Motile and non-motile sperm diagnostic manipulation using optoelectronic tweezers

Lab Chip. 2010 Dec 7;10(23):3213-7. doi: 10.1039/c0lc00072h. Epub 2010 Sep 8.

Abstract

Optoelectronic tweezers was used to manipulate human spermatozoa to determine whether their response to OET predicts sperm viability among non-motile sperm. We review the electro-physical basis for how live and dead human spermatozoa respond to OET. The maximal velocity that non-motile spermatozoa could be induced to move by attraction or repulsion to a moving OET field was measured. Viable sperm are attracted to OET fields and can be induced to move at an average maximal velocity of 8.8 ± 4.2 µm s(-1), while non-viable sperm are repelled to OET, and are induced to move at an average maximal velocity of -0.8 ± 1.0 µm s(-1). Manipulation of the sperm using OET does not appear to result in increased DNA fragmentation, making this a potential method by which to identify viable non-motile sperm for assisted reproductive technologies.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Cryopreservation
  • DNA Fragmentation
  • Equipment Design
  • Humans
  • Male
  • Optical Tweezers*
  • Reproductive Techniques, Assisted
  • Sperm Count
  • Sperm Injections, Intracytoplasmic / methods
  • Sperm Motility*
  • Sperm Retrieval
  • Spermatozoa / pathology
  • Spermatozoa / physiology