The present invention relates to an artificial contractile tissue generally devised to be used in the medical field. Such a tissue may be advantageously used to assist muscular contraction, in particular atrial contraction of patients with atrial fibrillation.
Artificial supports to assist muscular contraction are disclosed in Japanese patent applications JP 2001112796 and JP 7008515.
The devices described in this prior art act as muscle fibers and are therefore not adapted to completely replace a muscle tissue.
US patent application US 2005/0020871 discloses an artificial beating tissue based on nanotechnology actuators as source of one or more spatially oriented forces which are used to exert an extra pressure on the cardiac region to be assisted. To this effect, a network of contractile elements connected with longitudinal elements is provided. The network is embedded in an elastomeric material. Activation of the contractile elements causes a reduction in their length that is associated to the contraction of the web.
The objective of the present invention is to provide an improved artificial contractile tissue.
This objective has been reached according to the present invention by an artificial contractile tissue comprising a structure and several fibers of variable length which are fixed at their ends to the structure. The fibers are made of a contractile material which can be activated by an activator, e.g. an electric current/voltage, in such a way as to provide a tissue in a rest or in an activated position, the rest position being defined with non-rectilinear fibers and the activated position being defined with fibers of reduced length. The transition from the rest towards the activated position or vice-versa is defined by a fiber movement along a lateral direction which is perpendicular with respect to the fiber length.
In one embodiment, the structure is rigid and forms a closed line, the ends of each fibers being fixed to two separate points of the structure.
The closed line may be comprised in a plane and may form any shape, regular or not, for instance a circle, an ellipse, a square or a triangle.
In a preferred embodiment, the structure has an annular shape and each fiber forms a diameter of the annular structure. This means that all fibers are crossing each other at the center of the annular structure. At this point, the fibers are advantageously glued to each other.
In another embodiment, the structure has an annular shape and each fiber forms a loop around a central piece, called pivot hereafter, which is located at the center of the annular structure.
On one or both sides of the tissue, a membrane, e.g. made of silicone, may cover the fibers.
When using a planar structure, at rest position, the plane preferably forms an angle of 20 to 35° with the fiber ends.
Advantageously the external surface of the structure comprises a sewing surface, for instance a Dacron™ coating.
In another embodiment the structure is a flexible sheet, for instance woven or knitted tissue containing Kevlar™ or carbon fibers. In this case the contractile fibers may be distributed and fixed at their ends to appropriate locations on the sheet.
In a preferred embodiment several protrusions are distributed on the sheet surface, each protrusion being adapted to hold a fiber middle part, in such a way that activation of the fiber results in a lateral movement of the protrusion and therefore a contraction of the sheet.
In another embodiment the contractile fibers are knitted in the flexible sheet, on both sides, in such a way that the flexible sheet itself avoids shortcuts when an electric current is used to activate the contractile fibers. The fiber activation results in a movement of the flexible sheet ends in any desired direction.
If the activator is an electric current an isolating substance preferably covers the fibers. For instance, fibers may be inserted in ePTFE tubes.
Any suitable material can be used for the fibers, in particular Electro Active Polymers (EAP), Electro Active Ceramics (EAC), Shape Memory Alloys (SMA).
SMA undergo changes in shape and hardness when heated or cooled, and do so with great force. The mechanism of the shape memory effect is a diffusionless phase transformation as a solid, in which atoms move cooperatively, often by shear like mechanisms. SMA have a uniform crystal structure that radically changes to a different structure at a specific temperature, When the SMA is below this transition temperature (martensitic state) it can be stretched and deformed without permanent damages. After the SMA has been stretched, if it is heated (i.e. electrically) above its transition temperature (austenite state), the alloy recovers to the un-stretched shape and completely reverses the previous deformation.
Moreover, SMA are capable to lift thousand times their own weight. SMA have the ability to recover from plastic deformation, which is sustained below critical temperature, by heating, and they can work under tension, compression, bending or torsion.
Table 1 below shows a comparison of the properties of materials which may be used for artificial muscles: Electro Active Polymers, Shape Memory Alloys and Electro Active Ceramics.
Even if the energetic efficiency of these materials is lower than conventional electric and magnetic pumps (only 5% of the electricity potential for work becomes a usable physical force with 95% lost as heat), their high strength-to-weight ratio, small size and low operating voltages, allow the development of devices that would be difficult or impossible to make using conventional motors with overall better performance than other systems.
A suitable SMA material for the contractible fibers is Nitinol™. In this case the fibers can be stretched by as much as 4% when below the transition temperature, and when heated, they contract, recovering thereby to their original, shorter length with a usable amount of force in the process. Temperature range is 37-50° C.
Other particularly interesting materials are Biometal fibers (BMF) and Biometal helix (BMX) commercialized by Toki Corporation Inc., Japan. Those materials are able to reversibly contract upon a controlled heating caused by the supply of an electric current/voltage.
The invention is discussed below in a more detailed way with examples illustrated by the following figures:
The embodiment illustrated on
The ring may be made of plastic, e.g. Delrin™ and may have other shapes than a circular (ellipse, eight shape, etc. . . . ).
Bench tests have demonstrated that a 55 mm dome made of BMX200 can pump 80 ml of water against a pressure of 15 mmHg each time it is activated (contraction). With a rate of contractions of 60 times per minute, a total volume of 480 ml per minute of water may be pumped.
In order to avoid shortcuts, fibers a are isolated, e.g. inserted in ePTFE tubes having an inner diameter which may be of 400 μm. The ePTFE tubes are preferably glued together at the apex c.
Another mean to avoid shortcuts is to insert a pivot j at the apex c as illustrated in
A thin silicone membrane d, e.g. 100 μm thick, covers the inner and outer part of the dome to provide thermo isolation of the dome thereby reducing the risk of burn lesions on the heart surface.
On the external surface of the ring b, a coating, e.g. made of Dacron™, is fixed to provide a sewing surface e for the connection to the heart.
Advantageously the dome is sutured on the external surface of the upper chamber of the heart (atrium) in the rest position in such a way the atrium completely fills the inner part of the dome.
It should be pointed out at this stage that in the present invention, “flexible sheet” does not mean “elastomeric material” as disclosed in prior art application US 2005/0020871. A flexible sheet as presently defined can be folded but not extended or contracted.
In this embodiment (see
In another embodiment a flexible sheet f is partially and schematically illustrated on
Several matrix can be joined together in parallel (to increase the pulling force) and/or serial (to increase the length of the displacement) configuration for different clinical applications.
The working principle of the previous cited embodiment will be discussed below and illustrated on
When electrically activated, the fibers g reach their transitional temperature and may shrink 4% of their length, pulling consequently protrusions h down to the wave's midline. Because protrusions h are fixed to the matrix, fiber's activation results in matrix movement.
The axe of the movement of the matrix is orthogonal with respect to the fiber movement. Synchronous activation of the 26 fibers causes the matrix shrinking of about 25% as illustrate in
The matrix discussed here is able to develop about 240 gf over 6 mm displacement which corresponds to 0.1 W.
A Drive Unit (DU) and a Power Source (PS) are necessary to control and power matrix movement.
The DU is basically a microprocessor that distributes current to fibers. Intensity, width and rate of the electrical stimuli are determined according to the application of the matrix.
The PS may be a rechargeable battery.
The present invention has several applications in the medical field, in particular:
The drive unit is similar to that currently used for single chamber cardiac pacemakers: it detects ventricular electrical activity thanks to an epicardial electrode and provides control of current direction, intensity and frequency of activation of contractile elements: the contraction can be synchronous, asynchronous, sequential or others in order to have the most appropriate three dimensional deformations to compress atria and achieve the optimal ventricular filling. Lithium-manganese dioxide batteries (500 mA for 3.2V) provide the power supply and can last for 6 h. A percutaneous energy transfer supply can be developed for battery recharge during the night, as routinely done with other ventricular assist devices like LionHeart.
Number | Date | Country | Kind |
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PCT/IB2006/050033 | Jan 2006 | IB | international |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/IB06/55044 | 12/28/2006 | WO | 00 | 9/25/2008 |