US20160067084A1 - Optic Nerve Implants - Google Patents

Abstract

Methods and devices for delivering therapeutic substances into the eye. An implant containing the therapeutic substance is implanted at least partially within the optic nerve and the therapeutic substance then elutes from the implant. The implant may have a lumen or it may be solid.

Description

RELATED APPLICATIONS
• This application is a continuation of copending U.S. patent application Ser. No. 13/226,436 filed Sep. 6, 2011 and issuing as U.S. Pat. No. 9,138,345 on Sep. 22, 2015, which is a continuation of U.S. patent application Ser. No. 12/099,127 filed Apr. 7, 2008 and now issued as U.S. Pat. No. 8,012,115 Apr. 7, 2008, which is a continuation in part of U.S. patent application Ser. No. 10/781,343 filed Feb. 18, 2004 and now issued as U.S. Pat. No. 7,354,416 which claims priority to U.S. Provisional Patent Application No. 60/447,999 filed on Feb. 18, 2003, the entirety of each such application being expressly incorporated herein by reference.
FIELD OF THE INVENTION
• This invention relates generally to medicine and surgery, and more particularly to methods and devices for lowering intraocular pressure and delivering drugs or therapeutic substances to the optic nerve in human or veterinary patients.
BACKGROUND OF THE INVENTION
• In normal adults the ocular globe is approximately spherical, with a diameter averaging 24.5 mm. The cornea is a transparent tissue inserted into the sclera at the limbus, the anterior chamber is behind the cornea. The iris is the anterior extension of the ciliary body, it presents as a flat surface with a centrally situated round aperture, the pupil. The iris lies in contiguity with the anterior surface of the lens, dividing the anterior chamber from the posterior chamber, each of which contains aqueous humor. The lens is a biconvex, avascular, colorless and almost completely transparent structure about 4 mm thick and 9 mm in diameter. The lens is suspended behind the iris by the zonules, which connect it with the ciliary body. Anterior to the lens is the aqueous humor and posterior to the lens is the vitreous. The “vitreous body” which occupies approximately four fifths of the cavity of the eyeball, behind the lens. The vitreous body is formed of gelatinous material, known as the vitreous humor. Typically, the vitreous humor of a normal human eye contains approximately 99% water along with 1% macromolecules including: collagen, hyaluronic acid, soluble glycoproteins, sugars and other low molecular weight metabolites.
• The retina is essentially a layer of nervous tissue formed on the inner posterior surface of the eyeball. The retina is surrounded by a layer of cells known as the choroid layer. The retina may be divided into a) an optic portion which participates in the visual mechanism and b) a non-optic portion which does not participate in the visual mechanism. The optic portion of the retina contains the rods and cones, which are the effectual organs of vision. A number of arteries and veins enter the retina at its center, and splay outwardly to provide blood circulation to the retina. The posterior portion of the vitreous body is in direct contact with the retina. Networks of fibrillar strands extend from the retina and permeate or insert into the vitreous body so as to attach the vitreous body to the retina.
• The optic nerve provides communication between the retina and the brain. The optic nerve is primarily composed of axons from the retinal ganglion cells along with glial support cells and other tissue. The optic nerve begins at the optic nerve head or disc and passes through the sclera in the area of the lamina cribrosa. The optic nerve then passes through the orbit and optic canal to the optic chiasm. Posterior to the lamina cribrosa, the optic nerve is surrounded by a three-layered meningeal sheath similar to the central nervous system which consists of a dura mater (optic nerve sheath), arachnoid mater, and pia mater. The subarachnoid space surrounding the optic nerve is in direct communication with the subarachnoid space of the central nervous system.
• The term “glaucoma” encompasses a group of diseases that cause progressive damage to the optic nerve and resultant optical field defects, vision loss and, in some cases, blindness. Glaucoma is typically, but not always, accompanied by abnormally high intraocular pressure. There are three basic types of glaucoma—primary, secondary and congenital. The primary type of glaucoma is most common. Cases of primary glaucoma are classified as either open angle or closed angle. Secondary glaucoma occurs as a complication of a variety of other conditions, such as injury, inflammation, vascular disease and diabetes. Congenital glaucoma is elevated eye pressure present at birth due to a developmental defect in the eye's drainage mechanism.
• As well as being an important marker of the presence and advancement of glaucoma, the structure of the optic nerve head may play a role in the pathogenesis of glaucoma. Two main theories exist for the mechanism of optic nerve damage in glaucoma. One theory, known as the mechanical IOP related theory, suggests that the pressure head acts directly on the lamina cribosa. The lamina cribosa is not well supported superiorly and inferiorly at the disk and, as a result, initial damage occurs superiorly and inferiorly to produce the characteristic arcuate defects. Variations in the ganglion cell support at the disk may explain the variations between IOP susceptibilities of individuals with similar IOP's. The second theory, known as the vascular mechanism of damage theory, suggests that changes occur within the microcirculation of the disk capillaries and such microvascular changes are responsible for glaucomatous changes.
• Irrespective of the type of glaucoma a patient suffers from, controlling IOP through the use of drugs and/or surgery is a mainstay of treatment. It is generally acknowledged that lowering intraocular pressure in glaucoma patients can prevent or lessen the irreversible glaucoma-associated destruction of optic nerve fibers and the resultant irreversible vision loss.
• Presently the use of topically applied glaucoma medications consisting of mainly beta blockers, prostaglandin analogues, alpha-2 agonists, and carbonic anhydrase inhibitors are short acting, prone to deleterious side effects, prone to compliance issues, and must be used for life. Also, at present, the use of argon laser trabeculoplasty as a means for treating glaucoma is limited in clinical response, lasts only approximately 1-2 years, and is limited by the number of applications per eye. Also, at present, the performance of trabeculectomy procedures with or without antimetabolites allows for the external drainage of aqueous humor from the eye. However, trabeculectomy procedures can be technically difficult, fraught with early hypotony, late failure, and high rate of endophthalmitis leading to permanent loss of the eye.
• Another surgical approach to the treatment of glaucoma involves the implantation of a shunt to drain aqueous humor from the anterior chamber of the eye. Examples of glaucoma shunts of the prior art include those described in the following United States Patents: U.S. Pat. No. 5,626,558 entitled “Adjustable Flow Rate Glaucoma Shunt and Method of Using Same;” No. 6,007,510 entitled “Implantable Devices and Methods for Controlling the Flow of Fluids Within the Body;” U.S. Pat. No. 6,007,511 entitled “Shunt Valve and Therapeutic Delivery System for Treatment of Glaucoma and Methods and Apparatus for its Installation;” U.S. Pat. No. 6,142,969 entitled “Sutureless Implantable Device and Method for Treatment of Glaucoma” and U.S. Pat. No. 6,626,858 entitled “Shunt Device and Method for Treating Glaucoma.” The entire disclosure of each of these United States patents is expressly incorporated herein by reference.
• Thus, there remains a need in the art for the development of new methods and apparatus for lowering IOP and/or for draining fluid from the posterior chamber of the eye for treatment of glaucoma or other disease states.
SUMMARY OF THE INVENTION
• The present invention provides devices and methods for draining fluid from the posterior chamber of the eye into the optic nerve and/or the subarachnoid space. The posterior chamber of the eye is in direct fluidic communication with the anterior chamber of the eye. Thus, the methods and devices of the present invention may be used to treat diseases that are characterized by excess production and/or impaired drainage of aqueous humor (e.g., glaucoma) as well as other vitreoretinal disease states (e.g., for clearance of vitreous hemorrhage).
• In accordance with the invention, there is provided a method for draining fluid from the posterior chamber of the eye by creating a passageway between the posterior chamber of the eye and either i) a location within the optic nerve or ii) a location within the subarachnoid space. Contiguous communication between the anterior chamber, posterior chamber and subarachnoid space may be achieved by additionally performing either a) complete or partial surgical removal of the vitreous humor (e.g., a vitrectomy) or b) liquefaction of all or a portion of the vitreous humor (e.g., pharmacologic vitreolysis by intravitreal administration of urea; a urea derivative; a compound having a urea group; hyaluronidase or any other enzyme or agent that causes vitreal liquefaction). The passageway by which the fluid drains from the posterior chamber into the subarachnoid space may simply comprise a hole or puncture made in the lamina cribosa or other suitable location. Alternatively, the passageway may comprise a tubular shunt device that is implanted so as to drain fluid from the posterior chamber into the optic nerve or into the subarachnoid space. Fluid which first drains into the optic nerve will diffuse into the subarachnoid space where it becomes mixed with CSF. Fluid which drains directly into the subarachnoid space will mix with CSF within the subarachnoid space. In applications of the method wherein a shunt device is employed, the shunt device may alternatively extend between the anterior chamber and subarachnoid space such that it bypasses the posterior chamber or vitreous cavity (i.e., the shunt device may extend through a subconjunctival or subscleral tunnel), furthermore the shunting device may also incorporate a system of communication between the anterior chamber and subarachnoid space that bypasses the vitreous humor by passing directly through it (e.g., a tube that extends through the vitreous body).
• Further in accordance with the invention, there is provided a shunt device for draining fluid from the posterior chamber of the eye into the optic nerve or subarachnoid space. Such shunt device comprises a tube having a proximal end, a distal end and a lumen extending longitudinally therethrough, a substantially tissue penetrating tip on the distal end of the tube, a plurality of openings formed at or near the distal end of the tube to allow fluid to drain out of the lumen of the tube and at least one tissue engaging member configured to allow the shunt device to be advanced, tip member first, into tissue but to engage said tissue in such a manner as to subsequently deter retraction of the shunt out of the tissue. Optionally, the shunt device may additionally include a pressure control and/or one-way valve to control the magnitude of the pressure head required to cause fluid to drain from the eye through the shunt device and/or to prevent unwanted backflow of fluid into the eye through the shunt device. Also, optionally, the shunt device may comprise a shielding member, such as a semi-permeable membrane, to prevent or deter clogging of the shunt device by foreign matter and or tissue in-growth.
• Still further in accordance with the present invention, there is provided a system that comprises a shunt device of the above-described character in combination with an introducer that is insertable into the eye and useable to implant the shunt device at its desired implantation position within or adjacent to the optic nerve. Such introducer may comprise a tubular cannula through which the shunt device may be passed and/or an elongate member which may be used to drive or advance the shunt device to its intended location. In some embodiments, the elongate member may be used without the tubular cannula. In other applications, the shunt device will be initially loaded into the lumen of the tubular cannula and the elongate member (e.g., a solid or tubular pusher rod) may be used to push the shunt device out of the distal end of the cannula and to its intended site of implantation.
• Still further in accordance with the invention, there are provided methods and devices for delivering therapeutic substances (e.g., drugs, biologics, etc.) into the eye. An implant which contains the substance is implanted in the optic nerve and a therapeutic amount of the substance subsequently elutes from the implant.
• Further aspects and elements of the present invention will become apparent to those of skill in the relevant art upon reading and considering the following detailed description and the accompanying drawings to which it refers.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a longitudinal sectional view of one embodiment of an ocular shunt implantation system of the present invention.
• FIG. 1A is a perspective view of the cannula component of the ocular shunt implantation assembly ofFIG. 1.
• FIG. 1B is a perspective view of the shunt component of the ocular shunt implantation assembly ofFIG. 1.
• FIG. 1B is a partial cut-away/sectional view of a shunt device of the present invention incorporating an optional one-way valve to deter backflow and optional shielding member (e.g., a semi-permeable membrane) to deter clogging of the shunt due to debris or cellular tissue ingrowth.
• FIG. 1C a perspective view of the pusher component of the shunt implantation assembly ofFIG. 1.
• FIG. 2A is a cross-sectional view of a human eye into which an ocular shunt implantation system of the present invention has been inserted and positioned for advancement/implantation of the shunt.
• FIG. 2B is a cross-sectional view of a human eye into which an ocular shunt of the present invention has been implanted to shunt fluid from the posterior chamber of the eye into the body of the optic nerve.
• FIG. 20 is a cross-sectional view of a human eye into which an ocular shunt of the present invention has been implanted to shunt fluid from the posterior chamber of the eye into the area outside of the optic nerve.
DETAILED DESCRIPTION
• The following detailed description and the accompanying drawings are provided for the purpose of describing certain non-limiting examples or embodiments of the invention only. This detailed description is not intended to describe all possible examples and embodiments of the invention and, thus, shall not limit the scope of the claimed invention in any way.
• FIGS. 1-1C show one embodiment of asystem10 for implantation of ashunt device12 in accordance with the present invention. Thissystem10 generally comprises theshunt device12, acannula14, and apusher16. As shown inFIG. 1, theshunt device12 is initially positioned within thelumen18 of thecannula14 and thepusher16 is positioned in thelumen18 of thecannula14 behind theshunt device12 such that thepusher16 may be used to push theshunt device12 out of the distal end DE of the of thecannula14. One way of performing this shunt-expulsion procedure is shown inFIG. 2A and is explained in detail hereblow.
• The particular embodiment of theshunt12 shown inFIG. 1B comprises atube22 having alumen24 extending longitudinally therethrough. Atip member26 is positioned on the distal end of thetube22. Thetip member26 of this embodiment is generally conical in shape, but it will be understood that the tip member may be beveled, tapered, trocar tipped or of any other shape that will allow it to advance through tissue as explained herebelow.Apertures28 are formed in the side wall of thetip member26 to allow fluid to drain out of thelumen24 of thetube22. Optionaltissue engaging members30, such as barbs, hooks, undercuts, adhesive regions, tissue in-growth receiving areas, etc., may be formed on theshunt12 to deter unwanted movement or retraction of theshunt12 after it has been advanced to its intended implantation position. Also, optionally, a flange (e.g., any laterally extending member or area or increased diameter) may be formed on the proximal end of thetube22 to engage the lamina cribosa or other tissue in a manner that deters advancement of the tube beyond its intended position. Theshunt device12 may have a diameter or cross-dimension at its widest point of about 1 micron to about 2000 and preferably of about 50 microns to about 400 microns.
• FIG. 1B shows an alternative embodiment of the shunt device12awhich has the same construction as theshunt device12 shown inFIG. 1B but additionally includes an optional oneway valve23 and anoptional shielding member29 which covers theapertures28 to prevent or deter the entry of foreign matter or issue ingrowth throughapertures28. The oneway valve23 serves to allow fluid flow in the distal direction (Arrow DD) while preventing or substantially deterring backflow in the proximal direction (Arrow PD). The one way valve may be a duckbill type valve comprising a plurality offlexible leaflets25, as shown, or may comprise any other suitable type of check valve or one-way valve, such as a ball type check valve, a flapper, or any of the valves typically used as hemostatic valves on small medical catheters of a size similar to this shunt device12a.Also, this one-way valve23 may be constructed to open only when the pressure of fluid within thelumen24 proximal to thevalve23 exceeds a predetermined maximum, thereby providing for control of the intraocular pressure and preventing the drainage of too much fluid from the eye as may result in hypotony or other untoward sequale.
• Thecannula14 may comprise a tube having a generallycylindrical wall14, alumen18 extending longitudinally therethrough between an open proximal end PE and an open distal end DE.
• Thepusher16 may comprise a solid or tubularelongate member34 having a proximal end PE and a distal end DE. Optionally, ahandle38 may be positioned on the proximal end of theelongate member34. Also, optionally, theelongate member34 may have an outer diameter that is sized to be received within thelumen24 of theshunt device12 and the distal end DE of theelongate member34 may be tapered, as shown inFIG. 1C, to seat within the taperedtip member26 of theshunt device12.
• Some or all of the components of thesystem10 may be formed of silicon, polyethylene, polypropylene, polycarbonate, stainless steel or other biologically compatible materials. In the particular embodiment shown in the figures, theshunt device12 or12amay be substantially formed of silicon material. Theshunt device12 or12amay also involve an active pumping system or may incorporate a wick like system to move fluid in the required direction.
• FIG. 2A-2C show the system ofFIGS. 1-1C in its currently intended mode of operation. Prior to implantation of theshunt device12 or12a,a vitrectomy device may be inserted into the posterior chamber PC and a vitrectomy performed to remove at least a portion of the vitreous body from the posterior chamber PC. Alternatively, all or a portion of the vitreous body may be liquefied. Such vitreal liquefaction may be accomplished by intravitreal administration (e.g., intravitreal injection) of one or more agents that cause liquefaction of the vitreous humor. Examples of such agents include but are not limited to; urea, urea derivatives, compounds having urea groups, hyaluronidase and other enzymes or other substances that cause vitreal liquefaction. Descriptions of these and other substances that cause vitreal liquefaction, as well as dosage information and associated methods for administration, are found in U.S. Pat. Nos. 5,292,509 (Hagman): 6,551,590 (Karageozian et al.); 6,610,292 (Karageozian et al.) and 6,462,071 (Karageozian at al., the entireties of which are expressly incorporated herein by reference.
• As shown inFIG. 2A, a small opening such as a needle puncture is made in the pars plana PP and thesystem10 of the present invention is inserted through that opening and through a region of the poster chamber PC from which the vitreous body has been removed (e.g., by vitrectomy) or in which the vitreous body has been liquefied (e.g., by intravitreal injection of a vitreous liquefying agent as described above). Thesystem10 is advanced to position where the distal end DE of thecannula14 is positioned immediately anterior to the lamina cribosa. Thepusher16 is then advanced in the distal direction (Arrow DD) while thecannula14 is held stationary, thereby pushing theshunt device12 or12aout of the distal end DE of thecannula14 and causing thedistal tip member26 of theshunt device12 or12ato penetrate through the lamina cribosa and optic nerve ON tissue. Thepusher16 is advanced until resistance is felt due to the impingement of theflange member32 of theshunt device12 or12awith the optic nerve head. At this point, theshunt member12 or12ahas been advanced to its intended implantation site and thepusher16 andcannula14 may be removed from the eye, leaving theshunt device12 or12ain place. Depending on the angle at which theshunt device12 or12aa is advanced, itsoutflow apertures28 may be positioned at a subdural location within the body of the optic nerve ON (as shown inFIG. 23) or within the subarachnoid space adjacent to the optic nerve ON (as shown inFIG. 2C). In instances where theoutflow apertures28 are positioned within the body of the optic nerve ON (as shown inFIG. 2B), fluid that drains out of theoutflow apertures28 will subsequently diffuse and/or be transported though the optic nerve and into the subarachnoid space where it will mix with cerebrospinal fluid. In instances where the outflow apertures are located within the subarachnoid space, fluid that flows out of theoutflow apertures28 will mix with cerebrospinal fluid that resides within the subarachnoid space. In either case, the typical backpressure of fluid adjacent to theoutflow apertures28 will be low enough to facilitate drainage of excess fluid from the eye and in the distal direction (arrow DD) through theshunt device12 or12a.
Optic Nerve Drug Delivery System
• Theshunt device12,12amay, in some embodiments, additionally function as a substance delivery device for sustained delivery of a therapeutic substance directly to the optic nerve.
• Macular edema is the accumulation of fluid and small molecules in the retinal tissues. As this fluid accumulates in the outer plexiform and the inner nuclear layers of the retina, it results in macular thickening which may be accompanied by deposits of lipoprotein. Chronic macular edema can result in loss of sight is it becomes severe or affects the center of the macula.
• Various agents have been proposed for treatment of macular edema. Several agents have been developed that specifically target a particular inflammatory cytokine. Existing monoclonal antibodies have activity against TNF-α, IL-2 and VEGF. Of these, the anti-VEGF agents have been the most extensively studied. Several animal and clinical studies have shown that anti-VEGF agents can decrease vascular permeability and inhibit angiogenesis. Several studies are under way to determine the clinical utility of intravitreal injections of these agents in the treatment of diabetic macular edema. Early results from clinical trials with ranibizumab (Lucentis, Genentech), bevacizumab (Avastin, Genentech) and pegaptanib sodium (Macugen, (OSI) Eyetech) appear favorable.
• Corticosteroids act on a broad range of processes that are known to contribute to the pathophysiology of macular edema. For example, corticosteroids are known to inhibit prostaglandin and leukotriene synthesis and to interfere with the actions and/or production of ICAM-1, IL-6, VEGF-α and stromal-derived factor 1 (SDF 1). Corticosteroids may also increase the expression of genes that code for “tight junction proteins” which may also be helpful in treating macular edema. Repeated intravitreal injection of 25 mg of the corticosteroid triamcinolone acetonide has been reported to increase in visual acuity in patients with exudative age-related macular degeneration, with the peak in visual acuity and intraocular pressure elevation occurring about 2 to 5 months after each injection. Jonas, J., et al., Intravitreal Reinjection of Triamcinolone for Exudative Age-Related Macular Degeneration; Archives of Ophthalmology, Vol. 122, No. 22, pp 218-222 (2004). Additionally, the I-vation TA Sustained Drug Delivery System (Surmodics, Eden Prarie, Minn.) is a helical metal implant coated with a commercially available drug delivery polymer that contains triamcinolone acetonide the (Bravo™ Drug Delivery Polymer, Surmodics, Eden Prarie, Minn.). Also, polysaccharide and other drug delivery coatings that may be useable for delivery of corticosteroids such as triamcinolone acetonide are described in United States Patent Application Publication No. 2005/0255142, which is expressly incorporated herein by reference.
• Theshunt12,12aof the present invention may be coated with a drug delivery coating, such as those mentioned above, containing a suitable amount of a therapeutic substance (e.g., from about 1 to about 100 mg triamcinolone acetonide) which is effective to treat macular degeneration or other disorders and inflammation of the optic nerve, retina or macula.
• The hydrophilic or hydrophobic drug substances (e.g., agents for wet macular degeneration, agents for prevention of macular edema, anti-proliferative substances, agents for prevention of dry macular degeneration) may be combined with a coating that is applied to the surface of theshunt12,12aor could be applied as a gel like material to theshunt device12,12awhich would contain polymeric materials that will help the time release of the drugs over an extended period of time. In some embodiments intended for drug deliver only, thedevice12,12amay be devoid of a lumen and will not necessarily perform a shunting function.
• Thedevice12,12acontaining the therapeutic substance may be implanted in the optic nerve as described above without the need to perform a vitrectomy. Implantation may be performed by delivering thedevice12,12athrough a small caliber (27 Gauge, 25 Gauge, or 23 Gauge) needle inserted through the intact vitreous. This variant of the procedure will be recommended when highly diffusible drugs are employed and the drug needs to get to the delivery site very fast. Also another variant that could be performed if vitrectomy is not realized is the administration of a substance that can produce vitreous liquefaction or vitreous detachment previous the insertion of thedevice12,12a(24 to 48 hrs). Theoretically if there is not vitreous attached to the optic nerve possibilities of scarring tissue could be prevented mainly in those cases in which implants will not release anti-proliferative substances.
• When used for delivery of a therapeutic substance (e.g., from about 1 to about 100 mg triamcinolone acetonide) thedevice12,12amay be implanted either at the periphery of the optic nerve or in the center of the optic nerve. Insertion at the periphery will avoid damage of nerve fiber layer but could reach at the same time the lamina cribrosa. Insertion in the center of the optic nerve will implie penetration of the lamina cribrosa which will help to anchors thedevice12,12a.Based on topographic features, one suitable area for insertion, either in the periphery of the optic nerve or in the center of the optic nerve, is the nasal area. Insertion of thedevice12,12aat the nasal area will prevent damage of ganglion cell axons belonging to the macula area.
• When used for delivery of a therapeutic substance, the length of thedevice12,12amay vary depending on the elution and diffusion characteristics of the drug. Low diffusion drugs that need to reach the optic nerve may best be delivered using a long (e.g., more than 3 mm in length)device12,12a.High diffusion drugs that are intended to reach macula and other parts of the retina may be delivered by ashorter device12,12a(e.g., one that is less that 3 mm in length). A luminal or canulated embodiment of thedevice12,12amay allow drug delivery as well as drainage of aqueous humor and will typically be 3 mm or more in length.
• The shape of thedevice12,12amay vary and it may have be solid or canulated (i.e., having a lumen). Either solid or canulated will have the ability to harbor one or more compartments for drugs, gels, polymers, and or substances that will be released. Materials that will be used as a therapeutic substances may be also incorporated on the walls of thedevice12,12aas a coating or paint which by the time will be released slowly. Canulated embodiments of thedevice12,12amay have the ability to work also as a draining system for aqueous humor; aqueous humor may be drained through the optic nerve. This drainage may be achieved either through the sub-arachnoidal space or the intra-orbital space. Intraocular pressure is higher than the pressure in the SNC that gradient will allow fluid (aqueous humor) to drain in the sub-arachnoidal space or at the optic nerve. Thecanulated device12,12aalso can drain aqueous humor to the orbit. A small caliber device will prevent high rate of drainage preventing hypotony. Drugs belonging to thedevice12,12awill prevent formation and deposition of tissue inside the lumen of the canula. Thedevice12,12amay have a head and tail. The head will be used to manipulate thedevice12,12aand will remain visible on the surface of the optic nerve after insertion, the tail will be buried in the stroma of the nerve, will penetrate lamina cribrosa and can have different shapes to be anchored in either tissue or lamina cribrosa: arrow like, harpoon like, etc,
• Biodegradable and non biodegradable embodiments of thesubstance delivering device12,12amay be used. Biodegradable embodiments will release therapeutic substances as long as they remain in the optic nerve and will not require manual removal. Non-biodegradable embodiments may be formed of bocompatible metallic or non metallic materials such as polymers, plastics or silicone and may or may not be removed after all of the therapeutic substance has eluted from the device.
• The foregoing description is directed to certain embodiments and examples of the invention only and does not necessarily include or expressly mention each and every possible embodiment or example of the invention that is within the scope of the following claims.

Claims (15)

What is claimed is:

1. A method for delivering a therapeutic substance into the eye of a human or animal subject, said method comprising the steps of:

A) providing an implant that contains a quantity of the substance; and

B) inserting the implant into the optic nerve such that a therapeutic amount of the substance will elute from the implant.

2. A method according toclaim 1 wherein the implant has a lumen and additionally functions as a tubular shunt such that fluid from the interior of the eye will enter one end of the shunt and said fluid will exit the other end of the shunt either i) at a location within the optic nerve or ii) at a location within the subarachnoid space.

3. A method according toclaim 2 wherein the implant comprises a tube having a proximal end, a distal end and least one tissue engaging member formed on the implant to deter unwanted movement of the implant after it has been implanted.

4. A method according toclaim 3 wherein the at least one tissue engaging member comprises a barb or barb like structure that allows the shunt to be advanced through tissue in a distal direction but engages the tissue in a manner that deters subsequent retraction of the shunt in a proximal direction.

5. A method according toclaim 2 wherein the implant comprises a tube having a proximal end, a distal end and a flange member formed on the proximal end thereof.

6. A method according toclaim 2 wherein the implant comprises a tube having a valve associated therewith, said valve being operative to perform at least one valving function selected from the group consisting of a) allowing fluid to flow out of the eye but deterring fluid form backflowing into the eye and b) allowing fluid to flow out of the eye only when the fluid pressure exceeds a predetermined maximum pressure.

7. A method according toclaim 2 wherein the implant comprises a tube having a proximal end, a distal end and at least one shielding member associated therewith to deter foreign matter or cells from clogging the tube.

8. A method according toclaim 7 wherein the shielding member comprises a semi-permeable membrane constructed and positioned such that fluid flowing out of the distal end of the tube will diffuse outwardly through the membrane but foreign matter and cells will not diffuse inwardly through the membrane and into the distal end of the tube.

9. A method according toclaim 1 wherein the plant is devoid of a lumen.

10. A method according toclaim 1 wherein the therapeutic substance comprises a corticosteroid.

11. A method according toclaim 1 wherein the implant contains from about 1 to about 100 mg triamcinolone acetonide.

2. A method according toclaim 1 wherein the method is carried out to treat macular degeneration.

13. A method according toclaim 1 wherein step B is performed without a vitrectomy.

14. A method according toclaim 13 wherein step B is performed by delivering the implant through a needle that is inserted into the optic nerve through the in tact vitreous.

15. An apparatus for delivering a substance to the eye of a human or animal subject, said apparatus comprising:

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