Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Ester doai
Reexamination Certificate
1999-07-23
2001-10-23
Pak, John (Department: 1616)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Ester doai
C514S546000, C514S769000, C514S772000, C514S784000, C514S788000, C514S919000, C514S937000, C514S944000, C514S970000, C514S971000, C514S972000, C424S405000, C424SDIG005, C424SDIG001
Reexamination Certificate
active
06306905
ABSTRACT:
The present invention relates to a stable aqueous formulation of the substance ethyl 3-(N-butyl-acetamino)propionate.
As is known, the substance ethyl 3-(N-butyl-acetamino)propionate has an insect-repelling action and is also used in this role. The insect repellent can be obtained commercially, for example from Merck KGaA, Darmstadt.
For people, insects are an annoyance or even a threat in a number of respects. As well as the damage caused by some types of insects (for example the destruction of whole harvests), people and many animals alike are annoyed, stung and otherwise troubled in one way or another by a large variety of insects. This can lead to infections and to the transmission of dangerous diseases.
The main weapons in the fight against insects are insecticides, although their use and toxicity profile are not always without problems. Measures such as the use of insect eradicators are, however, not necessarily required to prevent direct annoyance.
Since nowadays environmental protection is very much at the fore, preventive measures are preferably used.
Thus insect repellents are now likely to be preferred to insecticides for controlling insects, since the former are merely intended to prevent insects from settling on a host.
The requirements for an insect repellent are high and manifold. Above all, effective protection of the skin against insects must be ensured. Lasting repellency over a number of hours, even under climatically unfavourable conditions, is important. The repellent should have as broad an activity spectrum as possible.
Other requirements are maximum skin and mucosa compatibility without toxic, allergenic or sensitizing properties, although there should be no penetration of the skin.
In addition, the substance should have high chemical stability, i.e. should not undergo hydrolysis or (photo)oxidation, high thermal stability and high perspiration resistance.
Furthermore, an insect repellent must be readily compatible and miscible with common cosmetic and pharmaceutical formulation bases.
The insect repellent ethyl 3-(N-butyl-acetamino)propionate satisfies this multiplicity of requirements.
It has however been established that this substance is degraded in aqueous formulations during the storage period. This degradation is speeded up under the influence of elevated temperatures. Even a temperature increase of 10° C. can double the rate of degradation.
This must be considered a disadvantage, since it is often the case that corresponding insect repellent formulations are stored for years after their manufacture and sale, or are only used now and again over a long period. In addition, higher temperatures (certainly 50° C. and above) are frequently encountered during the storage of cosmetic formulations in summer, especially in southern countries. It is thus possible that the insect repellent will already have been so severely degraded that its effect is considerably diminished.
It therefore appears desirable to provide aqueous or hydrous formulations of improved stability which have an unchanged content of ethyl 3-(N-butyl-acetamino)propionate over a long period, even at elevated temperatures.
Surprisingly, it has been found that the stability of aqueous formulations comprising ethyl 3-(N-butylacetamino)propionate can be considerably increased if formulations having a higher pH, preferably buffered solutions, are used.
Base formulations for cosmetic or pharmaceutical preparations are often prepared on the basis of aqueous alcoholic solutions. Such formulations are also known in connection with the insect repellent ethyl 3-(N-butylacetamino)propionate. However, there are no indications at all in the literature that formulations having a higher pH, in particular buffered formulations, are being used to improve stability.
The invention provides a stable aqueous formulation of the insect repellent ethyl 3-(N-butylacetamino)propionate which is characterized in that solutions having a higher pH, preferably buffered solutions, are used for stabilization.
The pH of these solutions is in a pH range greater than 3.0, preferably in the range from 3.5 to 7.9. In addition to acids and bases, such as, for example, citric acid or sodium hydroxide solution, buffers can also be used for adjusting the pH.
Suitable buffer system include any known buffer solutions in this pH range. Such buffers are generally known to the person skilled in the art and require no further explanation here.
According to the invention, a buffer selected from the following group of buffer systems is preferred. This group of buffer systems is merely given by way of example and is in no way limiting with respect to the formulations according to the invention: citric acid/disodium hydrogenphosphate, effective in a pH range from 2.2 to 7.8 (preferably 0.1 M citric acid/0.2 M Na
2
HPO
4
), tris(hydroxymethyl)aminomethane/HCl, effective in the pH range around 7.2 to 9.0 (preferably 0.2 M/0.1 M), disodium citrate/HCl, effective in the pH range from 1.2 to 5.0 (preferably 0.1 M/0.1 M), potassium hydrogenphthalate/NaOH, effective in the pH range from 4.2 to 6.2 (preferably 0.1 M/0.1 M), disodium citrate/NaOH, effective in the pH range from 5.2 to 6.6 (preferably 0.1 M/0.1 M), potassium dihydrogenphosphate/disodium hydrogenphosphate, effective in the pH range from 5.0 to 8.0 (preferably both 1/15 mol/l), or also triethanolamine+Titriplex III/HCl, effective in the pH range from 7.0 to 8.8 (preferably 0.5 mol/l/0.05 mol/l).
The invention also provides for the use of solutions adjusted or buffered using, for example, citric acid or sodium hydroxide solution for stabilizing hydrous formulations of the insect repellent ethyl 3-(N-butylacetamino)propionate. The pH of these solutions is in the range greater than 3.0. The pH is preferably in the range from 3.5 to 7.9.
Examples of suitable hydrous formulations are, inter alia, lotions, emulsions, like cream or milk (W/O or O/W), gels and also solid sticks.
In addition to other additives, UV filters can also be incorporated into these hydrous formulations, giving sunscreens or UV-protection formulations which can be applied to the skin and, if desired, also to the hair. Examples of suitable UV filters obtainable commercially are, inter alia, Eusolex 6300®, Eusolex 4300®, Eusolex 9020®, Eusolex 232®, Eusolex 2292®, Eusolex OCR®, Eusolex HMS®, Eusolex 6007®, PABA and Uvinul T 150®. UV filters can be incorporated individually or in combination with others into the formulations according to the invention in concentrations of from 0.5 to 10% by weight.
An emulsion according to the invention in the form of an insect repellent cream or milk can, in addition to the insect-repelling substance ethyl 3-(N-butylacetamino)propionate in solution or in solution with a suitable buffer, further comprise for example the following substances: fatty alcohols, fatty acid esters, fatty acids, lanolin, natural or synthetic oils or waxes and emulsifiers in the presence of water.
Lotions according to the invention comprise, inter alia, natural or synthetic oils and waxes, lanolin, fatty acid esters, low molecular weight alcohols or polyols.
Most gels further comprise thickeners, such as, for example, silica.
The solid sticks consist of natural or synthetic waxes and oils, fatty alcohols, fatty acids, fatty acid esters and lanolin in addition to the additives according to the invention.
The formulations according to the invention can also be in the form of aerosols, in which case the usual propellants, such as alkanes, fluoroalkanes and fluorochloroalkanes, are used as a rule.
The composition and preparation of such hydrous formulations are generally known to the person skilled in the art and require no further explanation here.
In another preferred embodiment, the pH in the formulations according to the invention is in the range from 4.5 to 8.0, and a particularly strong stabilization effect is displayed by formulations having a pH between 6.5 and 7.9.
The content of ethyl 3-(N-butylacetamino)-propionate in the formulations according to the invention is 1 to 50% by weight, preferably 10 to
Hitzel Sabine
Jalalian Mohammad
Kurz Thekla
Wille Dorothee
Merck Patent Gesellschaft mit beschrankter Haftung
Millen White Zelano & Branigan P.C.
Pak John
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