7 March 2006New styrene-b-isobutylene-b-styrene (SIBS) glaucoma drainage implant
Marcia Orozco, Ana C. Acosta, Edgar M. Espana, Leonard Pinchuk, Bruce A. Weber, Stewart Davis, Esdras Arrieta, Sander Dubovy, Francisco Fantes, Mohamed Aly, Yonghua Zhou, Jean-Marie Parel
Marcia Orozco,1,2 Ana C. Acosta,1 Edgar M. Espana,1 Leonard Pinchuk,1,2,3 Bruce A. Weber,3 Stewart Davis,3 Esdras Arrieta,1 Sander Dubovy,1 Francisco Fantes,1 Mohamed Aly,1 Yonghua Zhou,3 Jean-Marie Parel1,2,4
1Bascom Palmer Eye Institute, Miller School of Medicine, Univ. of Miami (United States) 2Univ. of Miami (United States) 3InnFocus, LLC (United States) 4Univ. of Liege (Belgium)
PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.
Purpose: To design and test the Miami-InnFocus Drainage Implant (MiDi) as a glaucoma shunt that is biocompatible,
flexible, and significantly smaller than existing commercial implants in order to prevent postoperative hypotony, inflammation, scarring, erosion, and extrusion.
Methods: A new biomaterial composed of styrene-b-isobutylene-b-styrene (SIBS) was used in a novel design for a glaucoma drainage implant. The implant consists of a tube 11mm long with an inner diameter of 70, 100, and 150 μm
and outer diameter of 250 μm with a 1mm2 tab located 4.5mm from the proximal tip to prevent migration. The device
was implanted in 15 New Zealand White rabbits for biocompatibility and efficacy testing. A similarly designed implant
made of polydimethylsiloxane was implanted in 6 other animals as a pseudo-control. Typical GDI implantation
technique was modified for this device. The proximal end of the new SIBS implant was inserted 2mm into the anterior
chamber and the distal end placed in a subconjunctival space created by the surgeon. Biocompatibility of the device was
studied by slit-lamp follow-up and intraocular pressure (IOP) measurements recorded periodically. Results:
Biocompatibility of the MiDi was excellent. A low and diffuse bleb was observed with these devices. All SIBS tubes
were patent 9 months after insertion. Immunostaining demonstrated non-continuous deposition of collagen with virtually
no encapsulation. No macrophages or myofibroblast were visible around the SIBS polymer which was found more
bioinert than the control PDMS.
Conclusion: This newly designed glaucoma implant is clinically biocompatible in the rabbit model and maintained
100% patency at 9 months.
PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.
The alert did not successfully save. Please try again later.
Marcia Orozco, Ana C. Acosta, Edgar M. Espana, Leonard Pinchuk, Bruce A. Weber, Stewart Davis, Esdras Arrieta, Sander Dubovy, Francisco Fantes, Mohamed Aly, Yonghua Zhou, Jean-Marie Parel, "New styrene-b-isobutylene-b-styrene (SIBS) glaucoma drainage implant," Proc. SPIE 6138, Ophthalmic Technologies XVI, 61380U (7 March 2006); https://doi.org/10.1117/12.652297