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Mini drug pump for ophthalmic use
To evaluate the feasibility of developing a novel mini drug pump for ophthalmic use. Using principles of microelectromechanical systems engineering, a mini drug pump was fabricated. The pumping mechanism is based on electrolysis, and the pump includes a drug refill port as well as a check valve to c...
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Published in: | Transactions of the American Ophthalmological Society 2009-12, Vol.107, p.60-70 |
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creator | Saati, Saloomeh Lo, Ronalee Li, Po-Ying Meng, Ellis Varma, Rohit Humayun, Mark S |
description | To evaluate the feasibility of developing a novel mini drug pump for ophthalmic use.
Using principles of microelectromechanical systems engineering, a mini drug pump was fabricated. The pumping mechanism is based on electrolysis, and the pump includes a drug refill port as well as a check valve to control drug delivery. Drug pumps were tested first on the benchtop and then after implantation in rabbits. For the latter, we implanted 4 elliptical (9.9 x 7.7 x 1.8 mm) non-electrically active pumps into 4 rabbits. The procedure is similar to implantation of a glaucoma seton. To determine the ability to refill and also the patency of the cannula, at intervals of 4 to 6 weeks after implantation, we accessed the drug reservoir with a transconjunctival needle and delivered approximately as low as 1 microL of trypan blue solution (0.06%) into the anterior chamber. Animals were followed up by slit-lamp examination, photography, and fluorescein angiography.
Benchtop testing showed 2.0 microL/min delivery when using 0.4 mW of power for electrolysis. One-way valves showed reliable opening pressures of 470 mm Hg. All implanted devices refilled at 4- to 6-week intervals for 4 to 6 months. No infection was seen. No devices extruded. No filtering bleb formed over the implant.
A prototype ocular mini drug pump was built, implanted, and refilled. Such a platform needs more testing to determine the long-term biocompatibility of an electrically controlled implanted pump. Testing with various pharmacologic agents is needed to determine its ultimate potential for ophthalmic use. |
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Using principles of microelectromechanical systems engineering, a mini drug pump was fabricated. The pumping mechanism is based on electrolysis, and the pump includes a drug refill port as well as a check valve to control drug delivery. Drug pumps were tested first on the benchtop and then after implantation in rabbits. For the latter, we implanted 4 elliptical (9.9 x 7.7 x 1.8 mm) non-electrically active pumps into 4 rabbits. The procedure is similar to implantation of a glaucoma seton. To determine the ability to refill and also the patency of the cannula, at intervals of 4 to 6 weeks after implantation, we accessed the drug reservoir with a transconjunctival needle and delivered approximately as low as 1 microL of trypan blue solution (0.06%) into the anterior chamber. Animals were followed up by slit-lamp examination, photography, and fluorescein angiography.
Benchtop testing showed 2.0 microL/min delivery when using 0.4 mW of power for electrolysis. One-way valves showed reliable opening pressures of 470 mm Hg. All implanted devices refilled at 4- to 6-week intervals for 4 to 6 months. No infection was seen. No devices extruded. No filtering bleb formed over the implant.
A prototype ocular mini drug pump was built, implanted, and refilled. Such a platform needs more testing to determine the long-term biocompatibility of an electrically controlled implanted pump. Testing with various pharmacologic agents is needed to determine its ultimate potential for ophthalmic use.</description><identifier>ISSN: 0065-9533</identifier><identifier>EISSN: 1545-6110</identifier><identifier>PMID: 20126483</identifier><language>eng</language><publisher>United States: The American Ophthalmological Society</publisher><subject>Animals ; Anterior Chamber - surgery ; Coloring Agents - administration & dosage ; Cornea - pathology ; Drug Delivery Systems - instrumentation ; Electrolysis - instrumentation ; Equipment Design ; Feasibility Studies ; Fluorescein Angiography ; In Vitro Techniques ; Microscopy, Electron ; Ophthalmic Solutions - administration & dosage ; Ophthalmologic Surgical Procedures ; Prostheses and Implants ; Rabbits ; Swine ; Trypan Blue - administration & dosage</subject><ispartof>Transactions of the American Ophthalmological Society, 2009-12, Vol.107, p.60-70</ispartof><rights>American Ophthalmological Society 2009</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2814560/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2814560/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20126483$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saati, Saloomeh</creatorcontrib><creatorcontrib>Lo, Ronalee</creatorcontrib><creatorcontrib>Li, Po-Ying</creatorcontrib><creatorcontrib>Meng, Ellis</creatorcontrib><creatorcontrib>Varma, Rohit</creatorcontrib><creatorcontrib>Humayun, Mark S</creatorcontrib><title>Mini drug pump for ophthalmic use</title><title>Transactions of the American Ophthalmological Society</title><addtitle>Trans Am Ophthalmol Soc</addtitle><description>To evaluate the feasibility of developing a novel mini drug pump for ophthalmic use.
Using principles of microelectromechanical systems engineering, a mini drug pump was fabricated. The pumping mechanism is based on electrolysis, and the pump includes a drug refill port as well as a check valve to control drug delivery. Drug pumps were tested first on the benchtop and then after implantation in rabbits. For the latter, we implanted 4 elliptical (9.9 x 7.7 x 1.8 mm) non-electrically active pumps into 4 rabbits. The procedure is similar to implantation of a glaucoma seton. To determine the ability to refill and also the patency of the cannula, at intervals of 4 to 6 weeks after implantation, we accessed the drug reservoir with a transconjunctival needle and delivered approximately as low as 1 microL of trypan blue solution (0.06%) into the anterior chamber. Animals were followed up by slit-lamp examination, photography, and fluorescein angiography.
Benchtop testing showed 2.0 microL/min delivery when using 0.4 mW of power for electrolysis. One-way valves showed reliable opening pressures of 470 mm Hg. All implanted devices refilled at 4- to 6-week intervals for 4 to 6 months. No infection was seen. No devices extruded. No filtering bleb formed over the implant.
A prototype ocular mini drug pump was built, implanted, and refilled. Such a platform needs more testing to determine the long-term biocompatibility of an electrically controlled implanted pump. Testing with various pharmacologic agents is needed to determine its ultimate potential for ophthalmic use.</description><subject>Animals</subject><subject>Anterior Chamber - surgery</subject><subject>Coloring Agents - administration & dosage</subject><subject>Cornea - pathology</subject><subject>Drug Delivery Systems - instrumentation</subject><subject>Electrolysis - instrumentation</subject><subject>Equipment Design</subject><subject>Feasibility Studies</subject><subject>Fluorescein Angiography</subject><subject>In Vitro Techniques</subject><subject>Microscopy, Electron</subject><subject>Ophthalmic Solutions - administration & dosage</subject><subject>Ophthalmologic Surgical Procedures</subject><subject>Prostheses and Implants</subject><subject>Rabbits</subject><subject>Swine</subject><subject>Trypan Blue - administration & dosage</subject><issn>0065-9533</issn><issn>1545-6110</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNpVkM1KxDAAhIMobl19BaknT4X8p7kIsugqrHjRc0jbZBtpm5g0gm9vwVX0NDAzfANzBArEKKs4QvAYFBByVklGyAqcpfQGIREE8VOwwhBhTmtSgKsnN7myi3lfhjyG0vpY-tDPvR5G15Y5mXNwYvWQzMVB1-D1_u5l81DtnrePm9tdFVAN58rUCBpkurazmIu6I7a1lEkkmLGNFYvJKYUCQ80bKjtDcaOJkFo0WDBsWrIGN9_ckJtx4ZhpjnpQIbpRx0_ltVP_k8n1au8_FK4RZRwugOsDIPr3bNKsRpdaMwx6Mj4nJQiRTHAul-bl36nfjZ9byBfKA192</recordid><startdate>20091201</startdate><enddate>20091201</enddate><creator>Saati, Saloomeh</creator><creator>Lo, Ronalee</creator><creator>Li, Po-Ying</creator><creator>Meng, Ellis</creator><creator>Varma, Rohit</creator><creator>Humayun, Mark S</creator><general>The American Ophthalmological Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20091201</creationdate><title>Mini drug pump for ophthalmic use</title><author>Saati, Saloomeh ; Lo, Ronalee ; Li, Po-Ying ; Meng, Ellis ; Varma, Rohit ; Humayun, Mark S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p180t-e810e1edcdf2678d3fcf459175efbf7f266440720a6b49de42ba379a7b2752ec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Anterior Chamber - surgery</topic><topic>Coloring Agents - administration & dosage</topic><topic>Cornea - pathology</topic><topic>Drug Delivery Systems - instrumentation</topic><topic>Electrolysis - instrumentation</topic><topic>Equipment Design</topic><topic>Feasibility Studies</topic><topic>Fluorescein Angiography</topic><topic>In Vitro Techniques</topic><topic>Microscopy, Electron</topic><topic>Ophthalmic Solutions - administration & dosage</topic><topic>Ophthalmologic Surgical Procedures</topic><topic>Prostheses and Implants</topic><topic>Rabbits</topic><topic>Swine</topic><topic>Trypan Blue - administration & dosage</topic><toplevel>online_resources</toplevel><creatorcontrib>Saati, Saloomeh</creatorcontrib><creatorcontrib>Lo, Ronalee</creatorcontrib><creatorcontrib>Li, Po-Ying</creatorcontrib><creatorcontrib>Meng, Ellis</creatorcontrib><creatorcontrib>Varma, Rohit</creatorcontrib><creatorcontrib>Humayun, Mark S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Transactions of the American Ophthalmological Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saati, Saloomeh</au><au>Lo, Ronalee</au><au>Li, Po-Ying</au><au>Meng, Ellis</au><au>Varma, Rohit</au><au>Humayun, Mark S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mini drug pump for ophthalmic use</atitle><jtitle>Transactions of the American Ophthalmological Society</jtitle><addtitle>Trans Am Ophthalmol Soc</addtitle><date>2009-12-01</date><risdate>2009</risdate><volume>107</volume><spage>60</spage><epage>70</epage><pages>60-70</pages><issn>0065-9533</issn><eissn>1545-6110</eissn><abstract>To evaluate the feasibility of developing a novel mini drug pump for ophthalmic use.
Using principles of microelectromechanical systems engineering, a mini drug pump was fabricated. The pumping mechanism is based on electrolysis, and the pump includes a drug refill port as well as a check valve to control drug delivery. Drug pumps were tested first on the benchtop and then after implantation in rabbits. For the latter, we implanted 4 elliptical (9.9 x 7.7 x 1.8 mm) non-electrically active pumps into 4 rabbits. The procedure is similar to implantation of a glaucoma seton. To determine the ability to refill and also the patency of the cannula, at intervals of 4 to 6 weeks after implantation, we accessed the drug reservoir with a transconjunctival needle and delivered approximately as low as 1 microL of trypan blue solution (0.06%) into the anterior chamber. Animals were followed up by slit-lamp examination, photography, and fluorescein angiography.
Benchtop testing showed 2.0 microL/min delivery when using 0.4 mW of power for electrolysis. One-way valves showed reliable opening pressures of 470 mm Hg. All implanted devices refilled at 4- to 6-week intervals for 4 to 6 months. No infection was seen. No devices extruded. No filtering bleb formed over the implant.
A prototype ocular mini drug pump was built, implanted, and refilled. Such a platform needs more testing to determine the long-term biocompatibility of an electrically controlled implanted pump. Testing with various pharmacologic agents is needed to determine its ultimate potential for ophthalmic use.</abstract><cop>United States</cop><pub>The American Ophthalmological Society</pub><pmid>20126483</pmid><tpages>11</tpages></addata></record> |
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subjects | Animals Anterior Chamber - surgery Coloring Agents - administration & dosage Cornea - pathology Drug Delivery Systems - instrumentation Electrolysis - instrumentation Equipment Design Feasibility Studies Fluorescein Angiography In Vitro Techniques Microscopy, Electron Ophthalmic Solutions - administration & dosage Ophthalmologic Surgical Procedures Prostheses and Implants Rabbits Swine Trypan Blue - administration & dosage |
title | Mini drug pump for ophthalmic use |
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