Literature DB >> 12499038

Magnetic resonance imaging to determine the distribution of a vaginal gel: before, during, and after both simulated and real intercourse.

E Scott Pretorius1, Kelly Timbers, Dan Malamud, Kurt Barnhart.   

Abstract

To provide effective contraception and protection against sexually transmitted disease, vaginal gels should maximally cover the cervical os and the vaginal epithelium before, during and after intercourse. To non-invasively monitor the intravaginal distribution of an applied intravaginal gel, we performed high-resolution magnetic resonance imaging (MRI) of the female pelvis before, during and after both real and simulated sexual intercourse. We sought to determine whether simulated intercourse with a plastic phallus could be used as a surrogate for real intercourse for such experiments. Dilute gadolinium chelate solution was mixed with Gynol-II gel and introduced intravaginally to volunteer female human subjects using a conventional applicator. MRI was performed at 1.5 Tesla with a surface coil. Imaging of the female pelvis was performed: (1) immediately after insertion of the gel; (2) during real intercourse with a male partner (2 subjects) or simulated intercourse with a plastic phallus (4 subjects); and (3) after completion of real or simulated intercourse. Subjects were studied after application of both 3 mL and 5 mL of vaginal gel. Measurements of gel thickness covering the vaginal mucosa were made digitally using electronic calipers. The bolus of gel is initially located in the upper vaginal canal, superior to the urogenital diaphragm. Both real and simulated intercourse dramatically increases the spread of gel to the lower vagina. The cervix appears to be adequately covered with gel both before and after intercourse. Increasing the volume of the gel increases initial vaginal mucosal coverage but also increases leakage from the introitus. No statistically significant differences in vaginal mucosal coverage were found between patients having undergone real vs. simulated intercourse, or on post-intercourse scans of 3 mL versus 5 mL. MRI is a sensitive, reproducible means of tracking the spread of intravaginal medications. Copyright 2002 Elsevier Science Inc.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12499038     DOI: 10.1016/s0010-7824(02)00412-2

Source DB:  PubMed          Journal:  Contraception        ISSN: 0010-7824            Impact factor:   3.375


  9 in total

1.  Distribution of cell-free and cell-associated HIV surrogates in the female genital tract after simulated vaginal intercourse.

Authors:  Nicolette A Louissaint; Edward J Fuchs; Rahul P Bakshi; Sridhar Nimmagadda; Yong Du; Katarzyna J Macura; Karen E King; Richard Wahl; Arthur J Goldsmith; Brian Caffo; Ying Jun Cao; Jean Anderson; Craig W Hendrix
Journal:  J Infect Dis       Date:  2012-01-25       Impact factor: 5.226

2.  Dynamics of HIV neutralization by a microbicide formulation layer: biophysical fundamentals and transport theory.

Authors:  Anthony R Geonnotti; David F Katz
Journal:  Biophys J       Date:  2006-06-30       Impact factor: 4.033

3.  Transport theory for HIV diffusion through in vivo distributions of topical microbicide gels.

Authors:  Bonnie E Lai; Marcus H Henderson; Jennifer J Peters; David K Walmer; David F Katz
Journal:  Biophys J       Date:  2009-11-04       Impact factor: 4.033

4.  The ins and outs of sexual imaging.

Authors:  M Castillo
Journal:  AJNR Am J Neuroradiol       Date:  2014-03-27       Impact factor: 3.825

5.  Optical imaging and analysis of human vaginal coating by drug delivery gels.

Authors:  Marcus H Henderson; Grace M Couchman; David K Walmer; Jennifer J Peters; Derek H Owen; Matthew A Brown; Michael L Lavine; David F Katz
Journal:  Contraception       Date:  2006-10-31       Impact factor: 3.375

6.  A Pilot Study Measuring the Distribution and Permeability of a Vaginal HIV Microbicide Gel Vehicle Using Magnetic Resonance Imaging, Single Photon Emission Computed Tomography/Computed Tomography, and a Radiolabeled Small Molecule.

Authors:  Edward J Fuchs; Jill L Schwartz; David R Friend; Jenell S Coleman; Craig W Hendrix
Journal:  AIDS Res Hum Retroviruses       Date:  2015-08-05       Impact factor: 2.205

7.  An exploratory, randomized, crossover MRI study of microbicide delivery with the SILCS diaphragm compared to a vaginal applicator.

Authors:  Sara Pentlicky; Mark Rosen; Patricia S Coffey; M Kilbourne-Brook; A Shaunik; Courtney A Schreiber; Kurt Barnhart
Journal:  Contraception       Date:  2012-08-13       Impact factor: 3.375

8.  Vaginal microbicides: detecting toxicities in vivo that paradoxically increase pathogen transmission.

Authors:  Richard A Cone; Timothy Hoen; Xixi Wong; Raed Abusuwwa; Deborah J Anderson; Thomas R Moench
Journal:  BMC Infect Dis       Date:  2006-06-01       Impact factor: 3.090

9.  Deducing Mucosal Pharmacokinetics and Pharmacodynamics of the Anti-HIV Molecule Tenofovir from Measurements in Blood.

Authors:  Sachin Govil; David F Katz
Journal:  Sci Rep       Date:  2019-01-14       Impact factor: 4.379

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.