Studies on vaginal malodor. I. Study in humans

Forty-two percent of collagen sponges tested as an intravaginal barrier contraceptive method developed malodor when retained for 5 days. Only 4% developed odor when the sponge was removed within 24 hours after intercourse, rinsed, and reinserted. While sexually active volunteers found odor in 37% of the sponges, odor formed only in 4% of the sponges worn by sexually inactive users. No difference in the rate of odor formation was found when neutral pH (7.0) and acid pH (3.4) collagen sponges were tested, although we believe that a pH 3.4 is too acid and promotes odor formation. The optimal pH of the sponge should be 4.5 to 5.5. Malodor was efficiently extracted from sponges by washing in acid milieu of tap water and vinegar or 0.1 M acetate buffer, pH 4.0. Alkali extraction procedures were ineffective, and lukewarm water was slightly less effective than acid extraction of odor. At the time of malodor development, the high content of polyamines (putrescine, spermine, spermidine) in the ejaculate decreased to undetectable values. We conclude that the ejaculate is the major source of malodor formation in intravaginally worn collagen sponges. Removal, rinsing optimally in vinegar solution, and reinsertion within 24 hours after intercourse reduces the chance of malodor formation.

Medienart:

Artikel

Erscheinungsjahr:

1978

Erschienen:

1978

Enthalten in:

Zur Gesamtaufnahme - volume:52

Enthalten in:

Obstetrics and gynecology - 52(1978), 1 vom: 24. Juli, Seite 88-93

Sprache:

Englisch

Beteiligte Personen:

Chvapil, M [VerfasserIn]
Eskelson, C [VerfasserIn]
Jacobs, S [VerfasserIn]
Chvapil, T [VerfasserIn]
Russell, D H [VerfasserIn]

Themen:

9007-34-5
Barrier Methods--side effects
Biology
Clinical Research
Collagen
Contraception
Contraceptive Methods--side effects
Family Planning
Genitalia
Genitalia, Male
Human Volunteers
Journal Article
Physiology
Polyamines
Research Methodology
Semen
Seminal Vesicles
Urogenital System
Vaginal Barrier Methods--side effects
Vaginal Sponge--side effects

Anmerkungen:

Date Completed 18.10.1978

Date Revised 23.11.2016

published: Print

Citation Status MEDLINE

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM000295051