Evaluation of Tissue Interactions with Mechanical Elements of a Transscleral Drug Delivery Device

The goal of this work was to evaluate tissue-device interactions due to implantation of a mechanically operated drug delivery system onto the posterior sclera. Two test devices were designed and fabricated to model elements of the drug delivery device—one containing a free-spinning ball bearing and...

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Main Authors: Jeffrey T. Borenstein, Evangelos S. Gragoudas, Joan W. Miller, Christopher M. Andreoli, Mark Keegan, Robison V. Paul Chan, Sarah J. Cohen
Format: Article
Language:English
Published: MDPI AG 2012-03-01
Series:Pharmaceutics
Subjects:
Online Access:http://www.mdpi.com/1999-4923/4/1/212/
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author Jeffrey T. Borenstein
Evangelos S. Gragoudas
Joan W. Miller
Christopher M. Andreoli
Mark Keegan
Robison V. Paul Chan
Sarah J. Cohen
author_facet Jeffrey T. Borenstein
Evangelos S. Gragoudas
Joan W. Miller
Christopher M. Andreoli
Mark Keegan
Robison V. Paul Chan
Sarah J. Cohen
author_sort Jeffrey T. Borenstein
collection DOAJ
description The goal of this work was to evaluate tissue-device interactions due to implantation of a mechanically operated drug delivery system onto the posterior sclera. Two test devices were designed and fabricated to model elements of the drug delivery device—one containing a free-spinning ball bearing and the other encasing two articulating gears. Openings in the base of test devices modeled ports for drug passage from device to sclera. Porous poly(tetrafluoroethylene) (PTFE) membranes were attached to half of the gear devices to minimize tissue ingrowth through these ports. Test devices were sutured onto rabbit eyes for 10 weeks. Tissue-device interactions were evaluated histologically and mechanically after removal to determine effects on device function and changes in surrounding tissue. Test devices were generally well-tolerated during residence in the animal. All devices encouraged fibrous tissue formation between the sclera and the device, fibrous tissue encapsulation and invasion around the device, and inflammation of the conjunctiva. Gear devices encouraged significantly greater inflammation in all cases and a larger rate of tissue ingrowth. PTFE membranes prevented tissue invasion through the covered drug ports, though tissue migrated in through other smaller openings. The torque required to turn the mechanical elements increased over 1000 times for gear devices, but only on the order of 100 times for membrane-covered gear devices and less than 100 times for ball bearing devices. Maintaining a lower device profile, minimizing microscale motion on the eye surface and covering drug ports with a porous membrane may minimize inflammation, decreasing the risk of damage to surrounding tissues and minimizing disruption of device operation.
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spelling doaj.art-9938b80dda424e2496029e4f2a6bb9422022-12-22T04:03:40ZengMDPI AGPharmaceutics1999-49232012-03-014121222910.3390/pharmaceutics4010212Evaluation of Tissue Interactions with Mechanical Elements of a Transscleral Drug Delivery DeviceJeffrey T. BorensteinEvangelos S. GragoudasJoan W. MillerChristopher M. AndreoliMark KeeganRobison V. Paul ChanSarah J. CohenThe goal of this work was to evaluate tissue-device interactions due to implantation of a mechanically operated drug delivery system onto the posterior sclera. Two test devices were designed and fabricated to model elements of the drug delivery device—one containing a free-spinning ball bearing and the other encasing two articulating gears. Openings in the base of test devices modeled ports for drug passage from device to sclera. Porous poly(tetrafluoroethylene) (PTFE) membranes were attached to half of the gear devices to minimize tissue ingrowth through these ports. Test devices were sutured onto rabbit eyes for 10 weeks. Tissue-device interactions were evaluated histologically and mechanically after removal to determine effects on device function and changes in surrounding tissue. Test devices were generally well-tolerated during residence in the animal. All devices encouraged fibrous tissue formation between the sclera and the device, fibrous tissue encapsulation and invasion around the device, and inflammation of the conjunctiva. Gear devices encouraged significantly greater inflammation in all cases and a larger rate of tissue ingrowth. PTFE membranes prevented tissue invasion through the covered drug ports, though tissue migrated in through other smaller openings. The torque required to turn the mechanical elements increased over 1000 times for gear devices, but only on the order of 100 times for membrane-covered gear devices and less than 100 times for ball bearing devices. Maintaining a lower device profile, minimizing microscale motion on the eye surface and covering drug ports with a porous membrane may minimize inflammation, decreasing the risk of damage to surrounding tissues and minimizing disruption of device operation.http://www.mdpi.com/1999-4923/4/1/212/age-related macular degenerationdrug deliverytransscleral
spellingShingle Jeffrey T. Borenstein
Evangelos S. Gragoudas
Joan W. Miller
Christopher M. Andreoli
Mark Keegan
Robison V. Paul Chan
Sarah J. Cohen
Evaluation of Tissue Interactions with Mechanical Elements of a Transscleral Drug Delivery Device
Pharmaceutics
age-related macular degeneration
drug delivery
transscleral
title Evaluation of Tissue Interactions with Mechanical Elements of a Transscleral Drug Delivery Device
title_full Evaluation of Tissue Interactions with Mechanical Elements of a Transscleral Drug Delivery Device
title_fullStr Evaluation of Tissue Interactions with Mechanical Elements of a Transscleral Drug Delivery Device
title_full_unstemmed Evaluation of Tissue Interactions with Mechanical Elements of a Transscleral Drug Delivery Device
title_short Evaluation of Tissue Interactions with Mechanical Elements of a Transscleral Drug Delivery Device
title_sort evaluation of tissue interactions with mechanical elements of a transscleral drug delivery device
topic age-related macular degeneration
drug delivery
transscleral
url http://www.mdpi.com/1999-4923/4/1/212/
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