| US 7,579,442 B2 | ||
| Method for stromal corneal repair and refractive alteration | ||
| Joseph J. Bango, New Haven, Conn. (US); and John B. Fenn, Richmond, Va. (US) | ||
| Assigned to Ocugenics, LLC, Orangevale, Calif. (US) | ||
| Filed on Apr. 16, 2003, as Appl. No. 10/414,796. | ||
| Claims priority of provisional application 60/373725, filed on Apr. 16, 2002. | ||
| Prior Publication US 2003/0193118 A1, Oct. 16, 2003 | ||
| This patent is subject to a terminal disclaimer. | ||
| Int. Cl. A61K 38/17 (2006.01); B29C 47/02 (2006.01) | ||
| U.S. Cl. 530—356 [264/465] | 7 Claims |
| 1. A method of producing a controlled corneal collagen fibril matrix with a controlled cross-hatch pattern of fibril strands
of collagen on a conductive target for transfer to a cornea, comprising the steps of:
A) providing a conductive spraying needle having a conductive needle tip, and a conductive target,
B) forming a solution of collagen using a solvent, and loading the solution of collagen in the conductive spraying needle
having a conductive needle tip,
C) providing a power source having an alternating output voltage adjustable over a range extending from 1000 to 20,000 volts,
the output voltage being coupled to produce an electric field between the conductive target and the conductive needle tip,
D) adjusting the alternating output voltage of the power source to produce a strand of collagen fiber from a Taylor Cone from
the solution of collagen passing from the conductive needle tip to the conductive target when the electric field exceeds the
surface tension of the solution of collagen fluid in the conductive needle tip,
E) directing the strand of collagen fiber from the Taylor Cone onto the conductive target from the conductive needle tip,
F) moving said conductive spraying needle having a conductive needle tip in a linear direction for a fixed distance and then
reversing such motion with respect to said conductive target while at the same time indexing the target utilizing a precision
positioner, to deposit a first collagen mat of collagen fibril strands laid down on said conductive target, and then
rotating the target ninety degrees and repeating the process to obtain a second mat of collagen fibril strands laid down on
said first collagen mat of collagen fibril strands on said conductive target, the first and second mat forming a controlled
corneal collagen fibril matrix with a controlled cross-hatch pattern,
G) evaporating said solvent from said controlled corneal collagen fibril matrix with a controlled cross-hatch pattern on said
conductive target,
H) repeating steps E-G to obtain
the controlled corneal collagen fibril matrix with a controlled cross-hatch pattern of collagen fibril strands having a thickness
sufficient for transfer to a cornea.
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