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Modulation of Viscoelasticity and HIV Transport as a Function of pH in a Reversibly Crosslinked Hydrogel
Authors:Julie I Jay  Shetha Shukair  Kristofer Langheinrich  Melissa C Hanson  Gianguido C Cianci  Todd J Johnson  Meredith R Clark  Thomas J Hope  Patrick F Kiser
Affiliation:1. Department of Pharmaceutics and Pharmaceutical Chemistry University of Utah Salt Lake City, UT 84112‐5820 (USA);2. Department of Cell and Molecular Biology, Feinberg School of Medicine Northwestern University Chicago, IL 60611 (USA);3. Department of Bioengineering University of Utah Salt Lake City, UT 84112‐5820 (USA)
Abstract:Materials that respond to physiological stimuli are important in developing advanced biomaterials for modern therapies. The reversibility of covalent crosslinks formed by phenylboronate (PBA) and salicylhydroxamate (SHA) has been exploited to provide a pH‐responsive gel for application to the vaginal tract. Dynamic rheology reveals that the gel frequency‐dependent viscoelastic properties are modulated by pH. At pH 4.8 the viscous component dominates throughout most of the frequency range. As the pH increases, the characteristic relaxation time continues to increase while the GPlateau levels off above pH 6. At pH 7.5, the elastic component dominates throughout the frequency sweep and is predominately independent of frequency. Particle tracking assesses the transport of both fluorescently labeled HIV‐1 and 100‐nm latex particles in the PBA–SHA crosslinked gel as a function of pH. At pH 4.8 the ensemble‐averaged mean squared displacement at lag times greater than three seconds reveals that transport of the HIV‐1 and 100‐nm particles becomes significantly impeded by the matrix, exhibiting diffusion coefficients less than 0.0002 µm2 s?1. This pH‐responsive gel thus displays properties that have the potential to significantly reduce the transport of HIV‐1 to susceptible tissues and thus prevent the first stage of male‐to‐female transmission of HIV‐1.
Keywords:HIV transport inhibition  Microbicides  pH responsive materials  Stimuli‐responsive materials
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