Drug – bio-affecting and body treating compositions – Anti-perspirants or perspiration deodorants
Reexamination Certificate
1999-05-06
2003-07-01
Dodson, Shelley A. (Department: 1616)
Drug, bio-affecting and body treating compositions
Anti-perspirants or perspiration deodorants
C424S059000, C424S076100, C424S400000, C424S401000, C512S001000
Reexamination Certificate
active
06585964
ABSTRACT:
BACKGROUND OF THE INVENTION
This invention relates to a method for preventing or minimizing biodegradation of a substance which normally contains a naturally occurring optical isomer. More particularly, this invention relates to a process for rendering a substance or surface supporting microorganisms, or subject to deliberate or accidental contamination with microorganisms, odoriferous, e.g., fragrant, for an extended period of time.
Next to sight, the sense of smell is reported to be that sense most widely appreciated. It plays an important role in our everyday lives. For this reason, the fragrance industry has grown to its present enormous size. Commercially sold fragrances are based on natural products and synthetic ones. The latter have become of increasing importance as the science of chemistry has become more inventive. Natural fragrances have also been synthesized. However, many of the most pleasant, or otherwise desired odors are highly transient, requiring frequent re-applications, or disappearing after periods shorter than desired for the intended uses.
Fragrant or odoriferous preparations generally consist of two functional components: the odor-producing compound or material, and a vehicle which serves as a carrier for the fragrant molecules. Such vehicles have served their purpose when the fragrance has been adequately disseminated. These vehicles are generally short-chain organic compounds which then evaporate quite quickly. This leaves the generally longer-chain fragrant molecules in situ in the desired locations from which they, in turn, volatilize, although somewhat more slowly. The sustained volatilization of these fragrant molecules achieves the desired effect by contacting the olfactories of the target persons or animals in the affected area.
While the fragrant compound applied to the site will ultimately be completely exhausted through volatilization, the full potential of this effective time is seldom, if ever, realized. This is because the fragrant molecules may be biodegradable and they are generally applied to areas rich in microorganisms. An application is to skin, which is well known to be heavily laden with microorganisms. However, all other common surfaces are also heavily populated with microorganisms. The interests of economy and personal appearance require that perfumes, for example, be applied sparingly. The biodegradability of the organic fragrance molecules results in the microbial populations attacking these molecules, metabolizing them and rendering the remains non-fragrant, less fragrant, or even of an undesirable odor. The otherwise expected useful time of the application of the product is thus effectively reduced.
In recent years, there has been a continuing replacement of natural fragrances with chemically synthesized molecules. Some are identical to natural fragrances, but are made synthetically more cheaply than can otherwise be obtained. Others are novel compounds, but these are also generally biodegradable. Both types of products suffer the same fate as described above for the natural fragrances.
SUMMARY OF THE INVENTION
In accordance with this invention, there is provided a method for preventing or minimizing biodegradation of a substance which normally contains a naturally occurring optical isomer, which process comprises replacing the naturally occurring optical isomer with the corresponding unnatural optical isomer. Examples of such substances include fragrances, substances which contain fragrances, and nonfragrant substances which contain optical isomer(s), such as body lotions, soaps, deodorants, and dyes and paints.
In a preferred embodiment of this invention, there is provided a process for prolonging emanation of odor(s) from a substance or surface containing one or more odoriferous optically isomeric compounds and which substance or surface also contains or becomes contaminated with microorganisms, which process comprises selecting (an) unnatural optical isomer(s) of the compound(s) to prevent or delay biodegradation of the odoriferous compound(s).
More particularly, it has now been found that an odoriferous compound applied to a substance or surface such as skin, may render the desired odor for an extended period of time by selecting its non-naturally occurring optical stereoisomer for use on the surface. The resulting substance or surface will remain odoriferous for a longer period of time than if the naturally occurring optical stereoisomer had been applied. This is because the non-naturally occurring optical stereoisomer is non-biodegradable, or is of greatly reduced biodegradability since the microbial enzymes necessary to the biodegradation process can cope only with the naturally occurring optical stereoisomer.
DETAILED DESCRIPTION OF THE INVENTION
Some of the organic molecules synthesized for fragrance purposes, and some of the natural fragrance molecules which can be synthesized have structures which contain carbon atoms bonded to four different atomic groups. The four atomic groups can assume one of two opposite configurations about their central carbon atom. For the purpose of chemical reactions, these configurations behave identically. Although little used as fragrances, amino acids and carbohydrates are important examples of chirality, the occurrence of optical stereoisomers of the same molecule, and serve to illustrate the point. Virtually all amino acids in nature are of the optically stereoisomeric form designated “left handed”, while natural carbohydrates occur almost exclusively in the optically stereoisomeric form called “right handed”. (These common designations derive from their mirror images which demonstrate the chemical identity, but not superimposability of the two forms of the same molecule.) The reason for the natural preference of one optical stereoisomer over its opposite form is unknown, but all known life forms follow this preference in their consumption and production of chiral organic compounds.
Some natural chemicals used in perfumery, and which have optical isomers, are listed in Table 1.
TABLE 1
Some Fragrances and their optical Isomers
NATURAL OPTICAL ISOMER
UNNATURAL OPTICAL ISOMER
(1R,2S,5R)-(−)-Menthol
(1S,2R,5S)-(+)-Menthol
(R)-(+)-Citronellal
(S)-(−)-Citronellal
(−)-Linalool
(+)-Linalool
(−)-Menthone
Four isomers
(1R)-(−)-Menthyl Acetate
(1S)-(+)-Menthyl Acetate
The strong preference, or specificity, for natural optical isomers displayed by biological entities is because virtually all biological reactions are conducted through the participation of enzymes. From the time life originated, its first enzymes have consistently passed on their optical isomeric specificity to all life forms evolved down through the eons. Enzymes, being templates which position molecules for specific reactions, do distinguish between, or among, optical isomers of the same molecule. Not being able to fit physically to the other optical isomer of the reactive molecular species, an enzyme cannot induce the reaction with the unnatural optical isomer.
The sense of smell has been attributed to enzymatic reactions: “Olfactory transduction begins with the binding of an odorant ligand to a protein receptor of the olfactory neuron cell surface, initiating a cascade of enzymatic reactions . . . ”(Breer, H.,
Semin. Cell Biol
5, 25, 1994; Sheppard, G. M.,
Neuron
13, 771, 1994, cited by Zhao, H. et al,
Science
, 279, 237, 1998). A fundamental characteristic of enzymatic reactions is their specificity for the molecule they catalyze into reaction. “Perhaps the most striking aspect of the specificity of enzymes is their ability to select between enantiomorphous compounds. This may be termed stereochemical specificity. For example, carboxypeptidase, which catalyzes the hydrolysis of carbobenzoxyglycyl-L-phenalalanine, has no measurable action on carbobenzoxyglycyl-D-phenalalanine. . . . These examples of stereochemical specificity involve an absolute discrimination between enantiomorphs.” (General Biochemistry, Fruton and Simmonds, eds, 3rd printing, p. 277, John Wiley
Levin Gilbert V.
Pinchot Roy B.
Biospherics Incorporated
Dodson Shelley A.
Roylance Abrams Berdo & Goodman L.L.P.
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