Patent Application
20240315826
Briefly summarized, embodiments disclosed herein are directed to an implantable prosthesis, or graft, having an integrated therapeutic delivery system. Providing medications, drugs, or similar therapeutic agents directly into the blood stream can increase the efficacy of the treatments. Further, when placing grafts, stents, or similar intravascular prostheses, drugs may be required to prevent rejection of the prosthesis, restenosis, or similar unwanted side effects. Administering such drugs systemically can reduce the efficacy of the drugs at the target site, or affect areas other than the target site.
Vascular prostheses have been developed that include drug eluting structures. These structures can provide therapeutic agents directly to the target site, increasing the efficacy of the treatment and extending the lifespan of the prosthesis. However, even these slow-release, drug-eluting structures still only have a finite efficacy time. Embodiments, disclosed herein are directed to an implantable graft having an integrated therapeutic delivery system that can be replenished indefinitely to increase the lifespan of the prosthesis.
Disclosed herein is a drug delivery graft including, a graft body defining a graft lumen extending between a first end and a second end, an implantable access port, a delivery line coupled to the graft body, and defining a delivery line lumen in fluid communication with the implantable access port, and a plurality of channels extending through a wall of the graft body and communicating between the graft lumen and the delivery line lumen.
In some embodiments, a portion of the delivery line is coupled to an outer surface of the graft body or embedded within the wall of the graft body, or partially embedded within the wall of the graft body. In some embodiments, the delivery line extends helically about the graft body. In some embodiments, the delivery line extends laterally, longitudinally, or radially along the graft body. In some embodiments, the plurality of channels are spaced equidistant throughout the graft body. In some embodiments, the plurality of channels have an equal lumen diameter. In some embodiments, a distance between a first channel and a second channel of the plurality of channels disposed proximate the first end, is larger than a distance between a third channel and a fourth channel of the plurality of channels disposed proximate the second end.
In some embodiments, a diameter of the first channel of the plurality of channels disposed proximate the first end is smaller than a diameter of the fourth channel of the plurality of channels disposed proximate the second end. In some embodiments, the implantable access port is coupled to the delivery line proximate the second end. In some embodiments, the diameter of the delivery line proximate the second end is larger than the diameter of the delivery line proximate the first end. In some embodiments, one or both of the graft body and the delivery line is formed of an impermeable material. In some embodiments, one or both of the first end or the second end are trimmable from an original length to a second selected length, shorter than the original length.
Also disclosed is a method of infusing a drug including, accessing a subcutaneous access port with an access needle, inserting a predetermined amount of therapeutic fluid into the port, flowing the therapeutic fluid through a delivery line, the delivery line coupled to a surface of a graft body, and flowing the therapeutic fluid through a plurality of channels into a lumen of the graft body.
In some embodiments, a portion of the delivery line is coupled to an outer surface of the graft body or embedded within the wall of the graft body, or partially embedded within the wall of the graft body. In some embodiments, the delivery line extends helically about the graft body. In some embodiments, the delivery line extends laterally, longitudinally, or radially along the graft body. In some embodiments, the plurality of channels are spaced equidistant throughout the graft body. In some embodiments, the plurality of channels have an equal lumen diameter. In some embodiments, one or both of the graft body and the delivery line is formed of an impermeable material.
A more particular description of the present disclosure will be rendered by reference to specific embodiments thereof that are illustrated in the appended drawings. It is appreciated that these drawings depict only typical embodiments of the invention and are therefore not to be considered limiting of its scope. Example embodiments of the invention will be described and explained with additional specificity and detail through the use of the accompanying drawings in which:
Before some particular embodiments are disclosed in greater detail, it should be understood that the particular embodiments disclosed herein do not limit the scope of the concepts provided herein. It should also be understood that a particular embodiment disclosed herein can have features that can be readily separated from the particular embodiment and optionally combined with or substituted for features of any of a number of other embodiments disclosed herein.
Regarding terms used herein, it should also be understood the terms are for the purpose of describing some particular embodiments, and the terms do not limit the scope of the concepts provided herein. Ordinal numbers (e.g., first, second, third, etc.) are generally used to distinguish or identify different features or steps in a group of features or steps, and do not supply a serial or numerical limitation. For example, “first,” “second,” and “third” features or steps need not necessarily appear in that order, and the particular embodiments including such features or steps need not necessarily be limited to the three features or steps. Labels such as “left,” “right,” “top,” “bottom,” “front,” “back,” and the like are used for convenience and are not intended to imply, for example, any particular fixed location, orientation, or direction. Instead, such labels are used to reflect, for example, relative location, orientation, or directions. Singular forms of “a,” “an,” and “the” include plural references unless the context clearly dictates otherwise.
To assist in the description of embodiments described herein, as shown in
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by those of ordinary skill in the art.
In an embodiment, the graft body 110 can be disposed within a vasculature of a patient, such as arteries, veins, capillaries, or the like. However it will be appreciated that embodiments disclosed herein can be used within any tubular structure within the patient, including but not limited to, the lymph system, uro-excretory system, or the like. In an embodiment, the graft system 100 can be used with various other vascular medical devices, (e.g. stents, or the like) either disposed within the graft lumen 112, or disposed abluminally on an outer surface of the graft body 110. The port 120 can be disposed subcutaneously, adjacent a skin surface with a portion of the delivery line 130 providing fluid communication between the port 120 and the graft body 110.
In an embodiment, the graft body 110 can be formed of an impervious material, such as polypropylene (PP), non-porous polytetrafluoroethylene (PTFE), fluoroethylene polymer (FEP), or similar implantable polymer or plastic Advantageously, the impervious material can maintain the therapeutic agent within the lumen 112 of the graft body 110 to allow the therapeutic agent to fully mix with the blood stream. Further, the impervious graft body 110 can mitigate reabsorption of the therapeutic agent proximate the locus of introduction. As such, the graft body 110 can promote a more uniform dispersion of the therapeutic agent throughout the graft body 110 and/or downstream thereof.
As will be appreciated the longitudinal length of the graft body 110 can vary depending on the requirements of the treatment. In an embodiment, one of the first end 114 or the second end 116 can be trimmable from an original length to a second, selected length. In an embodiment, the graft body 110 can be formed of a porous or semi-porous material, such as expanded polytetrafluoroethylene (ePTFE), or similar porous implantable polymer or plastic. Further details and embodiments of which can be found in U.S. Pat. No. 6,355,063 which is herein incorporated by reference in its entirety.
In an embodiment, the port 120 can include a reservoir 122 having a needle penetrable septum 124 disposed thereover. The septum 124 can provide percutaneous access to the reservoir 122 by an access needle. For example, an access needle (e.g. Huber needle, non-coring needle, or the like) can penetrate the skin surface and underlying tissues and penetrate the septum 124 to access the reservoir 122. The access needle can define a lumen to provide fluid communication with the reservoir. In an embodiment, the port 120 can be coupled to the delivery line 130 by way of an interference fit, press-fit, snap-fit engagement, or can be coupled to a stem of the port 120 using a cathlock or similar mechanism. In an embodiment, the delivery line 130 can be formed integrally with the port 120 or coupled thereto by adhesive, bonding, welding, combinations thereof, or the like. In an embodiment, the port 120 can provide fluid communication between the reservoir 122 and a lumen 132 of the delivery line 130. It will be appreciated that the port 120 is an exemplary access device and various subcutaneous or supra-cutaneous access devices can be used with the graft system 100, for example the devices disclosed in U.S. Pat. Nos. 8,998,860; 9,642,986; 10,307,581; U.S. Patent Publication No. 2019/0232035; and WO 2020/028847, each of which is incorporated by reference in its entirety into this application.
The delivery line 130 can be a tubular structure defining a lumen 132 in fluid communication with the port 120. The delivery line 130 can extend from the port 120 to the graft body 110 and can be coupled with an outer surface of the graft body 110 by adhesive, bonding, welding, or can be formed integrally therewith. The delivery line 130 can extend over at least a portion of an outer surface of the graft body 110. As shown in
In an embodiment, the delivery line 130 can extend from the port 120 to a first end 114 of the graft body 110 and then to a second end 116 of the graft body 110. However, it will be appreciated that the delivery line 130 can extend from the port 120 to the graft body 110 to either the first end 114, the second end 116, or to a point disposed therebetween, as described in more detail herein. In an embodiment, the delivery line 130, or a portion thereof, can extend over an outer surface of the graft body 110. In an embodiment, the delivery line 130, or a portion thereof, can be embedded within the wall of the graft body 110, i.e. extending through a wall of the graft body 110. In an embodiment, as shown in
As shown in
In an embodiment, a diameter of the channel lumen 142 can be modified to vary the concentration of therapeutic agents released into the graft lumen 112. For example, a relatively larger diameter of the channel lumen 142 can provide a higher rate of infusion and higher concentration of the therapeutic agent. Similarly, a relatively smaller diameter of the channel lumen 142 can provide a lower rate of infusion and a lower concentration of the therapeutic agent.
In an embodiment, as shown in
In an embodiment, as shown in
In an embodiment, the graft body 110 can be formed of an impervious material. As such, the therapeutic agents can be released into the graft lumen 112 through one or more channel lumen 142. Advantageously, the number and diameter of channels 142 can be modified to provide an accurate, predetermined, rate of infusion of therapeutic agent into the lumen 112 of the graft body 110. Further, the impervious delivery line 130 and/or graft body 110 can ensure uniform dissemination of the therapeutic agent along the length of the graft body 110.
In an embodiment, as shown in
For example, as shown in
As such, a counter current infusion rate can be predetermined across the length (L1) of the graft body 110. Proximate the first end 114, upstream of the blood flow 80 a concentration of therapeutic agents within the graft lumen 112 is relatively low. As such, a lower infusion rate (i.e. greater spacing of channels 140, relatively smaller channel lumen 142 diameter, or smaller delivery line lumen diameter) is required to achieve an infusion rate. As the blood flows downstream through the graft lumen 112 towards second end 116, the concentration of therapeutics increases and, as such, a larger flow rate is required to infuse the therapeutics at the same rate.
Alternatively, as shown in
While some particular embodiments have been disclosed herein, and while the particular embodiments have been disclosed in some detail, it is not the intention for the particular embodiments to limit the scope of the concepts provided herein. Additional adaptations and/or modifications can appear to those of ordinary skill in the art, and, in broader aspects, these adaptations and/or modifications are encompassed as well. Accordingly, departures may be made from the particular embodiments disclosed herein without departing from the scope of the concepts provided herein.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US21/40930 | 7/8/2021 | WO |
