This application is a continuation of Ser. No. 10/204,968 filed Aug. 27, 2002 as the national stage of PCT/EP01/01289 filed on Feb. 7, 2001 and also claims Paris Convention priority of DE 100 10 572.6 filed Mar. 3, 2000.
BACKGROUND OF THE INVENTION The invention relates to a bristle with an antimicrobial finish, which is mainly of thermoplastic material and which is doped with an antimicrobial substance, which during use diffuses to the bristle surface. The invention is also directed at brushware having such bristles and to a pack for such bristles or brushware.
Bristles having an antimicrobial finish have long been known, but have scarcely been used in practice. Thus, at a very early date the known antimicrobial action of silver in colloidal form and its possibility of use in toothbrushes was recognized (GB 446 303), in that oligodynamic, colloidal silver was embedded in bristle monofilaments or applied to the bristle carrier. It is also known to embed in the bristle material or apply to the bristle monovalent or polyvalent ion forming agents, including silver and silver compounds (EP 678 548), silver being proposed in particle form <10 μm with a content of 100 ppm to 10 mass %. It is finally known (DE 195 08 539) to fill a bristle with particles of different size, the larger particles being of silver with the oxidation number 0 and having a size of 1 to 50 μm.
It is also known (EP 413 833) to coat bristle monofilaments with a solution or emulsion of a polymer with free acid radicals and a mixed in, cationic antibactericide, e.g. chlorohexidine and to then dry the coating. Production is very complicated and the adhesion of the coating to the bristle core is inadequate. The antibactericide also diffuses out too rapidly.
It is also known in textile fiber technology to bind silver to carrier materials, e.g. zeolite (U.S. Pat. No. 4,525,410, EP 275 047) and to disperse the thus doped zeolite in particle form in the polymer melt for the monofilament and extrude it with the latter. The fiber comprises a polymer core with a higher melting point and an outer layer of a polymer with a low melting point, which contains the silver-doped zeolite particles. It is also known (EP 116 865) to coextrude a fiber having a Nylon core and outer segments or layers, which contain silver-doped zeolite particles.
In all known systems the antimicrobial action is based on the fact that in a moist environment antimicrobially active cations diffuse out of the bristle or fiber and penetrate the thin cell wall of microorganisms, particularly bacteria and block their protein metabolism.
When used as bristles or in brushware monofilaments of the aforementioned type suffer from the disadvantage that if pure silver is used as the antimicrobial substance this necessarily leads to a correspondingly high filling of the bristle with the particulate silver. This leads to a reduction in the stability of the bristles and consequently to a deterioration of the use characteristics (flexibility, recovery capacity, etc.). Thus, such monofilaments have not been adopted in practice.
Other microbial substances, particularly in the form of metal salts or silver doped zeolite, due to the high ballast material percentage, also lead to a weakening of the bristle. This weakening can only be partly compensated by a diameter increase, which is highly undesired in the case of much brushware, particularly toothbrushes. This is often accompanied by an undesired, high bristle roughness. All the known proposals suffer from the further disadvantage that, even prior to use, particularly in a moist atmosphere, the antimicrobial substance is given off, so that the substance is used up prematurely.
SUMMARY OF THE INVENTION On the basis of the prior art of EP 413 833, the problem of the present invention is to propose a bristle for brushware, e.g. for toothbrushes, body care, cosmetic and hygienic brushes or the like, which has an adequate antimicrobial action and at the same time unchanged, highly satisfactory use characteristics. The invention must also ensure that the antimicrobial action is not prematurely used up.
According to the invention this problem is solved in that the bristle is produced in a multicomponent extrusion process and has at least one first cross-sectional area determining the mechanical use characteristics of the bristle of a plastic component and at least one further cross-sectional area of the other plastic component, and that the further cross-sectional area or the sum of all further cross-sectional areas controls the diffusion rate of the antimicrobial substance.
As a result of the construction according to the invention the first cross-sectional area guarantees the use characteristics of the bristle, whereas the further cross-sectional area or areas are of minor significance for the use characteristics of the bristle. The doping with the antimicrobial substance takes place exclusively or preponderantly in one of the cross-sectional areas, whereas the other cross-sectional area or areas act in diffusion-controlling manner for the antimicrobial substance. The control of the diffusion rate of the microbial substance can take place by different doping of the cross sectional areas with the substance or in that a non-doped cross-sectional area acts as a diffusion brake or as a reflector for the ionized atoms or molecules. This makes it possible to simultaneously control the action period of the antimicrobial substance.
The use characteristics of the bristle on the one hand and the diffusion rate on the other can also be influenced in that the cross-sectional areas are made from different or differently finished plastics or have different cross-sectional surfaces and/or different cross-sectional contours.
Preferably the further and appropriately smaller cross-sectional area of the bristle is doped with the substance in high concentration, so that an adequate charge carrier quantity diffuses into the moist atmosphere. In this embodiment this can be further assisted in that the larger cross-sectional area acts as a diffusion brake, so that the substance mainly diffuses out at the surface of the highly doped cross-sectional area and only with a significant time lag at the surface of the large cross-sectional area.
The large cross-sectional area of the monofilament can also be doped with the substance in a concentration not impairing its mechanical use characteristics, the further, smaller cross-sectional area acting exclusively as a microbially inert diffusion brake and for regulating the active substance delivery from the larger cross-section. However, the smaller cross-section can also be highly doped with the antimicrobial substance and then there is also diffusion into the larger cross-sectional area, so that the ions diffusing out there on the surface are constantly replaced from the other cross-sectional area. However, at the same time the large cross-sectional area forms a diffusion brake, because the ions preferably pass out at the free surface of the smaller cross-sectional area, where the lower diffusion resistance exits.
According to a preferred development, the further cross-sectional area is located on the circumference of the large cross-sectional area and either forms part of the bristle surface or completely embraces the bristle. This on the one hand ensures a comparatively rapid delivery of the ions at the free surface of the smaller cross-sectional area and on the other hand the cross-sectional area decisive for the stability and bending behavior of the bristle is only slightly weakened, so that even very thin bristles can be adequately doped with antimicrobial substance. In the case of thin bristles, particularly with diameters smaller than 0,75 mm, the bristle can be completely surrounded by a thin layer acting as a diffusion brake.
The further, smaller cross-sectional area can form a sector in the larger cross-sectional area or also a layer on the surface thereof. In the first case said further cross-sectional area can be highly doped, whereas when constructed in the form of a layer it acts exclusively as a diffusion brake through a corresponding material choice. This layer can be extruded with the monofilament or can be subsequently applied.
In another embodiment the further, smaller cross-sectional area can be located in the interior of the large cross-sectional area, e.g. in the form of coextruded, thin monofilaments with a random cross-sectional shape (circular, polygonal, cruciform, etc.). The further cross-sectional area can also subdivide the large cross-sectional area into sectors, e.g. can be in the form of a star-shaped layer of limited thickness. In this embodiment the diffusion of the antimicrobial substance also takes place into the larger cross-sectional area. To the extent that the surface of the smaller cross-sectional area is exposed, an increased diffusing out takes place.
Preferably at least one further cross-sectional area has silver of oxidation level0 as the antimicrobial substance. Instead of this or in addition thereto the large cross-sectional area can contain silver of oxidation level0 and then preferably the further, smaller cross-sectional area has the same substance in a higher concentration.
An advantageous embodiment is characterized in that the large cross-sectional area has silver of oxidation level0 with a content of 0<c<50,000 ppm and the further cross-sectional area a content of c<100%.
In a preferred development the further, smaller cross-sectional area has silver of oxidation level0 with a content of 500<c<100,000 ppm. Practical tests with such a bristle have shown that the combination of a high concentration in the further, smaller cross-sectional area and a lower concentration in the large cross-sectional area ensures a diffusion of the antimicrobial substance at an adequate speed and over an adequate period of time roughly corresponding to the use period of a toothbrush.
Another embodiment of the invention is characterized in that at least one cross-sectional area has silver ofoxidation level1 and it can be in the form of silver halides, sulphates, carbonates or organic silver salts, in which cation formation takes place as a function of the solubility product to a greater extent.
The aforementioned antimicrobial substances can also be combined with one another in such a way that one cross-sectional area has silver of oxidation level0 and at least one further cross-sectional area silver ofoxidation level1.
If silver of oxidation level0 is used, it can be contained in the further, smaller cross-sectional area in the form of at least one thread, which, during the extrusion of the monofilament, also follows. Preferably the silver ofoxidation level0 or1 is present in disperse form in the plastic matrix and is extruded together with the plastic melt. For this purpose it is possible to use a granulate, which already contains the particles. Instead of this silver-containing polymer particles can be extruded together with the polymer. Since as a result of the silver content the polymer particles have a better dimensional stability, they largely maintain their particle form. Bristles of this type without an antimicrobial finish and their production are e.g. described in WO 17/09906, the entire disclosure of which is hereby incorporated by reference.
Instead of this it is possible for the silver of oxidation level0 to be applied to one of the cross-sectional areas in layer form.
All the cross-sectional areas of the bristle can comprise the same thermoplastic material. However, it is also possible to form the further, smaller cross-sectional area from a thermoplastic elastomer, which has a lower diffusion resistance to the antimicrobial substance.
In order to provide a use indication, the cross-sectional areas can also be differently surface or through-dyed, wherein increasing wear on the free bristle end or bristle jacket is indicated by a corresponding color change.
The preferred thermoplastic materials are those having a water absorptivity of at least 0.1 mass % and more particularly polyamides, polyesters and polyurethanes.
The diffusion rate can also be controlled in that the cross-sectional areas of the bristle or the polymers forming them have different water absorptivity, so that the cations are more rapidly formed in the cross-sectional area with the higher water absorptivity and more rapidly diffuse out than in the other cross-sectional area.
The cross-sectional areas of the bristle can also be formed by two or more combined monofilaments, whereof each forms one of the cross-sectional areas.
The invention also relates to brushware having a plastic bristle carrier and bristles constructed according to the invention. Such brushware is characterized in that also the bristle carrier is at least zonally antimicrobially finished. Thus, in the case of toothbrushes, the invention takes account of the scientifically proven finding that as a result of the permanently moist atmosphere, as well as the cavities which have evolved in the bristle configuration area, a relatively high bacterial attack occurs on the bristle carrier.
If, as is usually the case, the bristle carrier is made from plastic, it preferably has particulate silver ofoxidation level0 or1.
If, as is also known, the bristle carrier is made from two different or different types of plastic, which are produced by multicomponent injection molding, at least one of the components is filled with particulate silver ofoxidation level0 or1.
In a preferred development the bristle carrier is solely or preponderantly filled in the vicinity of the fastening of the bristles with particulate silver ofoxidation level0 or1, i.e. in the area which is particularly endangered by bacterial attack and the establishment of bacteria.
Finally, in the case of such brushware, the bristles are preferably individually fastened to or in the bristle carrier, which compared with a bundle-like arrangement of the bristles aids free diffusion, because on the one hand moisture has uniformly rapid access to all the bristles and on the other the bristle configuration dries more rapidly after use, which prevents bacterial attack and blocks diffusion.
Moreover, either individually or in bundle form, the bristles are joined to the bristle carrier in gap-free manner by thermal processes in order to prevent the establishment of bacteria and in order to prevent excessively rapid consumption of the antimicrobial substance. Such processes more particularly include injecting in, welding or thermal bonding.
Bristles and brushware, particularly when used for hygienic purposes, such as toothbrushes, cosmetic brushes, etc., reach the processor or final consumer in packs. Frequently they are in the form of plastic packs or blister packs with a cardboard support and a transparent plastic blister. As packing cannot take place under sterile clean room conditions, it is also not possible to exclude that during packing germs can enter the pack. Despite the air-tight seal germ growth can occur if moisture is present in the pack, particularly if as a result of temperature changes the moisture condenses on the inside of the pack and which reacts more rapidly to temperature changes than the actual packed article.
To prevent contamination of the packed bristles or brushware with germs, according to the invention the pack is characterized in that it is finished with an antimicrobial substance. Said substance is preferably silver or silver salts and can be incorporated in disperse form into the material of the pack or can be applied in layer form to the inside of the pack.
The invention is described in greater detail hereinafter relative to embodiments represented in the drawings.
BRIEF DESCRIPTION OF THE DRAWINGFIG. 1 shows a cross section through a bristle in a first embodiment of the invention;
FIG. 2 shows a perspective view of the bristle ofFIG. 1;
FIG. 3 shows a cross section through a bristle in a second embodiment of the invention;
FIG. 4 shows a cross section through a bristle in a third embodiment of the invention;
FIG. 5 shows a cross section through a bristle in a fourth embodiment of the invention;
FIG. 6 shows a cross section through a bristle in a fifth embodiment of the invention;
FIG. 7 shows a cross section through a bristle in a sixth embodiment of the invention;
FIG. 8 shows a cross section through a bristle in a seventh embodiment of the invention;
FIG. 9 shows a cross section through a bristle in an eighth embodiment of the invention;
FIG. 10 shows a cross section through a bristle in a ninth embodiment of the invention;
FIG. 11 shows a cross section through a bristle in a tenth embodiment of the invention; and
FIG. 12 shows a cross section through a bristle in an eleventh embodiment of the invention.
DESCRIPTION OF THE PREFERRED EMBODIMENTFIG. 1 is a cross section through abristle1, whose first, largercross-sectional area2 comprises a thermoplastic material, e.g. polyamide, polyester or polyurethane and which has a furthercross-sectional area3 with a much smaller cross-section and which forms a partly cylindrical sector of the overall cross-section. Thecross-sectional area2 has the use characteristics necessary for a bristle with respect to the bending behavior and recovery capacity and at least to a limited extent this is aided bycross-sectional area3.Cross-sectional area3 can be made from a different plastic, particularly a different thermoplastic or an elastomer.
As can be gathered fromFIG. 2, the smallercross-sectional area3 passes over the entire length of thebristle1 and production preferably takes place by the extrusion of both material components forcross-sectional areas2 and3. The smallercross-sectional area3 is filled with an antimicrobial substance in particle form, preferably silver ofoxidation level0 or1. A high doping of the antimicrobial substance takes place. The largercross-sectional area2 can also be filled with anantimicrobial substance5 in particle form. The thermoplastic material of the largercross-sectional area2 forms in this embodiment a diffusion brake for the highly doped, antimicrobial substance in the smallercross-sectional area3 and which diffuses out more rapidly on its free surface, whereas the substance from the larger cross-sectional area diffuses out at a lower speed and more slowly due to the longer diffusion paths.
The bristle1 according toFIG. 3 once again has a largecross-sectional area2, which determines the use characteristics thereof. In saidcross-sectional area2 the smallcross-sectional area3 is present as a core and is produced, optionally together with the largercross-sectional area2, by coextrusion. It can once again comprise a different plastic and is in this case highly doped with theantimicrobial substance4. In this case the largercross-sectional area2 acts as a diffusion brake or conversely the smallercross-sectional area3 forms a slow and continuously flowing source of antimicrobial substance.
In the embodiment according toFIG. 4 the largercross-sectional area2 determining the bristle use characteristics contains three smallercross-sectional areas3 in the form of strands and which are once again highly doped with the antimicrobial substance. Once again the largercross-sectional area2 acts as a diffusion brake.
In the embodiment according toFIG. 5 the further, smallercross-sectional area3 is incorporated in the form of a cruciform cross-section in the largercross-sectional area2. In this embodiment the cruciformcross-sectional area3 is highly doped and the largercross-sectional area2 less highly doped with the antimicrobial substance.
FIG. 6 shows an embodiment in which the largercross-sectional area2 is subdivided in star-like manner into sectors by the smallercross-sectional area3 and only the smallercross-sectional area3 is highly doped with the antimicrobial substance.
FIG. 7 shows a bristle6 with a polygonal, namely square cross-section leading to a higher mechanical cleaning action than with a circular bristle. The bristle6 once again has a largercross-sectional area2 of a thermoplastic material and a smallercross-sectional area3 in the form of a segment, which is more highly doped with the antimicrobial substance than the largecross-sectional area2. The bristle7 according toFIG. 8 differs from that ofFIG. 7 only in that it has two segmental, smallercross-sectional areas3 at diagonally positioned corners. In both cases the antimicrobially acting cations are mainly delivered at the free surface of the smallercross-sectional area3. However, part thereof is diffused into the largercross-sectional area2 and to this extent a diffusion brake is formed, because the cations must firstly migrate through this cross-sectional area in order to arrive at the free surface thereof.
In the embodiment according toFIG. 9 the smallercross-sectional area3 forms a layer on the largercross-sectional area2 only extending over a small part of the circumference. Thecross-sectional area3 is preferably diffusion-tight with respect to theantimicrobial substance4 in the largecross-sectional area2, so that the inherently slow diffusion on the larger, free surface ofcross-sectional area2 is intensified. According toFIG. 10 this can optionally take place in locally oriented form, in that theouter layer3 forming the diffusion brake covers a larger part of the circumference of the largecross-sectional area2 or, as in the embodiment ofFIG. 11, the entire circumference. In both cases the antimicrobial substance is exclusively housed in the largecross-sectional area2.
FIG. 12 shows a star-shaped bristle8, whose bearingcross-sectional area2 has a four-arm construction. At the ends of each arm are located the smallercross-sectional areas3, which are highly doped with theantimicrobial substance4, whereas thecross-sectional area2 is less highly doped.