May 2004
Volume 45, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2004
Development of Microelectromechanical Systems(MEMS) forceps for intraocular surgery.
Author Affiliations & Notes
  • D.D. S. Pereira
    Ophthalmology, UCSF School of Medicine, San Francisco, CA
  • C. Keller
    Berkeley Sensor and Actuator Center, University of California Berkeley, Berkeley, CA
  • R.B. Bhisitkul
    Ophthalmology, UCSF School of Medicine, San Francisco, CA
  • Footnotes
    Commercial Relationships  D.D.S. Pereira, None; C. Keller, MEMS Precision Instruments E, P; R.B. Bhisitkul, None.
  • Footnotes
    Support  That Man May See Foundation, Grant #989004
Investigative Ophthalmology & Visual Science May 2004, Vol.45, 2021. doi:
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      D.D. S. Pereira, C. Keller, R.B. Bhisitkul; Development of Microelectromechanical Systems(MEMS) forceps for intraocular surgery. . Invest. Ophthalmol. Vis. Sci. 2004;45(13):2021.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Abstract: : Purpose: To develop silicon microforceps for intraocular surgery using MEMS technology, the application of microchip fabrication techniques to produce movable, controllable three–dimensional devices on the micron scale. Methods: A variety of MEMS forceps prototypes were manufactured of single crystal silicon at the microfabrication facility of the Berkeley Sensor and Actuator Center. Designs using both thermoelectric actuators and conventional mechanical handles were employed to open and close the forceps. Forceps were tested for functionality in human cadaver eyes and rabbit eyes in vivo using standard vitreoretinal surgery. Results: MEMS forceps were constructed with tip sizes ranging from 200 microns to 2 mm. Scanning electron microscopy confirmed accurate construction of microfeatures such as forceps teeth designed as small as 10 microns. Surgical videos demonstrated that in cadaveric and rabbit eyes the forceps tips were sufficiently durable and rigid for repetitive vitreoretinal surgical maneuvers, including grasping retinal membranes and excising tissue. Heat dispersion plates in the thermoelectric actuator design were found to malfunction due to surface protein coagulation; mechanical spring–activated handles were successful in the environment of the vitreous cavity. While handheld operation was possible, the precision of the forceps was best exploited when mounted on a 3–axis micromanipulator. Conclusions: MEMS microforceps are feasible for conventional vitreoretinal surgery, and offer advances in small scale and precision.

Keywords: vitreoretinal surgery • retina • microscopy: electron microscopy 
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