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Triamcinolone acetonide derivative |
| RE29799 |
Triamcinolone acetonide derivative
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| Patent Drawings: | |
| Inventor: |
Agusti |
| Date Issued: |
October 10, 1978 |
| Application: |
05/822,695 |
| Filed: |
August 8, 1977 |
| Inventors: |
Agusti; Agustin (Barcelona, ES)
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| Assignee: |
J. Uriach & Cia S.A. (Barcelona, ES) |
| Primary Examiner: |
Roberts; Elbert L. |
| Assistant Examiner: |
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| Attorney Or Agent: |
Striker; Michael J. |
| U.S. Class: |
514/174; 552/566; 552/602 |
| Field Of Search: |
260/397.45; 424/241 |
| International Class: |
C07J 71/00 |
| U.S Patent Documents: |
3626063 |
| Foreign Patent Documents: |
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| Other References: |
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| Abstract: |
.[.Triamcinolone.]. .Iadd.Bis(triamcinolone .Iaddend.acetonide.Iadd.) .Iaddend.4,4'-methylene-bis(3-methoxy-2-naphthoate), method of preparing the same by preparing a reactive derivative of 4,4'-methylene-bis(3-methoxy-2-naphthoic) acid and reacting such derivative with triamcinoline acetonide. The triamcinolone acetonide derivative is particularly suitable for use in the treatment of dermatosis, eczema, neurodermatitis, impetigo, psoriasis, pruritis, erythema and the like. |
| Claim: |
I claim:
1. A pharmaceutical preparation comprising as active ingredients .[.triamcinolone acetonide.]. .Iadd.bis(triamcinolone acetonide).Iaddend.4,4'-methylene-bis(3-methoxy-2-naphthoate); and a pharmaceutically acceptable carrier.
2. A pharmaceutical preparation according to claim 1 in the form of a cream.
3. A pharmaceutical preparation according to claim 2 wherein said active ingredient is present in an amount of 0.1 to 0.5 percent.
4. A method of treating allergic and inflammatory dermatoses which comprises applying to affected areas of the skin a therapeutically effective amount of a pharmaceutical preparation according to claim 1.
5. A method according to claim 4 which comprises applying said pharmaceutical preparation as 0.1 to 0.5 percent cream 2 or 3 times daily.
6. A method of treating arthritis, bursitis, tendinitis and synovitis which comprises administering to the patient having such condition a therapeutically effective amount of a pharmaceutical preparation according to claim 1. |
| Description: |
This invention relates to a new triamcinolone acetonide derivative, and methods for making and using the same. More particularly the invention relates to .[.triamcinolone acetonide.]. .Iadd. bis(triamcinoloneacetonide) .Iaddend.4,4'-methylene-bis(3-methoxy-2-naphthoate) and the use thereof in treating a broad range of dermatological conditions.
It is well known that triamcinolone acetonide, or 9.alpha.-fluoro-11.beta.,21-dihydroxy-16.alpha.,17.alpha.-isopropylidenedi oxy-1,4-pregnadiene-3,20-dione, has proved particularly useful in the treatment of dermatological conditions. Thecompound has been proved to have marked efficacy in the treatment of dermatosis, eczema, neurodermitis, impetigo, psoriasis, pruritis and other related diseases. However, in the long term topical treatment of large areas, especially with children andwhere there are skin lesions, there arise a great variety of general secondary reactions due to the percutaneous absorption of the corticoid. Thus the drug is known to induce .[.naturesis.]. .Iadd.natriuresis .Iaddend.negative sodium balance withweight loss in most patients. Nearly every side effect seen with hydrocortisone has been seen with triamcinolone acetonide but the relative frequencies are less. These undesirable results are particularly associated with long therapy.
Triamcinolone acetonide is a fluorinated derivative of prednisone, the fluorine atom in the 9.alpha. position of the corticosteroid ring system increasing the activity of the glucocorticoid and reducing the action on the metabolism ofelectrolytes.
Triamcinolone acetonide is the cyclic 16,17-acetal of triamcinolone with acetone and has the following formula: ##STR1##
The compound of the above formula is prepared by reacting triamcinolone (9-fluoro-11.beta.,16.alpha.,17,21-tetrahydroxypregna-1,4-diene-3,20-dione ) with acetone and perchloric acid followed by neutralization and vacuum concentration.
Triamcinolone can be synthesized from hydrocortisone acetate via the 3,20-bis ketal by treatment with thionyl chloride, refluxing with potassium hydroxide and acetylation to give 21-acetoxy-4,9,11(16)-pregnatriene-3,20-dione. Oxidation withosmium tetroxide to the 16.alpha.,17.alpha.-dihydroxy derivative and subsequent insertion of the 9.alpha.-fluoro and 11.beta.-hydroxy groups for instance by treatment with N-bromoacetamide and perchloric acid to give the 9.alpha.-bromo-118.beta.-hydroxycompound followed by abstraction of HBr with potassium acetate to form the 9.beta.,11.beta.-epoxy derivative which by treatment with HF in a halogenated hydrocarbon yields the 9.alpha.-fluoro-11.beta.-hydroxy analog, gives a product lacking only a doublebond at the 1-position. This latter step is accomplished by incubation with Norcardia corallina followed by saponification of the acetate to yield triamcinolone.
In copending British application 38795/71 (now British Pat. No. 1,332,058) a method has been described whereby the undesirable side effects of prednisone may be decreased or avoided by reacting the prednisone with an acid (particularly with anacid chloride) to form an ester which has decreased or zero absorption with respect to prednisone. The new ester has the desired anti-inflammatory properties of prednisone but may be administered without side effects resulting from absorption when giventopically, orally or by injection i.e., intramuscular or intravenous routes. The acid with which the prednisone is reacted is 4,4'-methylene-bis(3-methoxy-2-naphthoic) acid.
The preparation of the just-mentioned acid has been described in Spanish patent application No. 385,254.
In accordance with the invention it has now been found that .[.triamcinolone acetonide.]. .Iadd. bis(triamcinolone acetonide) .Iaddend.4,4-methylene-bis(3-methoxy-2-naphthoate) which is a new compound .Iadd.is .Iaddend.suitable for use indermatological applications. It is intended for local application, in which circumstances it is more efficaceous than triamcinolone and triamcinolone .[.acetonamide.]. .Iadd.acetonide .Iaddend.and is more potent. It is particularly adapted for use inthe treatment of allergic and inflammatory dermatoses, pruritis, arthritis, .[.bursititis.]. .Iadd.bursitis .Iaddend.tendinitis and synovitis.
The naphthoate of the invention may be made by preparing a reactive derivative of 4,4'-methylene-bis(3-methoxy-2-naphthoic) acid and thereafter reacting the derivative with triamcinolone acetonide.
In the preparation of the naphthoate, the acid is preferably reacted with a halogenating agent such as thionyl chloride to form two acid halide moieties on the molecule i.e. ##STR2## where X is halogen and preferably chlorine. This reactionshould be carried out in an anhydrous medium.
The acid halide thus obtained is then reacted with triamcinolone acetonide, the preparation of which is carried out in the known manner, for instance as described above in the presence of an agent for fixing the hydracid which is formed duringthe reaction, so as to obtain the final product, corresponding to the formula: ##STR3## where R is the radical of triamcinolone acetonide.
As hydracid fixation agent, an organic base may be used. An example of a particularly suitable base is pyridine, which acts both as base and as a solvent for the reaction.
The following Example is given in order to illustrate theinventio but is in nowise to be construed as limitative thereof.
EXAMPLE
15 Grams of 4,4'-methylene-bis-(3-methoxy-2-naphthoic) acid were mixed with 55 ml of thionyl chloride. The resultant mixture was heated on a water bath for 2 hours, after which the excess of thionyl chloride was distilled off until a solid wasobtained. The solid was purified by recrystallization from anhydrous benzene. 4,4'-Methylene-bis(3-methoxy-2-naphthoic) acid chloride was thusly obtained in the form of a yellow solid material.
______________________________________ Melting point 170-173.degree. C Yield 95% ______________________________________
Elementary Analysis:
.[.Calculated.]. .Iadd.Found.Iaddend.: C = 66.23% H = 4.02% Cl = 15.64%
.[.Found.]. .Iadd.Calculated.Iaddend.: C = 66.80% H = 4.10% Cl = 15.66%
10 Grams of the acid chloride were treated with 19.2 gm of triamcinolone acetonide in 150 ml pyridine. The mixture was heated for 3 hours at 90.degree. C and the resultant solution added to 3 liters water. The product thus formed was recoveredby filtration and was then washed with water. It was then vacuum dried at between 40.degree. C and 50.degree. C. Triamcinolone acetonide 4,4'-methylene bis(3-methoxy-2-naphthoate) was obtained in 90 percent yield.
After recrystallization from a mixture of acetone and water the product was found to have the following properties:
______________________________________ Melting point 220.degree. C (decomposition) ______________________________________
Elementary Analysis:
Calculated: C = 69.5% H = 6.25% F = 3.08%
Found: C = .[.70.13%.]. .Iadd.70.18.Iaddend. % H = 6.29% F = 3.04%
Clinical tests have established that the product was absorbed neither orally nor topically (even over large skin areas). In particular it was discovered that oral administration of the product did not alter the urinary excretion rates of17-ketosteroids, sodium or potassium ions, whereas these values changed significantly when related corticoids were administered in the same dosages and under the same conditions.
However, other evaluating methods showed that the product of the invention had the same anti-flammatory activity as triamcinolone acetonide and was about 200 times as active as prednisone.
The compound may be administered in any suitable form together with a pharmaceutically acceptable carrier. For example, for topical application, it may suitably be made up in a concentration of 0.1 to 0.5 percent and preferably of 0.3 percent inthe form of a cream or pomade. When the cream is applied three times daily in the conventional manner to affected areas, substantially total healing was reported in 100 percent of cases having various dermatological diseases as for instance contact.[.dermatits.]. .Iadd.dermatitis .Iaddend.and related allergies, eczema and physical, chemical and medical origin, flexural and housewive's eczema, impetigo, psoriasis and erythema, without any danger of secondary complaints .[.cased.]. .Iadd.caused.Iaddend.by absorption of the active material.
The lack of absorption provides a further advantage of the compound, namely that there is no danger of overdosages when the medicament is applied to the skin or mucosa, or even from occlusive dressings applied directly onto affected areas.
The compound can be applied topically as a 0.1 percent solution, lotion, or aerosol or as a 0.1 to 0.5 percent cream applied 2 or 3 times daily. The compound can be administered intrasynovially, 2.5 to 15, mg as a 1 percent suspension atintervals of 1 to several weeks. Orally the compound is administered in amounts of 2 to 10 ml 3 to 4 times daily.
The lotion is made up in a suitable aqueous vehicle. The ointment is made up in a suitable hydrophilic ointment base. The suspension is a sterile suspension in a suitable aqueous medium.
An example of a hydrophilic base is hydrophilic petrolatum:
______________________________________ Cholesterol 30 grams Stearyl alcohol 30 grams White wax 80 grams White petrolatum 860 grams to make 1000 grams ______________________________________
Another hydrophilic ointment base has the following composition:
______________________________________ Methylparaben 0.25 grams Propylparaben 0.15 grams Sodium laurylsulfate 10.00 grams Propylene glycol 120.00 grams Stearyl alcohol 250.00 grams White petrolatum 250.00 grams Purified water 370.00 grams to make 1000 grams ______________________________________
The preparations, lotions, ointments or otherwise may further contain anesthetics, antiseptics, germicides, protective or screening agents, pigments, etc.
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