US20080154204A1 - Method and device for subretinal drug delivery - Google Patents

Abstract

Devices and methods for the treatment of the eye are disclosed. Preferred devices of the invention include a piercing member that is inserted into the eye to create a pathway for a cannula. The cannula is slidably mounted to the piercing member and is adapted to reach a treatment site within the eye at which material is injected into and/or withdrawn from the eye. The outer diameter of the piercing member is small enough to allow for self-sealing of the insertion site of the device upon the device's withdrawal therefrom. Also disclosed are methods for the utilizing the devices to treat the eye.

Description

• This application is a divisional application of U.S. patent application Ser. No. 09/888,079, filed Jun. 22, 2001, which is incorporated by reference herein in its entirety.
BACKGROUND OF THE INVENTION
• 1. Field of the Invention.
• The present invention relates generally to the delivery of medicaments, and more particularly, to devices and methods for delivering therapeutic agents directly to intraocular tissue and for withdrawing materials from within areas of the eye, such as the vitreous humor. These devices and methods are advantageous for many reasons, among which is that insertion of such a device into the eye necessitates forming an insertion site that is small enough to require no sutures to close, i.e., that is self-sealing, following post-treatment removal of the device.
• 2. Background
• The delivery of drugs to the eye, especially the retina, presents many challenges, most of which are owed to the geometry, delicacy and/or behavior of the eye and its components.
• For example, it is known in the art that ocular absorption of systemically administered pharmacological agents and medicaments is limited by the blood ocular barrier, i.e., tight junctions of the retinal pigment epithelium and vascular endothelial cells. And although high systemic doses of such medicaments and agents are capable of penetrating this barrier in relatively small amounts, a realistic risk of systemic toxicity accompanies such a course of treatment.
• Topical delivery of pharmacological agents and medicaments, although involving fewer risks, has proven to be an equally ineffective treatment method. Not only do the complex hydrophobic/hydrophilic properties of the cornea and sclera hamper absorption of topically delivered agents, but data also indicates that it is not unusual for up to 85% of topically-applied agents to be removed by the eye's blink mechanism/reflex.
• Intravitreal injection of a drug is an effective means of delivering the drug to the posterior segment of the eye in high concentrations, but it necessarily requires follow-up injections in order to maintain an adequate therapeutic concentration. This, in turn, presents problems because each additional intraocular injection carries with it a realistic risk of infection, hemorrhage and/or retinal detachment.
• Moreover, even if intravitreal injection techniques were not otherwise problematic, such techniques have also proven inadequate for performing cell transplantation and gene therapy, which require, respectively, subretinal placement of cells and subretinal delivery of gene vectors.
• Several specific prior art techniques for subretinal delivery of agents are known, e.g., those described in U.S. Pat. Nos. 5,273,530 and 5,409,457. Another such approach is discussed inInvestigative Ophthalmology and Visual Science30:1684 (1989), which details a microspatula device for administering cells to the eye through a trans-scleral or trans-corneal incision. Yet another instrument employed by those in the art is a glass pipette, which is used to replace cells in the retina by being introduced the eye anteriorly through an incision via the scleral route (Investigative Ophthalmology and Visual Science28:1131(1987)).
• Still other systems for subretinal drug injection, and for gene delivery are described inHuman Gene Therapy11:449 (2000) andInvestigative Ophthalmology and Visual Science35:2535 (1994). And yet another instrument known in the art to serve this purpose is a glass micro cannula.
• A common feature of these techniques/instruments is that they necessarily require the creation of a surgical incision at the outset of a procedure, and/or the use of sutures following completion of the procedure. This, in turn, increases the duration, cost, and realistic risks of corneal ulceration, cataract formation, intraocular infection, and/or vitreous loss that accompany these procedures.
SUMMARY OF THE INVENTION
• The present invention provides novel devices and methods for the delivery of agents to the eye. More particularly, the present invention relates to methods and devices for introducing materials (e.g., therapeutic agents/medicaments such as genes, proteins, cells, small molecule pharmaceuticals such as steroids and the like, and sterile solutions) into the subretinal space of the eye. The present device may also be used to effectuate the removal of intravitreal fluid from the eye.
• The devices and methods of the invention also are employed to provide a localized deposit of a pharmaceutical agent within the eye, particularly subretinally. For instance a steroidal composition can be administered subretinally, wherein the steroid resides as a solid (e.g. from an initial suspension administration) and diffuses or otherwise is absorbed by the patient over time.
• In an exemplary aspect of the present invention, the device includes a piercing member that has adequate sharpness to penetrate the sclera of a patient's eye. The piercing member may be connected to a handle or gripping element, which facilitates grasping of the device prior to and during use thereof.
• The device further includes a cannula, which, in one aspect of the invention, is slidably disposed within a passageway defined within the device, and which, in another aspect of the invention, is connected to, and positioned within a rigid member disposed within this passageway. In the former aspect of the invention, the cannula is directly connected to a distal end of a quantity of tubing, while in the latter aspect, the rigid member is connected to the distal end of the tubing.
• In both aspects of the invention, the proximal end of the quantity of tubing is attached to an externally located injection/removal device. This device is adapted to supply and/or withdraw fluid through the cannula, a distal end of which protrudes from the piercing element and into proximity of a treatment/target site within the eye.
• In accordance with an exemplary method of the present invention, the piercing member is advanced into and through the sclera transconjunctively. The device is then advanced towards a target/treatment site (e.g. the retina) until the distal end of the cannula pierces the site.
• Thereafter, the external device connected to the proximal end of the tubing is activated to either inject material (e.g., an agent/medicament) into the target site or to remove material therefrom. Upon completion of the injection and/or removal of material, the device is withdrawn from the target/treatment site, and then from the patient's eye by reversing the steps of its insertion.
• During withdrawal of the device, the piercing member is removed from the eye. Preferably, the piercing member is small enough in size that the insertion site fashioned by the piercing member is self-sealing (i.e., requiring no sutures to close) following post-treatment removal of the piercing member therethrough.
• In a preferred aspect of the invention, the device delivers an agent directly into the subretinal space of the patient's eye. In such an embodiment, the device is directed towards the retina such that the distal end of the cannula is advanced into, but not beyond, the subretinal space. Accuracy of placement of the device can be ensured/verified by techniques known in the art, e.g., by injecting agent through the cannula until the formation of a retinal detachment is observed. Injection of agent into this dome-shaped retinal detachment also enables the delivered agent to enjoy a prolonged residence time within the subretinal space. This, in turn, allows the agent to provide a greater therapeutic effect, without adversely affecting either intraocular pressure or neighboring retinal cells.
• The present subretinal injection device is a self-contained system. Specifically, no separate surgical cannula systems are required during use of a device in accordance with the present invention. This allows for ease of handling of the device, which, coupled with the fact that the insertion site is self-sealing upon removal of the piercing member of the device, allows devices in accordance with the present invention to be uniquely suited for office-based procedures, which are comparatively less expensive, shorter in duration, and carry with them fewer risks than treatments necessitated by prior art systems and devices.
• Moreover, because the insertion site is self-sealing upon removal of the piercing member, use of this device is a preferred treatment method as compared to currently known intraretinal transplantation procedures, which require the creation of a surgical incision prior to the treatment, and then the suturing of the incision following completion of the treatment. Specifically, in intraretinal transplantation techniques, a pars plana incision is required to insert a glass micropipette or similar instrument through the globe into the subretinal space. Upon completion of such techniques, scleral and conjunctival sutures, neither of which is required in accordance with the present invention, must be used to close the incision.
• Moreover, once an eye has been entered, an operator can utilize the device of the present invention to treat multiple target sites simply by varying the angle of the entry of the device, thus avoiding the need for creation of multiple entry sites. Even in the event, however, that multiple entry sites were required, each entry site would be self-sealing as described above.
• Further, because agents are delivered directly to the subretinal space by the device of the present invention, it follows that higher concentrations of the agent are delivered to the choroidal vessels and retinal pigment epithelial cells as compared to intravitreal injection and intraocular implants that introduce drugs into the vitreous humor. Injection into the subretinal space may also provide for a more sustained delivery of the agent/medicament to the retinal cells, thus avoiding a more rapid clearance rate from the vitreous. In addition, this type of local delivery may reduce the risk of elevated intraocular pressure associated with prior devices, which provide sustained drug delivery to the vitreous.
• Other aspects of the invention are disclosed infra.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a side view of an exemplary embodiment of a device in accordance with the present invention;
• FIG. 2 is a side view of an alternate embodiment of the device ofFIG. 1 in which the cannula is unsupported by a rigid member;
• FIG. 3A is a schematic view of the device ofFIG. 2 following puncture of the sclera of the eye by the piercing member of the device;
• FIG. 3B is a schematic view of the device of FIG.2/3A following piercing of the retina by the cannula of the device.
• FIG. 4A is a schematic view of the device of FIG.2/3A depicting use of the device to treat multiple treatment sites by varying the angle of the portion of the device that lies outside of the eye.
• FIG. 4B is a schematic view of the device of FIG.2/4A following piercing of the retina by the cannula of the device.
DETAILED DESCRIPTION OF THE INVENTION
• As stated above, new devices and methods are provided for delivery of agents to the eye.
• Referring now to the various figures of the drawings, wherein like reference characters refer to like parts, there are depicted inFIGS. 1-4 various views ofsurgical devices10,10′ in accordance with the present invention.
• As shown inFIG. 1, a first exemplary embodiment of thedevice10 of the present invention includes a piercingmember12, which has aproximal end14 and adistal end16, with a lumen defined therebetween. Thedistal end16 of the piercingmember12 is pointed (e.g., beveled) to allow for the piercing member to pierce and penetrate a target/treatment site as will be described below.
• In an exemplary embodiment of the present invention, the piercingmember12 has an outer diameter of about 25 gage (0.5 millimeter) or less and a length, P, in the range of about 6 millimeters to 25 millimeters, preferably in the range of about 15 millimeters to 20 millimeters.
• The piercing member lumen should have a substantially constant diameter, which generally is in the range of about 0.152 millimeter to 0.305 millimeter.
• The piercingmember12 may be made of a variety of biocompatible materials, including, but not limited to, polymers, metals and composites. Generally however, the piercingmember12 is made of a stainless steel.
• Theproximal end14 of the piercingmember12 is connected, via a technique known in art (e.g., press fitting, and/or via an adhesive or an epoxy) to afirst connection element18.
• Thefirst connection element18 has aproximal end20 and adistal end22 and a lumen defined therebetween. The first connection element lumen should have a diameter that is substantially identical to that of the piercing member lumen such that, upon connection of theproximal end16 of the piercingmember12 to thedistal end22 of thefirst connection element18, these lumen are substantially longitudinally aligned to create a fluid tight passageway.
• Thefirst connection element18 may be made of a variety of biocompatible materials, including, but not limited to, polymers, metals and composites. Generally, theelement18 is made of titanium, stainless steel, nitinol or, preferably, delrin.
• Optionally, but preferably, aseal24 is connected to thefirst connection element18, and substantially surrounds at least a portion of the first connection member lumen in order to further enhance the integrity of the fluid tight passageway. Theseal24 may be slidably connected to thefirst connection element18 and/or may be connected via techniques known in the art, e.g., via an adhesive or an epoxy. Theseal24 can be made of a variety of materials, but is generally made of silicone.
• The fluid tight passageway is sized to accommodate arigid member26, which adds physical stability to thedevice10. Therigid member26 has aproximal end28 and adistal end30, and a lumen defined therebetween. Thedistal end30 of therigid member26 extends distal to thedistal end16 of the piercing member, while theproximal end28 of the rigid member extends proximate to theseal24.
• Acannula44 is disposed within therigid member26. Preferably, thecannula44 is physically connected to the rigid member26 (e.g., via adhesive, sealant, or epoxy or via other techniques known in the art) such that any distal-to-proximal or proximal-to-distal movement of the rigid member effects corresponding movement of the cannula, and such that any distal-to-proximal movement of the cannula effects corresponding movement of the rigid member.
• Thecannula44 has a length, C, such that, when disposed within therigid member26, adistal portion46 of the cannula is distal to thedistal end30 of the rigid member, while aproximal end48 of the cannula extends proximal to thedistal end34 of thetubing32.
• It is understood, however, that the length, C, of thecannula44 may be shorter or longer than depicted inFIG. 1. For example, thedistal portion46 of the cannula may extend further beyond thedistal end30 of therigid member26, and/or theproximal end48 of the cannula may extend further proximately within the tubing or beyond theproximal end42 of the tubing.
• The length, C, of thecannula44 is generally in the range of about 35 millimeters to 75 millimeters with itsdistal portion46 generally having a length in the range of about 1 millimeter to 3 millimeters.
• Generally, the outer diameter of the rigid member is about 28 gage (0.32 mm) or less, while the outer diameter of thecannula44 in the range of about 38 gage (0.128 millimeter) to 45 gage (0.0457) millimeter.
• Both therigid member26 and thecannula44 can be made of a variety of biocompatible materials, including, but not limited to, polymers, metals and composites. In an exemplary embodiment of the present invention, thecannula20 is made of polyimide tubing, while therigid member26 is made of either polyimide, titanium, nitinol, or, preferably, stainless steel.
• As shown inFIG. 1, therigid member26 extends into a quantity oftubing32 such that theproximal end28 of the rigid member is proximal to thedistal end34 of the tubing. In an exemplary embodiment of the present invention, thetubing32 and therigid member26 also are physically connected to each other (e.g., via an adhesive, a sealant, an epoxy or via other techniques known in the art) such that any distal-to-proximal or proximal-to-distal movement of the tubing effects corresponding movement of the rigid member (and, therefore, of the cannula as well), and such that any distal-to-proximal movement of either the rigid member or the cannula effects corresponding movement of the tubing.
• Preferably, asecond connection element36 surrounds adistal portion38 of thetubing32 and aproximal portion40 of therigid member26 in order to maintain the connection between the tubing and rigid member. The second connection element is connected to thetubing32 and rigid member by a suitable technique known in the art, e.g., press fitting and/or via use of an adhesive or an epoxy.
• Thesecond connection element36 may be made of a variety of biocompatible materials, including, but not limited to, polymers, metals and composites. Generally, thesecond connection element36 is made of titanium, polyimide, nitinol, stainless steel or, preferably, delrin.
• Thetubing32 includes aproximal end42, which is in communication with an external supply or withdrawal device (not shown) either directly or via a connection element (e.g., a luer fitting). This connection allows for material (e.g., fluid, air, etc.) to be supplied into, or withdrawn from the tubing, each as will be discussed below.
• Exemplary materials of which the tubing may be formed include, but are not limited to, a polymer, with preferred materials being silicon and polyimide.
• Referring now toFIG. 2, it depicts an alternate embodiment of thedevice10 ofFIG. 1. Thedevice10′ is similar in both structure and operation to thedevice10 ofFIG. 1, but includes ahandle50 and does not utilize arigid member26.
• Thedevice10′ ofFIG. 2 includes a piercingmember12′ substantially as described above except that the length of the piercing member is preferably in the range of about 22 millimeters to 30 millimeters.
• Theproximal end14′ of the piercingmember12′ is connected to thedistal end52 of ahandle50, which has aproximal end54 that is connected to a quantity oftubing32′. By virtue of its connection to both the piercingmember12′ and thetubing32′, thehandle50 is not only effective to facilitate initial and continued grasping of thedevice10′, but also to stabilize and provide support to thedevice10′.
• Each of thehandle50, the piercingmember12′ and thetubing32′ has a lumen defined therebetween, thus defining a pathway between thedistal end16′ of the piercing member and theproximal end42′ of the tubing.
• A cannula is disposed within, and, preferably, connected to thelumen60 defined within thetubing32′. Thetubing32′ andcannula44′ may be connected as is generally known in the art, e.g., via an adhesive, a sealant or an epoxy. By virtue of this connection, distal-to-proximal and proximal-to-distal movement of thetubing32′ will result in corresponding movement of thecannula44′, and vice versa.
• Thecannula44′ generally has identical length and outer diameter parameters to thecannula44 ofFIG. 1, and generally is made of the same material as well.
• Thehandle50 also includes anactuating element56 that sits within a slot (not shown) or other opening. Theactuating element56 is in communication with ahousing58, which is in communication with thedistal end34′ of thetubing32′ as shown inFIG. 2. By virtue of this arrangement, distal-to-proximal or proximal-to-distal movement of theactuating element56 within the slot causes substantially corresponding movement of the housing, which, in turn, causes substantially corresponding movement of the tubing and, therefore, of thecannula44′ as well.
• Exemplary materials from which thehandle50 andhousing58 may be made include, but are not limited to, biocompatible materials such as polymers (e.g., acetal, polyphenylene sulfide, polypropylene, ABS plastic), metals (e.g., stainless steel), and composites. Preferably, thehandle50 is made of acetal. Thehousing58 may also be made of teflon or nylon. In an exemplary embodiment of the present invention, thehandle50 and thehousing58 are made of the same material.
• The devices ofFIGS. 1 and 2 are used to treat one or more target/treatment sites, each of which is generally located within an eye. Although the description ofFIGS. 3A-B and4A-B below refer to use of the device ofFIG. 2, these descriptions also are applicable to use of the device ofFIG. 1. Also, all common elements of thedevices10,10′ ofFIGS. 1 and 2 will be referred to in these descriptions by theirFIG. 2 reference numbers.
• Referring now toFIG. 3A, in preparation for its use, thedevice10′ gains access to thevitreous humor102 of ahuman eye100. This occurs by placing enough pressure onto thedevice10′ such that the sharpdistal end18′ of the piercingmember12′ penetrates thesclera104 of theeye100, thus creating a continuous passageway (not shown) between the device and thevitreous humor102 of theeye100.
• The piercingmember12′ has a length, P (seeFIG. 1) such that once itsproximal end16′ is in contact with a portion of the outer periphery of thesclera104, it is ensured that thedistal end18 of the piercing instrument is within thevitreous humor102 of theeye100. Once inserted as such, the piercingmember12′ can be angled by gently tilting any portion of thedevice10′ that lies outside of theeye100. This allows thedevice10′ to treat multiple target sites within theeye38 without necessitating multiple, separate insertions of the device into the eye.
• It is understood that although the process of inserting the piercingmember12′ into thevitreous humor102 is depicted inFIG. 3 as occurring while thecannula44′ is partially inserted within thedevice10, the process may occur either with or without the cannula being entirely or partially within the device.
• Once a passageway into theeye100 is created as such, thecannula44′ and attachedtubing32′ (or, in the case of thedevice10 ofFIG. 1, therigid member26 with attachedcannula44 positioned therewithin) is advanced into and through thedevice10′ and to a treatment/target site. InFIGS. 3B and 4B, the target site is theretina110 of theeye100, but it is understood that the target site may be any portion of the eye.
• In an embodiment in which theretina110 is the target site, thecannula44′ is guided through thedevice10′ until adistal portion46′ of the cannula emerges from the guidingmember12′, and into thevitreous humor102.
• Thecannula44′ is further advanced within theeye100 until thedistal portion46′ of the cannula enters theretina110. An operator of thedevice10′ is able to determine that thedistal portion46′ of thecannula44′ has entered, but not traveled completely through, theretina48 by virtue of techniques generally known in the art.
• For example, once an operator estimates that thedistal portion46′ of the cannula is approaching the retina, s/he can inject an agent through thecannula44′. In order to simplify this estimation, thecannula44′ can include one or more markings that serve as visual and/or tactile indicators of the relative position of the cannula with respect to the retina. If, following this injection, the formation of a retinal detachment is observed, the operator can safely deduce that thedistal portion46′ of thecannula44′ has entered, and still remains within, theretina110 and can halt the distal advancement of the cannula.
• Once proper positioning of thedistal portion46′ of thecannula44′ at/within the treatment/target site110 is ensured, the device may be utilized either to deliver or withdraw material from theeye100. This occurs by activation of an externally located supply or withdrawal device (not shown) connected to theproximal end42′ of thetubing32′. Preferably, this externally located device is connected to thetubing32′ by a connection device (not shown), e.g., a luer fitting or other connection device known in the art.
• In an embodiment in which material is supplied to a treatment site, the material is infused into theproximal end42′ of thetubing32′ via an externally located supply device. The material travels through thetubing32′, wherein a quantity of the material is forced into theproximal end48′ of thecannula44′, through which it travels until it exits thedistal portion46′ of the cannula.
• In an embodiment in which material is withdrawn from a treatment site, an aspiration force is supplied through thetubing32′. A sufficient amount of this force enters theproximal end48′ of thecannula44′ to enable material to be drawn into thedistal portion46′ of thecannula44′ from the treatment site. This material then travels though thecannula44′, out itsproximal end48′, into thetubing32′, and out theproximal end42′ of the tubing to an externally located collection device (not shown).
• In an embodiment wherein material is delivered to the retina through an externally located supply device (e.g., a syringe), such material is generally a therapeutic agent or medicament, but may be any entirely or partially liquid-based or airborne material. Exemplary medicaments/agents include, but are not limited to, small molecule therapeutics, genes, proteins, or cells.
• Among the uses for these agents/medicaments that are supplied to theretina10 are for treatment of such problems/disorders as retinal detachment, vascular occlusions, proliferative retinopathy, diabetic retinopathy, inflammations such as uveitis, choroiditis and retinitis, degenerative disease, vascular diseases and various tumors including neoplasms.
• It is understood that the amount of agent/medicament required to be delivered to the treatment site will vary depending on the treatment circumstances and will be readily calculable by one of ordinary skill in the art without undue experimentation.
• In an exemplary embodiment in which materials are removed via thedevice10′, the treatment site may be thevitreous humor102 of theeye100. For example, portions of thevitreous humor102 may be removed through thedevice10′ during a vitrectomy—a procedure often used to treat a variety of eye diseases, ocular injuries and complicated retinal detachments.
• In accordance with an exemplary method of the present invention, the piercingmember12′ is advanced into and through the sclera104 (e.g., transconjunctively), thereby penetrating theeye100. Thecannula44′ (which is connected to therigid member26 in the embodiment ofFIG. 1, and connected to thetubing32′ in the embodiment ofFIG. 2) is then advanced through thedevice10′, then into and through thevitreous humor102 to a target site, (e.g. the retina110), such that thedistal portion46′ of thecannula44′ pierces the target site.
• An infusion or aspiration device (not shown) connected to theproximal end42′ of thetubing32′ is then activated to either inject material into the target site or to remove material therefrom as described above.
• Upon completion of the injection and/or removal step, thecannula44′ is withdrawn from theeye100 by reversing the steps of its insertion, after which the piercingmember12′ is removed from the eye. Preferably, the piercing member has a small enough outer diameter, e.g., about 25 gage (0.4547 millimeters) or less, that the incision made by the piercing member to gain entry into and through theeye100 is self-sealing, i.e., requiring no sutures for post-treatment closure.
• In a particularly preferred embodiment, thedevice10′ is used to deliver an agent directly into thesubretinal space110 of a patient'seye100. Once thedistal portion46′ of thecannula44′ is properly positioned within thesubretinal space110, medicament is injected therein, thus raising a dome-shaped retinal detachment (not shown) that allows for the delivered medicament to enjoy a prolonged residence time within the subretinal space. This, in turn, allows the medicament to provide a greater therapeutic effect, without adversely affecting intraocular pressure or neighboring retinal cells, both of which are problems that plague procedures in which drugs are administered directly into thevitreous humor102.
• The presentsubretinal injection device10′ is a self-contained system, i.e., no additional devices other than those discussed in accordance with the embodiments described above must be employed during use of the device. Moreover, the insertion site of the piercingmember12′ is self-sealing, also as discussed above.
• These features of the present invention allow thedevice10′ to be uniquely suited to office-based procedures (i.e., procedures that are not required to take place in a hospital setting). Such office-based procedures are comparatively less expensive, shorter in duration, and carry with them less risk than treatments necessitated by prior art systems and devices.
• Moreover, because the area of entry of thedevice10′ is self-sealing upon removal of the device, use of this device is a preferred treatment method as compared to intraretinal transplantation, which requires surgically opening the eye. Specifically, in intraretinal transplantation techniques, a pars plana incision is required to insert a glass micropipette or similar instrument through the globe and into the subretinal space. Upon completion of the procedure, scleral and conjunctival sutures are required to close the incision. As indicated above, this results in a prolonged procedure and/or an increased risk of infection, problems which are avoided due to the insertion site for the piercingmember12′ of the present invention being self-sealing.
• Another advantage of adevice10′ of the present invention is that an operator may use it to treat multiple treatment sites simply by varying the angle of the portion of the device that lies outside of theeye100, for example, as depicted inFIGS. 3A-4B, thus avoiding the need for creation of multiple entry sites. Even in the event, however, that multiple entry sites were required, each entry site would be self-sealing as described above.
• Further, because the agents are delivered directly to the subretinal space by thedevice10′ of the present invention, it follows that higher concentrations of the agent/medicament are delivered to the choroidal vessels and retinal pigment epithelial cells as compared to intravitreal injection and intraocular implants that introduce drugs into the vitreous humor. Moreover, the local delivery accomplished by thepresent device10′ and methods may also reduce the risk of elevated intraocular pressure associated with prior devices that provide sustained drug delivery to the vitreous humor.
• The present device further provides a method for direct intraretinal injection of therapeutics. Properly designed formulations delivered in such a manner result in sustained local delivery to retinal tissues, while reducing the risk of affecting intraocular pressure that accompanies intravitreal implants.
• The present invention also includes kits (not shown) that comprise one ormore devices10′ in accordance with the invention. Such kits also may include equipment (e.g., one or more containers, and aerosol canisters) for use with the device(s)10′, and/or written instructions for use of the device(s) and/or the equipment.
• The invention also includes kits that comprise one or more devices of the invention, preferably packaged in sterile condition. Kits of the invention may include, e.g., one or more piercing members with contained cannula, preferably packaged in sterile condition, and/or written instructions for use of the device and other components of the kit.
• The foregoing description of the invention is merely illustrative thereof, and it is understood that variations and modifications can be effected without departing from the scope or spirit of the invention as set forth in the following claims. All documents mentioned herein are incorporated by reference herein in their entirety.

Claims (22)

1. A device for treating an eye comprising:

a piercing member having a length, an outer diameter, a proximal end, a distal end, and a lumen extending between the proximal and distal ends, the distal end being of sufficient sharpness to cause a penetration of the eye conjunctiva and sclera; and

a cannula having a proximal end, a distal end, a lumen extending between the proximal and distal ends, and an outer diameter, wherein the cannula is slidably disposed within the lumen of the piercing member and wherein the distal end of the cannula is extendable beyond the distal end of the piercing member;

wherein the outer diameter of the piercing member is sized to allow the length of the piercing member to be advanced through the penetration, and for self sealing of the penetration upon removal of the piercing member from the eye.

2. The device ofclaim 1 wherein the length of the piercing member is such that the distal end of the piercing member is capable of accessing any treatment site within the eye when the length of the piercing member is inserted in the eye.

3. The device ofclaim 2 wherein the length of the piercing member is in the range of 22 mm to 30 mm.

4. The device ofclaim 1 wherein the outer diameter of the piercing member is 0.5 mm or less.

5. The device ofclaim 1 wherein a proximal portion of the device is provided to remain outside of the eye after penetration by the piercing member, and wherein angling of the proximal portion of the device outside of the eye provides the distal end of the cannula with access to multiple treatment sites via the penetration.

6. The device ofclaim 5 wherein the proximal portion of the device comprises a handle having a length, a proximal end, a distal end, and a substantially hollow portion, the distal end of the handle being mounted to the piercing member.

7. The device ofclaim 1 wherein the cannula has a length such that when the cannula is advanced through the lumen of the piercing member, the proximal end of the cannula is capable of accessing any treatment site within the eye.

8. The device ofclaim 1 wherein the outer diameter of the cannula is in the range of 0.128 mm to 0.0457 mm.

9. The device ofclaim 1 wherein the cannula comprises polyimide.

10. The device ofclaim 6 further comprising a quantity of tubing having a proximal end, a distal end, and a lumen extending therebetween, the distal end of the tubing being disposed within the substantially hollow portion of the handle.

11. The device ofclaim 10 wherein the quantity of tubing is in fluid connection with the cannula.

12. The device ofclaim 10 wherein the proximal end of the tubing is adapted to be connected to a supply device.

13. The device ofclaim 10 wherein the proximal end of the tubing is adapted to be connected to a syringe.

14. The device ofclaim 1 further comprising a rigid member having a proximal end, a distal end, and a lumen therebetween, wherein the rigid member is in connection with the cannula such that distal-to-proximal movement and proximal-to-distal movement of the rigid member affects movement of the cannula correspondingly.

15. The device ofclaim 14 wherein the cannula comprises polyimide tubing.

16. The device ofclaim 14 wherein the proximal end of the rigid member is connected to the distal end of the tubing,

17. The device ofclaim 16 wherein an epoxy is used to connect the proximal end of the rigid member to the distal end of the tubing, and the distal end of the rigid member to the proximal end of the cannula.

18. The device ofclaim 1 further comprising a housing disposed in the substantially hollow portion of the handle, the housing movable in distal-to-proximal and proximal-to-distal directions.

19. The device ofclaim 18 wherein the housing that is movable in distal-to-proximal and proximal-to-distal directions causes corresponding movement of the cannula in distal-to-proximal and proximal-to-distal directions.

20. The device ofclaim 19 wherein the housing is connected to an actuating element, which can be manipulated by an operator to cause corresponding movement of the housing.

21. A device for treating an eye comprising:

a piercing member having a length, an outer diameter, a proximal end, a distal end, the distal end being of sufficient sharpness to cause a penetration in the eye conjunctiva and sclera;

a handle having a length, a proximal end, a distal end, and a substantially hollow portion, the distal end of the handle being mounted to the piercing member, wherein the piercing member and the handle have a lumen therebetween, defining a pathway between the proximal end of the handle and distal end of the piercing member; a rigid member and cannula slidably disposed within the lumen of the piercing member and the handle, wherein rigid member has a proximal end, a distal end, and a lumen therebetween, and the cannula has a proximal end, a distal end, and a lumen therebetween, and the distal end of the rigid member is connected to the proximal end of the cannula; and

a quantity of tubing having a proximal end, a distal end, and a lumen extending therebetween, the distal end of the tubing being disposed within the lumen of the handle and being connected to the proximal end of the rigid member.

22. A device for treating an eye comprising:

a piercing member having a length, an outer diameter, a proximal end, a distal end, and a lumen extending between the proximal and distal ends, the distal end being of sufficient sharpness to cause a penetration in the eye conjunctiva and sclera wherein the outer diameter of the piercing member is sized to allow the length of the piercing member to be advanced through the penetration, and for self sealing of the penetration upon removal of the piercing member from the eye;

a fluid conduit comprising a cannula having a proximal end, a distal end, a lumen extending between the proximal and distal ends, and an outer diameter; and a rigid member having a proximal end, a distal end, and a lumen therebetween, wherein the cannula is disposed within the lumen of the rigid member, and wherein the rigid member and cannula are both slidably disposed within the lumen of the piercing member, and wherein the distal end of the cannula is extendable beyond the distal end of the piercing member and the distal end of the rigid member;

wherein distal-to-proximal movement and proximal-to-distal movement of the rigid member affects movement of the cannula correspondingly.

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