DENTAL TREATMENT FILMS INCORPORATING UNMIXED REACTIVE INGREDIENTS
20180206960 ยท 2018-07-26
Inventors
Cpc classification
A61K8/65
HUMAN NECESSITIES
A61K2800/412
HUMAN NECESSITIES
A61K9/16
HUMAN NECESSITIES
A61K8/8129
HUMAN NECESSITIES
A61K8/8123
HUMAN NECESSITIES
A61K9/50
HUMAN NECESSITIES
A61K6/20
HUMAN NECESSITIES
A61K8/8111
HUMAN NECESSITIES
A61C19/063
HUMAN NECESSITIES
A61K9/006
HUMAN NECESSITIES
International classification
A61K9/70
HUMAN NECESSITIES
Abstract
A two-part treatment film may include a barrier layer, a gelatinous composition layer, and at least one active ingredient adhered to the gelatinous composition layer. The barrier layer may be a flexible film that is insoluble in water. In some embodiments, the at least one active ingredient may be in the form of dried particles. In other embodiments, the at least one active ingredient may be in the form of microspheres filled with an active ingredient.
Claims
1. A two-part treatment film comprising: a barrier layer; a gelatinous composition layer; and at least one active ingredient adhered to the gelatinous composition layer.
2. The two-part treatment film of claim 1, wherein the barrier layer is insoluble in water.
3. The two-part treatment film of claim 2, wherein the barrier layer comprises a flexible film.
4. The two-part treatment film of claim 1, wherein the gelatinous composition layer comprises a dehydrated surface skin.
5. The two-part treatment film of claim 1, wherein the at least one active ingredient comprises dried particles.
6. The two-part treatment film of claim 1, wherein the at least one active ingredient comprises microspheres filled with an active ingredient.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0008] In order to describe the manner in which the above-recited and other advantages and features of the invention can be obtained, a more particular description of the invention briefly described above will be rendered by reference to specific example embodiments thereof which are illustrated in the appended drawings. Understanding that these drawings depict only typical embodiments of the invention and are not therefore to be considered to be limiting of its scope, the invention will be described and explained with additional specificity and detail through the use of the accompanying drawings.
[0009]
[0010]
[0011]
DETAILED DESCRIPTION
[0012] Embodiments of the present invention utilize a barrier layer that is comprised of a polymeric sheet. An ideal barrier layer may be thin, flexible and insoluble in water. The barrier layer may constitute a first layer in the manufacture of a treatment film; it is on one surface of the barrier layer that a second treatment layer is adhered. Examples of barrier layer materials include but are not limited to: parafilm, polyethylene sheet, polypropylene sheet, PVC sheet, polyurethane sheet, nylon sheet, PVA sheet, and the like. [0013] One embodiment of the present invention comprises three layers: [0014] A. Barrier layer [0015] B. Gelatinous composition layer [0016] C. Surface adhered active ingredient particulates/granules
[0017]
[0018] The resulting film/strip is activated when it is applied to a moist treatment area within the oral cavity. Upon application, the saliva dissolves the dry ingredients of the active ingredient particulates layer C and at the same time hydrates the surface skin layer D; this allows the separated components to begin mixing after being placed adjacent the treatment site. The patient may aid the mixing of the layers while hand applying the strip/film to the teeth or tissue; the pressure applied against the barrier layer A will produce forces that squish the layers together that further mix the two-part system. Furthermore, the active forces within the oral cavity will aid the mixing of the layers while the regime continues, i.e. increased temperature to about 37 degrees C., mild occlusal forces, and continuous interactions between cheeks and teeth. Upon mixing, the two-part system becomes activated delivering the desired reaction chemicals or shelf unstable compounds to the treatment site in a convenient manner.
[0019] Another embodiment of the present invention is shown in
[0020] By design, the hollow shells of the layer C can be made of materials that readily dissolve in water or saliva; thus the internal active ingredients are released when placed against a wet treatment surface and the outer shell is readily dissolved. The released compounds then mix with the active ingredients contained within a layer B. Upon mixing, the two-part system becomes activated delivering the desired reaction chemicals or shelf unstable compounds to the treatment site in a convenient manner.
[0021] By design, the micro-spheres of the layer C can be made of materials that have a low crush strength. When the layer C is placed against the treatment site the force of application causes the micro-spheres to become ruptured releasing their contents to readily mix with the layer B. Upon mixing, the two-part system becomes activated delivering the desired reaction chemicals or shelf unstable compounds to the treatment site in a convenient manner.
[0022] Another embodiment of the present invention is shown in
[0023] Upon practical application of the embodiments of the present invention many other embodiments that fall under the scope of this patent become evident.