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The rational design and development of a dual chamber vaginal/rectal microbicide gel formulation for HIV prevention.

Publication ,  Journal Article
Ham, AS; Nugent, ST; Peters, JJ; Katz, DF; Shelter, CM; Dezzutti, CS; Boczar, AD; Buckheit, KW; Buckheit, RW
Published in: Antiviral research
August 2015

The DuoGel™ was developed for safe and effective dual chamber administration of antiretroviral drugs to reduce the high incidence of HIV transmission during receptive vaginal and anal intercourse. The DuoGel™s containing IQP-0528, a non-nucleoside reverse transcriptase inhibitor (NNRTI), were formulated from GRAS excipients approved for vaginal and rectal administration. The DuoGel™s were evaluated based upon quantitative physicochemical and biological evaluations defined by a Target Product Profile (TPP) acceptable for vaginal and rectal application. From the two primary TPP characteristics defined to accommodate safe rectal administration three DuoGel™ formulations (IQB3000, IQB3001, and IQB3002) were developed at pH 6.00 and osmolality ⩽400mmol/kg. The DuoGel™s displayed no in vitro cellular or bacterial toxicity and no loss in viability in ectocervical and colorectal tissue. IQB3000 was removed from consideration due to reduced NNRTI delivery (∼65% reduction) and IQB3001 was removed due to increase spread resulting in leakage. IQB3002 containing IQP-0528 was defined as our lead DuoGel™ formulation, possessing potent activity against HIV-1 (EC50=10nM). Over 12month stability evaluations, IQB3002 maintained formulation stability. This study has identified a lead DuoGel™ formulation that will safely deliver IQP-0528 to prevent sexual HIV-1 transmission in the vagina and rectum.

Duke Scholars

Published In

Antiviral research

DOI

EISSN

1872-9096

ISSN

0166-3542

Publication Date

August 2015

Volume

120

Start / End Page

153 / 164

Related Subject Headings

  • Virology
  • Pyrimidinones
  • Humans
  • HIV-1
  • HIV Infections
  • Gels
  • Female
  • Excipients
  • Drug Stability
  • Chemoprevention
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Ham, A. S., Nugent, S. T., Peters, J. J., Katz, D. F., Shelter, C. M., Dezzutti, C. S., … Buckheit, R. W. (2015). The rational design and development of a dual chamber vaginal/rectal microbicide gel formulation for HIV prevention. Antiviral Research, 120, 153–164. https://doi.org/10.1016/j.antiviral.2015.06.010
Ham, Anthony S., Sean T. Nugent, Jennifer J. Peters, David F. Katz, Cory M. Shelter, Charlene S. Dezzutti, Ashlee D. Boczar, Karen W. Buckheit, and Robert W. Buckheit. “The rational design and development of a dual chamber vaginal/rectal microbicide gel formulation for HIV prevention.Antiviral Research 120 (August 2015): 153–64. https://doi.org/10.1016/j.antiviral.2015.06.010.
Ham AS, Nugent ST, Peters JJ, Katz DF, Shelter CM, Dezzutti CS, et al. The rational design and development of a dual chamber vaginal/rectal microbicide gel formulation for HIV prevention. Antiviral research. 2015 Aug;120:153–64.
Ham, Anthony S., et al. “The rational design and development of a dual chamber vaginal/rectal microbicide gel formulation for HIV prevention.Antiviral Research, vol. 120, Aug. 2015, pp. 153–64. Epmc, doi:10.1016/j.antiviral.2015.06.010.
Ham AS, Nugent ST, Peters JJ, Katz DF, Shelter CM, Dezzutti CS, Boczar AD, Buckheit KW, Buckheit RW. The rational design and development of a dual chamber vaginal/rectal microbicide gel formulation for HIV prevention. Antiviral research. 2015 Aug;120:153–164.
Journal cover image

Published In

Antiviral research

DOI

EISSN

1872-9096

ISSN

0166-3542

Publication Date

August 2015

Volume

120

Start / End Page

153 / 164

Related Subject Headings

  • Virology
  • Pyrimidinones
  • Humans
  • HIV-1
  • HIV Infections
  • Gels
  • Female
  • Excipients
  • Drug Stability
  • Chemoprevention