The present disclosure relates generally to a MEMS (Micro Electro-Mechanical Systems) check valve and associated systems and methods, and more particularly, to a MEMS check valve usable in a pump platform. The pump platform may be used in ophthalmic treatments.
Glaucoma, a group of eye diseases affecting the retina and optic nerve, is one of the leading causes of blindness worldwide. Most forms of glaucoma result when the intraocular pressure (IOP) increases to pressures above normal for prolonged periods of time. IOP can increase due to high resistance to the drainage of the aqueous humor relative to its production. Left untreated, an elevated IOP causes irreversible damage to the optic nerve and retinal fibers resulting in a progressive, permanent loss of vision.
The eye's ciliary body continuously produces aqueous humor, the clear fluid that fills the anterior segment of the eye (the space between the cornea and lens). The aqueous humor flows out of the anterior chamber (the space between the cornea and iris) through the trabecular meshwork and the uveoscleral pathways, both of which contribute to the aqueous humor drainage system. The delicate balance between the production and drainage of aqueous humor determines the eye's IOP.
One method of treating glaucoma includes implanting a drainage device in a patient's eye. The drainage device allows fluid to flow from the interior chamber of the eye to a drainage site, relieving pressure in the eye and thus lowering IOP. In order to provide desired treatments to patients, it may be important to regulate the drainage flow through the drainage device. However, drainage devices with flow regulation devices can be large and unwieldy when implanted in the eye. Such devices may not provide desired levels of comfort to the patient and may result in tissue irritation or other discomforts. In addition, implantation of larger implants can be challenging to secure.
The system and methods disclosed herein overcome one or more of the deficiencies of the prior art.
In one exemplary aspect, the present disclosure is directed to a MEMS check valve including a supporting portion having a first perforation therethrough sized to permit fluid flow and a displaceable portion having a second perforation therethrough sized to permit fluid flow. The displaceable portion may be moveable relative to the supporting portion between a closed position inhibiting fluid flow through the valve and an open position permitting fluid flow through the valve. The first and second perforations are offset to inhibit fluid flow when the displaceable portion is in the first position, and fluid may flow through the first and second perforations when the displaceable portion is in the second position.
In one aspect, the supporting portion includes a body portion, and the displaceable portion abuts the supporting portion such that the second perforation is aligned with the body portion when the displaceable portion is in the closed position.
In another exemplary aspect, the present disclosure is directed to a MEMS check valve chip including a first side and an opposing second side. A first passage extends from the first side to the second side, and a second passage extends from the first side to the second side. A first fluid restriction on the first side may be associated with the first passage, with the fluid restriction being configured to inhibit fluid flow into the first passage and permitting fluid flow out of the first passage. A second fluid restriction on the first side may be associated with the second passage. The second fluid restriction may be being configured to inhibit fluid flow out of the second passage and permit fluid flow into the second passage.
In one aspect, the second fluid restriction comprises a MEMS check valve having a supporting portion and a displaceable portion. The displaceable portion may be moveable relative to the supporting portion between a closed position inhibiting fluid flow through the valve and an open position permitting fluid flow through the valve.
In another exemplary aspect, the present disclosure is directed to a method including forming a fluid passageway through a MEMS chip having a first side and a second side, and including creating a displaceable member on the first side of the chip over the passageway. The displaceable member may be having at least one displaceable member perforation therethrough configured to permit the flow of a fluid. The method may also include creating a supporting portion over the displaceable member on the first side of the chip. The supporting portion may have at least one supporting portion perforation therethrough configured to permit the flow of a fluid therethrough. The displaceable member perforation may be aligned with a solid portion of the supporting portion when the displaceable member is in a first position to inhibit fluid flow through the displaceable member perforation, and the displaceable member perforation may be spaced from the solid portion of the supporting portion when the displaceable member is in a second position to permit fluid flow through the displaceable member perforation.
In one aspect, the method includes forming a second fluid passageway through the MEMS chip, and creating a second displaceable member on the first side of the chip over the second fluid passageway. The displaceable member may include at least one displaceable member perforation therethrough configured to permit the flow of a fluid therethrough. In one aspect, the method may include stacking the MEMS chip on a second MEMS chip to form a chamber therebetween.
It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory in nature and are intended to provide an understanding of the present disclosure without limiting the scope of the present disclosure. In that regard, additional aspects, features, and advantages of the present disclosure will be apparent to one skilled in the art from the following detailed description.
The accompanying drawings illustrate embodiments of the devices and methods disclosed herein and together with the description, serve to explain the principles of the present disclosure.
For the purposes of promoting an understanding of the principles of the present disclosure, reference will now be made to the embodiments illustrated in the drawings, and specific language will be used to describe the same. It will nevertheless be understood that no limitation of the scope of the disclosure is intended. Any alterations and further modifications to the described devices, instruments, methods, and any further application of the principles of the present disclosure are fully contemplated as would normally occur to one skilled in the art to which the disclosure relates. In particular, it is fully contemplated that the features, components, and/or steps described with respect to one embodiment may be combined with the features, components, and/or steps described with respect to other embodiments of the present disclosure. For simplicity, in some instances the same reference numbers are used throughout the drawings to refer to the same or like parts.
The present disclosure relates generally to a MEMS check valve that may be formed on a chip to regulate fluid flow through a flow passage. The MEMS check valve may be formed on the side of the chip into which the fluid enters the passage. Because of its arrangement, the check valve disclosed herein may be formed on the same side of a chip as a second check valve, and the two check valves may restrict fluid flow in opposite directions. Accordingly, when used in a MEMS pump, fluid may flow through the first check valve formed on the first side of the chip into a chamber and may be restricted from exiting the chamber through the first check valve, but may be permitted to exit the chamber through the second check valve formed on the first side of the chip. Because the MEMS check valve may be formed at the entrance to the flow passage through the chip on the first side of the chip, chip processing may be easier and may be less expensive. In addition, since the entrance valve and the exit valve are able to be formed on the same side of the chip, the overall stack size of the pump may be reduced because fewer chips are needed when compared to a device that uses one check valve per chip. Thus, implants formed from the chips may be smaller making them more comfortable for the patient, potentially easier to implant, improving the overall clinical result. In addition because fewer chips are required, the resulting devices may be less expensive to manufacture.
The plate 102 is configured to fit at least partially within the subconjunctival space and is sized for example within a range between about 15 mm×12 mm to about 30 mm×15 mm and has a thickness less than about 2 mm thick and preferably less than about 1 mm thick. The plate 102 may be formed to the radius of the eye globe (about 0.5 inches). In some embodiments, the plate 102 is rigid and preformed with a curvature suitable to substantially conform to the globe or it may be flexible to conform to the globe. Some embodiments have relatively planar outer surfaces. Some of these are small enough that conforming to the globe provides little benefit in comfort or implantation technique. The above dimensions are exemplary only, and other sizes and arrangements are contemplated. When implanted, the plate 102 may be located in the subconjunctival pocket between the conjunctiva and sclera. It may be generally located on an ocular quadrant commonly used for conventional glaucoma drainage devices with plates; that is, it may be centered such that it is equidistant from the neighboring ocular muscles that define the ocular quadrant chosen for implantation.
The drainage tube 104 is sized to bridge the anterior chamber and the plate 102 in the subconjunctival pocket to provide an auxiliary flow path for aqueous humor, bypassing the flow-resistive conventional pathway through the trabecular meshwork and shunting aqueous humor directly to a drainage site. In the example shown, the drainage tube 104 is a single tube having a single lumen. Other embodiments include a plurality of drainage tubes or a plurality of lumens cooperating together to permit fluid to flow through the implantable system 100. The drainage tube 104 is sized to extend from the plate 102 to the anterior chamber of the eye, as shown in
The one or more sensors 152 may be configured to detect a parameter relating to the condition of the patient or the condition of the implantable device 100. In one embodiment, the one or more sensors 152 are pressure sensors disposed about the implantable device 100 and configured to detect pressure or variations in pressure. For example, the sensors may be used to detect pressures for calculation of IOP. Data from the sensors may be communicated to the processor 156 for processing.
The power source 154, which provides power to the system 150, is typically a rechargeable battery, such as a lithium ion or lithium polymer battery, although other types of power sources may be employed such as capacitors. The power source can be recharged or the power source can exist external of the system 150 via inductive coupling such as an RFID (Radio Frequency Identification Device) link or other type of magnetic coupling.
The processor 156 is typically an integrated circuit with power, input, and output pins capable of performing logic functions. In various embodiments, the processor 156 may be a targeted device controller or a microprocessor configured to control more than one component of the device. It may receive and process data and may issue control signals to the flow system or other components.
The memory 158, which is typically a semiconductor memory such as RAM (Random Access Memory), FRAM (Ferroelectric Random Access Memory), or flash memory, interfaces with the processor 156. As such, the processor 156 can write to and read from the memory 158, and perform other common functions associated with managing semiconductor memory. In this manner, a series of IOP readings can be stored in the memory 158.
The flow system 160 controls the amount of drainage flow through the implantable device 100. In one embodiment, it is responsive to signals from the processor 156 to increase flow, decrease flow, or maintain flow.
The flow system 160 may be controlled by the processor 156 based on input data received from, by way of non-limiting example, sensors or data or a programmed treatment plan. A desired pressure differential can be maintained by controlling the operation of the flow system 160. Likewise, various intraocular pressure parameters, such as, by way of non-limiting example, the desired IOP, the IOP change rate, and/or the bleb pressure may be controlled by controlling the operation of flow system 160.
As can be seen in
The valve chip 162 also includes an inlet check valve 180 and an outlet check valve 182. Here, the inlet and outlet check valves 180 and 182 are formed on the same side of a single chip. Accordingly, even with two check valves arranged to restrict flow in opposite directions, manufacturing processing may be performed on the same side of the same chip. Also, because of the arrangement of the check valves on the same side of the chip, the pump functionality may be formed using only two chips, whereas devices formed with a single check valve on a side of the chip would use at least an additional chip. This may reduce the stack size required to carry out the operation of the flow system 160.
The inlet check valve 180 comprises a flexible portion 186 that spans the opening of the inlet passageway on the upper side 168. The flexible portion 186 may be a membrane formed of an elastically deformable material including without limitation, materials such as a silicone, silicon nitride, silicone elastomer, polyimide, parylene and others. In the example shown, the flexible portion 186 is a circular material secured at its periphery to the chip 162. In other embodiments, the chip 162 and the flexible portion 186 are formed so that the membrane has a non-circular shape, including oval, substantially rectangular, or square, for example. Other shapes are also contemplated.
In the embodiment shown, the flexible portion 186 includes one or more flow apertures 188 and a sealing portion 189. The flow apertures 188, in this embodiment are disposed off-center, and the sealing portion 189 is disposed in a central region. In this embodiment, fluid may flow into the chamber 166 through the inlet passageway 174 and through the flow apertures 188. If pressure in the chamber 166 is greater than the inlet pressure, the flexible portion 186 may deflect so that the sealing portion 189 abuts against a seat 190 and the flexible portion 186 may restrict fluid from exiting the chamber 166 through the inlet passageway 174.
The flow apertures 188 are formed as through holes in the flexible portion 186. In some embodiments, the flow apertures 188 are formed of a mesh or screen material that permits a fluid to flow therethrough. The flow apertures 188 may be of any shape and of any size that permits the fluid to pass into the chamber 166. In some embodiments, the flexible portion 186 includes a solid central portion and the flow apertures, as a screen or porous material forms the entire periphery of the flexible portion 186. Other arrangements are also contemplated.
The outlet check valve 182 will be described with reference to
In one embodiment, the enclosure structure 191 is formed of flexible media, such as for example, the same material as the flexible membrane portion 186 discussed above. In one embodiment, for example, the enclosure structure 191 may be made of parylene. In other embodiments, the enclosure structure 191 is formed of a rigid material, such as, for example, silicon, gold, titanium, or some other rigid structure material.
The enclosure structure 191 also includes one or more perforations 198 formed therethrough that permit the passage of liquid from the chamber 166 to the outlet passageway 176. In the embodiment shown, the perforations 198 include one or more through holes in a hole pattern located about where the leg portion 194 and the body portion 196 meet. In other embodiments, the perforations 198 may be formed elsewhere on the enclosure structure 191. For example, in some embodiments the perforations 198 are formed in the body structure while in other embodiments, the perforations are formed in the leg structures. In still other embodiments, the perforations are formed through a mesh-like structure or other arrangement that still allows fluid to flow from the chamber 166 to the outlet passageway 176. In addition to having the perforations, as can be understood by the above description, the enclosure structure includes some regions of non-perforations. In the embodiments shown these are found along the leg and body portions 194, 196.
The flexible portion 192 may be similar in some respects to the flexible portion 186 discussed above and the description above applies to the flexible portion 192 also. The flexible portion 192 connects to the upper surface 168 of the valve chip 162 and lies adjacent to the enclosure structure. As can be seen, the flexible portion 192 includes perforations 200 therethrough that are sized and configured to permit fluid flow therethrough. The perforations 200 may be similar to those discussed above with reference to the perforations 188 in
When the outlet check valve 182 is in the closed position shown in
When the outlet check valve 182 is in the open position shown in
In the embodiment shown, fluid may flow out of the chamber 166 through the outlet passageway 176 when the outlet check valve 182 is open. If pressure in the chamber 166 is higher than the pressure in the outlet passageway 176, then the fluid will act on the exposed membrane portion and force the outlet check valve to the open position. In the open position, the fluid may flow from the chamber 166 through the perforations 198 in the enclosure structure 191 and through the perforations 200 in the flexible portion 192 and into the outlet passageway 176. When pressure in the outlet passageway 176 is greater than the pressure in the chamber 166, the flexible portion 192 displaces to the closed position, and the perforations 200 in the flexible portion 192 are blocked by the solid portion of the enclosure structure 191. At the same time, the perforations 198 in the enclosure structure 191 are blocked by the solid portions of the flexible portion 192. As can be seen in
In the embodiment shown in
In another example, instead of having the electrolysis actuator disposed on the pump chip, the electrolysis actuator is disposed on the upper surface 168 of the valve chip 162. Accordingly, in this embodiment, all the displaceable members and/or membranes are formed on the same chip reducing the quantity of chips with flexible material processes.
A method of manufacturing the MEMS outlet check valve 182 includes forming a passageway through the chip for the passage of a fluid. The passageway may extend from an upper side 168 to a lower side 170. The flexible portion 192 may include at least one perforation 200 therethrough. In addition, the flexible portion 192 may include at least one solid region that does not readily permit flow therethrough under normal operating conditions.
The enclosure structure 191 may then be formed over the flexible portion 192. Perforations 198 in the enclosure structure 191 may be formed in locations on the enclosure structure that are offset or not aligned with perforations 200 in the flexible portion 192 when the valve is in a closed position.
In some embodiments, a MEMS inlet check valve 180 is formed on the same side of the chip as the MEMS outlet check valve 182. The inlet check valve 180 may be formed in manner similar to that described above, with an inlet passageway 174 formed through the chip and a flexible portion 186 formed over the entrance to the passageway 174. The flexible portion 186 may have perforations allowing fluid flow therethrough. Under pressure, the flexible portion 186 is configured to displace and seat on the seat 190 and prevent fluid flow out of the inlet chamber 166.
The outlet check valve disclosed herein creates new opportunities for creating flow systems, such as a fluid valve or a pump system, in a smaller and/or thinner package. The unique design of the MEMS outlet check valve allows the MEMS outlet check valve to be formed on the same side of a chip as the inlet valve. Accordingly, an entire chip layer may be eliminated from the flow system, resulting in a shorter stack of chips for the flow system. This may result in a thinner plate that may be more comfortable for the patient. In addition, since complex material deposition processing may occur on a single side of the chip, processing may be simplified and costs may be reduced.
Persons of ordinary skill in the art will appreciate that the embodiments encompassed by the present disclosure are not limited to the particular exemplary embodiments described above. In that regard, although illustrative embodiments have been shown and described, a wide range of modification, change, and substitution is contemplated in the foregoing disclosure. It is understood that such variations may be made to the foregoing without departing from the scope of the present disclosure. Accordingly, it is appropriate that the appended claims be construed broadly and in a manner consistent with the present disclosure.
This application claims the benefit of priority of U.S. Provisional Patent Application Ser. No. 61/737,964 titled “MEMS CHECK VALVE,” filed on Dec. 17, 2012, whose inventors are Cesario Pereira Dos Santos and Leslie A. Field, which is hereby incorporated by reference in its entirety as though fully and completely set forth herein.
Number | Name | Date | Kind |
---|---|---|---|
4089329 | Couvillon, Jr. et al. | May 1978 | A |
4182355 | Briel | Jan 1980 | A |
4206762 | Cosman | Jun 1980 | A |
4457757 | Molteno | Jul 1984 | A |
4560375 | Schulte et al. | Dec 1985 | A |
4604087 | Joseph | Aug 1986 | A |
4656827 | Puillet | Apr 1987 | A |
4750901 | Molteno | Jun 1988 | A |
4869282 | Sittler et al. | Sep 1989 | A |
4922913 | Waters, Jr. et al. | May 1990 | A |
5005577 | Frenkel | Apr 1991 | A |
5083742 | Wylie et al. | Jan 1992 | A |
5171132 | Miyazaki et al. | Dec 1992 | A |
5178604 | Baerveldt et al. | Jan 1993 | A |
5179953 | Kursar | Jan 1993 | A |
5397300 | Baerveldt et al. | Mar 1995 | A |
5433701 | Rubinstein | Jul 1995 | A |
5466233 | Weiner et al. | Nov 1995 | A |
5476445 | Baerveldt et al. | Dec 1995 | A |
5558629 | Baerveldt et al. | Sep 1996 | A |
5573646 | Saito et al. | Nov 1996 | A |
5626558 | Suson | May 1997 | A |
5681275 | Ahmed | Oct 1997 | A |
5702618 | Saaski et al. | Dec 1997 | A |
5707643 | Ogura et al. | Jan 1998 | A |
5722948 | Gross | Mar 1998 | A |
5891097 | Saito et al. | Apr 1999 | A |
5910110 | Bastable | Jun 1999 | A |
6007511 | Prywes | Dec 1999 | A |
6048328 | Haller et al. | Apr 2000 | A |
6050970 | Baerveldt | Apr 2000 | A |
6056269 | Johnson et al. | May 2000 | A |
6240962 | Tai et al. | Jun 2001 | B1 |
6251090 | Avery et al. | Jun 2001 | B1 |
6261256 | Ahmed | Jul 2001 | B1 |
6443893 | Schnakenberg et al. | Sep 2002 | B1 |
6447449 | Fleischman et al. | Sep 2002 | B1 |
6468283 | Richter et al. | Oct 2002 | B1 |
6533733 | Ericson et al. | Mar 2003 | B1 |
6579235 | Abita et al. | Jun 2003 | B1 |
6589198 | Soltanpour et al. | Jul 2003 | B1 |
6682500 | Soltanpour et al. | Jan 2004 | B2 |
6712764 | Jeffries et al. | Mar 2004 | B2 |
6719750 | Varner et al. | Apr 2004 | B2 |
6726676 | Stegmann et al. | Apr 2004 | B2 |
6749568 | Fleischman et al. | Jun 2004 | B2 |
6939299 | Petersen et al. | Sep 2005 | B1 |
6962573 | Wilcox | Nov 2005 | B1 |
6976982 | Santini, Jr. et al. | Dec 2005 | B2 |
7025740 | Ahmed | Apr 2006 | B2 |
7137952 | Leonardi et al. | Nov 2006 | B2 |
7169106 | Fleischman et al. | Jan 2007 | B2 |
7252006 | Tai et al. | Aug 2007 | B2 |
7304334 | Agarwal et al. | Dec 2007 | B2 |
7354416 | Quiroz-Mercado et al. | Apr 2008 | B2 |
7409863 | Bateman et al. | Aug 2008 | B2 |
7544176 | Rodgers et al. | Jun 2009 | B2 |
7565744 | Matsui et al. | Jul 2009 | B2 |
7612328 | Kaiser | Nov 2009 | B2 |
7648465 | Gordon | Jan 2010 | B2 |
7756559 | Abreu | Jul 2010 | B2 |
7824699 | Ralph et al. | Nov 2010 | B2 |
8123687 | Dacquay et al. | Feb 2012 | B2 |
8182435 | Dacquay et al. | May 2012 | B2 |
8206440 | Guarnieri | Jun 2012 | B2 |
8256465 | Christenson et al. | Sep 2012 | B2 |
8257295 | Rickard et al. | Sep 2012 | B2 |
8419673 | Rickard | Apr 2013 | B2 |
8545431 | Rickard | Oct 2013 | B2 |
8549925 | Tai et al. | Oct 2013 | B2 |
8579848 | Field et al. | Nov 2013 | B2 |
8584703 | Kobrin et al. | Nov 2013 | B2 |
8585631 | Dacquay | Nov 2013 | B2 |
8585664 | Dos Santos et al. | Nov 2013 | B2 |
8603024 | Bohm et al. | Dec 2013 | B2 |
8652085 | Gelvin et al. | Feb 2014 | B2 |
8721580 | Rickard et al. | May 2014 | B2 |
8753305 | Field et al. | Jun 2014 | B2 |
8814820 | Bergheim et al. | Aug 2014 | B2 |
8840578 | Dos Santos et al. | Sep 2014 | B2 |
8858491 | Field et al. | Oct 2014 | B2 |
8864701 | Dos Santos et al. | Oct 2014 | B2 |
8986240 | Dos Santos et al. | Mar 2015 | B2 |
9072588 | Bohm et al. | Jul 2015 | B2 |
9125721 | Field | Sep 2015 | B2 |
9132034 | Dos Santos | Sep 2015 | B2 |
20010000527 | Yaron et al. | Apr 2001 | A1 |
20020013545 | Soltanpour et al. | Jan 2002 | A1 |
20020013546 | Grieshaber et al. | Jan 2002 | A1 |
20020019607 | Bui | Feb 2002 | A1 |
20020049374 | Abreu | Apr 2002 | A1 |
20020087111 | Ethier et al. | Jul 2002 | A1 |
20020099359 | Santini, Jr. et al. | Jul 2002 | A1 |
20020103412 | Trimmer | Aug 2002 | A1 |
20020139947 | Wang | Oct 2002 | A1 |
20020143284 | Tu et al. | Oct 2002 | A1 |
20020156413 | Williams et al. | Oct 2002 | A1 |
20020156461 | Joshi | Oct 2002 | A1 |
20020165478 | Gharib et al. | Nov 2002 | A1 |
20020169468 | Brown | Nov 2002 | A1 |
20020175191 | Joshi et al. | Nov 2002 | A1 |
20020193674 | Fleischman et al. | Dec 2002 | A1 |
20030014036 | Varner et al. | Jan 2003 | A1 |
20030078487 | Jeffries et al. | Apr 2003 | A1 |
20030225318 | Montegrande et al. | Dec 2003 | A1 |
20030234376 | Cabuz et al. | Dec 2003 | A1 |
20040013702 | Glover | Jan 2004 | A1 |
20040059248 | Messner et al. | Mar 2004 | A1 |
20040073137 | Lloyd et al. | Apr 2004 | A1 |
20040073156 | Brown | Apr 2004 | A1 |
20040111050 | Smedley et al. | Jun 2004 | A1 |
20040116794 | Fink et al. | Jun 2004 | A1 |
20040186367 | Fresco | Sep 2004 | A1 |
20040228734 | Jeon et al. | Nov 2004 | A1 |
20040254438 | Chuck et al. | Dec 2004 | A1 |
20040254517 | Quiroz-Mercado et al. | Dec 2004 | A1 |
20050016866 | Kramer et al. | Jan 2005 | A1 |
20050049578 | Tu et al. | Mar 2005 | A1 |
20050067029 | Henning et al. | Mar 2005 | A1 |
20050159660 | Montegrande et al. | Jul 2005 | A1 |
20050271704 | Tu et al. | Dec 2005 | A1 |
20050273033 | Grahn et al. | Dec 2005 | A1 |
20060041220 | Boukhny et al. | Feb 2006 | A1 |
20060131350 | Schechter et al. | Jun 2006 | A1 |
20060189916 | Bas | Aug 2006 | A1 |
20070019156 | Fink | Jan 2007 | A1 |
20070032757 | Medow et al. | Feb 2007 | A1 |
20070077270 | Wen | Apr 2007 | A1 |
20070106199 | Krivoy et al. | May 2007 | A1 |
20070106200 | Levy | May 2007 | A1 |
20070109117 | Heitzmann et al. | May 2007 | A1 |
20070123767 | Montegrande et al. | May 2007 | A1 |
20070129623 | Fleischman et al. | Jun 2007 | A1 |
20070156079 | Brown | Jul 2007 | A1 |
20070212397 | Roth | Sep 2007 | A1 |
20070243111 | Momose | Oct 2007 | A1 |
20070255262 | Haase | Nov 2007 | A1 |
20080015421 | Penner | Jan 2008 | A1 |
20080027478 | Connors et al. | Jan 2008 | A1 |
20080035875 | Tai | Feb 2008 | A1 |
20080077127 | Gao et al. | Mar 2008 | A1 |
20080097276 | Bertrand et al. | Apr 2008 | A1 |
20080125691 | Yaron et al. | May 2008 | A1 |
20080129486 | Jeckelmann et al. | Jun 2008 | A1 |
20080147021 | Jani | Jun 2008 | A1 |
20080228127 | Burns et al. | Sep 2008 | A1 |
20080257915 | Wold | Oct 2008 | A1 |
20090069648 | Irazoqui et al. | Mar 2009 | A1 |
20090076367 | Sit et al. | Mar 2009 | A1 |
20090143713 | Van Dam et al. | Jun 2009 | A1 |
20090196903 | Kliman | Aug 2009 | A1 |
20090227933 | Karageozian | Sep 2009 | A1 |
20090240215 | Humayun et al. | Sep 2009 | A1 |
20090275924 | Lattanzio et al. | Nov 2009 | A1 |
20090312742 | Pang et al. | Dec 2009 | A1 |
20100010416 | Juan, Jr. et al. | Jan 2010 | A1 |
20100042209 | Guarnieri | Feb 2010 | A1 |
20100114006 | Baerveldt | May 2010 | A1 |
20100121248 | Yu et al. | May 2010 | A1 |
20100121348 | van der Burg et al. | May 2010 | A1 |
20100174272 | Weiner | Jul 2010 | A1 |
20100222769 | Meng et al. | Sep 2010 | A1 |
20100222770 | Gordon et al. | Sep 2010 | A1 |
20100234717 | Wismer | Sep 2010 | A1 |
20100249691 | Van Der Mooren et al. | Sep 2010 | A1 |
20100253167 | Charnley et al. | Oct 2010 | A1 |
20100280349 | Dacquay et al. | Nov 2010 | A1 |
20100305550 | Meng et al. | Dec 2010 | A1 |
20110046536 | Stegmann et al. | Feb 2011 | A1 |
20110071454 | Dos Santos et al. | Mar 2011 | A1 |
20110071456 | Rickard | Mar 2011 | A1 |
20110071458 | Rickard | Mar 2011 | A1 |
20110071459 | Rickard et al. | Mar 2011 | A1 |
20110071505 | Rickard et al. | Mar 2011 | A1 |
20110077626 | Baerveldt et al. | Mar 2011 | A1 |
20110082385 | Diaz et al. | Apr 2011 | A1 |
20110144617 | Meng et al. | Jun 2011 | A1 |
20110203700 | Scholten et al. | Aug 2011 | A1 |
20110248671 | Dos Santos et al. | Oct 2011 | A1 |
20110282328 | Ambati et al. | Nov 2011 | A1 |
20120004528 | Li et al. | Jan 2012 | A1 |
20120022505 | Dacquay et al. | Jan 2012 | A1 |
20120022506 | Rickard et al. | Jan 2012 | A1 |
20120039770 | Namkoong et al. | Feb 2012 | A1 |
20120296258 | Rickard et al. | Nov 2012 | A1 |
20120302861 | Marshall et al. | Nov 2012 | A1 |
20120316492 | Chappel | Dec 2012 | A1 |
20130000765 | Fernandes et al. | Jan 2013 | A1 |
20130085440 | Bohm et al. | Apr 2013 | A1 |
20130144202 | Field et al. | Jun 2013 | A1 |
20130150774 | Field et al. | Jun 2013 | A1 |
20130150775 | Dos Santos et al. | Jun 2013 | A1 |
20130150777 | Bohm et al. | Jun 2013 | A1 |
20130150778 | Dos Santos | Jun 2013 | A1 |
20130158381 | Rickard | Jun 2013 | A1 |
20130204177 | Field et al. | Aug 2013 | A1 |
20130211311 | Field | Aug 2013 | A1 |
20130211312 | Gelvin | Aug 2013 | A1 |
20130218064 | Rickard | Aug 2013 | A1 |
20130317413 | Field et al. | Nov 2013 | A1 |
20130338564 | Rickard et al. | Dec 2013 | A1 |
20140039374 | Dos Santos et al. | Feb 2014 | A1 |
20140107557 | Dos Santos et al. | Apr 2014 | A1 |
20140163448 | Lind et al. | Jun 2014 | A1 |
20140166140 | Santos et al. | Jun 2014 | A1 |
20140171777 | Sanchez et al. | Jun 2014 | A1 |
20140172090 | Gunn | Jun 2014 | A1 |
20150057523 | Gunn | Feb 2015 | A1 |
20150057592 | Gunn | Feb 2015 | A1 |
20150057593 | Johnson et al. | Feb 2015 | A1 |
20150057595 | Gunn et al. | Feb 2015 | A1 |
20150057596 | Lind et al. | Feb 2015 | A1 |
20150150720 | Gunn et al. | Jun 2015 | A1 |
20150230982 | Gunn et al. | Aug 2015 | A1 |
20150230984 | Gunn | Aug 2015 | A1 |
Number | Date | Country |
---|---|---|
101360523 | Feb 2009 | CN |
101466299 | Jun 2009 | CN |
4438201 | May 1996 | DE |
0102747 | Mar 1984 | EP |
1195523 | Apr 2002 | EP |
1296067 | Mar 2006 | EP |
1917987 | May 2008 | EP |
03049775 | Aug 1992 | JP |
2005535392 | Nov 2005 | JP |
2007512866 | May 2007 | JP |
WO9303665 | Mar 1993 | WO |
WO9803665 | Jan 1998 | WO |
WO9803809 | Jan 1998 | WO |
WO9938470 | Aug 1999 | WO |
WO0174427 | Oct 2001 | WO |
WO0194784 | Dec 2001 | WO |
WO02056758 | Jul 2002 | WO |
WO03001991 | Jan 2003 | WO |
WO03102632 | Dec 2003 | WO |
WO2004014218 | Feb 2004 | WO |
WO2005079204 | Sep 2005 | WO |
WO2005088417 | Sep 2005 | WO |
WO2007127305 | Nov 2007 | WO |
WO2007136993 | Nov 2007 | WO |
WO2008060649 | May 2008 | WO |
WO2008061043 | May 2008 | WO |
WO2008084350 | Jul 2008 | WO |
WO2008094672 | Aug 2008 | WO |
WO2009010799 | Jan 2009 | WO |
WO2009026499 | Feb 2009 | WO |
WO2009049686 | Apr 2009 | WO |
WO2009081031 | Jul 2009 | WO |
WO2010129446 | Nov 2010 | WO |
WO2010136071 | Dec 2010 | WO |
WO2011034727 | Mar 2011 | WO |
WO2011034738 | Mar 2011 | WO |
WO2011034740 | Mar 2011 | WO |
WO2011034742 | Mar 2011 | WO |
WO2011035218 | Mar 2011 | WO |
WO2012012017 | Jan 2012 | WO |
WO2013052332 | Apr 2013 | WO |
WO2013058943 | Apr 2013 | WO |
WO2013085894 | Jun 2013 | WO |
WO2013085895 | Jun 2013 | WO |
WO2013090006 | Jun 2013 | WO |
WO2013090231 | Jun 2013 | WO |
WO2013123142 | Aug 2013 | WO |
Entry |
---|
International Search Report and Written Opinion issued for PCT/US2013/074113 dated Apr. 18, 2014, 12 pgs. |
International Searching Authority, International Search Report, PCT/US2012/66709, Apr. 19, 2013, 4 pages. |
International Searching Authority, Written Opinion of the International Searching Authority, PCT/US2012/66709, Apr. 19, 2013, 5 pages. |
Byunghoon Bae, Hongseok Kee, Seonho Kim, Yeon Lee, Taeseok Sim, Yongkweon Him and Kyihwan Park; “In Vitro Experiment of the Pressure Regulating Valve for a Glaucoma Impact”; Journal of Micromechanics and Microengineering, 13 (2003); pp. 613-619. |
Eggers, T., et al, “Wireless Intra-Ocular Pressure Monitoring System Integrated Into an Artificial Lens,” 1st Annual Int'l IEEE-EMBS Special Topic Conference on Microtechnologies in Medicine & Biology, Oct. 12-14, 2000, pp. 466-469, Lyon, France. |
Greene, M.E. and Gilman, B.G., “Intraocular Pressure Measurement With Instrumented Contact Lenses,” Investigative Ophthalmology & Visual Science (IVOS), Apr. 1974, pp. 299-302, vol. 13, No. 4, IVOS. |
Hjortdal, Jesper and Jensen, Peter, “In Vitro Measurement of Corneal Strain, Thickness, and Curvature Using Digital Image Processing,” Acta Ophthalmologica Scandinavica, 1995, pp. 5-11, vol. 73, Denmark. |
International Searching Authority, International Search Report, PCT/US2010/033329, Jul. 13, 2010, 4 pages. |
International Searching Authority, Search Report and Written Opinion of the International Searching Authority, PCT/US2010/033329, Jul. 13, 2010, 8 pages. |
International Searching Authority, International Search Report, PCT/US2010/047429, Nov. 1, 2010, 4 pages. |
International Searching Authority, Written Opinion of the International Searching Authority, PCT/US2010/047429, Nov. 1, 2010, 7 pages. |
International Searching Authority, International Search Report, PCT/US2010/047600, Dec. 14, 2010, 5 pages. |
International Searching Authority, Written Opinion of the International Searching Authority, PCT/US2010/047600, Dec. 14, 2010, 7 pages. |
International Searching Authority, International Search Report, PCT/US2010/049424, Nov. 26, 2010, 6 pages. |
International Searching Authority, Written Opinion of the International Searching Authority, PCT/US2010/049424, Nov. 26, 2010, 8 pages. |
International Searching Authority, International Search Report, PCT/US2011/036742, Aug. 17, 2011, 2 pages. |
International Searching Authority, Written Opinion of the International Searching Authority, PCT/US2011/036742, Aug. 17, 2011, 5 pages. |
Lam, Andrew K.C. and Douthwaite, William A., “The Effect of an Artificially Intraocular Pressure on the Central Corneal Curvature,” Ophthalmic and Physiological Optics, 1997, pp. 18-24, vol. 17, No. 1, Elsevier Science, Ltd., Great Britain. |
Leonardi, Matteo, et al., “A Soft Contact Lens With a Mems Strain Gage Embedded for Intraocular Pressure Monitoring,” In Proc. 12th Int'l Conference on Solid State Sensors, Actuators and Microsystems, Jun. 8-12, 2003, pp. 1043-1046, Vol. 2, Boston, MA. |
Leonardi, Matteo, et al., “First Steps Toward Noninvasive Intraocular Pressure Monitoring with a Sensing Contact Lens,” Investigative Ophthalmology & Visual Science (IVOS), 2004, pp. 3113-3117, vol. 45, No. 9, IVOS. |
McLaren, Jay W., et al, “Continuous Measurement of Intraocular Pressure in Rabbits by Telemetry,” Investigative Ophthalmology & Visual Science (IVOS), May 1996, pp. 966-975, vol. 37, No. 6, IVOS. |
Puers, Robert, “Linking Sensors with Telemetry: Impact on the System Design,” In Proc. 8th Int'l Conference of Solid State Sensors, Actuators, Eurosens, Jun. 25-29, 1995, pp. 169-174, Stockholm, Sweden. |
Schnakenberg, U., et al, “Initial Investigations on Systems for Measuring Intraocular Pressure,” Sensors and Actuators, 2000, p. 287-291, vol. 85, Elsevier Science B.V., Germany. |
Stangel, Karsten, et al, “A Programmable Intraocular CMOS Pressure Sensor System Implant,” IEEE Journal of Solid-State Circuits, Jul. 2001, pp. 1094-1100, vol. 36, No. 7, IEEE, Germany. |
Ullerich, Stella, et al, “Micro Coils for an Advanced System for Measuring Intraocular Pressure,” 1st Annual Int'l IEEE-EMBS Special Topic Conference on Microtechnologies in Medicine & Biology, Oct. 12-14, 2000, pp. 470-474, Lyon, France. |
Van Schuylenbergh, K., et al, “An Implantable Telemetric Tonometer for Direct Intraocular Pressure Measurements,” 1st European Conference on Biomedical Engineering, Feb. 1991, pp. 194-195, vol. 17, No. 20, Nice, France. |
Walter, Peter; Intraocular Pressure Sensor: Where Are We—Where Will We Go? Journal Graefe's Archive for Clinical and Experimental Ophthalmology; Publisher Springer Berline/Heidelberg; ISSN 0721-832X (Print) 1435-702X (Online); Issue vol. 240, No. 5/May 2002 DOI 10.1007/s00417-002-0474-y; pp. 335-336; Subject Collection Medicine. |
Neagu Cristina R.; “A Medical Microactuator Based on an Electrochemical Principle”; Thesis at the Twente University,the Netherlands, Enschede; Aug. 28, 1998; pp. 1-162. |
Saloomeh Saati M.D., et al.; “Mini Drug Pump for Ophthalmic Use”; TRANS Am Ophthalmol Soc 2009; 107; pp. 60-71. |
Stemme et al.; “A Valveless Diffuser/Nozzle-Based Fluid Pump”; ScienceDirect; Sensors and Actuators A, 39; pp. 159-167 (1993). |
Nisar, et al.; MEMS-Based Micropumps in Drug Delivery and Biomedical Applications; ScienceDirect; Sensors and Actuators B 130; pp. 917-942 (2008). |
International Searching Authority, International Search Report, PCT US2010/047605; Dec. 16, 2010, 7 pages. |
International Searching Authority, Written Opinion of the International Searching Authority, PCT US2010/047605; Dec. 16, 2010, 9 pages. |
International Searching Authority, International Search Report, PCT/US2010/047612; Dec. 21, 2010, 7 pages. |
Internationl Searching Authority, Written Opinion of the International Searching Authority, PCT/US2010/047612; Dec. 21, 2010, 10 pages. |
Driot et al.; “Ocular pharmacokinetics of fluocinolone acetonide after RetisertTM intravitreal implantation mplantation in rabbits over a 1-year period”; J. Ocular Pharm; 20; 3;pp. 269-275. |
Kuppermann B D et al., 2006, “Efficacy and safety of a novel intravitreous dexamethasone drug-delivery system after applicator or incisional placement in patients with macular edema”, IOVS, 47 ARVO E-Abs 5913. |
Miyamoto H et al., 1997, Biodegradable scleral implant for intravitreal controlled release of fluconazole, Curr Eye Res, 16(9), 930-935. |
Mruthyunjaya P et al., 2003, “An intravitreal sustained release fluocinolone acetonide device to treat severe experimental uveitis”, IOVS, 44, ARVO E-Abs 4215. |
Ratanapakorn T et al., 2005, “Helical intravitreal triamcinolone implant: An explanation survival study”, IVOS 46 E-Abs 484. |
Rego MGR et al., 2004, “In vitro evaluation of sustained-release intravitreal dexamethasone implants”, IOVS, 45 E-Abs 5060. |
Sakurai E et al., 2001, “Scleral plug of biodegradable polymers containing ganciclovir for experimental cytomegalovirus retinitis”, IOVS, 42(9), 2043-2048. |
See R F et al., 2006, “Safety and drug release profile of injectable intravitreal sustained-release fluocinolone acetonide device”, IOVS, 47, ARVO E-Abs 5119. |
Tano R et al., 2005, Helical intravitreal implant: surgical method development and outcomes, IOVS, 46, ARVO E-Abs 483. |
Varner S E et al., 2003, “Development of a minimally invasive intravitreal implant for drug delivery”, IOVS, 44, ARVO E-Abs 4214. |
Weiner A L, 2007, “Drug Delivery Systems in Ophthalmic Applications, In: Ocular Therapeutics; Eye on New Discoveries; T. Yorio, A. Clark, M.Wax, Eds, Elsevier Press/Academic Press, New York”, pp. 7-43. |
Yasukawa T et al., 2001, “Biodegradable scleral plugs for vitreoretinal drug delivery”, Adv. Drug Del Rev., 52(1), 25-36. |
International Searching Authority, International Search Report, PCT/US2013/026066, Apr. 17, 2013, 5 pages. |
International Searching Authority, Written Opinion of the International Searching Authority, PCT/US2013/026066, Apr. 17, 2013, 8 pages. |
Parkhutik, Vitali, et al., The Role of Hydrogen in the Formation of Porous Structures in Silicon, Materials Science & Engineering, 1999, B58, 95-99, Elsevier Science, S.A. |
Dacquay, Bruno, Intraocular Pressure Sensor, Prosecution History, U.S. Appl. No. 12/434,709, filed May 4, 2009, 566 pages. |
Rickard, Matthew J.A., Lumen Clearing Valve for Glaucoma Drainage Device, Prosecution History, U.S. Appl. No. 12/609,043, filed Oct. 30, 2009, 1507 pages. |
Rickard, Matthew, Intraocular Pressure Sensor with External Pressure Compensation, Prosecution History, U.S. Appl. No. 12/563,244, filed Sep. 21, 2009, 562 pages. |
Dos Santos, Cesario, Power Generator for Glaucoma Drainage Device, Prosecution History, U.S. Appl. No. 12/685,772, filed Jan. 12, 2010, 517 pages. |
Dacquay, Bruno, Closed Loop Glaucoma Drug Delivery System, Prosecution History, U.S. Appl. No. 13/109,155, filed May 17, 2011, 238 pages. |
Field, Leslie, Active Drainage Systems with Pressure-Driven Valves and Electronically-Driven Pump, Prosecution History, U.S. Appl. No. 13/315,329, filed Dec. 9, 2011, 1620 pages. |
Rickard, Matthew J.A., Power Saving Glaucoma Drainage Device, Prosecution History, U.S. Appl. No. 12/837,803, filed Jul. 16, 2010, 1725 pages. |
Dos Santos, Cecario P., Multilayer Membrane Actuators, Prosecution History, U.S. Appl. No. 13/315,905, filed Dec. 9, 2011, 1652 pages. |
Rickard, Matthew, Intraocular Pressure Sensor with External Pressure Compensation, Prosecution History,U.S. Appl. No. 14/267,443, filed May 1, 2014, 53 pages. |
Rickard, Matthew, Intraocular Pressure Sensor with External Pressure Compensation, Prosecution History, U.S. Appl. No. 13/565,907, filed Aug. 3, 2012, 1652 pages. |
Barton, Keith, et al., “The Ahmed Baerveldt Comparison Study,” Journal of Ophthalmology, Jul. 15, 2010, vol. 118, No. 3, Elsevier, Inc., USA. |
International Searching Authority, Search Report of the International Searching Authority, PCT/US2012/057261, Jan. 23, 2013, 7 pages. |
International Searching Authority, Written Opinion of the International Searching Authority, PCT/US2012/057261, Jan. 23, 2013, 8 pages. |
International Searching Authority, International Search Report, PCT/US2014/039582, Oct. 22, 2014, 3 pages. |
International Searching Authority, Written Opinion, PCT/US2014/039582, Oct. 22, 2014, 3 pages. |
Mokwa et al., “Mircro-Transponder Systems for Medical Applications”, IEEE Transactions on Instrumentation and Measurement, vol. 50, No. 6, Dec. 2001, 5 pgs. |
Number | Date | Country | |
---|---|---|---|
20140166140 A1 | Jun 2014 | US |
Number | Date | Country | |
---|---|---|---|
61737964 | Dec 2012 | US |