Devices and methods for targeted delivery of a substance
A device for applying a bubble of a substance to a tissue surface, the device comprising a cannula, a distal tip at the distal end portion of the cannula, the distal tip having a bubble support surface and an exit port extending through the bubble support surface, an expansion fluid passageway extending through the cannula to the exit port, a source of an expansion fluid and an actuator therefor. In some arrangements, the distal tip can be configured to support a layer of the substance thereon over the distal port and the device can be configured such that the advancement of the expansion fluid from the fluid source through the exit port causes at least one bubble of the substance to form on the distal tip, wherein the at least a portion of the bubble can be transferred to the tissue surface to treat a defect on the tissue surface.
1. A device for applying a bubble of a bioadhesive substance to a tissue surface of an eye, the device comprising:
a cannula comprising a proximal end portion, a distal end portion, and an intermediate portion extending therebetween;
a distal tip at the distal end portion of the cannula configured for insertion into the eye, the distal tip having an outer, longitudinally extending surface, the distal tip having a wall with an inner surface defining a lumen of a first diameter for passage of an expansion gas, the wall having a thickness between the distal tip outer surface and the wall inner surface, the distal tip defining an exit port in fluid communication with the lumen, the exit port having a diameter that is smaller than the lumen first diameter, the exit port circumvented by a rim that extends from the distal tip outer surface inward relative to the wall inner surface, the rim having a flat, circumferential face forming a distal most surface of the distal tip, an entirety of the circumferential face being flat, the flat, circumferential face having a width between an outer diameter and an inner diameter of the flat, circumferential face that is larger than the wall thickness, the rim configured to support a layer of the bioadhesive substance on the flat, circumferential face;
a bioadhesive pathway for introducing the bioadhesive substance to the flat, circumferential face of the rim;
an expansion gas passageway extending through at least the intermediate portion and the distal end portion of the cannula, the expansion gas passageway being in fluid communication with the distal tip lumen and being configured to provide a passageway for the expansion gas separate from the bioadhesive pathway along a length of the intermediate and distal end portions of the cannula all the way to the exit port, the expansion gas passageway being coaxial with the bioadhesive pathway; and
an actuator configured to couple with a source of the expansion gas and configured to selectively advance the expansion gas through the expansion gas passageway and the distal tip lumen upon actuation of the actuator and to direct the expansion gas to the layer of the bioadhesive substance to form the bubble of the bioadhesive substance on the flat, circumferential face of the rim with the layer of the bioadhesive substance at least partially surrounding a volume of the expansion gas.
2. The device of claim 1 , comprising a handle portion at a proximal end of the device, the handle portion configured to support at least the actuator and the source of expansion gas.
3. The device of claim 1 , wherein the device is configured to form a bubble that comprises a spherically shaped film of the bioadhesive substance at least partially enclosing the expansion gas.
4. The device of claim 1 , wherein the actuator comprises a compressible bladder configured to expel the expansion gas from the source of the expansion gas within the bladder through the expansion gas passageway.
5. The device of claim 1 , wherein the actuator comprises a wheel moveable along a compressible bladder configured to expel the expansion gas from the source of the expansion gas within the bladder through the expansion gas passageway.
6. The device of claim 1 , wherein the bioadhesive pathway surrounds the expansion gas passageway.
7. The device of claim 1 , wherein the bioadhesive pathway comprises an elongate body comprising a proximal end and a distal end having a distal tip with at least one opening therein, the elongate body being advanceable through the expansion gas passageway to the distal tip at the distal end portion of the cannula.
8. The device of claim 1 , wherein the bioadhesive pathway is internal to or surrounded by at least a portion of the expansion gas passageway of the cannula.
9. The device of claim 1 , further comprising a cautery component configured to increase the temperature of at least the distal tip of the device.
10. The device of claim 1 , wherein the flat, circumferential face of the rim is not beveled perpendicular to a longitudinal extent of the cannula.
11. The device of claim 1 , wherein the flat, circumferential face of the rim is beveled.
12. The device of claim 1 , wherein the width of the flat, circumferential face is in the range of 0.1 mm to 0.5 mm.
13. The device of claim 1 , wherein the width of the flat, circumferential face is in the range of 0.5 mm to 1 mm.
14. The device of claim 1 , wherein the distal tip defines a single exit port.
15. The device of claim 1 , further comprising a manifold surrounding the exit port, the bioadhesive pathway being in fluid communication with the manifold.
16. The device of claim 1 , wherein the distal tip comprises a hydrophobic material.
17. The device of claim 1 , wherein the rim is configured to support the layer of the bioadhesive substance on an entirety of the flat, circumferential face.
18. A handheld device for applying a bioadhesive bubble to a retina of an eye, comprising:
an elongate body comprising a first end and a second end, the first end comprising a handle, the second end comprising a cannula configured for insertion into the eye and having a wall with an outer, longitudinally extending surface, the cannula defining a lumen and having an exit port and a rim having a flat face at a distal most surface of the cannula, an entirety of the rim face being flat, the exit port having a smaller diameter than the lumen and the flat face extending inward from the outer surface into the lumen a distance greater than a thickness of the cannula wall adjacent the flat face;
a bioadhesive reservoir configured for containing a liquid bioadhesive;
a first passageway in communication with the exit port and configured to selectively communicate a supply of an expansion gas through the exit port; and
a second passageway in communication with the bioadhesive reservoir and configured to selectively communicate a supply of the bioadhesive from the bioadhesive reservoir to the second end of the elongate body, wherein the second passageway completely surrounds the first passageway at least at a distal end of the cannula all the way to the exit port;
wherein:
the first passageway is configured to direct the supply of the expansion gas through a layer of the bioadhesive that is received on the flat face to produce the bioadhesive bubble;
the first passageway is configured to maintain the supply of the expansion gas out of contact with the bioadhesive until the expansion gas is directed through the bioadhesive at the flat face;
the flat face is configured to maintain the bioadhesive bubble on the second end when the expansion gas stops flowing through the exit port; and
the second end is configured to release the bioadhesive bubble when the bioadhesive bubble is brushed against a retina or when the expansion gas flows again through the exit port.
19. The handheld device of claim 18 , wherein the elongate body further comprises a joining portion, the joining portion comprising a coupling end configured to interact with a proximal portion of the cannula, and wherein the proximal portion of the cannula is configured to reversibly interact with the coupling end of the elongate body.
20. The device of claim 18 , wherein the flat face has a width in the range of 0.1 mm to 0.5 mm.
21. The device of claim 18 , wherein the flat face has a width in the range of 0.5 mm to 1 mm.
22. The device of claim 18 , wherein the distal tip defines a single exit port.
23. The device of claim 18 , further comprising a manifold surrounding the exit port, the bioadhesive pathway being in fluid communication with the manifold.
24. The device of claim 18 , wherein the distal tip comprises a hydrophobic material.
25. A device for applying a bubble of a bioadhesive substance to a tissue surface, the device comprising:
a cannula comprising a proximal end portion, a distal end portion, and an intermediate portion extending therebetween along a longitudinal axis;
a distal tip at the distal end portion of the cannula, the distal tip having an outer longitudinally extending surface, the distal tip having a wall of a first thickness defining a lumen of a first diameter for passage of an expansion gas, the distal tip defining only a single exit port, the exit port having a smaller diameter than the lumen first diameter, the exit port circumvented by a rim of larger dimension than the first thickness, the rim having a circumferential face extending inward from the distal tip outer surface, the circumferential face oriented at an acute angle to the longitudinal axis along an entirety of the circumferential face, the rim configured to support a layer of the bioadhesive substance on the circumferential face;
a bioadhesive pathway for introducing the bioadhesive substance to the circumferential face of the rim;
an expansion gas passageway extending through at least the intermediate portion and the distal end portion of the cannula, the expansion gas passageway being in fluid communication with the distal tip lumen and being configured to provide a passageway for the expansion gas separate from the bioadhesive pathway along a length of the intermediate and distal end portions of the cannula, the expansion gas passageway and bioadhesive pathway remaining separate all the way to the exit port; and
an actuator configured to couple with a source of the expansion gas and configured to selectively advance the expansion gas through the expansion gas passageway and the distal tip lumen upon actuation of the actuator and to direct the expansion gas to the layer of the bioadhesive substance to form the bubble of the bioadhesive substance on the circumferential face of the rim with the layer of the bioadhesive substance at least partially surrounding a volume of the expansion gas.
26. The device of claim 25 , wherein the circumferential face has a width in the range of 0.1 mm to 0.5 mm.
27. The device of claim 25 , wherein the circumferential face has a width in the range of 0.5 mm to 1 mm.
28. The device of claim 1 , further comprising a manifold surrounding the exit port, the bioadhesive pathway being in fluid communication with the manifold.
29. The device of claim 25 , wherein the distal tip comprises a hydrophobic material.
30. The device of claim 25 , wherein the distal tip is configured for insertion into the eye.
31. The device of claim 25 , wherein the rim is configured to support a layer of the bioadhesive substance on the entirety of the circumferential face.
32. The device of claim 25 , wherein an entirety of the circumferential face is flat.
33. A device for applying a bubble of a bioadhesive substance to a tissue surface, the device comprising:
a cannula comprising a proximal end portion, a distal end portion, and an intermediate portion extending therebetween along a longitudinal axis;
a distal tip at the distal end portion of the cannula, the distal tip having a wall of a first thickness defining a lumen of a first diameter, the distal tip defining an exit port in fluid communication with the lumen, the exit port having a smaller diameter than the lumen first diameter, and a deflector extending into the lumen and having a distal facing surface located within the distal tip;
a bioadhesive pathway for introducing the bioadhesive substance to the distal facing surface of the deflector;
an expansion gas passageway defined by a member extending through at least the intermediate portion and the distal end portion of the cannula, the expansion gas passageway being in fluid communication with the lumen and being configured to provide a passageway for the expansion gas separate from the bioadhesive pathway along a length of the intermediate and distal end portions of the cannula, the deflector configured to direct flow of the bioadhesive substance radially inwardly about a distal end of the member defining the passageway for the expansion gas, the distal end of the member spaced proximal of the deflector; and
an actuator configured to couple with a source of the expansion gas and configured to selectively advance the expansion gas through the expansion gas passageway and the lumen upon actuation of the actuator and to direct the expansion gas to a layer of the bioadhesive substance to form the bubble of the bioadhesive substance on the distal facing surface of the deflector with the layer of the bioadhesive substance at least partially surrounding a volume of the expansion gas.
34. The device of claim 33 , wherein the distal tip is configured for insertion into the eye.
35. A device for applying a bubble of a bioadhesive substance to a tissue surface of an eye, the device comprising:
a cannula comprising a proximal end portion, a distal end portion, and an intermediate portion extending therebetween;
a distal tip at the distal end portion of the cannula configured for insertion into the eye, the distal tip having an outer, longitudinally extending surface, the distal tip having a wall with an inner surface defining a lumen of a first diameter for passage of an expansion gas, the wall having a thickness between the distal tip outer surface and the wall inner surface, the distal tip defining an exit port in fluid communication with the lumen, the exit port having a diameter that is smaller than the lumen first diameter, the exit port circumvented by a rim that extends from the distal tip outer surface inward relative to the wall inner surface, the rim having a flat, circumferential face forming a distal most surface of the distal tip, an entirety of the circumferential face being flat, the flat, circumferential face having a width between an outer diameter and an inner diameter of the flat, circumferential face that is larger than the wall thickness, the rim configured to support a layer of the bioadhesive substance on the flat, circumferential face;
a bioadhesive pathway for introducing the bioadhesive substance to the flat, circumferential face of the rim;
an expansion gas passageway having a central axis extending through at least the intermediate portion and the distal end portion of the cannula, the expansion gas passageway being in fluid communication with the distal tip lumen and being configured to provide a passageway for the expansion gas separate from the bioadhesive pathway along a length of the intermediate and distal end portions of the cannula all the way to the exit port, the central axis of the expansion gas pathway being aligned with a center of the exit port; and
an actuator configured to couple with a source of the expansion gas and configured to selectively advance the expansion gas through the expansion gas passageway and the distal tip lumen upon actuation of the actuator and to direct the expansion gas to the layer of the bioadhesive substance to form the bubble of the bioadhesive substance on the flat, circumferential face of the rim with the layer of the bioadhesive substance at least partially surrounding a volume of the expansion gas.
36. The device of claim 35 , wherein the flat face has a width in the range of 0.1 mm to 0.5 mm.
37. The device of claim 35 , wherein the flat face has a width in the range of 0.5 mm to 1 mm.
38. The device of claim 35 , wherein the distal tip defines a single exit port.
39. The device of claim 38 , wherein the distal tip defines only the single exit port.
40. The device of claim 35 , further comprising a manifold surrounding the exit port, the bioadhesive pathway being in fluid communication with the manifold.
41. The device of claim 35 , wherein the distal tip comprises a hydrophobic material.
42. The device of claim 35 , wherein the rim is configured to support the layer of the bioadhesive substance on an entirety of the flat, circumferential face.