EP4065181A1

EP4065181A1 - Device and method for determining, analytically and by sensing, the release of an active substance from a release system

Info

Publication number: EP4065181A1
Application number: EP19812968.6A
Authority: EP
Inventors: Edison Diaz; Isabel LANFERMANN; Katharina MICHELS; Marco SINGER; Patrick OSTERMANN; Achim Schumann; Fabian UDE
Original assignee: Symrise AG
Current assignee: Symrise AG
Priority date: 2019-11-27
Filing date: 2019-11-27
Publication date: 2022-10-05
Also published as: US20220412937A1; JP2023503371A; JP7445760B2; WO2021104624A1; BR112022010089A2; CN115003343A

Abstract

The present invention relates to a device and to a method for determining, analytically and/or by sensing, the release of an active substance or a plurality of active substances from a release system. In particular, the present invention relates to a device and to a method for determining the release of an active substance or a plurality of active substances, in particular a fragrance or flavoring substance or a fragrance or aroma mixture, from a capsule or a precursor. The present invention further relates to a device and to a method for determining the properties of a release system, in particular a capsule or a precursor. Finally, the present invention relates to the use of the device according to the invention and of the method according to the invention to determine, analytically and/or by sensing, the release of an active substance or a plurality of active substances from a release system.

Description

Device and method for the analytical and sensory determination of the release of an active ingredient from a release system

Field of invention

The present invention relates to a device and a method for the analytical and / or sensory determination of the release of an active ingredient or several active ingredients from a release system. In particular, the present invention relates to a device and a method for determining the release of an active ingredient or more active ingredients, in particular a fragrance or flavor or a fragrance or flavor mixture, from a capsule or a precursor. In addition, the present invention relates to a device and a method to determine the properties of a release system, in particular a capsule or a precursor. Ultimately, the present invention relates to the use of the device according to the invention and the method according to the invention for the analytical and / or sensory determination of the release of an active ingredient or several active ingredients from a release system.

A release system within the meaning of the invention is a solid preparation, for example particles or capsules, which contains one or more active ingredients.

Another example of such release systems are so-called precursors or precursors. With such precursors or precursors is / are by a chemical or physical impulse, for example by chemical reaction with an agent, temperature, humidity, change in pH , Oxygen (oxidation), light, for example UV radiation, enzymes, microorganisms, etc., one or more active ingredients are released. For example, in fragrance production, precursors are molecules with a weak inherent odor that release at least one new fragrance molecule, when external factors such as temperature, oxygen (oxidation), light, enzymes, microorganisms, chemical reactions (e.g. hydrolysis), changes in pH or moisture act on them. As a result, over the life span of such a fragrance precursor, new fragrance notes are released again and again and a slightly varying odor is created.

The term “encapsulation” is generally understood by those skilled in the art to mean a technique with which finely dispersed solid, liquid or gaseous substances, for example active ingredients, are surrounded with a film-forming shell made of polymeric and / or inorganic wall materials and are thus immobilized.

The substances or active ingredients enclosed in the capsules are generally referred to as core material.

Depending on the wall or shell material and the degree of crosslinking, individual properties of the microcapsules can be achieved in this way.

The aim is to protect the active components referred to as active ingredients from reactions with the environment, for example moisture or oxidation, but also reaction with other substances, and / or to be able to release them in a targeted manner at a defined point in time.

In the case of encapsulation, depending on the phase morphologies, a distinction is made between capsules of the matrix type or of the core / shell type. In matrix encapsulation, the active ingredient (s) is / are mixed homogeneously with the shell component (“matrix”) and a particle is created in which the active ingredient (s) is / are evenly distributed. Matrix systems are also known as microparticles. The active ingredient (s) is usually released either by diffusion of the active ingredient (s) into the environment or by degradation of the matrix.

In the case of core / shell encapsulation, the active substance (s) that form the core is / are enveloped with a shell material. The result is a real capsule with one or more shells. Usually creates a mechanical stress, for example pressure or shear, a complete release of the core material. However, it is also possible to specifically release the core material or the active ingredient (s) by means of alternative opening mechanisms, for example temperature, change in the pH value, UV radiation, microwaves or ultrasound.

In addition to macroscopic particles with diameters in the range up to 1 cm, microcapsules in particular are of interest. The person skilled in the art understands this to mean spherical particles with a diameter in the range from about 0.0001 to about 5 and preferably from 0.005 to 0.5 mm.

The term "microcapsules" is understood according to the invention particles and aggregates which contain an inner space or core which is filled with a solid, gelled, liquid or gaseous medium and enclosed (encapsulated) by a continuous shell of film-forming polymers . In addition, the microscopic capsules can contain one or more cores distributed in the continuous encapsulation material, consisting of one or more layers.

The shell of such microcapsules can consist of natural, semi-synthetic or synthetic materials. Natural shell materials are, for example, gum arabic, agar-agar, agarose, maltodextrins, alginic acid or their salts, e.g. sodium or calcium alginate, fats and fatty acids, cetyl alcohol, collagen, chitosan, lecithins, gelatin, albumin, shellac, polysaccharides such as starch or Dextran, polypeptides, protein hydrolysates, sucrose and waxes. Semi-synthetic casing materials include chemically modified celluloses, in particular cellulose esters and ethers, e.g. cellulose acetate, ethyl cellulose, hydroxypropyl cellulose, hydroxypropylmethyl cellulose and carboxymethyl cellulose, as well as starch derivatives, in particular starch ethers and esters. Synthetic shell materials are, for example, polymers such as polyacrylates, polyamides, polyvinyl alcohol, aminoplasts, phenoplasts or polyvinylpyrrolidone.

Depending on the use of different wall and core materials, there are many possible uses. The production of microcapsules has been described in detail in the literature of the prior art and is accessible by means of known reactive and non-reactive processes, such as solvent evaporation, precipitation processes, coacervation, interfacial polycondensation,

High pressure encapsulation processes etc ..

Examples of prior art microcapsules are the following commercial products (the shell material is indicated in brackets in each case): Hallcrest Microcapsules (gelatin, gum arabic), Coletica Thalaspheres (maritime collagen), Lipotec Millicapsules (alginic acid, agar-agar), Induchem Unispheres (lactose, microcrystalline cellulose, hydroxypropylmethyl cellulose); Unicerin C30 (lactose, microcrystalline cellulose, hydroxypropylmethylcellulose), Kobo Glycospheres (modified starch, fatty acid esters, phospholipids), Softspheres (modified agar-agar) and Kuhs Probiol Nanospheres (phospholipids) as well as Primaspheres and Primasponges (phospholipides) and alginates . As well as capsules made from synthetic polymers Micronal <®> (BASF), microcapsules 500 and 560 (Koehler SE), Folco Smart-caps <®>, Enfinit <®>, Ensensa <®>.

Due to their properties, capsules, in particular microcapsules, which include one or more active ingredient (s), including in the printing industry (eg scented varnishes), the food industry (eg vitamins, flavors, plant extracts, enzymes, microorganisms), agrochemicals (eg Fertilizers, pesticides), the feed industry (e.g. minerals, vitamins, enzymes, drugs, microorganisms), the pharmaceutical industry, the detergent industry and the cosmetics industry.

Many everyday items such as cleaning agents, fabric softeners, washing powder, liquid detergents, shower gels, shampoos, deodorants, body lotions, etc. are now perfumed with encapsulated fragrances or fragrance mixtures. In particular, the capsules, preferably microcapsules, are used for the production of, for example, perfume extracts, eau de perfumes, eau de toilettes, aftershave, eau de colognes, pre-shave products, splash colognes, acidic, alkaline and neutral Cleaning agents, such as floor cleaners, window glass cleaners, dishwashing detergents, bathroom and sanitary cleaners, scouring milk, solid and liquid toilet cleaners, powder and foam-form carpet cleaners, liquid detergents, powder-form detergents,

Laundry pretreatment agents such as bleaches, soaking agents and stain removers, fabric softeners, laundry soaps, washing tablets, disinfectants, surface disinfectants and air fresheners in liquid, gel-like or solid carrier form, aerosol sprays, waxes and liquid polishes such as furniture polishes, floor waxes such as body and shoe polishes, for example Soaps, shower gels, shampoos, shaving soaps, shaving foams, bath oils, cosmetic emulsions of the oil-in-water, of the water-in-oil and of the water-in-oil-in-water type such as skin creams and lotions, Face creams and lotions, sunscreen creams and lotions, after-sun creams and lotions, hand creams and lotions, foot creams and lotions, depilatory creams and lotions, after shave creams and lotions, tanning creams and lotions, hair care products such as Hair sprays, hair gels, setting hair lotions, hair conditioners, permanent and semi-permanent Hair coloring agents, hair shaping agents such as cold waves and hair straighteners, hair lotions, hair creams and lotions, deodorants and antiperspirants such as armpit sprays, roll-ons, deodorant sticks, deodorant creams, decorative cosmetics products such as eye shadow, nail varnish, make-up, lipsticks, mascara, Care wipes, baby wipes, intimate wipes, refreshing wipes, as well as candles, lamp oils, incense sticks, insecticides, repellants, fuels.

The encapsulation of an active ingredient or several active ingredients with a suitable shell material can take place for several reasons:

Conversion of liquids into a manageable powder form (e.g.

Encapsulation of vegetable oils, fats); Time-controlled or delayed release of substances (dosage control, depot effect for pharmaceuticals, pesticides and fertilizers);

Flavor, smell and color masking (e.g. bitter or pungent aromas);

Protection against light, oxidation, heat, acids or bases (e.g. vitamins, aromatic substances, etc.)

Moisture protection from e.g. hygroscopic salts or minerals; Reduction of the evaporation rate of volatile components (e.g. flavorings); Prevention of premature chemical reactions with other mixture components; better handling before or during processing (e.g. optimized flow properties, avoidance of the formation of fine dusts);

Protection of personnel from harmful or unpleasant materials (chemicals, flavor concentrates); or better dispersibility.

A particular use of microcapsules are, for example, detergents and cleaning agents for the controlled or delayed release of fragrances on textile surfaces. During washing, microcapsules containing a fragrance or perfume oil spread on the laundry and adhere to the fabric. When the clothing is worn, the capsules burst due to the friction or pressure that occurs and release the fragrance or perfume oil.

The contents of microcapsules can be released in various ways. Four typical mechanisms can be considered:

The capsule walls are mechanically destroyed by crushing or shearing. This mechanism is used, for example, in reaction copy paper.

The capsule walls are destroyed by melting the wall material. According to this mechanism, ingredients such as raising agents or flavors in baking mixes are only released during the baking process. The capsule walls are destroyed by dissolving the wall material. This mechanism comes into play with washing powder, for example, so that encapsulated ingredients such as enzymes are only released during the washing process.

The capsules are retained, the contents of the capsule are gradually released by diffusion through the capsule wall. According to this mechanism, for example, a slow and steady release of active pharmaceutical ingredients in the body can be achieved.

In order to be able to take suitable measures in the development, production and use of such active substance release systems, in particular capsules or precursors, it is important to determine the release rate of active substances, for example the concentration of an active substance or several active substances, the release rate, the release profile of an active ingredient or several active ingredients, etc. as well as their properties, such as mechanical stability of the capsule shell, breaking strength, retardation behavior, etc. to be in the picture.

The determination of the release of an active ingredient or several active ingredients, in particular a fragrance or flavor, from a capsule, in particular from a microcapsule, is carried out by a sensory-analytical evaluation using different methods. Specifically trained test persons / panels are used for this.

Descriptive sensory analyzes, ie the descriptive sensory methods, are considered to be the most demanding sensory methods due to their diversity and complexity. They are traditionally based on the sensory perception of appropriately qualified people, result in detailed product profiles, but are time-consuming and costly. Specially trained testers are used for the tasks in the context of a classic descriptive analysis, such as the identification, description and quantification of objectively sensory perceptible product properties. The aim of these procedures is to obtain a detailed product description that can be compared with other products or can also be implemented in product recipes. In addition to the multi-stage sensory process, the complex training process for examiner qualification in classic profile analyzes is a major point of criticism.

[0025] Cost and time pressure in the case of innovations as well as ever shorter product life cycles increasingly require information relevant to decision-making to be available more quickly. Short-term procedures, so-called descriptive rapid methods, can represent an alternative in this regard, as they also enable untrained test persons to be used, but are also associated with a loss of information.

Although the trend is towards standardizing the sensory evaluation by improving the methods or by better training the test subjects, the evaluation remains a subjective evaluation that cannot be equated with an objective or standardized analytical method based on specific criteria .

The release of the active ingredients from a release system, in particular from a capsule, takes place in the sensory analysis usually by manual friction without normalization for the pressure applied, for example pressure intensity, on the release system, in particular the capsule, so that the result of the release of the Active ingredient or the active ingredients is subject to strong fluctuations.

The primary object of the present invention was therefore to overcome the problems mentioned above and to provide a device and a method for performing an objective and standardized, ie standardized, analytical method which enables reproducible, qualitative and / or quantitative statements to be made to make the release of an active ingredient or more active ingredients, in particular qualitative and / or quantitative information about the released active ingredient or active ingredients, and / or about the properties of an active ingredient release system, in particular a capsule. In particular, it was the object of the present invention to provide a standardized method for the analytical and / or sensory determination of the release of an active ingredient or several active ingredients from a release system, in particular an active ingredient or several active ingredients from a capsule or a precursor.

It was also an object of the present invention that the device has a simple structure and the method is easy to use and can be used variably for a large number of different release systems or active ingredients.

Ultimately, it was the object of the present invention that the device can be combined with standard analytical instruments in order to enable the measurements to be identified and quantified.

Surprisingly, it has been found that the aforementioned objects are achieved by a device and / or a method in which an active ingredient or several active ingredients are released from a release system 6 by a physical or chemical impulse, for example pressure and / or friction, preferably from a capsule 6 or a precursor 6, is / are released, the released active ingredient or the several released active ingredients is / are supplied to a detection device and the released active ingredient is ultimately determined analytically.

The procedural advantage is that with the device and / or the method according to the invention, an objective analysis method is provided under normalized, ie standardized conditions, which allows, for example, analysis values from different release systems to be compared with one another, and that the release the active ingredients can be measured continuously online. Above all, the device according to the invention and the method according to the invention allow a determination of the concentration of the released active ingredient or active ingredients, a determination of the release rate of the active ingredient or active ingredients or the determination of the release profile of one or more active ingredients.

On the other hand, the device according to the invention and the method according to the invention allow a determination of the properties of a release system, in particular a capsule, for example the mechanical stability and the breaking strength of the capsule or the retardation behavior, for example a capsule after storage for a certain period of time.

With the device according to the invention and the method according to the invention, it is also possible to check the distribution and adhesion of a release system, in particular a capsule (6) or a precursor (6), on a substrate, and / or the substantivity of a To analyze the active substance or several active substances after the release from the release system (6), in particular from a capsule (6) or a precursor (6), on a substrate; and / or to analyze the influence of physical or chemical factors, for example temperature, light, UV radiation, pH value, on the mechanical stability and breaking strength of a release system and / or to analyze the release of an active ingredient or several active ingredients from a release system ; and / or to check the release of one or more active ingredients and the properties of a delivery system during the development and manufacture of a delivery system.

Summary of the invention

In a first aspect, the present invention relates to a device 1 which is suitable for the analytical and / or sensory determination of the release of an active ingredient or several active ingredients from a release system 6, in particular an active ingredient or several active ingredients from a capsule 6 or a precursor 6, and / or to determine the properties of a Release system 6, in particular a capsule 6 or a precursor 6, which is located on a sample carrier 7 on a support surface 8, comprising:

(a) a skeleton 2;

(b) an activation device 3 which is connected to the basic structure 2 and which is set up to open or activate the release system 6, in particular the capsule 6 or the precursor 6, and to release the active ingredient contained therein or the several active ingredients contained therein; and

(c) a detection device 5, set up for the analytical determination of the released active ingredient or active ingredients, and designed in such a way that the released active ingredient or the several released active ingredients can be fed to the detection device 5.

In a further aspect, the present invention is directed to a method for the analytical and / or sensory determination of the release of an active ingredient or several active ingredients from a release system 6, in particular from a capsule 6 or a precursor 6, and / or for determining the Properties of a release system 6, in particular a capsule 6 or a precursor 6, which comprises the following steps:

(i) providing a release system 6, in particular a capsule 6 or a precursor 6, which comprises the one or more active ingredients, on a sample carrier 7 or on a support surface 8;

(ii) positioning the activation device 3 with an activator 31 above the release system 6, in particular above the capsule 6 or the precursor 6;

(iii) Lowering the activation device 3;

(iv) releasing the active ingredient or the plurality of active ingredients from the release system 6, in particular from the capsule 6 or the precursor 6, by means of the activator 31;

(v) collecting and supplying the released active ingredient or active ingredients to a detection device 5; and (vi) analytical determination of the released active ingredient or active ingredients.

Ultimately, the present invention is directed to the use of the device according to the invention and the method according to the invention for the analytical and / or sensory determination of the release of an active ingredient or several active ingredients, in particular the concentration, the release rate or the release profile from a release system 6, in particular from a capsule 6 or a precursor 6; to determine properties, for example the mechanical stability, the breaking strength or the retardation behavior, of a release system 6, in particular a capsule 6 or a precursor 6, in particular the mechanical stability, the breaking strength or the retardation behavior, of capsules 6 made of different capsule materials and different active ingredients; for analyzing the distribution and adhesion of a release system 6, in particular a capsule 6 or a precursor 6, on a substrate, in particular after washing and drying textiles; for analyzing the substantivity of an active ingredient or several active ingredients after the release from the release system 6, in particular from a capsule 6 or a precursor 6, on a substrate; to analyze the influence of physical or chemical factors, for example temperature, light, UV radiation, pH value, on the mechanical stability and breaking strength of a release system, in particular a capsule or a precursor 6 and / or on the release of an active ingredient or of several active ingredients from a release system 6, in particular from a capsule 6 or a precursor 6; for the analytical determination of the release of an active ingredient or several active ingredients and for the determination of the properties of a release system 6, in particular a capsule 6 or a precursor 6, during the production of the release system 6. These and other aspects, features, and advantages of the present

Invention will become apparent to those skilled in the art from a study of the following detailed description and claims. Each feature from one aspect of the invention can in principle be used in any other aspect of the invention. Furthermore, it goes without saying that the examples contained herein are intended to describe and illustrate the invention, but not to limit it, and in particular the present invention is not limited to these examples.

The term “at least one” as used in the context of the present

Description used refers to one or more, for example one, two, three, four, five, six, seven, eight, nine or more. For example, the term “at least one positioning unit” means that at least one positioning unit is detected, but also two or more

Positioning units can be included.

characters

FIG. 1 shows a schematic plan view of a preferred variant of the device according to the present invention.

FIG. 2 is a schematic cross section through a preferred variant of an activation device of the device according to the present invention.

FIG. 3 is a perspective detailed view of a preferred variant of the device according to the present invention.

FIG. 4 is a perspective view of a preferred variant of the device in an overall view with a detection system and feed lines according to the invention.

FIG. 5 is a schematic representation of the steps of the analysis method according to the present invention. FIG. 6 shows an exemplary course of a continuous measurement of the capsule burst of a capsule containing perfume oil.

FIG. 7 shows a comparison of the fragrance release from core / shell perfume oil capsules based on methylformamide with different wall thicknesses

Detailed description of the invention

In the following, the device according to the invention, variants of the device and preferred embodiments thereof will be described in more detail with reference to the accompanying FIGS.

The device 1 for analytical and / or sensory determination is not only to be understood for the analytical determination of the release of an active ingredient or several active ingredients from a capsule, but is generally intended for the analytical and / or sensory determination of the release of an active ingredient or several active ingredients configured a delivery system comprising an active ingredient.

A release system in the context of the present invention is understood to mean a solid preparation, for example particles or capsules, which contains one or more active ingredients. A preferred delivery system is a capsule, preferably a microcapsule, of the matrix type or of the core / shell type. In matrix encapsulation, the active ingredient (s) is / are mixed homogeneously with the filling component (“matrix”) and a particle is created in which the active ingredient (s) is / are evenly distributed. The active ingredient (s) are usually released from this type of capsule either by diffusion of the active ingredient (s) into the environment or by the rate of degradation of the matrix. In the case of core-shell encapsulation, the active substance (s) that form the core is / are enveloped with a shell material. The result is a real capsule with one or more shells. Usually generated a mechanical stress, for example pressure or shear, a complete release of the core material. However, it is also possible to specifically release the core material through alternative opening mechanisms, for example temperature, pH values, UV light, microwaves or ultrasound.

In connection with the present invention, a suitability of the device 1 according to the invention for the analytical determination of the release of an active ingredient from a capsule, such as, for example, from flart capsules, soft capsules (soft-shelled capsules), macrocapsules, microcapsules, capsule slurries, capsule emulsions, in particular prefers.

A release system in the context of the present invention is also understood to mean a precursor or a precursor substance. With such a precursor or a precursor substance, a chemical or physical impulse, for example by temperature, oxygen (oxidation), light, enzymes, microorganisms, chemical reaction (for example hydrolysis), change in the pH value or moisture, etc. Active ingredient or more active ingredients released. Precursors used according to the invention are, for example, fragrances with a weak inherent odor, which release at least one new fragrance molecule when they come into contact with external factors such as light, water or oxygen. As a result, new fragrance notes are released over and over again over the life of a fragrance and a slightly varying odor is created.

In the context of the present invention, the term “release system” preferably encompasses capsules, in particular microcapsules, as well as precursors or precursor substances. The terms “release system”, “capsule”, “microcapsule”, “precursor or precursor compound” are used in the following description with equal value next to one another and interchangeably so that one term includes the other and vice versa. The terms “capsule” and “microcapsule” include both a matrix type and a core / shell type capsule. In a first aspect, the present invention consequently relates to a device 1 for the analytical and / or sensory determination of the release of an active ingredient or several active ingredients from a release system 6, preferably an active ingredient or several active ingredients from a capsule 6 or a precursor.

By release is meant the release or generation of an active ingredient from the formulation, i.e. from the release system 6, preferably the capsule 6 or the precursor 6.

Under analytical determination is generally a qualitative (identification of the active ingredient) and / or quantitative (amount of the active ingredient) analysis of a released or generated from the release system 6, in particular one or more from a capsule 6 or a precursor 6 or released or generated active ingredient or released or generated active ingredients understood. By means of the analytical determination, the concentration of the released active ingredient or active ingredients and the release rate, i.e. the release of the active ingredient or active ingredients over time, can be determined.

When determining the release rate, it is measured how, i.e. with what intensity and / or in what concentration, the active ingredient or the several active ingredients are released from the capsule over time.

In addition, the analytical determination can also be used to determine the release profile, ie a rapid or delayed release, of an active ingredient or a plurality of active ingredients, both qualitatively and quantitatively. The determination of the release profile is particularly important in the case of mixtures of active substances, for example perfume oils, fragrance mixtures or flavor mixtures. The release profile can be used to determine how, ie with what intensity and / or in what concentration over time, the individual components of a fragrance mixture or flavor mixture are released from the release system, in particular from a capsule 6 or from a precursor 6. In addition, the device 1 is configured to determine the properties of a release system 6, in particular a capsule 6. Determination of the properties of a release system is understood to mean an analysis of the functional properties, such as mechanical stability, breaking strength or retardation behavior, in particular after storage for a certain period of time, etc. of the release system or the capsule.

By analyzing the released active ingredient or active ingredients, information about the concentration of the released active ingredient, about the rate of release of the active ingredient (rapid vs. delayed release), about the release profile, for example of an active ingredient mixture, or about how stable the capsule shell is, what burst behavior (break-open behavior) the capsule shell has, what retardation properties the capsule shell has, for example after storage of the release system for a certain period of time, etc.

The material or core material or active ingredient contained in the release system 6, preferably the capsule 6, distributed in the matrix is solid, liquid or gaseous substances. Preferably, the core material of the release system 6 is a volatile substance that is volatile at room temperature.

The selection of the active ingredients which are used in the release system described above depends essentially on the intended use of the release system.

Preferably, in the release system 6, preferably the capsule 6, active ingredients from the fields of detergents and cleaning agents, adhesives, coating compositions such as. B. paints and varnishes, binders, materials such as plastics, paper, textiles, lubricants, building materials, dyes, organic and inorganic powders, pigment dispersions, phase transition materials, flame retardants, but also agrochemicals Active ingredients from the cosmetic and pharmaceutical sectors used.

The release system 6, preferably the capsule 6, preferably contains at least one active ingredient selected from the group consisting of: fragrances, flavorings, perfume oils, fragrance mixtures, aromas, vitamins, minerals, antioxidants, anthocyanins, coenzyme IO, Adhesives, mineral oils, waxes and fats, biocides, fungicides, flerbicides, pesticides, insecticides, fertilizers, disperse dyes and dye solutions or monomers for the synthesis of plastics.

The one or more active ingredients are preferably fragrances, flavorings, perfume oils, fragrance mixtures or aromas. These active ingredients are predominantly volatile substances that are volatile at room temperature.

The preferably used fragrances or flavors or fragrance mixtures or flavor mixtures which comprise two, three, four, five or even many more other fragrance or flavor components are selected from the group consisting of: (1) hydrocarbons; (2) aliphatic alcohols; (3) aliphatic aldehydes and their acetals; (4) aliphatic ketones and their oximes; (5) aliphatic sulfur-containing compounds; (6) aliphatic nitriles; (7) esters of aliphatic carboxylic acids; (8) acyclic terpene alcohols; (9) acyclic terpene aldehydes and ketones; (10) cyclic terpene alcohols; (11) cyclic terpene aldehydes and ketones; (12) cyclic alcohols; (13) cycloaliphatic alcohols; (14) cyclic and cycloaliphatic ethers; (15) cyclic and macrocyclic ketones; (16) cycloaliphatic aldehydes; (17) cycloaliphatic ketones; (18) esters of cyclic alcohols; (19) esters of cycloaliphatic alcohols; (20) esters of cycloaliphatic carboxylic acids; (21) araliphatic alcohols; (22) esters of araliphatic alcohols and aliphatic carboxylic acids; (23) araliphatic ethers; (24) aromatic and araliphatic aldehydes; (25) aromatic and araliphatic ketones; (26) aromatic and araliphatic carboxylic acids and their esters; (27) nitrogen-containing aromatic compounds; (28) phenols, Phenyl ethers and phenyl esters; (29) heterocyclic compounds; (30) lactones; as well as any mixtures thereof.

The choice of fragrances or flavors is very extensive; corresponding substances can be found z. B. in "S. Arctander, Perfume and Flavor Chemicals, Vol. I and II, Montclair, N. J., 1969, self-published "or" H. Surburg and J. Panten, Common Fragrance and Flavor Materials, 6th edition, Wiley-VCH, Weinheim, 2016 “.

The following are specifically mentioned:

Extracts from natural raw materials: This group stands for essential oils, concretes, absolutes, resins, resinoids, balms, tinctures such as. B. Ambré tincture; Amyris oil; Angelica seed oil; Angelica root oil; Anise oil; Valerian oil; Basil oil; Tree moss absolute; Bay oil; Mugwort oil; Benzoeresine; Bergamot oil; Beeswax absolute; Birch tar oil; Bitter almond oil; Savory oil; Bucco leaf oil; Cabreuva oil; Cade oil; Calamus oil; Camphor oil; Cananga oil; Cardamom oil; Cascarilla oil; Cassia oil; Cassie absolute; Castoreum absolute; Cedar leaf oil; Cedarwood oil; Cistus oil; Citronella oil; Lemon oil; Copaiva balsam; Copaiva balsam oil; Coriander oil; Costus root oil; Cumin oil; Cyprus oil; Davana oil; Dill herb oil; Dill seed oil; Eau de brouts absolute; Oakmoss absolute; Elemi oil; Tarragon oil; Eucalyptus citriodora oil; Eucalyptus oil; Fennel oil; Spruce needle oil; Galbanum oil; Galbanum resin; Geranium oil; Grapefruit oil; Guaiac wood oil; Gurjun balm; Gurjun balm oil; Helichrysum absolute; Helichrysum oil; Ginger oil; Orris root absolute; Orris root oil; Jasmine absolute; Calamus oil; Chamomile oil blue; Roman chamomile oil; Carrot seed oil; Cascarilla oil; Pine needle oil; Spearmint oil; Caraway seed oil; Labdanum oil; Labdanum absolute; Labdanum resin; Lavandin absolute; Lavandin oil; Lavender absolute; Lavender oil; Lemongrass oil; Lovage oil; Distilled lime oil; Pressed lime oil; Linaloe oil; Litsea cubeba oil; Bay leaf oil; Mace oil; Marjoram oil; Mandarin oil; Massoirinden oil; Mimosa absolute; Musk seed oil; Musk tincture; Muscatel sage oil; Nutmeg oil; Myrrh absolute; Myrrh oil; Myrtle oil; Clove leaf oil; Clove blossom oil; Neroli oil; Olibanum absolute; Olibanum oil; Opopanax oil; Orange blossom absolute; Orange oil; Origanum oil; Palmarosa oil; Patchouli oil; Perilla oil; Balsam oil of Peru; Parsley leaf oil; Parsley seed oil; Petitgrain oil; Peppermint oil; Pepper oil; Allspice oil; Pine oil; Poley oil; Rose absolute; Rosewood oil; Rose oil; Rosemary oil; Dalmatian sage oil; Spanish sage oil; Sandalwood oil; Celery seed oil; Spiclavender oil; Star anise oil; Styrax oil; Marigold oil; Pine needle oil; Tea tree oil; Turpentine oil; Thyme oil; Tolu balsam; Tonka absolute; Tuberose absolute; Vanilla extract; Violet leaf absolute; Verbena oil; Vetiver oil; Juniper berry oil; Wine yeast oil; Wormwood oil; Wintergreen oil; Ylang oil; Hyssop oil; Civet absolute; Cinnamon leaf oil; Cinnamon bark oil and fractions thereof or ingredients isolated from it.

Individual fragrances: Individual fragrances can be divided into a large number of classes, namely:

Hydrocarbons such as 3-carene; a-pinene; ß-pinene; a-terpinene; g-terpinene; p-cymene; Bisabolene; Camphene; Caryophyllene; Cedren; Ferns; Limonene; Longifolene; Myrcene; Ocimen; Valencene; (E, Z) ~ 1, 3,5-undecatriene; Styrene; Diphenylmethane;

Aliphatic alcohols such as hexanol; Octanol; 3-octanol; 2,6-dimethylheptanol; 2-methyl-2-heptanol; 2-methyl-2-octanol; (E) - 2-flexenol; (E) - and (ZJ-3-hexenol; 1- octen-3-ol; mixture of 3,4,5,6,6-pentamethyl-3/4-hepten-2-ol and 3, 5,6, 6- Tetramethyl-4-methyleneheptan-2-ol; (E, ZJ-2,6-nonadienol; 3,7-dimethyl-7-methoxy-octan-2-ol; 9-decenol; 10-undecenol; 4-methyl -3-decen-5-ol;

Aliphatic aldehydes and their acetals such as hexanal; Heptanal; Octanal; Nonanal; Decanal; Undecanal; Dodecanal; Tridecanal; 2-methyloctanal; 2-methyl nonanal; (EJ-2-hexenal; (J-4-heptenal; 2,6-dimethyl-5-heptenal; 10-undecenal; (E) - 4-decenal; 2-dodecenal; 2,6,10-trimethyl-9- undecenal; 2,6,10-trimethyl-5,9-undecadienal; heptanal diethyl acetal; 1,1-dimethoxy-2,2,5-trimethyl-4-hexene;

Citronellyloxyacetaldehyde; 1 - (1-methoxy-propoxy) - (E, Z) -3-hexene;

Aliphatic ketones and their oximes, such as, for example, 2-heptanone; 2-octanone; 3-octanone; 2-nonanone; 5-methyl-3-heptanone; 5-methyl-3-heptanone oxime; 2,4,4,7-tetramethyl-6-octen-3-one; 6-methyl-5-hepten-2-one; Aliphatic sulfur-containing compounds such as, for example, 3-methylthio-hexanol; 3-methylthiohexyl acetate; 3-mercaptohexanol; 3-mercaptohexyl acetate; 3-mercaptohexyl butyrate; 3-acetylthiohexyl acetate; 1-menthen-8-thiol;

Aliphatic nitriles such as 2-nonenoic acid nitrile; 2-undecenoic acid nitrile; 2-tridecenoic acid nitrile; 3,12-tridecadienoic acid nitrile; 3,7-dimethyl-2,6-octadiene-acid nitrile; 3,7-dimethyl-6-octenoic acidithl;

Esters of aliphatic carboxylic acids such as (E) - and (ZJ-S-hexenyl formate; ethyl acetoacetate; isoamyl acetate; hexyl acetate; 3,5,5-trimethylhexyl acetate; 3-methyl-2-butenyl acetate; ('Ej-2-hexenyl acetate; (E ) - and (j-3-hexenyl acetate; octyl acetate; 3-octyl acetate; 1-octen-3-ylacetate; ethyl butyrate; butyl butyrate; isoamyl butyrate; hexyl butyrate; (E) - and (ZJ-3-hexenyl isobutyrate; hexyl crotonate; ethyl isovalerate; Ethyl 2-methylpentanoate; ethyl hexanoate; allyl hexanoate; ethyl heptanoate; allyl heptanoate; ethyl octanoate; ethyl decadienoate; methyl 2-octinate; methyl 2-nonynate; allyl 2-isoamyloxyacetate; methyl 3,7-dimethyl 2,6-octadienoate; 4-methyl-2-pentyl crotonate;

Acyclic terpene alcohols such as. B. Citronellol; Geraniol; Nerol; Linalool; Lavadulol; Nerolidol; Farnesol; Tetrahydrolinalool; Tetrahydrogeraniol; 2,6-dimethyl-7-octen-2-ol; 2,6-dimethyloctan-2-ol; 2-methyl-6-methylen-7-octen-2-ol; 2,6-dimethyl-5,7-octadien-2-ol; 2,6-dimethyl-3,5-octadien-2-ol; 3,7-dimethyl-4,6-octadien-3-ol; 3,7-dimethyl-1,5,7-octatrien-3-ol; 2,6-dimethyl-2,5,7-octatrien-1-ol; and their formates, acetates, propionates, isobutyrates, butyrates, isovalerianates, pentanoates, hexanoates, crotonates, tiglinates and 3-methyl-2-butenoates;

Acyclic terpene aldehydes and ketones such. B. Geranial; Neral; Citronellal; 7-hydroxy-3,7-dimethyloctanal; 7-methoxy-3,7-dimethyloctanal; 2,6,10-trimethyl-9-undecenal; Geranylacetone; as well as the dimethyl and diethyl acetals of geranial, neral, 7-hydroxy-3,7-dimethyloctanal; Cyclic terpene alcohols such as. B. menthol; Isopulegol; alpha-terpineol; Terpinenol-4; Menthan-8-ol; Menthan-1-ol; Menthan-7-ol; Borneol; Isoborneol; Linalool oxide; Nopoly; Cedrol; Ambrinol; Vetiverol; Guajol; and their formates, acetates, propionates, isobutyrates, butyrates, isovalerianates, pentanoates, hexanoates, crotonates, tiglinates and 3-methyl-2-butenoates;

Cyclic terpene aldehydes and ketones such. B. menthone; Isomenthone; 8-mercaptomenthan-3-one; Carvone; Camphor; Fenchone; alpha-ionon; beta-ionon; alpha- n-methylionone; beta-n-methylionone; alpha-isomethylionone; beta-isomethylionone; alpha-lron; alpha damascone; beta damascone; beta-damascenone; delta damascone; gamma damascone; 1 - (2,4,4-trimethyl-2-cyclohexen-1-yl) -2-buten-1-one; 1, 3,4,6,7,8a- Flexahydro-1, 1, 5,5-tetramethyl-2H-2,4a-methanonaphthalen-8 (5H) -one; 2-methyl-4- (2,6, 6-trimethyl-1-cyclohexen-1-yl) -2-butenal; Nootkatone; Dihydronootkatone; 4,6,8-megastigmathen-3-one; alpha-sinensal; beta-sinensal; acetylated cedar wood oil (methyl cedryl ketone);

Cyclic alcohols such as 4-tert-butylcyclohexanol; 3,3,5-trimethylcyclohexanol; 3-isocamphylcyclohexanol; 2,6,9-trimethyl-Z2, Z5, E9-cyclododecatrien-1-ol; 2-isobutyl-4-methyltetrahydro-2FI-pyran-4-ol;

Cycloaliphatic alcohols such as alpha, 3,3-trimethylcyclohexylnnethanol; 1- (4-isopropylcyclohexyl) ethanol; 2-methyl-4- (2,2,3-trimethyl-3-cyclopent-1 -yl) butanol; 2-methyl-4- (2,2,3-trimethyl-3-cyclopent-1-yl) -2-buten-1-ol; 2-ethyl-4- (2,2,3-trimethyl-3-cyclopent-1 -yl) -2-buten-1-ol; 3-methyl-5- (2,2,3-trimethyl-3-cyclopent-1-yl) -pentan-2-ol; 3-methyl-5- (2,2,3-trimethyl-3-cyclopent-1-yl) -4-penten-2-ol; 3,3-dimethyl-5- (2,2,3-trimethyl-3-cyclopent-1-yl) -4-penten-2-ol; 1 - (2,2,6-trimethylcyclohexyl) pentan-3-ol; 1 - (2,2,6-trimethylcyclohexyl) hexan-3-ol;

Cyclic and cycloaliphatic ethers such as cineole; Cedryl methyl ether; Cyclododecyl methyl ether; 1,1-dimethoxycyclododecane;

(Ethoxymethoxy) cyclododecane; alpha cedrene epoxide; 3a, 6, 6,9a-

Tetramethyldodecahydronaphtho [2,1 -b] furan; 3a-ethyl-6,6,9a- trimethyldodecahydronaphtho [2,1-b] furan; 1,5,9-trimethyl-13-oxabicyclo [10.1.0] trideca-4,8-diene; Rose oxide; 2- (2,4-dimethyl-3-cyclohexen-1 -yl) -5-methyl-5- (1-methylpropyl) -1,3-dioxane;

Cyclic and macrocyclic ketones such as 4-tert-butylcyclohexanone; 2,2,5-thmethyl-5-pentylcydopentanone; 2-heptylcyclopentanone; 2-pentylcyclopentanone; 2-hydroxy-3-methyl-2-cyclopenten-1-one; 3-methyl-cis-2-penten-1-yl-2-cyclopenten-1 - one; 3-methyl-2-pentyl-2-cyclopenten-1-one; 3-methyl-4-cyclopentadecenone; 3-methyl-

5-cyclopentadecenone; 3-methylcyclopentadecanone; 4- (1-ethoxyvinyl) -3, 3,5,5-tetramethylcyclohexanone; 4-tert-pentylcyclohexanone; 5-cyclohexadecen-1-one; 6,7-dihydro-1, 1, 2,3,3-pentamethyl-4 (5H) -indanone; 8-cyclohexadecen-1-one; 9-

Cycloheptadecen-1-one; Cyclopentadecanone; Cyclohexadecanone;

Cycloaliphatic aldehydes such as 2,4-dimethyl-3-cyclohexenecarbaldehyde; 2-methyl-4- (2,2,6-trimethyl-cyclohexen-1-yl) -2-butenal; 4- (4-hydroxy-4-methylpentyl) -3-cyclohexenecarbaldehyde; 4- (4-methyl-3-penten-1-yl) -3-cyclohexenecarbaldehyde;

Cycloaliphatic ketones such as. B. 1- (3,3-Dimethylcyclohexyl) -4-penten-1-one; 2,2-dimethyl-1 - (2,4-dimethyl-3-cyclohexen-1 -yl) -1-propanone; 1 - (5,5-dimethyl-1-cyclohexen-1-yl) -4-penten-1-one; 2,3,8,8-tetramethyl-1, 2,3,4,5,6,7,8-octahydro-2-naphthalenyl methyl ketone; Methyl 2,6,10-trimethyl-2,5,9-cyclododecathenyl ketone; tert-butyl- (2,4-dimethyl-3-cyclohexen-1-yl) ketone;

Esters of cyclic alcohols such as 2-tert-butylcyclohexyl acetate; 4-tert-butylcyclohexyl acetate; 2-tert-pentylcyclohexyl acetate; 4-tert-pentylcyclohexyl acetate; 3,3,5-trimethylcyclohexyl acetate; Decahydro-2-naphthyl acetate; 2-cyclopentylcyclopentylcrotonate; 3-pentyl tetrahydro-2H-pyran-4-ylacetate; Decahydro-2,5,5,8a-tetramethyl-2-naphthyl acetate; 4,7-methano-3a, 4,5,6,7,7a-hexahydro-5 or 6-indenyl acetate; 4,7-methano-3a, 4,5,6,7,7a-hexahydro-5 or 6-indenyl propionate; 4,7-methano-3a, 4,5,6,7,7a-hexahydro-5 or 6-indenyl isobutyrate; 4,7-methanooctahydro-5, or

6-indenyl acetate; Esters of cycloaliphatic alcohols such as, for example, 1-cyclohexylethyl crotonate;

Esters of cycloaliphatic carboxylic acids such as. B. allyl 3-cyclohexyl propionate; Allylcyclohexyloxyacetate; cis and trans methyl dihydrojasmonate; cis and trans methyl jasmonate; Methyl 2-hexyl-3-oxocyclopentanecarboxylate; Ethyl 2-ethyl-6,6-dimethyl-2-cyclohexenecarboxylate; Ethyl 2,3,6,6-tetramethyl-2-cyclohexene carboxylate; Ethyl 2-methyl-1,3-dioxolane-2-acetate;

Araliphatic alcohols such as benzyl alcohol; 1-phenylethyl alcohol; 2-phenylethyl alcohol; 3-phenylpropanol; 2-phenylpropanol; 2-phenoxyethanol; 2,2-dimethyl-3-phenylpropanol; 2,2-dimethyl-3- (3-methylphenyl) propanol; 1,1-dimethyl-2-phenyl-ethyl alcohol; 1,1-dimethyl-3-phenylpropanol; 1-ethyl-1-methyl-3-phenylpropanol; 2-methyl-5-phenylpentanol; 3-methyl-5-phenylpentanol; 3-phenyl-2-propen-1-ol; 4-methoxybenzyl alcohol; 1- (4-isopropylphenyl) ethanol;

Esters of araliphatic alcohols and aliphatic carboxylic acids such as benzyl acetate; Benzyl propionate; Benzyl isobutyrate; Benzyl isovalerate; 2-phenylethyl acetate; 2-phenylethyl propionate; 2-phenylethyl isobutyrate; 2-phenylethyl isovalerate; 1-phenylethyl acetate; alpha-trichloromethylbenzyl acetate; alpha, alpha-dimethylphenylethyl acetate; alpha, alpha-dimethylphenylethyl butyrate; Cinnamyl acetate; 2-phenoxyethyl isobutyrate; 4-methoxybenzyl acetate;

Araliphatic ethers such as 2-phenylethyl methyl ether; 2-phenylethyl isoamyl ether;

2-phenylethyl-1-ethoxyethyl ether; Phenyl acetaldehyde dimethyl acetal;

Phenylacetaldehyde diethyl acetal; Hydratropaaldehyde dimethyl acetal;

Phenylacetaldehyde glycerol acetal; 2,4,6-trimethyl-4-phenyl-1,3-dioxane; 4, 4a, 5, 9b-tetrahydroindeno [1, 2-d] -m-dioxin; 4,4a, 5,9b-tetrahydro-2,4-dimethylindeno [1,2-d] -m-dioxin;

Aromatic and araliphatic aldehydes such as. B. benzaldehyde; Phenylacetaldehyde;

3-phenylpropanal; Hydratropaaldehyde; 4-methylbenzaldehyde; 4-methylphenyl acetaldehyde; 3- (4-ethylphenyl) -2,2-dimethylpropanal; 2-methyl-3- (4-isopropylphenyl) - propanal; 2-methyl-3- (4-tert-butylphenyl) propanal; 2-methyl-3- (4-isobutylphenyl) propanal; 3- (4-tert-butylphenyl) propanal; Cinnamaldehyde; alpha-butyl cinnamaldehyde; alpha-amylcinnamaldehyde; alpha-hexyl cinnamaldehyde; 3-methyl-5-phenylpentanal; 4-methoxybenzaldehyde; 4-hydroxy-3-methoxybenzaldehyde; 4-hydroxy-3-ethoxybenzaldehyde; 3,4-methylenedioxybenzaldehyde; 3,4-dimethoxybenzaldehyde; 2-methyl-3- (4-methoxyphenyl) propanal; 2-methyl-3- (4-methylenedioxyphenyl) propanal;

Aromatic and araliphatic ketones such as acetophenone; 4-methylacetophenone; 4-methoxyacetophenone; 4-tert-butyl-2,6-dimethylacetophenone; 4-phenyl-2-butanone; 4- (4-hydroxyphenyl) -2-butanone; 1- (2-naphthalenyl) ethanone; 2-benzofuranylethanone; (3-methyl-2-benzofuranyl) ethanone; Benzophenone; 1,1, 2,3,3, 6-hexamethyl-5-indanyl methyl ketone; 6-tert-butyl-1,1-dimethyl-4-indanyl methyl ketone; 1 - [2,3-dihydro-1, 1, 2,6-tetramethyl-3- (1-methylethyl) -1H-5-indenyl] ethanone; 5 ‘, 6‘, 7 ‘, 8‘-tetrahydro-

3 ‘, 5‘, 5 ‘, 6‘, 8 ‘, 8‘-hexamethyl-2-acetonaphthone;

Aromatic and araliphatic carboxylic acids and their esters such as benzoic acid; Phenylacetic acid; Methyl benzoate; Ethyl benzoate; Hexyl benzoate; Benzyl benzoate; Methylphenyl acetate; Ethyl phenyl acetate; Geranyl phenyl acetate; Phenylethyl phenyl acetate; Methylcinnmat; Ethyl cinnamate; Benzyl cinnamate; Phenylethyl cinnamate; Cinnamyl cinnamate; Allyl phenoxy acetate; Methyl salicylate; Isoamyl salicylate; Hexyl salicylate; Cyclohexyl salicylate; Cis-3-hexenyl salicylate; Benzyl salicylate; Phenylethyl salicylate; Methyl 2,4-dihydroxy-3,6-dimethylbenzoate; Ethyl 3-phenyl glycidate; Ethyl 3-methyl-3-phenyl glycidate;

Nitrogen-containing aromatic compounds such as 2,4,6-trinitro-1,3-dimethyl-5-tert-butylbenzene; 3,5-dinitro-2,6-dimethyl-4-tert-butyl acetophenone; Cinnamonitrile; 3-methyl-5-phenyl-2-pentenoic acid nitrile; 3-methyl-5-phenylpentanoic acid nitrile;

Methyl anthranilate; Methyl N-methyl anthranilate; Schiff's bases of methyl anthranilate with 7-hydroxy-3,7-dimethyloctanal, 2-methyl-3- (4-tert-butylphenyl) propanal or 2,4-dimethyl-3-cyclohexenecarbaldehyde; 6- Isopropylquinoline; 6-isobutylquinoline; 6-sec-butylquinoline; 2- (3-phenylpropyl) pyridine; Indole; Skatole; 2-methoxy-3-isopropylpyrazine; 2-isobutyl-3-methoxypyrazine;

Phenols, phenyl ethers and phenyl esters such as estragole; Anethole; Eugenol; Eugenyl methyl ether; Isoeugenol; Isoeugenyl methyl ether; Thymol; Carvacrol; Diphenyl ether; beta-naphthyl methyl ether; beta-naphthyl ethyl ether; beta-naphthyl isobutyl ether; 1,4-dimethoxybenzene; Eugenyl acetate; 2-methoxy-4-methylphenol; 2-ethoxy-5- (1-propenyl) phenol; p-cresylphenyl acetate;

Heterocyclic compounds such as 2,5-dimethyl-4-hydroxy-2H-furan-3-one; 2-ethyl-4-hydroxy-5-methyl-2H-furan-3-one; 3-hydroxy-2-methyl-4H-pyran-4-one; 2-ethyl-3-hydroxy-4H-pyran-4-one;

Lactones such as 1,4-octanolide; 3-methyl-1,4-octanolide; 1,4-nonanolide; 1,4-decanolide;

8-decen-1,4-olide; 1, 4-undecanolide; 1,4-dodecanolide; 1,5-decanolide; 1,5-dodecanolide; 4-methyl-1,4-decanolide; 1, 15-pentadecanolide; cis- and trans-11-pentadecen-1, 15-olide; cis- and trans-12-pentadecen-1, 15-olide; 1, 16-hexadecanolide;

9-hexadecen-1, 16-olide; 10-oxa-1, 16-hexadecanolide; 11-oxa-1, 16-hexadecanolide;

12-oxa-1, 16-hexadecanolide; Ethylene 1, 12-dodecanedioate; Ethylene 1,13-tridecanedioate; Coumarin; 2,3-dihydrocoumarin; Octahydrocoumarin; and any mixtures of the aforementioned fragrances or flavorings.

Also suitable and preferred as active ingredient are so-called precursor compounds or precursors, preferably fragrance precursors or fragrance precursors. This class of compounds are compounds that are formed by breaking a chemical bond, for example by chemical reaction, temperature, humidity, change in the pH value, oxygen (oxidation), light, in particular UV light, enzymes or microorganisms, releases a desired odor and / or fragrance molecule. Typically, to form a pro-fragrance, a desired fragrance raw material is chemically combined with a carrier, preferably a slightly volatile or moderately volatile one Carrier, connected. The combination results in a less volatile and more hydrophobic fragrance precursor with improved substantivity on fabrics. The fragrance is then released by breaking the bond between the fragrance raw material and the carrier, for example by changing the pH value (e.g. through perspiration when wearing), humidity, heat and / or sunlight during storage or drying on the Clothes line.

Such fragrance precursors or fragrance precursors are described, for example, in Herrmann, Andreas, Controlled release of volatiles under mild reaction conditions: from nature to everyday products, Angew. Chem., Int. Ed., 2007, 46, pages 2 - 30, the disclosure of which in this regard is incorporated into the present application in its entirety by reference.

The device 1 according to the present invention preferably consists of a basic frame 2. The basic frame can have any shape and construction which is set up to receive an activation device (3).

In a preferred variant of the device according to the invention, the basic structure comprises at least one X-axis 21 and one Y-axis 22. In a further preferred variant, the basic structure 2 consists of two legs which run parallel to one another. The X-axis 21 is supported, preferably at a 90 ° angle, on the basic framework and is set up in such a way that an activation device 3 is horizontal and in the X-direction relative to the support surface 8 or the plane on which the sample to be analyzed lies, to move. The device according to the present invention preferably has two X-axes 21 which are mounted on the basic structure at a distance from and parallel to one another.

On the two X-axes 22, in turn, a Y-axis 22, which is set up in such a way, is supported, preferably at a 90 ° angle, an activation device 3 horizontally and in the Y-direction relative to the support surface 8 or the plane on which the sample to be analyzed lies. By means of the two X-axes 21 and the Y-axis 22, the activation device 3 can be set to predetermined coordinates of the support surface 8 on which the sample carrier 7 or the direct sample lies, or in the direction of the sample 6 to be analyzed move towards it and position it exactly over the sample.

The device 1 for the analytical and / or sensory determination of an active ingredient or several active ingredients from a release system 6, in particular from a capsule 6 or a precursor 6, according to the first aspect of the present invention further comprises an activation device 3. The activation device 3 is used to open the release system 6, in particular the capsule 6 or the precursor 6, for example to break open or activate it, in order to release the active ingredient or the several active ingredients from the release system. The activation device of the device according to the invention is preferably arranged on the basic frame 2, in particular on the Y-axis 22, and connected to it. For movement and positioning in relation to the sample 6, the activation device 3 is fastened to the basic framework 2, in particular so that it can move freely in three dimensions.

The movement and positioning of the activation device 3 horizontally and in the X and Y positions relative to the sample carrier 7 or the support surface 8 on which the sample 6 to be analyzed, ie the release system 6, lies, is carried out by means of X / Y positioning units (41; 42) reached. The positioning units are either a drive, by means of which the coordinates of the activation device 3 can be set manually, or can be set using an electric motor that is controlled by an EDP. The positioning unit is preferably an electric motor which controls the coordinates of the sample 6 to be analyzed by means of an EDP control and positions the activation device 3 above the sample 6 to be analyzed.

For the analytical and / or sensory determination, the sample 6, ie the active ingredient release system 6 to be analyzed, is preferably the one to capsule 6 to be analyzed or the precursor 6 to be analyzed on a sample carrier 7, which in turn is preferably located on a support surface 8. The support surface 8 is usually a surface on which the device 1 according to the invention is also located. In an alternative variant, the sample 6, ie the active ingredient release system to be analyzed, preferably the capsule 6 to be analyzed or the precursor 6 to be analyzed, can also be located directly on the support surface 8. Both the sample carrier 7 and the support surface 8 can also be part of the device 1.

The sample carrier 7 or the support surface 8 on which the sample 6 to be analyzed is located is preferably arranged within the basic framework 2 of the device according to the invention.

The support surface 8 is preferably a mat with a smooth surface, preferably made of plastic. The support surface 8 is preferably a rubber mat which prevents the sample carrier 7 from slipping during the analysis process.

For example, in order to test the distribution or adhesion of an active ingredient release system on a specific substrate, the sample carrier 7 can also be a fabric, for example clothing, linen, etc. made of cotton, linen, wool, viscose, polyacrylic, polyamide, polyester, or another organic or inorganic substrate or its surface, for example tiles, linoleum, wood, glass, metal, hair, etc. or can be a fiber cover.

In the alternative variant, in which the sample 6 is located directly on the support surface 8, for example in the case of a floor cleaning agent with an encapsulated active ingredient 6 or a precursor 6, the device according to the invention for analyzing the active ingredient can be positioned directly above the support surface and the analysis can be carried out on the surface of the support surface 8. In such a case, the support surface 8 can also be a fabric, for example clothing, linen, etc. made of cotton, linen, wool, viscose, polyacrylic, polyamide, Polyester, or another organic or inorganic substrate or its surface, for example tiles, linoleum, wood, glass, metal, hair, etc., or it can be a fiber cover.

In addition, the device for the analytical and / or sensory determination of an active ingredient or several active ingredients from a release system, in particular from a capsule 6 or a precursor 6, according to the first aspect of the present invention comprises a detection device or an analysis device 5 for analytical determination of the released active ingredient or of the several released active ingredients. The detection device or analysis device 5 is designed in such a way that the released active ingredient or the plurality of released active ingredients can be fed to the detection device 5 via a detection line 35.

The detection device or analysis system 5 is a measuring device which enables a qualitative and / or quantitative analysis of the released active ingredient or active ingredients.

The detection device or analysis device 5 is preferably selected from the group consisting of gas chromatograph (GC), gas chromatograph / mass spectrometer (GC / MS), ion mobility spectrometry (IMS), FAIMS (high field asymmetric waveform ion mobility spectrometry) , GC-FAIMS and GC-MS-FAIMS or combinations of the aforementioned measuring devices.

Preferably used as detection device or analysis device 5, IMS (ion mobility spectrometry), FAIMS (high field asymmetric waveform ion mobility spectrometry), GC-FAIMS and GC-MS-FAIMS or a combination of the aforementioned measuring devices for analysis.

The detection device or analysis device FAIMS (high field asymmetric waveform ion mobility spectrometry) is most preferred. The FAIMS enables the detection and analysis of volatile chemical substances directly from a gas flow or from the gas phase over a liquid or a solid Sample. There are two mechanisms for adding the sample to the FAIMS unit: single sampling or continuous sampling. When taking individual samples, a defined volume of the gaseous analyte, ie the released active ingredient, is collected or adsorptively enriched in a preceding step and fed to the FAIMS. With continuous sampling, the gaseous analyte, ie the released active ingredient, is continuously fed to the FAIMS by means of a carrier gas. The sampling is preferably carried out continuously, whereby the analytical determination of the released active ingredient or active ingredients can be carried out in real time. This enables an analytical determination of the real-time release, which is particularly advantageous when determining the release of fragrance or flavoring mixtures.

In addition, it is possible with the device 1 according to the invention to bind the released active ingredient or the several released active ingredients to an adsorbent, for example in a Tenax tube, in order to concentrate them and then to measure them by means of GC-MS (dynamic Fleadspace method). With the dynamic fleadspace technique, the active ingredient released during the measurement or the several active ingredients released during the measurement are transferred to a suitable adsorber material via a continuous air flow, for example generated by the FAIMS or for which an additional external pump is used, or an inert gas , for example in a Tenax tube, or in a cold trap. For this purpose, the adsorbent-containing glass tube can either be integrated directly into the air flow from the CBA, or the active substance (s) is / are first (if the air flow is too high for the direct method) into a closed container (e.g. a plastic bag), in order to then guide the active ingredient (s) onto the adsorbent with less air flow. Then the Tenax tube (adsorber) or the trap is heated up and the enriched analytes reach the FAIMS or the column for gas chromatographic analysis, for example. In a preferred variant, the detection device or analysis device 5 has an alternative output for an olfactometer and / or an olfactory detection port (ODP) (sniffing port system) 52, with which a sensory determination of the released active ingredient or the released active ingredients is possible, so that in addition to the qualitative and / or quantitative analysis, a sensory analysis of the active ingredient can be carried out. Such a combination allows a correlation to be established between the analytical and sensory determination.

The sniffing port system can be arranged in the device according to the invention both in front of the detection device 5 and behind the detection device 5. The arrangement of the sniffing port system behind the detection device 5 is particularly advantageous when the detection device 5 is a FAIMS or an IMS, since the FAIMS or the IMS does not destroy the analytes and these are still available at the output of the FAIMS or the IMS stand. With such an arrangement, a correlation between the measured data and the sensory evaluation of the released active ingredients can be established particularly well.

In a most preferred variant of the device according to the invention, the FAIMS is equipped with a gas chromatograph (GC) and / or mass spectrometer (MS) and / or an olfactometer and / or an olfactory detection port (ODP) (sniffing port system) ( 52) combined.

The activation device 3 of the device according to the first aspect of the present invention comprises an activator 31. The activator 31 is preferably designed in the form of a stamp and is arranged at the lower end of the axis of the activation device 3 and perpendicular to the plane of the support surface 8. The activator 31 is connected to a Z-positioning unit 32. The Z-positioning unit 32 enables the activator to be lowered and raised perpendicular to the sample carrier 7 or to the support surface 8. By means of the Z-positioning unit 32, the activator 31 can be perpendicular to the sample carrier 7 or to the support surface 8 and thus perpendicular to the sample 6, ie to the active ingredient release system to be analyzed, preferably to the capsule to be analyzed or the precursor 6 to be analyzed, on the sample carrier 7 or the support surface 8 and positioned.

The Z-positioning unit 32 is either a positioning unit, by means of which the activator 31 can be lowered manually, or it can be lowered over the sample to be analyzed via an electric drive / motor which is controlled by an EDP. The positioning unit is preferably an electric motor which controls the coordinates of the samples to be analyzed by means of an EDP control and lowers the activator 31 over the sample to be analyzed.

The activator 31 is configured to exert a physical and / or chemical impulse on the sample 6 to be analyzed, ie the release system 6, preferably the capsule 6 or the precursor 6, so as to, in the event that the release system has a The capsule is to open the capsule or, in the case that the release system is a precursor, to activate the precursor and to release the active substance contained therein.

The physical and / or chemical pulse is an action on the release system through pressure, friction, temperature, change in the pFI value, UV radiation, ultrasound, microwave or a chemical reaction by means of which the capsule is opened or the precursor is activated. For this purpose, the activator 31 is designed accordingly, for example as a friction head, UV lamp, pipetting module, etc.

If the release system is a capsule, it can be opened by various opening mechanisms, as a result of which the capsule contents or the active ingredient (s) are released. In the majority of cases, the release system or the capsule is opened by mechanical stress, for example by pressure or shear. Alternative opening mechanisms, with which the active ingredient or the active ingredients can be released from the release system or the capsule are temperature, change in the pH value, microwaves, light energy, for example UV radiation or ultrasound.

Mechanical pressure and / or friction is preferably exerted perpendicularly on the sample 6 by means of the activator 31 in order to break the release system, preferably the capsule, and to release the active ingredient or ingredients contained therein. The mechanical pressure is generated by a pressure sensor 33. The pressure sensor 33 can be used to set the pressure that is applied to the active ingredient release system, preferably the capsule, in order to open it, i.e. to make it burst or break.

In order to generate friction, which also leads to breaking or improving of the active ingredient release system, the activation device comprises a rotation unit 38. The activator 31 is in direct connection with the rotation unit 38, which is driven by an electric motor. The rotation unit 38 sets the activator 31 in motion, for example by means of a concentric, eccentric or isometric movement. With the concentric movement, the activator performs rotating circular movements on the sample 6 to be analyzed, the circles having different radii. In the case of the eccentric movement, the activator performs rotating circular movements on the sample 6 to be analyzed, which are outside the center of the circle. During the isometric movement, the activator moves back and forth like a slide on the sample 6 to be analyzed in the X and Y directions.

By one of the above-mentioned movements, the activator 31 moves over the sample 6 to be analyzed and generates friction, as a result of which the active ingredient is released from the active ingredient release system, preferably the capsule.

In an alternative variant of the activation device 3, the rotation unit is an oscillator unit 38 which makes the activator 31 vibrate. By vibrating the activator over the sample to be analyzed 6 friction is generated, as a result of which the active ingredient is released from the active ingredient delivery system, preferably the capsule.

The activator 31 preferably performs a concentric, eccentric or isometric movement on the sample 6 to be analyzed.

The surface of the activator 31 facing the sample 6 to be analyzed can be smooth or rough. In a preferred variant, the activator 31 has a rough surface. The rough surface increases the friction of the activator 31 on the release system, preferably the capsule. The surface material of the activator 31 is selected from the group consisting of Teflon, felt, sponge, terry cloth and other textiles, molton, glass, metal and Plexiglas. The preferred surface material of the activator 31 is Teflon. Most preferred is felt because it creates high friction.

In an alternative variant, the activator 31 is designed in such a way that it can be used to generate other opening mechanisms in order to open the release system, preferably the capsule. For example, the activator 31 is configured in such a way that it can be used to generate temperature, UV radiation, magnetic radiation, ultrasound or microwaves which, when acted upon, then open the release system, preferably the capsule, and release the capsule contents.

If the release system is a precursor or a precursor substance, it can be changed by means of the activator 31 by triggering a chemical or physical impulse such as temperature, oxygen (oxidation), light, enzymes, microorganisms, chemical reactions (for example hydrolysis) the pH value or moisture, etc. are activated, whereby an active ingredient, preferably a fragrance, is released.

In a preferred variant, the released active ingredient or the released active ingredients are a volatile substance (s). The activation device 3 further comprises a detection line 35. The released active ingredient or the plurality of released active ingredients, which are preferably present as a gas phase, are captured by means of a detection line 35 and supplied to the detection device 5. In a preferred variant, the activation device is set up in such a way that the active ingredient or active ingredients released from the release system are sucked in by means of an integrated suction mechanism and fed to the detection device 5.

In an alternative and preferred embodiment, the activation device 3 also comprises a collecting container 34 at its lower end, which can enclose the sample 6 to be analyzed and the activator 31 when the collecting container is placed on the sample carrier 7 or the support surface 8. The collecting container 34 has a detection line 35 for collecting a released active substance and a flushing line 36.

In order to prevent a released active ingredient, in particular a gaseous or volatile active ingredient, for example a fragrance or a flavoring substance, from escaping from the area of the surface of the sample carrier 7 or the support surface 8 covered by the collecting container 34 without going to the detection device or the analysis device 5, the collecting container 34 is preferably designed in such a way that it is closed on the sides and at its upper end and open at its lower end and the end facing the sample to be analyzed. When the activation device 3 is lowered over the sample to be analyzed and placed on the sample carrier 7 or the support surface 8, the collecting container with the covered surface closes in a gas-tight manner.

In a preferred variant, the collecting container 34 has a bell shape.

In order to further avoid that a released active ingredient from the area covered with the collecting container or the bell 34 of the surface of the Sample carrier 7 or the support surface 8 escapes without reaching the detection device or the analysis device 5, the collecting container or the bell 34 can be provided with a round edge, which can be flush with the support surface below, or a sealing arrangement which a tight fit of the bell on the covered area enables the released active substance to be analyzed to escape exclusively via the detection line 35 and thus inevitably be fed to the detection device or the analysis device. For example, the collecting container can have a sealing ring which can be formed from a fluoroelastomer.

The collecting container or the bell 34 can be made of a transparent material such as glass or plastic. The transparency of the collecting container or the bell 34 has the advantage that while the opening or activation of the release system, preferably the capsule 6 or the precursor 6, the release of the active ingredient or the several active ingredients and the analysis are carried out with the collecting container or The surface covered by the bell 34 can be inspected.

The collecting container or the bell 34 is arranged on the activation device 3 in such a way that it can be lowered or moved upwards together with the activator 31 by means of the Z-positioning unit 32 perpendicular to the sample carrier 8 or to the support surface 8.

A transparent collecting container 34 also has the advantageous effect that, alternatively, an opening or activation of the release system, preferably the capsule 6 or the precursor 6, and the release of one or more active ingredients by means of light or UV radiation, instead of the Activator, can be done by direct irradiation through the collecting container 34 through on the sample to be analyzed.

In a further embodiment of the device according to the invention, the collecting container or the bell 34 can be independent of the Z-positioning of the Activator 31 is lowered perpendicular to the sample carrier 8 or to the support surface 8 or moved upwards.

In an alternative and preferred variant, the activation device 3 comprises a detection line 35 which is connected to the collecting container or the bell 34. The detection line 35 is designed in such a way that it feeds the active substance or the active substances released from the release system to the detection device 5. The detection line is preferably made of metal or a plastic polymer.

The released active ingredient to be analyzed is preferably a volatile substance, for example a volatile odorous or flavoring substance, or a mixture of volatile odorous or flavoring substances, which is / are passed directly to the detection device 5 and arrives there for analysis / reach. In a preferred variant, the volatile substance or the volatile substances are sucked in via an integrated suction mechanism by means of the detection power 35 and supplied to the detection device 5. Otherwise, and in an alternative variant, the released active substance arrives at the detection device or analysis device 5 by expelling it with an inert gas, for example nitrogen or helium. For this purpose, inert gas is supplied via a line that is connected to the collecting container or the bell 34 Gas introduced into the collecting container, whereby the volatile substance or the volatile substances is expelled and passed to the detection device 5 / are.

The activation device 3 optionally comprises a flushing line 36 which is connected to the collecting container or the bell 34. The flushing line 36 is set up to supply a flushing gas or a flushing liquid to the system after the opening, releasing and analysis process has ended, in order to flush the collecting container or the bell 34 and / or the detection line 35. Rinsing removes traces of active ingredients so that the system is free of contamination for the next analysis. The purge gas is preferably selected from air, nitrogen or helium. The rinsing liquid is preferably water or polar or non-polar solvents, preferably ethanol, acetone, isopropanol, heptane, or aqueous cleaning agent solutions, the latter optionally used in combination with a subsequent further rinsing step. Otherwise you wait between two analysis runs until the residues of volatile active ingredients have evaporated.

With a fan 39, which is optionally part of the activation device 3, residual flushing gas or flushing liquid, residual active ingredients of the encapsulated active ingredient and other sample residues can be blown off from the activation device 3, preferably from the collecting container 34 and / or from the activator 31.

The device according to the first aspect of the present invention also comprises an EDP system 51 with suitable software for controlling and positioning the device 1 and for evaluating and storing the measurement results.

In a preferred variant, the X / Y positioning units (4) of the device according to the first aspect of the invention comprise a positioning laser (43). The positioning laser (43) is part of the positioning unit of the EDP system or of the computer 51, via which the movement of the X-axis 21, the X-axis 22 and the activation device 3 are controlled.

The sample carrier 7 preferably has a grid of evenly spaced horizontal and vertical lines, through which a grid of uniform sample fields is created. A sample field forms the (surface) on which the sample to be analyzed is applied or positioned.

For the positioning and movement of the activation device 3 over the sample carrier 7, the start and end measurement points of the sample fields and the number of horizontal and vertical sample fields on the sample carrier 7 are required for the adjustment (teaching) of the device 1. These positions are determined via a position laser 41 and via the EDP system in the device 1 saved. Starting from the determined and stored start and end measurement points of the sample fields, which were defined by means of the position laser, the activation device 3 can be positioned exactly over the sample field to be analyzed and a sample field can be traversed.

At the start of a measurement or a series of measurements or before the start of the break-up, release and analysis process, the X-axis 21, the Y-axis 22 and the activation device 3 are each set to the “zero points”, ie the Starting points of the basic framework 2 approached. As soon as the "zero points" are reached, a signal is sent to the computer. Using these "zero" points, in combination with the movement of the positioning units, the start and end points can each be assigned to a coordinate. Using these coordinates in connection with the number of measurements in the horizontal and vertical, a coordinate can be calculated for each measuring point and approached accordingly automatically.

With the device 1 for the analytical and / or sensory determination of a release system and / or an encapsulated active ingredient according to the first aspect of the present invention, a system is provided which enables an objective and standardized analysis method to be carried out. This in turn enables objective qualitative and / or quantitative statements about the release of an active ingredient or several active ingredients, for example the concentration of the released active ingredient, the release rate or the release profile and / or statements about the properties of an active ingredient release system, preferably a capsule or a precursor, for example, the mechanical stability, breaking strength or the retardation behavior of a capsule after storage for a certain period of time.

In addition, the device 1 according to the first aspect of the present invention works fully automatically. The fully automatic device 1 has the advantage that it enables the following, for example, to be set exactly Analysis parameters allowed: pressure, time lengths of the pressure-free measurement, application of pressure without friction, friction process and the friction-free detection time, rotation speed, rotation duration or flushing time. By means of the device 1 according to the invention, an analytical and / or sensory determination can be carried out at the same time, whereby a correlation of the measurement results obtained is possible. In addition, the device 1 according to the invention enables an analysis of the real-time analysis of the release of an active ingredient or several active ingredients from a release system used according to the invention.

In addition, the device 1 according to the invention enables, for the first time, a reproducible, objective analytical and / or sensory determination of the burst behavior of encapsulated active substances, for example fragrances or aromatic substances. This enables new capsule technologies and capsule developments to be screened for capsules with the best burst behavior, without a large expenditure of time and personnel and without negative influences on the subjectivity of a sensor panel.

In a second aspect, the present invention is therefore directed to a method for the analytical and / or sensory determination of the release of an active ingredient or several active ingredients from a release system, preferably from a capsule or a precursor.

A release system 6 in the context of the present invention is understood to mean a solid preparation, for example particles or a capsule 6, which contains one or more active ingredient (s), or a precursor 6 or a precursor substance, as defined above .

The capsules 6 which are analyzed with the method according to the invention are preferably those which are selected from the group consisting of hard capsules (hard-shelled capsules), soft capsules (soft shelled capsules), macrocapsules, microcapsules, capsule slurries and capsule emulsions.

The active ingredient contained in the release system, preferably the active ingredient contained in the capsule or the active ingredient released from the precursor, are solid, liquid or gaseous substances.

The active ingredient of the release system is preferably a volatile substance which is volatile at room temperature and which is preferably selected from the group consisting of fragrances, flavorings, perfume oils, fragrance mixtures, flavoring mixtures, aromatic substances,

Plant extracts, essential oils, cosmetic active ingredients, cooling active ingredients and pharmaceutical active ingredients. As far as the individual active ingredients are concerned, reference is made to the above description.

In a first step of the method according to the invention, a sample 6, namely a release system 6 to be analyzed, which comprises one or more active ingredients, is provided on a sample carrier 7 which is located on a support surface 8.

In order to test, for example, the distribution or adhesion of an active substance release system on a specific substrate, the sample carrier 7 can also be a fabric, for example clothing, linen, etc. made of cotton, linen, wool, viscose, polyacrylic, polyamide, polyester, or another organic or inorganic substrate or its surface, for example tiles, linoleum, wood, glass, metal, hair, etc. or can be a fiber cover.

As an alternative to this, the release system 6, preferably a capsule 6 or a precursor 6, is located directly on the support surface 8 in the method according to the invention. In the alternative variant, where the sample 6 is located directly on the support surface 8, for example in the case of a floor cleaning agent with an encapsulated active ingredient 6 or a precursor 6, the device according to the invention is positioned directly above the support surface and the analysis is carried out directly on the Surface of the support surface 8 are carried out.

The applied amount of the release system 6, preferably the capsule 6 or the precursor 6, on the sample carrier 7 is variable and is depending on the material and diameter of the rubbing head, the application of the capsule or the precursor and the active ingredient content in the capsule or . of the precursor. The application to the sample carrier is preferably carried out in the form of a capsule slurry, preferably in a concentration close to the application, for example taking into account the concentration in a standard washing liquor in a washing machine and taking into account the average flaking of the capsules on the laundry in a washing process. The amount applied is 0.1 mg to 2.0 mg capsule or precursor per measurement field or sample field, even more preferably 0.3 to 1.8 mg and most preferably 0.5 to 1.0 mg capsule or precursor per measurement field or sample field on the sample carrier.

As an alternative to this, for example, when the adhesion of a release system to a tissue is determined after a machine washing process, the amount of the release system is adapted to the application.

The sample carrier 7 preferably has a grid of uniformly spaced horizontal and vertical lines, whereby a grid of uniform measurement or sample fields is created. The sample 6 to be analyzed, ie the release system 6 to be analyzed, preferably the capsule 6 or the precursor 6, is applied to the sample carrier 7 within a specific measurement or sample field which has individual coordinates. By teaching the device according to the invention (via the laser) and specifying rows and columns before the start of a measurement, the grid coordinates of the EDP is calculated and controlled independently. The activation device 3 can thus be controlled to the corresponding sample field on which the sample to be analyzed is applied or positioned.

In a next step of the method according to the invention, the activation device 3 is positioned with an activator 31 over the release system 6, in particular the capsule 6 or the precursor 6. The movement and positioning of the activation device 3 with the activator 31 takes place via the X-axis 21 and the Y-axis 22 or via the X-positioning unit / the X-positioning drive 41 and the Y-positioning unit / the Y-positioning drive horizontally and in the X and Y directions relative to the sample carrier 7 or the support surface 8 on which the sample to be analyzed lies.

In a further step of the method according to the second aspect of the invention, the activation device 3 is lowered so that the activator 31 maintains a distance from the release system 6, in particular from the capsule or the precursor, or slightly touches the release system 6. This takes place as a function of the pulse used to open or activate the release system. In the case of opening or activation by means of pressure and / or friction, the activator 31 touches the release system, while in the case of opening or activation by means of UV radiation, a distance from the release system can be maintained.

Next, in the method according to the invention, the active ingredient or the plurality of active ingredients is / are released from the release system 6, preferably the capsule 6 or the precursor 6, by means of the activator. The active ingredient or the several active ingredients are released by a physical and / or chemical impulse. If the release system is a capsule, the active ingredient is released by opening the capsule using pressure, friction, temperature, changes in the pFI value, UV radiation, microwaves and ultrasound. If the release system 6 is a precursor 6, the active ingredient is released from the precursor substance by chemical reaction, temperature, humidity, Change in pH value, oxygen (oxidation), light, e.g. UV radiation, enzymes and microorganisms.

In a preferred variant of the method, the active ingredient or the several active ingredients are released from a capsule by means of the activator by applying pressure to the sample 6 to be analyzed and / or rubbing the sample 6 to be analyzed thin capsule wall or in the case of an unstable capsule material, in an alternative variant of the method according to the invention the capsule is broken open only by applying pressure and without friction.

The mechanical pressure is generated via a pressure sensor 33. The pressure sensor 33 can be used to set the pressure that is applied to the active ingredient release system, preferably the capsule, in order to cause it to burst or break. The pressure in the method according to the invention, which acts on the active substance release system, preferably the capsule, in order to break it and release the active substance, is> 0 Pa. Even a pressure of 0 Pa, i.e. when the activator 31 is simply brought up to the sample 6 to be analyzed, is demonstrably sufficient to break the first capsules. The method is preferably carried out at a pressure in the range from 1000 Pa to 30000 Pa, even more preferably at a pressure in the range from 2500 Pa to 25000 Pa, on the active ingredient release system, preferably the capsule, or the sample carrier 7. These values are preferably based on a radius of 2 cm. By changing the radii of the activator or selecting the rubbing head material, the above-mentioned minimum and maximum pressures are adjusted.

In order to generate friction, which also leads to the breaking or improving of the active ingredient release system, the activation device comprises a rotation unit 38. The activator 31 is in direct connection with the rotation unit 38, which is driven by an electric motor. The rotation unit 38 sets the activator 31 in motion, for example by means of a concentric, eccentric or isometric movement. With the concentric Movement, the activator performs rotating circular movements on the sample 6 to be analyzed, the circles having different radii. In the case of the eccentric movement, the activator performs rotating circular movements on the sample 6 to be analyzed, which are outside the center of the circle. During the isometric movement, the activator moves back and forth like a slide on the sample 6 to be analyzed in the X and Y directions.

As a result of one of these movements, the activator 31 moves over the sample 6 to be analyzed and generates friction, as a result of which the active substance is released from the release system, preferably the capsule.

In an alternative variant of FIG. 4, the activator 31 is an oscillator unit 38 which makes the activator 31 oscillate. The vibration of the activator above the sample 6 to be analyzed generates friction, as a result of which the active ingredient is released from the release system, preferably the capsule.

In a further alternative variant, the direction of rotation of the activator can be changed at short time intervals during the measurement, as a result of which the active ingredient is released from the active ingredient release system, preferably the capsule.

The release of the active ingredient from the release system 6, in particular from the capsule 6, by means of the activator 31 in the method according to the invention takes place at a rotational speed of the activator 31 when the encapsulated active ingredient 6 and / or the sample carrier 7 is touched from 0 rpm , preferably at a rotation speed of 50 rpm to 1,000 rpm, and more preferably a rotation speed of 200 rpm to 1,000 rpm.

The rubbing time in the method according to the invention is variable. It is preferably 0 to 30 seconds.

The process parameters pressure and friction have the greatest influence on the breaking of the capsule. Advantageously, these two Set the process parameters exactly with the automated process according to the invention. Due to the setting of different process parameters, it is also possible to break capsules of different sizes and capsule walls of different thicknesses. In addition, an increase in pressure enables, for example, a faster release of the active ingredient or ingredients from the release system, which means that stronger intensities can be measured in the subsequent analytical and / or sensory determination so that the stability of a capsule can be seen.

In a preferred variant, the released active ingredient or the released active ingredients are a volatile substance (s).

In a further step of the method according to the invention, the released active ingredient or the several released active ingredients, which are preferably present in the gas phase, are captured by means of a detection line 35 and supplied to the detection device 5. In a preferred variant, in the method according to the invention, the active ingredient or active ingredients released from the release system are sucked in by means of an integrated suction mechanism, preferably the pump of a FAIMS, and fed to the detection device 5.

In a preferred variant of the method according to the invention, in order to avoid that a released active ingredient, in particular a gaseous or volatile active ingredient, for example a fragrance or a flavor, can escape during the analytical and / or sensory determination, the surface of the Sample carrier 7 or the support surface 8 on which the sample is located, covered with a collecting container 34, which preferably has a bell shape and which is arranged at the lower end of the activator 31. For this purpose, the collecting container 34 is preferably designed in such a way that it is closed laterally and at its upper end and open at its lower end and that end facing the sample to be analyzed. When lowering the activation device 3 over the sample to be analyzed and the support on the sample carrier 7 or the support surface 8 is sealed by the collecting container with the covered surface in a gas-tight manner. This prevents a released active ingredient, in particular a volatile active ingredient, for example a fragrance or a flavoring substance, from escaping from the area of the surface of the sample carrier 7 or the support surface 8 covered by the collecting container 34 without reaching the detection device or the analysis device 5 reach.

In an optional variant, the released active substance can be sucked in from the collecting container or the bell to the detection device or the analysis device 5 by means of a pump. This has the advantage that the released active ingredient can be detected after just a few seconds.

The active ingredient released from the release system, preferably the capsule or the precursor, is fed in a further step of the method according to the invention to a detection device or an analysis device 5 for the analytical and / or sensory determination of the released active ingredient.

In a further step of the method according to the invention, the detection device or analysis device 5 is used to carry out the analytical and / or sensory determination of the active substance released from the release system.

Analytical determination and / or determination is understood to mean a sensory, qualitative (identification of the active ingredient) and / or quantitative (amount of active ingredient) analysis of an active ingredient released from the release system 6, in particular from a capsule 6 or a precursor 6. The method according to the invention can advantageously be used to analyze the type and amount of the active ingredient or the active ingredients of a release system, for example the encapsulated active ingredient or the encapsulated active ingredients. The detection device or analysis device 5 is a measuring device which enables a qualitative and / or quantitative analysis of the released active substance.

For the qualitative and / or quantitative analysis of the released active ingredient or active ingredients, detection devices or analysis devices 5 are preferably used, which are preferably selected from the group consisting of gas chromatograph (GC), gas chromatograph / mass spectrometer (GC / MS ), Ion Mobility Spectrometry (IMS), FAIMS (high field asymmetric waveform ion mobility spectrometry), GC-FAIMS and GC-MS-FAIMS or combinations of the aforementioned measuring devices.

Preferably, the detection device or analysis device 5 used for the analysis is IMS (ion mobility spectrometry), FAIMS (high field asymmetric waveform ion mobility spectrometry), GC-FAIMS and GC-MS-FAIMS or a combination of the aforementioned measuring devices.

Most preferably, in the method according to the invention, the analytical determination of the released active ingredient is carried out by means of FAIMS (high field asymmetric waveform ion mobility spectrometry). The FAIMS enables the detection and analysis of volatile chemical substances directly from a gas flow or from the gas phase over a liquid or a solid sample. There are two mechanisms for adding the sample to the FAIMS unit: single sampling or continuous sampling. When taking individual samples, a defined volume of the gaseous analyte, ie the released active ingredient or active ingredients, is collected or adsorptively enriched in a preceding step and fed to the FAIMS. With continuous sampling, the gaseous analyte, ie the released active substance, is continuously fed to the FAIMS by means of a carrier gas, for example purified air or argon. The sampling is preferably carried out continuously, whereby the analytical determination of the released active ingredient or active ingredients can be carried out in real time. This enables an analytical determination of the real-time release, which is particularly the case with the Determining the release of fragrance or flavor mixtures is beneficial.

In an alternative variant of the method according to the invention, the released active ingredient or the released active ingredients are bound to an adsorbent, for example in a Tenax tube, in order to concentrate them and then measured by means of GC-MS (dynamic headspace method). With the dynamic headspace technique, the active ingredient released during the measurement or the several active ingredients released during the measurement are transferred to a suitable air flow via a continuous air flow, which is generated, for example, by the FAIMS or for which an additional external pump is used, or an inert gas Adsorber material, for example in a Tenax tube, or in a cold trap. For this purpose, the adsorbent-containing glass tube can either be integrated directly into the air flow from the CBA, or the active substance (s) are first (if the air flow is too high for the direct method) into a closed container (e.g. a plastic bag) and then to direct the active ingredient (s) onto the adsorbent with a lower air flow. Then the Tenax tube (adsorber) or the trap is heated up and the enriched analytes reach the FAIMS or the column for gas chromatographic analysis, for example.

In a preferred variant of the method according to the invention, in addition to the qualitative and quantitative determination of the released active ingredient, a sensory determination of the released active ingredient using an olfactometer and / or an olfactory detection port (ODP) (sniffing port system) (52) which is connected to the detection device or analysis device 5 via an alternative output. Such a combination allows a correlation to be established between the analytical and sensory determination.

The sniffing port system can be arranged in the device according to the invention both in front of the detection device 5 and behind the detection device 5. The location of the sniffing port The system behind the detection device 5 is particularly advantageous when the detection device 5 is a FAIMS or an IMS, since the FAIMS or the IMS does not destroy the analytes and these are still available at the output of the FAIMS or the IMS. With such an arrangement, a correlation between the measured data and the sensory evaluation of the released active ingredients can be established particularly well.

The measurement results obtained are fed to an EDP system 51 with suitable software and are evaluated and stored by means of the software.

In a final step of the method according to the invention, the device 1 is reset, the device 1 being reset comprising the following steps: First, the activation device 3 is started up by means of the Z-positioning unit 32.

Optionally, the method according to the invention comprises a step in which the activator 31 and / or the detection line 35 and / or the detection device are flushed with a flushing gas or a flushing liquid after the opening, releasing and analysis process has ended. The rinsing removes residues of released active substances or other sample residues, so that the system is free of contamination for the next analysis process. The purge gas is preferably selected from air, nitrogen or helium. The rinsing liquid used is preferably water or polar or non-polar solvents, preferably ethanol, acetone, isopropanol, heptane, or aqueous cleaning agent solutions, the latter optionally in combination with a subsequent further rinsing step. Otherwise, you wait between two analyzes until the residues of the released active ingredients have evaporated.

With a fan 39, which is an optional component of the activation device 3, in the method according to the invention, residual purge gas or Rinsing liquid, residual active ingredients of the encapsulated active ingredient and other sample residues are blown off from the activation device 3, preferably from the activator 31 and / or from the collecting container 34.

A schematic overview of the steps of the method according to the invention is shown in FIG.

With the method according to the second aspect of the present invention it is possible to analyze active ingredients from release systems, preferably capsules or precursors, objectively and under standardized conditions, i.e. with the setting of defined process parameters. With the analysis method according to the invention, active ingredient release systems, preferably capsules or precursors, can be broken open under clearly defined conditions (e.g. pressure), i.e. standardized and controlled, and the capsule contents can be analyzed quantitatively and / or qualitatively at the same time. This enables a standardized, standardized and reproducible analysis method in which the conditions of its applicability and its sequence are defined in such a way that the same results can be expected under the same conditions. This also makes it possible to compare measurement results from different capsule samples or precursors with one another. Such an analytical and / or sensory determination under reproducible release conditions is not yet known.

The reproducible, objective analytical and / or sensory determination of the burst behavior of encapsulated active ingredients by the method according to the invention in turn enables the screening of new capsule technologies and capsule developments for capsules with the best burst behavior, without great expenditure of time and personnel and without negative influences on subjectivity a sensor panel.

In addition, the method according to the invention enables, for the first time, a continuous on-line measurement of the release of one or more active substances Active ingredients from a capsule or from a precursor, whereby the time sequence of the release can be recorded directly, ie parallel to the release. Such an on-line measurement is shown by way of example in FIG.

FIG. 6 shows the course of a continuous measurement of the capsule burst of a capsule containing perfume oil. The capsule is a multilayer capsule with a liquid perfume oil core. Measurement parameters: 10 s rubbing at 60 rpm at 1.0 N; 30 s post rub time.

The capsule burst (capsule break) and the release of the perfume oil are particularly visible after lifting the grating head. The maximum of the release curve is reproducible and can be used to compare different capsules.

The method according to the invention also enables continuous operation in which several samples can be analyzed one after the other, for example using the same method parameters. This allows the analysis values to be compared directly with one another. In addition, via a combination of detection device 5 with an alternative output for an olfactometer and / or an olfactory detection port (ODP) (sniffing port system) 52, improved sensory evaluations and comparisons of different samples can take place through the reproducible release method. In addition, the analytical and sensory measurement results obtained in this way can be correlated with one another.

Due to the advantages described above, the device according to the invention and the method according to the invention are preferably suitable for the analytical and / or sensory determination of the release of an active ingredient from a release system 6, preferably from a capsule 6 or a precursor 6, in order to determine the composition of the active ingredient to be analyzed in terms of type and quantity. The method according to the invention can also be used to analyze the mechanical stability and the breaking behavior of different capsule materials, in particular in the development and manufacture of new capsules. In addition, the method according to the invention allows the determination of the retardation behavior of capsules to be analyzed, preferably after the capsules have been stored for a certain period of time.

The method according to the invention also enables a comparison of the release behavior of different active ingredients, for example different smells or flavors or fragrance or aroma mixtures, from a release system, preferably from a capsule or a precursor.

The method according to the invention also allows the analysis of the distribution and adhesion of microcapsules on surfaces, for example the distribution and adhesion of microcapsules which contain a fragrance, after textiles have been washed and dried.

The method according to the invention also enables the substantivity of an active ingredient or several active ingredients to be analyzed after the release from the release system 6, in particular from a capsule 6 or a precursor 6, on a substrate;

In addition, with the method according to the invention, the influence of physical or chemical factors, for example temperature, light, UV radiation, pH value, on the mechanical stability and breaking strength of a release system, in particular a capsule or a precursor 6 and / or on the Release of an active ingredient or of several active ingredients from a release system 6, in particular from a capsule 6 or a precursor 6 can be analyzed.

In addition, the method according to the invention can be used during the development and production of the release system 6 for the analytical determination of the Release of an active ingredient or several active ingredients and used to determine the properties of a release system 6, in particular a capsule 6 or a precursor 6.

In a final aspect, the present invention therefore relates to the use of the device according to the invention and the method according to the invention for the analytical and / or sensory determination of the release of an active ingredient or several active ingredients, in particular the concentration, the release rate or the release profile from a release system (6 ), in particular from a capsule (6) or a precursor (6); to determine the properties, in particular the mechanical stability, the breaking strength and the retardation behavior, of a release system (6), in particular a capsule (6) or a precursor (6), in particular the mechanical stability, the breaking strength or the retardation behavior, of capsules (6 ) from different capsule materials and different active ingredients; for analyzing the distribution and adhesion of a release system (6), in particular a capsule (6) or a precursor (6), on a substrate, in particular after textiles have been washed and dried; for analyzing the substantivity of an active ingredient or several active ingredients after the release from the release system 6, in particular from a capsule 6 or a precursor 6, on a substrate; to analyze the influence of physical or chemical factors, for example temperature, light, UV radiation, pH value, on the mechanical stability and breaking strength of a release system, in particular a capsule or a precursor 6 and / or on the release of an active ingredient or of several active ingredients from a release system 6, in particular from a capsule 6 or a precursor 6; and for the analytical determination of the release of one or more active ingredients and for the determination of the properties of a release system 6, in particular a capsule 6 or a precursor 6, during the development and manufacture of a release system 6.

Example 1: Comparison of the fragrance release from different capsule technologies

Comparison of the analytical burst behavior of different capsule types. Type A to type D are core / shell perfume oil capsules based on methylformamide and differ in their wall thickness (decreasing wall thickness from A to D). All capsule types were loaded with the same perfume oil with the same dosage. The measurement was carried out at 2.5 N for 15 s; Friction: 100 rpm.

The results of the maximum burst intensity are shown in FIG. The burst intensity is highest in the type D capsule with the thinnest wall thickness.

List of reference symbols:

1 device

2 basic structure

21 X axis

22 Y-axis

3 activation device

31 activator

32 Z positioning unit

33 pressure sensor

34 Collecting container / bell

35 detection line

36 flushing line

37 rinsing pump

38 rotation unit

39 fan

4 X / Y positioning units

41 X positioning unit / X positioning drive

42 Y positioning unit / Y positioning drive

43 Positioning Lasers

5 detection device / analysis device

51 IT system

52 Sniffing Port System

6 sample / delivery system / capsule / precursor

7 sample carriers

8 support surface

Claims

1. Device (1) suitable for the analytical and / or sensory determination of the release of an active ingredient or several active ingredients from a release system (6), in particular from a capsule (6) or a precursor (6), and / or for determining the properties of a Release system (6), in particular a capsule (6) or a precursor (6), which is located on a sample carrier (7) or a support surface (8), comprising:

(a) a basic structure (2);

(b) an activation device (3) which is connected to the basic structure (2) and which is set up to open or activate the release system (6), in particular the capsule (6) or the precursor (6), and the To release active ingredient; and

(c) a detection device (5), set up for the analytical determination of the released active ingredient or active ingredients, and designed in such a way that the released active ingredient or the several released active ingredients can be fed to the detection device (5).

2. Device (1) according to claim 1, wherein the activation device (3) comprises:

(i) an activator (31) which is connected to a Z-positioning unit (32) and can be moved perpendicular to the support surface (8) via the Z-positioning unit (32) and which is designed to apply a physical or chemical impulse to the To exercise the release system (6), in particular on a capsule (6) or a precursor (6), on the sample carrier (7) in order to release the active ingredient or the several active ingredients;

(ii) a detection line (35) which is set up to collect the released active ingredient or the plurality of released active ingredients and to guide them to the detection device (5); and (iii) optionally a flushing line (36) which is connected to the detection line (35) and is set up to supply a flushing gas or a flushing liquid to the detection line (35).

3. Device according to claim 1 or 2, wherein the physical or chemical impulse on the capsule (6) is selected from the group consisting of pressure, friction, temperature, change in pH, UV radiation, microwaves and Ultrasound, or the physical or chemical impulse on the precursor (6), is selected from the group consisting of chemical reaction, temperature, humidity, change in pH value, oxygen (oxidation), light, enzymes and microorganisms.

4. Device according to one of claims 1 to 3, wherein the activator (31) comprises a collecting container (34) which contains the release system (6), in particular the capsule (6) or the precursor (6), and the activator (31) can enclose when the collecting container is placed on the sample carrier (7) or the support surface (8).

5. Device according to one of claims 1 to 4, wherein the activator (31) has a rough surface.

6. Device according to one of claims 1 to 5, wherein the

Activation device (3) has a rotation unit (38) which triggers concentric, eccentric or isometric movement in the activator (31).

7. Device according to one of claims 1 to 6, wherein the device further comprises: at least one X and / or Y positioning unit (41, 42) which is connected to the basic structure (2) and which is set up, the activation device (3) to move relative to the sample carrier.

8. Device according to one of claims 1 to 7, wherein the positioning unit (4) comprises a positioning laser (43).

9. A method for the analytical and / or sensory determination of the release of an active ingredient or several active ingredients from a release system (6), in particular from a capsule (6) or a precursor (6), which comprises the following steps:

(i) Providing a release system (6), in particular a capsule (6) or a precursor (6), which comprises one or more active ingredients, on a sample carrier (7) or on a support surface (8);

(ii) positioning the activation device (3) with an activator (31) above the release system (6), in particular above the capsule (6) or the precursor (6);

(iii) Lowering the activation device (3);

(iv) releasing the active ingredient or the plurality of active ingredients from the release system (6), in particular from the capsule (6) or the precursor (6), by means of the activator (31);

(v) collecting and feeding the released active ingredient or the plurality of released active ingredients to a detection device (5); and

(vi) analytical and / or sensory determination of the released active ingredient or the several released active ingredients, in particular the concentration, the release rate or the release profile from a release system (6), in particular from a capsule (6) or a precursor (6); and or

Determination of the properties, in particular the mechanical stability, the breaking strength and the retardation behavior, of a release system (6), in particular a capsule (6) or a precursor (6), in particular the mechanical stability, the breaking strength or the retardation behavior of capsules (6) different capsule materials and different active ingredients; and or Analysis of the distribution and adhesion of a release system (6), in particular a capsule (6) or a precursor (6), on a substrate, in particular after textiles have been washed and dried; and or

Analysis of the substantivity of an active ingredient or several active ingredients after the release from the release system (6), in particular from a capsule (6) or a precursor (6), on a substrate; and / or analysis of the influence of physical or chemical factors, for example temperature, light, UV radiation, pH value, on the mechanical stability and breaking strength of a release system (6), in particular a capsule (6) or a precursor (6) and / or the release of an active ingredient or of several active ingredients from a release system (6), in particular from a capsule (6) or a precursor (6); and / or analytical determination of the release of an active ingredient or several active ingredients and for determining the properties of a release system (6), in particular a capsule (6) or a precursor (6), during the development and manufacture of a release system (6).

10. The method according to claim ^ wherein after step (vi) the following step takes place:

(vii) resetting the device, wherein resetting the device comprises one or more of the following steps:

(A) starting up the activation device (3); and optionally (ß) rinsing the activator (31) and / or the detection line (35) and / or the detection device (5) with a rinsing gas or a rinsing liquid; and optional

(y) blowing off residues of the released active ingredient or of the several released active ingredients and / or other sample residues from the activation device (3), in particular by the activator (31), preferably by a fan (39).

11. The method according to claim 9 or 10, wherein the release of the active ingredient or the plurality of active ingredients by means of the activator (31) takes place by a physical or a chemical pulse.

12. The method according to claim 11, wherein the physical or chemical impulse on the capsule (6) is selected from the group consisting of pressure, friction, temperature, change in pH, UV radiation, microwaves and ultrasound, or the physical or chemical impulse on the precursor (6) is selected from the group consisting of chemical reaction, temperature, humidity, change in pH value, oxygen (oxidation), light, enzymes and microorganisms.

13. The method according to claim 9 to 12, in which the release of the active ingredient or the plurality of active ingredients by means of the activator (31) is carried out at a pressure from 0 Pa, in particular at a pressure of 1000 Pa to 30000 Pa.

14. The method according to any one of claims 9 to 13, in which the release of the active ingredient or the plurality of active ingredients by means of the activator (31) at a rotational speed of the activator (31) when the release system (6) and / or the sample carrier (7 ) from 0 rpm, in particular from 50 rpm to 1,000 rpm.

15. The method according to any one of claims 9 to 14, wherein the release system (6) is selected from the group consisting of: hard capsules (hard-shelled capsules), soft capsules (soft-shelled capsules), macrocapsules, microcapsules, capsule slurries and Capsule emulsions.

16. The method according to any one of claims 9 to 15, wherein the encapsulated active ingredient is selected from the group consisting of fragrances, Flavors, perfume oils, fragrance mixtures,

Flavor mixtures, aromatic substances, plant extracts, essential oils, cosmetic active ingredients, cooling active ingredients, pharmaceutical active ingredients.

17. Use of the device according to one of claims 1 to 8 and the method according to one of claims 9 to 16 for the analytical and / or sensory determination of the release of an active ingredient or several active ingredients, in particular the concentration, the release rate or the release profile from a release system ( 6), in particular from a capsule (6) or a precursor (6); and / or to determine the properties, in particular the mechanical stability, the breaking strength and the retardation behavior, of a release system (6), in particular a capsule (6) or a precursor (6), in particular the mechanical stability, the breaking strength or the retardation behavior of capsules (6) made of different capsule materials and different active ingredients; and / or for analyzing the distribution and adhesion of a release system (6), in particular a capsule (6) or a precursor (6), on a substrate, in particular after textiles have been washed and dried; and / or for analyzing the substantivity of an active ingredient or several active ingredients after the release from the release system (6), in particular from a capsule (6) or a precursor (6), on a substrate; and / or to analyze the influence of physical or chemical factors, for example temperature, light, UV radiation, pH value, on the mechanical stability and breaking strength of a release system (6), in particular a capsule (6) or a precursor (6) and / or the release of an active ingredient or of several active ingredients from one Release system (6), in particular from a capsule (6) or a precursor (6); and / or for the analytical determination of the release of an active ingredient or several active ingredients and for the determination of the properties of a release system (6), in particular a capsule (6) or a precursor (6), during the development and manufacture of a release system (6).