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Antibiotics (Basel). 2015 Dec;4(4):617-626. doi: 10.3390/antibiotics4040617. Epub 2015 Nov 24.

Pharmacokinetic/Toxicity Properties of the New Anti-Staphylococcal Lead Compound SK-03-92.

Antibiotics (Basel, Switzerland)

William R Schwan, Jill M Kolesar, M Shahjahan Kabir, Edmund J Elder, Jeffrey B Williams, Rachel Minerath, James M Cook, Christopher M Witzigmann, Aaron Monte, Tricia Flaherty

Affiliations

  1. Department of Microbiology, University of Wisconsin-La Crosse, 1725 State St., La Crosse, WI 54601, USA; Emerging Technology Center for Pharmaceutical Development, University of Wisconsin-La Crosse, 1725 State St., La Crosse, WI 54601, USA.
  2. Carbone Comprehensive Cancer Center, University of Wisconsin-Madison, Madison, WI 53706, USA.
  3. Department of Chemistry and Biochemistry, University of Wisconsin-Milwaukee, Milwaukee, WI 53211, USA.
  4. Zeeh Pharmaceutical Experiment Station, University of Wisconsin-Madison, Madison, WI 53705, USA.
  5. Department of Microbiology, University of Wisconsin-La Crosse, 1725 State St., La Crosse, WI 54601, USA.
  6. Emerging Technology Center for Pharmaceutical Development, University of Wisconsin-La Crosse, 1725 State St., La Crosse, WI 54601, USA; Department of Chemistry and Biochemistry, University of Wisconsin-La Crosse, 1725 State St., La Crosse, WI 54601, USA.

PMID: 26877886 PMCID: PMC4748848 DOI: 10.3390/antibiotics4040617

Abstract

Because of the potential of a new anti-staphylococcal lead compound SK-03-92 as a topical antibiotic, a patch, or an orally active drug, we sought to determine its safety profile and oral bioavailability. SK-03-92 had a high IC

Keywords: Staphylococcus; drug formulation; pharmacokinetics; safety testing

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