Preclinical evaluation of sodium cellulose sulfate (Ushercell) as a contraceptive antimicrobial agent

RA Anderson, KA Feathergill, XHUI DIAO… - Journal of …, 2002 - Wiley Online Library
RA Anderson, KA Feathergill, XHUI DIAO, MD Cooper, R Kirkpatrick, BC Herold, GF Doncel…
Journal of andrology, 2002Wiley Online Library
The spread of sexually transmitted infections (STIs) and limited methods for control of
pregnancies presents high risks to the reproductive health of women. Methods controlled by
women and directed toward disease prevention and contraception are needed. We report
on preclinical studies of the biological properties of sodium cellulose sulfate (Ushercell)
currently being developed for use as a topical contraceptive antimicrobial agent. Ushercell
was evaluated with tests designed to identify its contraceptive and antimicrobial properties …
Abstract
The spread of sexually transmitted infections (STIs) and limited methods for control of pregnancies presents high risks to the reproductive health of women. Methods controlled by women and directed toward disease prevention and contraception are needed. We report on preclinical studies of the biological properties of sodium cellulose sulfate (Ushercell) currently being developed for use as a topical contraceptive antimicrobial agent. Ushercell was evaluated with tests designed to identify its contraceptive and antimicrobial properties. Ushercell inhibits hyaluronidase (reversible; IC50 = 1.7 mg/mL), impairs sperm penetration of cervical mucus (approximately 70% inhibition at 1 mg/mL), and acts as a stimulus for acrosomal loss (IC50 = 52 ng/mL). It prevents conception in rabbits when added to spermatozoa (approximately 95% inhibition at 1 mg/mL) or when vaginally applied (complete contraception by 45 mg) before insemination. However, up to 50 mg/mL, Ushercell does not irreversibly immobilize spermatozoa, suggesting that Ushercell is not cytotoxic. Ushercell has a broad spectrum of antimicrobial activity in vitro. Inhibited microbes include human immunodeficiency viruses (different laboratory strains and clinical isolates; IC50 values range from 3 to 78 μg/mL), herpes viruses, HSV‐1 (IC50 = 59 ng/mL) and HSV‐2 (IC50 = 24 ng/mL), Neisseria gonorrhoeae (IC50 = 2 μg/mL), and Chlamydia trachomatis (IC50 = 78 μg/mL). In contrast, Ushercell does not inhibit growth of beneficial vaginal bacteria, Lactobacillus gasseri, at 5 mg/mL. These results suggest that the antimicrobial effects of Ushercell are selective, and not likely mediated by nonspecific cytotoxic mechanisms. These data provide the basis for further clinical development of Ushercell as a vaginal agent to prevent unplanned pregnancy and STIs.
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