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

Antiviral Res. 2015 Aug:120:153-64. doi: 10.1016/j.antiviral.2015.06.010. Epub 2015 Jun 17.

Abstract

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.

Keywords: Formulation; HIV prevention; Microbicides; Pyrimidinedione; Rectal gel; Vaginal gel.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Administration, Intravaginal
  • Administration, Rectal
  • Anti-Infective Agents / pharmacology*
  • Chemistry, Pharmaceutical
  • Chemoprevention / methods*
  • Drug Stability
  • Excipients
  • Female
  • Gels / pharmacology*
  • HIV Infections / prevention & control*
  • HIV-1 / drug effects*
  • Humans
  • Pyrimidinones / pharmacology*

Substances

  • Anti-Infective Agents
  • Excipients
  • Gels
  • IQP-0528
  • Pyrimidinones