초록 ▼

A device for delivering a biocompatible material to a surgical site includes a cannula having proximal and distal portions and at least a first interior lumen disposed therebetween through which the biocompatible material is delivered. The device further includes an initiation member for initiating

A device for delivering a biocompatible material to a surgical site includes a cannula having proximal and distal portions and at least a first interior lumen disposed therebetween through which the biocompatible material is delivered. The device further includes an initiation member for initiating cross-linking of the biocompatible material while the biocompatible material is within the cannula. The cannula may include a heating element to thermally initiate cross-linking. Alternately, the cannula may include a second lumen for transmitting light from a light source. A movable blocking element controls the amount of light that passes into the first lumen. A method of delivering a curable biocompatible material to a surgical site includes positioning a distal portion of a cannula adjacent the surgical site and introducing the biocompatible material through a first lumen of the cannula. Cross-linking of the biocompatible material is then initiated while the biocompatible material is within the cannula.

대표청구항 ▼

What is claimed is: 1. A device, comprising: an elongate cannula having a proximal portion adapted to be located outside a body during a surgical procedure, and a distal portion adapted to be located within the body during the surgical procedure and adjacent a surgical site to which a curable bioco

What is claimed is: 1. A device, comprising: an elongate cannula having a proximal portion adapted to be located outside a body during a surgical procedure, and a distal portion adapted to be located within the body during the surgical procedure and adjacent a surgical site to which a curable biocompatible material is to be delivered, the cannula comprising: an outer wall; a first interior lumen disposed between the proximal and distal portions through which the biocompatible material is delivered, a wall of the first lumen including a first wall portion capable of transmitting light therethrough; a second interior lumen disposed adjacent the first interior lumen and adapted to transmit light within the second lumen, a wall of the second lumen including a second wall portion capable of transmitting light therethrough, the first and second wall portions being generally aligned so that light from the second lumen may pass through the first and second wall portions to photo initiate cross-linking of the biocompatible material in the first lumen; a blocking element positioned in at least one of the first or second lumens and movable between a first position wherein light from the second lumen may pass through at least a part of the first and second wall portions to the first lumen, and a second position wherein less light may pass through at least one of the first and second wall portions than in the first position; and an end of the cannula to be located adjacent a surgical site. 2. The device of claim 1, further comprising: a fiber optic bundle positioned in the second lumen for generating light to be transmitted within the second lumen, the fiber optic cable terminating proximal the second wall portion. 3. The device of claim 1, further comprising: a light source for generating light to be transmitted within the second lumen. 4. The device of claim 3, wherein the light source is selected from the group consisting of a visible and an ultraviolet light source. 5. The device of claim 1, wherein the outer wall is opaque to protect body tissue from light exposure. 6. The device of claim 1, further comprising: a controller adapted to move the blocking element between the first and second positions and control the amount of light transmitted through the first and second wall portions. 7. The device of claim 6, wherein the controller is coupled to a supply of the biocompatible material and capable of varying the rate at which the biocompatible material flows through the cannula. 8. A method of delivering a curable biocompatible material to a surgical site in the body, comprising: positioning a distal portion of a cannula adjacent the surgical site; introducing the biocompatible material through a first lumen of the cannula; and initiating cross-linking of the biocompatible material prior to delivery to the surgical site while the biocompatible material is within the cannula, wherein initiating cross-linking comprises: transmitting light through a second lumen of the cannula to the first lumen to photo initiate cross-linking of the biocompatible material; and moving a blocking element between a first and a second position to control the amount of light transmitted from the second lumen to the first lumen. 9. The method of claim 8, wherein light is transmitted by a fiber optic bundle positioned in the second lumen of the cannula. 10. The method of claim 8, further comprising: controlling wherein light transmitted from the second lumen is selected from the group consisting of visible and ultraviolet light. 11. The method of claim 8, further comprising: protecting body tissue from exposure to light transmitted from the second lumen to the first lumen. 12. The method of claim 11, wherein at least a portion of the cannula is opaque. 13. The method of claim 8, wherein the blocking element is moved by a controller. 14. The method of claim 13, wherein the controller is coupled to a supply of the biocompatible material and capable of varying the rate at which the biocompatible material flows through the cannula.