USPatent applicationPatented

Storage-stable ophthalmic compositions comprising diclofenac and ofloxacin

Granted 12 Aug 2003 · 3 office actions

Application· this page
9462731
filed 20 Mar 2000
Publication
Not published
not published
Patent
US 6,605,295
granted 12 Aug 2003

Life of the application

11 dated events
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Abstract

The invention relates to stable ophthalmic preparations including the penetrant antiphlogistic diclofenac or salts thereof and the penetrant antibiotic ofloxacin present in the form of the racemate, an enantiomer, particularly levofloxacin, or the corresponding hydrochloride thereof. The preparations may be used for treating eye infections and/or inflammations and for preventing infections before and after eye surgery.

Description

6 parts
›This application is a 371 of PCT/EP98/04267 filed…

This application is a 371 of PCT/EP98/04267 filed Jul. 9, 1998.

The invention pertains to storage-stable ophthalmic compositions containing diclofenac or its salts and ofloxacin in the form of a racemate, one of its enantiomers, in particular of levofloxacin, or of the corresponding hydrochloride. In addition, the invention pertains to the use of such ophthalmic compositions to treat eye inflammations and/or infections as well as to the prophylaxis of infection before and after eye operations.

Both the individual as well as the combined administration of antibiotics and antiphlogistics for the simultaneous treatment of inflammations and infections of the front section of the eye have been known for a long time. In this regard, the administration of appropriate composition preparations has proven especially advantageous.

It must be ensured with such composition preparations that the components do not affect one another negatively in so far as their effectiveness and stability are concerned or even enter into chemical reactions with one another which could result in undesirable by-products.

Ophthalmic composition preparations made of antibiotics and steroidal antiphlogistics which meet these criteria are disclosed in PCT application WO90/01933. Ofloxacin in combination with dexamethasone or rimexolon, among others, is mentioned as an active ingredient. Although the compatibility of the components and the storage stability of these compositions are satisfactory, they are tainted with the known disadvantages caused by the steroid components, such as an increase in intraocular pressure. In addition, dexamethasone is only a weakly penetrating antiphlogistic.

In order to overcome the disadvantages of known composition preparations caused bythe steroid components, the Spanishpatent specification ES 2065846 proposed combining a non-steroidal antiphlogistic with an antibiotic from the gyrase inhibitor group instead of a steroidal antiphlogistic. Ophthalmic suspensions and ointments containing the active-ingredient combinations clobetason/lomefloxacin, fluorometholon/norfloxacin, dexamethasone/ciprofloxacin, and indomethacin/norfloxacin are given as examples.

European patent application EP 0711546 discloses composition preparations for ophthalmology and otology which include the non-steroidal antiphlogistic diclofenac or its salts and the antibiotic tobramycin. The formulations described have substantial stability problems attributable to the poor solubility of diclofenac, on the one hand, and to chemical interactions between the active ingredients, on the other. It was possible to overcome the stability problems observed through careful adjustment of the active-ingredient concentrations and of the pH-value by using suitable solubilizers. A disadvantage of this composition is to be found in the fact that tobramycin cannot penetrate into the eye; therefore, it is suitable solely to treat superficial infections.

From a therapeutic point of view, an ophthalmic composition preparation made from a penetrating antiphlogistic and a penetrating antibiotic is desirable. Diclofenac or its salts and ofloxacin in the form of its racemate, one of its enantiomers, especially of levofloxacin, or of the corresponding hydrochloride, would be considered suitable active ingredients in this case.

During the first fundamental studies on this invention it was discovered that in formulating a composition medication with the active ingredients diclofenac and ofloxacin, unexpected stability problems occur in such a way that a decomposition product of ofloxacin, ofloxacin-N-oxide, is produced to a greater degree than is the case with ofloxacin in monopreparations. After a storage period of only 6 months, 2% ofloxacin-N-oxide is produced where diclofenac is present, whereas with pure solutions of ofloxacin, i.e. in the absence of diclofenac, the oxide content is less than 0.2% even after a long storage period.

The objective of this invention is to make available a stable composition preparation containing diclofenac or its salts and ofloxacin in the form of its racemate or one of its enantiomers, especially of levofloxacin, or of the corresponding hydrochloride, which can be used to treat eye inflammations and/or infections as well as a prophylaxis against infection before and after eye operations.

In accordance with the invention, the achievement of this objective is made possible through the features of the independent claims.

The dependent claims define advantageous forms of the invention.

Surprisingly, it was established that the formation of ofloxacin-N-oxide or levofloxacin-N-oxide respectively, which is described above, can be restrained through the use of antioxidation agents normally used in ophthalmic preparations.

A stable pH-value greater than 7 is to be maintained to keep the diclofenac in solution. The pH-value of ophthalmic preparations is normally adjusted by means of buffer systems.

In this case, however, it was observed that where solutions containing diclofenac and ofloxacin were buffered, precipitates were produced during the storage period, even where an oxidation agent was present, these precipitates presumably being attributable to the high salt concentration of the buffered system. These precipitates could not be prevented by adding the usual solubilizers, either.

In accordance with the invention, it was now found that stable composition preparations containing the active ingredient diclofenac or its salts and ofloxacin in the form of its racemate, one of its enantiomers, or of the corresponding hydrochloride, can be obtained by adding the usual antioxidants and doing without a buffer system, i.e. the pH-value is adjusted solely with acids or alkalis.

The inventive formulations contain 0.001-0.15% by weight, preferably 0.01-0.13% by weight, by preference 0.08-0.12% by weight, diclofenac or its salts and 0.001-0.5% by weight, preferably 0.01-0.35% by weight, by preference 0.1-0.3% by weight, ofloxacin in the form of its racemate, one of its enantiomers, especially of levofloxacin, or of the corresponding hydrochloride.

›The inventive compositions contain ascorbic acid, citric acid…

The inventive compositions contain ascorbic acid, citric acid, tartaric acid, sodium sulphite, orsodium disulphite in quantities of 0.001-0.02% by weight, preferably 0.005-0.015% by weight, by preference 0.008-0.012% by weight, as suitable antioxidants. In a formulation which is especially preferred, the inventive compositions contain sodium disulphite in concentrations between 0.008 and 0.012% by weight.

HCl and NaOH are preferably used to adjust the pH-value. The inventive compositions may contain normal solubilizers, like povidone, etc. in concentrations of 0-5% by weight, preferably 2-4% by weight and by preference 2.5-3.5% by weight, and/or polysorbate, etc. in a concentration of 0-2% by weight, preferably 0.1-1% by weight and by preference 0.3-0.7% by weight.

The inventive compositions may contain the following as further normal additives:

isotonization agents, like sodium chloride in quantities of 0-5% by weight, preferably 0.3-2% by weight, by preference 0.5-1.25% by weight, or sorbitol in quantities of 0-10% by weight, preferably 2-6% by weight, by preference 3-5% by weight;

chelating agents, like EDTA or its sodium salt in quantities of 0-0.002% by weight, preferably 0.0008-0.0012% by weight;

preservatives, like benzalkonium chloride in quantities of 0-1.0% by weight, preferably 0.01-0.5% by weight, by preference 0.02-0.04% by weight.

The inventive formulations may be formulated as eyedrops, suspensions, ointments, or gels. The formulation as eyedrops is especially preferred.

The following embodiments serve only to explain the invention and do not represent any kind of restriction.

›Examples4
EXAMPLE 1
EXAMPLE 2
EXAMPLE 3
›EXAMPLE 4

The compositions presented as examples were stable for a long period and exhibited only low ofloxacin-N-oxide contents, which did not increase during the storage period.

The stable, inventive compositions may by used to treat eye infections and/or inflammations as well as for prophylaxis against infection before and after operations.

The results of various test series are compared in the following Table I.

In test series 1, a composition was tested which, in addition to the active ingredients diclofenac-Na and ofloxacin, contains the buffer system boric acid/sodium tetraborate as well as the adjuvants Kollidon 25 and Tween 80 SD. Although a clear solution resulted, 1.6-1.9% ofloxacin-N-oxide was produced after only 4 months.

As test series 2 shows, it was possible to clearly restrain the production of ofloxacin-N-oxide by adding sodium disulphite; however, precipitation occurred with the compositions tested in this test series.

As test series 3, 4, and 5 show, in accordance with the invention clear solutions containing minor amounts of ofloxacin-N-oxide can be produced if sodium disulphite is added and at the same time the buffer system is not used.

›Tables in the description — 5
Batch size: 20 l
ComponentsQuantity
Diclofenac-sodium0.020 kg
Ofloxacin0.060 kg
Kollidon 250.600 kg
Sodium disulphite0.002 kg
Sodium chloride0.150 kg
1 N HCl to adjust the pH-value
1 N NaOh to adjust the pH-value
Water19.404 kg
Batch size: 20 l
ComponentsQuantity
Diclofenac-sodium0.020 kg
Levofloxacin0.060 kg
Sodium edetate0.002 kg
Kollidon 250.600 kg
Sodium disulphite0.002 kg
Sodium chloride0.150 kg
Polysorbate0.100 kg
1 N HCl to adjust the pH-value
1 N NaOH to adjust the pH-value
Water19.304 kg
Batch size: 20 l
ComponentsQuantity
Diclofenac-sodium0.020 kg
Ofloxacin0.060 kg
Kollidon 250.600 kg
Sodium disulphite0.002 kg
Sorbitol0.800 kg
Polysorbate0.100 kg
1 N HCl to adjust the pH-value
1 N NaOH to adjust the pH-value
Water18.838 kg
Batch size: 20 l
ComponentsQuantity
Diclofenac-sodium0.020 kg
Ofloxacin0.060 kg
Kollidon 250.600 kg
Sodium disulphite0.002 kg
Sorbitol0.800 kg
Benzalkonium chloride0.006 kg
Polysorbate0.100 kg
1 N HCl to adjust the pH-value
1 N NaOH to adjust the pH-value
Water18.832 kg
TABLE I — Test Series using Various Formulations
Test 1,Test 2,Test 3,
ChemicalChemicalChemical
designation:designation:designation:Test 4,Test 5,
Formula,#950501#960107#970201ChemicalChemical
components#950502#960108#970202designation:designation:
in %#950503#960109#970203#970817#971203
Diclofenac-0.10.10.10.10.1
Na
Ofloxacin0.30.30.30.30.3
Boric acid1.51.5———
Sodium0.450.45———
tetraborate x
10 H 2 O
Kollidon 253.03.03.03.03.0
Tween 80 SD0.50.5—0.50.5
Sodium—0.010.010.010.01
disulphite
NaCl—0.750.70.7
N-oxide formt = 4 months,t = 6 months,t = 3 months,t = 8 months,t = 4 months,
t = x, 21° C.,1.6-1.9%0.4%0.4%0.48%0.34%
max. 1%
Appearancet = 19 monthst = 6 monthst = 3 monthst = 8 monthst = 4 months
T = xsolution:precipitationsolution:clearclear
clearclear
RemarksTerminationTermination———
of testof test
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Classifications

15 codes
IPC · International Patent Classification
Section A — Human necessities
  • A61K31/535
  • A61K31/196
  • A61P27/02
  • A61K47/12
  • A61K31/198
  • A61K47/14
  • A61K31/5383
  • A61K47/22
  • A61K47/18
  • A61K9/00
  • A61K47/02
Section C — Chemistry; metallurgy
  • C07D498/06
USPC · US Patent Classification
424/427514/914514/912

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1,860 days filing → grant
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Examiner
James M. Spear
art unit 1615 · TC 1600
Citations: 11 back · 17 forward

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