The present invention relates to an electrical connector arrangement and, more particularly, to an implantable electrical connector arrangement.
Implantable connectors play an important role in the manufacture and implantation of active implantable medical devices (AIMD). These typically consist of a housing that contains control electronics and a battery, implantable electrodes (or electrode arrays) and cables for establishing electrical contact with the electrodes and the electronics.
Reversibly detachable connectors (hereinafter also referred to as connectors), which are integrated into the cables, make it possible to separate the individual parts. This makes implantation easier and also creates the possibility of replacing defective, improved, or consumed parts (e.g. the battery in a pacemaker, which only has a lifespan of 3 to 7 years).
Such implants and connectors are shown e.g. in publications J. E. Letechipia, P. H. Peckham, M. Gazdik, and B. Smith, “In-Line lead connector for use with implanted neuroprosthesis,” “IEEE Trans. Biomed” Engl., vol. 38, no. 7, pages 707-709, 1991; M. Cocco, P. Dario, M. Toro, P. Pastacaldi, and R. Sacchetti, “An implantable neural connector incorporating microfabricated components,” “J. Micromech. Microeng.”, vol. 3, no. 4, pages. 219-221, 1993; as well as R. G. Hauser and B. J. Maron, “Lessons from the failure and recall of an implantable cardioverterdefibrillator,” (Engl), “Circulation”, vol. 112, no. 13, pages 2040-2042, 2005.
Depending on the desired number of channels and the desired integration density, the size of the connector increases, which in turn can have negative effects on the surrounding tissue. With conventional connector concepts, the insertion force is proportional to the number of contacts desired. In the case of miniaturized implantable connectors, the electrical insulation between the individual adjacent contacts of different channels is also a problem because a saturated, 100% moist environment prevails due to the use in the body. The electrical insulation must also be implemented and requires additional materials and forces. In order to ensure adequate electrical insulation, the distance between adjacent contacts in known connector arrangements must furthermore be comparatively large so that the integration density is not sufficiently high. The number of channels is therefore relatively limited and is at a maximum of 16 for known arrangements.
Once the two connector partners have been joined, adhesive must be applied in some known connector arrangements in order to create an insulation from the exterior. An example is the “Craggs connector” from Finetech Medical, see P. E. Donaldson, “The Craggs connector: A termination for Cooper cable,” (Engl), “Medical & biological engineering & computing”, vol. 23, no. 2, pages 195-196, 1985.
An implantable electrical connector arrangement electrically connects a first electrical component and a second electrical component. The connector arrangement includes a first connector having a first terminal and a first coupling electrode connected to the first terminal and a second connector having a second terminal and a second coupling electrode connected to the second terminal. The first connector and the second connector are connectable to each other such that the first terminal and the second terminal are capacitively connectable via the first coupling electrode and the second coupling electrode in a connected state. A defined separation gap is formed between the first coupling electrode and the second coupling electrode in the connected state.
The invention will now be described by way of example with reference to the accompanying Figures, of which:
For better understanding of the present invention, it shall be explained in detail by way of embodiments with reference to the figures. Same elements are there designated with same reference numerals and same component designations. Furthermore, some features or combinations of features from the different embodiments shown and described can also be independent inventive solutions by themselves or solutions according to the invention.
An implantable electrical connector arrangement 100 according to a first embodiment of the present invention shall first be explained in more detail below with reference to
The electrically insulating material of both substrates 106, 110 can be flexible or rigid depending on the configuration, but should not be electrically conductive. In the case of electrically conductive material, additional insulation layers must be introduced. For example, polyimide, PDMS, ceramic, and all other materials that are used for electrical circuit carriers are suitable.
Second coupling electrode 112 is electrically connected to a second terminal 122, as shown in
In the connected state shown in
Coupling electrodes 108, 112 can be formed by alloys such as platinum-iridium or MP35N®. MP35N® is a registered trademark of Standard Pressed Steel Technologies, Inc. The components of MP35N® ensure excellent corrosion resistance of the alloy, as all four alloy components, nickel, cobalt, chromium and molybdenum, increase corrosion resistance in almost all stainless steel, nickel, and cobalt alloys employed in the industry. The proportion of 20% chromium improves the resistance to oxidation, sulphidation, and chemical reactions with salt at elevated temperatures. Any other electrically conductive electrode material can of course also be used.
For electrical insulation and for protection against the external environment, an electrically insulating passivation layer 118, 120 is provided on first and second connector 102, 104, respectively, as shown in
The present invention is based on the idea that capacitive coupling (displacement current) is used instead of galvanic faradic transmission (line current). Since the electrical coupling of the two connectors 102, 104 is capacitive, low frequencies are blocked. An additional smoothing capacitor can be integrated in order to nevertheless obtain low stimulation frequencies at the electrode in the case of use with a stimulation electrode. The actuation circuit outputs an excitation signal that has a higher frequency than a signal that is output to the implantable electrode.
According to the invention, the separating gap 132 can be filled with water or electrolyte during operation, so that an improved dielectric is created between two coupling electrodes 108, 112. In this case, separating gap 132 fills with liquid from the surrounding medium and/or with water which emerges from first and second passivation layers 118, 120 during operation.
In general, silicone rubber (polydimethylsiloxane, PDMS) is typically chosen as the insulator material, such as fort the passivation layers 118, 120, for use in implantable components. PDMS has the sufficient long-term stability that must be demanded for years of use in an aqueous or moist environment, as is present for an active implantable assembly. In the event that the separating gap 132 is at least in part defined by silicone material, it was possible to show that osmosis effects in the implanted state cause condensation water to escape from the silicone material and fill the separating gap 132. Such a layer of water with a high relative dielectric constant represents a good dielectric for the capacitive coupling. In addition, no measures have to be taken to prevent the ingress of liquid into the connector arrangement 100. This increases the long-term stability of the connection and thereby reduces the likelihood of failure.
Due to this type of connection, no contact pressure needs to be applied for establishing an electrical connection. The gap 132 with precisely defined dimensions is instead provided between the two contact 108, 112. According to an advantageous further development of the present invention, the separating gap 132 is not hermetically sealed off from the outside environment. When the connector arrangement 100 is implanted, water condenses in the separating gap 132. The significantly higher dielectric constant of water (σ, H2O=80) compared to air (εr, air=1) supports the capacitive coupling via the gap 132.
As indicated schematically in
In another embodiment, an implantable electrode arrangement according to the present invention comprises at least one implantable electrode and one implantable connector arrangement 100, where the at least one first terminal 116 is respectively connected to the at least one electrode and the at least one second terminal 122 is connectable to a control circuit.
A further advantageous embodiment of connector arrangement 100 according to the invention shall be explained below with reference to
In the embodiment shown in
In contrast to ohmic contacts, the electrically conductive coupling electrodes 108, 112 do not need to be opened; i.e. the layer of insulating material 134, 136 can remain thereon. It can consist e.g. of polymers (Parylene-C, PDMS), oxides (TiOx) or other materials. Parylene-C, for example, is a material approved for human implantation and is electrically tight at a thickness of Various oxides achieve this electrical tightness already with significantly lower layer thicknesses and have a higher dielectric constant (e.g. εr, TiO2=63.7; εr, Paryiene-c=3.1). Both factors promise an increase in the coupling capacity and, accordingly, a better coupling. If no insulation is used, then the electrical coupling can be capacitive and resistive by way of accumulated water. In this case, however, adjacent contacts must be isolated from one another. The insulating material 134, 136 can but does not need to differ from the remainder of the encapsulation material of the connector (depending on the configuration, it is sufficient to provide different thicknesses for the insulating material and the encapsulation material for obtaining a directional capacitive coupling). In this way, the dielectric between the two coupling electrodes can be optimized for a particularly efficient capacitive coupling.
In the case of ohmic contacts, crosstalk between adjacent channels typically arises due to electrical leakage paths caused by the accumulation of water in voids that are present unintentionally. Such a resistive leakage path to adjacent channels is prevented due to the fact that a capacitive coupling is used in the concept according to the invention.
According to a first embodiment, the capacitive connector arrangement comprises only first and second connector 102, 104. In this case, a schematic cross section looks as shown in
As shown in
In another embodiment, the second connector 104 also comprises coupling electrodes on its rear side. As shown in
The multilayer arrangement shown in
In addition to the simple planar arrangements that were explained with reference to
According to a further advantageous embodiment of implantable connector arrangement 300, shown in
The spatial geometries of connectors 302, 304 can also be designed completely differently in other embodiments. Another example of such a three-dimensional connector-like structure is illustrated in
A further variant of connector arrangement 300 with pins and sockets is shown in
In summary, the present invention provides a capacitive, implantable, reversible, and multi-channel connection. Condensed or ingressing water at the point of coupling is used as a desired effect for capacitive coupling of two connectors. This arrangement advantageously provides the scalability of the number of electrical channels at a constant insertion force. A multi-channel, reversible, and implantable connection can thus be realized without the need for electrical insulation structures between two or more channels. The ingress of water cannot cause short circuits and therefore does not have to be prevented. The connector according to the embodiments of the invention is reusable, whereby the part connected to the implanted electrode can remain in situ when the components connected to the other part need to be repaired.
The implantable connector arrangement according to the present invention allows even densely packed contact arrays to be connected reliably as well as with long-term electrical and mechanical stability. The connector arrangement is inexpensive and, moreover, is biocompatible and certifiable for chronic use.
Number | Date | Country | Kind |
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10 2018 219 831.4 | Nov 2018 | DE | national |
This application is a continuation of PCT International Application No. PCT/EP2019/081630, filed on Nov. 18, 2019, which claims priority under 35 U.S.C. § 119 to German Patent Application No. 102018219831.4, filed on Nov. 20, 2018.
Number | Date | Country | |
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Parent | PCT/EP2019/081630 | Nov 2019 | US |
Child | 17323473 | US |