The present invention relates generally to tubes in which pressurized fluid flows, and particularly to a multiple lumen tube for pressurized fluid flow, which may form part of a prosthesis, such as but not limited to, an inflatable penile prosthesis.
Inflatable penile prostheses are used in the treatment of erectile dysfunction (ED) or impotence. An example of an inflatable penile prosthesis is described in PCT Patent Application PCT/IB2016/057892. The penile prosthesis is implantable within the penis and achieves a penile erection upon fluid flowing from a fluid reservoir and inflating an inflatable tubular member. An axial penile pump of such a prosthesis requires both inlet for low pressure and outlet for high pressure in order to evacuate fluid from the reservoir to implant cylinders and achieve erection. The high pressure lumen also enables the deflation of the penile cylinders back to the reservoir for returning to the flaccid state.
The present invention, relates, in some embodiments thereof, to a multiple lumen tube for pressurized fluid flow, which may form part of a prosthesis, such as but not limited to, an inflatable penile prosthesis. The tubes are made of an elastomeric material with at least two longitudinal lumens formed in the elastomeric material. The lumens are surrounded by a coil embedded in the elastomeric material. The coil helps prevent the tube from kinking.
According to an aspect of the present invention, there is provided apparatus including a tubular body made of an elastomeric material, at least two longitudinal lumens formed in the elastomeric material of the tubular body, which extend through an entire length of the tubular body along a longitudinal axis of the tubular body, the lumens being separated from each other by a wall, and a coil embedded in the elastomeric material of the tubular body, the coil surrounding the lumens.
Without limitation, each of the lumens may be oval shaped.
Without limitation, each of the lumens may be oval shaped with a major length tilted at an angle with respect to the longitudinal axis of the tubular body. For example, each of the lumens may be oval shaped with a major length in a range of 1.3-1.9 mm and a minor length in a range of 0.4-0.9 mm. A thickness of the wall may be in a range of 0.2-0.5 mm at a center of the tubular body.
The tubular body may be coated with a hydrophilic material. The tubular body may be coated with an antibiotic material.
A pressurizing fluid may be fluidly connected to at least one of the lumens.
Some embodiments of the invention are herein described, by way of example only, with reference to the accompanying drawings. With specific reference now to the drawings in detail, it is stressed that the particulars shown are by way of example and for purposes of illustrative discussion of embodiments of the invention. In this regard, the description taken with the drawings makes apparent to those skilled in the art how embodiments of the invention may be practiced.
In the drawings:
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At least two longitudinal lumens 14 are formed in the elastomeric material of tubular body 12. The lumens extend through the entire length of tubular body 12 along a longitudinal axis 16 of body 12. In the illustrated embodiment, each lumen 14 has a cross-section which is oval shaped with a major length MJL, without limitation, in a range of 1.3-1.9 mm and a minor length MNL, without limitation, in a range of 0.4-0.9 mm. In one embodiment, the major length is perpendicular to the longitudinal axis 16 of body 12. Alternatively, the major length may be tilted at an angle other than 90° to the longitudinal axis 16 of body 12.
The lumens 14 are separated from each other by a wall 18. Without limitation, the thickness T of wall 18 is in a range of 0.2-0.5 mm at the center of tubular body 12, which is the point of minimum thickness of wall 18.
The lumens 14 are surrounded by a coil 20 embedded in the elastomeric material of tubular body 12. Coil 20 may be made from an elastic, flexible material, such as but not limited to, nylon, nitinol and others.
Tubular body 12 may be coated with a hydrophilic material to facilitate movement of the tube after implantation, and/or with an antibiotic material to prevent possible infections following implantation.
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