IP Library Granted Patent US 10,390,941
Granted Patent B2
US 10,390,941 · App. 15/233,527 · Granted Aug 27, 2019

Automated intraocular lens injector device

Inventors: David A. Downer (Fort Worth, TX); Tu Cam Tran (Grapevine, TX)
Assignee: Novartis AG
A61F2/1672A61B17/3468A61F2/167A61F2/1678A61F9/00736A61M37/0069A61B2017/00039A61B2017/00159A61B2017/00199A61B2017/00398A61B2017/00473A61B2017/00477A61B2090/034A61B2090/064A61B2090/0811
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Quick Facts
Patent No.
US 10,390,941
App. No.
15/233,527
Granted
Aug 27, 2019
Kind
B2
Abstract

An IOL injection device comprises a tubular housing with a plunger longitudinally disposed within the tubular housing. The device is configured so that when the plunger is translated towards the front of the device, its tip engages an intraocular lens insertion cartridge mounted at or near the front end of the housing. The IOL injection device further comprises a control circuit. The control circuit is configured to perform the steps of advancing the plunger to a critical point at which an axial compressive force on the lens suddenly increases, retracting the plunger from the critical point to a sufficient distance for material of the intraocular lens to relax, pausing to allow the material of the intraocular lens to relax, advancing the plunger to the critical point a second time, and continuing to advance the plunger beyond the critical point to implant the intraocular lens.

Claims (31)

1. A device for implanting an intraocular lens in the lens capsule of an eye, the device comprising:

a tubular housing having a primary axis extending between front and rear ends of the housing;

a plunger longitudinally disposed within the housing and having first and second ends, the first end being disposed towards the front end of the housing;

an electric drive system disposed within the housing, the electric drive system including an electric motor and configured to cause longitudinal translation of the plunger along the primary axis of the housing;

a cartridge mount at or near the front end of the housing and configured to accommodate a removable insertion cartridge in alignment with the plunger so that an intraocular lens disposed in the insertion cartridge is displaced from the insertion cartridge as the plunger is translated towards the front end of the housing; and

a control circuit, electrically connected to the electric motor and configured to: monitor a back EMF signal from the electric motor caused by the force on the plunger; advance the plunger;

detect, based on the back EMF signal exceeding a predetermined threshold level, a critical point at which an axial compressive force on the lens suddenly increases;

in response to the detection of the back EMF exceeding the predetermined threshold level, retract the plunger from the critical point to a sufficient distance for material of the intraocular lens to relax;

pause after the plunger is retracted to allow the material of the intraocular lens to relax;

advance the plunger to the critical point a second time; and

continue to advance the plunger beyond the critical point at an accelerated rate to implant the intraocular lens.

2. The device of claim 1 , wherein the control circuit is further configured to:

advance the plunger to fully compress the intraocular lens;

pause after the intraocular lens is fully compressed to allow the material of the intraocular lens to relax; and

advance the plunger to implant the lens.

3. The device of claim 1 , wherein the control circuit is further configured to pause the advancement of the plunger for at least five seconds.

4. The device of claim 1 , wherein, during the advance of the plunger to the critical point and the advance of the plunger to the critical point the second time, the plunger advances at a rate of 1.2 mm/s or less as it reaches the critical point.

5. A method of implanting an intraocular lens, comprising the steps of:

monitoring a back EMF signal from an electric motor caused by the force on a plunger;

advancing the plunger;

detecting, based on the back EMF signal exceeding a predetermined threshold level, a critical point at which an axial compressive force on the lens suddenly increases;

in response to the detection of the back EMF exceeding the predetermined threshold level, retracting the plunger from the critical point to a sufficient distance for material of the intraocular lens to relax;

pausing to allow the material of the intraocular lens to relax;

advancing the plunger to the critical point a second time; and

continuing to advance the plunger at an accelerated rate to implant the intraocular lens.

6. The method of claim 5 , wherein the step of continuing to advance the plunger further comprises:

advancing the plunger to fully compress the intraocular lens;

pausing after the intraocular lens is fully compressed to allow the material of the intraocular lens to relax; and

advancing the plunger to implant the lens.

7. The method of claim 5 , wherein the step of pausing comprises pausing at least five seconds.

8. The method of claim 5 , wherein, during the steps of advancing the plunger to the critical point and advancing the plunger to the critical point the second time, the plunger is advancing at a rate of 1.2 mm/s or less as it reaches the critical point.

Assignments (1)
CONFIRMATORY DEED OF ASSIGNMENT EFFECTIVE APRIL 8, 2019 Recorded Dec 10, 2019
From: NOVARTIS AG
To: ALCON INC.
Reel/Frame 051454/0788 →
Continuity (3)
Continuation 14223422 · Mar 24, 2014
Provisional Application 61808053 · Apr 3, 2013
Related Publication 20160346078A1 · Dec 1, 2016