1. Field of the Invention
The present invention relates to breast prostheses and, more specifically, to a multi-chamber breast prosthesis.
2. Description of the Related Art
Many women who have had a mastectomy wear a breast prosthesis at the affected site. Typically, a breast prosthesis is made to look like a natural breast. It is placed against the patient's chest and is typically supported by a brassiere.
A common type of breast prosthesis is made from a soft silicone gel. Such a prosthesis includes an envelope made from a thin plastic film into which uncured silicone gel is injected. The pouch and the uncured silicone gel are then placed in a metallic mold having an interior that is complementary in shape to the desired shape of the prosthesis. The mould is then placed in an oven, where the silicone gel is heated until it is cured.
The silicone gel must be cured until it has a firmness so that it will maintain the shape of a natural breast during regular use. However, prostheses having such firmness have two disadvantages: (1) they can be uncomfortable when placed against the chest of the user; and (2) their outer surface does not drape naturally, thereby giving user an unnatural, asymmetric appearance.
Therefore, there is a need for a breast prosthesis that is firm enough to maintain a natural breast form shape during regular use, but that is comfortable to wear and that gives a natural drape.
The disadvantages of the prior art are overcome by the present invention which, in one aspect, is a breast prosthesis that includes an outer first layer, a middle second layer and an inner third layer. The outer first layer includes a first material that has a first firmness. The first firmness allows for a 20 mm to a 25 mm penetration by a cone penetrometer. The first layer has a shape corresponding to a shape of a breast form. The middle second layer is disposed adjacent to the first layer and includes a second material that has a second firmness that is greater than the first firmness. The inner third layer is disposed adjacent to the second layer opposite from the first layer and includes a third material that has a third firmness that is less than the second firmness.
In another aspect, the invention is a breast form prosthesis that includes four films that are welded together at a single weld to form three chambers having a shape of a breast form footprint. The three chambers include: a first chamber, a second chamber and a third chamber. An outer first layer is disposed in the first chamber and includes a first material that has a first firmness. The first layer has a shape corresponding to a shape of a breast form. The first material includes a silicone gel with a first concentration of a methyl hydrosiloxane polymer cross-linker The middle second layer is disposed adjacent to the first layer in the second chamber and includes a second material that has a second firmness that is greater than the first firmness. The second material includes a silicone gel with a second concentration, greater than the first concentration, of a methyl hydrosiloxane polymer cross-linker. The inner third layer is disposed in the third chamber and adjacent to the second layer opposite from the first layer. The inner third layer includes a third material that has a third firmness that is less than the second firmness. The third material includes a silicone gel with a third concentration, less than the second concentration, of a methyl hydrosiloxane polymer cross-linker.
In yet another aspect, the invention is a method of making a breast prosthesis, in which four flexible films are welded together with a single weld so as to form a breast form envelope. The breast form envelope includes a first chamber, a second chamber and a third chamber. Each chamber has a shape of a breast form footprint. The breast form envelope is placed into a mold having a shape that is complementary in shape to a breast form. A first material is injected into the first chamber. The first material has a first firmness that allows for a 20 mm to a 25 mm penetration by a cone penetrometer when cured. A second material is injected into the second chamber. The second material has a second firmness when cured. The second firmness is greater than the first firmness. A third material is injected into the third chamber. The third material has a third firmness when cured. The third firmness is less than the second firmness. The mold, the breast form envelope, the first material, the second material and the third material are heated to a temperature sufficient to cure the first material to the first firmness, the second material to the second firmness and the third material to the third firmness.
These and other aspects of the invention will become apparent from the following description of the preferred embodiments taken in conjunction with the following drawings. As would be obvious to one skilled in the art, many variations and modifications of the invention may be effected without departing from the spirit and scope of the novel concepts of the disclosure.
A preferred embodiment of the invention is now described in detail. Referring to the drawings, like numbers indicate like parts throughout the views. Unless otherwise specifically indicated in the disclosure that follows, the drawings are not necessarily drawn to scale. As used in the description herein and throughout the claims, the following terms take the meanings explicitly associated herein, unless the context clearly dictates otherwise: the meaning of “a,” “an,” and “the” includes plural reference, the meaning of “in” includes “in” and “on.”
U.S. Pat. Nos. 4,247,351 and 4,249,975 disclose prostheses of silicone gel encased in polyurethane film and, therefore, are incorporated herein by reference. U.S. Pat. Nos. 4,950,291, 5,895,423, 5,922,023 and 7,759,354 disclose multi-chambered breast prosthesis and methods of making the same and are also, therefore, incorporated herein by reference.
One embodiment of a breast prosthesis includes three layers of silicone gel enclosed in polyurethane film. The shape of the prosthesis conforms to the shape of a female breast. The layers of silicone are arranged such that a layer of soft conformable silicone is closest to the chest of the wearer and can conform to any irregularities in the chest. The middle layer of silicone is firm and provides support for the prosthesis, and the third layer of silicone positioned in the front of prosthesis (furthest away from the body) is soft and provides a natural drape to the prosthesis, which gives the wearer's chest a natural look and a symmetric appearance.
As shown in
In one embodiment, a first polyurethane film 110, a second polyurethane film 112, a third polyurethane film 114 and a fourth polyurethane film 116 are welded together along a single weld 126 to form three chambers. The single weld 126 has the footprint of a breast form. The first material of the first layer120 is placed in a first of the three chambers. The second material of the second layer 122 is placed in a second of the three chambers. The third material of the third layer 124 is placed in a third of the three chambers.
The first material, the second material and the third material can each include silicone gels. In one embodiment, the silicone gels include a two-component addition-cure silicone gel composition that includes a first combination, including a vinyl polymer, a silicone oil and a cross-linker, and a second combination, including a vinyl polymer, a silicone oil and a catalyst (such as a platinum and silicone complex). (One example of suitable silicon gels include prosthesis gels manufactured by Wacker Chemie GmbH.) A typical cross-linker includes a methyl hydrosiloxane polymer.
In one embodiment the exterior layer 120 and the interior layer 124 have a firmness that allows for a 20 mm to a 26 mm penetration by a cone penetrometer when cured and the middle layer 122 has a firmness that allows for a 10 mm to a 13 mm penetration by a cone penetrometer when cured. In one embodiment, micro-spheres can be added to one or all of the silicone gels to reduce the weight of the resulting prosthesis 100. Similarly, pigments can be added to give the prosthesis a natural look.
In one experimental embodiment, all silicone gel penetrations were determined on a Humboldt H1200 penetrometer. The probe employed a 65 mm diameter cone (the dimensions corresponded to part number 18-0122 from Petrolab Company) and the total probe weight was 24.9 g.
This breast prosthesis 100 provides a soft back layer 124 that conforms to the chest of the wearer and also a soft front layer 120 that provides a natural drape and fit. The middle layer 122 has sufficient firmness to maintain the shape of the breast form during regular use.
In one embodiment of a method of making a breast form, as shown in
Once in the mold 230, the first material 212 is injected into the first chamber through the first sprue 111, the second material 214 is injected into the second chamber through the second sprue 113 and the third material 216 is injected into the third chamber through the third sprue 117. This forms an uncured breast form 210, from which any air is removed. The sprues (111, 113 and 117) are sealed and the mold 230 with the uncured breast form 210 therein is placed in an oven 240 and heated to a sufficient temperature for a sufficient amount of time to cure the first material 212, the second material 214 and the third material 216, thereby forming a cured breast form 220. The exact temperature and time depend on the specific mixture of silicone gel used; however, it can readily be determined from the manufacturer's data sheet. The cured breast form 220 is removed from the oven 240, is allowed to cool, removed from the mold 230 and any excess film is trimmed away from the weld, resulting in a breast prosthesis 100.
The final prosthesis 100 includes a layer 124 closest to the patient that is soft and conforms to the chest of the wearer for comfort. The middle layer 122 is firm and provides a stable structure to the prosthesis. The front layer 120 is soft enough to provide a natural drape to the prosthesis 100 so as to give it an appearance of natural breast tissue.
The above described embodiments, while including the preferred embodiment and the best mode of the invention known to the inventor at the time of filing, are given as illustrative examples only. It will be readily appreciated that many deviations may be made from the specific embodiments disclosed in this specification without departing from the spirit and scope of the invention. Accordingly, the scope of the invention is to be determined by the claims below rather than being limited to the specifically described embodiments above.
This application claims the benefit of U.S. Provisional Patent Application Ser. No. 61/383,558, filed Sep. 16, 2010, the entirety of which is hereby incorporated herein by reference. This application is a divisional of, and claims the benefit of U.S. patent application Ser. No. 13189747, filed Jul. 25, 2011, the entirety of which is hereby incorporated herein by reference.
Number | Date | Country | |
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61383558 | Sep 2010 | US |
Number | Date | Country | |
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Parent | 13189747 | Jul 2011 | US |
Child | 14034101 | US |