Abstrict An insert for a bra, wherein the insert adaptable to the inner
shape of the cup comprises at least one zone storing an active ingredient
and delivering to the skin, and at least one breathing compensation
zone, wherein the zones selectively deliver active ingredients only
or act in a compensating manner, or carry out both functions simultaneously.
Claims What is claimed is:
1. An insert for a bra, the insert (1) shaped generally in the
form of a bra cup, the insert comprising a layer having at least
one zone (4) storing an active ingredient and delivering the active
ingredient to the skin, the layer further having at least one active
ingredient free breathing compensation zone wherein the breathing
compensation zone (6) absorbs substances given up by the skin.
2. An insert according to claim 1 characterised in that the zone
storing the active ingredient is at the same time a breathing zone.
3. An insert according to claim 1 characterised in that total
surface of the zones (4 6) corresponds essentially to the total
surface of the insert (2).
4. An insert according to claim 1 characterised in that a multitude
of active ingredient zones (4) and a multitude of compensation zones
(6) are arranged alternately about the periphery of the insert.
5. An insert according to claim 1 characterised in that a multitude
of zones of the one type, that is of active ingredient zones (4)
or of compensation zones (6) are arranged separated from one another
and the regions therebetween form the zone of the other type, i.e.
a compensation zone (6) or an active ingredient zone (4).
6. An insert according to claim 1 characterised in that zones
are arranged strip-shaped in the circumferential direction or the
longitudinal direction.
7. An insert according to claim 6 characterised in that the zones
arranged separated from one another comprise a round circumferential
shape.
8. An insert according to claim 1 characterized in that the insert
(2) comprises several layers of which one contains the active ingredient
and compensation zone (4 6).
9. An insert according to claim 8 characterised in that the insert
(2) comprises a layer, externally bordering the layer containing
the active ingredient and compensation zones (4 6), which is breathing
and at least in the regions neighbouring the active ingredient zones
(4) is permeable to fluid.
10. An insert according to claim 8 characterised in that the insert
(2) comprises a layer, internally bordering the active ingredient
and compensation zones (4 6), which is for transmitting the active
ingredients (22) or substances to be absorbed by the compensation
zones.
11. An insert according to claim 8 characterised in that the insert
(2) comprises a removable protective film as an innermost layer.
12. An insert according to claim 1 characterised in that the border
surfaces (20) between active ingredient zones and compensation tones
(4 6) bordering one another have a limited permeability.
13. An insert according to claim 1 characterised in that the insert
(2) consists of flexible material.
14. An insert according to claim 1 characterised in that it comprises
thermoplastic material at least on the inner side, which with body
surface temperature adapts to the skin and ensures a good skin contact.
15. An insert according to claim 1 characterised in that the insert
(2) is a rolled up flat strip with a self-adhesing closure.
16. An insert according to claim 15 characterised in that the
flat strip comprises weakening lines for shortening the strip.
17. An insert according to claim 1 characterised in that the insert
(2) in the longitudinal direction comprises a separating line and
two lateral regions (8 10) adjustably overlap along the line.
18. An insert according to claim 1 characterised in that the insert
(2) comprises recesses (16) in the longitudinal direction.
19. An insert according to claim 1 characterised in that the insert
(2) externally comprises at least a self-adhesing region for fastening
to the bra.
20. An insert according to claim 1 characterised in that the active
ingredient zones (4) are hygroscopic.
21. An insert according to claim 1 characterised in that it is
constructed such that there exists a pressure difference between
the active ingredient zones (4) and the skin.
22. An insert according to claim 1 characterised in that it is
so constructed and the active ingredient is so incorported that
the active ingredient transport to the skin is effected by falls
in concentration (controlled release).
23. An insert according to claim 1 characterised in that a toil
battery is arranged in such a manner that an electrical voltage
(28 30) is applied over the thickness of the active ingredient
zones (4).
24. An insert according to claim 1 characterised in that the active
ingredient zones (4) on the inner side are limited by a diaphragm-like
separating layer.
25. An insert according to claim 1 characterised in that the active
ingredients (22) are located in a substance or form a substance
which liquifies on heating.
26. An insert according to claim 1 characterised in that the active
ingredients (22) are located in a substance or form a substance
which is thixotropic.
27. An insert according to claim 1 characterised in that the active
ingredient zones (4) on the inside are limited by a membrane whose
permeability to the active ingredients (22) increases on heating.
28. An insert according to claim 1 characterised in that the active
ingredient zones on the inside are limited by a membrane whose permeability
to the active ingredients (22) increases with the effect of force
by changes in movement of the insert (2).
29. An insert according to claim 1 characterised in that the active
ingredient zones (4) are border surface systems with border-surface-active
active ingredients (22).
30. The insert of claim 1 having a generally frustoconical shape.
31. The insert of claim 1 wherein the layer comprising the zone
storing an active ingredient and the breathing zone is a skin contacting
layer.
Description The invention relates to an insert adapting to the cup shape for
a bra.
For the care of the female breast there are active ingredient preparations,
for example creams or fluids which are applied to the skin of the
breasts in order to act over a longer period of time. With the direct
application on the skin a metering of the active ingredient preparations
is possible only with difficulty or is very time consuming, for
example by repeated application of small amounts. A uniform metering
over a longer period of time may be achieved in this manner only
to a certain extent.
Inserts for bras are known which serve various purposes. There
are for example breastfeeding inserts (see G 81 19 845.0 DE 32
06 371 A1 or G 8315 729.9) and shape-inserts (see DE 31 20 875 C2).
It is the object of the invention to provide an insert for a bra,
via which active ingredients, for the care of the female breast
or for its therapeutic treatment in a comfortable manner and with
a constant metering, can be brought into contact with the skin.
The object is achieved in that the insert adaptable to the inner
shape of the cup comprises a zone which stores the active ingredients
and delivers to the skin, and at least one breathing compensation
zone.
Advantages of the insert are that the active ingredient zones serve
as reservoirs for the active ingredient prepearations and simultaneously
deliver one or more active ingredients to the skin, wherein the
delivery quantity is co-determined by the nature of the active ingredient
zones, as is described below. Furthermore the compensation zone
of the insert serves as a breathing region, in particular for avoiding
the formation of sweat. It is however also possible without further
ado that the active ingredient zone is at the same time a breathing
region.
The insert advantageously covers essentially the whole inner surface
of the cup. In order to maximise the effect of the insert, preferably
the size of the active ingredient and compensation zones is selected
such that their total surface corresponds essentially to the total
surface of the insert. In an advantageous embodiment of the invention
a multitude of active ingredient zones and a multitude of compensation
zones are provided which are arranged alternately. With this the
zones of one type may be separated from one another, arranged in
an island manner within the zone of the other type. It is favourable
when the zones run strip-shaped in the circumferential direction
or in the longitudinal direction. If the zones are arranged in an
island manner within another zone, a round circumferential shape
of the zones arranged in an island-like manner may be advantageous.
According to a further advantageous embodiment the insert comprise
several layers, of which one contains the active ingredient zones
and the compensation zones. On this layer a further layer may be
connected which lies further outside, which is breathing and is
fluid permeable at least in the regions bordering the active ingredient
zones. In this way it is achieved that the active ingredient preparation
which as a rule is fluid or viscous or the carrier substance in
which the active ingredients are contained, these being contained
in the active ingredient zones, cannot exit into the bra. Towards
the inside a further layer may be connected to the storing layer,
this further layer able to serve for the transmission of the active
ingredient and also for transmission of the body substances to be
taken up by the compensation zones. On application of such a transmission
layer, this comes into direct contact with the skin in place of
the storing layer. Also the transmission zone may comprise various
zones which are congruent with the active ingredient zones or the
compensation zones and comprise various transmission properties
corresponding to these. So that an active ingredient preparation,
already added on manufacture of the insert, may not exit the insert
already before its use or may not lose its effectiveness, as an
innermost layer a removable protective film which is airtight may
be provided. Alternatively the whole insert after its manufacture
may be sealed by an encompassing foil. It may also be provided that
the active ingredient zones are not provided already on manufacture
of the insert with an active ingredient preparation, but that the
active ingredient zones are provided with an active ingredient preparation
by the user, for example by introducing drop by drop. Furthermore
it may also be provided that the user after use of the insert, refills
active ingredient preparations into the active ingredient zones.
In particular when the total surfaces of the active ingredient
zones and the compensation zones are to be a maximum, the various
zones may directly border onto one another. Preferably then the
bordering surfaces are so created between the zones that they have
a limited permeability. For the active ingredient preparation and
the carrier substance there should be practically no permeabilty.
If the active ingredient zones or the compensation zones do not
directly border one another, between these zones there may lie further
zones which are "neutral". Preferably these "neutral"
zones, similar to the bordering areas between directly bordering
active ingredient and compensation zones, have practically no permeability
for the active ingredient preparation and the carrier fluid.
So that the insert may be well adapted to the shape of a bra cup,
the insert is preferably manufactured from a flexible material.
On the inner side the insert may act thermoplastically in order
to provide an inner contact given the skin surface temperature.
The insert may be a flat strip, which is rolled up and closed with
a self-adhesing closure. The flat strip may be so formed that it
has a conical form on its rolling up. Additionally or alternatively,
the material of the flat strip may be so soft that the rolled up
flat strip adapts very easily to the cup shape. This flat strip
may comprise weakening lines along which part of the flat strip
may be removed for its shortening, in order to adapt the size of
the insert to the cup. The insert then when it is a rolled-up flat
strip as well as when it is manufactured initially in the cup shape,
may comprise a separating line in the longitudinal direction, wherein
the two lateral regions along the line adjustably overlap for changing
the size. An adaptation of the insert to bra cups of various sizes
may also be achieved in that the insert comprises recesses in the
longitudinal direction which extent from the largest circumferential
line so that the wall segments located between these may bend towards
the inside without folds forming. Further on the outside the insert
may comprise one or more self-adhesing regions which serve the fastening
in the bra cup. Preferably this insert may have a dimensional stability
of its own so that it comprises a cup shape without being connected
to the bra.
An insert which has such a predetermined shape may be used on its
own, that is without combination with a bra. This may for example
occur for therapeutic purposes.
In the following various embodiments of the active ingredient zones
are described which are designed with properties for metering the
active ingredients. In particular when the active ingredient comprises
a relatively high viscosity, the active ingredient zones may be
formed hygroscopically in order for example by way of the uptake
of body moisture to gradually thin or let the fluid become more
fluid. A further possibility for the metering of the active ingredient
may consist of providing a pressure difference between the active
ingredient regions and the skin, by way of which ions or molecules
of the active ingredient preparation exert a certain pressure on
the skin. By way of varying concentrations of the active ingredient
a transport in the direction of the skin can be effected (controlled
release). A deposition of certain ions or molecules on the skin
may be achieved in that an electrical voltage is applied at least
over the thickness of the active ingredient zones, i.e. by way of
a foil battery, by which means it is achieved that certain ions
or molecules dependent on charge accumulate at one electrode which
borders the skin or is insulated by the skin. According to a futher
embodiment of the invention the active ingredient zones on the inner
side may be limited by a diaphragm-like separating layer, so that
the active ingredients may act osmotically on the skin. The applied
active ingredient preparation may further be so formed that the
active ingredients are located in a carrier substance which liquifies
when heated up, or the active ingredients may themselves form a
substance which has this property. The heating up is effected by
the body temperature. There may also be provided substances which
are thixotropic. A further possibility for metering the active ingredients
lies in limiting the active ingredient zones at their inner side
by a membrane whose permeability to the active ingredient increases
on heating. There may also be provided a membrane whose permeability
to the active ingredient increases on the effect of force by movement
changes of the insert, i.e. with body movements. The active incredients
may also be materials lowering the interfacial tension (capillary
active) which for example accumulate on the border surfaces between
the active ingredient zones and the skin. The active ingredient
zones with this embodiment are formed as border surface systems.
The invention is described in more detail by way of the subsequent
drawings. The drawings show:
FIG. 1 a perspective view of an insert adjustable in size;
FIGS. 2a and 2b lateral views of inserts with strip-shaped active
ingredient zones and compensation zones;
FIG. 3 a perspective view of an insert with recesses and wall segments
for adapting the size of the insert;
FIG. 4 a schematic part section view of an arrangement of active
ingredient zones and compensation zones and of a bordering bra material;
FIG. 5 a part section view of an active ingredient zone with a
bordering transmission zone and an applied electrical voltage.
In all figures the same parts are indicated with the same reference
numerals.
FIG. 1 shows an insert 2 with a multitude of active ingredient
zones 4 which have a round circumferential shape. The active ingredient
zones are arranged over the whole surface of the insert, but are
not shown on the left side of the insert for reasons of clarity.
Regions between the active ingredient zones together form a compensation
zone 6. The insert comprises in the longitudinal direction a separating
line, and two lateral regions 8 10 along the line which overlap,
wherein the thickness of the overlapping as is shown by the double
arrow P, is adjustable in order to be able to adapt the size of
the insert to the size of the cup. The insert comprises at the front
end an opening 12 which serves so that the nipple does not come
into contact with the insert.
It is however also possible that the zones 4 may simultaneously
be breathing compensation zones.
The FIGS. 2a and 2b show inserts with strip-shaped active ingredient
zones 4 and essentially strip-shaped compensation zones 6. With
the insert of FIG. 2a the strips 4 6 are arranged in the circumferential
direction, in FIG. 2b on the other hand they are arranged in the
longitudinal direction. Both inserts are, in contrast to the insert
shown in FIG. 1 closed at the front end. Whilst the insert of FIG.
2a is formed with a compensation zone at the front end, the insert
of FIG. 2b at the front end neither comprises a compensation zone
nor an active ingredient zone. The front end represents a further
zone of a "neutral" zone 14 within a layer containing
the active ingredient zones and the compensation zones.
FIG. 3 shows an insert with active ingredient zones 4 and compensation
zones 6 which are arranged as with the insert of FIG. 1. For size
adaptation of the insert 2 to the size of a cup there are three
recesses 16 extending in the longitudinal direction from the border
edge, these having a wedge-like and rounded shape tapering towards
the front end of the insert. With these recesses the insert is subdivided
into three wall segments 18 which are connected to one another via
the front end of insert, and which on lateral pressure can bend
inwards by which means the circumference of the insert may be reduced
without folds forming.
FIG. 4 explains the functioning principle of the active ingredient
zones 4 and the compensation zones 6. With the arrangement shown
in FIG. 4 of these two zone types, these alternately directly border
onto one another. They are separated by border surfaces 20 which
are not permeable to the active ingredient preparation present in
the active ingredient zone. On a longitudinal side which forms the
outer side, the zones rest against a bra material. This material
is selected such that the active ingredient particles 22 may only
exit through the longitudinal side lying opposite, thus inwardly
towards the skin from the active ingredient zones as is shown by
the straight arrows. In the opposite direction through the same
longitudinal side substances given up by the skin may enter into
the breathing compensation zones, as is indicated by the arrows
24.
FIG. 5 shows a part of an active ingredient zone 4 and a part of
a transmission zone 26 bearing on this on the inside. Over the whole
width of these two zones an electrical voltage is so applied that
the outer side of the active ingredient zone 28 is negatively poled
and the inner side of the transmission zone 30 is positively poled.
This voltage may for example be applied with the help of a foil
battery. Negative active ingredient ions or molecules migrate as
is indicated by the arrows 32 from the active ingredient zone into
the transmision zone towards the positive pole 30.
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