Objective: To identify prospective oxidants that rapidly immobilize human s
perm upon contact with human semen.
Design: Inorganic, organic, and enzymatically-generated oxidants were mixed
with human semen and spermicidal activity was tracked by a modified Sander
-Cramer assay.
Setting: Commercial and university-based laboratories.
Patient(s): Semen samples obtained through a university-based andrology lab
oratory.
Intervention(s): Not applicable.
Main Outcome Measures(s): Quantitation of spermicidal activity of test oxid
ants.
Result(s): Sperm lost motility within 20 seconds of exposure to enzymatical
ly generated free iodine (I,). Toluidine blue, phenazine methosulfate, or m
ethylene blue exhibited some, albeit much less, spermicidal activity. Oxida
nts formed by mixing ascorbic acid with Fe(III)-EDTA, xanthine with xanthin
e oxidase, or by exposing sperm to the nitric oxide generator, SIN-1 (3-mor
pholinosydnonimine hydrochloride), were far less potent spermicidal agents.
Conclusion(s): Free I, formed in situ and presented to semen is an extremel
y potent spermicide. Additional studies on methods of generating de novo I,
may be beneficial in developing a novel new class of nondetergent-based sp
ermicides. (C) 2001 by American Society for Reproductive Medicine.