| Literature DB >> 26093158 |
Anthony S Ham1, Sean T Nugent2, Jennifer J Peters3, David F Katz3, Cory M Shelter4, Charlene S Dezzutti5, Ashlee D Boczar2, Karen W Buckheit2, Robert W Buckheit2.
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.Entities:
Keywords: Formulation; HIV prevention; Microbicides; Pyrimidinedione; Rectal gel; Vaginal gel
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Year: 2015 PMID: 26093158 PMCID: PMC4492852 DOI: 10.1016/j.antiviral.2015.06.010
Source DB: PubMed Journal: Antiviral Res ISSN: 0166-3542 Impact factor: 5.970