 Reissued May 14, 1974 ABSTRACT OF THE DISCLOSURE [This application is a continuation of copending application Ser. No. 864,526, which was filed Oct. 7, 1969, in the name of Matthew C. Urbin, now abandoned] This is a Reissue of Pat. No. 3,639,579, issued Feb. I 1972, which is a continuation of copending application Ser. No. 864,526, now abandoned.
BACKGROUND OF THE INVENTION The enzyme names used in the following specification are drived from Recommendations 1964 of the International Union of Biochemistry published in Comprehensive Biochemistry, Marcel Florkin, Elsevier, Amsterdam, NY. (1965).
In the practice of the present invention, these amines are destroyed by the application of suitable oxidase enzymes and by the presence of a catalase enzyme which will provide the necessary oxygen. The catalase enzyme may in some instances be present in the tissue, or it may be supplied as an ingredient of the preparation.
The action when, for example, a monoamine oxidase is used, may be represented as follows:
Monoamine RCH: NH: or H20 ---0 (Amine) Oxldase 115:0 mo. NH.
The following references are give for the isolation of monoamine oxidase and diamine oxidase. They are typical of the prior art isolation procedures for these enzymes.
Purification monoamine oxidase:
(a) Human Plasma Monoamine Oxidase, Charles M. McEwen, Ir. Journal of Biol. Chem. 240, 2003-10 (1965) (b) Monoamine Oxidase" Hideaki Yamada and Kerry T. Yasunobu Journal of Biol. Chem. 237, 1511-16 (1962) Purification Diamine Oxidase:
(a) Diamine Oxidase, Herbert Tabor, Journal of Biol.
Chem. 188, 125-36 (1951) (b) Purification and Identification of Hog-Kidney Histaminase, R. Kapeller-Adler and H. MacFarland, Biochim. Biophys. Acta 67, 542-65 (1963) (c) Purification of Pig-Kidney Diamine Oxidase and its Identity with Histaminase, B. Mondovi, G. Rotilo, A. Finazzi, and A. Scioscia-Santoro, Biochem. J. 91, 408- 15 (1963) (d) Diamine Oxidase Chapter 11 by E. Albert Zeller, from The Enzymes, volume 8 editors P. D. Boyer, H, Lardy, K. Myrback, Academic Press, New York, 1963 (e) Reinvestigation of the Substrate Specificity of Pig Kidney Diamine Oxidase, W. G. Bardsley, C. M. Hill, and R. W. Lobley, Biochem. J., 117, 169-76 (1970) Recommended Other names not Reference No. Systematic name a1 name recommended 1.4.3.6 Dlamine: oxygen Diamine oxidase histamoxidoreductase inase.
(deaminattng). 1.4.8.4. Monomine: oxygen Monoamlne oxldase Tyramlnase:
oxldoreductase amine oxidase. (dearninatlng). 1.11.1.6 Hydrogen-peroxide: Catslase ydrogen peroxide oxiporeduetase.
All of the enzymes referred to in the following specification, and particularly with respect to the specific formulations, were purchased from Sigma Chemical Co., 3500 DeKalb St., St. Louis, Mo., 63118.
(a) D 7876 Diamine Oxidase Grade II: From Hog Kidney (b) Monoamine Oxidase: Type 1: Crude; From Beef Plasma (c) Catalase: Stock No. C-10 Purified Powder.
The prior art pharmaceutical preparations for the treatment of hemorrhoids are generally not completely satisfactory due primarily to the lack of complete understanding in the prior art as to the cause and cure of hemorrhoids. It has been determined that the cause of itching and swelling in the region of the colon which produces 70 hemorrhoids is due primarily to the formation of amines by bacteria in the colon.
DETAILED DESCRIPTION OF SPECIFIC EMBODIMENTS OF THE INVENTION The following formulations have been made and have proven to be completely satisfactory in immediately terminating itching caused by hemorrhoids, and in reducing the swelling within one or two days.
3 FORMULATION A (a) An ointment base and an enzyme stabilizing agent was compounded by melting 50 grams polyethylene glycol 6000 with 30 grams of polyethylene glycol 1540, and by then cooling the mixture to 50 C.
(b) Five milligrams of monoamine oxidase (Sigma Type 1: crude beef plasma) was then dissolved in 20 cc. of 0.1 molar phosphate buffer (pH 7.2), the phosphate buffer serving to hold the pH of the preparation in a predetermined range and to prevent the preparation from assuming the pH of the area being treated. The tentative activity is as follows:
1 mg. will produce an initial change in the optical density (OD) of about 0.1/minute at 25 C. in a threemilliliter reaction mixture containing benzylamine. Reference-Taber et al. Journal of Biological Chemists, 208 645 (1964).
(c) The formulation was prepared by mixing (a) and (b) and by allowing the mixture to solidify.
On the basis of the monoamine oxidase in the Formulation A, it was speculated that the addition of catalase may well have a synergistic effect on the reaction by removing the most noxious of the end products, and it would also serve as an agent for supplying one of the necessities for the reaction, namely oxygen. Accordingly, the following Formulation B was compounded, and found to be completely effective.
FORMULATION B (a) An ointment base and enzyme stabilizing action was compounded by melting 50 grams of polyethylene glycol (Carbowax) 6000 with 30 grams of polyethylene glycol (Carbowax) 1540, and by then cooling the mixture to 50 C.
(b) Five milligrams of catalase (Sigma stock #C-lO purified from beef plasma) (activity 2000-5000 sigma units/ gram) was then dissolved in 20 cc. of 0.1 M phosphate buffer (pH 7.2) (one Sigma unit will decompose one micromole of hydrogen peroxide per minute at pH 7.0 at 25 C. while the hydrogen peroxide concentration falls from 10.3 to 9.2 micromoles per milliliter of reaction mixture). The rate of disappearance of the hydrogen peroxide is followed by observing the rate of decrease in optical density at 240 micromoles).
(c) Mix (a) and (b) and allow the mixture to solidify.
The rationale of Formulation B may be represented by the following:
Monoarnlne o H R511 NH Oxldase 2 2 Catalese It has also been found that histamine, cadaverins and putrescine are formed in the colon, and these elements also are effective in the formation and stimulation of hemorrhoids. For that reason, in the following preparation, Formulation C, diamine oxidase is added to oxidize the aforesaid elements. For example, one milligram of diamine oxidase will oxidize approximately 0.7 micromole of putrescine per hour at a pH of 7.2 and at 37 C.
FORMULATION C Formulation C was found to be very effective in the treatment of hemorrhoids. Moreover, tests were made on all the preceding formulations, and they were found to maintain their activity indefinitely. For example, Formulation B was tested at two month intervals for almost a year and was found to lose none of its activity.
FORMULATION D (a) An ointment and enzyme stabilizing agent was compounded by melting 25 grams of polyethylene glycol (Carbowax) 6000 with 15 grams of polyethylene glycol (Carbowax) 1540, and by then cooling the mixture to 50 C.
(b) 2.5 milligrams of monoamine oxidase (Sigma Type 1: crude beef plasma); 2.5 milligrams diamine oxidase (Sigma Grade 11 from hog kidney); and 2.5 milligrams catalase (Sigma stock #Cl0purified powder from beef plasma) were then dissolved in 10 cc. of 0.1 M. phosphate buffer (pH 7.2).
(c) The formulation was prepared by mixing (a) and (b) and allowing the mixture to solidify.
FORMULATION E (a) An ointment and enzyme stabilizing agent was compounded by melting 25 grams of polyethylene glycol (Carbowax) 6000 with 15 grams of polyethylene glycol (Carbowax) 1540, and by then cooling the mixture to 50 C.
(b) As a second step, 2.5 milligrams diamine oxidase (Sigma Grade 11 from hog kidney), and 2.5 milligrams catalase (Sigma stock #C-10-purified powder from beef plasma) were then dissolved in 10 cc. of 0.1 molar phosphate buffer (pH 7.2).
(c) The formulation was prepared by mixing (a) and (b) allowing the mixture to solidify.
FORMULATION F (a) An ointment and enzyme stabilizing agent was compounded by melting 25 grams of polyethylene glycol (Carbowax) 6000 with 15 grams of polyethylene glycol (Carbowax) 1540, and by then cooling the mixture to 50 C.
(h) Then, 2.5 milligrams of monoamine oxidase (Sigma Type 1: crude beef plasma); and 2.5 milligrams catalase (Sigma stock #C-l 0-purified powder from beef plasma) were dissolved in 10 cc. of 0.1 M phosphate buffer (pH 7.2).
(c) The formulation was prepared by mixing (a) and (b) allowing the mixture to solidify.
FORMULATION G (a) An ointment and enzyme stabilizing agent was compound by melting 25 grams polyethylene glycol (Carbowax) 4000 with 20 grams polyethylene glycol (Carbowax) 400 and by cooling the mixture to 50 C.
(b) 0.1 milligram of monoamine oxidase (Sigma Type 1: crude beef plasma); 0.1 milligram diamine oxidase (Signma Grade 11 from hog kidney); and 0.1 milligram catalase (Sigma stock #Cl0-purified powder from beef plasma) were then dissolved in 10 cc. of 0.1 M phosphate buffer (pH 7.2).
(c) The formulation was prepared by mixing (a) and (b) allowing the mixture to solidify.
FORMULATION H (a) An ointment and enzyme stabilizing agent was compounded by melting 25 grams polyethylene glycol (Carbowax) 4000 with 20 grams polyethylene glycol (Carbowax) 400 and by cooling the mixture to 50 C.
(b) 2.5 milligrams of monoamine oxidase (Sigma Type 1: crude beef plasma); 2.5 milligrams diamine oxidase (Sigma Grade 11 from hog kidney); and 2.5 milligrams catalase (Sigma stock #C-lO-purified powder from beef plasma) were then dissolved in 10 cc. of 0.1 M phosphate buffer (pH 7.2).
(c) The formulation was prepared by mixing (a) and (b) allowing the mixture to solidify.
FORMULATION I (a) An ointment and enzyme stabilizing agent was compounded by melting 25 grams polyethylene glycol (Carbowax) 4000 with 20 grams polyethylene glycol (Carbowax) 400 and by cooling the mixture to 50 C.
(b) 50.0 milligrams of monoamine oxidase (Sigma Type 1: crude beef plasma); 50.0 milligrams of diamine oxidase (Sigma Grade 11 from hog kidney); and 50.0 milligrams catalase (Sigma stock #C-l0purified powder from beef plasma) were then dissolved in cc. of 0.1 M phosphate buffer (pH 7.2).
(c) The formulation was prepared by mixing (a) and (b) and allowing the mixture to solidify.
The latter formulations were also found to be effective in the treatment of hemorrhoids. However, for universal application, and for most effective use, the Formulations C or D are considered to be the preferred formulations at present.
The invention provides, therefore, a formulation which is relatively simple and inexpensive to prepare, and which uses readily available and relatively inexpensive ingredients. The formulation is also easy to apply, and it has been found most effective in accomplishing its desired purpose.
It will be appreciated that although particular formulations have been shown and described, modifications may be made, and it is intended in the claims to cover all modifications which come within the spirit and scope of the invention.
What is claimed is:
1. A pharmaceutical formulation for the treatment of hemorrhoids, and which includes ingredients in approximately the following proportions: 0.l50 milligrams monoamine oxidase, and 10-20 cubic centimeters of a stabilizing buffer in which said oxidase is dissolved to prevent the formulation from assuming the pH of the area being treated.
2. A pharmaceutical formulation for the treatment of hemorrhoids, and which includes ingredients in approximately the following proportions: 0.1-50 milligrams monoamine oxidase derived from crude beef plasma and dissolved in 10-20 cubic centimeters of a phosphate buffer of a pH 7.2 and 0.1 molar, said phosphate buffer being selected to hold the pH of the formulation in a predetermined range and to prevent the formulation from assuming the pH of the area being treated.
3. The formulation defined in claim 2, and which includes an ointment base in approximately the following proportions: grams polyethylene glycol 6000 and 30 grams of polyethylene glycol 1540.
4. The formulation defined in claim 2, and which includes approximately 5 milligrams of catalase purified from beef plasma and dissolved in said phosphate buffer.
5. The formulation defined in claim 4, and which includes approximately 5 milligrams diamine oxidase derived from hog kidney and dissolved in said phosphate buffer to oxidize histamine, cadaverins, and putrescine formed in the colon.
6. A pharmaceutical preparation for the treatment of hemorrhoids, and which includes ingredients in approximately the following proportions: 0.1-50 milligrams diamine oxidase; 0.1-50 milligrams catalase; and 10-20 cubic centimeters of a stabilizing bufler in which said oxidase is dissolved to prevent the formulation from assuming the pH of the area being treated.
References Cited 1/1962 France 424-94 OTHER REFERENCES Chemical Abstracts (1), vol. 52, entry l2029d, 1958. Chemical Abstracts (2), vol. 66, entry 84507u, 1967. Chemical Abstracts (1), vol. 52, entr 12029d, 1958. Chemical Abstracts (2), vol. 66, entry 84507u, 1967.
RICHARD L. HUFF, Primary Examiner
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US30800072A | 1972-11-20 | 1972-11-20 |
Publications (1)
Publication Number | Publication Date |
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USRE28011E true USRE28011E (en) | 1974-05-14 |
Family
ID=23192099
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US28011D Expired USRE28011E (en) | 1972-11-20 | 1972-11-20 | Pharmaceutical preparation |
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US (1) | USRE28011E (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4945084A (en) | 1987-07-08 | 1990-07-31 | Norman Oksman | Method and composition for topically treating anorectal or other dermal wounds |
US5478814A (en) * | 1987-07-08 | 1995-12-26 | Norman H. Oksman | Hemorrhoidal, other compositions and methods of treatment |
WO2007065637A1 (en) | 2005-12-06 | 2007-06-14 | Andreas Kern | Orally administered antibiotics for the treatment of hemorrhoids |
-
1972
- 1972-11-20 US US28011D patent/USRE28011E/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4945084A (en) | 1987-07-08 | 1990-07-31 | Norman Oksman | Method and composition for topically treating anorectal or other dermal wounds |
US5478814A (en) * | 1987-07-08 | 1995-12-26 | Norman H. Oksman | Hemorrhoidal, other compositions and methods of treatment |
WO2007065637A1 (en) | 2005-12-06 | 2007-06-14 | Andreas Kern | Orally administered antibiotics for the treatment of hemorrhoids |
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